Abstract: Linear hydrofluorocarbons of the formula XCF.sub.2 (CF.sub.2).sub.n CH.sub.2 F where X is H or F, and n is 1 to 7 when X is H and 0 to 7 when X is F, are produced by a vapor phase catalytic reaction of HF with corresponding compounds of the formula XCF.sub.2 (CF.sub.2).sub.n CH.sub.2 OY where Y is --(CO)Cl or --SO.sub.2 Cl. Azeotropic compositions with HF (e.g., an azeotrope of CHF.sub.2 CF.sub.2 CH.sub.2 F and HF) are provided, and a portion of the linear hydrofluorocarbon product (e.g., a portion of the CHF.sub.2 CF.sub.2 CH.sub.2 F) may be recovered as an azeotropic composition and recycled.

Abstract: A process for the manufacture of pentafluorodimethyl ether is disclosed which involves contacting at least one starting compound selected from the group consisting of compounds having a formula (CF.sub.3 OCF.sub.2 CO.sub.2)A and compounds having he formula (CF.sub.3 OCF.sub.2 CO.sub.2).sub.2 A' wherein A is selected from the group consisting of hydrogen, ammonium, alkali metals (e.g., sodium or potassium) and R (wherein R is a C.sub.1 to C.sub.4 alkyl group) and A' is an selected from the group consisting of alkaline-earth metals (e.g., magnesium or calcium), with at least one hydroxylic compound selected from the group consisting of water, mono-alcohols of the formula R'OH (wherein R' is a C.sub.1 to C.sub.12 straight or branched chain alkyl group) and alkanediols of the formula R" (OH).sub.2 (wherein R" is a C.sub.2 to C.sub.8 alkylene group) at temperature of about 120.degree. C. to 170.degree. C.

Abstract: A process for the manufacture of hydrofluorocarbons by the reaction of selected relatively low modular weight saturated and unsaturated hydrocarbons and corresponding partially halogenated hydrocarbons with elemental fluorine in the vapor phase. By selecting the ratio of F.sub.2 / substrate in combination with reaction temperature and reactor residence time the extent of fluorination of a substrate and degree of overfluorination can be controlled. Thus, starting with 1,1,1-trifluoroethane, CH.sub.3 CF.sub.3 (HFC-143a), 1,1,1,2-tetrafluoroethane, CH.sub.2 FCF.sub.3 (HFC-134a) is produced by simple thermal fluorination even in the presence of simultaneous formation of pentafluoroethane HFC-125. The use of compounds highly reactive toward fluorine are shown to promote the selective fluorination of partially fluorinated substrates.

Abstract: This invention relates to chemical processes for preparing tetrafluoropropionate salts and selected derivatives thereof.

Abstract: This invention relates to a process for producing linear hydrofluorocarbons of the formula XCF.sub.2 (CF.sub.2).sub.n CH.sub.2 F, where X is H or F, and n is 1 to 7 when X is H, and n is 0 to 7 when X is F, by a vapor phase catalytic reaction of HF and phosgene or sulfuryl chloride with corresponding compounds of the formula XCF.sub.2 (CF.sub.2).sub.n CH.sub.2 OZ where Z is H or --C(O)OCH.sub.2 (CF.sub.2).sub.n CF.sub.2 X.

Abstract: Linear hydrofluorocarbons of the formula XCF.sub.2 (CF.sub.2).sub.n CH.sub.2 F where X is H or F, and n is 1 to 7 when X is H and 0 to 7 when X is F, are produced by a vapor phase catalytic reaction of HF with corresponding compounds of the formula XCF.sub.2 (CF.sub.2).sub.n CH.sub.2 OY where Y is --(CO)Cl or --SO.sub.2 Cl.

Abstract: Azeotropic mixtures of HFC-338pcc and an alcohol such as methanol, ethanol, isopropanol or N-propanol, or a ketone such as acetone, are disclosed that are useful as cleaning agents, refrigerants, aerosol propellants, heat transfer media, gaseous dielectrics, fire extinguishing agents, expansion agents for polyolefins and polyurethanes, power cycle working fluids, polymerization media, particulate removal fluids, carrier fluids, and displacement drying agents.

Abstract: A process for the preparation of chlorofluoropropanes of the formula C.sub.3 HCl.sub.2 F.sub.5 by contacting monofluorodichloromethane with tetrafluoroethylene in the presence of a modified aluminum chloride catalyst at a temperature of 0.degree. to 150.degree. C. The novel compound CF.sub.3 CCl.sub.2 CHF.sub.2 is also disclosed.

Abstract: Novel perfluoropolyethers, such as perfluorodipentaerythritol hexaethyl ether, and their intermediates exhibit excellent chemical and thermal stability and are useful as vapor phase soldering fluids and convection cooling liquids.

Abstract: A process for the preparation of 1,1-dichloro-1,2-difluoroethane (HCFC-132c) comprising contacting 1,1-dichloroethylene with lead dioxide and anhydrous hydrogen fluoride. Addition of fluorine to the double bond of vinylidene chloride can be achieved using inexpensive and readily available commercial raw materials.