A method for marking a petroleum hydrocarbon or a liquid biologically derived fuel; said method comprising adding to said petroleum hydrocarbon or liquid biologically derived fuel at least one compound that is a R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5, R.sup.6, R.sup.7 and R.sup.8—substituted dibenzofuran, wherein R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5, R.sup.6, R.sup.7 and R.sup.8 independently are hydrogen, hydrocarbyl, hydrocarbyloxy, aryl or aryloxy; provided that R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5, R.sup.6, R.sup.7 and R.sup.8 collectively have at least two carbon atoms; wherein each compound having formula (I) is present at a level from 0.01 ppm to 20 ppm.

The present invention relates to fuel derived from renewable resources. More specifically, the present invention provides a composition which can be used as a fuel and a mixture which can be added to one or more C.sub.8-22 fatty acid triglycerides in order to provide a fuel. In particular, the present invention concerns the reduction of decomposition of such fuels due to bacterial growth and oxidation.

A method for marking a petroleum hydrocarbon or a liquid biologically derived fuel; said method comprising adding to said petroleum hydrocarbon or liquid biologically derived fuel at least one compound that is a R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5, R.sup.6, R.sup.7, R.sup.8, R.sup.9 and R.sup.10-substituted xanthene, wherein R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5, R.sup.6, R.sup.7, R.sup.8, R.sup.9 and R.sup.10 independently are hydrogen, hydrocarbyl, hydrocarbyloxy, aryl or aryloxy; wherein each compound of formula (I) is present at a level from 0.01 ppm to 20 ppm.

The present invention aims a new diesel composition comprising a diesel fuel and from 0.01 to 0.8% by volume of a glycerol acetal or ketal. The new diesel composition shows a higher cetane number and better lubricity performances compared to known diesel compositions.

A method for marking a petroleum hydrocarbon or a liquid biologically derived fuel; said method comprising adding to said petroleum hydrocarbon or liquid biologically derived fuel at least one compound that is a R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5, R.sup.6, R.sup.7 and R.sup.8—substituted dibenzofuran, wherein R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5, R.sup.6, R.sup.7 and R.sup.8 independently are hydrogen, hydrocarbyl, hydrocarbyloxy, aryl or aryloxy; provided that R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5, R.sup.6, R.sup.7 and R.sup.8 collectively have at least two carbon atoms; wherein each compound having formula (I) is present at a level from 0.01 ppm to 20 ppm.

A method of manufacturing an octane-boosting fuel additive, the method comprises reacting n-butyraldehyde, iso-butyraldehyde, or a combination comprising at least one of the foregoing with glycerol in the presence of an acidic catalyst to obtain an octane-boosting product mixture comprising 2-propyl-5-hydroxy-1,3-dioxane, 2-isopropyl-5-hydroxy-1,3-dioxane, 2-propyl-5-hydroxymethyl-1,3-dioxolane, 2-isopropyl-5-hydroxymethyl-1,3-dioxolane, or a combination comprising at least one of the foregoing.

The present disclosure relates to methods for preparing cyclic acetals from the catalytic transformation of bio-derived aldehydes with 2,3-butanediol. The methods operate in a solvent-free reaction system and provide isolation of the product acetals through phase separation and subsequent decantation. The cyclic acetals exhibit excellent properties for blending with diesel fuel, including increased cetane number and density, and decreased viscosity, freezing point, and soot formation.

A method for marking a petroleum hydrocarbon or a liquid biologically derived fuel; said method comprising adding to said petroleum hydrocarbon or liquid biologically derived fuel at least one compound that is a R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5, R.sup.6, R.sup.7 , R.sup.8, R.sup.9 and R.sup.10-substituted xanthene, wherein R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5, R.sup.6, R.sup.7, R.sup.8, R.sup.9 and R.sup.10 independently are hydrogen, hydrocarbyl, hydrocarbyloxy, aryl or aryloxy; wherein each compound of formula (I) is present at a level from 0.01 ppm to 20 ppm.

According to embodiments disclosed herein, a method of reducing corrosion during petroleum transportation, petroleum storage, or both, may comprise inputting a corrosion inhibitor formulation into a petroleum pipeline, a petroleum storage tank, or both, wherein the corrosion inhibitor formulation consists essentially of solvent and a pyridinium hydroxyl alkyl ether compound.

A Liquid, comprising an hydrophobic flavonoid derivative electrochemically non-active, that is capable of restoring its electrochemical activity, the concentration of the flavonoid derivative being 10 ppm by weight or less, and an organic substance in an amount of 90% by weight or more.