Abstract: An oxidative halogenation process involving contacting a reactant hydrocarbon selected from methane, a halogenated C1 hydrocarbon, or a mixture thereof with a source of halogen and, preferably, a source of oxygen in the presence of a rare earth halide or rare earth oxyhalide catalyst, so as to form a halogenated C1 hydrocarbon having a greater number of halogen substituents as compared with the reactant hydrocarbon. Preferably, the product is a monohalogenated methane, more preferably, methyl chloride. The oxidative halogenation process to form methyl halide can be integrated with downstream processes to produce valuable commodity chemicals, for example, methyl alcohol and/or dimethyl ether; light olefins, including ethylene, propylene, and butenes; higher hydrocarbons, including gasolines; vinyl halide monomer, and acetic acid. Hydrogen halide, which is a co-product of these downstream processes, can be recycled to the oxidative halogenation process.

Abstract: Halohydrocarbons comprising at least 3 carbon atoms are obtained by batchwise reaction between a haloalkane and an olefin in the presence of a catalyst and a co-catalyst. The addition of at least some of the co-catalyst is carried out gradually. At least some of the co-catalyst is recovered with a view to its re-use.

Abstract: The present invention relates to a catalytic process for the preparation of alkylene glycols from alkylene oxide and water. Further, the invention relates to a method of preservation of catalysts in alkylene oxide containing systems. More in particular, it has been found that polycarboxylic acids, preferably oxalic acid, have a positive effect on the lifetime of catalyst systems based on anion exchange resins, and particularly those in the bicarbonate and oxalate forms.

Abstract: The invention relates to novel naphthopyran- and phenanthropyran-type compounds having a carbobicycle annelated in 5,6- position. These compounds have formula (I) given below: These compounds (I) have interesting photochromic properties. The invention also relates to their preparation, to their applications as photochromes, as well as to the compositions and (co)polymer matrices containing them.

Abstract: Halohydrocarbons comprising at least 3 carbon atoms are obtained by reaction between a haloalkane and a haloolefin, in the substantial absence of nitrile, and by introducing the reactants in a molar ratio between the haloalkane and the haloolefin of less than 2. 1,1,1,3,3-Pentachloropropane can thus be obtained in good voluminal yield.

Abstract: In a process for the treatment of a cracking gas formed by pyrolysis of 1,2-dichloroethane (EDC), in which the cracking gas is split into its principal components hydrogen chloride (HCl), vinyl chloride (VCM) and unreacted 1,2-dichloroethane (EDC), and these are formed in substantially pure form, where, in the first step of the treatment of the cracking gas, the solids are separated therefrom in a quench zone, the disadvantages of the prior art are intended to be reduced at least partly and in particular the energy losses which usually arise due to the substantial condensation of the quench gas and its re-heating for the purposes of distillative separation are avoided and, due to the circulation of the unreacted EDC at a higher temperature level, the original conversion in the pyrolytic cracking of EDC is intended to be subsequently increased.

Abstract: The invention relates to a process for preparing alkali metal alkoxides by reacting alkali metals with alcohols in the presence of a catalyst, preferably a transition metal salt and especially iron(III) chloride.

Abstract: A method for efficiently extracting a reaction product containing a target aromatic fluorine compound formed by the halogen exchange reaction of an aromatic chlorine compound with a fluorinating agent quickly from the reaction vessel without suffering part of the reaction product to remain as a residue inside the reaction vessel is disclosed. Specifically, the reaction product is extracted from the reactor subsequently to the halogen exchange reaction at a temperature in the range of 20-250° C. By this method, the reaction product formed in consequence of the halogen exchange reaction can be efficiently extracted quickly from the reaction vessel, and that without suffering occurrence of a residue of the reaction product.

Abstract: A gaseous process for obtaining pentafluoroethane by dismutation of chlorotetrafluoroethane in the presence of a supported catalyst, said catalyst being formed of a mixture of trivalent chromium oxide with at least an alkaline-earth metal oxide selected from Mg, Ca, Sr and Ba.

Abstract: An improved process for the manufacture of CF3CHF2 by contacting 1,2-dichloro-1,1,2-trifluoroethane (CClF2CHClF) or 1-chloro-1,1,2,2-tetrafluoroethane (CHF2CClF2) or mixtures of CF3CHCl2 and CClF2CHClF or mixtures of CF3CHClF and CHF2CClF2 with HF in the presence of a Cr2O3 catalyst prepared by pyrolysis of ammonium dichromate, the reaction being conducted under controlled conditions whereby the production of CF3CHF2 is maximized, and the formation of chloropentafluoroethane (CF3CClF2) and other perhalo derivatives is minimized. The subject hydrogen-containing compound is useful as a blowing agent, propellant, refrigerant, fire extinguishing agent, or sterilant carrier gas.

Abstract: In a process for the production of VCM, the gaseous reactants and an inert carrier gas are fed into an adiabatic reaction zone in the oxychlorination section, both reaction zones being associated with an integral fluidised bed, the cooled reaction zone containing a vertically coaxial hollow cooling rod bundle forming a passage. A balanced production of VCM is to be achieved, this being done by selecting a ratio of 1 to 6 inclusive between the equivalent diameter of the passage cross-sectional area and the mean gas bubble pocket diameter of the fluidised bed.

Abstract: Disclosed is a process for producing an iodinated aromatic compound, which comprises reacting an aromatic compound with an iodine compound in the presence of a chlorate as an oxidizing agent.

Abstract: Indane compounds of general formulae (1) to (4) and their pharmaceutical use, particularly to achieve mast cell stabilising activity and/or anti-inflammatory activity are described.

Abstract: A method of preparing pentafluoroethane wherein chlorine-containing carbon compounds are fluorinated in the presence of chromium catalysts that are in an amorphous state and wherein the main component is chromium compounds with the addition of at least one metal element selected from the group composed of indium, gallium, cobalt, nickel, zinc and aluminum and the average valence of the chromium in said chromium compounds is not less than +3.5 but not more than +5.0. And said chromium catalysts and a preparation method thereof. A method of preparing pentafluoroethane wherein the total yield of chlorofluoroethane by-products can be decreased without significantly deteriorating the generation activity of the pentafluoroethane and compounds which can be recycled in the reaction system. And to provide catalysts for this fluorination and a preparation method thereof.

Abstract: A method for producing inexpensively in a high yield a halogen-containing aromatic compound, particularly a halogen-containing aromatic compound incorporating therein a bromodifluoroalkyl group, and a halogen-containing naphthalene compound useful as a raw material for a resin excelling in heat resistance, chemical resistance and water repellency, and having a low dielectric constant and a low refractivity are provided.

Abstract: The work-up of the gaseous products from the thermal cracking of 1,2-dichloroethane is simplified if the cracking gases are cooled to a temperature range of about 150 to 180° C., only a subsidiary proportion, which comprises all the coke formed, being condensed and fed to a separate work-up.

Abstract: Continuous process for the preparation of pentafluoroethyl iodide from iodine, iodine pentafluoride and tetrafluoroethylene, which comprises dissolving the iodine in iodine pentafluoride and continuously feeding the resulting solution to a vertical bubble column (1), which is filled with iodine pentafluoride and at its lower end has a feed line for tetrafluoroethylene, where the reaction zone is maintained at from 85 to 95° C., preferably 90° C., and the pentafluoroethyl iodide formed escapes in gaseous form at the top of the reactor (1), is liquefied in a downstream cooled condenser and is drawn off into storage vessels.

Abstract: This invention relates to the production of an hexabromocyclododecane product, which process comprises brominating cyclododecatriene in the presence of a 1,4-dioxane and water based solvent and from about 0.5 to about 30 wt % bromide ion in the liquid phase of the reaction mass. Optional post-reaction heat treatment in a finishing step increases process yields if needed. The hexabromocyclododecane product is unrecrystallized and contains no more than about 1.5 wt % tetrabromocyclododecene impurities.

Abstract: The present invention discloses an improved process for the N-acylation of amino alcohols employing an organic acid in the form of an acid halogenide, wherein the acylation occurs in an organic solvent in the additional presence of water.

Abstract: The present invention is directed to a process for preparing 1,2-dichloroethane by reacting ethene with hydrogen chloride and oxygen over a copper-containing fluidized-bed catalyst. The discharge of the catalyst from the reactor per se is avoided if the catalyst is virtually completely retained in the upper part of the reactor by means of superfine filtration.