The present invention includes a fuel injection amount sensor for detecting an injection amount of oil, a pretreatment desulfurization agent injection amount sensor for detecting an injection amount of a pretreatment desulfurization agent, and a control panel for controlling and monitoring the injection amount of the pretreatment desulfurization agent so that the predetermined desulfurization agent is mixed with the fuel in a predetermined mixing ratio. The fuel injection amount sensor is disposed on a fuel supply line between a fuel tank and a marine engine, and the pretreatment desulfurization agent injection amount sensor is disposed between a downstream fuel supply line installed downstream of the fuel injection amount sensor and a pretreatment desulfurization agent tank.

Methods and compositions for flocculating solids are provided. The solids may be suspended in an organic liquid medium and a water in oil emulsion may be added to the liquid medium. The water in oil emulsion includes an emulsion polymer capable of flocculating the solids suspended in the organic liquid medium. The emulsion polymer may be added to the organic liquid medium in an inactive form and the polymer may subsequently become activated upon contacting the organic liquid medium. Once activated, the polymer may flocculate the suspended solids.

Methods and compositions for flocculating solids are provided. The solids may be suspended in an organic liquid medium and a water in oil emulsion may be added to the liquid medium. The water in oil emulsion includes an emulsion polymer capable of flocculating the solids suspended in the organic liquid medium. The emulsion polymer may be added to the organic liquid medium in an inactive form and the polymer may subsequently become activated upon contacting the organic liquid medium. Once activated, the polymer may flocculate the suspended solids.

Treatment of hydrocarbon streams, and in one non-limiting embodiment refinery distillates, with high pH aqueous reducing agents, such as borohydride, results in reduction of the sulfur compounds such as disulfides, mercaptans and thioethers that are present to give easily removed sulfides. 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.

The present technology provides a method that includes contacting a composition with a caustic solution to produce a caustic-treated composition; combining the caustic-treated composition with silica particles to produce a slurry; and removing the silica particles from the slurry to produce a treated composition; wherein the composition includes one or more of animal fats, animal oils, plant fats, plant oils, vegetable fats, vegetable oils, greases, and used cooking oil and the composition includes: at least about 10 wppm of total metals, at least about 8 wppm of phosphorus, at least about 10 wppm of chlorine, at least about 10 wppm of sulfur, at least about 20 wppm of nitrogen, at least about 5 wt. % of free fatty acids; and has an acid number from about 10 mg KOH/g to about 150 mg KOH/g, and the silica particles has a particle size from about 10 microns to about 50 microns, a BET surface area from about 200 m.sup.2/g to about 1000 m.sup.2/g.

A treatment process for preparing a remediated liquid from a contaminated liquid originally containing more than 5 ppm hydrogen sulfide (H.sub.2S) and substantially without formation of precipitate, includes steps of steps of adding an aqueous solution containing at least one hydroxide compound at a collective concentration of 35-55 wt % to the contaminated liquid to achieve a concentration of 125-5000 ppm of the hydroxide compounds in the contaminated liquid, adding a fulvic acid and/or a humic acid to the contaminated liquid to achieve a concentration of 0.01-10 ppm of the acid(s) in the contaminated liquid, and dispersing the aqueous solution and the at least one organic acid in the contaminated liquid and allowing the aqueous solution and the at least one organic acid to react with the contaminated liquid for a period of time until a concentration of hydrogen sulfide in the contaminated liquid is reduced to ≤5 ppm.

A treatment process for preparing a remediated liquid from a contaminated liquid originally containing more than 5 ppm hydrogen sulfide (H.sub.2S) and substantially without formation of precipitate, includes steps of steps of adding an aqueous solution containing at least one hydroxide compound at a collective concentration of 35-55 wt % to the contaminated liquid to achieve a concentration of 125-5000 ppm of the hydroxide compounds in the contaminated liquid, adding a fulvic acid and/or a humic acid to the contaminated liquid to achieve a concentration of 0.01-10 ppm of the acid(s) in the contaminated liquid, and dispersing the aqueous solution and the at least one organic acid in the contaminated liquid and allowing the aqueous solution and the at least one organic acid to react with the contaminated liquid for a period of time until a concentration of hydrogen sulfide in the contaminated liquid is reduced to ≤5 ppm.

The present technology provides a method that includes contacting a composition with a caustic solution to produce a caustic-treated composition; combining the caustic-treated composition with silica particles to produce a slurry; and removing the silica particles from the slurry to produce a treated composition; wherein the composition includes one or more of animal fats, animal oils, plant fats, plant oils, vegetable fats, vegetable oils, greases, and used cooking oil and the composition includes: at least about 10 wppm of total metals, at least about 8 wppm of phosphorus, at least about 10 wppm of chlorine, at least about 10 wppm of sulfur, at least about 20 wppm of nitrogen, at least about 5 wt. % of free fatty acids; and has an acid number from about 10 mg KOH/g to about 150 mg KOH/g, and the silica particles has a particle size from about 10 microns to about 50 microns, a BET surface area from about 200 m.sup.2/g to about 1000 m.sup.2/g.

Systems and methods for sulfur-compound removal from hydrocarbon liquids may include at least one tank defining a chamber with top and bottom ends, a gas inlet into the chamber, a gas outlet from the chamber, a fluid inlet into the chamber, and a fluid outlet from the chamber. A fluid circulation assembly creates a hydrocarbon liquid flow on a liquid path, and a gas circulation assembly circulates a gas flow along a gas path. The gas inlet and outlet and the fluid inlet and outlet of the tank may be arranged to create a crossflow and counterflow of the liquid and gas flows in the chamber of the tank such that sulfur-containing compounds are transferred from the liquid to the gas flow. A gas processor assembly may remove sulfur-containing compounds from the gas flow before recirculating the gas flow. The gas flow may be predominantly nitrogen (N2) gas.

Systems and methods for sulfur-compound removal from hydrocarbon liquids may include at least one tank defining a chamber with top and bottom ends, a gas inlet into the chamber, a gas outlet from the chamber, a fluid inlet into the chamber, and a fluid outlet from the chamber. A fluid circulation assembly creates a hydrocarbon liquid flow on a liquid path, and a gas circulation assembly circulates a gas flow along a gas path. The gas inlet and outlet and the fluid inlet and outlet of the tank may be arranged to create a crossflow and counterflow of the liquid and gas flows in the chamber of the tank such that sulfur-containing compounds are transferred from the liquid to the gas flow. A gas processor assembly may remove sulfur-containing compounds from the gas flow before recirculating the gas flow. The gas flow may be predominantly nitrogen (N2) gas.