A fuel composition comprising as an additive the reaction product of a polycarboxylic acid having no more than 5 carbon atoms per carboxylic acid group, or an anhydride thereof and an alcohol having at least 5 carbon atoms.

A fuel composition comprising as an additive the reaction product of a polycarboxylic acid having no more than 5 carbon atoms per carboxylic acid group, or an anhydride thereof and an alcohol having at least 5 carbon atoms.

Diesel fuel composition comprising a diesel base fuel and at least one blowing agent wherein the blowing agent is selected from ester compounds, oxalate compounds and diazene compounds and wherein the blowing agent has a solubility in diesel base fuel at 25° C. of 100 mg/kg or greater, a decomposition temperature in the range from 50° C. to 300° C. as measured by thermogravimetric analysis (TGA), and wherein the diesel fuel composition has an evaporation rate of greater than that of the diesel base fuel as measured by acoustic levitation.

Diesel fuel composition comprising a diesel base fuel and at least one blowing agent wherein the blowing agent is selected from ester compounds, oxalate compounds and diazene compounds and wherein the blowing agent has a solubility in diesel base fuel at 25° C. of 100 mg/kg or greater, a decomposition temperature in the range from 50° C. to 300° C. as measured by thermogravimetric analysis (TGA), and wherein the diesel fuel composition has an evaporation rate of greater than that of the diesel base fuel as measured by acoustic levitation.

The present invention relates to processes for producing industrial products such as hydrocarbon products from non-polar lipids in a vegetative plant part. Preferred industrial products include alkyl esters which may be blended with petroleum based fuels.

The present invention relates to processes for producing industrial products such as hydrocarbon products from non-polar lipids in a vegetative plant part. Preferred industrial products include alkyl esters which may be blended with petroleum based fuels.

A fuel for an internal combustion engine includes a C.sub.5 to C.sub.30 dialkoxyalkanoate corresponding to formula (I):

##STR00001##

wherein the R.sub.1 group is —H or a —CH.sub.3 group, the R.sub.2 and R.sub.2′ groups are alkyl groups independently selected to have 1 to 9 carbon atoms; and the R.sub.3 group is selected to have 1 to 9 carbon atoms. The compounds described herein may be used as neat fuels or mixed fuels (with diesel, biodiesel, jet fuel, marine fuel or other fuel compounds) in autoignition or spark ignition engines, such as diesel engines, gasoline (spark ignition) engines, MCCI, Homogeneous Charge Compression Ignition (HCCI) engines, or more generally in Low-Temperature Gasoline Combustion (LTGC) engines (using gasoline-like fuels), that have the high-efficiency advantages of HCCI but can operate with some level of charge inhomogeneities. Methods of making these compounds are environmentally friendly and can be done in a continuous manner.

A fuel for an internal combustion engine includes a C.sub.5 to C.sub.30 dialkoxyalkanoate corresponding to formula (I):

##STR00001##

wherein the R.sub.1 group is —H or a —CH.sub.3 group, the R.sub.2 and R.sub.2′ groups are alkyl groups independently selected to have 1 to 9 carbon atoms; and the R.sub.3 group is selected to have 1 to 9 carbon atoms. The compounds described herein may be used as neat fuels or mixed fuels (with diesel, biodiesel, jet fuel, marine fuel or other fuel compounds) in autoignition or spark ignition engines, such as diesel engines, gasoline (spark ignition) engines, MCCI, Homogeneous Charge Compression Ignition (HCCI) engines, or more generally in Low-Temperature Gasoline Combustion (LTGC) engines (using gasoline-like fuels), that have the high-efficiency advantages of HCCI but can operate with some level of charge inhomogeneities. Methods of making these compounds are environmentally friendly and can be done in a continuous manner.

A fuel for an internal combustion engine includes a C.sub.5 to C.sub.30 dialkoxyalkanoate corresponding to formula (I): ##STR00001## wherein the R.sub.1 group is —H or a —CH.sub.3 group, the R.sub.2 and R.sub.2′ groups are alkyl groups independently selected to have 1 to 9 carbon atoms; and the R.sub.3 group is selected to have 1 to 9 carbon atoms. The compounds described herein may be used as neat fuels or mixed fuels (with diesel, biodiesel, jet fuel, marine fuel or other fuel compounds) in autoignition or spark ignition engines, such as diesel engines, gasoline (spark ignition) engines, MCCI, Homogeneous Charge Compression Ignition (HCCI) engines, or more generally in Low-Temperature Gasoline Combustion (LTGC) engines (using gasoline-like fuels), that have the high-efficiency advantages of HCCI but can operate with some level of charge inhomogeneities. Methods of making these compounds are environmentally friendly and can be done in a continuous manner.

A fuel for an internal combustion engine includes a C.sub.5 to C.sub.30 dialkoxyalkanoate corresponding to formula (I): ##STR00001## wherein the R.sub.1 group is —H or a —CH.sub.3 group, the R.sub.2 and R.sub.2′ groups are alkyl groups independently selected to have 1 to 9 carbon atoms; and the R.sub.3 group is selected to have 1 to 9 carbon atoms. The compounds described herein may be used as neat fuels or mixed fuels (with diesel, biodiesel, jet fuel, marine fuel or other fuel compounds) in autoignition or spark ignition engines, such as diesel engines, gasoline (spark ignition) engines, MCCI, Homogeneous Charge Compression Ignition (HCCI) engines, or more generally in Low-Temperature Gasoline Combustion (LTGC) engines (using gasoline-like fuels), that have the high-efficiency advantages of HCCI but can operate with some level of charge inhomogeneities. Methods of making these compounds are environmentally friendly and can be done in a continuous manner.