Abstract: An improved gas-phase process for the manufacture of 1,1,1-trifluorodichloroethane and/or 1,1,1,2-tetrafluorochloroethane by contacting a suitable tetrahaloethylene with hydrogen fluoride in the presence of a selected metal in combination with a high fluorine content aluminum-containing compound, the reaction being conducted under controlled conditions whereby the production of pentafluoroethane is minimized.
Abstract: A process for preparing 1,1,1-trifluoro-2,2-dichloroethane by hydrofluorination, in the gas phase, of perchloroethylene in the presence of a catalyst comprising chrome oxides supported on AlF.sub.3 in the gamma and/or beta form.
Abstract: Process of the preparation of highly fluorinated alkanes by contacting halogenated alkenes or alkanes with at least the molar equivalent of HF in the presence of a catalyst selected from TaF.sub.5 and NbF.sub.5 in an amount of at least 0.25 molar equivalent at a temperature of 0.degree. C. to 175.degree. C.
Type:
Grant
Filed:
June 15, 1989
Date of Patent:
October 30, 1990
Assignee:
E. I. Du Pont de Nemours and Company
Inventors:
William H. Gumprecht, Wesley G. Schindel, Vinci M. Felix
Abstract: Process for the separation of hydrogen fluoride (HF), 2,2-dichloro-1,1,1-trifluoroethane (FC-123), and/or 2-chloro-1,1,1,2-tetrafluoroethane (FC-124) from mixtures containing them by controlling the molar ratio of HF/FC-123 in the mixture prior to subjecting the mixture to azeotropic distillation.
Type:
Grant
Filed:
August 1, 1988
Date of Patent:
July 31, 1990
Assignee:
E. I. DuPont de Nemours and Company
Inventors:
Leo E. Manzer, V. N. Mallikarjuna Rao, Richard T. Rockwell, Michael A. Sisk, Edwin J. Warwas, Roy Winteringham
Abstract: An improved process for the manufacture of 1,1,1,2-tetrafluoroethane, more particularly, a gas-phase reaction of a 1,1,1-trifluorochloroethane with hydrogen fluoride in the presence of a selected metal on aluminum fluoride or carbon.
Abstract: This invention relates to improved catalysts for gaseous phase fluoridation of aliphatic chlorinated and chlorofluorinated hydrocarbons by hydrofluoric acid. The catalysts comprise chromium salts or oxides complexed with aluminum phosphate and are characterized by a total specific surface area greater than about 200 m.sup.2 /g, but less than about 1000 m.sup.2 /g a surface area of pores of 40 to 50 .ANG. in radius above about 5 m.sup.2 /g, but less than about 150 m.sup.2 /g, a surface area of pores greater than or equal to 250 .ANG. in radius above about 2 m.sup.2 /g. but less than about 60 m.sup.2 /g. This invention also relates to gaseous phase fluoridation processes for chlorinated or chlorofluorinated derivatives utilizing these catalysts in fluidized bed reactors.
Abstract: An improved gas-phase process for the manufacture of 1,1,1-trifluorodichloroethane and/or 1,1,1,2-tetrafluorochloroethane by contacting a suitable tetrahaloethylene and/or pentahaloethane with hydrogen fluoride in the presence of Cr.sub.2 O.sub.3, prepared by pyrolysis of (NH.sub.4).sub.2 Cr.sub.2 O.sub.7, the reaction being conducted under controlled conditions whereby the production of pentafluoroethane is minimized.
Type:
Grant
Filed:
October 22, 1987
Date of Patent:
June 27, 1989
Assignee:
E. I. Du Pont de Nemours and Company
Inventors:
William H. Gumprecht, Leo E. Manzer, V. N. Mallikarjuna Rao
Abstract: A novel catalyst is prepared by codepositing hexavalent chromium oxide and a transition metal compound, preferably titanium trichloride, on alumina, followed by fluorinating the resulting combination. The catalyst is useful in the fluorination of a haloethylene of the formula CX.sub.2 .dbd.CHX (where the X's are chlorine or bromine or a combination of the two) in the vapor phase to form 1,1,1,2-tetrafluoroethane.
Abstract: An improved gas-phase process for the manufacture of 1,1-difluoro-1,2-dichloroethane and 1-fluoro-1,1,2-trichloroethane by contacting a suitable trihaloethylene and/or a tetrahaloethane with hydrogen fluoride in the presence of a metal in combination with a high fluorine content alumina, the reaction being preferably conducted under controlled conditions whereby the production of 1,1,1-trifluorochloroethane is minimized.
Abstract: A process for producing a hydrocarbon fluoride at a high selectivity with minimum formation of by-products is disclosed, which comprises reacting a hydrogen-containing hydrocarbon halide with anhydrous hydrogen fluoride in a liquid phase in the presence of a reaction product of (i) at least one of (a) an oxygen-containing compound selected from the group consisting of H.sub.2 O, H.sub.2 O.sub.2 and an oxygen-containing organic compound, and (b) a nitrogen-containing compound selected from the group consisting of NH.sub.3 and a nitrogen-containing organic compound, (ii) a tin compound selected from the group consisting of a stannic halide, a stannic oxyhalide and an organotin compound, and (iii) anhydrous hydrogen fluoride.
Abstract: An improved gas-phase process for the manufacture of 1,1,1-trifluorodichloroethane and 1,1,1,2-tetrafluorochloroethane by contacting a suitable tetrahaloethylene with hydrogen fluoride in the presence of a selected metal on a high fluorine content alumina support, the reaction being conducted under controlled conditions whereby the production of pentafluoroethane is minimized.
Abstract: This invention relates to a continuous gaseous-phase process for the preparation of trichlorotrifluoroethane, dichlorotetrafluoroethane and monochloropentafluoroethane, in predetermined proportions, from tetrachloroethylene, chlorine and hydrofluoric acid in the presence of a catalyst. The process is characterized by the combination of two chlorination-fluorination reactors in sequence, a parallel fluorination-dismutation reactor, and a separation unit for extracting the desired products and recycling recovered hydrofluoric acid and non-fluorinated or insufficiently fluorinated products. The process advantageously yields dichlorotetrafluoroethane containing less than 7% asymmetric isomer, and trichlorotrifluoroethane containing less than 2% asymmetric isomer.
Type:
Grant
Filed:
November 25, 1981
Date of Patent:
August 12, 1986
Assignee:
PCUK Products Chimiques Ugine Kuhlmann
Inventors:
Michel Abel, Francois Fine, Louis Foulletier, Yvan Verot
Abstract: A process is specified for preparing a chromium- and magnesium-containing catalyst for fluorination reactions by precipitating chromium(III) hydroxide. In this process, 1 mole of a water-soluble chromium(III) salt is reacted with at least 1.5 moles of magnesium hydroxide or magnesium oxide in the presence of water, and the reaction mixture--if necessary by evaporation--is converted into a paste which contains chromium(III) hydroxide and a magnesium salt. The paste is dried and treated with hydrogen fluoride at temperatures of 20.degree. to 500.degree. C.
Abstract: This invention relates to improved catalysts for gaseous phase fluorination of aliphatic chlorinated and chlorofluorinated hydrocarbons by hydrofluoric acid. The catalysts are characterized by an active carbon support having a total specific surface area greater than about 1000 m.sup.2 /g but less than about 2000 m.sup.2 /g, a surface area of pores of 40 to 50 .ANG. in radius above about 5 m.sup.2 /g but less than about 15 m.sup.2 /g, a surface area of pores greater than or equal to 250 .ANG. in radius above about 2 m.sup.2 /g but less than about 6 m.sup.2 /g, which has been impregnated with an aqueous chromium trioxide solution and dried. This invention also relates to gaseous phase fluorination processes for chlorinated or chlorofluorinated derivatives utilizing these catalysts in fluidized bed reactors.
Abstract: 1-Fluoro-1,1,2-trichloroethane is produced by a process which comprises the reaction of trichloroethylene with hydrogen fluoride using about 1.5 to 3.5 moles of hydrogen fluoride per mole of trichloroethylene, and conducting the reaction in the presence of a catalyst selected from the group consisting of CF.sub.3 SO.sub.3 H, TiCl.sub.4, MoCl.sub.5, WF.sub.6, NbCl.sub.5 and SnCl.sub.4 at a temperature in the range of 50.degree. to 150.degree. C. with a residence time of one quarter hour to five hours. The resulting product is relatively pure of overfluorinated by-products so as to be useful as a degreasing solvent.
Abstract: 1-Fluoro-1,1,2-trichloroethane is produced by a process which comprises the reaction of trichloroethylene with hydrogen fluoride using about 1.5 to 3.5 moles of hydrogen fluoride per mole of trichloroethylene, and conducting the reaction in the presence of a catalyst selected from the group consisting of CF.sub.3 SO.sub.3 H, TiCl.sub.4, MoCl.sub.5, WF.sub.6, NbCl.sub.5 and SnCl.sub.4 at a temperature in the range of 50.degree. to 150.degree. C. with a residence time of one quarter hour to five hours. The resulting product is relatively pure of overfluorinated by-products so as to be useful as a degreasing solvent.
Abstract: A halogenated alkene is reacted with HF in the presence of TaF.sub.5 or NbF.sub.5 to produce a fluorinated alkane. Exemplary is the reaction of tetrachloroethene with HF in the presence of TaF.sub.5 to produce 1,2,2-trichloro-1,1-difluoroethane and 1,1,2,2-tetrachloro-1-fluoroethane.