Abstract: A low temperature molten ionic liquid composition comprising a mixture of a metal halide and an alkyl-containing amine hydrohalide salt can be used in linear alkylbenzene formation. The metal halide is a covalently bonded metal halide which can contain a metal selected from the group comprised of aluminum, gallium, iron, copper, zinc, and indium, and is most preferably aluminum trichloride. The alkyl-containing amine hydrohalide salt may contain up to three alkyl groups, which are preferably lower alkyl, such as methyl and ethyl.

Abstract: A low temperature molten ionic liquid composition comprising a mixture of a metal halide and an alkyl-containing amine hydrohalide salt is described which is useful as a catalyst and a solvent in alkylation, arylation and polymerization reactions or as an electrolyte for batteries. The metal halide is a covalently bonded metal halide which can contain a metal selected from the group comprised of aluminum, gallium, iron, copper, zinc, and indium, and is most preferably aluminum trichloride. The alkyl-containing amine hydrohalide salt may contain up to three alkyl groups, which are preferably lower alkyl, such as methyl and ethyl.

Abstract: A process for forming a supported metal carbide catalyst, for example, a Group VIB transition metal carbide, such as tungsten carbide, which process comprises the calcination of a carbon support that has been impregnated with a metal carbide precursor comprising a water soluble salt of: (1) a cation comprising nitrogen-hydrogen bonded moieties, such as a guanidine cation; and (2) an anion, such as a tungstate anion, comprising metal-oxygen bonded moieties, so that upon calcination the product formed is the metal carbide and the by-products comprise ammonia and carbon dioxide.

Abstract: A process for forming a metal carbide catalyst, for example, a Group VIB transition metal carbide, such as tungsten carbide, which may be on a support, which process comprises the calcination of a precursor comprising a water soluble salt of: (1) a cation comprising nitrogen-hydrogen bonded moieties, such as a guanidine cation; and (2) an anion, such as a tungstate anion, comprising metal-oxygen bonded moieties, so that upon calcination the product formed is the metal carbide and the by-products comprise ammonia and carbon dioxide.

Abstract: Transition metal carbides, having high surface areas and catalytic activity for use in pollution control, isomerization and hydrodesulfurization procedures, can be formed by the calcination of a mixture of an acyclic compound containing carbon-nitrogen-hydrogen bonding and a metal salt. The acyclic compound is preferably a compound of guanidine or a derivative thereof such as a deammoniated derivative of guanidine. The metal salt is preferably a metal halide such as a metal chloride.

Abstract: Bimetallic oxynitrides and nitrides which have catalytic properties comprise two transition metals selected from Groups IIIB to VIII of the Periodic Table of the Elements. Preferably, one metal is either molybdenum or tungsten. The other can be tungsten or molybdenum, respectively, or another transition metal, such as vanadium, niobium, chromium, manganese, cobalt, or nickel. They have a face centered cubic (fcc) arrangement of the metal atoms and have a surface area of no less than about 40 m.sup.2 /gm.

Abstract: Chloromethane compounds including carbon tetrachloride and the chlorofluoromethane compounds, such as dichlorodifluoromethane, can be catalytically hydrodechlorinated, e.g., in the case of dichlorodifluoromethane to monochlorodifluoromethane and/or difluoromethane, by treatment with hydrogen in the presence of a transition metal carbide catalyst, for example, a Group IVB metal carbide, such as tungsten carbide, supported on an oxidic support, such as alumina, optionally with a passivating layer of ceramic, such as silicon carbide, between the oxidic support and catalyst. The catalyst preferably has a surface area of no less than about 1 m.sup.2 /gm.

Abstract: A process for reforming a hydrocarbon which comprises treating the hydrocarbon, while at elevated temperature, with a transition metal catalyst while in the presence of an effective amount of gaseous oxygen to improve the selectivity of the catalyst to aromatic formation and reduce the hydrogenolysis activity of the catalyst. The transition metal may be tungsten, and the transition metal catalyst may be supported on an oxidic support, optionally with a ceramic passivation layer lying between the support and the transition metal catalyst. The amount of gaseous oxygen used may be from about 50 ppm to about 5000 ppm, based upon the weight of the hydrocarbon.

Abstract: Supported non-oxide metal carbide-containing catalysts are provided which comprise: (a) an oxide support, such as alumina or cordierite; (b) a passivating layer of a ceramic, such as silicon carbide; and (c) a non-oxide metal ceramic catalytic component, such as a Group VI metal carbide or nitride, preferably tungsten carbide or molybdenum carbide.

Abstract: Tungsten carbide/zeolite catalysts useful in the hydrogenation of unsaturated sulfur containing compounds and in particular in the production of tetrahydrothiophene are provided.Also provided is a process for the production of tetrahydrothiophene from thiophene using the tungsten carbide/zeolite catalysts taught, which effects the selective production of tetrahydrothiophene without producing large quantities of H.sub.2 S and unwanted hydrocarbons.

Abstract: Nitriles can be hydrogenated to amines by heating the nitrile in the presence of hydrogen and a tungsten carbide catalyst, such as are formed by the calcination of a tungsten salt with an acyclic compound containing-nitrogen-hydrogen bonding.

Abstract: The addition of an aqueous solution containing one or more cations intended in a metal oxide ceramic product to a base to precipitate a calcinable metal oxide ceramic precursor reduces gelation problems during the precipitation of the precursor.

Abstract: Carbides of Group VIB metals, such as tungsten and molybdenum, can be formed by the pyrolysis of a salicylate of such metal. The salicylate can be formed by reaction of a Group VIB metal halide with salicylic acid.

Abstract: Mixed bimetallic alkoxide-caraboxylate compositions are formed by reaction of at least two metal alkoxides and a carboxylic acid with elimination of distillable ester by-product therefrom. Hydrolysis of said compositions produce bimetallic hydroxy-carboxylates which, upon calcination, give bimetallic oxides.

Abstract: Aluminum alkoxides can be formed by reaction of aluminum metal and alcohol in the presence of soluble titanium (e.g., derived from a titanium carboxylate) as the catalyst for the reaction.

Abstract: Stable metal oxide sols comprising an anhydrous alcohol having metal oxide particles colloidally dispersed therein is disclosed. This sol composition is formed by the hydrolysis of a metal alkoxide to form metal oxide particles, removal of the particles from the resulting mother liquor from such a reaction, and the redispersing of the metal oxide powders in an anhydrous alcohol solvent.

Abstract: Mixed heavy bimetallic alkoxide-carboxylate compositions are formed by reaction of a heavy metal tetraalkoxide (e.g., a zirconium alkoxide) and a heavy metal tricarboxylate (e.g., yttrium acetate) with elimination of distillable ester by-product therefrom. Hydrolysis of said compositions produced novel bimetallic hydroxy-carboxylates. Calcination of the hydrolysis products give bimetallic oxides.

Abstract: Metal oxide powders, which are chemically uniform and free-flowing, can be formed by dissolving a metal alkoxide in a non-polar organic solvent, adding water to the resulting composition and then emulsifying the blend of water and solvent containing the alkoxide to cause hydrolysis of the alkoxide. The hydrolysis reaction forms the desired metal oxide as a precipitate which can be recovered by a simple filtration process.

Abstract: Improved magnesium phosphate fast-setting cements comprising an effective amount of fiber to increase the impact strength of the cement. These fibers include glass, metal, organic and mixtures thereof.

Abstract: A fast-setting magnesium phosphate one-component adhesive/grout is used to bond tiles, e.g. ceramic tiles, to a substrate, e.g. sheet-rock. The grout comprises an activator prepared by e.g., mixing diatomaceous earth with at least a sufficient amount of an ammonium phosphate solution to form a paste then heating the paste to coat the pores of the diatomaceous earth and result in a dry solid which is then milled to yield the activator, magnesium oxide, diammonium phosphate, boric acid, and sufficient water to form a paste. This grout is applied to the surfaces to be bonded which are then brought together to form a composite which is allowed to set at ambient temperatures forming a durable bond in about three hours.