C10L1/191

PROCESS FOR THE PRODUCTION OF AN IMPROVED DIESEL FUEL

A method for the continuous production of an improved diesel fuel, having enhanced ignition characteristics, more particularly with a greater electric conductivity, enhanced cetane numbers and lubricity and with greater percentage of complete combustion, resulting in less soot production and NOx reduction at the same time in an internal combustion diesel engine, breaking the tradeoff in the emission of those two pollutants from an internal combustion diesel engine.

FUEL COMPOSITIONS WITH GDI DEPOSIT FLUIDIZING AGENTS AND METHODS OF USE THEREOF
20220098503 · 2022-03-31 ·

GDI deposit fluidizing additives, liquid fuel compositions including such additives and methods that improve a liquid fuel composition's GDI performance are provided. A liquid fuel composition may include a major amount of a base gasoline fuel; and 1 to 500 ppm of one or more polyether monohydroxy compounds, with the proviso that the liquid fuel composition is essentially free of fuel detergent additives. The liquid fuel composition provides at least 10% lower particulate emission as a function of time relative to a comparable liquid fuel composition not including the one or more polyether monohydroxy compounds. The GDI deposit fluidizing enhancing additive may include polyether monohydroxy compounds with the butane oxide and propene oxide in a variety of ratios and randomly distributed in the additive.

FUEL COMPOSITION WITH LUBRICITY ADDITIVES
20220064558 · 2022-03-03 ·

A fuel composition comprising a fuel and a lubricity additive package, where the lubricity additive package comprises (1) Dodecanoic acid and (2) 1-Lauroyl-rac-glycerol and the fuel is gasoline.

Lubricity and conductivity improver additive for ultra low sulfur diesel fuels

The present invention discloses a single package additive for improving lubricity and conductivity properties of ultra-low sulfur diesel fuels. The single package additive is a reaction product of a fatty acid composition, a glycerol tricarboxylates, a polysulfone, a polyamine, an alkylated benzene sulfonic acid and a phenol derivative. More specifically, the present invention discloses a reaction product of: a fatty acid composition in the range of 60-95% wt/wt; a glycerol tricarboxylate in the range of 0.1-10.0% wt/wt; a polysulfone in the range of 0.1-5.0% wt/wt; a polyamine in the range of 0.1-5.0% wt/wt; an alkylated benzene sulfonic acid in the range of 0.1-5.0% wt/wt; and a phenol derivative in the range of 0.1-10.0% wt/wt. The present invention also discloses a single-pot process for the preparation of said reaction product.

POLYMERIC ANTI-AGGLOMERANT HYDRATE INHIBITOR

A polymeric anti-agglomerant hydrate inhibitor useful for preventing the formation of hydrate agglomerates in a multi-phase oilfield fluid may be synthesized via a condensation reaction between a cyclic anhydride and a tertiary amine-diol in the presence of a condensation catalyst to form a polyester amine precursor and a reaction of the polyester amine polymer precursor with an organic acid.

LUBRICITY AND CONDUCTIVITY IMPROVER ADDITIVE FOR ULTRA LOW SULFUR DIESEL FUELS

The present invention discloses a single package additive for improving lubricity and conductivity properties of ultra-low sulfur diesel fuels. The single package additive is a reaction product of a fatty acid composition, a glycerol tricarboxylates, a polysulfone, a polyamine, an alkylated benzene sulfonic acid and a phenol derivative. More specifically, the present invention discloses a reaction product of: a fatty acid composition in the range of 60-95% wt/wt; a glycerol tricarboxylate in the range of 0.1-10.0% wt/wt; a polysulfone in the range of 0.1-5.0% wt/wt; a polyamine in the range of 0.1-5.0% wt/wt; an alkylated benzene sulfonic acid in the range of 0.1-5.0% wt/wt; and a phenol derivative in the range of 0.1-10.0% wt/wt. The present invention also discloses a single-pot process for the preparation of said reaction product.

MACROMOLECULAR CORROSION (MCIN) INHIBITORS: STRUCTURES, METHODS OF MAKING AND USING THE SAME
20210130722 · 2021-05-06 ·

Disclosed are multifunctional compounds represented by structural formula (I):

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methods of producing compounds represented by structural formula (I) and their use in inhibiting corrosion in corrodible material.

Methods of refining a grain oil composition to make one or more grain oil products, and related systems

The present disclosure is related to refining one or more grain oil composition streams (e.g., distillers corn oil or syrup) in a biorefinery to provide one or more refined grain oil products, where each grain oil product has targeted amounts of a free fatty acid component and the fatty acid alkyl ester component.

Fuel compositions
10995291 · 2021-05-04 · ·

Improved fuel compositions and fuel additive packages which serve to prolong stability at various ambient conditions and to increase fuel efficiency and fuel economy while also significantly reducing the level of multiple emissions constituents generated upon combustion of the fuels including CO.sub.2, NO.sub.X, SO.sub.X, Particulate Matter PM2.5, PM10 and Black Carbon. The fuels may include the hydrocarbon fuels gasolines, diesel fuels, biodiesel fuels, biomass diesel fuels, renewable fuels, synthetic fuels, algae-based fuels, kerosene fuel or heavy fuel oils, or may alternatively be hydrosols, and include an additive package having a sorbitan oleate, a polyoxyethylene alcohol, an alkylene glycol, and an amine. The fuels are mixed with an additive and are emulsified with clean, soft water having a water quality of 1 micron or less.

Modification of fats and oils for fuel and lubricating applications
10961472 · 2021-03-30 · ·

A bio-organic composition includes residues of a fatty acid glyceride-containing composition, residues of a first epoxide or glycol, and the residues of a second epoxide. The fatty acid glyceride-containing composition is characterized by the viscosity at room temperature. The first epoxide or glycol and second epoxides are present in a sufficient amount that the room temperature viscosity of the bio-organic composition is lower than the room temperature viscosity of the vegetable oil prior to formulation and/or the first epoxide or glycol and second epoxides are present in a sufficient amount that the pour point of the bio-organic composition is lower than the pour point of the fatty acid glyceride-containing composition prior to formulation.