Classifications

• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01D—SEPARATION
  • B01D53/00—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
  • B01D53/02—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
  • 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
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01D—SEPARATION
  • B01D5/00—Condensation of vapours; Recovering volatile solvents by condensation
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01D—SEPARATION
  • B01D53/00—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
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01D—SEPARATION
  • B01D53/00—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
  • B01D53/002—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 condensation
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01D—SEPARATION
  • B01D53/00—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
  • B01D53/02—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
• • C—CHEMISTRY; METALLURGY
  • C01—INORGANIC CHEMISTRY
  • C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
  • C01B7/00—Halogens; Halogen acids
  • C01B7/01—Chlorine; Hydrogen chloride
  • C01B7/03—Preparation from chlorides
  • C01B7/04—Preparation of chlorine from hydrogen chloride
• • C—CHEMISTRY; METALLURGY
  • C01—INORGANIC CHEMISTRY
  • C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
  • C01B7/00—Halogens; Halogen acids
  • C01B7/01—Chlorine; Hydrogen chloride
  • C01B7/07—Purification ; Separation
• • C—CHEMISTRY; METALLURGY
  • C01—INORGANIC CHEMISTRY
  • C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
  • C01B7/00—Halogens; Halogen acids
  • C01B7/01—Chlorine; Hydrogen chloride
  • C01B7/07—Purification ; Separation
  • C01B7/0706—Purification ; Separation of hydrogen chloride
  • C01B7/0718—Purification ; Separation of hydrogen chloride by adsorption
• • C—CHEMISTRY; METALLURGY
  • C01—INORGANIC CHEMISTRY
  • C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
  • C01B7/00—Halogens; Halogen acids
  • C01B7/01—Chlorine; Hydrogen chloride
  • C01B7/07—Purification ; Separation
  • C01B7/0706—Purification ; Separation of hydrogen chloride
  • C01B7/0718—Purification ; Separation of hydrogen chloride by adsorption
  • C01B7/0725—Purification ; Separation of hydrogen chloride by adsorption by active carbon
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01D—SEPARATION
  • B01D2253/00—Adsorbents used in seperation treatment of gases and vapours
  • B01D2253/10—Inorganic adsorbents
  • B01D2253/102—Carbon
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01D—SEPARATION
  • B01D2257/00—Components to be removed
  • B01D2257/20—Halogens or halogen compounds
  • B01D2257/206—Organic halogen compounds
  • B01D2257/2064—Chlorine
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01D—SEPARATION
  • B01D2257/00—Components to be removed
  • B01D2257/70—Organic compounds not provided for in groups B01D2257/00 - B01D2257/602
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01D—SEPARATION
  • B01D2257/00—Components to be removed
  • B01D2257/70—Organic compounds not provided for in groups B01D2257/00 - B01D2257/602
  • B01D2257/702—Hydrocarbons
  • B01D2257/7027—Aromatic hydrocarbons
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01D—SEPARATION
  • B01D2259/00—Type of treatment
  • B01D2259/40—Further details for adsorption processes and devices
  • B01D2259/40083—Regeneration of adsorbents in processes other than pressure or temperature swing adsorption
  • B01D2259/40088—Regeneration of adsorbents in processes other than pressure or temperature swing adsorption by heating
  • B01D2259/4009—Regeneration of adsorbents in processes other than pressure or temperature swing adsorption by heating using hot gas
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
  • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
  • Y02P20/00—Technologies relating to chemical industry
  • Y02P20/10—Process efficiency
  • Y02P20/129—Energy recovery, e.g. by cogeneration, H2recovery or pressure recovery turbines
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
  • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
  • Y02P20/00—Technologies relating to chemical industry
  • Y02P20/151—Reduction of greenhouse gas [GHG] emissions, e.g. CO2
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
  • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
  • Y02P20/00—Technologies relating to chemical industry
  • Y02P20/20—Improvements relating to chlorine production

Definitions

• the invention relates to a process for the treatment of gas streams contaminated with organic compounds by means of adsorption.
• the invention relates to the purification of hydrogen chloride-containing process gases.
• activated carbon is used as adsorber, which is regenerated after use. It is further proposed to regenerate the adsorber at elevated temperatures or under reduced pressure and optionally with the use of an inert gas.
• a disadvantage of this method is that the production process and HCl purification process for regeneration of the activated carbon bed must be interrupted.
• Another disadvantage of the method is that the regeneration is operated thermally or at reduced pressure, which is energetically unfavorable, or performed using an inert gas, which is costly.
• the object of the invention is to provide a more energetically more favorable process, which in particular reduces the use of costly inert gases in the workup of the adsorber and allows a continuous process.
• the adsorptive separation of mainly organic components from gas streams is widely used in the process industry.
• the adsorbent is usually heated and contacted with a regeneration gas stream. As a result, the adsorbed components dissolve in the regeneration gas stream and the adsorbent is discharged.
• the achievable purity of the gas stream depends essentially on the conceptual design of the regeneration of the loaded adsorbent.
• Conventional regeneration methods use heated inert gas or water vapor to simultaneously introduce the required heat energy and regeneration gas flow into the system.
• water vapor can only be used in cases where moisture can be tolerated within the process.
• it is attempted to avoid the introduction of water via the steam in order to prevent the corrosion of the product-contacting apparatus.
• inert gases e.g., nitrogen, etc.
• the amounts of gas to be supplied cause high costs in the simple use of an inert current.
• the components dissolved in the inert stream during the regeneration of the adsorber must be depleted before the stream is returned to the circulation. Otherwise, the regeneration would not be sufficient to achieve the required process gas purities in the next adsorption operation.
• the present invention aims to reduce the inert consumption of regenerative adsorption processes in process gas purification of organic compound contaminated gas streams.
• the invention relates to a regenerative adsorption process for removing organic components from an optionally hot crude gas stream with the steps:
• Inertgasnikstromes at a temperature of at most 0 0 C; K) subsequent adsorption of the residual organic components remaining in the inert gas circulating stream after the condensation J) in a second adsorption medium; L) optionally subsequent heat exchange between the inert gas circulating stream emerging from the adsorption K) and that entering the condensation J)
• Activated carbon zeolites, alumina, bentonite, silica gel or organometallic complexes are generally used as adsorbents. Activated carbon is preferred.
• Common types of apparatus for producing an intensive gas adsorbent Kunststoffes are simple fixed beds, fluidized beds, fluidized beds or as a whole movable fixed beds.
• a method which is characterized in that the cooling of the crude gas first takes place in a cooler to a temperature of at most 45 0 C is preferred. Further preferably, the cooling of the crude gas stream in a second step, in particular in a recuperator, to a temperature of at most 40 0 C.
• the heat exchange between the gas stream emerging from the adsorption C) and in the condensation B) entering raw gas stream in a recuperator is preferred.
• the cooling I) takes place in a first step in a cooler to a Temperature of at most 45 0 C and in a second step in a recuperator to a temperature of at most 40 0 C.
• a particularly preferred variant of the method is characterized in that the second adsorption medium mentioned under K) is regenerated with the aid of a further heated inert gas stream.
• the process is particularly preferably used when the raw gas stream to be purified essentially consists of hydrogen chloride and / or the inert gas for the inert gas circulating stream consists predominantly of nitrogen.
• organic compounds particularly preferred are substantially hydrocarbons or halogenated hydrocarbons, particularly preferred are aromatic hydrocarbons such as benzene, toluene, xylenes, and C 6 -C 2 aliphatics or chlorinated hydrocarbons such as phosgene, carbon tetrachloride hydrogen, vinyl chloride and dichloroethane, or chlorinated aromatic hydrocarbons such as hexachlorobenzene, monochlorobenzene and orthodichlorobenzene.
• Another particularly preferred variant of the process is characterized in that the adsorption mentioned under C) takes place in at least two adsorption stages.
• the adsorption medium of the first stage C) is particularly preferably regenerated with the aid of a partial stream of the crude gas stream, and the laden crude gas partial stream optionally combined with the crude gas stream entering the condensation B).
• a preferred modification of the method is characterized in that the adsorption medium of the first stage of the adsorption C) is regenerated from time to time by means of an inert gas, optionally in a single pass, alternating with the regeneration with the crude gas substream.
• an inert gas optionally in a single pass, alternating with the regeneration with the crude gas substream.
• the method is particularly preferably used when the hydrogen chloride-containing purified gas stream is used in a production process for the production of chlorine from hydrogen chloride and oxygen, in particular in a catalyzed gas phase oxidation of hydrogen chloride with oxygen or a non-thermal reaction of hydrogen chloride and oxygen.
• the coupling with the catalyzed gas phase oxidation of hydrogen chloride with oxygen is particularly preferred.
• the catalytic process known as the Deacon process is used in combination with the process according to the invention.
• hydrogen chloride is oxidized with oxygen in an exothermic equilibrium reaction to form chlorine, whereby water vapor is obtained.
• the reaction temperature is usually 150 to 500 0 C, the usual reaction pressure is 1 to 25 bar. Since it is an equilibrium reaction, it is expedient to work at the lowest possible temperatures at which the catalyst still has sufficient activity.
• oxygen in excess of stoichiometric amounts of hydrogen chloride. For example, a two- to four-fold excess of oxygen is customary. Since no loss of selectivity is to be feared, it may be economically advantageous to work at relatively high pressure and, accordingly, longer residence time than normal pressure.
• Suitable preferred catalysts for the Deacon process include ruthenium oxide, ruthenium chloride or other ruthenium compounds on silica, alumina,
• Titanium dioxide or zirconium dioxide as carrier.
• Suitable catalysts may for example by
• Suitable catalysts may, in addition to or instead of a ruthenium compound, also contain compounds of other noble metals, for example gold, palladium, platinum, osmium, iridium, silver, copper or rhenium. suitable
• Catalysts may further contain chromium (i ⁇ ) oxide.
• the catalytic hydrogen chloride oxidation may be adiabatic or preferably isothermal or approximately isothermal, batchwise, but preferably continuously or as a fixed bed process, preferably as a fixed bed process, more preferably in tube bundle reactors to heterogeneous catalysts at a reactor temperature of 180 to 500 0 C, preferably 200 to 400 0th C, more preferably 220 to 350 0 C and a pressure of 1 to 25 bar (1000 to 25000 hPa), preferably 1.2 to 20 bar, more preferably 1.5 to 17 bar and in particular 2.0 to 15 bar are performed ,
• Typical reactors in which the catalytic hydrogen chloride oxidation is carried out are fixed bed or fluidized bed reactors.
• the catalytic hydrogen chloride oxidation can preferably also be carried out in several stages.
• a suitable device for the method is that one uses a structured catalyst bed, in which the catalyst activity in Flow direction increases.
• Such Strukturierüng the catalyst bed can be done by different impregnation of the catalyst support with active material or by different dilution of the catalyst with an inert material.
• an inert material for example, rings, cylinders or balls of titanium dioxide, zirconium dioxide or mixtures thereof, alumina, steatite, ceramic, glass, graphite, stainless steel or nickel alloys can be used.
• the inert material should preferably have similar external dimensions.
• Suitable shaped catalyst bodies are shaped bodies with any desired shapes, preference being given to tablets, rings, cylinders, stars, carriage wheels or spheres, particular preference being given to rings, cylinders or star strands as molds.
• Ruthenium compounds or copper compounds on support materials are particularly suitable as heterogeneous catalysts, preference being given to optionally doped ruthenium catalysts.
• suitable carrier materials are silicon dioxide, graphite, rutile or anatase titanium dioxide, zirconium dioxide, aluminum oxide or mixtures thereof, preferably titanium dioxide, zirconium dioxide, aluminum oxide or mixtures thereof, particularly preferably ⁇ - or ⁇ -aluminum oxide or mixtures thereof.
• the copper or ruthenium-supported catalysts can be obtained, for example, by impregnation of the support material with aqueous solutions of CuCl 2 or RuCl 3 and optionally a promoter for doping, preferably in the form of their chlorides.
• the shaping of the catalyst can take place after or preferably before the impregnation of the support material.
• the catalysts are suitable as promoters alkali metals such as lithium, sodium, potassium, rubidium and cesium, preferably lithium, sodium and potassium, more preferably potassium, alkaline earth metals such as magnesium, calcium, strontium and barium, preferably magnesium and calcium, particularly preferably magnesium, Rare earth metals such as scandium, yttrium, lanthanum, cerium, praseodymium and neodymium, preferably scandium, yttrium, lanthanum and cerium, more preferably lanthanum and cerium, or mixtures thereof.
• alkali metals such as lithium, sodium, potassium, rubidium and cesium, preferably lithium, sodium and potassium, more preferably potassium, alkaline earth metals such as magnesium, calcium, strontium and barium, preferably magnesium and calcium, particularly preferably magnesium, Rare earth metals such as scandium, yttrium, lanthanum, cerium, praseodymium and neodymium, preferably scandium, yt
• the moldings can then be dried at a temperature of 100 to 400 0 C, preferably 100 to 300 0 C, for example, under a nitrogen, argon or air atmosphere and optionally calcined.
• the moldings are first dried at 100 to 150 0 C and then calcined at 200 to 400 0 C.
• the conversion of hydrogen chloride in a single pass may preferably be limited to 15 to 90%, preferably 40 to 85%, particularly preferably 50 to 70%. Unreacted hydrogen chloride can be partially or completely separated into the catalytic after separation Hydrogen chloride oxidation can be attributed.
• the volume ratio of hydrogen chloride to oxygen at the reactor inlet is preferably 1: 1 to 20: 1, preferably 1: 1 to 8: 1, particularly preferably 1: 1 to 5: 1.
• the heat of reaction of the catalytic hydrogen chloride oxidation can be used advantageously for the production of high-pressure steam. This can be used to operate a phosgenation reactor and / or distillation columns, in particular of isocyanate distillation columns.
• the chlorine formed is separated off.
• the separation step usually comprises several stages, namely the separation and optionally recycling of unreacted hydrogen chloride from the product gas stream of the catalytic hydrogen chloride oxidation, the drying of the obtained, substantially chlorine and oxygen-containing stream and the separation of chlorine from the dried stream.
• the separation of unreacted hydrogen chloride and water vapor formed can be carried out by condensation of aqueous hydrochloric acid from the product gas stream of hydrogen chloride oxidation by cooling. Hydrogen chloride can also be absorbed in dilute hydrochloric acid or water.
• FIG. 1 shows a process flow diagram of the crude gas purification with inert gas circulation
• FIG. 2 shows a process as in FIG. 1 with two serial adsorbers each
• an improved process concept also achieves a high purity of the regeneration gas and thus a high degree of regeneration of the adsorber while at the same time minimizing the consumption of inert gas.
• the regeneration gas stream is circulated, thus minimizing the inert consumption.
• the raw gas 1 (here hydrogen chloride gas from a TDI production) is pre-cooled in a cooler 21 and passed through the recuperator 22.
• Organic contaminants such as e.g. Hexachlorobenzene, monochlorobenzene or orthodichlorobenzene are condensed in the condenser 23 and removed as stream 8.
• the prepurified crude gas 2 is passed through an adsorbent bed 24 of activated carbon, the purified gas stream 3 passed from hydrogen chloride through the recuperator 22 for heat exchange with incoming raw gas 1, discharged as product stream 4 and oxidized in a (not shown) Deacon process to chlorine.
• the loaded adsorbent bed 24 ' which is operated in alternation with the adsorber bed 24, is cleaned with an inert gas 6, which is composed of fresh inert gas 5 and a return flow 10 and is heated in the heat exchanger 25.
• the laden regeneration gas stream After passing through the adsorber 24 ', the laden regeneration gas stream is cooled down in a precooler 27. Subsequently, a further cooling takes place in a recuperator 28. Subsequently, the regeneration gas stream is further cooled in a low-temperature condenser. During this cooling, an essential component of the organic components contained in the regeneration gas is already removed and combined with the stream 8. However, according to the thermodynamic equilibrium, a proportion of organic components corresponding to the vapor pressure of the respective organic components will still remain in the gas phase. This proportion can be reduced within limits by choosing correspondingly low temperatures or high process pressures.
• the circulating gas adsorber 30 is loaded, it is exchanged with the adsorber 31 and transferred to the regeneration mode. For this purpose, fresh inert gas 13 is heated in the heat exchanger 32 and directed against the flow direction during the loading phase on the adsorber 31.
• the loaded regeneration gas stream 12 is discharged from the system.
• the inventive regenerative adsorption process for removing organic components from gas streams allows a reduced inert gas consumption for the regeneration by the realization of a cycle gas method for the regeneration gas with high levels of regeneration due to the use of a Kreisgasadsorbers and thereby achieved high cycle gas purities.
• the use of a recirculating gas adsorber makes it possible to discharge components which can not be condensed during the low-temperature condensation and thus reduces or prevents their accumulation in the process.
• the Inertgaseinschleusung 5 shown in Fig. 1 in the regeneration cycle can be used for pressure maintenance, system flushing or the discharge of otherwise enriching components.
• the discharge takes place via stream 11.
• injection and discharge can also take place at any other positions in the regeneration gas cycle.
• the raw gas 1 also passes through the cooling and condensation stages 21, 22 and 23 already described in Example 1, in which part of the organic components contained in the gas stream is separated off.
• the prepurified crude gas 2 exiting from step 23 is passed into the two-stage adsorption 24, 26, in which the remaining organic components are completely or partially separated off.
• the concept requires a two-stage adsorption, since in the regeneration mode the first adsorption stage 24 'regenerates only partially with a heated partial stream 7 of the raw gas is and only in the second adsorption 26 'by an increased degree of regeneration, the required purities in the process gas can be achieved.
• the purified gas stream 3 is passed through the recuperator 22 for heat exchange with incoming raw gas 1, discharged as product stream 4 and oxidized in a (not shown) Deacon process to chlorine.
• a partial flow 7 of the still untreated raw gas is heated in the heat exchanger 34 and added to the first stage 24 'of the adsorption.
• the loaded partial stream 14 of the process gas used for the partial regeneration is added to the raw gas stream 1 again.
• the regeneration of the second adsorption stage is carried out with inert gas either in a single pass or in the recycle as shown in Fig. 2.
• the loaded adsorbent bed 26 ' which is operated in alternation with the adsorbent bed 26, cleaned with an inert gas 6, which is composed of fresh inert gas 5 and a return flow 10 and is heated in the heat exchanger 25.
• the loaded regeneration stream as in Example 1, passes through the cooling and condensation stages 27, 28 and 29.
• an essential constituent of the organic components contained in the regeneration gas is removed and combined with the stream 8.
• a proportion of organic components corresponding to the vapor pressure of the respective organic components will still remain in the gas phase. This proportion can be reduced within limits by choosing correspondingly low temperatures or high process pressures.
• the circulating gas adsorber 30 is loaded, it is exchanged with the adsorber 31 and transferred to the regeneration mode. For this purpose, fresh inert gas 13 is heated in the heat exchanger 32 and directed against the flow direction during the loading phase on the adsorber 31.
• the loaded regeneration gas stream 12 is discharged from the system.
• the Inertgaseinschleusung 5 is used in the regeneration cycle of pressure maintenance, system flushing or the discharge of otherwise enriching components.
• the discharge takes place via stream 11.
• injection and discharge can also take place at any other positions in the regeneration gas cycle.

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• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Inorganic Chemistry (AREA)
• Engineering & Computer Science (AREA)
• Analytical Chemistry (AREA)
• General Chemical & Material Sciences (AREA)
• Oil, Petroleum & Natural Gas (AREA)
• Separation Of Gases By Adsorption (AREA)
• Vaporization, Distillation, Condensation, Sublimation, And Cold Traps (AREA)

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• 2007
  • 2007-04-10 DE DE102007016973A patent/DE102007016973A1/de not_active Withdrawn
• 2008
  • 2008-03-26 EP EP08734761A patent/EP2136893A1/de not_active Withdrawn
  • 2008-03-26 WO PCT/EP2008/002360 patent/WO2008122363A1/de active Application Filing
  • 2008-03-26 KR KR1020097021123A patent/KR20100015469A/ko not_active Application Discontinuation
  • 2008-03-26 CN CN200880010636A patent/CN101652162A/zh active Pending
  • 2008-03-26 JP JP2010502434A patent/JP5036862B2/ja not_active Expired - Fee Related
  • 2008-04-10 US US12/100,456 patent/US7749307B2/en not_active Expired - Fee Related

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