Abstract: The formation of carbon on metals exposed to hydrocarbons in a thermal cracking process is reduced by contacting such metals with an antifoulant selected from the group consisting of a combination of elemental indium or an organic compound of indium and tin and a combination of elemental indium or an organic compound of indium and antimony.

Abstract: Cyclic polycarbonate oligomers are polymerized to linear polycarbonates by contact with a polycarbonate formation catalyst which has been modified by contacting the same with at least one diaryl carbonate, preferably diphenyl carbonate. Said modification decrease the polymerization rate or introduces an induction period into the polymerization reaction.

Abstract: A process is disclosed herein for preparing randomized copolymers of conjugated dienes and vinyl aromatic hydrocarbons having low vinyl contents by utilizing an anionic initiator system comprising alkali metal trihydrocarbyl magnesiates optionally together with an organolithium compound.

Abstract: Carrier-supported catalyst for making monocarboxylic anhydrides by subjecting a suitable ester or ether to carbonylation. The carrier supported catalyst has an organosilicon compound containing an alkoxy or halogen group and also an organonitrogen, organophosphorus, organoarsenic, organosulfur, mercapto or thioether group as a polyfunctional adhesion promoter additively combined with the carrier material on the one hand, and with the noble metal compound of the 8th subgroup of the Periodic System of the elements, on the other hand.

Abstract: A process and a catalyst system is disclosed herein for preparation of medium to high vinyl (co)polymers containing a 1,2-microstructure of between 30 and about 90 percent. The catalyst system which is employed in the production of the (co)polymer is an oligomeric oxolanyl alkane modifier and anionic initiator selected from (1) Na(R).sub.3 Mg or (2) Na(R).sub.3 Mg and an organolithium compound or (3) K(R).sub.3 Mg and an organolithium compound.

Abstract: There is disclosed a resin-metal (complex) catalyst, a method for its preparation, activation and use in carrying out Fischer-Tropsch reactions. The complex is a resin which has attached to it a coordination compound(s) and a metal(s). The complex has utility as a Fischer-Tropsch catalyst. More specifically, the complex is useful for the gaseous conversion of synthesis gas (carbon monoxide and hydrogen) to hydrocarbons.

Abstract: Olefin polymerization catalysts are described which are based on solid inorganic oxides (such as silica) and polychromium complexes (such as octakis(.mu.-trimethylsilylmethyl)tetrachromium(II)). Linear low density ethylene homopolymers with specific short chain branching as well as polymerization processes to make these polymers using the specific catalyst described are also disclosed.

Abstract: Olefins are hydroformylated with syngas in the presence of a novel organo metallic complex catalyst to form the corresponding aldehydes at high reaction rates and improved selectivity of linear aldehydes over branched aldehydes.The novel catalyst comprises an organo metallic complex formed from a mixture of:(1) a platinum (II) compound;(2) a ferrocene-derived ligand; and(3) a Group IVB metal halide.

Abstract: Olefins are hydroformylated with syngas in the presence of a novel organo metallic complex catalyst to form the corresponding aldehydes at high reaction rates and improved selectivity of linear aldehydes over branched aldehydes.The novel catalyst comprises an organo metallic complex formed from a mixture of:(1) platinum (II) acetylacetonate;(2) a Group IVB metal halide; and(3) a bidentate tertiary ligand of the formula ##STR1## wherein Q is arsenic, antimony, or phosphorus; and R.sub.1, R.sub.2 R.sub.3 and R.sub.4 are alkyl, alkoxyl, aryl, or aryloxyl groups, and may be the same or different; and m is an integer of from 3 to about 5; and n is an integer of from 2 to about 4.

Abstract: Stable, hydrocarbon-soluble organobarium-, organocalcium-, and organostrontium-containing polymerization initiators are prepared by reacting certain calcium, barium or strontium alkoxides with organolithium, diorganomagnesium or triorganoaluminum compounds and combinations thereof. By way of illustration, the barium alkoxides soluble in hydrocarbon or chlorinated hydrocarbon solvents are prepared by reacting a suspension of barium amide in a hydrocarbon or a chlorinated hydrocarbon solvent with stoichiometric quantities of certain alcohols, alone or in the presence of chelating tertiary di- or polyamines. Alcohols suitable for the preparation of hydrocarbon- or chlorinated hydrocarbon-soluble barium alkoxides are C.sub.4 -C.sub.12 aliphatic and cycloaliphatic alcohols possessing alkyl branches at the one or two-positions, or mixtures of such alcohols. Other suitable alcohols are 2-alkoxy-1-alkanols and .gamma.-alkoxy-poly(ethyleneoxy)-1-ethanols.

Abstract: Olefins are hydroformylated with syngas in the presence of a novel organo metallic complex catalyst to form the corresponding aldehydes at high reaction rates and improved selectivity of linear aldehydes over branched aldehydes.The novel catalyst comprises an organo metallic complex formed from a mixture of:(1) platinum (II) acetylacetonate;(2) a Group IVB metal halide; and(3) a bidentate tertiary ligand of the formula ##STR1## wherein Q is arsenic, antimony, or phosphorus; and R.sub.1, R.sub.2, R.sub.3 and R.sub.4 are alkyl, alkoxyl, aryl, or aryloxyl groups, and may be the same or different.

Abstract: The viscosity of hydrocarbon solutions of dialkylmagnesium compounds are reduced by using a reducing agent comprising a defined benzene derivative, a substance produced by reacting such a benzene derivative with magnesium or a dialkylmagnesium compound or a mixture of one of the foregoing with an organoaluminum viscosity reducing agent.

Abstract: Olefins are hydroformylated with syngas in the presence of a novel organo metallic complex catalyst to form the corresponding aldehydes at high reaction rate and improved selectivity of linear aldehydes over branched aldehydes.The novel catalyst comprises an organo metallic complex formed from a mixture of:(1) platinum (II) acetylacetonate;(2) a Group IVB metal halide; and(3) a bidentate tertiary ligand of the formulaR.sub.1 R.sub.2 Q(CH.sub.2).sub.m QR.sub.3 R.sub.4 ; or ##STR1## wherein Q is arsenic, antimony, or phosphorus; and R.sub.1,R.sub.2,R.sub.3 and R.sub.4 are alkyl, alkoxyl, aryl, or aryloxyl groups, and may be the same or different; and m is an integer of from 3 to about 5; and n is an integer of from 2 to about 4.

Abstract: Olefins are hydroformylated with syngas in the presence of a novel organo metallic complex catalyst to form the corresponding aldehydes at high reaction rates and improved selectivity of linear aldehydes over branched aldehydes.The novel catalyst comprises an organo metallic complex formed from a mixture of:(1) platinum (II) acetylacetonate;(2) a Group IVB metal halide; and(3) a bidentate tertiary ligand of the formula ##STR1## wherein Q is arsenic, antimony, or phosphorus; and R.sub.1, R.sub.2, R.sub.3 and R.sub.4 are alkyl, alkoxyl, aryl, or aryloxyl groups, and may be the same or different.

Abstract: Olefins are hydroformylated with syngas in the presence of a novel organometallic complex catalyst to form the corresponding aldehydes at high reaction rates and improved selectively of linear aldehydes over branched aldehydes.The novel catalyst comprises an organometallic complex formed from a mixture of(1) a platinum (O) complex containing two bidentate diphosphine, diarsine or distibine ligands; and(2) A Group IVB metal halide.

Abstract: Olefins are hydroformylated with syngas in the presence of a novel organo metallic complex catalyst to form the corresponding aldehydes at high reaction rates and improved selectivity of linear aldehydes over branched aldehydes.The novel catalyst comprises an organo metallic complex formed from a mixture of:(1) a platinum (II) compound;(2) a ferrocene-derived ligand; and(3) a Group IVB metal halide.

Abstract: Olefins are hydroformylated with syngas in the presence of a novel organometallic complex catalyst to form the corresponding aldehydes at high reaction rates and improved selectively of linear aldehydes over branched aldehydes.The novel catalyst comprises an organometallic complex formed from a mixture of(1) a platinum (O) complex containing two bidentate diphosphine, diarsine or distibine ligands; and(2) A Group IVB metal halide.

Abstract: Novel ligand materials and transition metal complexes thereof are disclosed which are useful as solvents and/or catalysts for various processes, including catalytic conversion processes for the conversion of hydrocarbons or carbon monoxide, such as the hydrocarbonylation of olefins, hydrogenation using H.sub.2 or CO and H.sub.2 O, dehydrogenation, hydrocarbon synthesis, alcohol synthesis, and water-gas disproportionation catalysis. Among the novel ligand materials disclosed are compositions containing phosphine and arsine coordinating groups along with, e.g., groups comprising fluorines, ethynyl or ethenyl groups, quaternary ammonium, arsonium and/or phosphonium groups. Ligands containing M-O-L linkages and complexes thereof are also disclosed wherein M is selected from, for example, Si or Ti and L is selected from P or As. Also, various ion-exchanged ligand compositions, photoreactive compositions and the uses of such compositions are also described.

Abstract: Conjugated dienes, in particular 1,3-conjugated dienes, can be polymerized or copolymerized using the catalyst system of this invention to polymers wherein the amount of 1,2-structure contained in the polymer is increased, and polymers can be prepared containing varying amounts of 1,2-structure as desired. Such desirable results can be obtained in accordance with the process of the present invention for polymerizing conjugated diene monomers which comprises the use of a catalyst system which comprises (a) at least one anionic initiator based on lithium, and (b) a modifier composition comprising at least one cyclic acetal of a glyoxal. ##STR1## wherein R and R' are each independently hydrogen, alkyl or aryl groups, and each A is independently an alkylene or an oxyalkylene group.In another embodiment, the catalyst system also contains at least one co-initiator selected from the group consisting of organomagnesium compounds, organoaluminum compounds, or mixtures thereof.

Abstract: The present invention relates to catalysts for the polymerization and copolymerization of ethylene, characterized in that they comprise a support based on magnesium chloride and possibly on aluminium chloride, of spheroidal shape, having a mean diameter by mass comprised between 10 and 100 microns and with a narrow particle size distribution, such that the ratio of the mean diameter by mass to the mean diameter by number is less than or equal to 3, on which support there has been precipitated a derivative of a transition metal of groups IV, V and VI of the Periodic Table of Elements, and a polymerization process utilizing the said catalysts.

Abstract: The present invention relates to catalyst supports for the polymerization and co-polymerization of alpha-olefins, especially ethylene and propylene, consisting essentially of magnesium chloride, characterized in that these supports contain a chlorinated compound of aluminium in a quantity such that the atomic ratio of Al/Mg is comprised between 0.001 and 0.1 and that they occur in the form of spheroidal particles having a mean diameter by mass comprised between 10 and 100 microns and a narrow and controllable particle size distribution such that the ratio of the mean diameter by mass to the mean diameter by number of particles is less than or equal to 3, and also a process for the preparation of these supports.

Abstract: Methyl acetate is prepared in good yield by reacting methanol with carbon monoxide in the presence of a homogeneous catalyst composition comprising a ruthenium-containing compound, a cobalt-containing compound and a quaternary onium salt or base, and heating the resulting mixture at an elevated temperature and pressure for sufficient time to produce the desired methyl acetate, and then recovering the same from the reaction mixture.

Abstract: A process and catalyst system is disclosed herein for the preparation of (co)polymers having a 1,2-microstructure ranging between about 20 and about 65 percent. These (co)polymers are prepared in a hydrocarbon or non-polar solvent from a monomer system which contains at least one 1,3-diene monomer and optionally other copolymerizable monomers. The catalyst system which is employed in the production of the (co)polymer is a combination of (1) an anionic initiator based on lithium; (2) a dialkyl magnesium compound or a trialkyl aluminum compound or a mixture thereof; and (3) a phosphine oxide modifier which is substituted with three saturated heterocyclic rings, each hetero ring containing one nitrogen atom and either four, five or six carbon atoms.

Abstract: A process for making mixed dialkylmagnesiums wherein magnesium metal is reacted with ethylene and an alkyl halide in the presence of a hydrocarbon solvent and in a substantially moisture-free and ether-free atmosphere, under relatively high pressure and at a relatively high temperature followed by separation of undissolved solids from the resulting solution. A composition of matter produced by the process comprising dialkylmagnesium compounds having at least four different alkyl groups, a hydrocarbon solvent and a small amount of an alkyl or alkoxy aluminum compound.

Abstract: Olefins are polymerized in the presence of (I) solid supported catalysts which are prepared by (A) reacting in the presence of a diluent such as n-hexane a mixture of (1) the reaction product of (a) an organomagnesium compound such as dibutyl magnesium and (b) a diol such as 1,8-octanediol and (2) a transition metal halide such as titanium tetrachloride and (B) recovering the solid precipitate such as by decanting and (C) washing the solid with a solvent such as n-hexane and (II) a suitable activating agent. The resultant polymers have a relatively broad molecular weight distribution.

Abstract: Process for oxidatively carbonylating toluene to toluic acid, at least 50 mol % of the toluic acid being the p-isomer, said process comprising contacting and reacting, at 110.degree.-250.degree. C., at a pressure of at least 500 psi (3.45 MPa), toluene, carbon monoxide, oxygen and the catalyst ingredients consisting essentially of(a) a compound of rhodium, iridium, ruthenium, platinum, palladium or osmium;(b) a sulfur oxy-acid or a Group Ia or IIa metal salt of a sulfur oxy-acid; and(c) an acid or acid mixture having a Hammett acidity value (--H.sub.o) of greater than 7.0,said catalyst ingredients containing 0.5-30 mol % of (a) and 70-99.5 mol % of (b+c), with the molar ratios of (b/a) and (c/a) each being at least 2, and recovering toluic acid.