Patent classifications
C07C17/087
Biosourced vinylidene difluoride monomer and polymers containing it
The invention relates to biosourced vinylidene difluoride. The invention also relates to methods for preparation of biosourced vinylidene difluoride from various renewable raw materials. The invention also relates to homopolymers of vinylidene difluoride obtained from polymerization of said monomer, and also copolymers obtained by copolymerization of said monomer with one or several compatible comonomers. Finally, the invention relates to the use of said homopolymers or copolymers in applications, such as chemical engineering or electronics, in particular mass-market electronic devices.
Biosourced vinylidene difluoride monomer and polymers containing it
The invention relates to biosourced vinylidene difluoride. The invention also relates to methods for preparation of biosourced vinylidene difluoride from various renewable raw materials. The invention also relates to homopolymers of vinylidene difluoride obtained from polymerization of said monomer, and also copolymers obtained by copolymerization of said monomer with one or several compatible comonomers. Finally, the invention relates to the use of said homopolymers or copolymers in applications, such as chemical engineering or electronics, in particular mass-market electronic devices.
Biosourced vinylidene difluoride monomer and polymers containing it
The invention relates to biosourced vinylidene difluoride. The invention also relates to methods for preparation of biosourced vinylidene difluoride from various renewable raw materials. The invention also relates to homopolymers of vinylidene difluoride obtained from polymerization of said monomer, and also copolymers obtained by copolymerization of said monomer with one or several compatible comonomers. Finally, the invention relates to the use of said homopolymers or copolymers in applications, such as chemical engineering or electronics, in particular mass-market electronic devices.
1,2,3,3,3-pentafluropropene production processes
A process is disclosed for making CF.sub.3CF═CHF. The process involves reacting CF.sub.3CClFCCl.sub.2F with H.sub.2 in a reaction zone in the presence of a catalyst to produce a product mixture comprising CF.sub.3CF═CHF. The catalyst has a catalytically effective amount of palladium supported on a support selected from the group consisting of alumina, fluorided alumina, aluminum fluoride and mixtures thereof and the mole ratio of H.sub.2 to CF.sub.3CClFCCl.sub.2F fed to the reaction zone is between about 1:1 and about 5:1. Also disclosed are azeotropic compositions of CF.sub.3CClFCCl.sub.2F and HF and azeotropic composition of CF.sub.3CHFCH.sub.2F and HF.
1,2,3,3,3-pentafluropropene production processes
A process is disclosed for making CF.sub.3CF═CHF. The process involves reacting CF.sub.3CClFCCl.sub.2F with H.sub.2 in a reaction zone in the presence of a catalyst to produce a product mixture comprising CF.sub.3CF═CHF. The catalyst has a catalytically effective amount of palladium supported on a support selected from the group consisting of alumina, fluorided alumina, aluminum fluoride and mixtures thereof and the mole ratio of H.sub.2 to CF.sub.3CClFCCl.sub.2F fed to the reaction zone is between about 1:1 and about 5:1. Also disclosed are azeotropic compositions of CF.sub.3CClFCCl.sub.2F and HF and azeotropic composition of CF.sub.3CHFCH.sub.2F and HF.
1,2,3,3,3-pentafluropropene production processes
A process is disclosed for making CF.sub.3CF═CHF. The process involves reacting CF.sub.3CClFCCl.sub.2F with H.sub.2 in a reaction zone in the presence of a catalyst to produce a product mixture comprising CF.sub.3CF═CHF. The catalyst has a catalytically effective amount of palladium supported on a support selected from the group consisting of alumina, fluorided alumina, aluminum fluoride and mixtures thereof and the mole ratio of H.sub.2 to CF.sub.3CClFCCl.sub.2F fed to the reaction zone is between about 1:1 and about 5:1. Also disclosed are azeotropic compositions of CF.sub.3CClFCCl.sub.2F and HF and azeotropic composition of CF.sub.3CHFCH.sub.2F and HF.
AZEOTROPE OR AZEOTROPE-LIKE COMPOSITIONS OF 2-CHLORO-3,3,3-TRIFLUOROPROPENE (HCFO-1233XF) AND WATER
Heterogenous azeotrope or azeotrope-like compositions comprising 2-chloro-3,3,3-trifluoropropene (HFCO-1233xf) and water which may include from about 0.09 wt. % to about 92.69 wt. % 2-chloro-3,3,3-trifluoropropene (HFCO-1233xf) and from about 7.31 wt. % to about 99.91 wt. % water and having a boiling point between about 12.0° C. and about 13.6° C. at a pressure of between about 12.5 psia and about 16.5 psia. The azeotrope or azeotrope-like compositions may be used to separate impurities, including water, from 2-chloro-3,3,3-trifluoropropene (HFCO-1233xf).
AZEOTROPE OR AZEOTROPE-LIKE COMPOSITIONS OF 2-CHLORO-3,3,3-TRIFLUOROPROPENE (HCFO-1233XF) AND WATER
Heterogenous azeotrope or azeotrope-like compositions comprising 2-chloro-3,3,3-trifluoropropene (HFCO-1233xf) and water which may include from about 0.09 wt. % to about 92.69 wt. % 2-chloro-3,3,3-trifluoropropene (HFCO-1233xf) and from about 7.31 wt. % to about 99.91 wt. % water and having a boiling point between about 12.0° C. and about 13.6° C. at a pressure of between about 12.5 psia and about 16.5 psia. The azeotrope or azeotrope-like compositions may be used to separate impurities, including water, from 2-chloro-3,3,3-trifluoropropene (HFCO-1233xf).
Method for preparing 1,1,1,2,2-pentafluoropropane
A method hydrofluorinates an olefin of the formula: RCX=CYZ to produce a hydrofluoroalkane of formula RCXFCHYZ or RCXHCFYZ, where X, Y, and Z are independently the same or different and are selected from the group consisting of H, F, Cl, Br, and C.sub.1-C.sub.6 alkyl which is partially or fully substituted with chloro or fluoro or bromo; and R is a C.sub.1-C.sub.6 alkyl which is unsubstituted or substituted with chloro or fluoro or bromo. The method includes reacting the olefin with HF in the vapor phase, in the presence of SbF.sub.5, at a temperature ranging from about −30° C. to about 65° C. and compositions formed by the process.
Method for preparing 1,1,1,2,2-pentafluoropropane
A method hydrofluorinates an olefin of the formula: RCX=CYZ to produce a hydrofluoroalkane of formula RCXFCHYZ or RCXHCFYZ, where X, Y, and Z are independently the same or different and are selected from the group consisting of H, F, Cl, Br, and C.sub.1-C.sub.6 alkyl which is partially or fully substituted with chloro or fluoro or bromo; and R is a C.sub.1-C.sub.6 alkyl which is unsubstituted or substituted with chloro or fluoro or bromo. The method includes reacting the olefin with HF in the vapor phase, in the presence of SbF.sub.5, at a temperature ranging from about −30° C. to about 65° C. and compositions formed by the process.