A treatment process for remediating H.sub.2S and other contaminants in liquids includes: partially filling a closed vessel with a contaminated liquid containing ≥5 ppm H.sub.2S with a head space above the liquid within the vessel where gasses released from the liquid from the liquid collect; separately providing a treatment composition in the head space so that the gasses from the liquid may contact the treatment composition; and permitting the contact between the vapors from the liquid and the treatment composition to continue until a collective concentration of H.sub.2S in the liquid and in the head space is <5 ppm. The treatment composition includes an aqueous solution containing at least one hydroxide compound, a collective concentration of the at least one hydroxide compound in the aqueous solution is in a range of 35-55 weight %, and the aqueous solution constitutes at least 80 weight % of the treatment composition.

This invention relates to a method and a system for abating hydrogen sulfide (H.sub.2S) and carbon dioxide (CO.sub.2) from H.sub.2S and CO.sub.2rich gas mixtures such as geothermal non-condensable gas mixtures (NCG). The H.sub.2S and CO.sub.2 gas is separated from the remaining gases contained in the H.sub.2S and CO.sub.2rich gas mixtures by pressurizing the gas stream and feeding it into an absorption column where H.sub.2S and CO.sub.2 are preferentially dissolved in a water stream, resulting in water stream rich in H.sub.2S and CO.sub.2. The H.sub.2S and CO.sub.2 rich water stream may then be re-injected into a geological reservoir or used for pH modification of another water stream of geological origin.

A system and method for removing hydrogen sulfide from natural gas using a triazine scavenger is described. The system includes a pre-treatment system that can be connected to an existing hydrogen sulfide removal system to more fully utilize the triazine scavenger. The pre-treatment system includes a contactor vessel in which sour natural gas is contacted with fresh and/or partially consumed scavenger to partially sweeten the sour gas by removing H.sub.2S. The partially sweetened gas then flows to the existing hydrogen sulfide removal system where it is fully sweetened.

A system and method for removing hydrogen sulfide from natural gas using a triazine scavenger is described. The system includes a pre-treatment system that can be connected to an existing hydrogen sulfide removal system to more fully utilize the triazine scavenger. The pre-treatment system includes a contactor vessel in which sour natural gas is contacted with fresh and/or partially consumed scavenger to partially sweeten the sour gas by removing H.sub.2S. The partially sweetened gas then flows to the existing hydrogen sulfide removal system where it is fully sweetened.

Systems and methods use bimetallic alloy particles for converting hydrogen sulfide (H.sub.2S) to hydrogen (H.sub.2) and sulfur (S), typically during multiple operations. In a first operation, metal alloy composite particles can be converted to a composite metal sulfide. In a second operation, composite metal sulfide from the first operation can be regenerated back to the metal alloy composite particle using an inert gas stream. Pure, or substantially pure, sulfur can also be generated during the second operation.

Systems and methods use bimetallic alloy particles for converting hydrogen sulfide (H.sub.2S) to hydrogen (H.sub.2) and sulfur (S), typically during multiple operations. In a first operation, metal alloy composite particles can be converted to a composite metal sulfide. In a second operation, composite metal sulfide from the first operation can be regenerated back to the metal alloy composite particle using an inert gas stream. Pure, or substantially pure, sulfur can also be generated during the second operation.

Processes, systems, and associated control methodologies are disclosed that control the flow of biogas during the biogas cleanup process to create a more consistent flow of biogas through the digester, while also optimizing the output and efficiency of the overall renewable natural gas facility. In representative embodiments, a biogas buffer storage system may be used during the cleanup process to control the pressure and flow rate of biogas. The biogas buffer storage system may monitor and control the biogas flow rate to either bring down or increase the digester pressure, thereby maintaining a normalized biogas flow rate.

Processes, systems, and associated control methodologies are disclosed that control the flow of biogas during the biogas cleanup process to create a more consistent flow of biogas through the digester, while also optimizing the output and efficiency of the overall renewable natural gas facility. In representative embodiments, a biogas buffer storage system may be used during the cleanup process to control the pressure and flow rate of biogas. The biogas buffer storage system may monitor and control the biogas flow rate to either bring down or increase the digester pressure, thereby maintaining a normalized biogas flow rate.

This invention provides a composition comprising I. at least one reaction product between a nitrogen-free monohydric alcohol and an aldehyde or ketone, and II. at least one reaction product between a monosaccharide having 3 to 6 carbon atoms and/or an oligosaccharide being formed by oligomerization of monosaccharides having 3 to 6 carbon atoms and an aldehyde or ketone, and optionally III. at least one reaction product from III.a) formaldehyde, and III.b) an amine, selected from the group consisting of primary alkyl amines having 1 to 4 carbon atoms, and primary hydroxy alkyl amines having 2 to 4 carbon atoms, and optionally IV. at least one solid suppression agent selected from the group consisting of IV(a). alkali or alkaline earth metal hydroxides IV(b). mono-, di- or tri-hydroxy alkyl, aryl or alkylaryl amines, IV(c). mono-, di- or tri-alkyl, aryl or alkylaryl primary, secondary and tertiary amines or IV(d). multifunctional amines and IV(e). mixtures of compounds of groups IV(a) to IV(c). wherein alkyl is C.sub.1 to C.sub.15, aryl is C.sub.6 to C.sub.15 and alkylaryl is C.sub.7 to C.sub.15.

This invention provides a composition comprising I. at least one reaction product between a nitrogen-free monohydric alcohol and an aldehyde or ketone, and II. at least one reaction product between a monosaccharide having 3 to 6 carbon atoms and/or an oligosaccharide being formed by oligomerization of monosaccharides having 3 to 6 carbon atoms and an aldehyde or ketone, and optionally III. at least one reaction product from III.a) formaldehyde, and III.b) an amine, selected from the group consisting of primary alkyl amines having 1 to 4 carbon atoms, and primary hydroxy alkyl amines having 2 to 4 carbon atoms, and optionally IV. at least one solid suppression agent selected from the group consisting of IV(a). alkali or alkaline earth metal hydroxides IV(b). mono-, di- or tri-hydroxy alkyl, aryl or alkylaryl amines, IV(c). mono-, di- or tri-alkyl, aryl or alkylaryl primary, secondary and tertiary amines or IV(d). multifunctional amines and IV(e). mixtures of compounds of groups IV(a) to IV(c). wherein alkyl is C.sub.1 to C.sub.15, aryl is C.sub.6 to C.sub.15 and alkylaryl is C.sub.7 to C.sub.15.