Abstract: An immobilized Lewis Acid catalyst system for the carbocationic polymerization of olefin monomer is provided. The catalyst comprises a porous polymer support having catalytically active Lewis Acid residue bonded to the surface of the support including the pore surfaces.

Abstract: The invention concerns the anionic polymerization of alkyl methacrylate in the presence of a priming system. The priming system comprises an organolithium primer and an organic compound of aluminum and pyridine. This priming system allows better polymerization control.

Abstract: Polyisoolefins are obtained using the process according to the invention by polymerising isoolefins, optionally with conjugated or unconjugated dienes and/or cationically polymerisable, mono- or polyunsaturated compounds at temperatures of -100.degree. C. to +100.degree. C. and pressures of 0.1 to 100 bar in solution, in suspension or in the gas phase in the presence of initiator systems consisting of certain hydrocarbons and open-chain and/or cyclic aluminoxane compounds.

Abstract: A inherently tacky pressure-sensitive adhesive copolymer is formed by copolymerizing at least one alkyl acrylate in the presence of a positive amount up to 50 percent by weight of the monomers of a polar acrylate monomer which, when homopolymerized, have a glass transition temperature less than 50.degree. C.

Abstract: A process for preparing hyperbranched polymers from AB monomers and C monomers Using a self-constructing approach is disclosed along with the hyperbranched polymers of a living-like character produced by such process.

Abstract: Transparent cycloolefin copolymers having a high tensile strength are obtained by polymerization of a polycyclic olefin, ethylene and, if desired, an acyclic olefin and/or a monocylcic olefin in the presence of a catalyst system which comprises a cocatalyst and an asymmetrical metallocene compound of the formula ##STR1## in which R.sup.16 is cyclopentadienyl and R.sup.17 is indenyl.

Abstract: A process for preparing hyperbranched polymers from AB monomers using a self constructing approach is disclosed. Hyperbranched polymers of a living-like character produced by such process are also disclosed.

Abstract: Immobilized Lewis Acid catalyst comprising polymer having at least one Lewis Acid immobilized within the structure therein, said polymer having monomer units represented by the structural formula:--[A].sub.a --[B].sub.b --[C].sub.c --whereina represents about 1 to about 99 mole %b represents about 0 to about 50 mole %c represents about 1 to about 99 mole %a+b+c is preferably about 100%; ##STR1## C is selected from the group consisting of: ##STR2## (III) combinations thereof, wherein D is OH, halide, OR.sup.4, NH.sub.2, NHR.sup.3, OM', or OM";E is the residue of the reaction of at least one Lewis Acid with the D substituent of monomer unit B;R.sup.1 represents proton, C.sub.1 -C.sub.24 alkyl group, or C.sub.3 -C.sub.24 cycloalkyl;R.sup.2 represents C.sub.1 -C.sub.24 alkylene group, C.sub.3 -C.sub.24 cycloalkylene, C.sub.6 -C.sub.18 arylene, or C.sub.7 -C.sub.30 alkylarylene;R.sup.3 represents C.sub.1 -C.sub.24 alkyl, C.sub.3 -C.sub.24 cycloalkyl, C.sub.1 -C.sub.24 aryl, or C.sub.7 -C.sub.30 alkylaryl;R.sup.

Abstract: Polyisoolefins are produced according to the invention by polymerizing isoolefins having 4 to 16 carbon atoms, optionally with conjugated diolefins having 4 to 6 carbon atoms and/or cationically polymerizable, mono- or polyunsaturated, organic compounds having 4 to 16 carbon atoms in the presence of mixtures of carbon dioxide and linear, branched and/or cyclic C.sub.4 -C.sub.8 alkanes and in the presence of catalysts at temperatures of -70.degree. C. to +20.degree. C. and pressures of 1 to 70 bar, wherein the weight ratio of carbon dioxide to alkanes is 10:90 to 90:10.The process according to the invention largely prevents the formation of fouling on the reactor walls, so ensuring better removal of heat. Moreover, in accordance with the process according to the invention, the polyisoolefins obtained may be directly chemically modified once the carbon dioxide has been removed.

Abstract: The production of C.sub.4 -C.sub.16 alkyl rubbers using the slurry process by copolymerisation of isoolefins having 4 to 16 carbon atoms with conjugated diolefins having 4 to 6 carbon atoms and/or cationically polymerisable, mono- or polyunsaturated organic compounds having 4 to 16 carbon atoms in the presence of methyl chloride and in the presence of Friedel-Crafts catalysts proceeds particularly advantageously by performing copolymerisation in the presence of linear, branched and/or cyclic alkanes.

Abstract: Alkylaluminoxanes having improved catalytic activity such as when they are used in combination with metallocenes for the polymerization of alpha-olefins, are prepared by treating an organic solvent solution of an alkylaluminoxane, such as methylaluminoxane, with anhydrous lithium halide.

Abstract: A living carbocationic catalyst composition comprising an initiator of a tertiary alkyl halide, a tertiary aralkyl halide or polymeric halide a co-initiator of a methylaluminum or methylboron compound, and a solvent medium with a dielectric constant between 2.5 and 7 is used to produce narrow molecular weight distribution polymers particularly isobutylene polymers.

Abstract: A living carbocationic catalyst composition comprising an initiator of a tertiary alkyl halide, a tertiary aralkyl halide or polymeric halide a co-initiator of an alkyl aluminum or alkyl boron, a proton scavenger and a solvent medium with a dielectric constant between 2.5 and 3.25 is used to produce narrow molecular weight distribution polymers particularly isobutylene polymers.

Abstract: A method for preparing a graft copolymer is here disclosed which is characterized by comprising the step of carrying out a living polymerization of at least one (meth)acrylic ester by the use of a polymeric compound as an initiator having one or more units represented by the following formula (I) in a molecular chain substantially in the absence of water in the presence of a Lewis acid or a donor compound of an anion selected from the group consisting of HF.sub.2.sup.-, (CH.sub.3).sub.3 SiF.sub.2.sup.- and F.sup.- : ##STR1## wherein R is hydrogen or an alkyl group having 1 to 6 carbon atoms, and R' is an alkyl group having 1 to 12 carbon atoms.

Abstract: A propylene (co) polymer terminated with a reactive group and a process for the preparation of the same.A graft copolymer having a specific side chain and a process for the preparation of the same.The propylene (co) polymer is usable as a radial- or ion-polymerizable propylene macromonomer or as an intermediate for the preparation of a block polymer. Examples of the application thereof include compatibizing agent for polymers, light- or laser-curable plastic, viscosity index and surface modifier.The graft copolymer is useful as a surface modifier or compatibilizing agent for polypropylene or a dispersant for fillers.

Abstract: A method of preparing homopolymers of conjugate dienes and copolymers of conjugate dienes with other dienes or with vinyl aromatic compounds, by means of which the aforementioned monomers are polymerised by using a complex catalytic composition basically comprising (a) an organomagnesium compound, (b) an organoaluminium compound and (c) an organic compound of phosphorus P(V) or P(III), of the metals barium, strontium or calcium. The method according to the invention is for producing homopolymers of 1,3-butadiene and copolymers of butadiene and styrene in random manner, with a high 1,4-trans addition content (above 70%) and vinyl addition below 5%. The method is also used to prepare block copolymers of the aforementioned monomers.

Abstract: The synthesis, and use as catalysts of chiral organolanthanide complexes for polymerization of substituted acrylates are disclosed, having the structure [(C.sub.5 R'.sub.4-x R*.sub.x) A (C.sub.5 R".sub.4-y R'''.sub.y) M Q.sub.p ].sup.m, where x and y represent the number of unsubstituted locations on the cyclopentadienyl ring; R', R", R''', and R* represent substituted and unsubstituted alkyl groups having 1-30 carbon atoms and R* is a chiral ligand; A is a fragment containing a Group 13, 14, 15, or 16 element of the Periodic Table; M is a Group 3, 4, 5, or lanthanide metal of the Periodic Table; and Q is a hydrocarbyl radical, aryl, hydrogen, amide radical, or halogen radical, with 3.gtoreq.p.gtoreq.o; and m=o or +1.

Abstract: A new class of macromolecular monomers (hereinafter called "macromonomers") comprises the polymerized product of at least one of an ethenylarene and a conjugated diene monomer, the product having a terminal omega-alkenyl group of at least four carbon atoms. The novel macromonomer can be copolymerized with ethylene and alpha-olefin monomers to form graft copolymers having pendant side-chains. The graft copolymers are useful as coating and molding compositions. The macromonomers can be useful as coatings on chromatographic supports for analytical and preparative separation of chemical mixtures.

Abstract: This system for priming the animic polymerization of (meth)acrylates includes at least one primer of the formula R--M (I) in which M represents a metal selected from alkaline and alkaline earth metals and R represents an alkyl radical with a straight or branched chain containing 2 to 6 atoms of carbon or an aryl radical or an arylalkyl radical. H is characterized in that it further contains at least one organic derivative of an alkaline metal, with the proviso that said organic derivative is neither an alcoholate nor a carboxyl acid ester substituted in position .alpha. by said metal. Applications in the anionic polymerization of (meth)acrylates.

Abstract: An isobutylene base polymer with a functional group having repeating units derived from isobutylene and at least one unit of the formula: ##STR1## wherein R.sup.1 is a hydrogen atom, a methyl group or an ethyl group and R.sup.2 is a divalent organic group, and a number average molecular weight of 500 to 500,000.

Abstract: A process for controlling the continuous gas-phase polymerization of one or more alpha-olefins in a fluidized and/or mechanically stirred bed reactor using a high activity catalyst based on a transition metal of groups IV, V or VI of the Periodic Table comprises introducing into the reactor, continuously and simultaneously, an activity retarder and an activator, in very small amounts, in a molar ratio and at flow rates which are varied with time in order to maintain substantially constant either the polymerization rate or the transition metal content of the polymer produced.

Abstract: The present invention provides a process for producing a polyacetylene.In the present process for producing a polyacetylene, acetylene is polymerized with a Ziegler-Natta catalyst consisting of a trialkylaluminum and an alkyl titanate, wherein there is used, as the trialkylaluminum, a trialkylaluminum having an alkyl group of 6 or more carbon atoms, or, as the alkyl titanate, an alkyl titanate having an alkyl group of 6 or more carbon atoms.The polyacetylene obtained according to the present invention is superior in mechanical properties, particularly stretchability.

Abstract: This invention relates to a process for the living cationic polymerization of vinylic unsaturated compounds containing electron donating substituents resulting in polymers of narrow molecular weight distribution.

Abstract: A polymerization process is provided for producing a butyl rubber with a bimodal molecular weight distribution which comprises introducing isobutylene, a conjugated diolefin monomer having from 4 to 8 carbon atoms, from about 1.times.10.sup.-5 to about 1.times.10.sup.-3 moles of an initiator component per mole of isobutylene, said initiator component being selected from the group consisting of an initiator component having the formula: ##STR1## in which R.sub.1, R.sub.2 and R.sub.3 are selected from the group consisting of alkyl, aryl and aralkyl groups and can be the same or different and i is a positive whole number from 2 to 6, and an initiator component having an adamantyl nucleus bearing from 2 to 4 hydroxyl groups an inert organic solvent and from about 1.times.10.sup.-4 to about 1.times.10.sup.-3 moles of water per liter of inert organic solvent into a suitable reaction vessel at a temperature of from about -120.degree. C. to about -50.degree. C., adding a solution of from about 5.times.10.sup.

Abstract: Ozone resistant vulcanizable copolymers of isoolefins with non-conjugated dienes of the general formula: ##STR1## where R.sub.1 is ##STR2## and R.sub.2 is alkyl of 1 to 6 carbon atoms and vulcanizates thereof. The copolymers are prepared by polymerization in the presence of Lewis acids.

Abstract: The invention relates to polyacrylates corresponding to formula (I) ##STR1## to their production in a quasi-ionic polymerization and to their use as monofunctional chain terminators, optionally in combination with typical other chain terminators, for the production of aromatic polycarbonates.The invention also relates to the polycarbonates or polycarbonate mixtures obtained using the compounds corresponding to formula (I) and to their use as additives for other thermoplastic polycarbonates.

Abstract: A family of ionic polyacetylenes containing long sequences of conjugated double bonds in the backbone with ionic charges adjacent to or in conjugation with the backbone, and a synthetic process for preparing them, are disclosed. These polymers, which are soluble in many solvents including water, are mono- and di-substituted polyacetylenes that are extensively conjugated. The charge density and geometry of charge distribution depends on the number and nature of the substituents.

Abstract: Liquid telechelic polymers are made from dienes and are produced via anionic polymerization. While having low molecular weight, for example less than 15,000, the telechelic polymers are generally gel-free, have high amounts of trans-1,4 structure, low vinyl unsaturation and low bulk viscosities. The liquid telechelic polymers are made utilizing a trimetallic initiator comprised of (1) an organopolylithium compound and (2) a complex of a trialiphatic substituted aluminum compound or derivative thereof and a barium salt of an organic alcohol.

Abstract: Methods of preparing storage stable components useful for metathesis bulk polymerization of cycloolefin monomers are provided. These components contain cycloolefins with norbornene-functional groups and cocatalysts activated with a halometal compound. In these methods, the cocatalyst is completely formed before the halometal activator is added to prevent the formation of unwanted hydrogen halides, which catalyze undesired crosslinking reactions which destabilize the cocatalyst component. Bulk polymerization systems are provided wherein these storage stable cocatalyst components are paired with catalyst components that together form the complete metathesis catalyst system. For some embodiments, storage stability is aided by the removal of water.

Abstract: Isobutylene homopolymers and copolymers are prepared using a catalyst system comprising a haloadamantane component and a Lewis acid. Branched polymers are prepared using polyhaloadamantanes, the branches being attached to the adamantane at the former location of the halide. The preferred catalyst systems are diethylaluminum chloride and bromoadamantane as well as polybromo, or polychloroadamantanes.

Abstract: Disclosed is a method of delaying the metathesis polymerization of strained ring cycloolefins by addition of certain phosphorus-containing compounds including various aryl phosphates, aliphatic phosphates, aliphatic phosphites, aryl phosphites, aryl phosphines and alkyl phosphines.

Abstract: A process for producing polyethylene of ultrahigh molecular weight having an intrinsic viscosity of 10-30 dl/g at 135.degree. C. in decalin is disclosed which comprises at least the following two stages of polymerization reaction: (a) a first reaction stage where in ethylene is polymerized with use of a catalyst comprising a solid component containing at least Mg, Ti and/or Va and in the absence or presence of hydrogen of reduced concentration to produce 70-99.5 weight parts of polyethylene having an intrinsic viscosity of 12-32 dl/g at 135.degree. C. in decalin; and (b) a second reaction stage wherein a fresh feed of ethylene is polymerized in the presence of hydrogen of higher concentration to produce 30-0.5 weight parts of polyethylene having an intrinsic viscosity of 0.1-5 dl/g at 135.degree. C. in decalin.

Abstract: A process for treating a polysilazane, characterized in that a polysilazane possessing on average at least two, and preferably at least three, hydrocarbon groups having aliphatic unsaturation per molecule is treated catalytically in the presence of a catalytically efficient amount of a co-ordination catalyst. The polysilazanes treated in this manner possess high thermal resistance and can be used, in particular, as precursors of ceramic products, with a high yield of inorganic product.

Abstract: Protection against molecular weight depression in the polymerization reaction producing polyisobutylene rubber or butyl rubber is achieved through addition of minor amounts of certain metal alkyls, particularly the lower alkyl aluminum compounds or lower alkyl aluminum hydrides which function as buffering, neutralizing or complexing agents against polymerization poisons and extraneous catalyst activators.

Abstract: A method of preparing a nodular polymer by preparing a copolymer chain and coupling it to a coupling agent. The coupling agent is a non-conjugated diene. Preferably the non-conjugated diene has both double bonds Ziegler catalyst polymerizable. The preferred product comprises a norbornadiene coupled ethylene copolymer wherein the ethylene copolymer has a M.sub.z /M.sub.m of less than 2.0 and a M.sub.w /M.sub.n of less than 1.8 before coupling.

Abstract: The invention relates to a continuous process for the manufacture of butyl rubber in which the monomers are polymerized using a halogenated polymerization medium in a self-cleaning screw extruder at a constant pressure under boiling plug-flow conditions by means of a modified aluminium halide catalyst which operates at high temperature (relative to prior art very low temperatures of e.g. -100.degree. C.). In contrast to prior art slurry processes, the polymerization mixture forms a sticky, highly viscous mass which is conveyed by screw action to the extruder outlet as polymerization proceeds. The butyl rubber product is separated at a high concentration from vapors of unreacted monomers and polymerization medium which are recycled.

Abstract: Isobutylene homopolymers and copolymers are prepared using a catalyst system comprising a haloadamantane component and a Lewis acid. Branched polymers are prepared using polyhaloadamantanes, the branches being attached to the adamantane at the former location of the halide. The preferred catalyst systems are diethylaluminum chloride and bromoadamantane as well as polybromo, or polychloroadamantanes.

Abstract: "Living" polymers and their preparation from acrylic-type or maleimide monomers and organosilicon, -tin or -germanium initiators.

Abstract: An optically active polymer is obtained by polymerizing a vinyl monomer in the presence of a catalyst which comprises an asymmetric ligand compound of the formula (I) or (II): ##STR1## in which R.sub.1 and R.sub.4 each are --O--R.sub.7, --S--R.sub.7, ##STR2## R.sub.2, R.sub.3, R.sub.5, R.sub.6, R.sub.7 and R.sub.8 each are an alkyl group having 1 to 10 carbon atoms; X is hydrogen, an alkyl group having 1 to 10 carbon atoms or a halogen; and n is a number of 1 to 4; and an anionic initiator to form a complex with said ligand compound.

Abstract: Disclosed is a process for polymerizing beta-pinene to a substantially colorless, hard beta-pinene resin, and to the beta-pinene resin thus produced.

Abstract: A process is provided for oligomerizing alpha-olefins comprising contacting in a reaction zone under reaction conditions: (a) alpha-olefins having at least three carbon atoms; (b) an aluminum compound having the formula R.sub.3 Al, wherein R is an hydrocarbyl group and (c) a cocatalyst which is hydrocarbyl halide having at least one halogen group reactive with said aluminum compound, elemental bromine or elemental iodine.

Abstract: Process for the production of a suspension of polyacetylene in the form of particles having a diameter of from 0.01 to 1 mm and having a great number of fibrous appendices comprising introducing acetylene in an organic suspending agent under constant stirring, in the presence of an aluminum-containing organometallic mixed catalyst in an amount corresponding to 10 to 100 m moles aluminium per liter suspending agent, at temperatures of from -100.degree. to 80.degree. C., until a maximum of 10 g, preferably 1 to 3 g of polyacetylene per liter of suspending agent have been formed.

Abstract: A new crystalline form (beta form) of MgCl.sub.2 is disclosed, as are methods for obtaining it by reaction of SOCl.sub.2 with hydrated MgCl.sub.2 at a temperature comprised between room temperature and the boiling point of SOCl.sub.2.

Abstract: A polymerization activator for polymerizing ethylene comprising a dialkylaluminum monofluoride mixed with minor amounts of at least one of dialkylaluminum hydride or halide and a trialkylaluminum. The activator preferably corresponds to the general formula (AlR.sub.2 F)(AlR.sub.2 H).sub.b (AlR.sub.3).sub.c or the general formula (AlR.sub.2 F)(AlR.sub.2 X).sub.a wherein R is an alkyl group having 1 to 12 carbon atoms, 0.1.ltoreq.b.ltoreq.0.4, 0.05.ltoreq.c.ltoreq.0.2, X is a halogen other than fluorine, and 0.1.ltoreq.a.ltoreq.0.4. The activator is used in a catalytic system including at least one halide of a transition metal of Group IVB to VIB, the valency of the metal in the halide being not more than 3 and the atomic ratio of aluminum in the activator to transition metal in the catalyst lying between 0.1 and 10. The catalytic system is used in a high pressure and temperature process for polymerizing or copolymerizing ethylene.

Abstract: The method and production of macromolecular monomers from cationically polymerizable monomers and vinyl-substituted hydrocarbon halides is disclosed. These cationically polymerizable monomers may react in the presence of a catalyst with the hydrocarbon halide to produce a macromer retaining a polymerizable headgroup. This compound may be used in a variety of copolymerization processes with a variety of copolymerizable monomers to form graft copolymers.

Abstract: Aluminum cyclopentadienyl compounds can be used to synthesize a variety of organic molecules containing the cyclopentadiene group, e.g., substituted cyclopentadiene compounds, polymer molecules with cyclopentadiene pendant groups, and polymer molecules with cyclopentadiene terminal groups.

Abstract: Age resistant resin which comprises a composition selected from (A) a composition having a softening point in the range of 0.degree. C. to about 140.degree. C. comprising units derived from selected aliphatic diolefins and aliphatic monoolefins, which can be modified with units derived from dicyclopentadiene, and certain vinyl aromatic compounds, and selected phenol or amine type compounds and (B) a composition having a softening point in the range of about 60.degree. C. to about 110.degree. C. comprising units derived from monoolefins and vinyl aromatic compounds, which can be modified with aliphatic diolefins, and selected phenol and amine type compounds. Such age resistant resins have particular utility when admixed with various rubbery materials and thermoplastics to create pressure sensitive adhesives and hot melt adhesives.

Abstract: The present invention relates to improved catalyst compositions used in the formation of substantially gel-free copolymers and terpolymers of isobutylene and one or more dienes having an Mn of about less than 500,000, a mole % unsaturation of about 8 to about 45, and a polydispersity value of about 3 to about 30, wherein the mixture of isobutylene and diene monomers and a cosolvent are contacted with the catalyst composition at polymerization conditions (-50.degree. to -100.degree. C.) wherein the improvement includes the hydrocarbon soluble catalyst composition being formed from the reaction product of a material of the formula:R.sub.m AlX.sub.

Abstract: Process for polymerizing olefinic hydrocarbons at a temperature from 0.degree. to 90.degree. C., preferably from 20.degree. to 80.degree. C. in the presence of a catalyst containing aluminum oxide and, per part by weight thereof, boron oxide in a proportion of 0.01 to 1, preferably 0.07 to 0.15 part by weight and halogen in a proportion of 0.5 to 20%, preferably 4 to 12%, said catalyst resulting from the reaction of an aluminum compound of formula AlX.sub.y R.sub.(3-y) where X is halogen, R is a hydrocarbon radical and y is selected from 1, 3/2, 2 and 3, with a carrier containing aluminum oxide and boron oxide in a proportion to aluminum oxide from 1 to 100%.

Abstract: Aluminum cyclopentadienyl compounds can be used to synthesize a variety of organic molecules containing the cyclopentadiene group, e.g., substituted cyclopentadiene compounds, polymer molecules with cyclopentadiene pendant groups, and polymer molecules with cyclopentadiene terminal groups.