In a process for removal of acid gases from a fluid stream the fluid stream is contacted with an absorbent to obtain a treated fluid stream and a laden absorbent. The absorbent comprises a diluent and a compound of the general formula (I) wherein R.sup.1 is C.sub.1-C.sub.3-alkyl; R.sup.2 is C.sub.1-C.sub.3-alkyl; R.sup.3 is selected from hydrogen and C.sub.1-C.sub.3-alkyl; and R.sup.4 is selected from hydrogen and C.sub.1-C.sub.3-alkyl. ##STR00001##

A system and method for processing unconditioned syngas first removes solids and semi-volatile organic compounds (SVOC), then removes volatile organic compounds (VOC), and then removes at least one sulfur containing compound from the syngas. Additional processing may be performed depending on such factors as the source of syngas being processed, the products, byproducts and intermediate products desired to be formed, captured or recycled and environmental considerations.

Hydrogen sulfide is removed from a gas stream by bubbling a gas stream having ≥100 ppm hydrogen sulfide through a scavenging mixture. The scavenging mixture includes: 1) at least one sweetener selected from the group consisting of triazines, oxazolidines, hemiacetals, and mixtures thereof, and 2) at least one reaction catalyst selected from the group consisting of dipropyl amine (DPA), diethyl amine (DEA), dimethyl amine (DMA), pyrrole, and mixtures thereof. The scavenging mixture interacts with the hydrogen sulfide to produce a cleaned gas stream having ≤ 5 ppm hydrogen sulfide.

Processes for separating carbon dioxide from a gas mixture that comprises CO.sub.2 and N.sub.2 that are based upon formation of gas hydrates, and systems useful for implementing such processes, are disclosed.

The present invention relates to a process for removing acid compounds contained in a gaseous effluent which consists in bringing a gaseous effluent into contact, in the absorption column, with an absorbent solution comprising water, between 20% and 28% by weight of pentamethyldipropylenetriamine and between 5% and 35% by weight of N-methyldiethanolamine.

This invention provides compositions and methods that inhibit formation of alkenyl sulfide polymers and allow the hydrogen sulfide to be removed when scavenging hydrogen sulfide by reaction with aldehydes.

A process is presented to treat a process gas stream containing hydrogen sulfide using a reverse jet absorber with a liquid treatment solution containing a chelated metal catalyst. A treat gas substantially free of the hydrogen sulfide is separated from a spent liquid treatment solution containing elemental sulfur which can then be regenerated in an oxidation vessel where it is contacted with an oxygen containing gas to convert the spent liquid treatment solution to a regenerated liquid treatment solution that can be recycled for introduction into the reverse jet absorber.

Disclosed is a process comprising: step a) contacting a feed stream comprising a contaminant with an absorbent stream in a counter-current flow to produce a contaminant depleted product stream depleted in the molar quantity of the contaminant relative to the molar quantity of said contaminant in the feed stream, and a contaminant enriched absorbent stream enriched in the molar quantity of the contaminant relative to the molar quantity of said contaminant in the absorbent stream; and step b) treating the contaminant enriched absorbent stream to form a gaseous stream comprising said contaminant and a regenerated absorbent stream lean in the molar quantity of said contaminant relative to the molar quantity of said contaminant in the contaminant enriched absorbent stream; herein said absorbent stream comprises at least 15 wt. % of at least one compound (A) of general formula (I) or a mixture (M) comprising at least one compound (B) of general formula (II) and at least one compound (C) of general formula (III).

Intensification techniques are described for enhancing biocatalytic CO.sub.2 absorption operations, and may include the use of a rotating packed bed, a rotating disc reactor, a zig-zag reactor or other reactors that utilize process intensification. Carbonic anhydrase can be deployed in the high intensity reactor free in solution, immobilized with respect to particles that flow with the liquid, and/or immobilized to internals, such as packing, that are fixed within the high intensity reactor.

Methods of sequestering carbon dioxide (CO.sub.2) are provided. Aspects of the methods include contacting an aqueous capture ammonia with a gaseous source of CO.sub.2 under conditions sufficient to produce an aqueous ammonium carbonate. The aqueous ammonium carbonate is then combined with a cation source under conditions sufficient to produce a solid CO.sub.2 sequestering carbonate and an aqueous ammonium salt. The aqueous capture ammonia is then regenerated from the from the aqueous ammonium salt. Also provided are systems configured for carrying out the methods.