Abstract: Acid gas purification processes for reducing nitrosamine precursor formation from a gas stream containing NOx, wherein the acid gas is selectively absorbed in an amine based wash solution comprising at least one secondary diamine. The processes generally include absorbing carbon dioxide from the gas stream containing NOx species with the amine-based wash solution comprising at least one secondary diamine to provide a carbon dioxide lean gas stream that is released into the surroundings, wherein absorbing the acid gas forms a rich amine solution; and regenerating the rich amine solution at an elevated temperature to release the carbon dioxide to form a regenerated lean amine solution, wherein absorbing and regenerating are configured to promote formation of carbamate species of at least one diamine.

Abstract: A method for the removal of CO2 from exhaust gases, e.g., exhaust gases from plants for pig-iron production or exhaust gases from synthesis-gas plants, includes removing CO2 using chemical and/or physical absorption, wherein the heat for regenerating the absorbent is obtained at least partially from an air separation plant. As a result, the CO2 can be separated from the exhaust gases to a greater extent than in the pressure-swing adsorption of other gases, but a lower-order energy carrier can additionally be used for this purpose.

Abstract: The invention relates to an absorbent, comprising an aqueous solution (A) of at least one amino acid salt of the formula (I), wherein R1 and R2 independently from each other represent alkyl or hydroxyalkyl, R is hydrogen, alkyl or hydroxyalkyl, or a group R together with R1 is alkylene, M is an alkali metal, and n an integer from 1 to 6, and (B) of at least one primary alkanolamine, which is substantially free of inorganic alkaline salts. The absorbent is used in a method for removing carbon dioxide from a gas flow, particularly combustion exhaust gases. Preferred amino acid salts (A) are N,N-dimethylamino acetic acid potassium salt, N,N-diethylamino acetic acid potassium salt and N-ethyl-N-methylamino acetic acid-potassium salt. Preferred alkanolamines (B) are 2-aminoethanol, 3-aminopropanol, 4-aminobutanol, 2-aminobutanol, 5-aminopentanol, 2-aminopentanol and 2-(2-aminoethoxy)ethanol.

Abstract: Novel solvent composition for selective removal of COS from a gas stream containing same, said composition comprising a) at least one polyalkylene glycol alkyl ether of the formula R1O-(Alk-O)n—R2??(I) or 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone or a mixture of N-formylmorpholine and N-acetylmorpholine wherein R1 is an alkyl group having from 1 to 6 carbon atoms; R2 is hydrogen or an alkyl group having from 1 to 4 carbon atoms; Alk is an alkylene group, branched or unbranched, having from 2 to 4 carbon atoms, and n is from 1 to 10; and b) at least one alkanolamine compound of the formula R3NHR4OR6??(II) or at least one piperazine compound of formula wherein R3 is hydrogen, an alkyl group having from 1 to 6 carbon atoms, or the R4OH group; R4 is a branched or unbranched alkylene group having from 1 to 6 carbon atoms; R5, independently in each occurrence, is hydrogen or an hydroxyalkyl group having from 1 to 4 carbon atoms; and R6 is hydrogen, an alkyl group having from 1

Abstract: A method for separating methane and carbon dioxide from biogas and a device are intended for purifying biogas, wherein carbon dioxide is separated off from the biogas. The method is distinguished by an energetically favorable mode of operation. The biogas is passed under atmospheric pressure and standard temperature into an absorption column. While the biogas ascends through a packed bed, which has a surface area of 600 to 1200 m2/m3, and at a space velocity of 5 to 40 Nm3/m3h, carbon dioxide present in the biogas is bound in a wash liquid by chemosorption. The purified methane gas is taken off at the top of the absorption column at a defined flow velocity. Carbon dioxide bound in the wash liquid is removed by desorption at a relatively high pressure of 2 to 30 bar and a temperature of at least 120° C. Biogas may be separated into methane and CO2.

Abstract: An absorbent liquid according to the present invention is an absorbent liquid for absorbing CO2 or H2S or both from gas, in which the absorbent liquid includes an alkanolamine as a first compound component, and a second component including a nitrogen-containing compound having in a molecule thereof two members or more selected from a primary nitrogen, a secondary nitrogen, and a tertiary nitrogen or a nitrogen-containing compound having in a molecule thereof all of primary, secondary, and tertiary nitrogens. The absorbent liquid has an excellent absorption capacity performance and an excellent absorption reaction heat performance, as compared to an aqueous solution containing solely an alkanolamine and a nitrogen-containing compound in the same concentration in terms of wt %, and can recover CO2 or H2S or both from gas with smaller energy.

Abstract: Novel solvent composition for selective removal of COS from a gas stream containing same, said composition comprising a) at least one polyalkylene glycol alkyl ether of the formula R1O-(Alk-O)n—R2??(I) or 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone or a mixture of N-formylmorpholine and N-acetylmorpholine wherein R1 is an alkyl group having from 1 to 6 carbon atoms; R2 is hydrogen or an alkyl group having from 1 to 4 carbon atoms; Alk is an alkylene group, branched or unbranched, having from 2 to 4 carbon atoms, and n is from 1 to 10; and b) at least one alkanolamine compound of the formula R3NHR4OR6??(II) or at least one piperazine compound of formula wherein R3 is hydrogen, an alkyl group having from 1 to 6 carbon atoms, or the R4OH group; R4 is a branched or unbranched alkylene group having from 1 to 6 carbon atoms; R5, independently in each occurrence, is hydrogen or an hydroxyalkyl group having from 1 to 4 carbon atoms; and R6 is hydrogen, an alkyl group having from 1

Abstract: The present invention relates to a method of deacidizing a gaseous effluent, wherein the following stages are carried out: a) contacting the gaseous effluent with an absorbent solution so as to obtain a gaseous effluent depleted in acid compounds and an absorbent solution laden with acid compounds, the absorbent solution being selected for its property to form two separable phases when it absorbs an amount of acid compounds, b) separating the absorbent solution laden with acid compounds into two fractions: a first absorbent solution fraction depleted in acid compounds and a second absorbent solution fraction enriched in acid compounds, c) regenerating the second fraction so as to release part of the acid compounds, d) mixing a predetermined amount of water with the first absorbent solution fraction obtained in stage b) or with the regenerated absorbent solution fraction obtained in stage c), then e) recycling the first absorbent solution fraction and the regenerated absorbent solution as the absorbent solu

Abstract: A method and system for CO2 capture from flue gas uses an absorber vessel in which a flue gas stream containing CO2 is contacted with an ammoniated solution to remove CO2 from the flue gas, and a regenerator vessel in which CO2 is released from the ammoniated solution. Parasitic energy consumption of the system can be reduced by adding to the ammoniated solution a promoter effective to enhance the formation of ammonium bicarbonate within the ammoniated solution. The amount of ammoniated solution recycled from the regenerator vessel to the absorber vessel is less than that which would be required using the ammoniated solution without the promoter for removal of the same amount of CO2 from the flue gas.

Abstract: A contaminant-tolerant hybrid scrubbing solvent is provided for post-combustion CO2 capture and removal, the scrubbing solvent including an amine and a low fraction of ammonia. A stripping carrier having a low latent energy is included for solvent regeneration. In one embodiment, the amine is MEA and the stripping chemical having low latent energy is pentane or an isomer thereof. Processes and apparatus for CO2 removal from post-combustion gases and for solvent regeneration are described.

Abstract: An absorbing solution according to the present invention is an absorbing solution that absorbs CO2 or H2S in gas or both of CO2 and H2S. The absorbing solution is formed by adding desirably 1 to 20 weight percent of tertiary monoamine to a secondary-amine composite absorbent such as a mixture of secondary monoamine and secondary diamine. Consequently, it is possible to control degradation in absorbing solution amine due to oxygen or the like in gas. As a result, it is possible to realize a reduction in an absorption loss, prevention of malfunction, and a reduction in cost. This absorbing solution is suitably used in an apparatus for removing CO2 or H2S or both of CO2 and H2S.

Abstract: A method is described for separating CO2 and/or H2S from a mixed gas stream by contacting the gas stream with a non-aqueous, liquid absorbent medium of a primary and/or secondary aliphatic amine, preferably in a non-aqueous, polar, aprotic solvent under conditions sufficient for sorption of at least some of the CO2. The solution containing the absorbed CO2 can then be treated to desorb the acid gas. The method is usually operated as a continuous cyclic sorption-desorption process, with the sorption being carried out in a sorption zone where a circulating stream of the liquid absorbent contacts the gas stream to form a CO2-rich sorbed solution, which is then cycled to a regeneration zone for desorption of the CO2 (advantageously at <100° C.). Upon CO2 release, the regenerated lean solution can be recycled to the sorption tower. CO2:(primary+secondary amine) adsorption molar ratios >0.5:1 (approaching 1:1) may be achieved.

Abstract: A CO2 amine scrubbing process uses an absorbent mixture consisting of an alkanolamine CO2 sorbent in combination with a non-nucleophilic base. The alkanolamine has oxygen and nitrogen sites capable of nucleophilic attack at the CO2 carbon atom. The nucleophilic addition is promoted in the presence of the non-nucleophilic, relatively stronger base, acting as a proton acceptor. The non-nucleophilic base promoter, which may also act as a solvent for the alkanolamine, can promote reaction with the CO2 at each of the reactive hydroxyl and nucleophilic amine group(s) of the alkanolamines. In the case of primary amino alkanolamines the CO2 may be taken up by a double carboxylation reaction in which two moles of CO2 are taken up by the reacting primary amine groups.

Abstract: The present application includes a method for inhibiting amine degradation during CO2 capture from flue gas streams. Particularly, the present disclosure relates to a method of inhibiting O2- and/or SO2-induced degradation of amines using sodium sulfite (Na2SO3), potassium sodium tartrate tetrahydrate (KNaC4H4O6.4H2O), ethylenediaminetetraacetic acid (EDTA) or hydroxylamine (NH2OH), or analogs or mixtures thereof during CO2 capture by amines.

Abstract: The invention describes an integrated process for capturing CO2 emitted by at least a portion of the flue gas coming from the regeneration zone of a catalytic cracking unit using a unit for amine treatment of said flue gas, in which the catalytic cracking unit is equipped with an external exchanger using as the hot fluid a portion of the catalyst removed from the regeneration zone, the heat necessary for the amine treatment unit being supplied integrally by the catalytic cracking unit using the steam generated by said external exchanger.

Abstract: In a method for removing acid gases from a fluid stream, the fluid stream, which is in contact with an absorption medium within an absorber, is passed through a first absorption zone in the absorber to remove a majority of acid gases from the fluid stream. The fluid stream is susequently passed through a second absorption zone in the absorber to further remove acid gases from the fluid stream. The loaded absorption medium is passed into a first regeneration zone to obtain a partially regenerated absorption medium, and a part of the partially regenerated absorption medium is passed into the first absorption zone. The other part of the partially regenerated absorption medium is passed into a second regeneration zone to obtain a regenerated absorption medium. A part of the regenerated absorption medium is passed into the first absorption zone and the other part is passed into the second absorption zone.

Abstract: A description is given of an absorption medium for removing carbon dioxide from gas streams which comprises aqueous solution of an amine of the formula I HNR2??(I) where one or both radicals R are and the other radical R is hydrogen. The absorption medium is distinguished by particular oxidation resistance.

Abstract: An aqueous carbon dioxide-absorbent solution comprising at least one alkanolamine and at least one quaternary ammonium salt is disclosed. A method of recovering carbon dioxide from a carbon dioxide-containing gaseous mixture and a method of reducing metal corrosion in an alkanolamine-based exhaust gas treating process are also disclosed.

Abstract: This invention relates to a method and plant for energy-efficient removal of CO2 from a gas phase by means of absorption. The invention is particularly suitable for use in connection with thermal power plants fired by fossil fuels, and is also well-suited for retrofitting in existing thermal power plants. A processing plant according to the invention comprises three sections: a primary CO2-generating process that serves as main product supplier; a CO2-capture and separation plant based on absorption and desorption of CO2 respectively by/from at least one absorbent; and a second CO2-generating process where combustion of carbonaceous fuel in pure oxygen atmosphere serves as energy supply to at least a part of the thermal energy necessary to drive the regeneration of the absorbent in the desorption column(s).

Abstract: Systems, methods, and apparatus for capturing CO2 using a solvent are provided. A gas that includes carbon dioxide may be mixed with a solvent that is operable to absorb at least a portion of the carbon dioxide from the gas. The solvent containing the carbon dioxide may be provided to at least one removal system operable to remove at least a portion of the liquid contained in the solvent. The solvent output by the removal system may be stripped to extract at least a portion of the carbon dioxide from the solvent.

Abstract: A sour gas sweetening solution comprises an aqueous solution of a silicon-containing compound and an amine-containing compound. The silicon-containing compound is preferably maintained at a concentration less than or equal to 500 parts per million (“ppm”) more preferably less than or equal to 400 ppm, and most preferably between about 100 ppm and 300 ppm as SiO2. The silicon-containing compound can be MxSiyOz, wherein “M” is a metal and “x”, “y” and “z” are numbers greater than zero. The amine-containing compound can be selected from the group consisting of primary amines, secondary amines and tertiary amines.

Abstract: Carbon dioxide and other acid gases are removed from gaseous streams using aqueous absorption and stripping processes. By replacing the conventional stripper used to regenerate the aqueous solvent and capture the acid gas with a matrix stripping configuration, less energy is consumed. The matrix stripping configuration uses two or more reboiled strippers at different pressures. The rich feed from the absorption equipment is split among the strippers, and partially regenerated solvent from the highest pressure stripper flows to the middle of sequentially lower pressure strippers in a “matrix” pattern. By selecting certain parameters of the matrix stripping configuration such that the total energy required by the strippers to achieve a desired percentage of acid gas removal from the gaseous stream is minimized, further energy savings can be realized.

Abstract: A process to capture and sequester an impurity gas from a fluid stream. The impurity gas capture is accomplished by contacting the fluid stream with an impurity removing mixture, the mixture comprising an ionic liquid and an amine compound under conditions sufficient to reduce the amount of impurity gas from said fluid stream. The captured impurity gas is sequestered by reacting the impurity gas with a sequestration material.

Abstract: A process for the removal of hydrogen sulfide from a gas stream in which the gas stream is first passed through a Claus unit operating at a sub-stoichiometric ratio (H2S:SO2) of greater than 2:1 to produce a tail gas stream comprising less than 2000 vppm SO2. This tail gas stream is then treated to increase the sulfur recovery to at least 99.5% by first directly cooling the tail gas stream by contact with water as a coolant, followed by contacting the gas stream with a circulating stream of a dilute, absorbent solution of a severely sterically hindered secondary aminoether alcohol to further cool the gas stream, and then removing the H2S from the stream using a stronger absorbent solution of a severely sterically hindered secondary aminoether alcohol.

Abstract: A chilled ammonia based CO2 capture system and method is provided. A promoter is used to help accelerate certain capture reactions that occur substantially coincident to and/or as a result of contacting a chilled ammonia based ionic solution with a gas stream that contains CO2.

Abstract: Novel solvent composition for selective removal of COS from a gas stream containing same, said composition comprising a) at least one polyalkylene glycol alkyl ether of the formula (I) or 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone or a mixture of N-formylmorpholine and N-acetylmorpholine Wherein R1 is an alkyl group having from 1 to 6 carbon atoms; R2 is hydrogen or an alkyl group having from 1 to 4 carbon atoms; Alk is an alkylene group, branched or unbranched, having from 2 to 4 carbon atoms, and n is from 1 to 10; and b) at least one alkanolamine compound of the formula (II) or at least one piperazine compound of formula (III) wherein R3 is hydrogen, an alkyl group having from 1 to 6 carbon atoms, or the R4OH group; R4 is a branched or unbranched alkylene group having from 1 to 6 carbon atoms; R5, independently in each occurrence, is hydrogen or an hydroxyalkyl group having from 1 to 4 carbon atoms; and R6 is hydrogen, an alkyl group having from 1 to 6 carbon atoms or an hydroxyalkyl group having f

Abstract: An process for efficiently deacidizing a gaseous mixture is described. The process utilizes a self-concentrating absorbent that absorbs an acid gas at reduced overall energy costs for the deacidizing operation.

Abstract: The present invention describes a method for recovery of high purity carbon dioxide, which is substantially free of nitrogen oxides. The present invention also discloses a plant for recovery of said high purity carbon dioxide comprising an absorption column, a flash column, a stripper column, and a purification unit.

Abstract: A process for maintaining a low carbon monoxide content in a carbon dioxide product that is made in a synthesis gas purification process is disclosed. More particularly, the invention involves an improved process in which a portion of a loaded solvent is sent through a carbon dioxide absorber instead of to a series of carbon dioxide flash drums.

Abstract: Systems and processes utilize one or more methods of providing overhead waste process heat to increase the feed temperature of the hot solvent stripping regeneration loop in an acid gas removal process. A heated rich solvent stream can be the primary feed for the hot solvent stripping regeneration loop, and one or more slip streams can be heated and then combined with the heated rich solvent stream to form a combined rich solvent stream prior to further processing in downstream units to remove acid gas from the solvent. A first slip stream can be heated in a stripper gas heat exchanger by heat exchange with a stripped gas stream. A second slip stream can be heated in a regenerator exchanger by heat exchange with an acid gas stream. A third slip stream can be heated in a recycle gas exchanger by heat exchange with a compressed recycle gas stream.

Abstract: A process for the removal of an amine capturable gas from a feed gas stream using an amine solvent, the process comprises (a) contacting the feed gas stream with a lean amine solvent to form a rich amine solvent, wherein heat stable salts are present in the rich amine solvent; (b) stripping amine capturable gas from the rich amine solvent to form the lean amine solvent and an overhead reflux stream; (c) periodically contacting at least a portion of one or both of the lean amine solvent and the rich amine solvent with an anion exchange resin to form a first heat stable salt lean amine solvent; (d) periodically regenerating the anion exchange resin, wherein during the regeneration of the anion exchange resin, at least a portion of the reflux stream is used to wash the amine solvent from the anion exchange resin to produce a second heat stable salt lean amine solvent; and, (e) recycling at least a portion of the first and the second heat stable salt lean amine solvent for use in capturing the amine capturable ga

Abstract: A sorbent system includes a porous polymer support and a sorbent within the porous polymer support. For example, the sorbent includes a tertiary amine, such as triethanolamine.

Abstract: The present invention relates to a process for removing carbon dioxide and optionally hydrogen sulphide and/or COS from a gas stream containing these compounds by washing the gas with an aqueous washing solution containing water, sulfolane and a secondary or tertiary amine derived from ethanolamine. More particularly the invention relates to the process described above, the process being carried out in the presence of a primary or secondary amine compound in an amount between 0.5 and 15 wt. % based on water, sulfolane and amine. The invention further relates to an absorbent liquid to be used in the above process.

Abstract: A treating unit that comprises an absorber unit for contacting a regenerated solvent with a gas stream loaded with contaminants to yield a treated gas stream and a loaded solvent stream; a regenerator unit for stripping the loaded solvent stream to yield a loaded gas stream and the regenerated solvent; and a device for smoothing contaminant peak concentrations in the loaded solvent stream and for receiving the loaded solvent stream. The device comprises a first hold-up tank having a first inlet and a first outlet, a second hold-up tank having a second inlet and a second outlet, and an inlet distributor that is operatively connected to the first inlet and to the second inlet and that provides for directing flow of the loaded solvent stream to either the first hold-up tank or the second hold-up tank.

Abstract: Disclosed is a method for deacidifying a fluid stream containing acidic gases as contaminants, according to which the fluid stream is brought into intimate contact with a washing liquid in at least one absorption step. Said washing liquid represents an aqueous solution containing a) tertiary aliphatic alkanolamines (alkanolamine A), at least 30 percent by weight of said tertiary aliphatic alkanolamines being 3-dimethylamino-1-propanol, and b) secondary aliphatic amines (activator B), at least 20 percent by weight of said secondary aliphatic amines being piperazin. The fluid stream which has been essentially purified of the acidic gases is then separated from the washing liquid that is loaded with acidic gases.

Abstract: A method for removing CO2 in a exhaust gas from combustion of carbonaceous material, in which method the exhaust gas is brought in countercurrent flow with a liquid CO2 absorbent in a contact section of an absorption column, to produce a CO2 depleted exhaust gas that is released into the atmosphere and a CO2 rich absorbent that is withdrawn from the absorption column, wherein the exhaust gas is introduced into the absorption column at a temperature above about 90 and the exhaust gas is cooled in the absorption column by countercurrent flow of the liquid absorbent in the absorption column, is described.

Abstract: An absorption medium for deacidifying fluid streams which has improved oxidation stability includes at least one aliphatic amine, and at least one non-hydroquinoid antioxidant. The absorption medium may be employed in deacidifying a fluid stream, in particular an oxygen-containing fluid stream, when the fluid stream is brought into intimate contact with the absorption medium in at least one absorption step.

Abstract: Apparatus comprising an absorber device provided with a plurality of sequentially adjacent sections for flowing a gas stream therethrough. A conduit infrastructure comprising a section configured to ingress, communicate with and egress from each section of the absorber device, and a recovery and regeneration section, is configured with a plurality of heat exchange and cooling equipment. A process wherein a liquid solvent provided with at least one chemical compound selected for reacting with the selected gaseous component, is counter-flowed against and commingled with the gas stream. The liquid solvent temperature is controllably manipulated between each section of the column to provide: (a) thermodynamic-driven mass transfer at the front end of the absorber device, and (b) kinetic-driven mass transfer at the back end of the absorber device. The heat generated during the recovery of the gaseous component from the absorption liquid solvent system is recovered for use in regenerating solvent system.

Abstract: The invention relates to a fluid separating device with a lower section with a fluid feeding device and a liquid discharging device, an upper section with a fluid feeding device and a gas discharging device, a contact device which is constructed in such a manner that gas, which rises from the lower section into the upper section, comes into contact with liquid which sinks from the upper section into the lower section. Thereby, the rising gases can be depleted of components which are soluble in said liquid. Furthermore, a measuring device for determining the quantity of liquid and/or the alterations thereof is provided.

Abstract: A method for obtaining an acid gas stream having a pressure of from 3 to 30 bar by removal of acid gases from a fluid stream containing H2S, the molar fraction of H2S based on the total amount of acid gases being at least 50 mol %, the method comprising bringing the fluid stream into intimate contact with a liquid absorption medium, thus producing a fluid stream substantially freed from acid gases and an acid-gas-loaded liquid absorption medium; separating the fluid stream and the liquid absorption medium; separating, by heating and optionally by expansion or stripping, the liquid absorption medium into an acid gas stream and a regenerated liquid absorption medium; passing the regenerated liquid absorption medium into a heat exchanger and cooling it there by using part of its thermal energy to heat up the acid-gas-loaded liquid absorption medium; and recirculating the regenerated liquid absorption medium.

Abstract: A process for the removal of hydrogen sulfide and mercaptans from a gas stream containing a high ratio of mercaptans to hydrogen sulfide, wherein the first step removes hydrogen sulfide by washing the gas stream with an aqueous washing solution comprising water, a physical solvent and a chemical solvent. The first removal step is followed by a second removal step by which mercaptans are removed from the washed gas stream by means of molecular sieves.

Abstract: A process for the abatement of hydrogen sulphide in refinery gases by means of a liquid-ring compressor (10) uses, as service liquid, an aqueous solution of amines already available in the refinery itself. The process also comprises a stage of washing of the gas discharged by the compressor, by means of a column (20) mounted on a three-phase separator supplied with a regenerated solution of amines. The treatment in the liquid-ring compressor enables an effective abatement of the amount of hydrogen sulphide to be achieved, which can be further improved by washing using a regenerated amine solution supplied to the column set above the liquid/gas separator (18) downstream of the compressor.

Abstract: An acid gas removal plant includes an absorber that provides a rich solvent to two regenerators that independently generate a lean and a semi-lean solvent, wherein the semi-lean solvent is produced in one of the regenerators using heat and/or steam derived from the other regenerator. Further heat integration is particularly contemplated with power plants in which the power plant provides high-level heat to the acid gas removal plant and wherein the power plant receives low-level heat from the acid gas removal plant.

Abstract: The disclosure relates to an absorbent for removing acid gases from fluids. The absorbent contains at least one tertiary amine, an amine which is selected from hydroxyethylpiperazine, bis(hydroxyethylpiperazine) or a mixture of these and piperazine. The absorbent may optionally contain a physical solvent for the acid gases.

Abstract: A method of treating an acidic component in an exhaust gas includes contacting the exhaust gas with an aqueous solution including a water-soluble amine that produces a water-soluble salt when reacted with the acidic component of the exhaust gas.

Abstract: This invention relates to a process for cleaning gas, in particular hydrocarbonaceous gas such as e.g. natural gas, which is contaminated with sulfur in the form of H2S and mercaptans as well as CO2. To remove the undesired sulfur-containing substances in the form of H2S and mercaptan from crude gas, it is proposed in accordance with the invention that the crude gas is introduced into an absorption and regeneration column and washed therein, three gas streams being withdrawn from this absorption and regeneration column, a first exhaust gas stream being introduced into a Claus plant, a second sour gas stream with a low H2S concentration being introduced into another absorption plant, and a third gas stream, the valuable gas with the mercaptans, being cooled and supplied to an adsorption plant, that from this adsorption plant a cleaned valuable gas is withdrawn, and a mercaptan-containing gas stream is subjected to washing, that this concentrated mercaptan-containing gas is supplied to the Claus plant.

Abstract: A hydrocarbon gas containing H2S, mercaptans and CO2 is fed to an absorption plant operated at a pressure of 20 to 80 bar and supplied with a selective solvent, a solvent stream loaded with H2S and a roughly desulfurized gas stream are withdrawn, the H2S loaded solvent stream is charged to a regeneration plant and the roughly desulfurized gas stream is charged to an absorption and regeneration plant operated at a pressure of 20 to 80 bar, a large first gas stream of H2S and CO2 and an unloaded solvent stream are withdrawn from the absorption regeneration plant, and the large first gas steam of H2S and CO2 is supplied to a Claus plant, and a valuable hydrocarbon gas stream is withdrawn from the absorption and regeneration plant.

Abstract: A process is described for removing acid gases from a gas stream in which an acid-gas-containing gas stream in which the sum of the partial pressures of the acid gases does not exceed 1,500 mbar is brought into contact with an aqueous absorbent in an absorption step and an absorbent is used which contains methyldiethanolamine and piperazine at a concentration of at least 8% by weight of the absorbent, an acid-gas-depleted gas stream and an acid-gas-loaded absorbent being obtained.

Abstract: A column of solvent containing foaming contaminants is provided. Gas is educted into the solvent in the column so as to generate foam in the column. The gas is educted into the column independently of the input flow of solvent into the solvent using a pumparound arrangement with the solvent. Foam generation continues so as to push the foam up in the column, wherein much of the solvent that is in the foam is allowed to drain back down into the column. The foam passes through concentrators which increase the residency time of the foam in the column to further dry the foam and to create larger bubbles. The drier foam is pushed out of the column and into a container. The foam is broken up into gas and the liquid foaming contaminants. The gas is recirculated for injection into the column even after foaming has stopped. The foaming contaminants are concentrated at the surface level of the solvent in the column. These contaminants are removed from the column.

Abstract: A description is given of the use of an alkylenediamine of the type R1HN—X—NHR2, where X is an alkylene radical having from 2 to 9 carbons, R1 is a hydrocarbon radical having from 1 to 6 carbons and R2 is a hydrocarbon radical having from 1 to 6 carbons or is hydrogen (H) for removing sour gases from a sour-gas-containing fluid stream, and of a process for deacidifying a fluid stream of this type and a wash liquid or absorption liquid for use in such a process. According to the invention, in at least one absorption step, the fluid stream is brought into intimate contact with a wash liquid, the wash liquid comprising an aqueous amine solution which comprises at least one tertiary aliphatic alkanolamine having from 2 to 12 carbons and an activator of the above type R1HN—X—NHR2. The fluid stream which is substantially freed from sour gases and the sour-gas-loaded wash liquid are then separated from one another.