Abstract: A regeneration solvent comprised of one or more ethylene amines may contact an adsorbent bed that has been used to remove sulfur compounds from a hydrocarbon stream to extract adsorbed sulfur compounds from the adsorbent material in the bed to regenerate it. The one or more ethyleneamines may have structure (I), (II), or (III): where R1, R2, R5 and R6 are, to the extent chemically possible, independently H, C1-C4 linear or branched alkyl, amido (RRNC?O), or hydroxyalkyl, where each R in the amido group is independently H or C1 alkyl, where R3 and R4 are alkylene of from 1 to 4 carbon atoms, where x ranges from 0 to 3, y ranges from 1 to 6. The regenerated adsorbent bed may be reused, either alone or in combination with a liquid-liquid extraction column, to remove sulfur compounds from a hydrocarbon stream.

Abstract: A solvent comprised of (1) a caustic and an alcohol, (2) a caustic and a quaternary ammonium hydroxide, or (3) a caustic, an alcohol, and a quaternary ammonium hydroxide may contact an adsorbent bed that has been used to remove sulfur compounds from a hydrocarbon stream to extract adsorbed sulfur compounds from the adsorbent material in the bed to regenerate it. The regenerated adsorbent bed may be reused, either alone or in combination with a liquid-liquid extraction column, to remove sulfur compounds from a hydrocarbon stream.

Abstract: Metals, such as mercury, may be removed from aqueous, hydrocarbon, or mixed oilfield or refinery fluids by: applying a sulfur compound having the general formula HS—X, where X is a heteroatom substituted alkyl, cycloalkyl, aryl, and/or alkylaryl group either alone or in combination with or as a blend with at least one demulsifier, a buffering agent, a pour point depressant, and/or a water clarifier to chelate the at least one metal and form a chelate complex of the sulfur compound with the at least one metal and then separating the chelate complex from the fluid.

Abstract: Metals, such as mercury, may be removed from aqueous, hydrocarbon, or mixed oilfield or refinery fluids by: applying a sulfur compound having the general formula HS-X, wherein X is a heteroatom substituted alkyl, cycloalkyl, aryl, and/or alkylaryl group either alone or in combination with or as a blend with at least one demulsifier, a buffering agent, a pour point depressant, and/or a water clarifier to chelate the at least one metal and form a chelate complex of the sulfur compound with the at least one metal and then separating the chelate complex from the fluid.

Abstract: Metals, such as mercury, may be removed from glycol fluids by applying a sulfur compound having the general formula HS—X, wherein X is a heteroatom-substituted alkyl, cycloalkyl, aryl, and/or alkylaryl group either alone or in combination with or as a blend with at least one antifoam additive, at least one demulsifier and/or a buffering agent, to chelate the at least one metal and form a chelate complex of the sulfur compound with the at least one metal and then separating the chelate complex from the fluid.

Abstract: Treatment of hydrocarbon streams, and in one non-limiting embodiment refinery distillates, with reducing agents, such as borohydride and salts thereof, alone or together with at least one co-solvent results in reduction of the sulfur compounds such as disulfides, mercaptans, thiophenes, and thioethers that are present to give easily removed sulfides. In one non-limiting embodiment, the treatment converts the original sulfur compounds into hydrogen sulfide or low molecular weight mercaptans that can be extracted from the distillate with caustic solutions, hydrogen sulfide or mercaptan scavengers, solid absorbents such as clay or activated carbon or liquid absorbents such as amine-aldehyde condensates and/or aqueous aldehydes.

Abstract: Metals, such as mercury, may be removed from aqueous, hydrocarbon, or mixed oilfield or refinery fluids by: applying a sulfur compound having the general formula HS-X, wherein X is a heteroatom substituted alkyl, cycloalkyl, aryl, and/or alkylaryl group either alone or in combination with or as a blend with at least one demulsifier, a buffering agent, a pour point depressant, and/or a water clarifier to chelate the at least one metal and form a chelate complex of the sulfur compound with the at least one metal and then separating the chelate complex from the fluid.

Abstract: An extraction solvent comprised of one or more ethyleneamines having structure (I), (II), or (III): where R1-R6 can independently be H, C1-C4 linear or branched alkyl, amido (RRNC?O), or hydroxyalkyl, where each R in the amido group independently H or C1 alkyl, and where x ranges from 1 to 6, may be contacted with a hydrocarbon stream to remove or extract non-acidic contaminants, such as thiophenes, benzothiophenes, alkyl sulfides, alkyl disulfides, mercaptans, aromatics, oxygenates, metals, olefins, and combinations thereof, from the hydrocarbon stream. The extraction solvent may include co-solvents and the hydrocarbon stream may be in gas and/or liquid form.

Abstract: Waste water streams from an oil or gas recovery or refinery operation contaminated with a metal such as a heavy metal (e.g. mercury) can be treated with a protein including chordin and chordin-like proteins so that ion bonding the protein with the metal occurs to give a metal protein complex. The metal protein complex is then removed from the aqueous stream by a process such as flocculation and/or filtration.

Abstract: Certain functionalized aldehydes scavengers may be used to at least partially scavenge sulfur-containing contaminants from fluid systems containing hydrocarbons and/or water. The contaminants scavenged or otherwise removed include, but are not necessarily limited to, H2S, mercaptans, and/or sulfides. Suitable scavengers include, but are not necessarily limited to, reaction products of glycolaldehyde with aldehydes; reaction products of glycolaldehyde with a nitrogen-containing reactant (e.g. an amine, a triazine, an imine, an aminal, and/or polyamines); non-nitrogen-containing reaction products of a hydrated aldehyde with certain second aldehydes; reaction products of 1,3,5-trioxane with hydroxyl-rich compounds (e.g. glyoxal, polyethylene glycol, polypropylene glycol, pentaerythritol, and/or sugars); and reaction products of certain aldehydes with certain phenols; and combinations of these reaction products.

Abstract: An extraction solvent comprised of one or more ethyleneamines having structure (I), (II), or (III): where R1-R6 can independently be H, C1-C4 linear or branched alkyl, amido (RRNC?O), or hydroxyalkyl, where each R in the amido group independently H or C1 alkyl, and where x ranges from 1 to 6, may be contacted with a hydrocarbon stream to remove or extract non-acidic contaminants, such as thiophenes, benzothiophenes, alkyl sulfides, alkyl disulfides, mercaptans, aromatics, oxygenates, metals, olefins, and combinations thereof, from the hydrocarbon stream. The extraction solvent may include co-solvents and the hydrocarbon stream may be in gas and/or liquid form.

Abstract: Treatment of crude oil with basic ionic liquids (ILs), results in scavenging of any hydrochloric acid (HCl) that is present to remove the HCl. The IL is a quaternary ammonium compound having the formula R4N+X? or R3N+R?N+R3, where R is independently an alkyl group, an alkylbenzyl group, a hydroxyalkyl group, or a hydroxyalkylbenzyl group, and R is straight or branched and has 1-22 carbon atoms, R? is a straight or branched alkylene or oxyalkylene having 1 to 10 carbon atoms, and where X? is selected from the group consisting of hydroxide, carbonate, alkylcarbonate, bicarbonate or alkoxide, where the alkyl group of the alkyl-carbonate or alkoxide, if present, is straight or branched and has 1 to 8 carbon atoms. The ILs are introduced into the crude oil after the refinery desalters and before the crude distillation tower to prevent or inhibit HCl from distilling to the crude tower overhead.

Abstract: It has been discovered that contaminants such as metals and/or amines can be transferred from a hydrocarbon phase to a water phase in an emulsion breaking process by using a composition that contains water-soluble C5-C12 polyhydroxy carboxylic acids, ammonium salts thereof, alkali metal salts thereof, and mixtures of all of these. The composition may also optionally include a mineral acid to reduce the pH of the desalter wash water. The method permits transfer of metals and/or amines into the aqueous phase with little or no hydrocarbon phase under-carry into the aqueous phase. Resolving the emulsion into the hydrocarbon phase and the aqueous phase occurs in a refinery desalting process using electrostatic coalescence. The composition is particularly useful in treating crude oil emulsions, and in removing calcium and other metals therefrom. The polyhydroxy carboxylic acid additionally inhibits metal corrosion of metal pipe or other equipment used in a crude unit.

Abstract: It has been discovered that contaminants such as metals and/or amines can be transferred from a hydrocarbon phase to a water phase in an emulsion breaking process by using a composition that contains water-soluble C5-C12 polyhydroxy carboxylic acids, ammonium salts thereof, alkali metal salts thereof, and mixtures of all of these. The composition may also optionally include a mineral acid to reduce the pH of the desalter wash water. The method permits transfer of metals and/or amines into the aqueous phase with little or no hydrocarbon phase under-carry into the aqueous phase. Resolving the emulsion into the hydrocarbon phase and the aqueous phase occurs in a refinery desalting process using electrostatic coalescence. The composition is particularly useful in treating crude oil emulsions, and in removing calcium and other metals therefrom. The polyhydroxy carboxylic acid additionally inhibits metal corrosion of metal pipe or other equipment used in a crude unit.

Abstract: An extraction solvent comprised of one or more ethyleneamines having structure (I), (II), or (III): where R1-R6 can independently be H, C1-C4 linear or branched alkyl, amido (RRNC?O), or hydroxyalkyl, where each R in the amido group independently H or C1 alkyl, and where x ranges from 1 to 6, may be contacted with a hydrocarbon stream to remove or extract non-acidic contaminants, such as thiophenes, benzothiophenes, alkyl sulfides, alkyl disulfides, mercaptans, aromatics, oxygenates, metals, olefins, and combinations thereof, from the hydrocarbon stream. The extraction solvent may include co-solvents and the hydrocarbon stream may be in gas and/or liquid form.

Abstract: Treatment of streams containing hydrogen and/or hydrocarbons, and in one non-limiting embodiment refinery distillates, with alkyl carbonates, such as dimethylcarbonate, alone or together with at least one solvent results in reduction or removal of hydrogen sulfide (H2S) that is present to give easily removed alkyl sulfides and/or mercaptans. In one non-limiting embodiment, the treatment converts the original hydrogen sulfide into alkyl sulfides and/or mercaptans that can be extracted from the stream with caustic solutions, mercaptan scavengers, solid absorbents such as clay or activated carbon or liquid absorbents such as amine-aldehyde condensates and/or aqueous aldehydes.

Abstract: Treatment of hydrocarbon streams, and in one non-limiting embodiment refinery distillates, with reducing agents, such as borohydride and salts thereof, alone or together with at least one co-solvent results in reduction of the sulfur compounds such as disulfides, mercaptans, thiophenes, and thioethers that are present to give easily removed sulfides. In one non-limiting embodiment, the treatment converts the original sulfur compounds into hydrogen sulfide or low molecular weight mercaptans that can be extracted from the distillate with caustic solutions, hydrogen sulfide or mercaptan scavengers, solid absorbents such as clay or activated carbon or liquid absorbents such as amine-aldehyde condensates and/or aqueous aldehydes.

Abstract: A method for scavenging hydrogen sulfide by introducing to a hydrogen sulfide contaminated fluid an additive comprising a zinc carboxylate complex and a viscosity improver selected from the group consisting of glycol ethers having from about 4 to about 10 carbons, alkyl alcohols having from about 1 to about 10 carbons, and combinations thereof.

Abstract: Treatment of hydrocarbon streams, and in one non-limiting embodiment refinery distillates, with reducing agents, such as borohydride and salts thereof, alone or together with at least one co-solvent results in reduction of the sulfur compounds such as disulfides, mercaptans, thiophenes, and thioethers that are present to give easily removed sulfides. In one non-limiting embodiment, the treatment converts the original sulfur compounds into hydrogen sulfide or low molecular weight mercaptans that can be extracted from the distillate with caustic solutions, hydrogen sulfide or mercaptan scavengers, solid absorbents such as clay or activated carbon or liquid absorbents such as amine-aldehyde condensates and/or aqueous aldehydes.

Abstract: Certain functionalized aldehydes scavengers may be used to at least partially scavenge sulfur-containing contaminants from fluid systems containing hydrocarbons and/or water. The contaminants scavenged or otherwise removed include, but are not necessarily limited to, H2S, mercaptans, and/or sulfides. Suitable scavengers include, but are not necessarily limited to, reaction products of glycolaldehyde with aldehydes; reaction products of glycolaldehyde with a nitrogen-containing reactant (e.g. an amine, a triazine, an imine, an aminal, and/or polyamines); non-nitrogen-containing reaction products of a hydrated aldehyde with certain second aldehydes; reaction products of 1,3,5-trioxane with hydroxyl-rich compounds (e.g. glyoxal, polyethylene glycol, polypropylene glycol, pentaerythritol, and/or sugars); and reaction products of certain aldehydes with certain phenols; and combinations of these reaction products.