Abstract: Fluorination process of halogenated organic compounds with gaseous anhydrous HF characterized in that a catalyst comprising a supported Cr(III) amorphous compound is used, wherein the support consists in an aluminum trifluoride (AlF.sub.3) having an high surface area and an high pore volume obtainable by fluorination with gaseous HF of alumina having surface area of at least 150 m.sup.2 /g and pore volume not lower than 0.3 cc/g and wherein said alumina comprises from 0.5 up to 15% by weight of silicon oxide, the chromium amount being comprised between 1 and 20% by weight.

Abstract: A fluorination catalyst based on of an amorphous Cr (III) compound and on a compound of another metal selected from Mg, Ca, Sr, Ba, Sc, Ti and Zr, wherein the atomic ratio of Cr/other metal is between 50:1 and 1:1, said compounds are supported on a AlF.sub.3 support and being prepared by impregnating the support with a concentrated aqueous solution containing a soluble Cr (III) salt and a soluble salt of the other metal. The catalyst can be used in gaseous phase reactions.

Abstract: 1,1,1,2-tetrafluoroethane (134a) is prepared by reacting, in the gas phase, trichloroethylene with 1,1,1-trifluorochloroethane (133a) and hydrofluoric acid with trichloroethylene/133a molar ratios ranging from 5/95 to 50/50, in the presence of a catalyst consisting of Cr.sub.2 O.sub.3 carried on AlF.sub.3.The process provides 134a yields higher than 90% and permits an exceptionally long life of the catalyst. In this way it is possible to realize a continuous process by recycling the unreacted trichloroethylene and 133a, thereby making up for the relatively low global conversion of the reagents.

Abstract: Process for preparing pentafluoroethane (125) containing amounts of 115 lower than 0.02% by weight wherein pentafluoroethane is obtained by a dismutation process of tetrafluorochloroethane CF.sub.3 CHClF (HCFC-124) in gaseous phase in the presence of a chrome oxide catalyst (CR.sub.2 O.sub.3) supported on a AlF.sub.3 support, wherein one operates at temperatures from 140.degree.-180.degree. C. for contact times comprised between 15-30 seconds, from >180.degree. C. to 240.degree. C. for contact times between 5 to 15 seconds, from >240.degree. C. to 260.degree. C. for contact times between 1 to 5 seconds, from >260.degree. to 300.degree. C. for contact times between 0.1 to 1 second.

Abstract: Process for the regeneration of a fluorination catalyst based on Cr(III) compounds optionally supported, which comprise a) treatment at 350.degree.-40.degree. C. with an air/inert gas mixture and b) treatment at 300.degree.-380.degree. C. with a mixture of an inert gas containing from 0.5 to 5% by volume of an aliphatic hydrocarbon C.sub.1 -C.sub.8.

Abstract: 1,1,1,2-tetrafluoroethane (134a) is prepared by reacting, in the gas phase, trichloroethylene with 1,1,1-trifluorochloroethane (133a) and hydrofluoric acid with trichloroethylene/133a molar ratios ranging from 5/95 to 50/50, in the presence of a catalyst consisting of Cr.sub.2 O.sub.3 carried on AlF.sub.3.The process provides 134a yields higher than 90% and permits an exceptionally long life of the catalyst. In this way it is possible to realize a continuous process by recycling the unreacted trichloroethylene and 133a, thereby making up for the relatively low global conversion of the reagents.

Abstract: 1,1,2-trifluoro-1,2-dichloroethane (Al23a) is isomerized to 1,1,1-tri-fluoro-2,2-dichloroethane (Al23) by contacting it with AlF.sub.3 at temperatures ranging from 180.degree. to 400.degree. C. Advantageously, it is operated with mixtures of Al23a with Al23 and/or other chlorofluorocarbons coming from the preparation of Al23 by hydrofluorination of perchloroethylene.

Abstract: 1,1,1-trifluoro-2-fluoroethane (CFC 134a) is purified from 1,1-difluoro-2-chloroethylene (CFC 1122) by reacting a mixture comprising said compounds with hydrofluoric acid, at temperatures from 200.degree. C. to 450.degree. C., in one presence of chrome oxide (Cr.sub.2 O.sub.3) in substantially crystalline form.

Abstract: 1,1,1-trifluoro-2-fluoroethane (CFC 134a) is purified from 1,1-difluoro-2-chloroethylene (CFC 1122) by reacting a mixture comprising said compounds with hydrofluoric acid, at temperatures from 200.degree. C. to 450.degree. C., in the presence of chrome oxide (Cr.sub.2 O.sub.3) in substantially crystalline form.

Abstract: 1,1,1,2-tetrafluoroethane (134a) is prepared by reacting, in the gas phase, trichloroethylene with 1,1,1-trifluorochloroethane (133a) and hydrofluoric acid with trichloroethylene/133a molar ratios ranging from 5/95 to 50/50, in the presence of a catalyst consisting of Cr.sub.2 O.sub.3 carried on AlF.sub.3.The process provides 134a yields higher than 90% and permits an exceptionally long life of the catalyst. In this way it is possible to realize a continuous process by recycling the unreacted trichloroethylene and 133a, thereby making up for the relatively low global conversion of the reagents.

Abstract: The 1,1,2-trifluoro-1,2-dichloroethane content is reduced or removed from 1,1,1-trifluoro-2,2-dichloroethane by contacting a gaseous mixture comprising said compounds with chrome oxide (Cr.sub.2 O.sub.3) either as such or supported, at temperatures from 180.degree. to 400.degree. C.

Abstract: Pentafluoroethane (HFC 125) is selectively prepared by dismutation of tetrafluorochloroethane (HCFC 124) effected by contacting the latter, in the gas phase, with a Cr.sub.2 O.sub.3 catalyst at temperatures ranging from 150.degree. to 330.degree. C. Along with HFC 125, also HCFC 123 substantially free from isomers 123a and 123b is obtained.

Abstract: Process for the preparation of a perfluoroacyl fluoride wherein the acyl radical is a propionyl or butyryl group, characterized in that perfluoroalkylvinylether wherein the alkyl radical is a methyl or ethyl group is thermally treated in the presence of a catalyst selected from the group consisting of:(A) a fluoride of Li, Na, K, Cs or Rb, or another compound of Li, Na, K, Cs or Rb which is easily fluorinated under the reaction conditions;(B) a fluoride of Be, Mg, Ca, Sr, or Ba, or another compound of Be, Mg, Ca, Sr, or Ba which is easily fluorinatable under the reaction conditions:(C) a fluoroaluminate, fluorosilicate, fluorotitanate or fluorometallate of an alkali metal, or of a metal belonging to group IIA of the Periodic Table, i.e.