Abstract: The invention relates to the synthesis of difluoromethane by gas-phase catalytic fluorination of methylene chloride. To lengthen the lifetime of the catalyst the operation is carried out in the presence of chlorine.

Abstract: In order to remove the impurities (in particular 1-chloro-2,2-difluoroethylene) present in crude 1,1,1,2-tetrafluoroethane (F134a), a gaseous mixture of crude F134a and hydrofluoric acid is treated in the gas phase, in the presence of a fluorination catalyst, at a temperature of between 200 and 380° C. and under a pressure between atmospheric pressure and 2.5 MPa, the HF/F134a molar ratio being between 0.05 and 0.5.

Abstract: The invention relates to the synthesis of difluoromethane by gas-phase catalytic fluorination of methylene chloride.

Abstract: The invention relates to the synthesis of difluoromethane by gas-phase catalytic fluorination of methylene chloride. To lengthen the lifetime of the catalyst the operation is carried out in the presence of chlorine.

Abstract: The invention relates to catalytic fluorination of perchloroethylene or of pentachloroethane in the gas phase by means of hydrofluoric acid.A mixed catalyst is employed, made up of nickel and chromium oxides, halides and/or oxyhalides deposited on a support consisting of aluminium fluoride or of a mixture of aluminium fluoride and alumina.

Abstract: In order to regenerate the activity of a catalyst for gas phase fluorination the spent catalyst is treated with chlorine and hydrogen fluoride, at a temperature of between 250.degree. and 450.degree. C.

Abstract: The invention relates to the manufacture of 1,1,1,2-tetrafluoroethane (F134a) by gas-phase catalytic fluorination of 1-chloro-2,2,2-trifluoroethane (F133a).A mixed catalyst is employed, composed of nickel and chromium oxides, halides and/or oxyhalides deposited on a support consisting of aluminium fluoride or of a mixture of aluminium fluoride and alumina.This mixed catalyst makes it possible to obtain an excellent selectivity for F134a with a high production efficiency.

Abstract: To remove the unsaturated impurities (in particular 1-chloro-2,2-difluoroethylene and polyfluoropropenes) present in crude 1,1,1,2-tetrafluoroethane (F134a), a gaseous mixture of crude F134a, of hydrofluoric acid and of chlorine is treated in gaseous phase in the presence of a fluorination catalyst at a temperature of between 100.degree. and 300.degree. C. and at a pressure between atmospheric pressure and 2.5 MPa, the molar ratio HF/F134a being between 0.05 and 0.5 and the molar ratio Cl.sub.2 /F134a between 0.0001 and 0.1.

Abstract: The invention relates to a process for the manufacture of 1,1,1,2-tetrafluoro-2-chloroethane and of pentafluoroethane.The process, which consists of the gas phase catalytic fluorination of at least one pentahaloethane of formula C.sub.2 HX.sub.2-n F.sub.3+n in which X denotes a chlorine or bromine atom and n the number 0 or 1 by means of hydrofluoric acid, is characterized in that there is used a mixed catalyst composed of oxides, halides and/or oxyhalides of nickel and chromium deposited on a support consisting of aluminium fluoride or a mixture of aluminium fluoride and alumina.

Abstract: The invention relates to mass catalysts based on chromium and nickel oxides, obtained from a sol of chromium and nickel hydroxides.These catalysts, in which the Ni/Cr atomic ratio is between 0.05 and 5, may be used from the fluorination of halogenated hydrocarbons by HF in the gas phase.

Abstract: The invention relates to the purification of pentafluoroethane (F125) containing chloropentafluoroethane (F15).The F-125-F115 mixture to be purified is subjected to a fluorination stage to convert F115 into hexafluoroethane (F116) which is then separated from F125, for example by distillation.

Abstract: In order to remove the olefinic impurities (in particular 1-chloro-2,2-difluoroethylene and polyfluoropropenes) present in crude 1,1,1,2-tetrafluoroethane (F134a), a gaseous mixture of crude F134a, hydrofluoric acid and oxygen or air is treated in the gas phase, in the presence of a fluorination catalyst, at a temperature between 200.degree. and 350.degree. C. and at a pressure between atmospheric pressure and 2.5 MPa, the HF/F134a molar ratio being between 0.05 and 0.5 and the O.sub.2 /F134a molar ratio being between 0.001 and 0.1.

Abstract: The invention relates to a process for the manufacture of 1,1,1,2-tetrafluorochloroethane and of pentafluoroethane.The process which consists of gas phase catalytic fluorination of at least one pentahaloethane of formula C.sub.2 HX.sub.2-n F.sub.3+n in which X denotes a chlorine or bromine atom and n the number 0 or 1, by hydrofluoric acid, is characterized in that a catalyst is employed consisting of a catalytic quantity of chromium in an oxidation state equal to or greater than 3 and of an activated charcoal as support.The selectivity for 1,1,1,2-tetrafluorochloroethane and pentafluoroethane reaches approximately 95% and even more.

Abstract: The invention relates to the selective manufacture of 1,1-dichloro-1,2,2,2-tetrafluoroethane by catalytic fluorination of 1,1,1-trichloro-2,2,2-trifluoroethane with anhydrous hydrofluoric acid.The reaction is carried out in the liquid phase at a temperature of between 70.degree. and 170.degree. C. and under a pressure of between 10 and 80 bars absolute, in the presence of an antimony-containing catalyst.

Abstract: The invention relates to the manufacture of chlorofluoroethanes of formula CF.sub.3 --CHF.sub.x Cl.sub.2-x, where x is equal to 0 or 1, by the catalytic hydrogenation of a perhaloethane of formula: CF.sub.3 --CF.sub.x Cl.sub.3-x. The use of a ruthenium-based catalyst deposited on a support enables the selectivity to be improved.

Abstract: The invention relates to a process for the manufacture of 1-chloro-1,1-difluoroethane in the liquid phase by reacting hydrofluoric acid with 1,1,1-trichloroethane and/or 1,1-dichloro-1-fluoroethane.The selectively is improved by using a perfluoroalkanesulphonic acid, in particular trifluoromethanesulphonic acid, as a catalyst.

Abstract: The invention relates to a gas phase process for the manufacture of chloropentafluoroethane by the action of hydrofluoric acid on dichlorotetrafluoroethane in the presence of a catalyst, the said catalyst being prepared by reacting, in a gaseous phase, an alumina in which the sodium oxide content is below 300 ppm and the volume of the pores having a radius equal to 40 angstroms or above is greater than 0.7 cm.sup.3 /g, with hydrofluoric acid or with a mixture of hydrofluoric acid and of air, nitrogen or a fluorinated compound.

Abstract: The process for synthesizing 2,2,2-trifluoroethanol by liquid phase catalytic hydrogenation of a compound of formula: ##STR1## in which R is a hydrogen atom or a linear or branched alkyl radical containing from 1 to 8 carbon atoms and optionally partially fluorinated, comprising carrying out the hydrogenation in the presence of a nickel catalyst and in the presence of an aliphatic tertiary amine as a cocatalyst.

Abstract: A process for producing 2,2,2-trifluoroethanol or 1,1,1,3,3,3-hexafluoroisopropanol which comprises hydrogenating a fluoro compound having the formula ##STR1## wherein R.sub.1 is hydrogen or CF.sub.3 and R.sub.2 is hydrogen or a straight- or branched-chain alkyl group, which can also be fluoro-substituted, in the liquid phase in the presence of a palladium-on-activated-carbon catalyst, and if desired a tertiary amine co-catalyst.

Abstract: The invention relates to the preparation of trifluoroacetyl chloride by catalytic chlorination of trifluoroacetaldehyde with chlorine. Catalysis is performed in the vapor phase in a fixed bed or a fluidized bed reactor with an activated carbon catalyst. Optionally, hydrochloric acid and/or an inert diluent can be present with the reactant without affecting the results of this process.