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.

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.

A method of upgrading a petroleum feedstock, the method comprising the steps of introducing a disulfide oil, a water feed, and a petroleum feedstock to a supercritical water upgrading unit, and operating the supercritical water upgrading unit to produce a product gas stream, a product oil stream, and a used water stream.

A method of upgrading a petroleum feedstock, the method comprising the steps of introducing a disulfide oil, a water feed, and a petroleum feedstock to a supercritical water upgrading unit, and operating the supercritical water upgrading unit to produce a product gas stream, a product oil stream, and a used water stream.

A scavenger comprising a formaldehyde sulfoxylate may be used to scavenge hydrogen sulfide (H.sub.2S) from systems that are brine or mixed production. Suitable formaldehyde sulfoxylates include, but are not necessarily limited to, sodium formaldehyde sulfoxylate, zinc formaldehyde sulfoxylate, and calcium formaldehyde sulfoxylate, potassium formaldehyde sulfoxylate, magnesium formaldehyde sulfoxylate, iron formaldehyde sulfoxylate, copper formaldehyde sulfoxylate, alkene aldehyde sulfoxylates, and combinations thereof.

A scavenger comprising a formaldehyde sulfoxylate may be used to scavenge hydrogen sulfide (H.sub.2S) from systems that are brine or mixed production. Suitable formaldehyde sulfoxylates include, but are not necessarily limited to, sodium formaldehyde sulfoxylate, zinc formaldehyde sulfoxylate, and calcium formaldehyde sulfoxylate, potassium formaldehyde sulfoxylate, magnesium formaldehyde sulfoxylate, iron formaldehyde sulfoxylate, copper formaldehyde sulfoxylate, alkene aldehyde sulfoxylates, and combinations thereof.

The present invention relates to a catalyst and a method for preparation of that catalyst for the selective hydrogenation of diolefins present in gasoline streams along with the shifting of lighter sulfur compounds in the feed stock to heavier sulfur compound by the reaction with olefinic compounds.

The present invention relates to a catalyst and a method for preparation of that catalyst for the selective hydrogenation of diolefins present in gasoline streams along with the shifting of lighter sulfur compounds in the feed stock to heavier sulfur compound by the reaction with olefinic compounds.

Hydrocracked bottoms fractions are treated to separate HPNA compounds and/or HPNA precursor compounds and produce a reduced-HPNA hydrocracked bottoms fraction effective for recycle, in a configuration of a single-stage hydrocracking reactor, series-flow once through hydrocracking operation, or two-stage hydrocracking operation. A process for separation of HPNA and/or HPNA precursor compounds from a hydrocracked bottoms fraction of a hydroprocessing reaction effluent comprises contacting the hydrocracked bottoms fraction with an effective quantity of a sulfonation agent to produce corresponding sulfonated HPNA compounds and/or sulfonated HPNA precursor compounds, and to form a sulfonated hydrocracked bottoms fraction. The sulfonated hydrocracked bottoms fraction is separated into an HPNA-reduced hydrocracked bottoms portion and a sulfonated HPNA portion. All or a portion of the HPNA-reduced hydrocracked bottoms portion is recycled within the hydrocracking operation.

Hydrocracked bottoms fractions are treated to separate HPNA compounds and/or HPNA precursor compounds and produce a reduced-HPNA hydrocracked bottoms fraction effective for recycle, in a configuration of a single-stage hydrocracking reactor, series-flow once through hydrocracking operation, or two-stage hydrocracking operation. A process for separation of HPNA and/or HPNA precursor compounds from a hydrocracked bottoms fraction of a hydroprocessing reaction effluent comprises contacting the hydrocracked bottoms fraction with an effective quantity of a sulfonation agent to produce corresponding sulfonated HPNA compounds and/or sulfonated HPNA precursor compounds, and to form a sulfonated hydrocracked bottoms fraction. The sulfonated hydrocracked bottoms fraction is separated into an HPNA-reduced hydrocracked bottoms portion and a sulfonated HPNA portion. All or a portion of the HPNA-reduced hydrocracked bottoms portion is recycled within the hydrocracking operation.