Provided is a carbon dioxide recovery device including an absorption part that produces a compound of carbon dioxide and an amine contained in an absorbing solution, and a regeneration part that includes an anode that desorbs the carbon dioxide from the compound to produce a complex compound of the amine, and a cathode that is electrically connected to the anode and regenerates the amine from the complex compound.

A gas separation system has system input inlet configured to receive a stream mixture including a target gas, one or more spray generators positioned to spray a non-sprayable liquid to change a concentration of the target gas in the non-sprayable liquid, one or more system outlets positioned to outlet an output material, wherein at least one of the system outlets outputs a material having a lower amount of the target gas than the input stream mixture, and a recirculating path connected to the one or more outputs and the input inlet to allow recirculation of the non-sprayable liquid. A method of performing gas separation includes absorbing a target gas from an input stream in a non-sprayable capture liquid, and releasing the target gas in an output gas stream by spraying the non-sprayable capture liquid into a heated volume using a spray generator. A method of performing gas separation includes receiving an input stream that includes a target gas, using one or more spray generators to apply a non-sprayable liquid as a spray to the input stream to change a concentration of the target gas in the liquid, and outputting the liquid with the changed concentration through an outlet.

An exhaust gas carbon dioxide capture and recovery system that may be mounted on a mobile vehicle or vessel. The system may include an exhaust absorber system, a solvent regenerator, a solvent loop, a carbon dioxide compressor, and a carbon dioxide storage tank, among other components. The system may be configured and integrated such that energy in the exhaust may be used to power and drive the carbon dioxide capture while having minimal parasitic effect on the engine.

A carbon dioxide (CO.sub.2) capture system to reduce CO.sub.2 emissions comprises an absorption zone and a regeneration zone. The absorption zone captures CO.sub.2 from exhaust gas by absorption in a liquid solvent separated from the exhaust gas by a separator. The liquid solvent comprises a blend of alkali metal salts of two or more amino or amino-sulfonic acids, thereby forming a first constituent and a second constituent. The first constituent is a primary or secondary amino or amino sulfonic acid with molar mass of less than 200 g/mol. The second constituent has a molar mass of less than 300 g/mol. The regeneration zone may rejuvenate the liquid solvent rich in captured CO.sub.2 by heating so that a resulting liquid solvent with a low concentration of CO.sub.2 is pumped back to the absorption zone. An on-board CO.sub.2 capture and storage system for a mobile internal combustion engine and a method for capturing CO.sub.2 are also described.

A process for capturing carbon dioxide (CO.sub.2) present in a gas stream is provided. The process includes providing a cooling tower that treats a gas stream. The gas stream including CO.sub.2 is introduced into the cooling tower. A liquid carbon-dioxide-capturing media is released into the gas stream in the cooling tower. The carbon-dioxide-capturing media absorbs the CO.sub.2 in the gas stream, and the carbon-dioxide-capturing media including the absorbed CO.sub.2 is collected. An absorber for capture of CO.sub.2 in a gas stream is also provided. The absorber includes a cooling tower for treatment of a gas stream including CO.sub.2. The cooling tower includes an input for the gas stream, an outlet for a treated gas stream, and a sprayer that releases liquid carbon-dioxide-capturing media into the cooling tower. The carbon-dioxide-capturing media absorbs the CO.sub.2 from the gas stream in the cooling tower. A collector collects the carbon-dioxide-capturing media including absorbed CO.sub.2.

Solid sorbents, and especially zeolites, are attractive candidates for CO.sub.2 direct air capture (DAC) and point source capture applications because of their potential for high selectivity, fast kinetics, and low energy CO.sub.2 capture cycles. A common issue with solid sorbents, including zeolites, is their low thermal conductivity, which makes them difficult to heat for regeneration without using complex and expensive heat transfer systems. This invention utilizes a modified TVSA process which utilizes the product CO.sub.2 gas itself as the heating medium for the adsorbent bed, alone or in conjunction with internal or external heaters. The use of CO.sub.2 as a heating medium allows efficient heating of the sorbent bed and enables high purity CO.sub.2 product.

The invention relates to an absorber column and to the use thereof for separation of unwanted, especially acidic, gas constituents, for example carbon dioxide and hydrogen sulfide, from a crude synthesis gas by absorption with an absorbent, especially under low load states of the absorber column in relation to the synthesis gas velocity. According to the invention, a defined concentration of carbon dioxide in the clean synthesis gas is established by mixing at least a portion of the absorbent regenerated by flash regeneration with the absorbent regenerated by means of hot regeneration prior to the recycling thereof into the absorber column.

An exhaust gas cleaning system comprises a first sub system including a scrubber unit comprising a scrubber arranged to wash the exhaust gas with a scrubber fluid, and a centrifugal separator arranged in communication with the scrubber unit for receiving the scrubber fluid after washing and separate it into a first and a second fraction, which second fraction is more polluted than the first fraction. The exhaust gas cleaning system further comprises a second sub system including a membrane filter arranged in communication with the centrifugal separator for receiving the first fraction output from the centrifugal separator and separating it into a third and a fourth fraction, which fourth fraction is more polluted than the third fraction. A method for cleaning exhaust gas onboard a ship involves cleaning an exhaust gas onboard a ship.

A process for recovering nitric acid or salts thereof, comprising: contacting, in the presence of water, an water-immiscible ionic liquid of the formula [A.sup.+][X.sup.−], wherein [A.sup.+] represents a phosphonium or ammonium cation and [X.sup.−] represents a counter anion which is NO.sub.3.sup.−, an halide anion displaceable by NO.sub.3.sup.−, or both, with a fluid which contains HNO.sub.3 and at least one more mineral acid, or precursors of said acids, and partition, under mixing, said acids between aqueous and organic phases and form nitrate-loaded ionic liquid of the formula [A.sup.+][NO.sub.3.sup.−].sub.z>0.25 where Z indicates a molar amount of nitrate held in the ionic liquid beyond the positions occupied by the nitrate counter ions; separating the so-formed mixture into an organic phase comprising a nitrate-loaded ionic liquid of the formula [A.sup.+][NO.sub.3.sup.−].sub.z>0.25 and an aqueous phase consisting of a nitrate-depleted aqueous solution that contains the other mineral acid(s); stripping the nitric acid from said nitrate-loaded ionic liquid to create an aqueous nitrate solution and regenerate ionic liquid of the formula [A.sup.+][NO.sub.3.sup.−].sub.z≥0 with reduced nitrate loading, or unloaded [A.sup.+][NO.sub.3.sup.−].sub.z=0 ionic liquid.

A method for recovering CO.sub.2 in the Rectisol process. The method includes at least the following steps: performing reduced-pressure flash distillation treatment on the CO.sub.2-rich methanol liquid, and outputing the CO.sub.2 desorbed gas obtained after the reduced-pressure flash distillation treatment as a product gas; performing heat exchange flash distillation treatment on a first methanol treatment liquid obtained after the reduced-pressure flash distillation treatment, and outputing the CO.sub.2 desorbed gas obtained after the heat exchange flash distillation treatment as a product gas; performing vacuum flash distillation treatment on a second methanol treatment liquid obtained after the heat exchange flash distillation treatment, and outputing the CO.sub.2 desorbed gas obtained after the vacuum flash distillation treatment as a product gas. Reduced-pressure flash distillation treatment, heat exchange flash distillation treatment and vacuum flash distillation treatment are sequentially performed on the CO.sub.2-rich methanol liquid in this method.