WO2005120680A1 - An improved two stage pressure swing adsorption process for producing enriched-oxygen - Google Patents

An improved two stage pressure swing adsorption process for producing enriched-oxygen Download PDF

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Publication number
WO2005120680A1
WO2005120680A1 PCT/CN2005/000640 CN2005000640W WO2005120680A1 WO 2005120680 A1 WO2005120680 A1 WO 2005120680A1 CN 2005000640 W CN2005000640 W CN 2005000640W WO 2005120680 A1 WO2005120680 A1 WO 2005120680A1
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Prior art keywords
pressure
stage
adsorption
swing adsorption
pressure swing
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PCT/CN2005/000640
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English (en)
French (fr)
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Yuwen Song
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Chengdu Tianli Chemical Engineering Technology Co Ltd
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Chengdu Tianli Chemical Engineering Technology Co Ltd
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Priority to ES05754843.0T priority Critical patent/ES2519443T3/es
Priority to PL05754843T priority patent/PL1769839T3/pl
Priority to EP05754843.0A priority patent/EP1769839B1/en
Priority to US11/570,415 priority patent/US8128734B2/en
Publication of WO2005120680A1 publication Critical patent/WO2005120680A1/zh
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    • C01B21/00—Nitrogen; Compounds thereof
    • C01B21/04—Purification or separation of nitrogen
    • C01B21/0405—Purification or separation processes
    • C01B21/0433—Physical processing only
    • C01B21/045—Physical processing only by adsorption in solids
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    • B01D53/047—Pressure swing adsorption
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    • B01D53/04—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by adsorption, e.g. preparative gas chromatography with stationary adsorbents
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    • C01B13/00—Oxygen; Ozone; Oxides or hydroxides in general
    • C01B13/02—Preparation of oxygen
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Definitions

  • the invention relates to a method for producing oxygen-enriched from air by using a two-stage pressure swing adsorption technology, in particular to an improved method for producing oxygen-rich air by two-stage pressure swing adsorption.
  • the invention is a further improvement of the two-stage pressure swing adsorption technology for producing oxygen-enriched patented technology from the air (patent publication number: CN1386565A), and also produces concentrated nitrogen, improves the recovery rate of oxygen and nitrogen, and makes the entire oxygen plant Power consumption and investment are further reduced. Disclosure of invention
  • the object of the present invention is to provide an improved two-stage pressure swing adsorption method for oxygen enrichment, which overcomes the above-mentioned problems of the prior art, greatly saves power consumption and investment, and improves the oxygen of the entire device compared with the prior art. Recovery rate.
  • the present invention uses two-stage pressure swing adsorption technology to separate nitrogen and oxygen from the air.
  • the product can be oxygen, nitrogen, or both oxygen and nitrogen.
  • This method uses a two-stage pressure swing adsorption device to operate in series.
  • the first stage A PSA device is used to remove carbon dioxide, water, and some nitrogen and to condense the nitrogen.
  • a PSA device in the second stage is used to further remove nitrogen from the intermediate gas flowing out of the adsorption step of the adsorption tower in the first stage.
  • the adsorption tower of the first stage pressure swing adsorption device undergoes adsorption, displacement P ', vacuum VC, two-stage gas reverse equal pressure boost 2ER, displacement in a cycle.
  • Adsorption process steps are used to remove carbon dioxide
  • the forward pressure equalization and pressure reduction ED process steps are added after the adsorption A process step, and the reverse pressure equalization and pressure reduction BD 'process step is added to the reverse boost ER process steps to increase the pressure.
  • the gas mixture of the ER process step comes from the step-down ED process step.
  • the pressure equalization and pressure reduction 2ED 'process steps at both ends are added after the adsorption A process step, and the pressure equalization boost 2ER' process is added after the two-stage gas reverse pressure equalization pressure boost 2ER process step is completed.
  • the mixed gas at both ends of the pressure-boosting 2ER 'process step comes from the pressure-boosting 2ED' process step.
  • a reverse depressurization BD process step is added after the P 'process step is replaced.
  • the mixed gas released from the second stage pressure swing adsorption device adsorption tower reverse pressure equalization and pressure reduction BD 'process steps Enter the buffer tank VI until the pressure is balanced.
  • the first stage of the PSA adsorption tower is performing the two-stage gas reverse equalizing pressure boost 2ER process step, the adsorption tower and the buffer tank VI communicate until the pressure is balanced.
  • the average concentration of oxygen in the outlet gas of the adsorption step of the adsorption tower of the first stage pressure swing adsorption device is greater than 5 21 ⁇ 80% (V).
  • the average concentration of oxygen in the outlet gas of the adsorption step of the adsorption tower of the first stage pressure swing adsorption device is greater than 21 ⁇ 25% (V).
  • IMPa ( ⁇ ⁇ ).
  • the pressure of the two-stage pressure swing adsorption device adsorption step A is 0. 001 ⁇ 0. IMPa (gauge pressure).
  • the adsorbent charged from the bottom to the top of the pressure swing adsorption device in the first stage is activated alumina and the fractional sieve; the adsorbent filled in the pressure swing adsorption device of the second stage is only a molecular sieve.
  • the number of reverse pressure equalization and pressure reduction ED 'of the adsorption tower of the second stage pressure swing adsorption device and the pressure equalization and pressure increase 2ER of the second stage gas of the pressure absorption tower of the first stage pressure swing adsorption device are greater than or equal to one.
  • the reverse pressure equalization pressure reduction ED 'of the adsorption tower of the second stage pressure swing adsorption device and the reverse pressure equalization pressure increase 2ER of the second stage gas pressure of the adsorption tower of the first pressure swing adsorption device are 3 to 7 times.
  • the invention is used to separate nitrogen and oxygen from the air.
  • the product can be either oxygen or nitrogen.
  • This method uses a two-stage pressure swing adsorption device to operate in series.
  • the first stage pressure swing adsorption device is used to remove carbon dioxide, water and part of the nitrogen and concentrate nitrogen, and the second stage pressure swing adsorption.
  • the device is used to further remove nitrogen in the intermediate gas flowing out of the adsorption step of the adsorption tower of the first stage pressure swing adsorption device, and increase the oxygen to a desired concentration.
  • the adsorption tower of the first stage pressure swing adsorption device is in a 0 cycle.
  • the present invention is used to separate nitrogen and oxygen from air.
  • the product can be oxygen, nitrogen, or both oxygen and nitrogen.
  • This method uses a two-stage pressure swing adsorption device to operate in series. The first stage
  • the PSA device is used to remove carbon dioxide, water and some nitrogen and to condense the nitrogen, and the PSA device in the second stage is used to feed nitrogen from the intermediate gas flowing out of the adsorption step of the adsorption tower in the first stage. 0 in one step and raise the oxygen to the required concentration.
  • the first stage of the adsorption tower of the PSA device undergoes adsorption A, pressure drop 2ED 'at both ends, vacuum VC, and second stage.
  • the first stage of the PSA adsorption tower increases pressure after 2ED 'pressure equalization and pressure reduction at both ends. Step-down BD process steps. Brief description of the drawings
  • FIG. 1 is an operation program table of the process steps of the first stage pressure swing adsorption device of the embodiment.
  • FIG. 2 is a process chart of the process steps of the second stage pressure swing adsorption device of the embodiment.
  • Fig. 3 is a process flowchart of the first embodiment. Best way to implement the invention
  • the raw material gas of the present invention is air, and its typical composition is as follows:
  • the present invention uses two-stage pressure swing adsorption technology to produce oxygen-rich air from the air.
  • This method uses a two-stage pressure swing adsorption device to operate in series.
  • the first stage pressure swing adsorption device is used to remove gaseous water, carbon dioxide and some nitrogen, and the adsorption tower.
  • the average concentration of oxygen in the outlet gas of the adsorption step is 21 ⁇ 80% (V), and the adsorbent filled from bottom to top in the adsorption tower is activated alumina and molecular sieve; the second stage pressure swing adsorption device is used to change the first stage
  • the nitrogen in the intermediate gas flowing out of the adsorption step of the adsorption tower of the pressure adsorption device is further removed, and 5 oxygen is increased to a desired concentration.
  • the adsorbent packed in the adsorption tower is a molecular sieve.
  • Two-stage pressure swing adsorption device adsorption step A pressure is 0. 001 ⁇ 0. IMPa (gauge pressure).
  • Each adsorption tower of the two-stage pressure swing adsorption device sequentially goes through the following steps in a cycle.
  • the first stage pressure swing adsorption device The first stage pressure swing adsorption device:
  • the adsorbent in the adsorption tower selectively adsorbs water, carbon dioxide, and some nitrogen components in the air in sequence, some nitrogen that is not adsorbed, and argon that is not easily adsorbed.
  • the other components flow out from the outlet and enter the second stage pressure swing adsorption device in the adsorption step.
  • the total amount of components such as water, carbon dioxide and some nitrogen adsorbed by the adsorbent continues to increase.
  • the adsorbent saturates the above components, the air intake is stopped, and the adsorption ends at this time. 5 (2) Voltage drop on both ends 2ED '
  • the oxygen concentration in the dead space gas in the adsorption tower is high, and this part of oxygen needs to be recycled.
  • the gas in the adsorption tower is depressurized from the upper and lower ends.
  • the dead space gas enters and exits from the adsorption tower; the outlet is discharged into this stage, and the corresponding adsorption tower that has completed the two-stage gas reverse equalizing pressure boosting 2ER step performs pressure boosting 2ER 'at both ends.
  • the number of pressure drops 2ED 'at both ends can be 1 or more times (such as 1 ⁇ 3 times).
  • the first step of evacuating the gas of the VC step from the adsorption tower is used.
  • the bottom of the reactor enters to replace the remaining oxygen in the tower, and the mixed gas replaced from the adsorption tower enters the corresponding adsorption tower that has completed the two-stage gas reverse equalizing pressure boosting 2ER step or the pressure equalizing pressure boosting 2ER step at both ends.
  • Replacement gas boost R ' is used.
  • this part of the gas is evacuated in the reverse direction from the bottom of the adsorption tower or used as a product.
  • the water, carbon dioxide and nitrogen adsorbed by the adsorbent were evacuated from the bottom of the adsorption tower with a vacuum pump, and the adsorbent was regenerated.
  • the second stage of the pressure swing adsorption device is used to complete the adsorption of the adsorption tower or the pressure is equalized to reduce the pressure.
  • the gas enters the adsorption tower that has completed the evacuation VC step in this stage to increase the pressure of the adsorption tower.
  • the two-stage gas reverse pressure equalization pressure boost 2ER can be 1 or more times (such as 1 ⁇ 7 times).
  • the gas discharged from the pressure equalizing and pressure reducing 2ED 'steps at both ends of the section is used to enter the adsorption tower from the inlet and outlet ends, so that the adsorption tower gradually increases the pressure, and the pressure is increased at both ends.
  • 2ER ' is equal to the number of pressure drops 2ED' at both ends.
  • the step of equalizing pressure boosting 2ER 'at both ends of the adsorption tower in this section is different from the ordinary pressure equalizing pressure increasing ER step.
  • the gas in the ordinary pressure equalizing pressure increasing ER step of the adsorption tower enters from the exit end of the adsorption tower, and The pressure at the two ends of the tower is equalized and pressure-boosted.
  • the 2ER 'step gas enters from the inlet and outlet ends of the adsorption tower.
  • the pressure at the outlet of the adsorption tower at the stage of the replacement P' step is used for pressure boosting.
  • the adsorption tower is used to pressurize the adsorption tower from the top until it reaches the adsorption pressure, and the raw material air can also be used to raise the adsorption tower to the adsorption pressure.
  • the outlet gas of the adsorption tower in the first stage of the PSA device in the adsorption step is sent to the adsorption tower in the second stage of the PSA device in the adsorption step.
  • the adsorbent in the adsorption tower selectively adsorbs nitrogen, which is difficult to adsorb oxygen and argon. Gas and other components are discharged from the outlet into the oxygen-rich buffer tank or the next section. With the passage of time, the total amount of nitrogen adsorbed by the adsorbent increases. When the adsorbed nitrogen is saturated, the intake of gas is stopped. At this time, the adsorption ends, and the oxygen concentration in the outlet gas is controlled at the level required by the product.
  • the dead space gas in the adsorption tower is discharged from the exit of the adsorption tower and enters the corresponding adsorption tower that has completed the step of reverse pressure equalization and pressure reduction BD 'in this section.
  • the pressure in the two towers may be equal or unequal to ensure that the product is rich.
  • the oxygen concentration meets the requirements.
  • the number of times of forward pressure equalization and pressure reduction ED can be 1 time or more (such as 1 ⁇ 3 times).
  • Adsorption or forward pressure equalization and decompression After the ED is completed, the gas in the tower is reversed from the bottom of the adsorption tower to the first stage of the VC which has been evacuated.
  • the second stage gas reverse equalization pressure boost 2ER is directly performed.
  • the number of reverse BDs can be 1 or more times (such as 1 ⁇ 7 times). .
  • the gas in the adsorption tower can also be put in the reverse direction first.
  • a buffer tank and then the gas in the buffer tank is sent to the first stage pressure swing adsorption device to evacuate the adsorption tower after the VC is completed.
  • the gas discharged from the forward pressure equalization and pressure reduction ED step is used to enter the adsorption tower from the outlet end to increase the pressure of the adsorption tower.
  • the source gas in this example is air.
  • the oxygen concentration in the first stage of the PSA device during the adsorption step is controlled to 21 ⁇ 23% (V), and the second stage of the PSA device is in the adsorption step:
  • the oxygen concentration in the gas at the exit of the attached tower is controlled at About 93% (V) (that is, the product is rich in oxygen).
  • a total of four adsorption towers A to D constitute a first stage pressure swing adsorption device.
  • the adsorbent filled from bottom to top in the adsorption tower is activated alumina and molecular sieve in turn.
  • a single-pressure adsorption equalization program is run.
  • the vacuum pump P1 is used to evacuate the adsorption tower by using the vacuum line G15.
  • the second stage pressure swing adsorption device The adsorbent packed in the adsorption tower is a molecular sieve, and a single-pressure adsorption equalization program is run.
  • the above-mentioned two-stage pressure swing adsorption device is operated in series.
  • the first stage pressure swing adsorption device removes gaseous water, carbon dioxide and some nitrogen in the air.
  • the nitrogen in the intermediate gas flowing out of the adsorption step of the adsorption tower of the first stage pressure swing adsorption device is further removed, and the oxygen is increased to a desired concentration.
  • the first and second stage pressure swing adsorption devices can also be combined with more than four adsorption towers.
  • the adsorbent in the adsorption tower selectively adsorbs the gaseous water, carbon dioxide, and some nitrogen components in the air in order. Components such as oxygen and argon are discharged from the outlet into the adsorption tower in the second stage pressure swing adsorption device.
  • the molecular sieve in the adsorption tower selectively adsorbs nitrogen, and components such as oxygen and argon that are not easily adsorbed are discharged from the outlet.
  • Product oxygen-rich buffer tank is provided to produce the outlet.
  • the oxygen concentration in the exit gas of the adsorption tower at the adsorption step is controlled to 21 ⁇ 23% (V), and its adsorption tower undergoes adsorption A, replacement P ', vacuum VC, and The stage gas reverse equal pressure boost 2ER, the replacement gas boost R ', and the final boost FR PSA process steps;
  • the second stage PSA device is in the adsorption tower outlet gas at the adsorption step to control the oxygen concentration at 93% (V ), Its adsorption tower sequentially undergoes the process steps of adsorption A, reverse pressure equalization and pressure reduction BD ′, and finally pressure-increasing FR pressure swing adsorption in a cycle.
  • Tower A has completed the final step-up FR step. Open the program-controlled valves 1A and 2A, and the air enters the adsorption tower A through the pipe Gi l.
  • the adsorbent selectively adsorbs water, carbon dioxide and Some components such as nitrogen, some non-adsorbed nitrogen and difficult-to-adsorb argon flow out from the outlet end and enter the adsorption tower of the second stage pressure swing adsorption device in the adsorption step.
  • the water adsorbed by the adsorbent The total amount of carbon dioxide, some nitrogen and other components is constantly increasing.
  • the adsorbent adsorbs the above components, the intake of gas is stopped. At this time, the adsorption ends, and the program control valves 1A and 2A are closed.
  • the nitrogen concentration in the outlet gas is controlled to 70 ⁇ 78 % (V).
  • the program-controlled valves 6A, 4A, and 4C are opened, and the gas at the outlet of the vacuum pump enters the C tower through the pipelines G 16 and G14 to perform the replacement gas boosting of the C tower (referred to as R ′). , Close the programmed valves 6A, 4A and 4C.
  • the program-controlled valve 5A was closed, and the water, carbon dioxide, and nitrogen adsorbed by the adsorbent were extracted from the bottom of the adsorption tower with a vacuum pump and vented or used as a product, and the adsorbent was regenerated.
  • the program-controlled valves 5a, 4A, and KV8 are opened, and the gas in the second stage of the pressure swing adsorption device adsorption tower a is used to reverse pressure equalize and depressurize BD 'to enter the adsorption tower A to pressurize the adsorption tower A.
  • the program-controlled valves KV6 and 3A are opened, and the -The outlet gas of the adsorption tower in the step is boosted from the top ⁇ A tower.
  • the program control valves KV6 and 3A are closed.
  • the tower a has completed the final step-up FR step, the program-controlled valves la, 2a are opened, and the intermediate mixed gas enters the adsorption tower a through the pipe G21.
  • the first stage pressure swing adsorption device is in the adsorption step of the adsorption.
  • the outlet gas from the tower is sent to the adsorption tower in the second stage pressure swing adsorption device in the adsorption step.
  • the adsorbent in the adsorption tower selectively adsorbs nitrogen, and the components such as oxygen and argon, which are not easily adsorbed, are discharged from the outlet into the oxygen-rich buffer tank. Or the next section.
  • the total amount of nitrogen adsorbed by the adsorbent continues to increase: when the nitrogen adsorbed by the adsorbent is saturated, the air intake is stopped, and the adsorption is completed at this time, and the program-controlled valves are closed.
  • the program-controlled valves 5a, 4A, and KV8 are opened, and the gas in the adsorption tower a is reversely discharged into the adsorption tower A to increase the pressure.
  • the program-controlled valves KV7 and 3a are opened, and the tower a is pressurized from the top using the adsorption tower outlet gas in the adsorption step.
  • the program-controlled valve KV7 is closed. And 3a.
  • Tower A has completed one cycle and can enter the next cycle.
  • the b ⁇ h adsorption tower has the same cycle steps as the a tower, except that the time is staggered with each other, as shown in Figure 2 and Figure 3.
  • the result of this example is that the oxygen concentration is greater than 93% (V), the nitrogen concentration is greater than 99.7% (V), and the oxygen recovery rate is greater than 98.5% (V).
  • Embodiment 2 of the present invention is a diagrammatic representation of Embodiment 2 of the present invention.
  • the source gas in this example is air.
  • the oxygen concentration in the outlet gas of the adsorption tower at the first stage of the pressure swing adsorption device in the adsorption step is controlled to 21 ⁇ 23% (V), and the oxygen concentration in the outlet gas of the adsorption tower at the second step of the pressure swing adsorption device in the adsorption step is controlled at 93 ° /. (V) around (that is, the product is rich in oxygen).
  • a total of 7 adsorption towers A to G constitute the first stage pressure swing adsorption device.
  • the adsorbent filled from bottom to top in the adsorption tower is activated alumina and molecular sieve in turn, and the three-phase adsorption three-pressure equalization program is run; a total of 7 adsorption towers a to g constitute a second-stage pressure swing adsorption device.
  • the adsorbent is a molecular sieve, and a five-column adsorption three-pressure equalization program is run.
  • the above-mentioned two-stage pressure swing adsorption device is operated in series.
  • the first-stage pressure swing adsorption device removes gaseous water, carbon dioxide and some nitrogen in the air, and the second-stage pressure swing adsorption device is used for first-stage pressure swing adsorption.
  • the nitrogen in the intermediate gas flowing out of the adsorption step of the device is further removed, and the oxygen is raised to the desired concentration.
  • the adsorbent in the adsorption tower selectively adsorbs the gaseous water, carbon dioxide, and some nitrogen components in the air in order. Components such as oxygen and argon are discharged from the outlet into the adsorption tower in the second stage pressure swing adsorption device.
  • the molecular sieve in the adsorption tower selectively adsorbs nitrogen, and components such as oxygen and argon that are not easily adsorbed are discharged from the outlet.
  • Product oxygen-rich buffer tank is provided to produce the outlet.
  • the oxygen concentration in the exit gas of the adsorption tower at the adsorption step is controlled to 21 ⁇ 23% (V), and its adsorption tower undergoes adsorption A, replacement P ', vacuum VC, and
  • the third stage gas reverses the third pressure equalization pressure boost 2ER3, the second stage gas reverses the second pressure equalization pressure boost 2ER2, the second stage gas reverses the first pressure equalization pressure boost 2ER1, the replacement gas pressure boost R ', and the final pressure boost FR changes Pressure adsorption process steps;
  • the second stage pressure swing adsorption device is in the adsorption step at the outlet gas of the adsorption tower to control the oxygen concentration at about 93% (V), and its adsorption tower undergoes adsorption A in turn in a cycle in turn.
  • the oxygen concentration is greater than 93% (V)
  • the nitrogen concentration is greater than 99.7% (V)
  • the oxygen recovery rate is greater than 98.5% (V).
  • Embodiment 3 of the present invention is a diagrammatic representation of Embodiment 3 of the present invention.
  • the source gas in this example is air.
  • the oxygen concentration in the outlet gas of the adsorption tower in the first stage of the pressure swing adsorption device in the adsorption step is controlled to 21 ⁇ 23% (V)
  • the oxygen concentration in the outlet gas of the adsorption tower in the second stage of the pressure swing adsorption device in the adsorption step is controlled to 93% (V) around (that is, the product is rich in oxygen).
  • a total of 7 adsorption towers A to G constitute the first stage pressure swing adsorption device.
  • the adsorbent filled from bottom to top in the adsorption tower is activated alumina and molecular sieve in turn, and the three-phase adsorption three-pressure equalization program is run; a total of 7 adsorption towers a to g constitute a second-stage pressure swing adsorption device.
  • the adsorbent is a molecular sieve, and a four-column adsorption three-pressure equalization program is run.
  • the above two-stage pressure swing adsorption device is operated in series.
  • the pressure swing adsorption device removes gaseous water, carbon dioxide and some nitrogen in the air
  • the second pressure swing adsorption device is used to further remove nitrogen in the intermediate gas flowing out of the adsorption step of the first pressure swing adsorption device adsorption tower, and Increase the oxygen to the desired concentration.
  • the adsorbent in the adsorption tower selectively adsorbs the gaseous water, carbon dioxide, and some nitrogen components in the air in order. Components such as oxygen and argon are discharged from the outlet into the adsorption tower in the second stage pressure swing adsorption device.
  • the molecular sieve in the adsorption tower selectively adsorbs nitrogen, and components such as oxygen and argon that are not easily adsorbed are discharged from the outlet.
  • Product oxygen-rich buffer tank is provided to produce the outlet.
  • the oxygen concentration in the exit gas of the first stage of the pressure swing adsorption device in the adsorption step is controlled to 21 ⁇ 23% (V), and its adsorption tower undergoes adsorption A, replacement P ', and vacuum VC in sequence in a cycle;
  • the second stage gas reverses the third equal pressure boost 2ER3, the second stage gas reverses the second equal pressure boost 2ER2, the second stage gas reverses the first equal pressure boost 2ER1, the replacement gas boost R ', and the final boost FR
  • the pressure swing adsorption process is rapid; the second stage pressure swing adsorption device is in the adsorption step, and the oxygen concentration in the outlet gas of the adsorption tower is controlled to about 93% (V), and its adsorption tower sequentially undergoes adsorption A and forward uniformity in a cycle.
  • the result of this example is that the oxygen concentration is greater than 93% (V), the nitrogen concentration is greater than 99.7% (V), and the oxygen recovery rate is greater than 98.5% (V).
  • Embodiment 4 of the present invention is a diagrammatic representation of Embodiment 4 of the present invention.
  • the source gas in this example is air.
  • the oxygen concentration in the outlet gas of the adsorption tower in the first stage of the pressure swing adsorption device in the adsorption step is controlled to 21 ⁇ 23% (V)
  • the oxygen concentration in the outlet gas of the adsorption tower in the second stage of the pressure swing adsorption device in the adsorption step is controlled to 93% (V) around (that is, the product is rich in oxygen).
  • the adsorbent charged from bottom to top in the pressure swing adsorption device of the first stage is activated alumina and molecular sieve in turn.
  • the adsorbent filled in the pressure swing adsorption device of the second stage is molecular sieve.
  • the above-mentioned two-stage pressure swing adsorption device is operated in series.
  • the first-stage pressure swing adsorption device removes gaseous water, carbon dioxide, and part of nitrogen in the air
  • the second-stage pressure swing adsorption device is used for first-stage pressure swing adsorption.
  • the nitrogen in the intermediate gas flowing out of the adsorption step of the device is further removed, and the oxygen is raised to the desired concentration.
  • the air enters the adsorption tower of the first stage pressure swing adsorption device in the adsorption step.
  • the adsorbent in the adsorption tower selectively adsorbs the gaseous water, carbon dioxide, and some nitrogen components in the air in sequence. Part of the nitrogen and components that are not easily adsorbed such as oxygen and argon are discharged from the outlet end into an adsorption tower in the second stage pressure swing adsorption device in the adsorption step.
  • the molecular sieve in the adsorption tower selectively adsorbs nitrogen, difficult to adsorb oxygen and argon, etc. The components are discharged from the outlet end into the product oxygen-rich buffer tank.
  • the oxygen concentration in the exit gas of the adsorption tower of the first stage pressure swing adsorption device in the adsorption step is controlled to 21 ⁇ 23% (V), and its adsorption tower sequentially undergoes adsorption A, replacement P ', and vacuum VC in a cycle;
  • the second stage gas reverses the third equal pressure boost 2ER3, the second stage gas reverses the second equal pressure boost 2ER2, the second stage gas reverses the first equal pressure boost 2ER1, the replacement gas boost R ', and the final boost FR Pressure swing adsorption process steps;
  • the second stage of the pressure swing adsorption device is in the adsorption step at the outlet gas of the adsorption tower to control the oxygen concentration at about 93% (V), and its adsorption tower sequentially undergoes adsorption A in a cycle and reverses the first time
  • the oxygen concentration is greater than 93% (V)
  • the nitrogen concentration is greater than 99.7% (V)
  • the oxygen recovery rate is greater than 98.5% (V).
  • Embodiment 5 of the present invention is a diagrammatic representation of Embodiment 5 of the present invention.
  • the source gas in this example is air.
  • the oxygen concentration in the outlet gas of the adsorption tower at the first stage of the pressure swing adsorption device in the adsorption step is controlled to 21 ⁇ 23% (V)
  • the oxygen concentration in the outlet gas of the adsorption tower at the second stage of the pressure swing adsorption device in the adsorption step is controlled to 93% (V) around (that is, the product is rich in oxygen).
  • the adsorbent charged from bottom to top in the pressure swing adsorption device of the first stage is activated alumina and molecular sieve in turn.
  • the adsorbent filled in the pressure swing adsorption device of the second stage is molecular sieve.
  • the above-mentioned two-stage pressure swing adsorption device is operated in series.
  • the first-stage pressure swing adsorption device removes gaseous water, carbon dioxide, and part of nitrogen in the air
  • the second-stage pressure swing adsorption device is used for first-stage pressure swing adsorption.
  • the nitrogen in the intermediate gas flowing out of the adsorption step of the device is further removed, and the oxygen is raised to the desired concentration.
  • the adsorbent in the adsorption tower selectively adsorbs the gaseous water, carbon dioxide, and some nitrogen components in the air in order. Components such as oxygen and argon are discharged from the outlet into the adsorption tower in the second stage pressure swing adsorption device.
  • the molecular sieve in the adsorption tower selectively adsorbs nitrogen, and components such as oxygen and argon that are not easily adsorbed are discharged from the outlet.
  • Product oxygen-rich buffer tank is provided to produce the outlet.
  • the oxygen concentration in the exit gas of the adsorption tower at the first stage of the pressure swing adsorption device in the adsorption step is controlled to 21 ⁇ 23% (V), and its adsorption tower sequentially undergoes adsorption A, replacement P ', and vacuum VC in a cycle;
  • the second stage gas reverses the third equalizing pressure boost 2ER3, the second stage gas reverses the second equalizing pressure boost 2ER2, the second stage gas reverses the first equalizing pressure boost 2ER1, Replacement gas boost R ', final boost FR PSA process steps;
  • the second stage PSA device is in the adsorption tower outlet gas at the adsorption step to control the oxygen concentration at about 93% (V), and its adsorption tower is in a cycle In the cycle, it experiences adsorption A, forward equalizing pressure drop ED, reverse first pressure equalizing pressure drop BID-, reverse second pressure equalizing pressure drop B2D ', reverse third pressure equalizing pressure drop B3D', reverse equalizing pressure Step-up ER
  • the oxygen concentration is greater than 93% (V)
  • the nitrogen concentration is greater than 99.7% (V)
  • the oxygen recovery rate is greater than 98.5% (V).
  • Embodiment 6 of the present invention is a diagrammatic representation of Embodiment 6 of the present invention.
  • the source gas in this example is air.
  • the oxygen concentration in the outlet gas of the adsorption tower at the first stage of the pressure swing adsorption device in the adsorption step is controlled to 21 ⁇ 23% (V)
  • the oxygen concentration in the outlet gas of the adsorption tower at the second stage of the pressure swing adsorption device in the adsorption step is controlled to 93% (V) around (that is, the product is rich in oxygen).
  • the adsorbent charged from bottom to top in the pressure swing adsorption device of the first stage is activated alumina and molecular sieve in turn.
  • the adsorbent filled in the pressure swing adsorption device of the second stage is molecular sieve.
  • the above-mentioned two-stage pressure swing adsorption device is operated in series.
  • the first-stage pressure swing adsorption device removes gaseous water, carbon dioxide, and part of nitrogen in the air
  • the second-stage pressure swing adsorption device is used for first-stage pressure swing adsorption.
  • the nitrogen in the intermediate gas flowing out of the adsorption step of the device is further removed, and the oxygen is raised to the desired concentration.
  • the adsorbent in the adsorption tower selectively adsorbs the gaseous water, carbon dioxide, and some nitrogen components in the air in order. Components such as oxygen and argon are discharged from the outlet into the adsorption tower in the second stage pressure swing adsorption device.
  • the molecular sieve in the adsorption tower selectively adsorbs nitrogen, and components such as oxygen and argon that are not easily adsorbed are discharged from the outlet.
  • Product oxygen-rich buffer tank is provided to produce the outlet.
  • the oxygen concentration in the exit gas of the adsorption tower in the adsorption step is controlled to 21 ⁇ 23% (V), and its adsorption tower sequentially undergoes adsorption A, pressure equalization and pressure drop 2ED ', Replacement of P ', vacuum VC, second stage gas reverse pressure equalizing pressure boost 2ER3, second stage gas reverse pressure equalizing pressure boost 2ER2, second stage gas reverse pressure equalizing pressure boost 2ER1, pressure equalization at both ends Step-up 2ER ', replacement gas step-up R', final step-up FR PSA process steps; the second stage PSA device is in the adsorption tower outlet gas at the adsorption step to control the oxygen concentration at about 93% (V), which In one cycle, the adsorption tower undergoes adsorption A in sequence, the first reverse pressure equalization pressure drop BiD ', the second reverse pressure equalization pressure drop B2D', the third reverse pressure equalization pressure drop B3D ', and the final boost
  • Embodiment 7 of the present invention is a diagrammatic representation of Embodiment 7 of the present invention.
  • the source gas in this example is air.
  • the oxygen concentration in the gas at the exit of the adsorption tower in the first stage of the PSA device during the adsorption step is controlled to 21 ⁇ 23% (V)
  • the oxygen concentration in the gas at the exit of the adsorption tower in the second stage of the PSA device during the adsorption step is controlled to 93% (V) (that is, the product is rich in oxygen).
  • the adsorbent charged from bottom to top in the pressure swing adsorption device of the first stage is activated alumina and molecular sieve in turn.
  • the adsorbent filled in the pressure swing adsorption device of the second stage is molecular sieve.
  • the above-mentioned two-stage pressure swing adsorption device is operated in series.
  • the first-stage pressure swing adsorption device removes gaseous water, carbon dioxide, and part of nitrogen in the air
  • the second-stage pressure swing adsorption device is used for first-stage pressure swing adsorption.
  • the nitrogen in the intermediate gas flowing out of the adsorption step of the device is further removed, and the oxygen is raised to the desired concentration.
  • the adsorbent in the adsorption tower selectively adsorbs the gaseous water, carbon dioxide, and some nitrogen components in the air in order. Components such as oxygen and argon are discharged from the outlet into the adsorption tower in the second stage pressure swing adsorption device.
  • the molecular sieve in the adsorption tower selectively adsorbs nitrogen, and components such as oxygen and argon that are not easily adsorbed are discharged from the outlet.
  • Product oxygen-rich buffer tank is provided to produce the outlet.
  • the oxygen concentration in the gas at the exit of the adsorption tower at the adsorption step is controlled to 21 ⁇ 23% (V), and its adsorption tower undergoes adsorption A, pressure equalization and pressure drop 2ED ', Replace P ', reverse BD, vacuum VC, second stage gas reverse pressure equalization pressure boost 2ER3, second stage gas reverse pressure equalization pressure boost 2ER2, second stage gas reverse pressure equalization pressure boost 2ER1, pressure equalization boost at both ends 2ER ', replacement gas boost R', and final pressure boost FR PSA process steps;
  • the second stage PSA device is in the adsorption tower outlet gas at the adsorption step to control the oxygen concentration at About 93% (V), the adsorption tower in this cycle undergoes adsorption A, reverse first pressure equalization pressure drop BID ', reverse second pressure equalization pressure drop B2D', and reverse third pressure equalization pressure B3D ', the final step-up FR pressure swing ad
  • the result of this example is that the oxygen concentration is greater than 93% (V), the nitrogen concentration is greater than 99.7% (V), and the oxygen recovery rate is greater than 98.5% (V).
  • Embodiment 8 of the present invention is a diagrammatic representation of Embodiment 8 of the present invention.
  • the source gas in this example is air.
  • the oxygen concentration in the outlet gas of the adsorption tower at the first stage of the pressure swing adsorption device is controlled at 21 ⁇ 23% (V), and the pressure swing adsorption device at the second stage is at the adsorption step.
  • the oxygen concentration in the exit gas of the tower is controlled at about 93% (V) (that is, the product is rich in oxygen).
  • the adsorbent charged from bottom to top in the pressure swing adsorption device of the first stage is activated alumina and molecular sieve in turn.
  • the adsorbent filled in the pressure swing adsorption device of the second stage is molecular sieve.
  • the above-mentioned two-stage pressure swing adsorption device is operated in series.
  • the first-stage pressure swing adsorption device removes gaseous water, carbon dioxide, and part of nitrogen in the air
  • the second-stage pressure swing adsorption device is used for first-stage pressure swing adsorption.
  • the nitrogen in the intermediate gas flowing out of the adsorption step of the device is further removed, and the oxygen is raised to the desired concentration.
  • the adsorbent in the adsorption tower selectively adsorbs the gaseous water, carbon dioxide, and some nitrogen components in the air in order. Components such as oxygen and argon are discharged from the outlet into the adsorption tower in the second stage pressure swing adsorption device.
  • the molecular sieve in the adsorption tower selectively adsorbs nitrogen, and components such as oxygen and argon that are not easily adsorbed are discharged from the outlet.
  • Product oxygen-rich buffer tank is provided to produce the outlet.
  • the oxygen concentration in the gas at the exit of the adsorption tower at the adsorption step is controlled to 21 ⁇ 23% (V), and its adsorption tower undergoes adsorption A, pressure equalization and pressure drop 2ED ', Replacement P ', vacuum VC, second stage gas reverse pressure equalizing pressure boost 2ER3, second stage gas reverse pressure equalizing pressure boost 2ER2, second stage gas reverse pressure equalizing pressure boost 2ER1, both ends are equal Pressure boost 2ER ', replacement gas boost R', and final boost FR PSA process steps;
  • the second stage PSA device is in the adsorption tower outlet gas at the adsorption step to control the oxygen concentration at about 93% (V), Its adsorption tower undergoes adsorption A, forward equalizing pressure drop ED, reverse first pressure equalizing pressure drop BID ', reverse second pressure equalizing pressure drop B2D', and reverse third pressure equalizing pressure in a cycle.
  • the result of this example is that the oxygen concentration is greater than 93% (V), the nitrogen concentration is greater than 99.7% (V), and the oxygen recovery rate is greater than 98.5% (V).
  • the source gas in this example is air.
  • the oxygen concentration in the gas at the exit of the adsorption tower in the first stage of the PSA device during the adsorption step is controlled at 21 ⁇ 23% (V)
  • the oxygen concentration in the gas at the exit of the adsorption tower in the second stage of the PSA device during the adsorption step is controlled at 93% (V) around (that is, the product is rich in oxygen).
  • the adsorbent charged from bottom to top in the pressure swing adsorption device of the first stage is activated alumina and molecular sieve in turn.
  • the adsorbent filled in the pressure swing adsorption device of the second stage is molecular sieve.
  • the above-mentioned two-stage pressure swing adsorption device is operated in series.
  • the first-stage pressure swing adsorption device removes gaseous water, carbon dioxide, and part of nitrogen in the air
  • the second-stage pressure swing adsorption device is used for first-stage pressure swing adsorption.
  • the nitrogen in the intermediate gas flowing out of the adsorption step of the device is further removed, and the oxygen is raised to the desired concentration.
  • the adsorbent in the adsorption tower selectively adsorbs the gaseous water, carbon dioxide, and some nitrogen components in the air in order. Components such as oxygen and argon are discharged from the outlet into the adsorption tower in the second stage pressure swing adsorption device.
  • the molecular sieve in the adsorption tower selectively adsorbs nitrogen, and components such as oxygen and argon that are not easily adsorbed are discharged from the outlet.
  • Product oxygen-rich buffer tank is provided to produce the outlet.
  • the oxygen concentration in the gas at the exit of the adsorption tower at the adsorption step is controlled to 21 ⁇ 23% (V), and its adsorption tower undergoes adsorption A, pressure equalization and pressure drop 2ED ', Replace P ', reverse BD, vacuum VC, second stage gas reverse pressure equalization pressure boost 2ER3, second stage gas reverse pressure equalization pressure boost 2ER2, second stage gas reverse pressure equalization pressure boost 2ER1, equal pressure boost at both ends 2ER ', replacement gas boost R', final boost FR PSA process steps;
  • the second stage PSA device is in the adsorption tower outlet gas at the adsorption step to control the oxygen concentration at 93% (V), in a cycle, its adsorption tower sequentially undergoes adsorption A, forward equalizing pressure drop ED, reverse first pressure equalizing pressure drop BID ', reverse second pressure equalizing pressure drop B2D', reverse Three pressure equalization and pressure reduction B3D ', reverse equalization
  • the result of this example is that the oxygen concentration is greater than 93% (V), the nitrogen concentration is greater than 99.7% (V), and the oxygen recovery rate is greater than 98.5% (V).
  • Embodiment 10 of the present invention is a diagrammatic representation of Embodiment 10 of the present invention.
  • the source gas in this example is air.
  • the oxygen concentration in the outlet gas of the adsorption tower at the first stage of the pressure swing adsorption device in the adsorption step is controlled to 21 ⁇ 23% (V)
  • the oxygen concentration in the outlet gas of the adsorption tower at the second stage of the pressure swing adsorption device in the adsorption step is controlled to 93% (V) around (that is, the product is rich in oxygen).
  • the adsorbent charged from bottom to top in the adsorption tower of the first stage pressure swing adsorption device is activated alumina and molecular sieve.
  • the adsorbent packed in the adsorption tower of the second stage pressure swing adsorption device is Molecular sieve.
  • This embodiment will The above-mentioned two-stage pressure swing adsorption device is operated in series.
  • the first-stage pressure swing adsorption device removes gaseous water, carbon dioxide and some nitrogen in the air
  • the second-stage pressure swing adsorption device is used to adsorb the first-stage pressure swing adsorption device adsorption tower.
  • the nitrogen in the intermediate gas flowing out of the step is further removed, and the oxygen is raised to the desired concentration.
  • the adsorbent in the adsorption tower selectively adsorbs the gaseous water, carbon dioxide, and some nitrogen components in the air in order. Components such as oxygen and argon are discharged from the outlet into the adsorption tower in the second stage pressure swing adsorption device.
  • the molecular sieve in the adsorption tower selectively adsorbs nitrogen, and components such as oxygen and argon that are not easily adsorbed are discharged from the outlet.
  • Product oxygen-rich buffer tank is provided to produce the outlet.
  • the oxygen concentration in the exit gas of the adsorption tower in the adsorption step is controlled to 2 to 23% (V), and its adsorption tower sequentially undergoes adsorption A, pressure equalization pressure drop 2ED ', Replace P ', reverse BD, vacuum VC, second stage gas reverse pressure equalization pressure boost 2ER3, second stage gas reverse pressure equalization pressure boost 2ER2, second stage gas reverse pressure equalization pressure boost 2ER1, equal pressure boost at both ends 2ER ', replacement gas boost R', final boost FR PSA process step;
  • the second stage PSA device is in the adsorption tower outlet gas at the adsorption step to control the oxygen concentration at 93 % (V), its adsorption tower in a cycle in turn undergoes adsorption A, forward equalizing pressure drop ED, reverse first pressure equalizing pressure drop BID ', reverse second pressure equalizing pressure drop B2D', reverse The third pressure equalization and pressure reduction B3D ', the reverse pressure
  • the result of this embodiment is that the oxygen concentration is greater than 93% (V) and the nitrogen concentration is greater than 99.9 ° /. (V), oxygen recovery rate is greater than 99% (V).
  • Embodiment 11 of the present invention is a diagrammatic representation of Embodiment 11 of the present invention.
  • the source gas in this example is air.
  • the oxygen concentration in the first stage of the pressure swing adsorption device in the adsorption tower outlet gas is controlled at 21 ⁇ 23% (V)
  • the oxygen concentration in the second stage of the pressure swing adsorption device in the adsorption tower outlet gas is controlled at 93. % (V) (that is, the product is rich in oxygen).
  • the adsorbent charged from bottom to top in the pressure swing adsorption device of the first stage is activated alumina and molecular sieve in turn.
  • the adsorbent filled in the pressure swing adsorption device of the second stage is molecular sieve.
  • the above-mentioned two-stage pressure swing adsorption device is operated in series.
  • the first-stage pressure swing adsorption device removes gaseous water, carbon dioxide, and part of nitrogen in the air
  • the second-stage pressure swing adsorption device is used for first-stage pressure swing adsorption.
  • the nitrogen in the intermediate gas flowing out of the adsorption step of the device is further removed, and the oxygen is raised to the desired concentration.
  • the agent selectively adsorbs components such as gaseous water, carbon dioxide, and some nitrogen in the air in sequence. Unadsorbed nitrogen and difficult-to-adsorb oxygen and argon components are discharged from the outlet into the second stage pressure swing adsorption device in the adsorption step.
  • the molecular sieve in the adsorption tower selectively adsorbs nitrogen, and the components such as oxygen and argon which are not easily adsorbed are discharged from the outlet end into the product oxygen-rich buffer tank.
  • the oxygen concentration in the gas at the exit of the adsorption tower at the adsorption step is controlled to 21 ⁇ 23% (V), and its adsorption tower undergoes adsorption A and pressure equalization and pressure reduction at both ends for the first time in a cycle.
  • the second stage PSA device is in the oxygen at the outlet of the adsorption tower in the adsorption step The concentration is controlled at about 93% (V), and its adsorption tower undergoes adsorption A, the first equalizing pressure drop E1D, the second equalizing pressure drop E2D, and the third time in a cycle.
  • Equalizing pressure reduction E3D Reverse pressure equalizing pressure reduction B1D ', Reverse pressure equalizing pressure reduction B2D', Reverse pressure equalizing pressure reduction B3D ', The third equalization rising E3R, second equalization rising reverse E2R, first equalization rising reverse E1R, final boosting FR pressure swing adsorption process steps.
  • the result of this example is that the oxygen concentration is greater than 93% (V), the nitrogen concentration is greater than 99.9% (V), and the oxygen recovery rate is greater than 99% (V).
  • Embodiment 12 of the present invention is a diagrammatic representation of Embodiment 12 of the present invention.
  • the source gas in this example is air.
  • the oxygen concentration in the outlet gas of the adsorption tower at the first stage of the pressure swing adsorption device in the adsorption step is controlled to 21 ⁇ 23% (V)
  • the oxygen concentration in the outlet gas of the adsorption tower at the second stage of the pressure swing adsorption device in the adsorption step is controlled to 93% (V) around (that is, the product is rich in oxygen).
  • the adsorbent charged from bottom to top in the pressure swing adsorption device of the first stage is activated alumina and molecular sieve in turn.
  • the adsorbent filled in the pressure swing adsorption device of the second stage is molecular sieve.
  • the above-mentioned two-stage pressure swing adsorption device is operated in series.
  • the first-stage pressure swing adsorption device removes gaseous water, carbon dioxide, and part of nitrogen in the air
  • the second-stage pressure swing adsorption device is used for first-stage pressure swing adsorption.
  • the nitrogen in the intermediate gas flowing out of the adsorption step of the device is further removed, and the oxygen is raised to the desired concentration.
  • the adsorbent in the adsorption tower selectively adsorbs the gaseous water, carbon dioxide, and some nitrogen components in the air in sequence. Part of the nitrogen and components that are not easily adsorbed such as oxygen and argon are discharged from the outlet end into an adsorption tower in the second stage pressure swing adsorption device in the adsorption step.
  • the molecular sieve in the adsorption tower selectively adsorbs nitrogen, difficult to adsorb oxygen and argon, etc. The components are discharged from the outlet end into the product with oxygen-rich buffering.
  • the concentration of oxygen in the exit gas of the adsorption tower in the adsorption step is controlled to 21 ⁇ 23% (V), and its adsorption tower sequentially undergoes adsorption A in one cycle, and the pressure at both ends is reduced by 2ED ', Replace P ', reverse BD, vacuum VC, second stage gas reverse pressure equalization pressure boost 2ER3, second stage gas reverse pressure equalization pressure boost 2ER2, second stage gas reverse pressure equalization pressure boost 2ER1, equal pressure boost at both ends 2ER ', replacement gas boost R', final boost FR 'PSA process steps; the second stage PSA device is in the adsorption tower outlet gas at the adsorption step to control the oxygen concentration at 93 % (V), in a cycle, the adsorption tower in turn undergoes adsorption A, the first pressure equalization pressure drop E1D, the second pressure equalization pressure drop E2D, and the third pressure equalization pressure drop.
  • the result of this example is that the oxygen concentration is greater than 93% (V), the nitrogen concentration is greater than 99.9% (V), and the oxygen recovery rate is greater than 99% (V).
  • the source gas in this example is air.
  • the oxygen concentration in the gas at the exit of the adsorption tower in the first stage of the PSA device during the adsorption step is controlled to 21 ⁇ 23% (V)
  • the oxygen concentration in the gas at the exit of the adsorption tower in the second stage of the PSA device during the adsorption step is controlled to 93% (V) around (that is, the product is rich in oxygen).
  • the adsorbent charged from bottom to top in the pressure swing adsorption device of the first stage is activated alumina and molecular sieve in turn.
  • the adsorbent filled in the pressure swing adsorption device of the second stage is molecular sieve.
  • the above-mentioned two-stage pressure swing adsorption device is operated in series.
  • the first-stage pressure swing adsorption device removes gaseous water, carbon dioxide, and part of nitrogen in the air
  • the second-stage pressure swing adsorption device is used for first-stage pressure swing adsorption.
  • the nitrogen in the intermediate gas flowing out of the adsorption step of the device is further removed, and the oxygen is raised to the desired concentration.
  • the adsorbent in the adsorption tower selectively adsorbs the gaseous water, carbon dioxide, and some nitrogen components in the air in order. Components such as oxygen and argon are discharged from the outlet into the adsorption tower in the second stage pressure swing adsorption device.
  • the molecular sieve in the adsorption tower selectively adsorbs nitrogen, and components such as oxygen and argon that are not easily adsorbed are discharged from the outlet.
  • Product oxygen-rich buffer tank is provided to produce the outlet.
  • the first stage pressure swing adsorption device is The oxygen concentration in the exit gas of the adsorption tower in the adsorption step is controlled at 21 ⁇ 23% (V), and its adsorption tower undergoes adsorption A, replacement P ', and vacuum VC in sequence in a cycle; the second stage gas is reversed for the third time.
  • the oxygen concentration in the gas at the exit of the adsorption tower at the adsorption step is controlled to about 93% (V), and its adsorption tower sequentially undergoes adsorption A, reverse first pressure equalization and pressure reduction BID ', reverse in a cycle.
  • the second pressure equalization and pressure reduction B2D ', the reverse third pressure equalization and pressure reduction B3D', the final step-up FR pressure swing adsorption process step, and the second stage pressure swing adsorption device reverses the first pressure equalization pressure reduction BID '.
  • the gas in buffer tank VI is used for pressure equalization, and then the gas in buffer tank VI is used for pressure equilibrium with the adsorption tower of the first stage pressure swing adsorption device to reverse the first pressure equalization pressure increase 2ER1 adsorption tower; the pressure swing adsorption in the second stage The adsorption tower of the device reverses the second pressure equalization and pressure reduction B2D 'gas into the buffer tank
  • the pressure is balanced in V2, and then the gas in the buffer tank V2 is used to reverse pressure with the adsorption tower of the first stage pressure swing adsorption device for the second pressure equalization and the pressure tower of 2ER2 is pressure-balanced.
  • the gas of the second pressure equalization and pressure reduction B3D ' is put into the buffer tank V3 for pressure equalization, and then the gas in the buffer tank V3 is used to reverse the pressure of the first pressure swing adsorption device adsorption tower and the third pressure equalization pressure 2ER3 adsorption tower for pressure balance .
  • the oxygen concentration is greater than 93% (V)
  • the nitrogen concentration is greater than 99.7% (V)
  • the oxygen recovery rate is greater than 98.5% (V).
  • Embodiment 14 of the invention is a diagrammatic representation of Embodiment 14 of the invention.
  • the source gas in this example is air.
  • the oxygen concentration in the outlet gas of the adsorption tower at the first stage of the pressure swing adsorption device in the adsorption step is controlled to 21 ⁇ 23% (V)
  • the oxygen concentration in the outlet gas of the adsorption tower at the second stage of the pressure swing adsorption device in the adsorption step is controlled to 93% (V) around (that is, the product is rich in oxygen).
  • the adsorbent charged from bottom to top in the pressure swing adsorption device of the first stage is activated alumina and molecular sieve in turn.
  • the adsorbent filled in the pressure swing adsorption device of the second stage is molecular sieve.
  • the above-mentioned two-stage pressure swing adsorption device is operated in series.
  • the first-stage pressure swing adsorption device removes gaseous water, carbon dioxide, and part of nitrogen in the air
  • the second-stage pressure swing adsorption device is used for first-stage pressure swing adsorption.
  • the nitrogen in the intermediate gas flowing out of the adsorption step of the device is further removed, and the oxygen is raised to the desired concentration.
  • the adsorbent in the adsorption tower selectively adsorbs the gaseous water, carbon dioxide, and some nitrogen components in the air in order. Components such as oxygen and argon are discharged from the outlet end into the second stage pressure swing adsorption device
  • the molecular sieve in the adsorption tower selectively adsorbs nitrogen, and difficult-to-adsorb oxygen and argon components are discharged from the outlet end into the product oxygen-rich buffer tank.
  • the oxygen concentration in the exit gas of the adsorption tower at the adsorption step is controlled to 21 ⁇ 23% (V), and its adsorption tower undergoes adsorption A, replacement P ', vacuum VC, and
  • the third stage gas reverses the third pressure equalization pressure boost 2ER3, the second stage gas reverses the second pressure equalization pressure boost 2ER2, the second stage gas reverses the first pressure equalization pressure boost 2ER1, the replacement gas pressure boost R ', and the final pressure boost FR changes Pressure adsorption process steps;
  • the second stage pressure swing adsorption device is in the adsorption step and the oxygen concentration in the outlet gas of the adsorption tower is controlled at about 93% (V), and its adsorption tower undergoes adsorption A and forward pressure drop in a cycle.
  • the second stage pressure swing adsorption device adsorption tower reverses the first pressure equalization and pressure reduction BID 'gas into the buffer tank VI for pressure equalization, and then uses the gas in the buffer tank VI and the first stage pressure swing adsorption device adsorption tower Reverse the first pressure equalization pressure boost 2ER1 adsorption tower for pressure balance; the second stage transforms the pressure The gas from the adsorption tower of the adsorption device reversed the second pressure equalization and pressure reduction B2D 'and put it into the buffer tank V2 for pressure equalization, and then the gas of the buffer tank V2 was used to reverse the pressure equalization and pressure increase of the adsorption tower of the first stage of the pressure swing adsorption device.
  • 2ER2 adsorption tower is pressure balanced; the second stage pressure swing adsorption device reverses the third pressure equalizing pressure drop B3D 'gas into buffer tank V3 for pressure equalization, and then uses the gas in buffer tank V3 to change with the first stage
  • the adsorption tower of the pressure adsorption device reverses the pressure of the third pressure equalization 2ER3 adsorption tower for pressure equilibrium.
  • the result of this example is that the oxygen concentration is greater than 93% (V), the nitrogen concentration is greater than 99.7% (V), and the oxygen recovery rate is greater than 98.5% (V).
  • Embodiment 15 of the present invention is a diagrammatic representation of Embodiment 15 of the present invention.
  • the source gas in this example is air.
  • the oxygen concentration in the gas at the exit of the adsorption tower in the first stage of the PSA device during the adsorption step is controlled at 21 ⁇ 23% (V)
  • the oxygen concentration in the gas at the exit of the adsorption tower in the second stage of the PSA device during the adsorption step is controlled at 93% (V) (that is, the product is rich in oxygen).
  • the adsorbent charged from bottom to top in the pressure swing adsorption device of the first stage is activated alumina and molecular sieve in turn.
  • the adsorbent filled in the pressure swing adsorption device of the second stage is molecular sieve.
  • the above-mentioned two-stage pressure swing adsorption device is operated in series.
  • the first-stage pressure swing adsorption device removes gaseous water, carbon dioxide, and part of nitrogen in the air
  • the second-stage pressure swing adsorption device is used for first-stage pressure swing adsorption.
  • the nitrogen in the intermediate gas flowing out of the adsorption step of the device is further removed, and the oxygen is raised to the desired concentration.
  • the agent selectively adsorbs components such as gaseous water, carbon dioxide, and some nitrogen in the air in sequence. Unadsorbed nitrogen and difficult-to-adsorb oxygen and argon components are discharged from the outlet into the second stage pressure swing adsorption device in the adsorption step.
  • the molecular sieve in the adsorption tower selectively adsorbs nitrogen, and the components such as oxygen and argon which are not easily adsorbed are discharged from the outlet end into the product oxygen-rich buffer tank.
  • the oxygen concentration in the exit gas of the adsorption tower in the adsorption step is controlled to 21 ⁇ 23% (V), and its adsorption tower sequentially undergoes adsorption A, pressure equalization and pressure drop 2ED ', Replacement P ', vacuum VC, second stage gas reverse pressure equalizing pressure boost 2ER3, second stage gas reverse pressure equalizing pressure boost 2ER2, second stage gas reverse pressure equalizing pressure boost 2ER1, both ends are equal Pressure boost 2ER ', replacement gas boost R', and final boost FR PSA process steps;
  • the second stage PSA device is in the adsorption tower outlet gas at the adsorption step to control the oxygen concentration at about 93% (V), Its adsorption tower sequentially undergoes adsorption A in one cycle, reverse first pressure equalization pressure drop B1D ', reverse second pressure equalization pressure drop B2D', reverse third pressure equalization pressure drop B3D ', and finally boost FR Pressure swing adsorption process steps.
  • the second stage of the pressure swing adsorption device reverses the pressure of the first pressure equalization and pressure drop BID 'into the buffer tank VI for pressure equalization, and then uses the gas in the buffer tank VI with the first stage of pressure swing adsorption.
  • the adsorption tower of the device reverses the pressure of the first pressure equalization 2ER1 adsorption tower for pressure balancing;
  • the second The pressure of the pressure swing adsorption device adsorption tower reverses the second pressure equalization and pressure drop B2D 'gas into the buffer tank V2 for pressure equalization, and then the gas in the buffer tank V2 and the first stage pressure swing adsorption device adsorption tower reverse the second pressure equalization
  • the pressure tower of 2ER2 boosts pressure balance;
  • the second stage of the pressure swing adsorption device reverses the pressure of the third pressure equalization and pressure drop B3D 'into buffer tank V3 for pressure equalization, and then uses the gas in buffer tank V3 and the first The stage pressure swing adsorption
  • the result of this embodiment is that the oxygen concentration is greater than 93% (V), the nitrogen concentration is greater than 99.7% (V), and the oxygen recovery rate is greater than 98.5 ° /. (V).
  • Embodiment 16 of the present invention is a diagrammatic representation of Embodiment 16 of the present invention.
  • the source gas in this example is air.
  • the oxygen concentration in the outlet gas of the adsorption tower at the first stage of the pressure swing adsorption device in the adsorption step is controlled to 21 ⁇ 23% (V)
  • the oxygen concentration in the outlet gas of the adsorption tower at the second stage of the pressure swing adsorption device in the adsorption step is controlled to 93% (V) around (that is, the product is rich in oxygen).
  • the adsorbent charged from bottom to top in the pressure swing adsorption device of the first stage is activated alumina and molecular sieve in turn.
  • the adsorbent filled in the pressure swing adsorption device of the second stage is molecular sieve.
  • the above-mentioned two-stage pressure swing adsorption device is operated in series.
  • the first-stage pressure swing adsorption device removes gaseous water, carbon dioxide, and part of nitrogen in the air
  • the second-stage pressure swing adsorption device is used for first-stage pressure swing adsorption.
  • Device adsorption The nitrogen in the intermediate gas flowing out of the column adsorption step is further removed and the oxygen is raised to the desired concentration.
  • the adsorbent in the adsorption tower selectively adsorbs the gaseous water, carbon dioxide, and some nitrogen components in the air in order. Components such as oxygen and argon are discharged from the outlet into the adsorption tower in the second stage pressure swing adsorption device.
  • the molecular sieve in the adsorption tower selectively adsorbs nitrogen, and components such as oxygen and argon that are not easily adsorbed are discharged from the outlet.
  • Product oxygen-rich buffer tank is provided to produce the outlet.
  • the oxygen concentration in the exit gas of the adsorption tower in the adsorption step is controlled to 21 ⁇ 23% (V), and its adsorption tower sequentially undergoes adsorption A, pressure equalization and pressure drop 2ED ', Replacement P ', vacuum VC, second stage gas reverse pressure equalizing pressure boost 2ER3, second stage gas reverse pressure equalizing pressure boost 2ER2, second stage gas reverse pressure equalizing pressure boost 2ER1, both ends are equal Pressure boost 2ER ', replacement gas boost R', and final boost FR pressure swing adsorption process steps; the second stage pressure swing adsorption device is in the adsorption tower outlet gas in which the oxygen concentration is controlled at about 93% (V), Its adsorption tower undergoes adsorption A, forward equalizing pressure drop ED, reverse first pressure equalizing pressure drop BID ', reverse second pressure equalizing pressure drop B2D', and reverse third pressure equalizing pressure in a cycle.
  • the result of this example is that the oxygen concentration is greater than 93% (V), the nitrogen concentration is greater than 99.7% (V), and the oxygen recovery rate is greater than 98.5% (V).
  • Embodiment 17 of the present invention is a diagrammatic representation of Embodiment 17 of the present invention.
  • the source gas in this example is air.
  • the oxygen concentration in the outlet gas of the adsorption tower at the first stage of the pressure swing adsorption device in the adsorption step is controlled to 21 ⁇ 23% (V)
  • the oxygen concentration in the outlet gas of the adsorption tower at the second stage of the pressure swing adsorption device in the adsorption step is controlled to 50% (V) (that is, the product is rich in oxygen).
  • a total of 7 adsorption towers A to G constitute the first stage pressure swing adsorption device.
  • the bottom of the adsorption tower is filled
  • the adsorbent is activated alumina and molecular sieve in turn, and the three-phase adsorption three pressure equalization program is run: 7 adsorption towers a to g constitute a second stage pressure swing adsorption device.
  • the adsorbent filled in the adsorption tower is molecular sieve, and the five- tower adsorption is run.
  • Three equalization procedures In this embodiment, the above-mentioned two-stage pressure swing adsorption device is operated in series.
  • the first-stage pressure swing adsorption device removes gaseous water, carbon dioxide and some nitrogen in the air, and the second-stage pressure swing adsorption device is used for first-stage pressure swing adsorption.
  • the nitrogen in the intermediate gas flowing out of the adsorption step of the device is further removed, and the oxygen is raised to the desired concentration.
  • the adsorbent in the adsorption tower selectively adsorbs the gaseous water, carbon dioxide, and some nitrogen components in the air in order. Components such as oxygen and argon are discharged from the outlet into the adsorption tower in the second stage pressure swing adsorption device.
  • the molecular sieve in the adsorption tower selectively adsorbs nitrogen, and components such as oxygen and argon that are not easily adsorbed are discharged from the outlet.
  • Product oxygen-rich buffer tank is provided to produce the outlet.
  • the oxygen concentration in the exit gas of the adsorption tower at the adsorption step is controlled to 21 ⁇ 23% (V), and its adsorption tower undergoes adsorption A, replacement P ', vacuum VC, and
  • the third stage gas reverses the third pressure equalization pressure boost 2ER3, the second stage gas reverses the second pressure equalization pressure boost 2ER2, the second stage gas reverses the first pressure equalization pressure boost 2ER1, the replacement gas pressure boost R ', and the final pressure boost FR changes Pressure adsorption process steps;
  • the second stage pressure swing adsorption device is in the adsorption step at the outlet gas of the adsorption tower to control the oxygen concentration at about 50% (V), and its adsorption tower sequentially undergoes adsorption A in a cycle, reverse the first time Pressure reduction pressure BID ', reverse pressure equalization pressure reduction B2D', reverse pressure equalization pressure reduction B3D ', and final step-up FR pressure swing adsorption process steps.
  • the oxygen concentration is greater than 50% (V)
  • the nitrogen concentration is greater than 99.7% (V)
  • the oxygen recovery rate is greater than 98.5% (V).
  • Embodiment 18 of the present invention is a diagrammatic representation of Embodiment 18 of the present invention.
  • the source gas in this example is air.
  • the oxygen concentration in the outlet gas of the adsorption tower at the first stage of the pressure swing adsorption device in the adsorption step is controlled to 21 ⁇ 23% (V)
  • the oxygen concentration in the outlet gas of the adsorption tower at the second stage of the pressure swing adsorption device in the adsorption step is controlled to 50% (V) around (that is, the product is rich in oxygen).
  • a total of 7 adsorption towers A to G constitute the first stage pressure swing adsorption device.
  • the adsorbent filled from bottom to top in the adsorption tower is activated alumina and molecular sieve in turn, and the three-phase adsorption three-pressure equalization program is run; a total of 7 adsorption towers a to g constitute a second-stage pressure swing adsorption device.
  • the adsorbent is a molecular sieve, and a four-column adsorption three-pressure equalization program is run.
  • the above-mentioned two-stage pressure swing adsorption device is operated in series.
  • the first-stage pressure swing adsorption device removes gaseous water, carbon dioxide and some nitrogen in the air, and the second-stage pressure swing adsorption device.
  • the device is used for further removing nitrogen in the intermediate gas flowing out of the adsorption step of the adsorption tower of the first pressure swing adsorption device, and increasing the oxygen to a desired concentration.
  • the adsorbent in the adsorption tower selectively adsorbs the gaseous water, carbon dioxide, and some nitrogen components in the air in order. Components such as oxygen and argon are discharged from the outlet into the adsorption tower in the second stage pressure swing adsorption device.
  • the molecular sieve in the adsorption tower selectively adsorbs nitrogen, and components such as oxygen and argon that are not easily adsorbed are discharged from the outlet.
  • Product oxygen-rich buffer tank is provided to produce the outlet.
  • the oxygen concentration in the exit gas of the adsorption tower at the adsorption step is controlled to 21 ⁇ 23% (V), and its adsorption tower undergoes adsorption A, replacement P ', vacuum VC, and
  • the third stage gas reverses the third pressure equalization pressure boost 2ER3, the second stage gas reverses the second pressure equalization pressure boost 2ER2, the second stage gas reverses the first pressure equalization pressure boost 2ER1, the replacement gas pressure boost R ', and the final pressure boost FR changes Pressure adsorption process steps;
  • the second stage pressure swing adsorption device is in the adsorption step at the outlet gas of the adsorption tower to control the oxygen concentration at about 50% (V), and its adsorption tower undergoes adsorption A, forward pressure equalization in a cycle.
  • Step-down ED first equalizing step-down BID ', inverse second step-down B2D', inverse third step-down B3D ', inverse step-up ER, final
  • the oxygen concentration is greater than 50% (V)
  • the nitrogen concentration is greater than 99.7% (V)
  • the oxygen recovery rate is greater than 98.5% (V).
  • Embodiment 19 of the invention is a diagrammatic representation of Embodiment 19 of the invention.
  • the source gas in this example is air.
  • the oxygen concentration in the exit gas of the adsorption tower in the first stage of the PSA device during the adsorption step is controlled to 21 ⁇ 23% (V)
  • the oxygen concentration in the exit gas of the adsorption tower in the second stage of the PSA device during the adsorption step is controlled to 50% (V) around (that is, the product is rich in oxygen).
  • the adsorbent charged from bottom to top in the pressure swing adsorption device of the first stage is activated alumina and molecular sieve in turn.
  • the adsorbent filled in the pressure swing adsorption device of the second stage is molecular sieve.
  • the above-mentioned two-stage pressure swing adsorption device is operated in series.
  • the first-stage pressure swing adsorption device removes gaseous water, carbon dioxide, and part of nitrogen in the air
  • the second-stage pressure swing adsorption device is used for first-stage pressure swing adsorption.
  • the nitrogen in the intermediate gas flowing out of the adsorption step of the device is further removed, and the oxygen is raised to the desired concentration.
  • the adsorbent in the adsorption tower selectively adsorbs the gaseous water, carbon dioxide, and some nitrogen components in the air in order. Components such as oxygen and argon are discharged from the outlet end into the second stage pressure swing adsorption device
  • the molecular sieve in the adsorption tower selectively adsorbs nitrogen, and difficult-to-adsorb oxygen and argon components are discharged from the outlet end into the product oxygen-rich buffer tank.
  • the first stage pressure swing adsorption device is
  • the oxygen concentration in the outlet gas of the adsorption tower in the adsorption step is controlled to 21 ⁇ 23% (V), and its adsorption tower undergoes adsorption A, pressure drop 2ED ', pressure displacement 2', and vacuum VC in a cycle.
  • the second stage gas reverses the third equalizing pressure boost 2ER3, the second stage gas reverses the second equalizing pressure boost 2ER2, the second stage gas reverses the first equalizing pressure boost 2ER1, and the two ends are equalized pressure boost 2ER ', replacement Gas pressure boost R ', final pressure boost FR pressure swing adsorption process steps;
  • the second stage pressure swing adsorption device is in the adsorption tower outlet gas at the adsorption step to control the oxygen concentration at about 50% (V), and its adsorption tower is in a cycle
  • adsorption A forward pressure equalization pressure drop ED, reverse first pressure equalization pressure drop BID ', reverse second pressure equalization pressure drop B2D', reverse third pressure equalization pressure drop B3D ', reverse pressure equalization Step-up ER, final step-up FR pressure swing adsorption process steps.
  • the oxygen concentration is greater than 50% (V)
  • the nitrogen concentration is greater than 99.7% (V)
  • the oxygen recovery rate is greater than 98.5% (V).
  • Embodiment 20 of the invention is a diagrammatic representation of Embodiment 20 of the invention.
  • the source gas in this example is air.
  • the oxygen concentration in the outlet gas of the adsorption tower at the first stage of the pressure swing adsorption device in the adsorption step is controlled to 21 ⁇ 23% (V)
  • the oxygen concentration in the outlet gas of the adsorption tower at the second stage of the pressure swing adsorption device in the adsorption step is controlled to 93% (V) around (that is, the product is rich in oxygen).
  • the adsorbent charged from bottom to top in the pressure swing adsorption device of the first stage is activated alumina and molecular sieve in turn.
  • the adsorbent filled in the pressure swing adsorption device of the second stage is molecular sieve.
  • the above-mentioned two-stage pressure swing adsorption device is operated in series.
  • the first-stage pressure swing adsorption device removes gaseous water, carbon dioxide, and part of nitrogen in the air
  • the second-stage pressure swing adsorption device is used for first-stage pressure swing adsorption.
  • the nitrogen in the intermediate gas flowing out of the adsorption step of the device is further removed, and the oxygen is raised to the desired concentration.
  • the adsorbent in the adsorption tower selectively adsorbs the gaseous water, carbon dioxide, and some nitrogen components in the air in order. Components such as oxygen and argon are discharged from the outlet into the adsorption tower in the second stage pressure swing adsorption device.
  • the molecular sieve in the adsorption tower selectively adsorbs nitrogen, and components such as oxygen and argon that are not easily adsorbed are discharged from the outlet.
  • Product oxygen-rich buffer tank is provided to produce the outlet.
  • the concentration of oxygen in the exit gas of the adsorption tower at the adsorption step is controlled to 21 ⁇ 23% (V), and its adsorption tower sequentially undergoes adsorption A in both cycles, and the pressure at both ends is reduced by 2ED ', Replacement P ', reverse decompression BD, vacuum VC, second stage gas reverse third pressure equalization pressure boost 2ER3, second stage gas reverse second pressure equalization pressure boost 2ER2,
  • the second stage gas reverses the first pressure equalization pressure boost 2ER1, the pressure equalization pressure boost 2ER 'at both ends, the replacement gas pressure boost R', and the final pressure boost FR PSA process steps;
  • the second stage PSA device is in the adsorption step
  • the oxygen concentration in the outlet gas of the adsorption tower is controlled at about 93% (V), and its adsorption tower undergoes adsorption A, the first equalizing pressure drop E1D, and the second equalizing pressure drop E2D in a cycle.
  • the oxygen concentration is greater than 93% (V)
  • the nitrogen concentration is greater than 99.9% (V)
  • the oxygen recovery rate is greater than 99% (V).
  • Embodiment 21 of the present invention is a diagrammatic representation of Embodiment 21 of the present invention.
  • the source gas in this example is air.
  • the oxygen concentration in the gas at the exit of the adsorption tower in the first stage of the PSA device during the adsorption step is controlled to 21 ⁇ 23% (V)
  • the oxygen concentration in the gas at the exit of the adsorption tower in the second stage of the PSA device during the adsorption step is controlled to 93% (V) around (that is, the product is rich in oxygen).
  • the adsorbent charged from bottom to top in the pressure swing adsorption device of the first stage is activated alumina and molecular sieve in turn.
  • the adsorbent filled in the pressure swing adsorption device of the second stage is molecular sieve.
  • the above-mentioned two-stage pressure swing adsorption device is operated in series.
  • the first-stage pressure swing adsorption device removes gaseous water, carbon dioxide, and part of nitrogen in the air
  • the second-stage pressure swing adsorption device is used for first-stage pressure swing adsorption.
  • the nitrogen in the intermediate gas flowing out of the adsorption step of the device is further removed, and the oxygen is raised to the desired concentration.
  • the adsorbent in the adsorption tower selectively adsorbs the gaseous water, carbon dioxide, and some nitrogen components in the air in order. Components such as oxygen and argon are discharged from the outlet into the adsorption tower in the second stage pressure swing adsorption device.
  • the molecular sieve in the adsorption tower selectively adsorbs nitrogen, and components such as oxygen and argon that are not easily adsorbed are discharged from the outlet.
  • Product oxygen-rich buffer tank is provided to produce the outlet.
  • the oxygen concentration in the gas at the exit of the adsorption tower in the adsorption step is controlled to 21 ⁇ 23% (V), and its adsorption tower undergoes adsorption A in turn, and the pressure at both ends is reduced.
  • the second stage PSA device is in the adsorption tower outlet gas at the adsorption step to control the oxygen concentration at 93 % (V), and its adsorption tower goes through in a cycle Adsorption A, the first pressure equalization pressure drop E1D, the second pressure equalization pressure drop E2D, the third pressure equalization pressure drop E3D, the first pressure equalization pressure drop BID ', the second pressure equalization Second equalizing voltage step-down B2D ', reverse third voltage equalizing step-down B3D', reverse third voltage equalizing step-up E3R, reverse second voltage equalizing step-up E2R, reverse first voltage equalizing step-up E1R, and
  • the pressure-reduced pressure B3D 'gas is put into the buffer tank V3 for pressure equalization, and then the gas in the buffer tank V3 is used with the first stage pressure swing adsorption device. Set the adsorption tower to reverse the pressure equalization for the third pressure equalization 2ER3 adsorption tower.
  • the oxygen concentration is greater than 93% (V)
  • the nitrogen concentration is greater than 99.9% (V)
  • the oxygen recovery rate is greater than 99.6% (V).
  • Embodiment 22 of the invention is a diagrammatic representation of Embodiment 22 of the invention.
  • the source gas in this example is air.
  • the oxygen concentration in the gas at the exit of the adsorption tower in the first stage of the PSA device during the adsorption step is controlled to 21 ⁇ 23% (V)
  • the oxygen concentration in the gas at the exit of the adsorption tower in the second stage of the PSA device during the adsorption step is controlled to 93% (V) around (that is, the product is rich in oxygen).
  • the adsorbent charged from bottom to top in the pressure swing adsorption device of the first stage is activated alumina and molecular sieve in turn.
  • the adsorbent filled in the pressure swing adsorption device of the second stage is molecular sieve.
  • the above-mentioned two-stage pressure swing adsorption device is operated in series.
  • the first-stage pressure swing adsorption device removes gaseous water, carbon dioxide, and part of nitrogen in the air
  • the second-stage pressure swing adsorption device is used for first-stage pressure swing adsorption.
  • the nitrogen in the intermediate gas flowing out of the adsorption step of the device is further removed, and the oxygen is raised to the desired concentration.
  • the adsorbent in the adsorption tower selectively adsorbs the gaseous water, carbon dioxide, and some nitrogen components in the air in order. Components such as oxygen and argon are discharged from the outlet into the adsorption tower in the second stage pressure swing adsorption device.
  • the molecular sieve in the adsorption tower selectively adsorbs nitrogen, and components such as oxygen and argon that are not easily adsorbed are discharged from the outlet.
  • Product oxygen-rich buffer tank is provided to produce the outlet.
  • the first stage pressure swing adsorption device is in the adsorption step and the oxygen concentration in the exit gas of the adsorption tower is controlled to 21 ⁇ 23% (V).
  • V the oxygen concentration in the exit gas of the adsorption tower
  • the oxygen concentration in the exit gas of the adsorption tower is controlled to 21 ⁇ 23% (V).
  • the cycle it experiences adsorption A, pressure equalization and pressure drop 2ED 'at both ends, displacement P', reverse pressure drop BD, second stage gas reverse pressure equalization 3rd pressure boost 2ER3, and second stage gas pressure reversed second pressure equalization 2ER2, the first stage of the two-stage gas reverse pressure equalization boost 2ER1, the two-stage pressure equalization pressure boost 2ER ', the replacement gas boost R', and the final boost FR PSA process steps; the second stage PSA device is located at The oxygen concentration in the outlet gas of the adsorption tower in the adsorption step is controlled at about 93% (V), and its adsorption tower sequentially undergoes
  • the gas of the second pressure equalization pressure drop BID ' is put into the buffer tank VI for pressure equalization, and then the gas in the buffer tank VI and the first stage pressure swing adsorption device are used.
  • the adsorption tower reverses the pressure of the first pressure equalization booster 2ER1 to perform pressure balancing; the second stage of the pressure swing adsorption device reverses the pressure of the second pressure equalization and pressure reduction B2D 'into the buffer tank ⁇ 2 for pressure equalization, and then uses
  • the gas in the buffer tank V2 is pressure-balanced with the adsorption tower of the first stage pressure swing adsorption device to reverse the pressure equalization 2ER2; the adsorption tower of the second stage pressure swing adsorption device reverses the pressure equalization pressure B3D '
  • the gas in the buffer tank V3 is used for pressure equalization, and then the gas in the buffer tank V3 is used to pressure-balance the adsorption tower of the first stage pressure swing adsorption device with the pressure equalization of the third pressure equalization 2ER3 adsorption tower.
  • the oxygen concentration is greater than 93% (V)
  • the nitrogen concentration is greater than 99.9% (V)
  • the oxygen recovery rate is greater than 99.6% (V).
  • Embodiment 23 of the present invention is a diagrammatic representation of Embodiment 23 of the present invention.
  • the source gas in this example is air.
  • the oxygen concentration in the gas at the outlet of the adsorption tower in the first stage of the pressure swing adsorption device is controlled at 21 ⁇ 23 ° /. (V).
  • the oxygen concentration in the gas at the outlet of the adsorption tower at the second stage of the PSA device is controlled at about 93% (V) (that is, the product is rich in oxygen).
  • a total of 7 adsorption towers A to G constitute the first stage pressure swing adsorption device.
  • the adsorbent filled from bottom to top in the adsorption tower is activated alumina and molecular sieve in turn, and the three-phase adsorption three-pressure equalization program is run; a total of 7 adsorption towers a to g constitute a second-stage pressure swing adsorption device.
  • the adsorbent is a molecular sieve, and a five-column adsorption three-pressure equalization program is run.
  • the above-mentioned two-stage pressure swing adsorption device is operated in series.
  • the first-stage pressure swing adsorption device removes gaseous water, carbon dioxide and some nitrogen in the air
  • the second-stage pressure swing adsorption device is used for first-stage pressure swing adsorption.
  • the nitrogen in the intermediate gas flowing out of the adsorption step of the adsorption tower of the device further Remove and raise oxygen to the desired concentration.
  • the adsorbent in the adsorption tower selectively adsorbs the gaseous water, carbon dioxide, and some nitrogen components in the air in order. Components such as oxygen and argon are discharged from the outlet into the adsorption tower in the second stage pressure swing adsorption device.
  • the molecular sieve in the adsorption tower selectively adsorbs nitrogen, and components such as oxygen and argon that are not easily adsorbed are discharged from the outlet.
  • Product oxygen-rich buffer tank is provided to produce the outlet.
  • the oxygen concentration in the exit gas of the adsorption tower in the adsorption step is controlled to 21 ⁇ 23% (V), and its adsorption tower sequentially undergoes adsorption A, pressure equalization and pressure drop 2ED ', Evacuation VC, the second stage gas reverses the third equalizing pressure boost 2ER3, the second stage gas reverses the second equalizing pressure boost 2ER2, the second stage gas reverses the first equalizing pressure boost 2ER1, and the both ends are equalized pressure boost 2ER ' ⁇
  • the result of this example is that the oxygen concentration is greater than 93% (V), the nitrogen concentration is greater than 99.7% (V), and the oxygen recovery rate is greater than 98.5%.
  • Embodiment 24 of the invention is a diagrammatic representation of Embodiment 24 of the invention.
  • the source gas in this example is air.
  • the oxygen concentration in the outlet gas of the adsorption tower in the first stage of the pressure swing adsorption device in the adsorption step is controlled to 21 ⁇ 23% (V)
  • the oxygen concentration in the outlet gas of the adsorption tower in the second stage of the pressure swing adsorption device in the adsorption step is controlled to 93% (V) around (that is, the product is rich in oxygen).
  • a total of 7 adsorption towers A to G constitute the first stage pressure swing adsorption device.
  • the adsorbent filled from bottom to top in the adsorption tower is activated alumina and molecular sieve in order, and the three-phase adsorption three pressure equalization program is run.
  • a total of 7 adsorption towers a to g constitute a second-stage pressure swing adsorption device.
  • the adsorbent is a molecular sieve, and a five-column adsorption three pressure equalization program is run.
  • the above-mentioned two-stage pressure swing adsorption device is operated in series.
  • the first-stage pressure swing adsorption device removes gaseous water, carbon dioxide and some nitrogen in the air, and the second-stage pressure swing adsorption device is used for first-stage pressure swing adsorption.
  • the nitrogen in the intermediate gas flowing out of the adsorption step of the device is further removed, and the oxygen is raised to the desired concentration.
  • the air enters the adsorption tower of the first stage pressure swing adsorption device in the adsorption step.
  • the adsorbent in the adsorption tower selectively adsorbs the gaseous water, carbon dioxide, and some nitrogen components in the air in sequence. Part of the nitrogen and components that are not easily adsorbed such as oxygen and argon are discharged from the outlet end into an adsorption tower in the second stage pressure swing adsorption device in the adsorption step.
  • the molecular sieve in the adsorption tower selectively adsorbs nitrogen, difficult to adsorb oxygen and argon, etc. The components are discharged from the outlet end into the product oxygen-rich buffer tank.
  • the concentration of oxygen in the exit gas of the adsorption tower in the adsorption step is controlled to 21 ⁇ 23% (V), and its adsorption tower undergoes adsorption A, pressure drop 2ED ', Reverse decompression BD, vacuum VC, two-stage gas reverse third pressure equalization boost 2ER3, two-stage gas reverse second pressure equalization boost 2ER2, two-stage gas reverse first pressure equalization boost 2ER1, both ends Equal pressure boost 2ER ', final step-up FR PSA process steps;
  • the second stage PSA device is in the adsorption tower outlet gas at the adsorption step to control the oxygen concentration at about 93% (V), and its adsorption tower is in a cycle During the cycle, the adsorption A, the first reverse pressure equalization pressure reduction BID ', the reverse second pressure equalization pressure reduction B2D', the reverse third pressure equalization pressure reduction B3D ', and the final step-up FR pressure swing adsorption
  • the result of this embodiment is that the oxygen concentration is greater than 93% (V), and the nitrogen concentration is greater than 99.7 ° /. (V), oxygen recovery rate is greater than 98.5%
  • Embodiment 25 of the present invention is a diagrammatic representation of Embodiment 25 of the present invention.
  • the source gas in this example is air.
  • the oxygen concentration in the exit gas of the adsorption tower in the first stage of the PSA device during the adsorption step is controlled to 21 ⁇ 23% (V)
  • the oxygen concentration in the exit gas of the adsorption tower in the second stage of the PSA device during the adsorption step is controlled to 93% (V) (that is, the product is rich in oxygen).
  • a total of 7 adsorption towers A to G constitute the first stage pressure swing adsorption device.
  • the adsorbents filled from bottom to top in the adsorption tower are activated alumina and molecular sieve in turn, and the three-phase adsorption three pressure equalization program is run;
  • a total of 7 adsorption towers a ⁇ -g constitute a second stage pressure swing adsorption device, and the adsorption tower is filled with
  • the adsorbent is molecular sieve, and a five-column adsorption three-pressure equalization program is run.
  • the above-mentioned two-stage pressure swing adsorption device is operated in series.
  • the first-stage pressure swing adsorption device removes gaseous water, carbon dioxide and some nitrogen in the air, and the second-stage pressure swing adsorption device is used for first-stage pressure swing adsorption.
  • the nitrogen in the intermediate gas flowing out of the adsorption step of the device is further removed, and the oxygen is raised to the desired concentration.
  • the adsorbent in the adsorption tower selectively adsorbs the gaseous water, carbon dioxide, and some nitrogen components in the air in order. Components such as oxygen and argon are discharged from the outlet into the adsorption tower in the second stage pressure swing adsorption device.
  • the molecular sieve in the adsorption tower selectively adsorbs nitrogen, and components such as oxygen and argon that are not easily adsorbed are discharged from the outlet.
  • Product oxygen-rich buffer tank is provided to produce the outlet.
  • the first stage pressure swing adsorption device is in The oxygen concentration in the outlet gas of the adsorption tower in the adsorption step is controlled to 21 ⁇ 23% (V), and its adsorption tower undergoes adsorption A, pressure equalization pressure drop 2ED 'at both ends, vacuum VC, and two-stage gas reverse in a cycle.
  • the second stage pressure swing adsorption device is in the adsorption step, the oxygen concentration in the exit gas of the adsorption tower is controlled at about 93% (V), and its adsorption tower undergoes adsorption A, forward pressure equalization and pressure reduction in a cycle.
  • ED first reverse pressure equalization pressure reduction BID ', reverse second pressure equalization pressure reduction B2D', reverse third pressure equalization pressure reduction B3D ', reverse pressure equalization pressure boost ER, final pressure boost FR pressure swing adsorption process step.
  • the result of this example is that the oxygen concentration is greater than 93% (V), the nitrogen concentration is greater than 99.7% (V), and the oxygen recovery rate is greater than 98.5%.
  • the invention can be widely used in the fields of chemical industry, petrochemical industry, metallurgy, building materials, environmental protection, and pharmaceuticals.

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Description

一种改进的两段变压吸附制富氧方法 技术领域
本发明涉及采用两段变压吸附技术从空气中生产富氧的方法,特别是一 种改进的两段变压吸附制富氧方法。 背景技术
本发明是对两段变压吸附技术从空气中生产富氧专利技术 (专利公开号 为 CN1386565A ) 的进一步改进, 同时还生产提浓氮气, 提高氧气和氮气的回 收率,使整个制氧装置的电耗和投资进一步降低。 发明的公开
本发明的目的就是提供一种改进的两段变压吸附制富氧方法, 该方法克 服了现有技术的上述问题, 与现有技术相比大幅度节省电耗和投资, 提高整 个装置的氧气回收率。
本发明的目的是这样来实施的。
本发明采用两段变压吸附技术从空气中分离氮气和氧气,产品可以是氧 气,也可以是氮气,还可以同时是氧气和氮气, 此方法采用二段变压吸附装置 串联操作, 第一段变压吸附装置用于脱除二氧化碳、 水和部分氮气并将氮气 提浓, 第二段变压吸附装置用于将第一段变压吸附装置吸附塔吸附步骤流出 的中间气中的氮进一步脱除, 并把氧提高至所需的浓度, 第一段变压吸附装 置的吸附塔在一个循环周期中依次经历吸附 、 置换 P '、 抽真空 VC、 二段气 逆向均压升压 2ER、 置换气升压 R'、最终升压 FR变压吸附工艺步骤; 第二段 变压吸附装置的吸附塔在一个循环周期中依次经历吸附 A、 逆向均压降压 BD '、 最终升压 FR变压吸附工艺步骤。
在第二段变压吸附装置吸附塔在吸附 A工艺步骤之后增加顺向均压降压 ED工艺步骤,同时在逆向均压降压 BD '工艺步骤完成后增加逆向升压 ER工艺 步骤,升压 ER工艺步骤的混合气来自降压 ED工艺步骤。
第一段变压吸附装置吸附塔在吸附 A 工艺步骤之后增加两端均压降压 2ED'工艺步骤, 同时在二段气逆向均压升压 2ER工艺步骤完成后增加均压升 压 2ER'工艺步骤, 两端均压升压 2ER'工艺步骤的混合气来自均压降压 2ED ' 工艺步骤。
第一段变压吸附装置吸附塔在置换 P'工艺步骤之后增加逆向降压 BD工 艺步骤。
第二段变压吸附装置吸附塔逆向均压降压 BD'工艺步骤放出的混合气进 入缓冲罐 VI,直到压力平衡为止,同时第一段变压吸附装置吸附塔在进行二 段气逆向均压升压 2ER工艺步骤时,吸附塔与缓冲罐 VI连通, 直到压力平衡 为止。
第一段变压吸附装置吸附塔吸附步骤出口气中氧气的平均浓度大于 5 21〜80% (V)。
第一段变压吸附装置吸附塔吸附步骤出口气中氧气的平均浓度大于 21〜25% ( V )。
两段变压吸附装置吸附步骤 A的压力为 0. 001〜0. IMPa (表压)。
第一段变压吸附装置吸附塔内由下到上装填的吸附剂为活性氧化铝及分 0 子筛; 第二段变压吸附装置吸附塔内装填的吸附剂只为分子筛。
第二段变压吸附装置吸附塔逆向均压降压 ED'和第一段变压吸附装置吸 附塔二段气逆向均压升压 2ER的次数大于或等于 1。
第二段变压吸附装置吸附塔逆向均压降压 ED'和第一段变压吸附装置吸 附塔二段气逆向均压升压 2ER的次数为 3〜7次。
5 本发明用于从空气中分离氮气和氧气,产品可以是氧气,也可以是氮气,
. 还可以同时是氧气和氮气, 此方法采用二段变压吸附装置串联操作, 第一段 变压吸附装置用于脱除二氧化碳、 水和部分氮气并将氮气提浓, 第二段变压 吸附装置用于将第一段变压吸附装置吸附塔吸附步骤流出的中间气中的氮进 一步脱除, 并把氧提高至所需的浓度, 第一段变压吸附装置的吸附塔在一个 0 循环周期中依次经历吸附 A、 两端均压降压 2ED 、 置换 P'、 逆向降压 BD、 二 段气逆向均压升压 2ER、 两端均压升压 2ER'、 置换气升压 R'、 最终升压 FR 变压吸附工艺步骤; 第二段变压吸附装置吸附塔在一个循环周期中依次经历 : 吸附 A、 顺向均压降压 ED、 逆向均压降压 BD'、 逆向均压升压 ER、 最终升压
FR变压吸附工艺步骤。
5 两段变压吸附装置吸附步骤 A的压力为 0. 3〜0. 6 Pa表压。
本发明用于从空气中分离氮气和氧气,产品可以是氧气,也可以是氮气, 还可以同时是氧气和氮气, 此方法采用二段变压吸附装置串联操作, 第一段
、 变压吸附装置用于脱除二氧化碳、 水和部分氮气并将氮气提浓, 第二段变压 吸附装置用于将第一段变压吸附装置吸附塔吸附步骤流出的中间气中的氮进 0 一步脱除, 并把氧提高至所需的浓度, 第一段变压吸附装置的吸附塔在一个 循环周期中依次经历吸附 A、 两端均压降压 2ED'、 抽真空 VC、 二段气逆向均 压升压 2ER、 两端均压升压 2ER'、 最终升压 FR变压吸附工艺步骤; 第二段变 压吸附装置的吸附塔在一个循环周期中依次经历吸附 A、 逆向均压降压 BD'、 ' 最终升压 FR变压吸附工艺步骤。
5 第一段变压吸附装置吸附塔在两端均压降压 2ED'工艺步骤之后增加逆 向降压 BD工艺步骤。 附图的简要说明
图 1是实施例第一段变压吸附装置的工艺步骤运行程序表。
5 图 2是实施例第二段变压吸附装置的工艺步骤运行程序表。
图 3是实施例 1的工艺流程图。 实现本发明的最佳方式
本发明原料气是空气, 其典型组成如下表:
Figure imgf000004_0001
0 本发明采用两段变压吸附技术从空气中生产富氧, 此方法采用二段变压 吸附装置串联操作, 第一段变压吸附装置用于脱除气态水、 二氧化碳及部分 氮气, 吸附塔吸附步骤出口气中氧气的平均浓度为 21〜80% (V ) , 吸附塔内 由下到上装填的吸附剂为活性氧化铝及分子筛; 第二段变压吸附装置用于将 第一段变压吸附装置吸附塔吸附步骤流出的中间气中的氮进一步脱除, 并把 5 氧提高至所需的浓度, 吸附塔内装填的吸附剂为分子筛。 两段变压吸附装置 吸附步骤 A的压力为 0. 001〜0. IMPa (表压)。 两段变压吸附装置的每个吸附 塔在一个循环中依次经历如下步骤。
第一段变压吸附装置:
(1) 吸附 A
0 将空气送入处于吸附步骤的吸附塔进料口, 吸附塔中的吸附剂选择性地 依次吸附空气中的水、 二氧化碳及部分氮气等组分, 未吸附的部分氮气和不 易吸附的氩气等组分从出口端流出进入第二段变压吸附装置处于吸附步骤的 . 吸附塔, 随着时间的推移, 吸附剂吸附的水、 二氧化碳及部分氮气等组分的 ' 总量不断增加, 当吸附剂吸附上述组分饱和时, 停止进气, 此时吸附结束。 5 (2) 两端均压降压 2ED'
吸附结束后, 吸附塔内死空间气体中氧气浓度较高, 这部分氧气需回收 利用, 为此, 把吸附塔内的气体从上下两端降压。 死空间气体从吸附塔进出 ; 口排出进入本段己完成二段气逆向均压升压 2ER步骤的相应吸附塔进行两端 升压 2ER'。 两端均压降压 2ED'次数可为 1次或 1次以上(如 1〜3次)。
0 吸附结束后, 还可以只顺向均压降压或逆向均压降压。
(3)置换 P'
两端均压降压 2ED'步骤结束后,用第一段抽真空 VC步骤的气体从吸附塔 的底部进入将塔内残留的氧气置换出去,从吸附塔置换出来的混合气进入本 段已完成二段气逆向均压升压 2ER步骤或两端均压升压 2ER '步骤的相应吸附 塔进行置换气体升压 R'。
(4)逆放 BD
置换 P'结束后,将这部分气体逆向从吸附塔底部放空或作为产品。
(5)抽真空 VC
置换 P'结束后, 从吸附塔底部用真空泵将吸附剂吸附的水、 二氧化碳和 氮抽出来放空, 使吸附剂得到再生。
(6)二段气逆向均压升压 2ER
抽真空 VC结束后,利用第二段变压吸附装置吸附塔吸附结束或顺向均压 降压 ED完成后的气体进入本段已完成抽真空 VC步骤的吸附塔, 对吸附塔升 压。 二段气逆向均压升压 2ER次数可为 1次或 1次以上(如 1〜7次)。
(7)两端均压升压 2ER'
二段气逆向均压升压 2ER结束后, 利用本段两端均压降压 2ED '步骤排出 的气体,从进出口端进入吸附塔,使吸附塔逐步升高压力,两端均压升压 2ER ' 与两端均压降压 2ED '的次数相等。 每次两端均压升压 2ER '的气体来自不同 吸附塔的两端均压降压 2ED '气体。 本段吸附塔两端均压升压 2ER'步骤与通 常的均压升压 ER步骤有所不同, 通常的吸附塔均压升压 ER步骤气体是从吸 附塔的出口端进入,而本段吸附塔两端均压升压 2ER '步骤气体是从吸附塔的 进出口两端进入。
(8)置换气升压 R'
两端均压升压 2ER'或二段气逆向均压升压 2ER结束后,用本段处于置换 P'步骤的吸附塔出口气体进行升压。
(9)最终升压 FR
置换气升压 R'结束后,利用处于吸附步骤的吸附塔出口气从顶端对吸附 塔进行升压, 直至升到吸附压力, 也可以利用原料空气对吸附塔升到吸附压 力。
第二段变压吸附装置
(1) 吸附 A
将第一段变压吸附装置处于吸附步骤的吸附塔出口气送入第二段变压吸 附装置处于吸附步骤的吸附塔, 吸附塔中的吸附剂选择性地吸附氮气, 不易 吸附的氧气和氩气等组分从出口端排出进入富氧缓冲罐或下一工段。 随着时 间的推移, 吸附剂吸附的氮气总量不断增加, 当吸附剂吸附氮气饱和时, 停 止进气, 此时吸附结束, 出口气中氧气浓度控制在产品要求的水平。
(2) 顺向均压降压 ED 吸附结束后, 吸附塔内死空间气体从吸附塔出口排出进入本段已完成逆 向均压降压 BD'步骤的相应吸附塔升压, 两塔压力可以相等, 也可以不相等, 以保证产品富氧浓度满足要求。顺向均压降压 ED次数可为 1次或 1次以上(如 1〜3次)。
5 (3)逆向均压降压 BD'
吸附或顺向均压降压 ED结束后,逆向从吸附塔底部将塔内的气体分次对 第一段已经完成抽真空 VC的吸附塔直接进行二段气逆向均压升压 2ER。逆向 均压降压 BD次数可为 1次或 1次以上(如 1〜7次)。。
在逆向从吸附塔底部将塔内的气体分次对第一段己经完成抽真空 VC 的 10 吸附塔进行二段气逆向均压升压 2ER 时,还可以将吸附塔内气体先逆向放入 一个缓冲罐, 然后再将缓冲罐中的气体送入第一段变压吸附装置抽真空 VC 结束后的吸附塔进行二段气逆向均压升压 2ER,缓冲罐的数量与逆向均压降 - 压 BD'的次数相等。
(4)逆向升压 ER
15 逆向均压降压 BD'结束后, 利用顺向均压降压 ED步骤排出的气体, 从出 口端进入吸附塔, 使吸附塔升高压力。
(5)最终升压 FR
■ 利用处于吸附步骤的吸附塔出口气从顶端对吸附塔进行升压, 直至升到 吸附压力。
0 本发明的实施例 1 :
本例的原料气为空气。 第一段变压吸附装置处于吸附步骤的吸附塔出口 气中氧气浓度控制在 21〜23% (V) , 第二段变压吸附装置处于吸附步骤的吸 : 附塔出口气中氧气浓度控制在 93% (V ) 左右 (即产品富氧)。
本实施例的空气组成如下:
Figure imgf000006_0001
温度: 45°C
压力: 0. 01 MPa (G )
如图 3所示, 吸附塔 A〜D共 4台组成第一段变压吸附装置。 吸附塔内由 下到上装填的吸附剂依次为活性氧化铝及分子筛, 运行单塔吸附一次均压程 序, 通过真空泵 P1利用真空管线 G15对吸附塔抽真空; 吸附塔 a〜d共 4台 组成第二段变压吸附装置。 吸附塔内装填的吸附剂为分子筛, 运行单塔吸附 一次均压程序。 本实施例将上述二段变压吸附装置串联操作, 第一段变压吸 附装置脱除空气中的气态水、 二氧化碳及部分氮气, 第二段变压吸附装置用 于将第一段变压吸附装置吸附塔吸附步骤流出的中间气中的氮进一步脱除, 并把氧提高至所需的浓度。 第一段和第二段变压吸附装置也可以采用四个以 上的吸附塔进行组合。
空气进入第一段变压吸附装置处于吸附步骤的吸附塔, 吸附塔中的吸附 剂选择性地依次吸附空气中的气态水、 二氧化碳及部分氮气等组分, 未吸附 的部分氮和不易吸附的氧和氩等组分从出口端排出进入第二段变压吸附装置 处于吸附步骤的吸附塔, 吸附塔中的分子筛选择性地吸附氮气, 不易吸附的 氧和氩等组分从出口端排出进入产品富氧缓冲罐。 第一段变压吸附装置处于 吸附步骤的吸附塔出口气中氧气浓度控制在 21〜23% ( V ) , 其吸附塔在一个 循环周期中依次经历吸附 A、 置换 P'、抽真空 VC、 二段气逆向均压升压 2ER、 置换气升压 R'、 最终升压 FR变压吸附工艺步骤; 第二段变压吸附装置处于 吸附步骤的吸附塔出口气中氧气浓度控制在 93% ( V ) 左右, 其吸附塔在一个 循环周期中依次经历吸附 A、 逆向均压降压 BD'、 最终升压 FR变压吸附工艺 步骤。 '
现以 A塔为例, 对照图 1和图 3, 说明本实施例第一段变压吸附装置吸附 塔在一个循环过程中的工艺步骤:
(1) 吸附 A
此时, A塔已完成最终升压 FR步骤, 打开程控阀 1A、 2A, 空气经管道 Gi l 进入吸附塔 A, 在吸附塔 A中, 吸附剂选择性地依次吸附空气中的水、 二氧化 碳及部分氮气等组分,未吸附的部分氮气和不易吸附的氩气等组分从出口端流 出进入第二段变压吸附装置处于吸附步骤的吸附塔, 随着时间的推移, 吸附剂 吸附的水、二氧化碳及部分氮气等组分的总量不断增加, 当吸附剂吸附上述组 分饱和时, 停止进气, 此时吸附结束, 关闭程控阀 1A、 2A, 出口气中氮气浓 度控制在 70〜78% ( V)。
(2)置换 P '
吸附结束后, 打开程控阀 6A、 4A和 4C, 用真空泵出口气体经管道 G 16和 G14进入 C塔对 C塔进行置换气升压(简称 R' ),当 A塔内的氮气浓度满足要求 后, 关闭程控阀 6A、 4A和 4C。
(3) 抽真空 VC
置换 P'结束后, 打幵程控阀 5A,从吸附塔底部用真空泵将吸附剂吸附的 水、 二氧化碳和氮抽出来放空或作为产品, 同时使吸附剂得到再生。
(4)二段气逆向均压升压 2ER
抽真空 VC结束后, 打开程控阀 5a、 4A和 KV8, 利用第二段变压吸附装 置吸附塔 a逆向均压降压 BD '步骤的气体进入吸附塔 A , 对吸附塔 A升压。
(5)最终升压 FR
二段气逆向均压升压 2ER结束后, 打开程控阀 KV6和 3A, 利用处于吸附 - 步骤的吸附塔出口气从顶端対 A塔进行升压, 当 A塔压力升至接近吸附压力 时, 关闭程控阀 KV6和 3A。
至此, A塔完成了一个循环, 又可进入下一个循环。 B〜D吸附塔与 A塔 的循环步骤一样, 只是时间上是相互错开的, 见图 1和图 3。
5 现以 a塔为例, 对照图 2和图 3, 说明本实施例第二段变压吸附装置吸 附塔在一个循环过程中的工艺步骤:
(1) 吸附 A
此时, a塔已完成最终升压 FR步骤, 打开程控阀 la、 2a, 中间混合气经 管道 G21进入吸附塔 a, 在吸附塔 a中, 将第一段变压吸附装置处于吸附步 骤的吸附塔出口气送入第二段变压吸附装置处于吸附步骤的吸附塔, 吸附塔 中的吸附剂选择性地吸附氮气, 不易吸附的氧气和氩气等组分从出口端排出 进入富氧缓冲罐或下一工段。 随着时间的推移, 吸附剂吸附的氮气总量不断 : 增加, 当吸附剂吸附氮气饱和时, 停止进气, 此时吸附结束, 关闭程控阀 l a、 2a
(2)逆向均压降压 BD'
吸附结束后, 打开程控阀 5a、 4A和 KV8, 将吸附塔 a内的气体逆放进入 吸附塔 A进行升压。
(3)最终升压 FR
逆向均压降压 BD'结束后, 打开程控阀 KV7和 3a, 利用处于吸附步骤的 吸附塔出口气从顶端对 a塔进行升压, 当 a塔压力升至接近吸附压力时, 关 闭程控阀 KV7和 3a。
至此, a塔完成了一个循环, 又可进入下一个循环。 b〜h吸附塔与 a塔 的循环步骤一样, 只是时间上是相互错开的, 见图 2和图 3。
本实施例结果为氧气浓度大于 93% ( V ) , 氮气浓度大于 99. 7% (V ) ,氧 气回收率大于 98. 5% ( V ) o
本发明的实施例 2 :
本例的原料气为空气。 第一段变压吸附装置处于吸附步骤的吸附塔出口 气中氧气浓度控制在 21〜23% ( V) , 第二段变压吸附装置处于吸附步骤的吸 附塔出口气中氧气浓度控制在 93°/。 (V) 左右 (即产品富氧)。
本实施例的空气组成如下:
Figure imgf000008_0001
45°C
压力: 0. 01 MPa (G) 吸附塔 A〜G共 7台组成第一段变压吸附装置。吸附塔内由下到上装填的 吸附剂依次为活性氧化铝及分子筛,运行三塔吸附三次均压程序;吸附塔 a〜 g共 7台组成第二段变压吸附装置,吸附塔内装填的吸附剂为分子筛,运行五 塔吸附三次均压程序。 本实施例将上述二段变压吸附装置串联操作, 第一段 变压吸附装置脱除空气中的气态水、 二氧化碳及部分氮气, 第二段变压吸附 装置用于将第一段变压吸附装置吸附塔吸附步骤流出的中间气中的氮进一步 脱除, 并把氧提高至所需的浓度。
空气进入第一段变压吸附装置处于吸附步骤的吸附塔, 吸附塔中的吸附 剂选择性地依次吸附空气中的气态水、 二氧化碳及部分氮气等组分, 未吸附 的部分氮和不易吸附的氧和氩等组分从出口端排出进入第二段变压吸附装置 处于吸附步骤的吸附塔, 吸附塔中的分子筛选择性地吸附氮气, 不易吸附的 氧和氩等组分从出口端排出进入产品富氧缓冲罐。 第一段变压吸附装置处于 吸附步骤的吸附塔出口气中氧气浓度控制在 21〜23% ( V ) , 其吸附塔在一个 循环周期中依次经历吸附 A、 置换 P'、 抽真空 VC、 二段气逆向第三次均压升 压 2ER3、二段气逆向第二次均压升压 2ER2、二段气逆向第一次均压升压 2ER1、 置换气升压 R'、 最终升压 FR变压吸附工艺步骤; 第二段变压吸附装置处于 吸附步骤的吸附塔出口气中氧气浓度控制在 93% (V )左右, 其吸附塔在一个 循环周期中依次经历吸附 A、 逆向第一次均压降压 BID'、 逆向第二次均压降 压 B2D'、 逆向第三次均压降压 B3D'、 最终升压 FR变压吸附工艺步骤。
本实施例结果为氧气浓度大于 93% ( V ) , 氮气浓度大于 99. 7% (V ) ,氧 气回收率大于 98. 5% (V)。
本发明的实施例 3 :
本例的原料气为空气。 第一段变压吸附装置处于吸附步骤的吸附塔出口 气中氧气浓度控制在 21〜23% (V ) , 第二段变压吸附装置处于吸附步骤的吸 附塔出口气中氧气浓度控制在 93% ( V ) 左右 (即产品富氧)。
本实施例的空气组成如下:
Figure imgf000009_0001
温度: 45°C
压力: 0. 01 MPa (G) .
吸附塔 A〜G共 7台组成第一段变压吸附装置。吸附塔内由下到上装填的 吸附剂依次为活性氧化铝及分子筛,运行三塔吸附三次均压程序;吸附塔 a〜 g共 7台组成第二段变压吸附装置,吸附塔内装填的吸附剂为分子筛,运行四 塔吸附三次均压程序。 本实施例将上述二段变压吸附装置串联操作' 第一段 变压吸附装置脱除空气中的气态水、 二氧化碳及部分氮气, 第二段变压吸附 装置用于将第一段变压吸附装置吸附塔吸附步骤流出的中间气中的氮进一步 脱除, 并把氧提高至所需的浓度。
空气进入第一段变压吸附装置处于吸附步骤的吸附塔, 吸附塔中的吸附 剂选择性地依次吸附空气中的气态水、 二氧化碳及部分氮气等组分, 未吸附 的部分氮和不易吸附的氧和氩等组分从出口端排出进入第二段变压吸附装置 处于吸附步骤的吸附塔, 吸附塔中的分子筛选择性地吸附氮气, 不易吸附的 氧和氩等组分从出口端排出进入产品富氧缓冲罐。 第一段变压吸附装置处于 吸附步骤的吸附塔出口气中氧气浓度控制在 21〜23% ( V), 其吸附塔在一个 循环周期中依次经历吸附 A、 置换 P'、 抽真空 VC;、 二段气逆向第三次均压升 压 2ER3、二段气逆向第二次均压升压 2ER2、二段气逆向第一次均压升压 2ER1、 置换气升压 R'、 最终升压 FR变压吸附工艺歩骤; 第二段变压吸附装置处于 吸附步骤的吸附塔出口气中氧气浓度控制在 93% ( V ) 左右, 其吸附塔在一个 循环周期中依次经历吸附 A、 顺向均压降压 ED、 逆向第一次均压降压 BID'、 逆向第二次均压降压 B2D'、 逆向第三次均压降压 B3D'、 逆向均压升压 ER、 最终升压 FR变压吸附工艺步骤。
本实施例结果为氧气浓度大于 93% ( V ) , 氮气浓度大于 99. 7% (V ) ,氧 气回收率大于 98. 5% (V) o
本发明的实施例 4:
本例的原料气为空气。 第一段变压吸附装置处于吸附步骤的吸附塔出口 气中氧气浓度控制在 21〜23% (V ) , 第二段变压吸附装置处于吸附步骤的吸 附塔出口气中氧气浓度控制在 93% (V) 左右 (即产品富氧)。
本实施例的空气组成如下:
Figure imgf000010_0001
温度: 45 °C
压力: 0. 02 MPa (G )
第一段变压吸附装置吸附塔内由下到上装填的吸附剂依次为活性氧化铝 及分子筛第二段变压吸附装置吸附塔内装填的吸附剂为分子筛。 本实施例将 上述二段变压吸附装置串联操作,第一段变压吸附装置脱除空气中的气态水、 二氧化碳及部分氮气, 第二段变压吸附装置用于将第一段变压吸附装置吸附 塔吸附步骤流出的中间气中的氮进一步脱除, 并把氧提高至所需的浓度。
空气进入第一段变压吸附装置处于吸附步骤的吸附塔, 吸附塔中的吸附 剂选择性地依次吸附空气中的气态水、 二氧化碳及部分氮气等组分, 未吸附 的部分氮和不易吸附的氧和氩等组分从出口端排出进入第二段变压吸附装置 处于吸附步骤的吸附塔, 吸附塔中的分子筛选择性地吸附氮气, 不易吸附的 氧和氩等组分从出口端排出进入产品富氧缓冲罐。 第一段变压吸附装置处于 吸附步骤的吸附塔出口气中氧气浓度控制在 21〜23% ( V ) , 其吸附塔在一个 循环周期中依次经历吸附 A、 置换 P'、 抽真空 VC;、 二段气逆向第三次均压升 压 2ER3、二段气逆向第二次均压升压 2ER2、二段气逆向第一次均压升压 2ER1、 置换气升压 R'、 最终升压 FR变压吸附工艺步骤; 第二段变压吸附装置处于 吸附步骤的吸附塔出口气中氧气浓度控制在 93% ( V )左右, 其吸附塔在一个 循环周期中依次经历吸附 A、 逆向第一次均压降压 BID'、 逆向第二次均压降 压 B2D'、 逆向第三次均压降压 B3D'、 最终升压 FR变压吸附工艺歩骤。
本实施例结果为氧气浓度大于 93% ( V ) , 氮气浓度大于 99. 7% (V ) ,氧 气回收率大于 98. 5% ( V)。
本发明的实施例 5 :
本例的原料气为空气。 第一段变压吸附装置处于吸附步骤的吸附塔出口 气中氧气浓度控制在 21〜23% ( V ), 第二段变压吸附装置处于吸附步骤的吸 附塔出口气中氧气浓度控制在 93% ( V ) 左右 (即产品富氧)。
本实施例的空气组成如下:
Figure imgf000011_0001
温度: 45°C
压力: 0. 02 MPa (G)
第一段变压吸附装置吸附塔内由下到上装填的吸附剂依次为活性氧化铝 及分子筛第二段变压吸附装置吸附塔内装填的吸附剂为分子筛。 本实施例将 上述二段变压吸附装置串联操作,第一段变压吸附装置脱除空气中的气态水、 二氧化碳及部分氮气, 第二段变压吸附装置用于将第一段变压吸附装置吸附 塔吸附步骤流出的中间气中的氮进一步脱除, 并把氧提高至所需的浓度。
空气进入第一段变压吸附装置处于吸附步骤的吸附塔, 吸附塔中的吸附 剂选择性地依次吸附空气中的气态水、 二氧化碳及部分氮气等组分, 未吸附 的部分氮和不易吸附的氧和氩等组分从出口端排出进入第二段变压吸附装置 处于吸附步骤的吸附塔, 吸附塔中的分子筛选择性地吸附氮气, 不易吸附的 氧和氩等组分从出口端排出进入产品富氧缓冲罐。 第一段变压吸附装置处于 吸附步骤的吸附塔出口气中氧气浓度控制在 21〜23% (V) , 其吸附塔在一个 循环周期中依次经历吸附 A、 置换 P'、 抽真空 VC;、 二段气逆向第三次均压升 压 2ER3、二段气逆向第二次均压升压 2ER2、二段气逆向第一次均压升压 2ER1、 置换气升压 R'、 最终升压 FR变压吸附工艺步骤; 第二段变压吸附装置处于 吸附步骤的吸附塔出口气中氧气浓度控制在 93% ( V )左右, 其吸附塔在一个 循环周期中依次经历吸附 A、 顺向均压降压 ED、 逆向第一次均压降压 BID -、 逆向第二次均压降压 B2D'、 逆向第三次均压降压 B3D'、 逆向均压升压 ER、 最终升压 FR变压吸附工艺步骤。 .
本实施例结果为氧气浓度大于 93% (V ) , 氮气浓度大于 99. 7% ( V ) ,氧 气回收率大于 98. 5% ( V)。
本发明的实施例 6 :
本例的原料气为空气。 第一段变压吸附装置处于吸附步骤的吸附塔出口 气中氧气浓度控制在 21〜23% (V), 第二段变压吸附装置处于吸附步骤的吸 附塔出口气中氧气浓度控制在 93% ( V ) 左右 (即产品富氧)。
本实施例的空气组成如下:
Figure imgf000012_0001
温度: 45 °C
压力: 0. 05 MPa ( G)
第一段变压吸附装置吸附塔内由下到上装填的吸附剂依次为活性氧化铝 及分子筛第二段变压吸附装置吸附塔内装填的吸附剂为分子筛。 本实施例将 上述二段变压吸附装置串联操作,第一段变压吸附装置脱除空气中的气态水、 二氧化碳及部分氮气, 第二段变压吸附装置用于将第一段变压吸附装置吸附 塔吸附步骤流出的中间气中的氮进一步脱除, 并把氧提高至所需的浓度。
空气进入第一段变压吸附装置处于吸附步骤的吸附塔, 吸附塔中的吸附 剂选择性地依次吸附空气中的气态水、 二氧化碳及部分氮气等组分, 未吸附 的部分氮和不易吸附的氧和氩等组分从出口端排出进入第二段变压吸附装置 处于吸附步骤的吸附塔, 吸附塔中的分子筛选择性地吸附氮气, 不易吸附的 氧和氩等组分从出口端排出进入产品富氧缓冲罐。 第一段变压吸附装置处于 吸附步骤的吸附塔出口气中氧气浓度控制在 21〜23% (V ) , 其吸附塔在一个 循环周期中依次经历吸附 A、 两端均压降压 2ED'、 置换 P'、 抽真空 VC、 二段 气逆向第三次均压升压 2ER3、二段气逆向第二次均压升压 2ER2、二段气逆向 第 次均压升压 2ER1、 两端均压升压 2ER'、 置换气升压 R'、 最终升压 FR变 压吸附工艺步骤; 第二段变压吸附装置处于吸附步骤的吸附塔出口气中氧气 浓度控制在 93% (V) 左右, 其吸附塔在一个循环周期中依次经历吸附 A、 逆 向第一次均压降压 BiD'、 逆向第二次均压降压 B2D'、 逆向第三次均压降压 B3D'、 最终升压 FR变压吸附工艺步骤。 本实施例结果为氧气浓度大于 93% (V ) , 氮气浓度大于 99. 7% ( V ) ,氧 气回收率大于 98. 5% ( V)。
本发明的实施例 7 :
本例的原料气为空气。 第一段变压吸附装置处于吸附步骤的吸附塔出口 气中氧气浓度控制在 21〜23% (V) , 第二段变压吸附装置处于吸附步骤的吸 附塔出口气中氧气浓度控制在 93% (V ) 左右 (即产品富氧)。
本实施例的空气组成如下:
Figure imgf000013_0002
Figure imgf000013_0001
压力: 0. 05 MPa ( G )
第一段变压吸附装置吸附塔内由下到上装填的吸附剂依次为活性氧化铝 及分子筛第二段变压吸附装置吸附塔内装填的吸附剂为分子筛。 本实施例将 上述二段变压吸附装置串联操作,第一段变压吸附装置脱除空气中的气态水、 二氧化碳及部分氮气, 第二段变压吸附装置用于将第一段变压吸附装置吸附 塔吸附步骤流出的中间气中的氮进一步脱除, 并把氧提高至所需的浓度。
空气进入第一段变压吸附装置处于吸附步骤的吸附塔, 吸附塔中的吸附 剂选择性地依次吸附空气中的气态水、 二氧化碳及部分氮气等组分, 未吸附 的部分氮和不易吸附的氧和氩等组分从出口端排出进入第二段变压吸附装置 处于吸附步骤的吸附塔, 吸附塔中的分子筛选择性地吸附氮气, 不易吸附的 氧和氩等组分从出口端排出进入产品富氧缓冲罐。 第一段变压吸附装置处于 吸附步骤的吸附塔出口气中氧气浓度控制在 21〜23% ( V ) , 其吸附塔在一个 循环周期中依次经历吸附 A、 两端均压降压 2ED'、 置换 P'、 逆向降压 BD、 抽 真空 VC、二段气逆向第三次均压升压 2ER3、二段气逆向第二次均压升压 2ER2、 二段气逆向第一次均压升压 2ER1、 两端均压升压 2ER'、 置换气升压 R '、 最 •终升压 FR变压吸附工艺步骤;第二段变压吸附装置处于吸附步骤的吸附塔出 口气中氧气浓度控制在 93% (V )左右, 其吸附塔在一个循环周期中依次经历 吸附 A、 逆向第一次均压降压 BID'、 逆向第二次均压降压 B2D'、 逆向第三次 均压降压 B3D'、 最终升压 FR变压吸附工艺步骤。
本实施例结果为氧气浓度大于 93% ( V ) , 氮气浓度大于 99. 7% ( V ) ,氧 气回收率大于 98. 5% (V ) o
本发明的实施例 8:
本例的原料气为空气。 第一段变压吸附装置处于吸附步骤的吸附塔出口 气中氧气浓度控制在 21〜23% (V ) , 第二段变压吸附装置处于吸附步骤的吸 附塔出口气中氧气浓度控制在 93% (V ) 左右 (即产品富氧)。
本实施例的空气组成如下:
Figure imgf000014_0001
温度: 45°C
压力: 0. 05 MPa ( G )
第一段变压吸附装置吸附塔内由下到上装填的吸附剂依次为活性氧化铝 及分子筛第二段变压吸附装置吸附塔内装填的吸附剂为分子筛。 本实施例将 上述二段变压吸附装置串联操作,第一段变压吸附装置脱除空气中的气态水、 二氧化碳及部分氮气, 第二段变压吸附装置用于将第一段变压吸附装置吸附 塔吸附步骤流出的中间气中的氮进一步脱除, 并把氧提高至所需的浓度。
空气进入第一段变压吸附装置处于吸附步骤的吸附塔, 吸附塔中的吸附 剂选择性地依次吸附空气中的气态水、 二氧化碳及部分氮气等组分, 未吸附 的部分氮和不易吸附的氧和氩等组分从出口端排出进入第二段变压吸附装置 处于吸附步骤的吸附塔, 吸附塔中的分子筛选择性地吸附氮气, 不易吸附的 氧和氩等组分从出口端排出进入产品富氧缓冲罐。 第一段变压吸附装置处于 吸附步骤的吸附塔出口气中氧气浓度控制在 21〜23% ( V ) , 其吸附塔在一个 循环周期中依次经历吸附 A、 两端均压降压 2ED'、 置换 P'、 抽真空 VC、 二段 气逆向第三次均压升压 2ER3、二段气逆向第二次均压升压 2ER2、二段气逆向 第一次均压升压 2ER1、 两端均压升压 2ER'、 置换气升压 R'、 最终升压 FR变 压吸附工艺步骤; 第二段变压吸附装置处于吸附步骤的吸附塔出口气中氧气 浓度控制在 93% ( V) 左右, 其吸附塔在一个循环周期中依次经历吸附 A、 顺 向均压降压 ED、 逆向第一次均压降压 BID'、 逆向第二次均压降压 B2D'、 逆 向第三次均压降压 B3D'、逆向均压升压 ER、最终升压 FR变压吸附工艺步骤。
本实施例结果为氧气浓度大于 93% ( V ) , 氮气浓度大于 99. 7% (V ) ,氧 气回收率大于 98. 5% (V ) o
' 本发明的实施例 9 :
本例的原料气为空气。 第一段变压吸附装置处于吸附步骤的吸附塔出口 气中氧气浓度控制在 21〜23% ( V ), 第二段变压吸附装置处于吸附步骤的吸 附塔出口气中氧气浓度控制在 93% ( V) 左右 (即产品富氧)。
本实施例的空气组成如下:
组 份 0, Ar CO, 其它 ∑
浓度 (%)
20. 93 78. 03 0. 932 0. 03 0. 078 100
( V) 温度: 45°C
压力: 0. 05 MPa (G )
第一段变压吸附装置吸附塔内由下到上装填的吸附剂依次为活性氧化铝 及分子筛第二段变压吸附装置吸附塔内装填的吸附剂为分子筛。 本实施例将 上述二段变压吸附装置串联操作,第一段变压吸附装置脱除空气中的气态水、 二氧化碳及部分氮气, 第二段变压吸附装置用于将第一段变压吸附装置吸附 塔吸附步骤流出的中间气中的氮进一步脱除, 并把氧提高至所需的浓度。
空气进入第一段变压吸附装置处于吸附步骤的吸附塔, 吸附塔中的吸附 剂选择性地依次吸附空气中的气态水、 二氧化碳及部分氮气等组分, 未吸附 的部分氮和不易吸附的氧和氩等组分从出口端排出进入第二段变压吸附装置 处于吸附步骤的吸附塔, 吸附塔中的分子筛选择性地吸附氮气, 不易吸附的 氧和氩等组分从出口端排出进入产品富氧缓冲罐。 第一段变压吸附装置处于 吸附步骤的吸附塔出口气中氧气浓度控制在 21〜23% ( V ) , 其吸附塔在一个 循环周期中依次经历吸附 A、 两端均压降压 2ED'、 置换 P'、 逆向降压 BD、 抽 真空 VC、二段气逆向第三次均压升压 2ER3、二段气逆向第二次均压升压 2ER2、 二段气逆向第一次均压升压 2ER1、 两端均压升压 2ER'、 置换气升压 R'、 最 终升压 FR变压吸附工艺步骤;第二段变压吸附装置处于吸附步骤的吸附塔出 口气中氧气浓度控制在 93% (V )左右, 其吸附塔在一个循环周期中依次经历 吸附 A、 顺向均压降压 ED、 逆向第一次均压降压 BID'、 逆向第二次均压降压 B2D'、 逆向第三次均压降压 B3D'、 逆向均压升压 ER、 最终升压 FR变压吸附 工艺步骤。
本实施例结果为氧气浓度大于 93% (V ) , 氮气浓度大于 99. 7% (V ) ,氧 气回收率大于 98. 5% ( V ) o
本发明的实施例 10:
本例的原料气为空气。 第一段变压吸附装置处于吸附步骤的吸附塔出口 气中氧气浓度控制在 21〜23% ( V ), 第二段变压吸附装置处于吸附步骤的吸 附塔出口气中氧气浓度控制在 93% ( V ) 左右 (即产品富氧)。
本实施例的空气组成如下:
Figure imgf000015_0001
温度: 45 °C
压力: 0. 1 MPa (G) - 第一段变压吸附装置吸附塔内由下到上装填的吸附剂依次为活性氧化铝 及分子筛第二段变压吸附装置吸附塔内装填的吸附剂为分子筛。 本实施例将 上述二段变压吸附装置串联操作,第一段变压吸附装置脱除空气中的气态水、 二氧化碳及部分氮气, 第二段变压吸附装置用于将第一段变压吸附装置吸附 塔吸附步骤流出的中间气中的氮进一步脱除, 并把氧提高至所需的浓度。
空气进入第一段变压吸附装置处于吸附步骤的吸附塔, 吸附塔中的吸附 剂选择性地依次吸附空气中的气态水、 二氧化碳及部分氮气等组分, 未吸附 的部分氮和不易吸附的氧和氩等组分从出口端排出进入第二段变压吸附装置 处于吸附步骤的吸附塔, 吸附塔中的分子筛选择性地吸附氮气, 不易吸附的 氧和氩等组分从出口端排出进入产品富氧缓冲罐。 第一段变压吸附装置处于 吸附步骤的吸附塔出口气中氧气浓度控制在 2卜 23% (V ) , 其吸附塔在一个 循环周期中依次经历吸附 A、 两端均压降压 2ED'、 置换 P'、 逆向降压 BD、 抽 真空 VC、二段气逆向第三次均压升压 2ER3、二段气逆向第二次均压升压 2ER2、 二段气逆向第一次均压升压 2ER1、 两端均压升压 2ER'、 置换气升压 R'、 最 终升压 FR变压吸附工艺歩骤;第二段变压吸附装置处于吸附步骤的吸附塔出 口气中氧气浓度控制在 93% ( V )左右, 其吸附塔在一个循环周期中依次经历 吸附 A、 顺向均压降压 ED、 逆向第一次均压降压 BID'、 逆向第二次均压降压 B2D'、 逆向第三次均压降压 B3D'、 逆向均压升压 £!^、.最终升压 FR变压吸附 工艺步骤。
本实施例结果为氧气浓度大于 93% ( V ) , 氮气浓度大于 99. 9°/。 ( V ) ,氧 气回收率大于 99% ( V)。
本发明的实施例 11 :
本例的原料气为空气。 第一段变压吸附装置处于吸附歩骤的吸附塔出口 气中氧气浓度控制在 21〜23% ( V ) , 第二段变压吸附装置处于吸附步骤的吸 附塔出口气中氧气浓度控制在 93% (V ) 左右 (即产品富氧)。
本实施例的空气组成如下:
Figure imgf000016_0001
温度: 45°C
压力: 0. 3 MPa (G )
第一段变压吸附装置吸附塔内由下到上装填的吸附剂依次为活性氧化铝 及分子筛第二段变压吸附装置吸附塔内装填的吸附剂为分子筛。 本实施例将 上述二段变压吸附装置串联操作,第一段变压吸附装置脱除空气中的气态水、 二氧化碳及部分氮气, 第二段变压吸附装置用于将第一段变压吸附装置吸附 塔吸附步骤流出的中间气中的氮进一步脱除, 并把氧提高至所需的浓度。
空气进入第一段变压吸附装置处于吸附步骤的吸附塔, 吸附塔中的吸附 剂选择性地依次吸附空气中的气态水、 二氧化碳及部分氮气等组分, 未吸附 的部分氮和不易吸附的氧和氩等组分从出口端排出进入第二段变压吸附装置 处于吸附步骤的吸附塔, 吸附塔中的分子筛选择性地吸附氮气, 不易吸附的 氧和氩等组分从出口端排出进入产品富氧缓冲罐。 第一段变压吸附装置处于 吸附步骤的吸附塔出口气中氧气浓度控制在 21〜23% ( V ), 其吸附塔在一个 循环周期中依次经历吸附 A、两端第一次均压降压 2E1D'、两端第二次均压降 压 2E2D'、 两端第三次均压降压 2E3D '、 置换 P '、 逆向降压 BD、 抽真空 VC、 二段气逆向第三次均压升压 2ER3、二段气逆向第二次均压升压 2ER2、二段气 逆向第一次均压升压 2ER1、 两端第三次均压升压 2E3R'、 两端第二次均压升 压 2E2R'、 两端第一次均压升压 2E1 R'、 置换气升压 R'、 最终升压 FR变压吸 附工艺步骤; 第二段变压吸附装置处于吸附步骤的吸附塔出口气中氧气浓度 控制在 93% ( V ) 左右, 其吸附塔在一个循环周期中依次经历吸附 A、 顺向第 一次均压降压 E1D、 顺向第二次均压降压 E2D、 顺向第三次均压降压 E3D、 逆 向第一次均压降压 B1D '、 逆向第二次均压降压 B2D'、 逆向第三次均压降压 B3D '、逆向第三次均压升压 E3R、逆向第二次均压升压 E2R、逆向第一次均压 升压 E1R、 最终升压 FR变压吸附工艺步骤。
本实施例结果为氧气浓度大于 93% ( V ) , 氮气浓度大于 99. 9% ( V ) ,氧 气回收率大于 99% ( V)。
本发明的实施例 12 :
本例的原料气为空气。 第一段变压吸附装置处于吸附步骤的吸附塔出口 气中氧气浓度控制在 21〜23% ( V ) , 第二段变压吸附装置处于吸附步骤的吸 附塔出口气中氧气浓度控制在 93% ( V ) 左右 (即产品富氧)。
本实施例的空气组成如下:
Figure imgf000017_0001
温度: 45 °C
压力: 0. 3 MPa ( G )
第一段变压吸附装置吸附塔内由下到上装填的吸附剂依次为活性氧化铝 及分子筛第二段变压吸附装置吸附塔内装填的吸附剂为分子筛。 本实施例将 上述二段变压吸附装置串联操作,第一段变压吸附装置脱除空气中的气态水、 二氧化碳及部分氮气, 第二段变压吸附装置用于将第一段变压吸附装置吸附 塔吸附步骤流出的中间气中的氮进一步脱除, 并把氧提高至所需的浓度。
空气进入第一段变压吸附装置处于吸附步骤的吸附塔, 吸附塔中的吸附 剂选择性地依次吸附空气中的气态水、 二氧化碳及部分氮气等组分, 未吸附 的部分氮和不易吸附的氧和氩等组分从出口端排出进入第二段变压吸附装置 处于吸附步骤的吸附塔, 吸附塔中的分子筛选择性地吸附氮气, 不易吸附的 氧和氩等组分从出口端排出进入产品富氧缓冲耀。 第一段变压吸附装置处于 吸附步骤的吸附塔出口气中氧气浓度控制在 21〜23% (V), 其吸附塔在一个 循环周期中依次经历吸附 A、 两端均压降压 2ED'、 置换 P'、 逆向降压 BD、 抽 真空 VC、二段气逆向第三次均压升压 2ER3、二段气逆向第二次均压升压 2ER2、 二段气逆向第一次均压升压 2ER1、 两端均压升压 2ER'、 置换气升压 R'、 最 终升压 FR '变压吸附工艺步骤;第二段变压吸附装置处于吸附步骤的吸附塔出 口气中氧气浓度控制在 93% (V)左右, 其吸附塔在一个循环周期中依次经历 吸附 A、 顺向第一次均压降压 E1D、 顺向第二次均压降压 E2D、 顺向第三次均 压降压 E3D、 逆向第一次均压降压 BID'、 逆向第二次均压降压 B2D'、 逆向第 三次均压降压 B3D'、 逆向第三次均压升压 E3R、 逆向第二次均压升压 E2R、 逆向第一次均压升压 E1R、 最终升压 FR变压吸附工艺步骤。
本实施例结果为氧气浓度大于 93% (V ) , 氮气浓度大于 99. 9% ( V ) ,氧 气回收率大于 99% ( V)。
' 本发明的实施例 13 :
本例的原料气为空气。 第一段变压吸附装置处于吸附步骤的吸附塔出口 气中氧气浓度控制在 21〜23% (V) , 第二段变压吸附装置处于吸附步骤的吸 附塔出口气中氧气浓度控制在 93% (V) 左右 (即产品富氧)。
本实施例的空气组成如下:
Figure imgf000018_0001
温度: 45°C
压力: 0. 01 MPa ( G )
第一段变压吸附装置吸附塔内由下到上装填的吸附剂依次为活性氧化铝 及分子筛第二段变压吸附装置吸附塔内装填的吸附剂为分子筛。 本实施例将 上述二段变压吸附装置串联操作,第一段变压吸附装置脱除空气中的气态水、 二氧化碳及部分氮气, 第二段变压吸附装置用于将第一段变压吸附装置吸附 塔吸附步骤流出的中间气中的氮进一步脱除, 并把氧提高至所需的浓度。
空气进入第一段变压吸附装置处于吸附步骤的吸附塔, 吸附塔中的吸附 剂选择性地依次吸附空气中的气态水、 二氧化碳及部分氮气等组分, 未吸附 的部分氮和不易吸附的氧和氩等组分从出口端排出进入第二段变压吸附装置 处于吸附步骤的吸附塔, 吸附塔中的分子筛选择性地吸附氮气, 不易吸附的 氧和氩等组分从出口端排出进入产品富氧缓冲罐。 第一段变压吸附装置处于 吸附步骤的吸附塔出口气中氧气浓度控制在 21〜23% ( V ) , 其吸附塔在一个 循环周期中依次经历吸附 A、 置换 P'、 抽真空 VC;、 二段气逆向第三次均压升 压 2ER3、二段气逆向第二次均压升压 2ER2、二段气逆向第一次均压升压 2ER1、 置换气升压 R'、 最终升压 FR变压吸附工艺步骤; 第二段变压吸附装置处于 吸附步骤的吸附塔出口气中氧气浓度控制在 93% ( V )左右, 其吸附塔在一个 循环周期中依次经历吸附 A、 逆向第一次均压降压 BID'、 逆向第二次均压降 压 B2D'、 逆向第三次均压降压 B3D'、 最终升压 FR变压吸附工艺步骤, 第二 段变压吸附装置吸附塔逆向第一次均压降压 BID'的气体放入缓冲罐 V I进行 均压,再用缓冲罐 VI的气体与第一段变压吸附装置吸附塔逆向第一次均压升 压 2ER1的吸附塔进行压力平衡;第二段变压吸附装置吸附塔逆向第二次均压 降压 B2D'的气体放入缓冲罐 V2进行均压,再用缓冲罐 V2 的气体与第一段变 压吸附装置吸附塔逆向第二次均压升压 2ER2的吸附塔进行压力平衡;第二段 变压吸附装置吸附塔逆向第三次均压降压 B3D'的气体放入缓冲罐 V3进行均 压,再用缓冲罐 V3的气体与第一段变压吸附装置吸附塔逆向第三次均压升压 2ER3的吸附塔进行压力平衡。
本实施例结果为氧气浓度大于 93% (V ) , 氮气浓度大于 99. 7% ( V ) ,氧 气回收率大于 98. 5% (V)。
本发明的实施例 14:
本例的原料气为空气。 第一段变压吸附装置处于吸附步骤的吸附塔出口 气中氧气浓度控制在 21〜23% ( V ) , 第二段变压吸附装置处于吸附步骤的吸 附塔出口气中氧气浓度控制在 93% ( V ) 左右 (即产品富氧)。
本实施例的空气组成如下:
Figure imgf000019_0001
温度: 45。C
压力: 0. 01 MPa (G )
第一段变压吸附装置吸附塔内由下到上装填的吸附剂依次为活性氧化铝 及分子筛第二段变压吸附装置吸附塔内装填的吸附剂为分子筛。 本实施例将 上述二段变压吸附装置串联操作,第一段变压吸附装置脱除空气中的气态水、 二氧化碳及部分氮气, 第二段变压吸附装置用于将第一段变压吸附装置吸附 塔吸附步骤流出的中间气中的氮进一步脱除, 并把氧提高至所需的浓度。
空气进入第一段变压吸附装置处于吸附步骤的吸附塔, 吸附塔中的吸附 剂选择性地依次吸附空气中的气态水、 二氧化碳及部分氮气等组分, 未吸附 的部分氮和不易吸附的氧和氩等组分从出口端排出进入第二段变压吸附装置 处于吸附步骤的吸附塔, 吸附塔中的分子筛选择性地吸附氮气, 不易吸附的 氧和氩等组分从出口端排出进入产品富氧缓冲罐。 第一段变压吸附装置处于 吸附步骤的吸附塔出口气中氧气浓度控制在 21〜23% (V ) , 其吸附塔在一个 循环周期中依次经历吸附 A、 置换 P'、 抽真空 VC、 二段气逆向第三次均压升 压 2ER3、二段气逆向第二次均压升压 2ER2、二段气逆向第一次均压升压 2ER1、 置换气升压 R'、 最终升压 FR变压吸附工艺步骤; 第二段变压吸附装置处于 吸附步骤的吸附塔出口气中氧气浓度控制在 93% ( V ) 左右, 其吸附塔在一个 循环周期中依次经历吸附 A、 顺向均压降压 ED、 逆向第一次均压降压 BID'、 逆向第二次均压降压 B2D'、 逆向第三次均压降压 B3D'、 逆向均压升压 ER、 最终升压 FR变压吸附工艺步骤, 第二段变压吸附装置吸附塔逆向第一次均压 降压 BID'的气体放入缓冲罐 V I进行均压,再用缓冲罐 VI 的气体与第一段变 压吸附装置吸附塔逆向第一次均压升压 2ER1的吸附塔进行压力平衡;第二段 变压吸附装置吸附塔逆向第二次均压降压 B2D'的气体放入缓冲罐 V2进行均 压,再用缓冲罐 V2的气体与第一段变压吸附装置吸附塔逆向第二次均压升压 2ER2的吸附塔进行压力平衡;第二段变压吸附装置吸附塔逆向第三次均压降 压 B3D'的气体放入缓冲罐 V3进行均压,再用缓冲罐 V3 的气体与第一段变压 吸附装置吸附塔逆向第三次均压升压 2ER3的吸附塔进行压力平衡。
本实施例结果为氧气浓度大于 93% (V ) , 氮气浓度大于 99. 7% ( V ) ,氧 气回收率大于 98. 5% (V) o
本发明的实施例 15 :
本例的原料气为空气。 第一段变压吸附装置处于吸附步骤的吸附塔出口 气中氧气浓度控制在 21〜23% ( V ), 第二段变压吸附装置处于吸附步骤的吸 附塔出口气中氧气浓度控制在 93% (V ) 左右 (即产品富氧)。
本实施例的空气组成如下:
Figure imgf000020_0001
温度: 45°C
压力: 0. 05 MPa (G)
第一段变压吸附装置吸附塔内由下到上装填的吸附剂依次为活性氧化铝 及分子筛第二段变压吸附装置吸附塔内装填的吸附剂为分子筛。 本实施例将 上述二段变压吸附装置串联操作,第一段变压吸附装置脱除空气中的气态水、 二氧化碳及部分氮气, 第二段变压吸附装置用于将第一段变压吸附装置吸附 塔吸附步骤流出的中间气中的氮进一步脱除, 并把氧提高至所需的浓度。
空气进入第一段变压吸附装置处于吸附步骤的吸附塔, 吸附塔中的吸附 剂选择性地依次吸附空气中的气态水、 二氧化碳及部分氮气等组分, 未吸附 的部分氮和不易吸附的氧和氩等组分从出口端排出进入第二段变压吸附装置 处于吸附步骤的吸附塔, 吸附塔中的分子筛选择性地吸附氮气, 不易吸附的 氧和氩等组分从出口端排出进入产品富氧缓冲罐。 第一段变压吸附装置处于 吸附步骤的吸附塔出口气中氧气浓度控制在 21〜23% (V ) , 其吸附塔在一个 循环周期中依次经历吸附 A、 两端均压降压 2ED'、 置换 P'、 抽真空 VC、 二段 气逆向第三次均压升压 2ER3、二段气逆向第二次均压升压 2ER2、二段气逆向 第一次均压升压 2ER1、 两端均压升压 2ER'、 置换气升压 R '、 最终升压 FR变 压吸附工艺步骤; 第二段变压吸附装置处于吸附步骤的吸附塔出口气中氧气 浓度控制在 93% ( V ) 左右, 其吸附塔在一个循环周期中依次经历吸附 A、 逆 向第一次均压降压 B1D'、 逆向第二次均压降压 B2D'、 逆向第三次均压降压 B3D'、最终升压 FR变压吸附工艺步骤, 第二段变压吸附装置吸附塔逆向第一 次均压降压 BID'的气体放入缓冲罐 VI进行均压,再用缓冲罐 VI 的气体与第 一段变压吸附装置吸附塔逆向第一次均压升压 2ER1的吸附塔进行压力平衡; 第二段变压吸附装置吸附塔逆向第二次均压降压 B2D'的气体放入缓冲罐 V2 进行均压,再用缓冲罐 V2的气体与第一段变压吸附装置吸附塔逆向第二次均 压升压 2ER2的吸附塔进行压力平衡;第二段变压吸附装置吸附塔逆向第三次 均压降压 B3D'的气体放入缓冲罐 V3进行均压,再用缓冲罐 V3 的气体与第一 段变压吸附装置吸附塔逆向第三次均压升压 2ER3的吸附塔进行压力平衡。
本实施例结果为氧气浓度大于 93% (V ) , 氮气浓度大于 99. 7% ( V ) ,氧 气回收率大于 98. 5°/。 (V)。
本发明的实施例 16 :
本例的原料气为空气。 第一段变压吸附装置处于吸附步骤的吸附塔出口 气中氧气浓度控制在 21〜23% ( V ) , 第二段变压吸附装置处于吸附步骤的吸 附塔出口气中氧气浓度控制在 93% (V) 左右 (即产品富氧)。
本实施例的空气组成如下:
Figure imgf000021_0001
45 C
压力: 0. 05 MPa ( G )
第一段变压吸附装置吸附塔内由下到上装填的吸附剂依次为活性氧化铝 及分子筛第二段变压吸附装置吸附塔内装填的吸附剂为分子筛。 本实施例将 上述二段变压吸附装置串联操作,第一段变压吸附装置脱除空气中的气态水、 二氧化碳及部分氮气, 第二段变压吸附装置用于将第一段变压吸附装置吸附 塔吸附步骤流出的中间气中的氮进一步脱除, 并把氧提高至所需的浓度。 空气进入第一段变压吸附装置处于吸附步骤的吸附塔, 吸附塔中的吸附 剂选择性地依次吸附空气中的气态水、 二氧化碳及部分氮气等组分, 未吸附 的部分氮和不易吸附的氧和氩等组分从出口端排出进入第二段变压吸附装置 处于吸附步骤的吸附塔, 吸附塔中的分子筛选择性地吸附氮气, 不易吸附的 氧和氩等组分从出口端排出进入产品富氧缓冲罐。 第一段变压吸附装置处于 吸附步骤的吸附塔出口气中氧气浓度控制在 21〜23% (V ) , 其吸附塔在一个 循环周期中依次经历吸附 A、 两端均压降压 2ED'、 置换 P'、 抽真空 VC、 二段 气逆向第三次均压升压 2ER3、二段气逆向第二次均压升压 2ER2、二段气逆向 第一次均压升压 2ER1、 两端均压升压 2ER'、 置换气升压 R'、 最终升压 FR变 压吸附工艺步骤; 第二段变压吸附装置处于吸附步骤的吸附塔出口气中氧气 浓度控制在 93% (V ) 左右, 其吸附塔在一个循环周期中依次经历吸附 A、 顺 向均压降压 ED、 逆向第一次均压降压 BID'、 逆向第二次均压降压 B2D'、 逆 向第三次均压降压 B3D'、逆向均压升压 ER、最终升压 FR变压吸附工艺步骤, 第二段变压吸附装置吸附塔逆向第一次均压降压 BID '的气体放入缓冲罐 VI 进行均压,再用缓冲罐 VI的气体与第一段变压吸附装置吸附塔逆向第一次均 压升压 2ER1的吸附塔进行压力平衡;第二段变压吸附装置吸附塔逆向第二次 均压降压 B2D'的气体放入缓冲罐 V2进行均压,再用缓冲罐 V2 的气体与第一 段变压吸附装置吸附塔逆向第二次均压升压 2ER2的吸附塔进行压力平衡;第 二段变压吸附装置吸附塔逆向第三次均压降压 B3D'的气体放入缓冲罐 V3进 行均压,再用缓冲罐 V3的气体与第一段变压吸附装置吸附塔逆向第三次均压 升压 2ER3的吸附塔进行压力平衡。
本实施例结果为氧气浓度大于 93% ( V ) , 氮气浓度大于 99. 7% ( V ) ,氧 气回收率大于 98. 5% (V )o
本发明的实施例 17 :
本例的原料气为空气。 第一段变压吸附装置处于吸附步骤的吸附塔出口 气中氧气浓度控制在 21〜23% ( V ) , 第二段变压吸附装置处于吸附步骤的吸 附塔出口气中氧气浓度控制在 50% (V ) 左右 (即产品富氧)。
本实施例的空气组成如下:
Figure imgf000022_0001
温度: 45 °C
压力: 0. 01 MPa (G)
吸附塔 A〜G共 7台组成第一段变压吸附装置。吸附塔内由下到上装填的 吸附剂依次为活性氧化铝及分子筛,运行三塔吸附三次均压程序:吸附塔 a〜 g共 7台组成第二段变压吸附装置,吸附塔内装填的吸附剂为分子筛,运行五 塔吸附三次均压程序。 本实施例将上述二段变压吸附装置串联操作, 第一段 变压吸附装置脱除空气中的气态水、 二氧化碳及部分氮气, 第二段变压吸附 装置用于将第一段变压吸附装置吸附塔吸附步骤流出的中间气中的氮进一步 脱除, 并把氧提高至所需的浓度。
空气进入第一段变压吸附装置处于吸附步骤的吸附塔, 吸附塔中的吸附 剂选择性地依次吸附空气中的气态水、 二氧化碳及部分氮气等组分, 未吸附 的部分氮和不易吸附的氧和氩等组分从出口端排出进入第二段变压吸附装置 处于吸附步骤的吸附塔, 吸附塔中的分子筛选择性地吸附氮气, 不易吸附的 氧和氩等组分从出口端排出进入产品富氧缓冲罐。 第一段变压吸附装置处于 吸附步骤的吸附塔出口气中氧气浓度控制在 21〜23% (V ) , 其吸附塔在一个 循环周期中依次经历吸附 A、 置换 P'、 抽真空 VC、 二段气逆向第三次均压升 压 2ER3、二段气逆向第二次均压升压 2ER2、二段气逆向第一次均压升压 2ER1、 置换气升压 R'、 最终升压 FR变压吸附工艺步骤; 第二段变压吸附装置处于 吸附步骤的吸附塔出口气中氧气浓度控制在 50% ( V )左右, 其吸附塔在一个 循环周期中依次经历吸附 A、 逆向第一次均压降压 BID'、 逆向第二次均压降 压 B2D'、 逆向第三次均压降压 B3D'、 最终升压 FR变压吸附工艺步骤。
本实施例结果为氧气浓度大于 50% ( V ) , 氮气浓度大于 99. 7% ( V ) ,氧 气回收率大于 98. 5% (V )。
本发明的实施例 18 :
本例的原料气为空气。 第一段变压吸附装置处于吸附步骤的吸附塔出口 气中氧气浓度控制在 21〜23% ( V ) , 第二段变压吸附装置处于吸附步骤的吸 附塔出口气中氧气浓度控制在 50% ( V) 左右 (即产品富氧)。
本实施例的空气组成如下:
Figure imgf000023_0001
温度: 45 °C
压力: 0. 01 MPa (G )
吸附塔 A〜G共 7台组成第一段变压吸附装置。吸附塔内由下到上装填的 吸附剂依次为活性氧化铝及分子筛,运行三塔吸附三次均压程序;吸附塔 a〜 g共 7台组成第二段变压吸附装置,吸附塔内装填的吸附剂为分子筛,运行四 塔吸附三次均压程序。 本实施例将上述二段变压吸附装置串联操作, 第 段 变压吸附装置脱除空气中的气态水、 二氧化碳及部分氮气, 第二段变压吸附 装置用于将第一段变压吸附装置吸附塔吸附步骤流出的中间气中的氮进一步 脱除, 并把氧提高至所需的浓度。
空气进入第一段变压吸附装置处于吸附步骤的吸附塔, 吸附塔中的吸附 剂选择性地依次吸附空气中的气态水、 二氧化碳及部分氮气等组分, 未吸附 的部分氮和不易吸附的氧和氩等组分从出口端排出进入第二段变压吸附装置 处于吸附步骤的吸附塔, 吸附塔中的分子筛选择性地吸附氮气, 不易吸附的 氧和氩等组分从出口端排出进入产品富氧缓冲罐。 第一段变压吸附装置处于 吸附步骤的吸附塔出口气中氧气浓度控制在 21〜23% ( V ) , 其吸附塔在一个 循环周期中依次经历吸附 A、 置换 P'、 抽真空 VC、 二段气逆向第三次均压升 压 2ER3、二段气逆向第二次均压升压 2ER2、二段气逆向第一次均压升压 2ER1、 置换气升压 R'、 最终升压 FR变压吸附工艺步骤; 第二段变压吸附装置处于 吸附步骤的吸附塔出口气中氧气浓度控制在 50% ( V )左右, 其吸附 '塔在一个 循环周期中依次经历吸附 A、 顺向均压降压 ED、 逆向第一次均压降压 BID'、 逆向第二次均压降压 B2D'、 逆向第三次均压降压 B3D'、 逆向均压升压 ER、 最终升压 FR变压吸附工艺步骤。
本实施例结果为氧气浓度大于 50% ( V ) , 氮气浓度大于 99. 7% ( V ) ,氧 气回收率大于 98. 5% (V )。
本发明的实施例 19:
本例的原料气为空气。 第一段变压吸附装置处于吸附步骤的吸附塔出口 气中氧气浓度控制在 21〜23% (V), 第二段变压吸附装置处于吸附步骤的吸 附塔出口气中氧气浓度控制在 50% ( V ) 左右 (即产品富氧)。
本实施例的空气组成如下:
Figure imgf000024_0001
温度: 45 °C
压力: 0. 05 MPa ( G)
第一段变压吸附装置吸附塔内由下到上装填的吸附剂依次为活性氧化铝 及分子筛第二段变压吸附装置吸附塔内装填的吸附剂为分子筛。 本实施例将 上述二段变压吸附装置串联操作,第一段变压吸附装置脱除空气中的气态水、 二氧化碳及部分氮气, 第二段变压吸附装置用于将第一段变压吸附装置吸附 塔吸附步骤流出的中间气中的氮进一步脱除, 并把氧提高至所需的浓度。
空气进入第一段变压吸附装置处于吸附步骤的吸附塔, 吸附塔中的吸附 剂选择性地依次吸附空气中的气态水、 二氧化碳及部分氮气等组分, 未吸附 的部分氮和不易吸附的氧和氩等组分从出口端排出进入第二段变压吸附装置 处于吸附步骤的吸附塔, 吸附塔中的分子筛选择性地吸附氮气, 不易吸附的 氧和氩等组分从出口端排出进入产品富氧缓冲罐。 第一段变压吸附装置处于
• 吸附步骤的吸附塔出口气中氧气浓度控制在 21〜23% (V ) , 其吸附塔在一个 循环周期中依次经历吸附 A、 两端均压降压 2ED'、 置换 P'、 抽真空 VC、 二段 气逆向第三次均压升压 2ER3、二段气逆向第二次均压升压 2ER2、二段气逆向 第一次均压升压 2ER1、 两端均压升压 2ER'、 置换气升压 R'、 最终升压 FR变 压吸附工艺步骤; 第二段变压吸附装置处于吸附步骤的吸附塔出口气中氧气 浓度控制在 50% ( V ) 左右, 其吸附塔在一个循环周期中依次经历吸附 A、 顺 向均压降压 ED、 逆向第一次均压降压 BID'、 逆向第二次均压降压 B2D'、 逆 向第三次均压降压 B3D'、逆向均压升压 ER、最终升压 FR变压吸附工艺步骤。
本实施例结果为氧气浓度大于 50% (V ) , 氮气浓度大于 99. 7% (V ) ,氧 气回收率大于 98. 5% (V)。
本发明的实施例 20:
本例的原料气为空气。 第一段变压吸附装置处于吸附步骤的吸附塔出口 气中氧气浓度控制在 21〜23% ( V ) , 第二段变压吸附装置处于吸附步骤的吸 附塔出口气中氧气浓度控制在 93% ( V) 左右 (即产品富氧)。
本实施例的空气组成如下:
Figure imgf000025_0001
温度: 45 °C
压力: 0. 6MPa ( G)
第一段变压吸附装置吸附塔内由下到上装填的吸附剂依次为活性氧化铝 及分子筛第二段变压吸附装置吸附塔内装填的吸附剂为分子筛。 本实施例将 上述二段变压吸附装置串联操作,第一段变压吸附装置脱除空气中的气态水、 二氧化碳及部分氮气, 第二段变压吸附装置用于将第一段变压吸附装置吸附 塔吸附步骤流出的中间气中的氮进一步脱除, 并把氧提高至所需的浓度。
空气进入第一段变压吸附装置处于吸附步骤的吸附塔, 吸附塔中的吸附 剂选择性地依次吸附空气中的气态水、 二氧化碳及部分氮气等组分, 未吸附 的部分氮和不易吸附的氧和氩等组分从出口端排出进入第二段变压吸附装置 处于吸附步骤的吸附塔, 吸附塔中的分子筛选择性地吸附氮气, 不易吸附的 氧和氩等组分从出口端排出进入产品富氧缓冲罐。 第一段变压吸附装置处于 吸附步骤的吸附塔出口气中氧气浓度控制在 21〜23% ( V), 其吸附塔在一个 循环周期中依次经历吸附 A、 两端均压降压 2ED'、 置换 P'、 逆向降压 BD、 抽 真空 VC、二段气逆向第三次均压升压 2ER3、二段气逆向第二次均压升压 2ER2、 二段气逆向第一次均压升压 2ER1、 两端均压升压 2ER'、 置换气升压 R'、 最 终升压 FR变压吸附工艺步骤;第二段变压吸附装置处于吸附步骤的吸附塔出 口气中氧气浓度控制在 93% ( V )左右, 其吸附塔在一个循环周期中依次经历 吸附 A、 顺向第一次均压降压 E1D、 顺向第二次均压降压 E2D、 顺向第三次均 压降压 E3D、 逆向第一次均压降压 BID'、 逆向第二次均压降压 B2D'、 逆向第 三次均压降压 B3P'、 逆向第三次均压升压 E3R、 逆向第二次均压升压 E2R、 逆向第一次均压升压 E1R、 最终升压 FR变压吸附工艺步骤。
本实施例结果为氧气浓度大于 93% ( V ) , 氮气浓度大于 99. 9% ( V ) ,氧 气回收率大于 99% ( V )。
本发明的实施例 21 :
本例的原料气为空气。 第一段变压吸附装置处于吸附步骤的吸附塔出口 气中氧气浓度控制在 21〜23% (V) , 第二段变压吸附装置处于吸附步骤的吸 附塔出口气中氧气浓度控制在 93% (V) 左右 (即产品富氧)。
本实施例的空气组成如下:
Figure imgf000026_0001
温度: 45°C
压力: 0. 6 MPa (G)
第一段变压吸附装置吸附塔内由下到上装填的吸附剂依次为活性氧化铝 及分子筛第二段变压吸附装置吸附塔内装填的吸附剂为分子筛。 本实施例将 上述二段变压吸附装置串联操作,第一段变压吸附装置脱除空气中的气态水、 二氧化碳及部分氮气, 第二段变压吸附装置用于将第一段变压吸附装置吸附 塔吸附步骤流出的中间气中的氮进一步脱除, 并把氧提高至所需的浓度。
空气进入第一段变压吸附装置处于吸附步骤的吸附塔, 吸附塔中的吸附 剂选择性地依次吸附空气中的气态水、 二氧化碳及部分氮气等组分, 未吸附 的部分氮和不易吸附的氧和氩等组分从出口端排出进入第二段变压吸附装置 处于吸附步骤的吸附塔, 吸附塔中的分子筛选择性地吸附氮气, 不易吸附的 氧和氩等组分从出口端排出进入产品富氧缓冲罐。 第一段变压吸附装置处于 吸附步骤的吸附塔出口气中氧气浓度控制在 21〜23% (V ) , 其吸附塔在一个 循环周期中依次经历吸附 A、 两端均压降压 .2ED'、 置换 P'、 逆向降压 BD、 抽 真空 VC、二段气逆向第三次均压升压 2ER3、二段气逆向第二次均压升压 2ER2、 二段气逆向第一次均压升压 2ER1、 两端均压升压 2ER'、 置换气升压 R '、 最 终升压 FR变压吸附工艺步骤;第二段变压吸附装置处于吸附步骤的吸附塔出 口气中氧气浓度控制在 93% (V )左右, 其吸附塔在一个循环周期中依次经历 吸附 A、 顺向第一次均压降压 E1D、 顺向第二次均压降压 E2D、 顺向第三次均 压降压 E3D、 逆向第一次均压降压 BID'、 逆向第二次均压降压 B2D '、 逆向第 三次均压降压 B3D'、 逆向第三次均压升压 E3R、 逆向第二次均压升压 E2R、 逆向第一次均压升压 E1R、 最终升压 FR变压吸附工艺步骤, 第二段变压吸附 装置吸附塔逆向第一次均压降压 BID'的气体放入缓冲罐 VI进行均压,再用缓 冲罐 VI的气体与第一段变压吸附装置吸附塔逆向第一次均压升压 2ER1的吸 附塔进行压力平衡;第二段变压吸附装置吸附塔逆向第二次均压降压 B2D'的 气体放入缓冲罐 V2迸行均压,再用缓冲罐 V2 的气体与第一段变压吸附装置 吸附塔逆向第二次均压升压 2ER2的吸附塔进行压力平衡:第二段变压吸附装 置吸附塔逆向第三次均压降压 B3D'的气体放入缓冲罐 V3进行均压,再用缓冲 罐 V3的气体与第一段变压吸附装置吸附塔逆向第三次均压升压 2ER3的吸附 塔进行压力平衡。
本实施例结果为氧气浓度大于 93% ( V ) , 氮气浓度大于 99. 9% (V ) ,氧 气回收率大于 99. 6% ( V)。
本发明的实施例 22:
本例的原料气为空气。 第一段变压吸附装置处于吸附步骤的吸附塔出口 气中氧气浓度控制在 21〜23% (V) , 第二段变压吸附装置处于吸附步骤的吸 附塔出口气中氧气浓度控制在 93% (V) 左右 (即产品富氧)。
本实施例的空气组成如下:
Figure imgf000027_0001
温度: 45°C
压力: ◦· 6 Pa (G)
第一段变压吸附装置吸附塔内由下到上装填的吸附剂依次为活性氧化铝 及分子筛第二段变压吸附装置吸附塔内装填的吸附剂为分子筛。 本实施例将 上述二段变压吸附装置串联操作,第一段变压吸附装置脱除空气中的气态水、 二氧化碳及部分氮气, 第二段变压吸附装置用于将第一段变压吸附装置吸附 塔吸附步骤流出的中间气中的氮进一步脱除, 并把氧提高至所需的浓度。
空气进入第一段变压吸附装置处于吸附步骤的吸附塔, 吸附塔中的吸附 剂选择性地依次吸附空气中的气态水、 二氧化碳及部分氮气等组分, 未吸附 的部分氮和不易吸附的氧和氩等组分从出口端排出进入第二段变压吸附装置 处于吸附步骤的吸附塔, 吸附塔中的分子筛选择性地吸附氮气, 不易吸附的 氧和氩等组分从出口端排出进入产品富氧缓冲罐。 第一段变压吸附装置处于 吸附步骤的吸附塔出口气中氧气浓度控制在 21〜23% ( V ) , 其吸附塔在一个 循环周期中依次经历吸附 A、 两端均压降压 2ED'、 置换 P'、 逆向降压 BD、 二 段气逆向第三次均压升压 2ER3、二段气逆向第二次均压升压 2ER2、二段气逆 向第一次均压升压 2ER1、 两端均压升压 2ER'、 置换气升压 R'、 最终升压 FR 变压吸附工艺歩骤; 第二段变压吸附装置处于吸附步骤的吸附塔出口气中氧 气浓度控制在 93% ( V ) 左右, 其吸附塔在一个循环周期中依次经历吸附 A、 顺向第一次均压降压 E1D、 顺向第二次均压降压 E2D、 顺向第三次均压降压 E3D、 逆向第一次均压降压 BID'、 逆向第二次均压降压 B2D'、 逆向第三次均 压降压 B3D'、 逆向第三次均压升压 E3R、 逆向第二次均压升压 E2R、 逆向第 —次均压升压 E1R、 最终升压 FR变压吸附工艺步骤, 第二段变压吸附装置吸 附塔逆向第一次均压降压 BID'的气体放入缓冲罐 V I进行均压,再用缓冲罐 V I 的气体与第一段变压吸附装置吸附塔逆向第一次均压升压 2ER1 的吸附塔进 行压力平衡; 第二段变压吸附装置吸附塔逆向第二次均压降压 B2D'的气体放 入缓冲罐 Ί2进行均压,再用缓冲罐 V2 的气体与第一段变压吸附装置吸附塔 逆向第二次均压升压 2ER2的吸附塔进行压力平衡;第二段变压吸附装置吸附 塔逆向第三次均压降压 B3D'的气体放入缓冲罐 V3进行均压,再用缓冲罐 V3 的气体与第一段变压吸附装置吸附塔逆向第三次均压升压 2ER3 的吸附塔进 行压力平衡。
本实施例结果为氧气浓度大于 93% (V ) , 氮气浓度大于 99. 9% ( V ) ,氧 气回收率大于 99. 6% ( V )。
本发明的实施例 23 :
本例的原料气为空气。 第一段变压吸附装置处于吸附步骤的吸附塔出口 气中氧气浓度控制在 21〜23°/。 (V), 第二段变压吸附装置处于吸附步骤的吸 附塔出口气中氧气浓度控制在 93% (V ) 左右 (即产品富氧)。
本实施例的空气组成如下:
Figure imgf000028_0001
温度: 45°C
压力: 0. 01 MPa (G )
吸附塔 A〜G共 7台组成第一段变压吸附装置。吸附塔内由下到上装填的 吸附剂依次为活性氧化铝及分子筛,运行三塔吸附三次均压程序;吸附塔 a〜 g共 7台组成第二段变压吸附装置,吸附塔内装填的吸附剂为分子筛,运行五 塔吸附三次均压程序。 本实施例将上述二段变压吸附装置串联操作, 第一段 变压吸附装置脱除空气中的气态水、 二氧化碳及部分氮气, 第二段变压吸附 装置用于将第一段变压吸附装置吸附塔吸附步骤流出的中间气中的氮进一步 脱除, 并把氧提高至所需的浓度。
空气进入第一段变压吸附装置处于吸附步骤的吸附塔, 吸附塔中的吸附 剂选择性地依次吸附空气中的气态水、 二氧化碳及部分氮气等组分, 未吸附 的部分氮和不易吸附的氧和氩等组分从出口端排出进入第二段变压吸附装置 处于吸附步骤的吸附塔, 吸附塔中的分子筛选择性地吸附氮气, 不易吸附的 氧和氩等组分从出口端排出进入产品富氧缓冲罐。 第一段变压吸附装置处于 吸附步骤的吸附塔出口气中氧气浓度控制在 21〜23% (V ) , 其吸附塔在一个 循环周期中依次经历吸附 A、 两端均压降压 2ED'、 抽真空 VC、 二段气逆向第 三次均压升压 2ER3、二段气逆向第二次均压升压 2ER2、二段气逆向第一次均 压升压 2ER1、 两端均压升压 2ER'、 最终升压 FR变压吸附工艺步骤; 第二段 变压吸附装置处于吸附步骤的吸附塔出口气中氧气浓度控制在 93% (V )左右, 其吸附塔在一个循环周期中依次经历吸附 \、 逆向第一次均压降压 BI D'、 逆 向第二次均压降压 B2D'、 逆向第三次均压降压 B3D'、 最终升压 FR变压吸附 工艺步骤。
本实施例结果为氧气浓度大于 93% ( V ) , 氮气浓度大于 99. 7% ( V ) ,氧 气回收率大于 98. 5%
本发明的实施例 24:
本例的原料气为空气。 第一段变压吸附装置处于吸附步骤的吸附塔出口 气中氧气浓度控制在 21〜23% (V ) , 第二段变压吸附装置处于吸附步骤的吸 附塔出口气中氧气浓度控制在 93% ( V ) 左右 (即产品富氧)。
本实施例的空气组成如下:
Figure imgf000029_0001
温度: 45。C
压力: 0. 1 Pa ( G)
吸附塔 A〜G共 7台组成第一段变压吸附装置。吸附塔内由下到上装填的 吸附剂依次为活性氧化铝及分子筛,运行三塔吸附三次均压程序;吸附塔 a〜 g共 7台组成第二段变压吸附装置,吸附塔内装填的吸附剂为分子筛,运行五 塔吸附三次均压程序。 本实施例将上述二段变压吸附装置串联操作, 第一段 变压吸附装置脱除空气中的气态水、 二氧化碳及部分氮气, 第二段变压吸附 装置用于将第一段变压吸附装置吸附塔吸附步骤流出的中间气中的氮进一步 脱除, 并把氧提高至所需的浓度。
空气进入第一段变压吸附装置处于吸附步骤的吸附塔, 吸附塔中的吸附 剂选择性地依次吸附空气中的气态水、 二氧化碳及部分氮气等组分, 未吸附 的部分氮和不易吸附的氧和氩等组分从出口端排出进入第二段变压吸附装置 处于吸附步骤的吸附塔, 吸附塔中的分子筛选择性地吸附氮气, 不易吸附的 氧和氩等组分从出口端排出进入产品富氧缓冲罐。 第一段变压吸附装置处于 吸附步骤的吸附塔出口气中氧气浓度控制在 21〜23% ( V ), 其吸附塔在一个 循环周期中依次经历吸附 A、 两端均压降压 2ED'、 逆向降压 BD、 抽真空 VC、 二段气逆向第三次均压升压 2ER3、二段气逆向第二次均压升压 2ER2、二段气 逆向第一次均压升压 2ER1、 两端均压升压 2ER'、 最终升压 FR变压吸附工艺 步骤; 第二段变压吸附装置处于吸附步骤的吸附塔出口气中氧气浓度控制在 93% (V ) 左右, 其吸附塔在一个循环周期中依次经历吸附 A、 逆向第一次均 压降压 BID'、 逆向第二次均压降压 B2D'、 逆向第三次均压降压 B3D'、 最终 升压 FR变压吸附工艺步骤。
本实施例结果为氧气浓度大于 93% ( V ) , 氮气浓度大于 99. 7°/。 (V ) ,氧 气回收率大于 98. 5%
本发明的实施例 25 :
本例的原料气为空气。 第一段变压吸附装置处于吸附步骤的吸附塔出口 气中氧气浓度控制在 21〜23% ( V) , 第二段变压吸附装置处于吸附步骤的吸 附塔出口气中氧气浓度控制在 93% (V ) 左右 (即产品富氧)。
本实施例的空气组成如下:
Figure imgf000030_0001
温度: 45Ό
压力: 0. 01 MPa ( G )
吸附塔 A〜G共 7台组成第一段变压吸附装置。吸附塔内由下到上装填的 吸附剂依次为活性氧化铝及分子筛,运行三塔吸附三次均压程序;吸附塔 a〜 - g共 7台组成第二段变压吸附装置,吸附塔内装填的吸附剂为分子筛,运行五 塔吸附三次均压程序。 本实施例将上述二段变压吸附装置串联操作, 第一段 变压吸附装置脱除空气中的气态水、 二氧化碳及部分氮气, 第二段变压吸附 装置用于将第一段变压吸附装置吸附塔吸附步骤流出的中间气中的氮进一步 脱除, 并把氧提高至所需的浓度。
空气进入第一段变压吸附装置处于吸附步骤的吸附塔, 吸附塔中的吸附 剂选择性地依次吸附空气中的气态水、 二氧化碳及部分氮气等组分, 未吸附 的部分氮和不易吸附的氧和氩等组分从出口端排出进入第二段变压吸附装置 处于吸附步骤的吸附塔, 吸附塔中的分子筛选择性地吸附氮气, 不易吸附的 氧和氩等组分从出口端排出进入产品富氧缓冲罐。 第一段变压吸附装置处于 吸附步骤的吸附塔出口气中氧气浓度控制在 21〜23% (V ) , 其吸附塔在一个 循环周期中依次经历吸附 A、 两端均压降压 2ED'、 抽真空 VC、 二段气逆向第 三次均压升压 2ER3、二段气逆向第二次均压升压 2ER2、二段气逆向第一次均 压升压 2ER1、 两端均压升压 2ER'、 最终升压 FR变压吸附工艺步骤; 第二段 变压吸附装置处于吸附步骤的吸附塔出口气中氧气浓度控制在 93% ( V )左右, 其吸附塔在一个循环周期中依次经历吸附 A、 顺向均压降压 ED、 逆向第一次 均压降压 BID'、 逆向第二次均压降压 B2D'、 逆向第三次均压降压 B3D'、 逆 向均压升压 ER、 最终升压 FR变压吸附工艺步骤。
本实施例结果为氧气浓度大于 93% ( V) , 氮气浓度大于 99. 7% ( V ) ,氧 气回收率大于 98. 5% 工业应用性
本发明可广泛应用于化工、 石化、 冶金、 建材、 环保、 制药等领域。

Claims

权 利 要 求
1、 一种改进的两段变压吸附制富氧方法, 其特征在于此方法用于 从空气中分离氮气和氧气,产品可以是氧气,也可以是氮气,还 可以周时是氧气和氮气, 此方法采用二段变压吸附装置串联操 作, 第一段变压吸附装置用于脱除二氧化碳、 水和部分氮气并 将氮气提浓, 第二段变压吸附装置用于将第一段变压吸附装置 吸附塔吸附步骤流出的中间气中的氮进一步脱除, 并把氧提高 至所需的浓度, 第一段变压吸附装置的吸附塔在一个循环周期 中依次经历吸附 4、 置换 P '、 抽真空 VC、 二段气逆向均压升压
2ER、 置换气升压 R'、 最终升压 FR变压吸附工艺步骤; 第二段 变压吸附装置的吸附塔在一个循环周期中依次经历吸附 A、逆向 均压降压 BD'、 最终升压 FR变压吸附工艺步骤。
2、 根据权利要求 1 所述的一种改进的两段变压吸附制富氧方法, 其特征在于在第二段变压吸附装置吸附塔在吸附 A 工艺步骤之 后增加顺向均压降压 ED工艺步骤, 同时在逆向均压降压 BD'工 艺步骤完成后增加逆向升压 ER工艺步骤,升压 ER工艺步骤的混 合气来自降压 ED工艺步骤。
3、 根据权利要求 1 或 2所述的一种改进的两段变压吸附制富氧方 法, 其特征在于第一段变压吸附装置吸附塔在吸附 A 工艺步骤 之后增加两端均压降压 2ED'工艺步骤, 同时在二段气逆向均压 升压 2ER工艺步骤完成后增加两端均压升压 2ER'工艺步骤, 两 端均压升压 2ER'工艺步骤的混合气来自均压降压 2ED '工艺步 骤。
4、 . 根据权利要求 3 所述的一种改进的两段变压吸附制富氧方法, 其特征在于第一段变压吸附装置吸附塔在置换 P '工艺步骤之; 3 增加逆向降压 BD工艺步骤。
5、 根据权利要求 1 或 2所述的一种改进的两段变压吸附制富氧方 法, 其特征在于第二段变压吸附装置吸附塔逆向均压降压 BD' 工艺步骤放出的混合气进入缓冲罐 V,直到压力平衡为止,同时 第一段变压吸附装置吸附塔在进行二段气逆向均压升压 2ER 工 艺步骤时,吸附塔与缓冲罐 V连通, 直到压力平衡为止。
6、 根据权利要求 3 所述的一种改进的两段变压吸附制富氧方法, 其特征在于第二段变压吸附装置吸附塔逆向均压降压 BD'工艺 步骤放出的混合气进入缓冲罐 V,直到压力平衡为止,同时第一 段变压吸附装置吸附塔在进行二段气逆向均压升压 2ER 工艺步 骤时,吸附塔与缓冲罐 V连通, 直到压力平衡为止。
7、 根据权利要求 4 所述的一种改进的两段变压吸附制富氧方法, 其特征在于第二段变压吸附装置吸附塔逆向均压降压 BD'工艺 步骤放出的混合气进入缓冲罐 V,直到压力平衡为止,同时第一 段变压吸附装置吸附塔在进行二段气逆向均压升压 2ER 工艺步 骤时,吸附塔与缓冲罐 V连通, 直到压力平衡为止。
8、 根据权利要求 1 或 2所述的一种改进的两段变压吸附制富氧方 法, 其特征在于第一段变压吸附装置吸附塔吸附步骤出口气中 氧气的平均浓度为 21〜80 V %。
9、 根据权利要求 3 所述的一种改进的两段变压吸附制富氧方法, 其特征在于第一段变压吸附装置吸附塔吸附步骤出口气中氧气 的平均浓度为 21〜80 V %。
10、 根据权利要求 5 所述的一种改进的两段变压吸附制富氧方法, 其特征在于第一段变压吸附装置吸附塔吸附步骤出口气中氧气 的平均浓度为 21〜80 V %0
11、 根据权利要求 9 所述的一种改进的两段变压吸附制富氧方法, 其特征在于第一段变压吸附装置吸附塔吸附步骤出口气中氧气 的平均浓度为 21〜25V%。 '
12、 根据权利要求 10所述的一种改进的两段变压吸附制富氧方法, 其特征在于第一段变压吸附装置吸附塔吸附步骤出口气中氧气 的平均浓度为 21〜25V%。
13、 根据权利要求 11所述的一种改进的两段变压吸附制富氧方法, 其特征在于第一段变压吸附装置吸附塔吸附步骤出口气中氧气 的平均浓度为 21〜25V%。 、 根据权利要求 1或 2所述的一种改进的两段变压吸附制富氧方 法,其特征在于两段变压吸附装置吸附步骤 A的压力为 0. 001〜
0. IMPa表压。 、 根据权利要求 3 所述的一种改进的两段变压吸附制富氧方法, 其特征在于两段变压吸附装置吸附步骤 k 的压力为 0. 001〜 0. 6MPa表压。 、 根据权利要求 4 所述的一种改进的两段变压吸附制富氧方法, 其特征在于两段变压吸附装置吸附步骤 A 的压力为 0. 001〜 0. 6MPa表压。 、 根据权利要求 1或 2所述的一种改进的两段变压吸附制富氧方 法, 其特征在于第一段变压吸附装置吸附塔内由下到上装填的 吸附剂为活性氧化铝及分子筛; 第二段变压吸附装置吸附塔内 装填的吸附剂只为分子筛。 、 根据权利要求 1或 2所述的一种改进的两段变压吸附制富氧方 法, 其特征在于第二段变压吸附装置吸附塔逆向均压降压 ED' 和第一段变压吸附装置吸附塔二段气逆向均压升压 2ER 的次数 大于或等于 1。 、 根据权利要求 3 所述的一种改进的两段变压吸附制富氧方法, 其特征在于第二段变压吸附装置吸附塔逆向均压降压 ED'和第 一段变压吸附装置吸附塔二段气逆向均压升压 2ER 的次数大于 或等于 1。 、 根据权利要求 4 所述的一种改进的两段变压吸附制富氧方法, 其特征在于第二段变压吸附装置吸附塔逆向均压降压 ED'和第 一段变压吸附装置吸附塔二段气逆向均压升压 2ER 的次数大于 或等于 1。 、 根据权利要求 18所述的一种改进的两段变压吸附制富氧方法, 其特征在于第二段变压吸附装置吸附塔逆向均压降压 ED '和第 一段变压吸附装置吸附塔二段气逆向均压升压 2ER的次数为 3〜 7次。 、 根据权利要求 19所述的一种改进的两段变压吸附制富氧方法, 其特征在于第二段变压吸附装置吸附塔逆向均压降压 ED'和第 一段变压吸附装置吸附塔二段气逆向均压升压 2ER的次数为 3〜 7次。 、 根据权利要求 20所述的一种改进的两段变压吸附制富氧方法, 其特征在于第二段变压吸附装置吸附塔逆向均压降压 ED '和第 一段变压吸附装置吸附塔二段气逆向均压升压 2ER的次数为 3〜 7次。 、 一种改进的两段变压吸附制富氧方法, 其特征在于此方法用于 从空气中分离氮气和氧气,产品可以是氧气,也可以是氮气,还 可以同时是氧气和氮气, 此方法采用二段变压吸附装置串联操 作, 第一段变压吸附装置用于脱除二氧化碳、 水和部分氮气并 将氮气提浓, 第二段变压吸附装置用于将第一段变压吸附装置 吸附塔吸附步骤流出的中间气中的氮进一步脱除, 并把氧提高 至所需的浓度, 第一段变压吸附装置的吸附塔在一个循环周期 中依次经历吸附八、两端均压降压 2ED'、置换 P '、逆向降压 BD、 二段气逆向均压升压 2ER、 两端均压升压 2ER'、 置换气升压 R'、 最终升压 FR变压吸附工艺步骤; 第二段变压吸附装置吸附塔在 一个循环周期中依次经历吸附 A、 顺向均压降压 ED、 逆向均压 降压 BD'、 逆向均压升压 ER、 最终升压 FR变压吸附工艺步骤。 、 根据权利要求 25所述的一种改进的两段变压吸附制富氧方法, 其特征在于两段变压吸附装置吸附步骤 A的压力为 0. 3〜0. 6MPa 表压。 、 一种改进的两段变压吸附制富氧方法, 其特征在于此方法用于 从空气中分离氮气和氧气,.产品可以是氧气,也可以是氮气,还 可以同时是氧气和氮气, 此方法采用二段变压吸附装置串联操 作, 第一段变压吸附装置用于脱除二氧化碳、 水和部分氮气并 将氮气提浓, 第二段变压吸附装置用于将第一段变压吸附装置 吸附塔吸附步骤流出的中间气中的氮进一步脱除, 并把氧提高 至所需的浓度, 第一段变压吸附装置的吸附塔在一个循环周期 中依次经历吸附八、 两端均压降压 2ED '、 抽真空 V (:、 二段气逆 向均压升压 2ER、 两端均压升压 2ER'、 最终升压 FR变压吸附工 艺步骤; 第二段变压吸附装置的吸附塔在一个循环周期中依次 经历吸附 A、 逆向均压降压 BD'、 最终升压 FR变压吸附工艺步 骤。 、 根据权利要求 27所述的一种改进的两段变压吸附制富氧方法, 其特征在于在第二段变压吸附装置吸附塔在吸附 A 工艺步骤之 后增加顺向均压降压 ED工艺步骤, 同时在逆向均压降压 BD'工 艺步骤完成后增加逆向升压 ER工艺步骤,升压 ER工艺步骤的混 合气来自降压 ED工艺步骤。 、 根据权利要求 27或 28所述的一种改进的两段变压吸附制富氧 方法, 其特征在于第一段变压吸附装置吸附塔在两端均压降压 2ED'工艺步骤之后增加逆向降压 BD工艺步骤。 、 根据权利要求 27或 28所述的一种改进的两段变压吸附制富氧 方法,其特征在于第二段变压吸附装置吸附塔逆向均压降压 BD ' 工艺步骤放出的混合气进入缓冲罐 VI,直到压力平衡为止,同时 第一段变压吸附装置吸附塔在进行二段气逆向均压升压 2ER 工 艺步骤时,吸附塔与缓冲罐 VI连通, 直到压力平衡为止。 、 根据权利要求 27或 28所述的一种改进的两段变压吸附制富氧 方法, 其特征在于两段变压吸附装置吸附步骤 A 的压力为 0. 005〜0. 6MPa表压。
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US8128734B2 (en) 2012-03-06
ES2519443T3 (es) 2014-11-07
PL1769839T3 (pl) 2015-03-31
US20090151561A1 (en) 2009-06-18
CN1597054A (zh) 2005-03-23
CN1287886C (zh) 2006-12-06
EP1769839A4 (en) 2008-11-19
EP1769839B1 (en) 2014-07-23
EP1769839A1 (en) 2007-04-04

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