EP4634335A1 - Procédé de craquage - Google Patents

Procédé de craquage

Info

Publication number
EP4634335A1
EP4634335A1 EP23814481.0A EP23814481A EP4634335A1 EP 4634335 A1 EP4634335 A1 EP 4634335A1 EP 23814481 A EP23814481 A EP 23814481A EP 4634335 A1 EP4634335 A1 EP 4634335A1
Authority
EP
European Patent Office
Prior art keywords
zone
hydrocarbon feed
heated sections
sections
heating
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.)
Pending
Application number
EP23814481.0A
Other languages
German (de)
English (en)
Inventor
Bernard Descales
Philippe Charles Yves LALANNE MAGNE
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Ineos Europe AG
Original Assignee
Ineos Europe AG
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Ineos Europe AG filed Critical Ineos Europe AG
Publication of EP4634335A1 publication Critical patent/EP4634335A1/fr
Pending legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
    • C10G9/00—Thermal non-catalytic cracking, in the absence of hydrogen, of hydrocarbon oils
    • C10G9/24—Thermal non-catalytic cracking, in the absence of hydrogen, of hydrocarbon oils by heating with electrical means
    • G—PHYSICS
    • G05—CONTROLLING; REGULATING
    • G05D—SYSTEMS FOR CONTROLLING OR REGULATING NON-ELECTRIC VARIABLES
    • G05D21/00—Control of chemical or physico-chemical variables, e.g. pH value
    • G05D21/02—Control of chemical or physico-chemical variables, e.g. pH value characterised by the use of electric means
    • G—PHYSICS
    • G05—CONTROLLING; REGULATING
    • G05D—SYSTEMS FOR CONTROLLING OR REGULATING NON-ELECTRIC VARIABLES
    • G05D23/00—Control of temperature
    • G05D23/19—Control of temperature characterised by the use of electric means
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
    • C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
    • C10G2300/40—Characteristics of the process deviating from typical ways of processing
    • C10G2300/4031—Start up or shut down operations

Definitions

  • the present invention relates to methods of cracking hydrocarbon feeds, and in particular in electrically heated furnaces.
  • the commercial cracking of hydrocarbons generally takes place at a temperature above 750°C. Prior to cracking at such temperatures the hydrocarbons to be cracked are vaporised, and for this reason the hydrocarbons are usually heated and vaporised in a convection section of a furnace before being passed to a burner section where the cracking occurs.
  • Steam cracking can be performed on different hydrocarbon feeds. These include “light”' hydrocarbon feeds, such as ethane, “medium” feeds, such as naphtha, and “heavy” feeds, such as pyrolysis oils.
  • the cracking of different feeds takes place at similar temperatures, typically above 750°C as already noted, although the optimum temperature tends to be slightly higher for lighter feeds than heavier ones, and the optimum residence lime also tends to be longer for lighter feeds. In contrast, it takes more energy to heat and vaporise medium and heavy feeds than it does light ones.
  • a “conventional” furnace designed to vaporise and crack a naphtha feed is generally not optimally designed for vaporising and cracking an ethane containing feed.
  • the number of tubes in the convection section required to fully vaporise naphtha tends to be more than are required to full vaporise ethane, but not sufficient to fully vaporise heavier feeds.
  • Steam cracking furnaces based on electrical heating rather than burners have been proposed. In such designs both the vaporisation and cracking steps can use electrical heating.
  • a particular advantage of electrical heating is that it can provide more control of the temperature of individual sections of the furnace/reactant tube.
  • US 7288690 describes a method and apparatus for steam cracking hydrocarbons in which cogeneration using combustion of a fuel is used to produce simultaneously both heat energy and mechanical work which is transformed into electricity, and wherein the mixture is initially subjected to heating using the heat energy supplied by the cogeneration and is subsequently heated to the desired cracking temperature by means of electrical heating using the electricity supplied by the cogeneration.
  • WO 2022/094455 discloses an electrically heated cracking furnace. According to this document different reactant coils may be fed with different hydrocarbons or a mix of hydrocarbon feeds and the heating can be varied depending on the feed to be cracked. This document also discloses that preheating can be provided outside of the main reactor to provide preheating to each feed.
  • a method for transitioning from a first process cracking a first hydrocarbon feed to a second process cracking a second hydrocarbon feed wherein: a) The first process comprises a. passing the first hydrocarbon feed to a reactant tube which reactant tube comprises a first zone and a second zone, downstream of the first zone, each zone comprising one or more electrically heated sections, b. heating the first hydrocarbon feed in the first zone in the one or more electrically heated sections to vaporise the first hydrocarbon feed, and c.
  • the transition comprises stopping the feeding of the first hydrocarbon feed to the reactant tube and starting the feeding of the second hydrocarbon feed to the same reactant tube, and c)
  • the second process comprises a. passing the second hydrocarbon feed to the reactant tube which reactant tube comprises a first zone and a second zone, downstream of the first zone, each zone comprising one or more electrically heated sections, b.
  • the first aspect of the present invention provides a method of transitioning.
  • the method being a “transition” is generally meant that the second hydrocarbon feed has a significantly different composition and/or boiling point range to the first hydrocarbon feed. (And because of this a change in the heat required to vaporise the feed is required.)
  • the final boiling point of the boiling point range of the second hydrocarbon feed is at least 20°C different (higher or lower) than the final boiling point of the boiling point range of the first hydrocarbon feed.
  • the second hydrocarbon feed may be of a different type to that of the first hydrocarbon feed.
  • cracking feeds may be generally characterised as either “ethane based”, ’’propane based”, ‘butane based”, “naphtha based” or “pyrolysis based” such as pyrolysis oil obtained from plastic recycling, and hence a change from one to another of these would be a transition.
  • the first process comprises passing the first hydrocarbon feed to a reactant tube.
  • the reactant tube has a total of n electrically heated sections. These heated sections are set up to provide a first zone having nl heated sections in which the first hydrocarbon feed is heated to vaporise the first hydrocarbon feed and a second zone having n2 heated sections in which the vaporised first hydrocarbon feed is further heated to crack the first hydrocarbon feed.
  • nl and n2 may each be one or more, and nl + n2 is equal to the total number of heated sections, n.
  • the term “electrically heated section” generally means a section of the reactant tube which is heated directly or indirectly by electrical energy.
  • Direct heating may comprise, for example, applying electrical energy directly to the reactant tube.
  • Indirect heating may comprise, for example, using one or more heating elements which heat the reactant tube through one or more of radiation and convection and induction.
  • each electrically heated section typically has one or more electric heaters associated with that section.
  • each heater on the reactant tube may define a single heated section. In this case there is one heater per heated section. For example, if the reactant tube has 20 heaters distributed along its length then this may be considered as 20 heated sections. However, a heated section may be heated by more than one electric heater. For example, a heated section may be heated by two or more heaters located on different sides of the same section. However the heated sections are set, the present invention simply requires that the number of said heated sections in the first zone and in the second zone is changed during the transition. Typically there are 4 to 30 heated sections in total (n is 4 to 30).
  • the hydrocarbon feed is heated in one or more electrically heated sections to vaporise the hydrocarbon feed.
  • the hydrocarbon feed is heated to a temperature which is sufficient to vaporise the feed but insufficient to cause cracking, or at least not significant levels of cracking.
  • the most preferred temperature will be different depending on the hydrocarbon feed, but the temperature at the exit of the first zone is typically less than 600°C. (This being applicable to the first and second hydrocarbon feeds.)
  • the vaporised hydrocarbon feed is further heated to crack the hydrocarbon feed.
  • the most preferred temperature for the cracking will be different depending on the hydrocarbon feed, but the temperature at the exit of the second zone is generally at least 700°C, and more usually (and preferably), at least 750°C. (These temperatures being applicable to the first and second hydrocarbon feeds.)
  • thermoelectric in the present invention refers to the temperature of the stream.
  • temperature refers to the temperature of the vaporised hydrocarbon at the end of the first zone or the cracked gas at the end of the second zone.
  • the heating applied in each zone, and in particular to each heated section, may be controlled by control of the electrical energy. This may be adjusted using a suitable process control system and based on the feed to be cracked.
  • a transition is performed from the first process cracking the first hydrocarbon feed to a second process cracking a second hydrocarbon feed.
  • the transition comprises stopping the feeding of the first hydrocarbon feed to the reactant tube and starting the feeding of the second hydrocarbon feed to the same reactant tube. (And in the situation where multiple reactant tubes are present, this step is usually performed for all reactant tubes.)
  • the number of heated sections in the first zone is increased during the transition (ml > nl).
  • the number of heated sections in the second zone is reduced (m2 ⁇ n2).
  • the number of heated sections in the first zone can be decreased during the transition (ml ⁇ nl) and the number of heated sections in the second zone can be increased (m2 > n2).
  • the specific “change” of a heating section so that is becomes part of the first zone rather than the second zone or vice versa may be achieved by adjusting the temperature in heating sections as required. For example, if during a transition, it is desired to increase the number of heating sections in the first zone, the electrical energy input can be adjusted so that the temperature in what was previous the first heating section of the second zone is reduced from a temperature sufficient for cracking to one that is sufficient only to vaporise the feed. This heating section then becomes part of the first zone.
  • process parameters other than the number of heating sections in each zone can also be adjusted.
  • hydrocarbon feed rate, and hence residence times in the first and second zones can also be adjusted depending on the hydrocarbon feed, as can the amount of heat energy applied to different heating sections.
  • the present invention takes advantage of the superior controllability of furnaces based on electrical heating compared to fired (burner based) furnaces.
  • the amount of heating from an individual electrical heater can be finely controlled between zero and the maximum rating of the heater, and thus the individual heated sections can be adapted easily to be used for either vaporisation or cracking.
  • each heated section in a zone may be heated by a single electric heater or by several electric heaters. Either way, “fine” adjustments can be made to the heat supplied to each zone and the cracking can therefore be optimised when the feed composition changes.
  • each heating section has its own electric heater or heaters, and the electric heater(s) on a particular section are different and distinct to electric heater(s) on a different section.
  • the first aspect arises from the ability to control the electric heating of the different sections and zones, and in particular to adjust the number of heating sections in each zone. This can also provide advantages in start-up and also in long term operation i.e. not just during a transition.
  • a method for starting a process for cracking a hydrocarbon feed comprising a) passing the hydrocarbon feed to a reactant tube which reactant tube comprises a first zone and a second zone, downstream of the first zone, the first zone comprising one or more electrically heated sections and the second zone comprising two or more electrically heated sections, b) heating the hydrocarbon feed in the first zone in the one or more electrically heated sections to vaporise the hydrocarbon feed, and c) heating the vaporised hydrocarbon feed in the second zone in the two or more electrically heated sections to crack the hydrocarbon feed, wherein the number of heated sections in the first zone is nl, the number of heated sections in the second zone is n2, and nl + n2 is equal to n, where n it the total number of heated sections, wherein the start-up of the process comprises a.
  • the number of heated sections used to provide each of the first and second zones is different at start-up than during steady state operation.
  • additional heating sections (si > nl) are provided for vaporising the feed during start-up than at steady state.
  • the product stream comprises hot cracked product from which heat can be recovered.
  • this heat/energy is used to provide pre-heating of incoming fresh hydrocarbon feed, which reduces the amount of heating required to vaporise the feed in the first zone.
  • the hydrocarbon stream exiting the reactor will generally be at lower temperatures than when at steady state, so can provide less energy for pre-heating the fresh feed.
  • additional heating sections are therefore provided to enable increased heating of the fresh feed in the first zone.
  • the number of sections in the first zone is reduced to nl required for steady state operation. (And correspondingly the number in the second zone is then increased, which enables higher cracking yield to be obtained.)
  • lower feed rates may be used initially than those at steady state, to increase the residence time of the hydrocarbon feed in the reactant tube, and in particular in the second zone, which has less heating sections than at steady state.
  • the number of heated sections in the first zone at start-up, si may be one more than the number of heated sections in the first zone at steady state, nl, or may be two or more (than nl).
  • si is two or more greater than nl at the start of the start-up then it will be apparent that there may be intermediate stages between the initial start-up and the steady state operation where the first zone has a number of heating sections between si and nl, and similarly for the second zone.
  • the cracking process comprises a quench section provided downstream of the heated sections of the reactant tube in which the cracked products (of first and second hydrocarbon feeds respectively) are cooled.
  • the cooling may be by indirect heat exchange, for example with water to generate steam.
  • the cracked product stream is cooled by indirect heat exchange with incoming (fresh) hydrocarbon feed. This provides preliminary pre-heating of the hydrocarbon feed which is then passed to the reactant tube and reduces the amount of energy for vaporisation in the upstream heated sections.
  • the first and/or second hydrocarbon feed may be analysed prior to entry to the first zone and/or between the first zone and the second zone. The electrical energy provided to the one or more electrically heated sections in the first zone and/or in the second zone may then be controlled based on the results of the analysis.
  • an analyser is located upstream of the first zone and operated to provide analysis on the hydrocarbon feed, and which can then be used to control the electrically heated sections in the first and second zones.
  • Suitable analysis methods include GC, Near-IR analysis and density measurements.
  • the analysis in this embodiment preferably provides information on the boiling point range of the hydrocarbon feed. This may be an actual boiling point range, or other information indicative thereof, such as a density measurement.
  • An alternative embodiment involves analysis to measure the presence of a liquid phase, for example with an ultrasound sensor, on the hydrocarbon feed between the first zone and the second zone.
  • the heating in the first zone may then be adapted accordingly, for example to increase the heating if liquid is observed.
  • the heating in the second zone for example in earlier sections of the second zone could also be adjusted based on such a measurement.
  • control of the electrical energy to control the electrically heated sections in the first and/or second zones will be adjusted using a suitable process control system i.e. the result of the analyses are passed to process control system for the cracking reaction, and this will adjust the energy inputs accordingly.
  • the methods of the present invention may be applied for cracking on any hydrocarbon feed which can be cracked in similar processes and methods. These include those discussed, for example, in US 7288690 and WO 2022/094455 already noted.
  • the present invention may be used to crack halogenated hydrocarbons, including cracking of dichloroethane.
  • Preferred cracking processes to which the present invention can be applied are processes for cracking of hydrocarbons to produce olefins.
  • Suitable hydrocarbon feeds for cracking, and in particular to produce olefins include ethane, propane, butane, naphtha, gasoil, gas condensate, pyrolysis oils, and mixtures thereof.
  • a particularly preferred cracking process to which the present invention can be applied is the steam cracking of hydrocarbons, and in particular of the hydrocarbon feeds noted above.
  • the general process conditions such as the feed flow rates, ratios of reactants, such as steam, residence times and cracking temperatures and the like are largely as for conventional processes.
  • the feeding systems and downstream systems such as quench systems and/or heat exchange of reactant and feed streams may all be present and applied as for conventional cracking processes.
  • the ‘"electrically heated section” can be heated directly or indirectly by electrical energy.
  • the reactant tube/heated sections thereof are provided inside a furnace or heating chamber.
  • a gas preferably an inert gas. may be provided inside the chamber.
  • suitable electrically heated furnaces can be found in WO 2022/094455 already noted, or WO 2020/002326.
  • Figure 1 shows in schematic form a reactant tube for use in the method of the present invention.
  • the reactant tube comprises a first zone ( 1 ) and a second zone (2), downstream of the first zone, each zone comprising a plurality of electrically heated sections.
  • the heated sections are schematically represented by individual heaters.
  • the first zone ( 1 ) has four heated sections/heatcrs. and the remaining heated sections/heaters form the second zone (2). (It is noted that not all sections of the second zone (2) are shown.)
  • This Example illustrates the change of the number of heating sections in the first zone and in the second zone when performing a transition.
  • the tube is 15 meters in length in total, with an internal diameter of 47mm and outer diameter of 53mm.
  • the reactant tube is formed of 15 electrically heated sections each 1 meter in length and each heated by an independently controlled electrical heater (i.e. one heater provided every meter of tube).
  • the tube metal temperature is measured by thermocouples.
  • Analysis of the feedstock is performed by a near infrared analyser correlated with an ASTM D86 laboratory analyser to provide a distillation temperature profile, and using a densimeter to measure the feedstock density.
  • the feedstock is a naphtha.
  • the analyses determine that the feedstock has a density of 0.715 g/cm3 and a distillation temperature profile as follows:
  • This naphtha at a flow rate is 250 kg/h is mixed with 75 kg/h of water steam, and is fed to the reactant tube.
  • the feedstock temperature at the inlet is 128°C and the pressure is 530 kPaa. It is determined from the analysis that the feedstock can be fully vaporised by provision of 30.9 kW of electrical power, and that this energy can be provided by a single electrically heated section (i.e. the first section) in the reactant tube. Thus, the first zone comprises the first heated section. The remaining 14 heated sections form a second zone in which the hydrocarbon feed can be cracked. Thus, in this process nl is 1, and n2 is 14. The feedstock is passed to the reactant tube under these conditions and cracked.
  • the gas temperature at the end of the vaporisation zone is 136°C.
  • the cracked gas temperature at the end of the cracking zone/end of the reactant tube is 820°C, this being a typical cracking temperature for naphtha.
  • the average heat transfer to the reactant tube is 150kW/m2.
  • This gas oil at a flow rate is 250 kg/h is mixed with 75 kg/h of water steam, and is fed to the reactant tube.
  • the feedstock temperature at the inlet is 120°C and the pressure is 530 kPaa. It is determined from the analysis that the feedstock can be fully vaporised by provision of 102.5 kW of electrical power, and in this process it is decided to use the first 6 metres of the reactant tube as a vaporisation zone (first zone).
  • the first zone comprises six heated sections. The remaining 9 heated sections form a second zone in which the hydrocarbon feed can be cracked.
  • ml is 6, and m2 is 9.
  • the electrical heat energy applied to the reactant tube between 2 and 6 m in length from the inlet is reduced so that these are converted from sections in the second zone to sections in the first zone for the second process.
  • the gas oil feedstock is passed to the reactant tube under these conditions and cracked.
  • the feedstock is fully vaporised in the vaporisation zone, with a gas temperature at the end of the vaporisation zone of 301 °C.
  • the cracked gas temperature at the end of the cracking zone/end of the reactant tube is 770°C, this being a typical cracking temperature for gas oil.
  • This Example illustrates the change of the number of heating sections in the first zone and in the second zone when starting a process.
  • Example 2 the initial conditions at start-up are taken as the conditions for cracking of the gas oil feed in Example 1.
  • the gas oil at a flow rate is 250 kg/h is mixed with 75 kg/h of water steam, and is fed to the reactant tube.
  • the feedstock temperature at the inlet is 120°C and the pressure is 530 kPaa.
  • the first zone comprises six heated sections. The remaining 9 heated sections form a second zone in which the hydrocarbon feed can be cracked.
  • si is 6, and s2 is 9.
  • this represents a process with a low level of pre-heating of the feed prior to the first zone, typical of a process start-up.
  • first zone can be reduced to comprise two heated sections.
  • the remaining 13 heated sections form a second zone in which the hydrocarbon feed can be cracked.
  • the cracking is altered to a process where, at steady state, nl is 2, and n2 is 13.
  • This process allows the optimum number of heating sections to be used for cracking at steady state whilst allowing for an improved start-up process.

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  • Physics & Mathematics (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • General Physics & Mathematics (AREA)
  • Automation & Control Theory (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Thermal Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)

Abstract

La présente invention se réfère à des procédés de craquage de charges d'hydrocarbures, et concerne en particulier un procédé de transition d'un premier processus de craquage d'une première charge d'hydrocarbures à un second processus de craquage d'une seconde charge d'hydrocarbures, dans lequel : a) le premier processus consistant à, a. faire passer la première charge d'hydrocarbures vers un tube de réactif, ledit tube de réactif comprenant une première zone et une seconde zone, en aval de la première zone, chaque zone comprenant une ou plusieurs sections chauffées électriquement, b. chauffer la première charge d'hydrocarbures de la première zone dans la ou les sections chauffées électriquement pour vaporiser la première charge d'hydrocarbures, et c. chauffer la première charge d'hydrocarbures vaporisée de la seconde zone dans la ou les sections chauffées électriquement pour craquer la première charge d'hydrocarbures, le nombre de sections chauffées dans la première zone étant n1, le nombre de sections chauffées dans la seconde zone étant n2, et n1 + n2 étant égal à n, n représentant le nombre total de sections chauffées ; b) la transition consistant à arrêter d'alimenter la première charge d'hydrocarbures vers le tube de réactif et à commencer à alimenter la seconde charge d'hydrocarbures vers le même tube réactif, et c) le second processus consistant à, a. faire passer la seconde charge d'hydrocarbures vers le tube de réactif, ledit tube de réactif comprenant une première zone et une seconde zone, en aval de la première zone, chaque zone comprenant une ou plusieurs sections chauffées électriquement, b. chauffer la seconde charge d'hydrocarbures de la première zone dans la ou les sections chauffées électriquement pour vaporiser la seconde charge d'hydrocarbures, et c. chauffer la seconde charge d'hydrocarbures vaporisée de la seconde zone dans la ou les sections chauffées électriquement pour craquer la seconde charge d'hydrocarbures, le nombre de sections chauffées dans la première zone étant ml, le nombre de sections chauffées dans la seconde zone étant m2, et m1 + m2 étant égal à n, et la seconde charge d'hydrocarbures étant différente de la première charge d'hydrocarbures, m1 ≠ n1 et m2 ≠ n2.
EP23814481.0A 2022-12-15 2023-11-30 Procédé de craquage Pending EP4634335A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP22213922 2022-12-15
PCT/EP2023/083763 WO2024126071A1 (fr) 2022-12-15 2023-11-30 Procédé de craquage

Publications (1)

Publication Number Publication Date
EP4634335A1 true EP4634335A1 (fr) 2025-10-22

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Country Link
EP (1) EP4634335A1 (fr)
JP (1) JP2025541255A (fr)
CN (1) CN120380114A (fr)
WO (1) WO2024126071A1 (fr)

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Publication number Priority date Publication date Assignee Title
TWI855572B (zh) * 2022-02-23 2024-09-11 南韓商Ｌｇ化學股份有限公司 流體加熱裝置

Family Cites Families (5)

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Publication number Priority date Publication date Assignee Title
FR2796078B1 (fr) 1999-07-07 2002-06-14 Bp Chemicals Snc Procede et dispositif de vapocraquage d'hydrocarbures
WO2020002326A1 (fr) 2018-06-29 2020-01-02 Shell Internationale Research Maatschappij B.V. Réacteur chauffé électriquement et procédé de conversion de gaz utilisant ledit réacteur
EP3730592A1 (fr) * 2019-04-24 2020-10-28 SABIC Global Technologies B.V. Utilisation d'énergie renouvelable dans la synthèse d'oléfine
KR102898701B1 (ko) 2020-11-02 2025-12-10 루머스 테크놀로지 엘엘씨 올레핀을 생성하기 위한 전기로
EP4056892A1 (fr) * 2021-03-10 2022-09-14 Linde GmbH Procédé et système de vapocraquage

Also Published As

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CN120380114A (zh) 2025-07-25
WO2024126071A1 (fr) 2024-06-20
JP2025541255A (ja) 2025-12-18

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