Abstract: A process for acyl substitution of an anhydride with an active-hydrogen-containing compound includes reacting the anhydride with the active-hydrogen-containing compound in the presence of a vanadyl salt catalyst to obtain a high yield of acyl substitution reaction product with high chemoselectivity.

Abstract: This invention discloses a process for making dilithium initiators in high purity. This process can be conducted in the absence of amines which is desirable since amines can act as modifiers for anionic polymerizations. The dilithium compounds made are highly desirable because they are soluble in aromatic solvents. The present invention more specifically discloses a process for synthesizing a dilithium initiator which comprises reacting disopropenylbenzene with a tertiary alkyl lithium compound in an aromatic solvent at a temperature which is within the range of about 0° C. to about 100° C. The present invention further discloses a process for synthesizing m-di-(1-methyl-3,3-dimethylbutyllithio)benzene which comprises reacting diisopropenylbenzene with tertiary-butyllithium in an aromatic solvent at a temperature which is within the range of about 0° C. to about 100° C.

Abstract: The invention relates to a polymer-supported carbonylation catalyst and its use in a process for preparing organic carboxylic acid or anhydride having n+1 carbon atoms. The invention relates also to a process for preparing organic carboxylic acid or anhydride having n+1 carbon atoms by carbonylating with monoxide, in the presence of the above-mentioned carbonylation catalyst, on alcohols having n carbon atoms, ethers having 2n carbon atoms or esters formed from said alcohols and acids. In particular, the invention relates to a process for preparing acetic acid by carbonylating methanol with carbon monooxide in the presence of said carbonylation catalyst. By using said carbonylation catalyst, the temperature for carbonylation can be lowered to about 160° C. with a reaction rate better than that of a traditional process, while the tendency of catalyst precipitation in the course of carbonylation can be improved also.

Abstract: Aluminoxanes are used as activators for the gas, solution or slurry phase polymerization of olefins in the presence of single site catalysts. Aluminoxanes contain residual aluminum alkyls which may poison the catalysts. The residual aluminum alkyls may be bound an/or removed from the aluminoxanes by treatment with carbohydrates such as cellulose, starch or sugar.

Abstract: The new metallocene catalysts according to the present invention are prepared by reacting a metallocene compound with a compound having at least two functional groups. The metallocene compound is a transition metal compound which a transition metal is coordinated with a main ligand such as cycloalkanedienyl group and an ancillary ligand. The functional groups of the compound having at least two functional groups are selected from the group consisting of a hydroxy group, a thiol group, a primary amine group, a secondary amine group, etc. The metallocene catalysts according to the present invention have a structure which an ancillary ligand of a metallocene compound is bonded with functional groups. A structure of the metallocene catalysts can be varied according to the metallocene compounds, the compound having at least two functional groups, and the molar ratio of each reactant. The metallocene catalyst is employed with a co-catalyst for styrene and olefin polymerization.

Abstract: A solid catalyst component for olefin polymerization prepared by a method which comprises contacting the following components (a), (b), (c) and (d): (a) a polymer carrier containing a carbonyl group; (b) an organometallic compound of metal of Group I, II or XIII of the Periodic Table; (c) a transition metal compound of Group IV of the Periodic Table; and (d) a phenol compound, a catalyst for olefin-polymerization comprising said solid catalyst component and an organoaluminum compound and/or organoaluminum oxide compound, and a method for producing an olefin polymer with said catalyst.

Abstract: A solid cocatalyst is prepared by reacting a suitable support base with an organoaluminum compound and then reacting that product with an activity promoting amount of water. The solid cocatalyst can be combined with a polymerization catalyst to form a catalyst system useful for the polymerization of olefins.

Abstract: Transition metal imine complexes can be prepared by reacting the imine precursors, a carbonyl compound and a primary amine, in the presence of a selected transition metal compound. The complexes may be used as catalysts for olefin polymerization.

Abstract: A method of producing metal fulvene insertion complexes, as well as new fulvene metal insertion complexes and the use thereof as catalysts for the polymerization of olefins and/or dienes and as hydrogenation catalysts.

Abstract: An acid-free, aqueous catalyst paste with a solids content of 30 to 70% by weight and containing dialkyltin oxide and a water-thinnable cationic binder vehicle and which can be used for cathodically depositable electro-dip lacquers, obtainable by a) dispersing dialkyltin oxide in an acid-free aqueous dispersion or solution of one or more hydroxycarboxylic acid salts of bismuth(III) in a weight ratio of tin to bismuth, calculated as the metal, from 1:3 to 3:1, and b) comminuting the preparation obtained with one or more cationic binder vehicles in a weight ratio of dialkyltin oxide plus hydroxycarboxylic acid salt of bismuth(III) to cationic binder vehicle from 0.5:1 to 6:1.

Abstract: A novel method for preparing a hydrogenation composition comprising organic polymer molecules having carbon--carbon double bonds, for removing hydrogen from the atmosphere within enclosed spaces and particularly from atmospheres within enclosed spaces that contain air, water vapor, oxygen, carbon dioxide or ammonia. The organic polymers molecules containing carbon--carbon double bonds throughout their structures, preferably polybutadiene, polyisoprene and derivatives thereof, intimately mixed with an insoluble noble metal catalyst composition. High molecular weight polymers may be added to the organic polymer/catalyst mixture in order to improve their high temperature performance. The hydrogenation composition is prepared by dispersing the polymers in a suitable solvent, forming thereby a solution suspension, flash-freezing droplets of the solution in a liquid cryogen, freeze-drying the frozen droplets to remove frozen solvent incorporated in the droplets, and recovering the dried powder thus formed.

Abstract: The present invention relates to a supported cobalt catalyst consisting of(a) cobalt compounds,(b) organoaluminium compounds,(c) water or OH-acidic compounds,(d) inorganic or polymeric organic support materials and(e) modifiers selected from the group comprising tertiary phosphines,to the production thereof and to the use thereof for the polymerization of unsaturated compounds, in particular of conjugated dienes, in the gas phase. With the assistance of the catalysts according to the invention, it is possible to achieve gas phase polymerization of conjugated dienes with an elevated content of lateral double bonds in the polymers.

Abstract: The present invention relates to a novel catalyst combination and a novel ocess for the synthesis of methanol and methyl formate (MF), and more specifically to the production of methanol and MF by contacting syngas under relatively mild conditions in a slurry phase with the novel catalyst combination comprising unreduced copper chromite prepared using specifical method, alkali alcoholates, a nonionics and a non-polar solvent. The nonionics, for example, C.sub.8 H.sub.17 --(C.sub.6 H.sub.4)--O--(C.sub.2 H.sub.4 O).sub.n H (where n is between 4 and 60) is used in the amount that is at least 5 vol. % of the slurry (liquid reaction medium). And the non-polar solvent having a dielectricity constant between 2 and 3 at 20.degree. C. is used in the amount that is at least 50 vol. % of the slurry. The present invention allows the synthesis of methanol and MF to occur in the temperature range of approximately 100-150.degree. C., and the pressure range of 3-8 MPa.

Abstract: A method for preparing an oil soluble catalytic precursor includes the steps of: providing a mixture of a catalytic metal salt in water, wherein the catalytic metal salt contains a catalytic metal selected from the group consisting of alkali metals, alkaline earth metals, transition metals, and mixtures thereof; providing a heavy hydrocarbon phase; forming a water in oil emulsion of the mixture in the heavy hydrocarbon phase; and heating the emulsion at a temperature sufficient to dehydrate the emulsion so as to provide a hydrocarbon containing an oil soluble compound containing the catalytic metal.

Abstract: Supported chromium catalysts are prepared by loading the support material with chromium compounds and calcining at from 400 to 1100.degree. C., and then treating the catalyst with a water-containing inert gas mixture.

Abstract: A composition suitable for safely removing hydrogen from gaseous mixtures containing hydrogen and oxygen, particularly those mixtures wherein the hydrogen concentration is within the explosive range. The composition comprises a hydrogenation catalyst, preferably Pd dispersed on carbon, wherein the concentration of Pd is from about 1-10 wt %, dispersed in a polymeric material matrix. As well as serving as a matrix to contain the hydrogenation catalyst, the polymeric material, which is substantially unreactive to hydrogen, provides both a diffusion restriction to hydrogen and oxygen, thereby limiting the rate at which the reactants (hydrogen and oxygen) can diffuse to the catalyst surface and thus, the production of heat from the recombination reaction and as a heat sink.

Abstract: A solid cocatalyst is prepared by combining (1) a first material capable of affixing an organoaluminum compound with (2) an organic liquid and then adding an organoaluminum compound and then contacting that product with water dispersed in an inert gas. Further catalyst compositions prepared from that cocatalyst and the use of such catalyst compositions to polymerize olefins is disclosed.

Abstract: A catalyst system for selective hydrogenation of sulfur-containing and nitrogen-containing compounds of a heteroaromatic organic phase includes a mixture of a noble metal selected from Group VIII of the Periodic Table of Elements and a water-soluble ligand. A process for preparing the catalyst system and hydrogenation process using the catalyst system are also provided.

Abstract: A vulcanization promoter for fluorine-containing elastomers prepared by (1) allowing 1.01 to 1.15 moles of a quaternary phosphonium salt to react with one mole of monoalkali metal salt of bisphenol AF in alcohol, (2) allowing 2.02 to 2.30 moles of a quaternary phosphonium salt to react with one mole of a dialkali metal salt of bisphenol AF in alcohol, (3) allowing one mole each of an alkali metal alkoxide and bisphenol AF to react with 1.01 to 1.15 moles of a quaternary phosphonium salt in alcohol or (4) subjecting one mole of bisphenol AF, 1.01 to 1.15 moles of a quaternary phosphonium salt and one mole of an alkali metal alkoxide to reaction in alcohol, each followed by further addition of the bisphenol AF thereto, or (5) allowing 1.01 to 1.15 moles of a quaternary phosphonium salt to react with one of 1/4alkali metal salt of bisphenol AF in alcohol gives much more improved vulcanization characteristics such as vulcanization speed, etc.

Abstract: The present invention relates to silica gel supported bis-cinchona alkaloid compounds of the formula: ##STR1## wherein Q is dihydroquininyl or dihydroquinindinyl; X is a compound having 4 carbon atoms; and R is methoxy, ethoxy or methyl; and methods of preparation and use thereof. The silica gel supported bis-cinchona alkaloid derivatives of this invention are useful re-useable catalysts for preparing vicinal diols by asymmetric dihydroxylation of olefins.

Abstract: This invention concerns modified fluorosulfonic acid compounds possessing a sulfonic acid fluoride, chloride or ester group or a sulfonic acid or a salt of a sulfonic acid group at one end and respectively a hydrolyzable or hydrolyzed silane group at the other end, said sulfonic group being adjacent a substantially fluorinated bidentate hydrocarbylene group which is in turn adjacent to a hydrocarbylenegroup linked to said hydrolyzable or hydrolyzed silane group. Self-condensation of the latter compounds provides novel siloxanes and polysiloxanes. This invention further concerns novel composites comprising a metal oxide network having incorporated therein a group having the formula: --O).sub.q Si(OH).sub.n-q R.sup.1.sub.m R.sup.2 R.sub.f SO.sub.3 Q, and compositions comprising a solid material having a reactive surface to which surface is attached at least one group having the formula: --O).sub.q Si(OH).sub.n-q R.sup.1.sub.m R.sup.2 R.sub.f SO.sub.3 Q.

Abstract: Porous microcomposites comprising a perfluorinated ion-exchange polymer (PFIEP) containing pendant metal cation exchanged sulfonate groups, metal cation exchanged carboxylate groups, or metal cation exchanged sulfonate and carboxylate groups, wherein the metal cation may be ligand coordinated, and optionally pendant sulfonic acid groups, carboxylic acid groups, or sulfonic acid and carboxylic acid groups, the PFIEP being entrapped within and highly dispersed throughout a network of metal oxide, a network of silica or a network of metal oxide and silica can be prepared from PFIEP and one or more precursors selected from the group consisting of a metal oxide precursor, a silica precursor, and a metal oxide and silica precursor using an in situ process. Preferred metal cations are Cr, Sn, Al, Fe, Os, Co, Zn, Hg, Li, Na, Cu, Pd or Ru. Such microcomposites have a first set of pores having a pore size diameter ranging from about 0.

Abstract: A solid catalyst component for the polymerization and copolymerization of ethylene and alpha- olefins, containing a metallocene supported on an inorganic solid carrier constituted by a porous silicon oxide, the supported metallocene having the formula (I): ##STR1## wherein M is a group of metal, R' and R" are dialkylamide groups, R'" has the same definition as R' or is a cyclopentadienyl consisting ligand, and A is an anion containing an .eta..sup.5 -cyclopentadienyl ring coordinated to metal M, and wherein a carbon atom of the .eta..sup.5 -cyclopentadienyl ring of anion A is covalently bonded to the surface of the porous inorganic solid carrier.

Abstract: A process is provided to modify an olefin production catalyst system which comprises contacting an olefin production catalyst system with ethylene prior to use. A process also is provided to trimerize and/or oligomerize olefins with the novel, modified olefin catalyst production system. The modified olefin production catalyst system produces less solids, such as, for example, polymer.

Abstract: An iridium-based solution is prepared by contacting components in a liquid phase containing (a) a carbonylated iridium compound, (b) hydriodic acid, a precursor of such an acid, or mixture thereof, and (c) a solvent; under a total pressure of between 1 and 10 bar at a temperature not greater than the boiling temperature of the solvent under conditions in which the components are brought into contact. The iridium-based solution can be used as a catalyst for carrying out carbonylation, hydroformylation or isomerization reactions.

Abstract: High-surface-area polyolefins grafted with certain fluoroalkylvinylether sulfonate or carboxylate monomers, and their method of preparation, are disclosed. Such materials are useful as catalysts and as membranes in electrochemical cells.

Abstract: This invention relates to supported metallocene catalyst systems and to methods for their production and use. Specifically, this invention relates to supported catalyst systems having unique, predetermined properties resulting from the designed distribution of catalyst components within and upon porous support particles. The designed distribution of catalyst components is obtained through sequential deposition of catalyst components with intervening removal of solvent.

Abstract: Catalytic solid for the (co)polymerisation of at least one olefin, comprising a coprecipitate of magnesium and of at least one transition metal, obtained by means of a process comprising the preparation of a mixture of a magnesium compound, such as the chloride or a magnesium alcoholate, and of a compound denoted by one of the formulae MY.sub.x (O--R').sub.t-x and M'O.sub.y (O--R").sub.s-2y and the treatment of the resulting mixture with a complex of formula M"(A)Al.sub.2 (X',X").sub.8 where X' and X" denote halogens, M and M' transition metals of groups IVB and VB, M" a transition metal of group IVB, A an aromatic hydrocarbon, Y a halogen or a group (O--R'"), and R', R" and R'" an alkyl, aryl or cycloalkyl group.

Abstract: A process for the polymerization of ethylene or the copolymerization of ethylene with an alpha-olefin, in suspension or in gas phase, in the presence of a catalyst consisting essentially of a cocatalyst and a catalytic component based on at least Mg, Ti and Cl, with the catalytic component being constituted of at least one derivative of magnesium and one chlorinated derivative of titanium in its form III and/or IV, which was subjected, prior to its use, to a reduction treatment and then to treatment with a chlorinated transition metal compound, with the said catalytic component being characterized in that the magnesium derivative is in the form MgCl.sub.2.MgO.

Abstract: A method for the preparation of a solid procatalyst suitable for the polymerization of olefins wherein the procatalyst comprises a transition metal compound reacted with a carrier by carrying out in the method the following consecutive steps: (a) feeding the transition metal compound and particles of the carrier into a vessel, which in its initial position has an essentially horizontal bottom sieve, (b) mixing and reacting the metal transitional compound and the particles of the carrier to produce raw procatalyst particles and a liquid reaction residue, (c) removing the liquid reaction residue through the bottom sieve of the vessel, (d) washing the raw procatalyst particles with a washing liquid, so that impurities in the raw procatalyst are removed through the bottom sieve, (e) drying the washed raw procatalyst particles by conducting an inert gas therethrough to give the solid procatalyst, and (f) removing the solid procatalyst from the vessel.

Abstract: The present invention relates to a storage-stable solution of a mixture of carbonated magnesium methoxide of the formula Mg(CH.sub.3 O).sub.2 (CO.sub.2).sub.n, carbonated magnesium ethoxide of the formula Mg(C.sub.2 H.sub.5 O).sub.2 (CO).sub.2).sub.n and a carbonated mixed alkoxide of the formula Mg(CH.sub.3 O).sub.x (C.sub.2 H.sub.5 O).sub.y (CO.sub.2).sub.n, in which 0<x, y<2 and x+y=2, in a combination of methanol and ethanol, and processes for the preparation thereof, the magnesium content of the solution being from 0.1 to 11% by weight, based on the total weight of the solution, and the CO.sub.2 content n being from 1.0 to 2.2. The present solutions are used, inter alia, for the preservation of paper and for the preparation of a catalyst for the polymerization of olefins.

Abstract: The present invention relates to a storage-stable solution of carbonated magnesium methoxide of the formula Mg(CH.sub.3 O).sub.2 (CO.sub.2).sub.n in methanol, and processes for their preparation by reacting metallic magnesium with methanol and CO.sub.2 or reacting magnesium methoxide in methanol with CO.sub.2, wherein the magnesium content of the solution is from 0.1 to 8% by weight, based on the total weight of the solution, and the CO.sub.2 content n is from 1 to 2.2. The present solution is used, inter alia, for the preservation of paper or for the preparation of a catalyst for the polymerization of olefins.

Abstract: The invention relates to a process for the preparation of alkylaluminoxanes immobilized on inert support materials, characterized in that alkylaluminoxanes present in the form of dispersions are fixed on inert support materials.

Abstract: A process for the preparation of complex salts with additional coordinated ligands comprising reacting with through mixing at 20.degree. to 200.degree. C. a complex-forming metal salt of a metal of the second and third main groups of the Periodic Table and the subgroups thereof with a stoichiometric amount of at least one member of the group consisting of a chelating ligand and a Lewis base in the absence of a solvent according to the equation:M.sub.m.sup.a+ (SR.sup.b-)n+xL.multidot.cH+yB.sup.- .fwdarw.m[M.sup.a+ (SR.sup.b-)(n-o)L.sub.x B.sub.y ]+o.multidot.SR.sup.b- +c.multidot.H.sup.+Iwherein M is a metal ion, SR is an acid radical of an organic or inorganic acid, B is a Lewis base, and L is a chelating ligand, m.multidot.a=b.multidot.(n-o)+c.multidot.x, wherein a=an integer of 1-8, b=an integer of 1-3, c=an integer of 0-4, m=an integer of 1-3, n=an integer of 1-8, o=an integer of 0-8, x=an integer of 0-4, y=and integer of 1-16, wherein (n-o)+x+y.ltoreq.

Abstract: A novel polymerization catalyst system comprising a diluent, a substrate, a nickel compound wherein the nickel is in a zero oxidation state and picolinic acid and a method for making such catalyst system is described. The polymerization catalyst system can be used in a process for the polymerization of polymerizable olefins.

Abstract: A polymer supported catalyst comprises Ziegler-Natta catalysts immobilized on a magnesium-modified polymer support. The catalyst support is prepared by (1) dissolving a carboxyl group-containing polymer in a solvent and precipitating the polymer in a polar non-solvent, (2) wet-grinding the precipitated polymer, and (3) mixing the ground polymer with an organomagnesium compound or a complex of an organomagnesium compound and an organoaluminum compound to give a magnesium-modified polymer support. Optionally, the resulting magnesium-modified support is treated with a halogen-containing silicon compound. The catalysts may be loaded onto the support by reacting the magnesium-modified support with a transition metal compound to form a catalyst constituent, and then combining the catalyst constituent with an appropriate organo-metallic compound.

Abstract: This invention relates to an improved polymerization free radical initiator delivery system for the polymerization of monomers containing olefinic unsaturation and to the preparation of the initiator which comprises dissolving a water insoluble free radical initiator and an excess amount of the polymeric product of the reaction in a mutual organic solvent having a boiling point below 140.degree. C., in the presence of between about 1.0 and 100 wt. % of a surfactant based on weight of initiator and mixing the resulting solution to achieve uniform molecular distribution of initiator and polymer molecules in the surfactant/solvent mixture; removing the solvent to provide coprecipitated initiator/polymer microparticles and then diluting the coprecipitated microparticles with water under vigorous agitation to form a microparticle emulsion of low viscosity which is suitable as the initiator feed for contact with monomer in a polymerization reaction.

Abstract: This invention relates to a process for preparing an improved polymerization free radical initiator delivery system for the polymerization of a monomer containing olefinic unsaturation which comprises uniformly dispersing a water insoluble free radical initiator, an excess amount of the polymeric product of the reaction and between about 1.0 and about 100 wt. % of a surfactant based on initiator in water to form an aqueous mixture containing between about 5 and about 40 wt. % solids; subjecting the dispersion to treatment at a temperature of between about -25.degree. C. and about 0.degree. C. under from about 50 to about 400 milli Tort vacuum for a period of from about 5 to about 24 hours to remove water and to form uniform coprecipitated initiator/polymer microparticles having an average particle diameter of between about 0.

Abstract: A cobalt based catalyst, and the method for preparing it, are disclosed. The catalyst is obtained from the reaction between NaCo(CO).sub.4 and s-trichloro triazine and is advantageously used in the processes of carbonylation of naphthalene mono- and disulfonates in order to yield naphthalene esters and acids.

Abstract: The present invention relates to the preparation of catalysts for heteroatom removal, particularly sulfur, from petroleum and synthetic fuel feedstocks. The catalyst is comprised of at least one Group VIII metal, and at least one Group VI metal, on a refractory support. The catalyst is prepared by: impregnating an inorganic oxide support material with a Group VI heteropolyacid; treating said impregnated support with an aqueous solution of a reducing agent which is capable of at least partially reducing the Group VI metal of the heteropolyacid; drying said treated support at a temperature from about 20.degree. C. to about 200.degree. C. at about atmospheric pressure; impregnating the treated support with a Group VIII metal salt of an acid having an acidity less than that of the Group VI heteropolyacid; drying said impregnated treated support at a temperature from about 20.degree. C. to about 200.degree. C. at about atmospheric pressure; and sulfiding said impregnated support, thereby forming the catalysts.

Abstract: A method for the preparation of catalysts for heteroatom removal, particularly sulfur, from petroleum and synthetic fuel feedstocks. The catalyst is comprised of at least one Group VIII metal, and at least one Group VI metal, on a refractory support. The present method for preparing said catalysts comprises impregnating the Group VIII metal onto the refractory support by use of a Group VIII metal salt of an acid, and impregnating the Group VI metal onto the support by way of a Group VI heteropolyacid, wherein the acid comprising the salt of the Group VIII metal is less acidic than the heteropolyacid. The catalysts are then subjected to a heat treatment which includes a first phase wherein the catalyst is dried of free water and a second phase wherein the catalyst is heated to a temperature up to about 300.degree. C. at a heating rate from about 0.15.degree. C./min to about 15.degree. C./min.

Abstract: 1 Process for producing a catalyst paste for cathodically separable electrophoretic dipping lacquers.2.1 Use was made of dibutyltin oxide by way of a catalyst paste for electrophoretic dipping lacquers, dispersed in pasting binders. An object is to provide a new process for producing such catalyst pastes while saving time and energy.2.2 A process is provided for producing a catalyst paste for cathodically separable electrophoretic dipping lacquers, wherein the dibutyltin oxide is first pre-dispersed with an organic solvent and an organic acid such as is commonly used for neutralizing cathodically separable electrophoretic dipping lacquers, whereupon it is dispersed with the pasting binder and water and ground.2.3 Cathodic electrophoretic dip lacquering making use of catalyst pastes containing dibutyltin oxide.

Abstract: The invention relates to a process for the preparation of lactide, in particular of optically pure L(-)- or D(+)-lactide, on an industrial scale.

Abstract: A process for isomerizing a chlorofluorocarbon of the formula:CClFYCClFXwherein X and Y are independently selected from chlorine and fluorine provided that X is not --Cl when Y is --Fto the compound of the formula:CCl.sub.2 YCF.sub.2 XThe process comprises contacting the chlorofluorocarbon with an activated aluminum trihalide catalyst. The catalyst is prepared by contacting the chlorofluorocarbon with anhydrous aluminum trichloride in the presence of a metal. The metal is selected from the group consisting of stainless steel, chromium, manganese, molybdenum, tungsten and combinations thereof.

Abstract: A catalyst prepared by (a) impregnating a catalyst carrier with an aqueous solution of a palladium salt and a salt of at least one metal selected from the group consisting of copper, lead, ruthenium and rhenium in an amount corresponding to 90 to 95% of the water absorption of the carrier, (b) treating the impregnated carrier with an aqueous solution of an alkali metal salt in an amount corresponding to 120 to 500% of the water absorption of the carrier to precipitate water-insoluble compounds of palladium and at least one metal selected from the group consisting of copper, lead, ruthenium and rhenium on the carrier, (c) treating the metal compounds-deposited carrier with a reducing agent to convert the compounds to the corresponding metals, and (d) further supporting an alkali metal acetate on the carrier, had a high catalytic activity for the reaction of forming allyl acetate by reacting propylene, acetic acid and oxygen in the gas phase, and the selectivity to allyl acetate is very high and the life of thi

Abstract: A process for the conversion of a heavy hydrocarbon oil in the presence of hydrogen and iron-petroleum coke catalyst is described in which the iron-petroleum coke catalyst is prepared by grinding petroleum coke particles and particles of an iron compound in oil to form an additive slurry or paste and mixing the petroleum coke-iron oil slurry or paste with the heavy hydrocarbon oil to form a feedstock to hydroconverter.

Abstract: According to the present invention, a zinc-containing solid catalyst prepared by contacting zinc oxide with an organic dicarboxylic acid in the presence of or in the absence of an organic solvent under a mechanical pulverization treatment is provided. The catalyst is in a good pulverized state and exhibits a high catalytic activity for polymerization of carbon dioxide with an epoxide to obtain a polyalkylene carbonate.

Abstract: There is provided layered oxides of aluminum and phosphorus or arsenic having pendant organic groups which protrude into the inner layer region of these layered materials. These materials may be prepared by reacting a suitable organoarsenic or organophosphorus compound, such as phenylphosphonic acid, with a suitable aluminum compound, such as alumina, in the presence of a suitable solvent, such as a mixture of ethanol and water, under conditions of elevated temperature.

Abstract: A process of isomerizing a chlorofluorocarbon of the formula: ##STR1## wherein X is chlorine or fluorine to the compound of the formula: ##STR2## The process comprises contacting the chlorofluorocarbon with an activated aluminum trichloride catalyst. The catalyst is prepared by contacting the chlorofluorocarbon with anhydrous aluminum trichloride in the presence of a metal. The metal is selected from the group consisting of stainless steel, chromium, manganese, molybdenum, tungsten and combinations thereof.

Abstract: A process for the conversion of a heavy hydrocarbon oil in the presence of hydrogen and iron-coal catalyst is described in which the iron-coal catalyst is prepared by grinding coal particles and particles of an iron compound in oil to form an additive slurry or paste and mixing the coal-iron oil slurry or paste with the heavy hydrocarbon oil to form a feedstock to a hydroconverter.