Patent classifications
C07C409/04
PREPARATION OF COMPOUNDS FROM LEVULINIC ACID
The present invention provides a method of making carboxylic acids from levulinic acid, such as succinic acid and 3-hydroxypropanoic acid, by reacting levulinic acid with an oxidant such as hydrogen peroxide under acidic or basic conditions.
PREPARATION OF COMPOUNDS FROM LEVULINIC ACID
The present invention provides a method of making carboxylic acids from levulinic acid, such as succinic acid and 3-hydroxypropanoic acid, by reacting levulinic acid with an oxidant such as hydrogen peroxide under acidic or basic conditions.
Method for concentrating a water-soluble organic peroxide
The present invention relates to a process for the concentration of a water-soluble organic peroxide, preferably an alkyl hydroperoxide, by reverse osmosis as well as to a process for the separation of a water-soluble organic peroxide and of a water-insoluble compound.
Method for concentrating a water-soluble organic peroxide
The present invention relates to a process for the concentration of a water-soluble organic peroxide, preferably an alkyl hydroperoxide, by reverse osmosis as well as to a process for the separation of a water-soluble organic peroxide and of a water-insoluble compound.
Upgrading paraffins to distillates and lubricant basestocks
A process for converting light paraffins (especially C.sub.3-C.sub.5) to middle distillate and higher boiling range liquid hydrocarbons by (1) oxygen or air oxidation of iso-paraffins to alkyl hydroperoxides; (2) conversion of alkyl hydroperoxides to dialkyl peroxides; (3) radical coupling of paraffins using the dialkyl peroxides as radical initiators forming heavier hydrocarbon products; and (4) fractionation of the heavy hydrocarbon products. The net reaction is catalytically converting light paraffins to heavier hydrocarbons using oxygen or air to effect the conversion.
Upgrading paraffins to distillates and lubricant basestocks
A process for converting light paraffins (especially C.sub.3-C.sub.5) to middle distillate and higher boiling range liquid hydrocarbons by (1) oxygen or air oxidation of iso-paraffins to alkyl hydroperoxides; (2) conversion of alkyl hydroperoxides to dialkyl peroxides; (3) radical coupling of paraffins using the dialkyl peroxides as radical initiators forming heavier hydrocarbon products; and (4) fractionation of the heavy hydrocarbon products. The net reaction is catalytically converting light paraffins to heavier hydrocarbons using oxygen or air to effect the conversion.
Purification of alkyl hydroperoxide by extractive distillation
The invention relates to a method for purifying an alkyl hydroperoxide from dialkyl peroxide thereof, comprising a step of distillation in the presence of alcohol and water followed by extraction of the condensates using a hydrocarbon or a hydrocarbon blend.
Purification of alkyl hydroperoxide by extractive distillation
The invention relates to a method for purifying an alkyl hydroperoxide from dialkyl peroxide thereof, comprising a step of distillation in the presence of alcohol and water followed by extraction of the condensates using a hydrocarbon or a hydrocarbon blend.
High octane gasoline and process for making same
A process for converting light paraffins to a high octane gasoline composition is disclosed. The process involves: (1) oxidation of iso-paraffins to alkyl hydroperoxides and alcohol; (2) conversion of the alkyl hydroperoxides and alcohol to dialkyl peroxides; and (3) radical coupling of iso-paraffins using the dialkyl peroxides as radical initiators, thereby forming gasoline-range molecules. Fractionation of the gasoline-range molecules can then be used to isolate high octane gasoline fractions having a road octane number [(RON+MON)/2] greater than 110.
High octane gasoline and process for making same
A process for converting light paraffins to a high octane gasoline composition is disclosed. The process involves: (1) oxidation of iso-paraffins to alkyl hydroperoxides and alcohol; (2) conversion of the alkyl hydroperoxides and alcohol to dialkyl peroxides; and (3) radical coupling of iso-paraffins using the dialkyl peroxides as radical initiators, thereby forming gasoline-range molecules. Fractionation of the gasoline-range molecules can then be used to isolate high octane gasoline fractions having a road octane number [(RON+MON)/2] greater than 110.