JPH0141372B2 - - Google Patents
Info
- Publication number
- JPH0141372B2 JPH0141372B2 JP56056615A JP5661581A JPH0141372B2 JP H0141372 B2 JPH0141372 B2 JP H0141372B2 JP 56056615 A JP56056615 A JP 56056615A JP 5661581 A JP5661581 A JP 5661581A JP H0141372 B2 JPH0141372 B2 JP H0141372B2
- Authority
- JP
- Japan
- Prior art keywords
- gas
- adsorbent
- amount
- intermittently
- temperature
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 239000003463 adsorbent Substances 0.000 claims description 38
- 238000010438 heat treatment Methods 0.000 claims description 18
- 238000000034 method Methods 0.000 claims description 13
- 238000000746 purification Methods 0.000 claims description 10
- 239000000126 substance Substances 0.000 claims description 10
- 238000003795 desorption Methods 0.000 claims description 9
- 239000007789 gas Substances 0.000 description 47
- 230000008929 regeneration Effects 0.000 description 10
- 238000011069 regeneration method Methods 0.000 description 10
- 238000001179 sorption measurement Methods 0.000 description 8
- 239000003960 organic solvent Substances 0.000 description 4
- 238000009835 boiling Methods 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 238000002485 combustion reaction Methods 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- 238000005485 electric heating Methods 0.000 description 2
- 238000010422 painting Methods 0.000 description 2
- 238000012805 post-processing Methods 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 238000007084 catalytic combustion reaction Methods 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical class C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000002336 sorption--desorption measurement Methods 0.000 description 1
Classifications
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F24—HEATING; RANGES; VENTILATING
- F24F—AIR-CONDITIONING; AIR-HUMIDIFICATION; VENTILATION; USE OF AIR CURRENTS FOR SCREENING
- F24F3/00—Air-conditioning systems in which conditioned primary air is supplied from one or more central stations to distributing units in the rooms or spaces where it may receive secondary treatment; Apparatus specially designed for such systems
- F24F3/12—Air-conditioning systems in which conditioned primary air is supplied from one or more central stations to distributing units in the rooms or spaces where it may receive secondary treatment; Apparatus specially designed for such systems characterised by the treatment of the air otherwise than by heating and cooling
- F24F3/14—Air-conditioning systems in which conditioned primary air is supplied from one or more central stations to distributing units in the rooms or spaces where it may receive secondary treatment; Apparatus specially designed for such systems characterised by the treatment of the air otherwise than by heating and cooling by humidification; by dehumidification
- F24F3/1411—Air-conditioning systems in which conditioned primary air is supplied from one or more central stations to distributing units in the rooms or spaces where it may receive secondary treatment; Apparatus specially designed for such systems characterised by the treatment of the air otherwise than by heating and cooling by humidification; by dehumidification by absorbing or adsorbing water, e.g. using an hygroscopic desiccant
- F24F3/1423—Air-conditioning systems in which conditioned primary air is supplied from one or more central stations to distributing units in the rooms or spaces where it may receive secondary treatment; Apparatus specially designed for such systems characterised by the treatment of the air otherwise than by heating and cooling by humidification; by dehumidification by absorbing or adsorbing water, e.g. using an hygroscopic desiccant with a moving bed of solid desiccants, e.g. a rotary wheel supporting solid desiccants
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F24—HEATING; RANGES; VENTILATING
- F24F—AIR-CONDITIONING; AIR-HUMIDIFICATION; VENTILATION; USE OF AIR CURRENTS FOR SCREENING
- F24F2203/00—Devices or apparatus used for air treatment
- F24F2203/10—Rotary wheel
- F24F2203/1012—Details of the casing or cover
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F24—HEATING; RANGES; VENTILATING
- F24F—AIR-CONDITIONING; AIR-HUMIDIFICATION; VENTILATION; USE OF AIR CURRENTS FOR SCREENING
- F24F2203/00—Devices or apparatus used for air treatment
- F24F2203/10—Rotary wheel
- F24F2203/1032—Desiccant wheel
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F24—HEATING; RANGES; VENTILATING
- F24F—AIR-CONDITIONING; AIR-HUMIDIFICATION; VENTILATION; USE OF AIR CURRENTS FOR SCREENING
- F24F2203/00—Devices or apparatus used for air treatment
- F24F2203/10—Rotary wheel
- F24F2203/1056—Rotary wheel comprising a reheater
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F24—HEATING; RANGES; VENTILATING
- F24F—AIR-CONDITIONING; AIR-HUMIDIFICATION; VENTILATION; USE OF AIR CURRENTS FOR SCREENING
- F24F2203/00—Devices or apparatus used for air treatment
- F24F2203/10—Rotary wheel
- F24F2203/1068—Rotary wheel comprising one rotor
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F24—HEATING; RANGES; VENTILATING
- F24F—AIR-CONDITIONING; AIR-HUMIDIFICATION; VENTILATION; USE OF AIR CURRENTS FOR SCREENING
- F24F2203/00—Devices or apparatus used for air treatment
- F24F2203/10—Rotary wheel
- F24F2203/1084—Rotary wheel comprising two flow rotor segments
Landscapes
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Combustion & Propulsion (AREA)
- Mechanical Engineering (AREA)
- General Engineering & Computer Science (AREA)
- Separation Of Gases By Adsorption (AREA)
Description
本発明はケースに収納の吸着体に対し、被吸着
物含有の第1気体と、脱着加熱用の第2気体とを
交互に通過させることを繰返して、第1気体の浄
化と、吸着体の再生とを行なう気体の浄化方法に
関する。
この種、気体の浄化方法においては、以下の様
な欠点を生じていた。
(i) 被処理気体が、塗装排気、印刷排気などのよ
うな有機溶剤を主体とするものでは、その大部
分の含有物質は吸着体への加熱エネルギーが比
較的小さい第2気体により容易に着脱しえるも
のである。この様な含有物質のみであるなら
ば、吸着、脱着の繰返し操作を長期間行なつて
も吸着体に残存蓄積するものは極く小量で、吸
着体の吸着性能の劣化は極く少ないものであ
る。
(ii) しかし、上記のような第1気体では、微量で
はあるが高沸点物質が含まれ、これは、上記の
様な少ない加熱エネルギーでは脱着されず、次
第に吸着体に蓄積されることとなるために、比
較的早期に吸着体の吸着性能が劣化してしまう
ものである。
(iii) この様な吸着体の劣化を防止するためには、
上記(i)に示すときの第2気体の加熱エネルギを
増大させれば良いのであるが、下表に示す通
り、第2気体の熱エネルギーは、吸着体に吸着
された溶剤などを加熱するために使用される量
は、全体の2〜10%程度である。
The present invention purifies the first gas and purifies the adsorbent by repeatedly passing a first gas containing an adsorbed substance and a second gas for desorption heating through an adsorbent housed in a case. The present invention relates to a gas purification method that performs regeneration. This type of gas purification method has the following drawbacks. (i) If the gas to be treated is mainly composed of organic solvents such as painting exhaust or printing exhaust, most of the contained substances can be easily attached and detached by the second gas, which requires relatively little heating energy to the adsorbent. It is something that can be taught. If only such substances are contained, even after repeated adsorption and desorption operations are performed for a long period of time, only a small amount will remain and accumulate on the adsorbent, and the adsorption performance of the adsorbent will deteriorate only slightly. It is. (ii) However, the first gas mentioned above contains a high boiling point substance, albeit in a small amount, and this is not desorbed by the small heating energy as mentioned above, but gradually accumulates in the adsorbent. Therefore, the adsorption performance of the adsorbent deteriorates relatively early. (iii) In order to prevent such deterioration of the adsorbent,
It is sufficient to increase the heating energy of the second gas when shown in (i) above, but as shown in the table below, the thermal energy of the second gas heats the solvent etc. adsorbed by the adsorbent. The amount used is about 2 to 10% of the total.
【表】
(iv) つまり高沸点物質を除去するために、加熱エ
ネルギーを増大させれば熱損矢がその分大幅に
増大するものであり、又、大部分の低沸点物質
は余分に加熱されるだけで、この分が熱損失と
なり、全体として大きな熱損失を生じざるを得
ないものであつた。
これとは反対に、第2気体からの一回の再生に
おける供給熱量を少なくすれば、熱量の損失を少
なくすることができるが充分な再生処理が行えな
くなり、使用開始から別途再生処理装置による再
生処理が必要になる期間(これを以後寿命と称す
る)が短かくなつて、稼働率が悪化する欠点が有
る。
このため、従来はこの熱損失と稼働率との関係
から適当な一定の供給熱量が設定されて、この設
定熱量を第2気体により1回の再生ごとに供給す
ることが行なわれていた。
しかし、この様な一定の供給熱量を適切に決定
することは実務上第1気体の湿度や含有被吸着物
の濃度の変動等の種々要因により極めて困難であ
る。
本発明は、この様な欠点に対し、従来の一定供
給熱量の設定によるもの以上に、寿命のわりには
熱量が少なくなるようにすることを目的とする。
この目的を達成するために、本発明は冒記した
気体の浄化方法において第2気体によつて前記吸
着体に与えられる熱量を所定回おきに間欠的に増
大させる構成を採用したものである。
この様に間欠的に第2気体による一回の供給熱
量を増大させることにより、この間に良好な脱着
を行ない、この間以外の供給熱量を通常よりも少
なくしておいても全体としては良好な再生状態を
維持しえるようになる。従つて、熱量の供給量に
比し、寿命は大幅に増大しえることとなつた。
次に本発明の実施例について説明する。
第1実施例(第2図参照)
第2図は本発明実施に使用する装置の1例であ
る連続吸着脱装置の配管等の系統図である。
回軸中心軸1周りにハンカム状の吸着体2、
(吸着物質としては、活性化炭素繊維あるいは、
粉末状の活性化炭素を使用し、これらを、繊維質
の物質と混合して形成した紙体にて形成してあ
る)を取付け、この吸着体2を覆うケース3に、
塗装ブースやあるいはその他の工場内の排気であ
る有機溶剤などを含有する気体(第1気体)4を
通過させる第1流域5と、ブロワー6にて吹き込
まれ、下記する加熱装置7にて加熱された加熱気
体(第2気体)8を通過させる第2流域9とに区
画する。
そして、前記吸着体2を中心軸1周りに一定速
度で一定方向に回転して、前記両流域5,9を順
次通過させ、前記第1気体4と第2気体8とを交
互に通過させるように構成してある。
前記加熱装置7には加熱温度調節構造(詳細は
下記する)が設けてあつて以下のパターンにより
第2気体8の温度を変更可能にしてある。
() 前記熱量Tに対応する低温度Toを100℃〜
150℃の内の一定温度とする。
() 前記熱量Thに対応する高温度Thoを前記
()の低温度Toよりも高温で125℃〜160℃の
内の一定温度とする。
() 低温度Toによる再生により、残留率Sが
大きくなつたとき、(これは、低温度Toの設定
により3回乃至100回ぐらいの再生後に生じ
る)、次回の再生温度を前記高温度Thとする。
この1回とは、前記吸着体2の1回の回転に
要する時間である。
この様なパターンで第2気体8の温度を変化さ
せるには、以下の様な構成を採用する。
第1気体4の温度、風量、並びに、被吸着物の
含有濃度が全体として安定している場合には上記
()乃至()のパターンをタイマーで制御す
る。
なお、前記加熱装置7は次の様なものである。
電熱式では、電気発熱体の本数や電気量を調
整して加熱温度を調整する。
ガスや石油バーナー式では、バーナー本数や
1本のバーナに対するガスあるいは石油などの
供給量を調整して加熱温度を調整する。
触媒式で、脱着後の第2気体8を加熱装置7
にもどして脱着した有機溶剤を触媒燃焼させ
て、第2気体8を加熱するものでは、触媒燃焼
前に供給する空気量や、燃焼後供給する空気量
を調整して、吸着体2通過時の第2気体8の温
度を調整する
なお、これらのいずれの手段においても吸着
体2への通過風量は略一定とする。
以上のようにして、第2気体8の温度を調整し
て、吸着体2への供給熱量を変更するものでは、
脱着時における吸着体2の温度が通常は高温化せ
ず、従つて、脱着温度の低い有機溶剤が高温にて
分解したり重合したりして吸着体2に強く付着
し、吸着体2の再生を不能とする劣化を早めるこ
とはなく、吸着体2の寿命を大幅に増進する効果
も有る。
なお、高温度Thoに連続して維持する時間は1
回の吸着体2の回転時間に限らず2回又は3回で
も良い。
又、両気体4,8の吸着体2の通過方向は、そ
の軸方向に限らず半径方向のものでも良い。
図中、10は第2気体8の後処理装置で、上記
に示すものでは、この後処理装置を加熱装置7
と兼用することとなる。
第2実施例(図示せず)
前記の様な温度の変更ではなく、第2気体8の
温度は略一定とし、風速を前記()、()、
()のパターにおける温度に変わつて変更する。
この具体的手段としてはブロワー6を可変形に
構成するとともに、前記(i)又は(ii)により風速を調
整し、かつ、この風速調整とともに前記乃至
によつて加熱量を調整して、第2気体8の温度を
略一定に保つ。
なお、この場合における第2気体8の温度は
100℃〜160℃の間のいずれかに安定させる。
第3実施例(図示せず)
前記第1、第2実施例のような温度や風速の変
動により、第2気体8による吸着体2への供給熱
量を変動するのではなく、吸着体2の回転速度を
変動して供給熱量を上記第1実施例のように変動
する。
具体的には、吸着体2の回転駆動装置に変速装
置を組込み、上記()、()、()のパターン
における温度にかわり、低温度相当時に所定の高
速回転し、高温度相当時に低速回転とする。
この場合には、ブロワー6や加熱装置7などの
制御が一般に行ないにくいものを変動調整しない
ので、調整作業が容易である。
第4実施例(図示せず)
複数の吸着材入り吸着塔ある吸着ブロツク入り
室に対し、所定順序で順次第1気体4と第2気体
8とを交互に供給して浄化を行なうバツヂ式の吸
着装置においても、前記第1乃至第2実施例を実
施することができる。
この様な場合、1回の脱着時間は、各塔あるい
は室夫々における1回の脱着時間を意味し、必ず
しも、複数の塔あるいは室を1循する時間と限定
して解釈する必要はない。しかし、複数の塔ある
いは室は、相互に同一の吸着能力を有せしめてあ
るのが一般的であるので、この様な場合は一循す
る時間を一回の吸着時間とすれば良い。
なお、第3実施例における方策とこの塔や室に
対し応用する場合は、各塔又は室における1回の
通過時間を間欠的に増大すれば良い。
なお、上記詳実施例において、第2気体8は空
気に限らず、蒸気や不燃性ガス(前記第1実施例
における、の加熱手段では、燃焼後の不燃焼
ガスを多く含み、実質的に不燃性ガスを第2気体
とすることとなる。)
又、第2気体8の温度と、風速又は温度と通過
時間(第1実施例では吸着体2の回転時間)又
は、風速と通過時間とを同時的に変動させるのも
良い。[Table] (iv) In other words, if heating energy is increased to remove high boiling point substances, the heat loss will increase significantly, and most low boiling point substances will be heated excessively. However, this amount becomes a heat loss, and a large heat loss cannot but be caused as a whole. On the contrary, if the amount of heat supplied in one regeneration from the second gas is reduced, the loss of heat can be reduced, but sufficient regeneration processing cannot be performed, and a separate regeneration processing device is required from the start of use. This has the disadvantage that the period during which treatment is required (hereinafter referred to as life span) becomes shorter and the operating rate deteriorates. For this reason, in the past, an appropriate fixed amount of heat to be supplied was set based on the relationship between the heat loss and the operating rate, and this set amount of heat was supplied by the second gas for each regeneration. However, it is extremely difficult in practice to appropriately determine such a constant amount of heat to be supplied due to various factors such as fluctuations in the humidity of the first gas and the concentration of adsorbed substances contained therein. SUMMARY OF THE INVENTION The present invention addresses these drawbacks and aims to reduce the amount of heat required over the lifespan compared to the conventional setting of a constant supply amount of heat. In order to achieve this object, the present invention employs a configuration in which the amount of heat given to the adsorbent by the second gas is intermittently increased at predetermined intervals in the gas purification method described above. By intermittently increasing the amount of heat supplied by the second gas in this way, good desorption is achieved during this period, and even if the amount of heat supplied other than this period is lower than usual, good regeneration is achieved overall. be able to maintain the condition. Therefore, the lifespan can be significantly increased compared to the amount of heat supplied. Next, examples of the present invention will be described. First Embodiment (See FIG. 2) FIG. 2 is a system diagram of piping, etc. of a continuous adsorption/desorption device, which is an example of the device used to carry out the present invention. A hunk-shaped adsorbent body 2 is placed around the rotation center axis 1.
(As the adsorbent, activated carbon fiber or
A paper body made of powdered activated carbon and mixed with a fibrous substance is attached to the case 3 that covers the adsorbent 2.
A gas (first gas) 4 containing organic solvents, which is exhaust gas from a painting booth or other factory, is blown into a first region 5 and a blower 6, and is heated by a heating device 7, which will be described below. and a second region 9 through which heated gas (second gas) 8 passes. Then, the adsorbent 2 is rotated around the central axis 1 at a constant speed in a constant direction, so that the two regions 5 and 9 are sequentially passed through, and the first gas 4 and the second gas 8 are passed alternately. It is structured as follows. The heating device 7 is provided with a heating temperature adjustment structure (details will be described below), and the temperature of the second gas 8 can be changed according to the following pattern. () The low temperature To corresponding to the above heat amount T is 100℃~
The temperature shall be constant within 150℃. () The high temperature Tho corresponding to the heat amount Th is set to be a constant temperature within 125°C to 160°C, which is higher than the low temperature To in the above (). () When the residual rate S increases due to regeneration at low temperature To (this occurs after approximately 3 to 100 regenerations depending on the setting of low temperature To), the next regeneration temperature is set to the high temperature Th. do. This one time is the time required for one rotation of the adsorbent 2. In order to change the temperature of the second gas 8 in such a pattern, the following configuration is adopted. When the temperature and air volume of the first gas 4 and the concentration of adsorbed substances are generally stable, the above patterns () to () are controlled by a timer. The heating device 7 is as follows. In the electric heating type, the heating temperature is adjusted by adjusting the number of electric heating elements and the amount of electricity. In a gas or oil burner type, the heating temperature is adjusted by adjusting the number of burners and the amount of gas or oil supplied to each burner. A heating device 7 uses a catalytic method to heat the second gas 8 after desorption.
In the case of heating the second gas 8 by catalytically combusting the organic solvent that has been returned and desorbed, the amount of air supplied before catalytic combustion and the amount of air supplied after combustion are adjusted to reduce the Adjusting the temperature of the second gas 8 Note that in any of these means, the amount of air passing through the adsorbent 2 is substantially constant. In the method described above, the temperature of the second gas 8 is adjusted to change the amount of heat supplied to the adsorbent 2,
The temperature of the adsorbent 2 during desorption usually does not rise to a high temperature, so organic solvents with low desorption temperatures decompose or polymerize at high temperatures and strongly adhere to the adsorbent 2, causing regeneration of the adsorbent 2. It does not accelerate deterioration that would make it impossible, and has the effect of significantly extending the life of the adsorbent 2. In addition, the time to maintain the high temperature Tho continuously is 1
The rotation time of the adsorbent 2 is not limited to 2 times or 3 times. Further, the direction in which the gases 4 and 8 pass through the adsorbent 2 is not limited to the axial direction, but may be in the radial direction. In the figure, 10 is a post-processing device for the second gas 8, and in the above example, this post-processing device is connected to the heating device 7.
It will be used for both. Second Embodiment (not shown) Instead of changing the temperature as described above, the temperature of the second gas 8 is kept approximately constant, and the wind speed is changed to (), (),
() Change the temperature in place of the putter. As a specific means for this, the blower 6 is configured to be variable, the wind speed is adjusted by the above (i) or (ii), and along with this wind speed adjustment, the heating amount is adjusted by the above, and the second The temperature of the gas 8 is kept approximately constant. In addition, the temperature of the second gas 8 in this case is
Stabilize anywhere between 100°C and 160°C. Third Embodiment (not shown) Instead of changing the amount of heat supplied to the adsorbent 2 by the second gas 8 due to fluctuations in temperature and wind speed as in the first and second embodiments, the amount of heat supplied to the adsorbent 2 is changed. By varying the rotational speed, the amount of heat supplied is varied as in the first embodiment. Specifically, a speed change device is incorporated into the rotary drive device of the adsorbent 2, and the temperature changes according to the pattern (), (), () above, and the rotation is performed at a predetermined high speed when the temperature corresponds to a low temperature, and at a low speed when the temperature corresponds to a high temperature. shall be. In this case, the adjustment work is easy because the blower 6 and the heating device 7, which are generally difficult to control, are not subject to fluctuation adjustment. Fourth Embodiment (not shown) A batch-type method in which purification is performed by alternately supplying the first gas 4 and the second gas 8 in a predetermined order to an adsorption block chamber containing a plurality of adsorption towers containing adsorbents. The first and second embodiments can also be implemented in an adsorption device. In such a case, one desorption time means one desorption time in each column or chamber, and does not necessarily need to be interpreted as limited to the time for one cycle through a plurality of columns or chambers. However, since a plurality of towers or chambers generally have the same adsorption capacity, in such a case, the time for one circulation may be considered as one adsorption time. In addition, when applying the measures in the third embodiment to this tower or chamber, it is sufficient to intermittently increase one passage time in each tower or chamber. In the detailed embodiment described above, the second gas 8 is not limited to air, but also steam or nonflammable gas (in the heating means of the first embodiment, it contains a large amount of noncombustible gas after combustion and is substantially nonflammable). In addition, the temperature of the second gas 8, the wind speed, the temperature and the passing time (in the first embodiment, the rotation time of the adsorbent 2), or the wind speed and the passing time. It is also good to change them simultaneously.
図面は本発明に係る気体の浄化方法の実施の態
様を示し、第1実施例を示すフローチヤートであ
る。
2……吸着体、3……ケース、4……第1気
体、8……第2気体。
The drawing shows an embodiment of the gas purification method according to the present invention, and is a flowchart showing a first embodiment. 2... Adsorbent, 3... Case, 4... First gas, 8... Second gas.
Claims (1)
含有の第1気体4と、脱着加熱用の第2気体8と
を交互に通過させることを繰返すとともに、前記
第2気体8によつて前記吸着体2に与えられる熱
量を所定回おきに間欠的に増大させる気体の浄化
方法。 2 ケース3は、前記吸着体2の存在箇所を、実
質的に第1気体4の通過域5と第2気体8の通過
域9とに区画されたもので、前記吸着体2は所定
方向に連続回転させられて、もつて、第1気体4
と第2気体8とを交互に通過させる特許請求の範
囲第1項に記載の気体の浄化方法。 3 前記第2気体8の温度を間欠的に高温化し
て、前記吸着体2への熱量を間欠的に増大させる
特許請求の範囲第1項又は第2項に記載の気体の
浄化方法。 4 前記第2気体8の一回の通過時間を間欠的に
増大して、前記吸着体2への熱量を間欠的に増大
させる特許請求の範囲第1項又は第2項に記載の
気体の浄化方法。 5 前記第2気体8の風速を間欠的に増大させ
て、前記吸着体2への熱量を間欠的に増大させる
特許請求の範囲第1項又は第2項に記載の気体の
浄化方法。 6 前記特許請求の範囲第2項に記載の気体の浄
化方法において、前記吸着体2の回転速度を間欠
的に低速化して、吸着体2に与えられる熱量を間
欠的に増大させる気体の浄化方法。[Scope of Claims] 1. Repeatedly passing a first gas 4 containing an adsorbed substance and a second gas 8 for desorption heating through an adsorbent 2 housed in a case 3, and 2. A gas purification method in which the amount of heat given to the adsorbent 2 by the gas 8 is intermittently increased at predetermined intervals. 2 Case 3 is one in which the location of the adsorbent 2 is substantially divided into a passage area 5 for the first gas 4 and a passage area 9 for the second gas 8, and the adsorbent 2 is moved in a predetermined direction. By being continuously rotated, the first gas 4
The method for purifying a gas according to claim 1, wherein the gas and the second gas 8 are passed alternately. 3. The gas purification method according to claim 1 or 2, wherein the temperature of the second gas 8 is intermittently increased to intermittently increase the amount of heat transferred to the adsorbent 2. 4. Gas purification according to claim 1 or 2, in which the time for one passage of the second gas 8 is intermittently increased to intermittently increase the amount of heat transferred to the adsorbent 2. Method. 5. The gas purification method according to claim 1 or 2, wherein the wind speed of the second gas 8 is intermittently increased to intermittently increase the amount of heat transferred to the adsorbent 2. 6. A gas purification method according to claim 2, in which the rotational speed of the adsorbent 2 is intermittently reduced to intermittently increase the amount of heat given to the adsorbent 2. .
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56056615A JPS57171420A (en) | 1981-04-14 | 1981-04-14 | Method for purifying gas |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56056615A JPS57171420A (en) | 1981-04-14 | 1981-04-14 | Method for purifying gas |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS57171420A JPS57171420A (en) | 1982-10-22 |
| JPH0141372B2 true JPH0141372B2 (en) | 1989-09-05 |
Family
ID=13032161
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP56056615A Granted JPS57171420A (en) | 1981-04-14 | 1981-04-14 | Method for purifying gas |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS57171420A (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3528122A1 (en) * | 1985-08-06 | 1987-02-12 | Richard Scheuchl | PLANT FOR RECOVERING SOLVENTS FROM A PROCESS GAS FLOW |
| DE19628796C1 (en) * | 1996-07-17 | 1997-10-23 | Daimler Benz Ag | System for removal of nitrogen oxide(s), carbon mon:oxide, etc. from engine exhaust gases |
| KR102786327B1 (en) * | 2022-01-20 | 2025-03-24 | 심근섭 | Automatic cleaning type continuous filtering apparatus |
-
1981
- 1981-04-14 JP JP56056615A patent/JPS57171420A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS57171420A (en) | 1982-10-22 |
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