Patent classifications
C07C69/52
Acid composition for processing fatty acids
The invention relates to a composition comprising: at least one alkane-sulphonic acid RSO.sub.3H wherein R represents a saturated, linear or branched, hydrocarbon chain comprising from 1 to 4 carbon atoms, which can or cannot be substituted by at least one halogen atom, at least one aryl-sulphonic acid; and optionally at least one solvent,
of which the proportions are as defined in the description. The invention also relates to the use of composition in a fatty acid esterification method.
Acid composition for processing fatty acids
The invention relates to a composition comprising: at least one alkane-sulphonic acid RSO.sub.3H wherein R represents a saturated, linear or branched, hydrocarbon chain comprising from 1 to 4 carbon atoms, which can or cannot be substituted by at least one halogen atom, at least one aryl-sulphonic acid; and optionally at least one solvent,
of which the proportions are as defined in the description. The invention also relates to the use of composition in a fatty acid esterification method.
Methods and apparatus for producing alkyl esters from lipid feed stocks, alcohol feedstocks, and acids
Embodiments herein relate to the production of alkyl esters from lipid feed stocks. In an embodiment, a process for producing alkyl esters is included. The process can include mixing a lipid feed stock with an alcohol, water, and at least one of carbon dioxide, carbon monoxide, and/or one or more acids to form a reaction mixture, and contacting the reaction mixture with a catalyst under supercritical conditions for the alcohol, the catalyst comprising a metal oxide. Other embodiments are also included herein.
Methods and apparatus for producing alkyl esters from lipid feed stocks, alcohol feedstocks, and acids
Embodiments herein relate to the production of alkyl esters from lipid feed stocks. In an embodiment, a process for producing alkyl esters is included. The process can include mixing a lipid feed stock with an alcohol, water, and at least one of carbon dioxide, carbon monoxide, and/or one or more acids to form a reaction mixture, and contacting the reaction mixture with a catalyst under supercritical conditions for the alcohol, the catalyst comprising a metal oxide. Other embodiments are also included herein.
Catalyst and method for biodiesel production from unrefined low-grade oil and crude aqueous alcohols
A catalyst for catalyzing transesterification of esters or esterification of fatty acids, the catalyst is selected from the group consisting of manganese (II) glycerolate, cobalt (II) glycerolate, iron (II) glycerolate, and any combination thereof. A method for transesterification reaction, includes: a) providing a catalyst, wherein the catalyst is selected from the group consisting of manganese (II) glycerolate, cobalt (II) glycerolate, iron (II) glycerolate, and any combination thereof; b) adding the catalyst, one or more alcohols, and a composition comprising one or more esters to a reactor to form a reaction mixture; and c) stirring while heating the reaction mixture for reaction to form transesterification products.
Catalyst and method for biodiesel production from unrefined low-grade oil and crude aqueous alcohols
A catalyst for catalyzing transesterification of esters or esterification of fatty acids, the catalyst is selected from the group consisting of manganese (II) glycerolate, cobalt (II) glycerolate, iron (II) glycerolate, and any combination thereof. A method for transesterification reaction, includes: a) providing a catalyst, wherein the catalyst is selected from the group consisting of manganese (II) glycerolate, cobalt (II) glycerolate, iron (II) glycerolate, and any combination thereof; b) adding the catalyst, one or more alcohols, and a composition comprising one or more esters to a reactor to form a reaction mixture; and c) stirring while heating the reaction mixture for reaction to form transesterification products.
METHOD FOR PREPARING LOW-GRADE UNSATURATED FATTY ACID ESTER
Provided is a method for preparing a lower unsaturated fatty acid ester, which comprises carrying out an aldol condensation reaction between dimethoxymethane (DMM) and a lower acid or ester with a molecular formula of R.sub.1CH.sub.2COOR.sub.2 on an acidic molecular sieve catalyst in an inert atmosphere to obtain a lower unsaturated fatty acid or ester(CH.sub.2C(R.sub.1)COOR.sub.2), wherein R.sub.1 and R.sub.2 are groups each independently selected from the group consisting of H- and C.sub.1-C.sub.4 saturated alkyl group.
PROCESS FOR THE PREPARATION OF UNSATURATED CARBOXYLIC ACIDS BY CARBONYLATION OF ALLYL ALCOHOLS AND THEIR ACYLATION PRODUCTS
The present invention relates to a process for carbonylating allyl alcohols at low temperature, low pressure and/or low catalyst loading. In an alternative embodiment, an acylation product of the allyl alcohol is used for the carbonylation. The present invention likewise relates to the preparation of conversion products of these carbonylation products and specifically of ()-ambrox.
PROCESS FOR THE PREPARATION OF UNSATURATED CARBOXYLIC ACIDS BY CARBONYLATION OF ALLYL ALCOHOLS AND THEIR ACYLATION PRODUCTS
The present invention relates to a process for carbonylating allyl alcohols at low temperature, low pressure and/or low catalyst loading. In an alternative embodiment, an acylation product of the allyl alcohol is used for the carbonylation. The present invention likewise relates to the preparation of conversion products of these carbonylation products and specifically of ()-ambrox.
METHOD OF PRODUCING PLANT BIOMASS-BASED BIOPLASTIC
This invention relates to the field of producing bioplastics. Specifically, it relates to a method of producing all key ingredients of bioplastic making from pumpkins and making of bioplastic with these ingredients. More specifically, glycerin and other chemicals are extracted from pumpkin seed oil and mixed with starches that in the pumpkin flesh to make bioplastic. The bioplastic produced with the method as disclosed in this invention possess superior properties in tensile strength and biodegradability compared to bioplastic.