Patent classifications
C07C303/04
Hydrolysis vessel used in a process for amidification of acetone cyanohydrin
The invention relates to an hydrolysis vessel (200) used during amidification step of acetone cyanohydrin (ACH), in the industrial process for production of a methyl methacrylate (MMA) or methacrylic acid (MAA). The hydrolysis vessel (200) is used for hydrolyzing acetone cyanohydrine with sulfuric acid to produce a mixture comprising -sulfatoisobutyramide (SIBAM). It comprises at least one cooling system (212; 244) on its internal annular periphery area and it is divided into at least two stages, preferably three, along its vertical wall, each stage (S1 to S3) comprising a ACH feeding inlet (201, 202, 203). Such vessel allows controlling both homogeneity and temperature of the mixture, and thus obtaining a high yield for the hydrolyzing reaction in very safe conditions.
Hydrolysis vessel used in a process for amidification of acetone cyanohydrin
The invention relates to an hydrolysis vessel (200) used during amidification step of acetone cyanohydrin (ACH), in the industrial process for production of a methyl methacrylate (MMA) or methacrylic acid (MAA). The hydrolysis vessel (200) is used for hydrolyzing acetone cyanohydrine with sulfuric acid to produce a mixture comprising -sulfatoisobutyramide (SIBAM). It comprises at least one cooling system (212; 244) on its internal annular periphery area and it is divided into at least two stages, preferably three, along its vertical wall, each stage (S1 to S3) comprising a ACH feeding inlet (201, 202, 203). Such vessel allows controlling both homogeneity and temperature of the mixture, and thus obtaining a high yield for the hydrolyzing reaction in very safe conditions.
Process for preparing a mixture of terpene alcohols
The present invention relates to a process for preparing a mixture of terpene alcohols comprising limonene-4-ol and terpinene-4-ol from terpinolene epoxide via an isomerization and/or hydrogenation reaction in the presence of a copper catalyst.
MICRO/NANO MATERIALS, PRODUCTS OBTAINED BY COVALENTLY MODIFYING SURFACE OF MICRO/NANO MATERIALS WITH HYDROPHILIC MATERIALS, AND METHOD FOR MAKING SAME
Micro-nano materials, products obtained by covalently modifying the surfaces of micro/nano materials with hydrophilic materials, and methods for making the same. The micro/nano materials on the surfaces have carboxyl groups or/and pro-carboxyl groups which are converted into their active esters. The products are covalently modified by forming amide bonds between the active esters on the surfaces and the modification agents; where the modification agents are hydrophilic compounds and/or hydrophilic polymers bearing primary and/or secondary aliphatic amines. Monomers bearing carboxyl groups and/or pro-carboxyl groups are used to produce an adequate number of carboxyl groups and/or pro-carboxyl groups on the surface of a polymer material to be modified. The carboxyl groups and/or pro-carboxyl groups are converted into active esters. A reasonably-sized modification agent bearing primary and/or secondary amines, zwitterions and hydrophilic linear spacer arms is used to form amide bonds and obtain a covalently modified surface layer.
MICRO/NANO MATERIALS, PRODUCTS OBTAINED BY COVALENTLY MODIFYING SURFACE OF MICRO/NANO MATERIALS WITH HYDROPHILIC MATERIALS, AND METHOD FOR MAKING SAME
Micro-nano materials, products obtained by covalently modifying the surfaces of micro/nano materials with hydrophilic materials, and methods for making the same. The micro/nano materials on the surfaces have carboxyl groups or/and pro-carboxyl groups which are converted into their active esters. The products are covalently modified by forming amide bonds between the active esters on the surfaces and the modification agents; where the modification agents are hydrophilic compounds and/or hydrophilic polymers bearing primary and/or secondary aliphatic amines. Monomers bearing carboxyl groups and/or pro-carboxyl groups are used to produce an adequate number of carboxyl groups and/or pro-carboxyl groups on the surface of a polymer material to be modified. The carboxyl groups and/or pro-carboxyl groups are converted into active esters. A reasonably-sized modification agent bearing primary and/or secondary amines, zwitterions and hydrophilic linear spacer arms is used to form amide bonds and obtain a covalently modified surface layer.
NOVEL ANIONIC SURFACTANTS AND WASHING AGENTS CONTAINING SAID SURFACTANTS
Surfactants of general formula (I), in which R.sup.1 denotes a linear or branched alkyl residue having 6 to 20, and in particular 8 to 14 carbon atoms, R.sup.2 denotes H or CH.sub.3, and M denotes hydrogen, an alkali metal or an N.sup.+R.sup.3R.sup.4R.sup.5 grouping, in which R.sup.3, R.sup.4 and R.sup.5, independently of one another, denote hydrogen, an alkyl group having 1 to 6 carbon atoms or a hydroxyalkyl group having 2 to 6 carbon atom, can be easily incorporated into washing or cleaning agents, have outstanding application-related properties, and can be produced based on renewable resources.
NOVEL ANIONIC SURFACTANTS AND WASHING AGENTS CONTAINING SAID SURFACTANTS
Surfactants of general formula (I), in which R.sup.1 denotes a linear or branched alkyl residue having 6 to 20, and in particular 8 to 14 carbon atoms, R.sup.2 denotes H or CH.sub.3, and M denotes hydrogen, an alkali metal or an N.sup.+R.sup.3R.sup.4R.sup.5 grouping, in which R.sup.3, R.sup.4 and R.sup.5, independently of one another, denote hydrogen, an alkyl group having 1 to 6 carbon atoms or a hydroxyalkyl group having 2 to 6 carbon atom, can be easily incorporated into washing or cleaning agents, have outstanding application-related properties, and can be produced based on renewable resources.
Industrial methods for producing arylsulfur pentafluorides
Industrial methods for producing arylsulfur pentafluorides are disclosed. Methods include reacting arylsulfur halotetrafluoride with hydrogen fluoride in the absence or presence of one or more additives selected from a group of fluoride salts, non-fluoride salts, and unsaturated organic compounds to form arylsulfur pentafluorides.
Low pH metal-free preparation of aminated organic acid
The invention provides a process for making compounds according to Formula I: ##STR00001##
where R.sup.1, R.sup.1a, R.sup.2, R.sup.2a, R.sup.3 and R.sup.3a are defined as set forth in the specification. Formula I compounds are useful as chelants and stabilizers of cations in aqueous media and the invention therefore provides a method for using the compounds in the treatment of subterranean formations, such as in acidizing operations.
Low pH metal-free preparation of aminated organic acid
The invention provides a process for making compounds according to Formula I: ##STR00001##
where R.sup.1, R.sup.1a, R.sup.2, R.sup.2a, R.sup.3 and R.sup.3a are defined as set forth in the specification. Formula I compounds are useful as chelants and stabilizers of cations in aqueous media and the invention therefore provides a method for using the compounds in the treatment of subterranean formations, such as in acidizing operations.