Abstract: The invention relates to a process for the preparation of composite material formed from a vulcanized elastomer, containing carboxylic acid or dicarboxylic acid anhydride groups, in combination with a thermoplastic elastomer containing polyamide blocks, which comprises vulcanizing an elastomer composition comprising said vulcanizable elastomer, a crosslinking system and, optionally, diverse adjuvants in a mold, one part of which is occupied by said thermoplastic elastomer containing polyamide blocks, the vulcanization temperature being between -15.degree. C. and +5.degree. C. with respect to the Vicat point of said thermoplastic elastomer containing polyamide blocks, the elastomer composition and the vulcanization kinetics being such that the material shows cohesive failure when subjected to stress for separation of the two elastomers.This process leads to composite materials which have excellent properties, in particular in respect of tensile strength (cohesive failure).

Abstract: Copolymers of ethylene, optionally substituted by a halogen atom, by two halogen atoms carried by the same carbon atom, or by a phenyl group, and of fluorinated (meth)acrylates of formula: ##STR1## in which: R is selected from hydrogen and methyl, andn is an integer greater than or equal to 1.Application of these copolymers to form, in particular, surfaces for gliding on snow or water.

Abstract: The present invention relates to a heat-sealable and peelable film for polystyrene containers, consisting of at least one thin film comprising a mixture (a) of polystyrene and (b) of one or more copolymer(s) of ethylene and of acrylic derivatives.It also relates to a process for sealing a polystyrene container by means of said film and to the heat-sealed polystyrene container thus obtained.

Abstract: A process is disclosed for the conversion of an ammonium or amine salt of an alkanesulfonic acid to its corresponding alkanesulfonamide by heating the salt to at least its melting point to remove the water by-product and recover an alkanesulfonamide.

Abstract: For the preparation of alkyl halodifluoroacetates, a 1,1-difluorotetrahaloethane is reacted with an alcohol in the presence of air and/or oxygen and a free-radical initiator, such as for example an azo compound, e.g., azobis(isobutyronitrile).

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 a polymer mixture which contains(A) 50 to 85 wt. % of a polyether block amide consisting of 30 to 60 wt. % of polyamide-12, polyamide-11 and/or polyamide-12,12 blocks and 70 to 40 wt. % of polyethylene glycol blocks,(B) 10 to 40 wt. % of a polyether block amide consisting of 65 to 85 wt. % of polyamide-12, polyamide-11 and/or polyamide-12,12 blocks and 35 to 15 wt. % of polyethylene glycol blocks, and(C) 5 to 40 wt. % of a poly(ethylene-co-vinylacetate-g-maleic anhydride) polymer consisting of 75 to 95 wt. % of ethylene, 5 to 25 wt. % of vinylacetate and 0.1 to 2 wt. % of maleic anhydride,wherein the data relating to wt. % for the constituents (A), (B) and (C) are with reference to the total amount of polymer mixture. The invention also relates to films produced from this polymer mixture and the use of these films to produce waterproof, water vapor permeable, wind resistant textile composite materials, dressing materials and hygiene items.

Abstract: A supported solid catalyst which can be used for the polymerization and clymerization of conjugated dienes having as its basis the reaction product of:A) a solid MgCl.sub.2 support,B) an ether, preferably THF, as swelling agent for the support,C) a metal salt selected from among metals having an atomic number of between 57 and 71 or 92 in the periodic table of elements and, if the metal salt is not a halide,D) a halogenation agent selected from the group consisting of a halogenated compound of aluminum and a halogenated compound not containing aluminum, the reaction solid being free from the swelling agent, plusE) an organic derivative of aluminum which is obligatory when the halogenation agent is not a halogenated compound of aluminum and optional when the halogenation agent is a derivative of aluminum.Also, a method of preparing this catalyst.

Abstract: Novel functionalized peroxides which may be used as crosslinking, grafting and curing agents, initiators for polymerization reactions and as monomers for condensation polymerizations to form peroxy-containing polymers, which in turn can be used to prepare block and graft copolymers, have the following Formula I: ##STR1## R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5, R.sup.6, R.sup.7, X, Y.sup.1, Y.sup.2, Y.sup.3, Z.sup.1, Z.sup.2, x, y and z are as defined in the Summary of the Invention. The compounds of Formula I may be prepared by reacting hydroxy-containing tertiary hydroperoxides with diacid halides, phosgene, dichloroformates, diisocyanates, anhydrides and lactones to form the functionalized peroxides. These reaction products may be further reacted, if desired, with dialcohols, diamines, aminoalcohols, epoxides, epoxy alcohols, epoxy amines, diacid halides, dichloroformates and diisocyanates to form additional functionalized peroxides.

Abstract: A compound (I) is prepared by reacting at least one (meth)acrylate (II) with a heterocyclic alcohol (III), in the presence of a catalyst consisting of a mixture formed (a) of at least one magnesium alkoxide and (b) of a component chosen from the chelates of calcium with 1,3-dicarbonyl compounds, dialkyltin oxides, dialkyltin alkoxides and dialkyltin diesters. ##STR1## R=C.sub.1 -C.sub.4 alkyl. R.sup.1 =H, CH.sub.3 ; A, B=straight or branched C.sub.2 -C.sub.5 hydrocarbon chain; R.sup.2 =C.sub.1 -C.sub.4 alkyl.

Abstract: A supported solid catalyst which can be used for the polymerization and copolymerization of conjugated dienes having as its basis the reaction product of:A) a solid MgCl.sub.2 support,B) an ether, preferably THF, as swelling agent for the support,C) a metal salt selected from among metals having an atomic number of between 57 and 71 or 92 in the periodic table of elements and, if the metal salt is not a halide,D) a halogenation agent selected from the group consisting of a halogenated compound of aluminum and a halogenated compound not containing aluminum, the reaction solid being free from the swelling agent, plusE) an organic derivative of aluminum which is obligatory when the halogenation agent is not a halogenated compound of aluminum and optional when the halogenation agent is a derivative of aluminum.Also, a method of preparing this catalyst.

Abstract: The invention relates to the preparation of alkanesulphonic acids by photooxidation of sulphur-containing derivatives (thiols, sulphides, disulphides).The operation is carried out in solution in aqueous or alcoholic acetonitrile, with a light source irradiating between 200 and 400 nm.

Abstract: A continuous non-catalytic process for the manufacture of 1,1-dichloro-1-fluoroethane/1-chloro-1,1-difluoroethane mixtures from 1,1-dichloro-1-fluoroethane is provided. Hydrogen fluoride and 1,1,1-trichloroethane are continuously feed a molar ratio of from about 3.0 to about 5.2 to form a liquid phase hydrofluorination reaction mixture. Vapor phase reaction product is continuously withdrawn from the reaction zone, and hydrogen fluoride is continuously selectively refluxed back to the reaction mixture. 1,1,1-Trichloroethane utilization approaches 100% , with selectivity for 1,1-dichloro-1-fluoroethane between 15% and 85%, based upon the amount of 1,1-dichloro-1-fluoroethane and 1-chloro-1,1-difluoroethane contained in the gaseous reaction product.

Abstract: To remove the traces of chlorofluoromethane present in a difluoromethane, the difluoromethane to be purified is passed over a 13X molecular sieve at a temperature of at least 60.degree. C.The sieve can be regenerated by washing with the aid of a solution of sodium or potassium carbonate and heating to high temperature under inert atmosphere or in vacuum.

Abstract: In this esterification, catalysed by H.sub.2 SO.sub.4, the crude reaction mixture comprising ester, butanol, acrylic acid, BuSO.sub.4 H and traces of H.sub.2 SO.sub.4 is obtained; BuSO.sub.4 H is hydrolysed (in R2) to H.sub.2 SO.sub.4 using pure water or water generated during the reaction; after hydrolysis, the medium is separated by settling (in D2) into an organic phase containing ester, butanol and part of the unconverted acid; and an aqueous phase containing H.sub.2 SO.sub.

Abstract: Stripping action of an alkaline paint stripper is improved when ammonia is partially or completely replaced with ammonium bicarbonate or chemical equivalent thereof which decomposes into ammonia and carbon dioxide. A benzyl alcohol solvent system containing at least ammonium bicarbonate is preferably a water-in-oil emulsion emulsified with oleic hydroxyethyl imidazoline and thickened with hydroxypropyl cellulose or hydroxypropyl methylcellulose. A mixture of ammonium carbamate and ammonium bicarbonate identified as ammonium carbonate is the preferred activator for this alkaline paint stripper. Improved stripping can also be provided by reacting ammonium bicarbonate and ammonia in situ within the water-in-oil emulsion.

Abstract: This invention relates to a flexible metal pipe covered with an impermeable sheath of a shrinkable, preferably semicrystalline polymer or polymers, characterized in that it incorporates between the shrinkable polymer sheath and the metal pipe an intermediate elastomer layer (8), optionally vulcanized or reticulated, and/or a TPE in the form of a continuous tubular sleeve (FIG. 3) or of a tape (FIG. 4 to 6). Sheathed pipes of this type are particularly suitable for flexible pipelines, optionally with suitable supports, for carrying oil and gas.

Abstract: Process for adiabatically hydrofluorinating hydrochlorocarbons and hydrochlorofluorocarbons in the gaseous phase in the presence of a catalyst that is active at the initial reaction temperature and remains highly selective at the maximum reaction temperature, e.g., a Cr catalyst. The molar ratio of HF to starting compound is at least about 2.5:1. The initial reaction temperature is selected such that the HF in the feed is partially associated but not completely (HF).sub.6. The catalyst may be unsupported or supported.

Abstract: Crystalline MgCl.sub.2 particulates, exhibiting the morphology of substantially regular polyhedra having an even number of from 10 to 18 face surfaces, are well suited as support substrate for olefin polymerization catalysts.

Abstract: For preparing sec-butyl acrylate, acrylic acid is reacted with 1-butene in the presence of a zirconium-based solid superacid as the catalyst, for example a calcined reaction product of 10-15 parts by weight of ammonium sulphate and 100 parts by weight of zirconium hydroxide.