Abstract: Non-phthalate compounds having a structure represented by the general formula and a method for using same are provided as electron donors in the Ziegler-Natta type catalyst system for the homopolymerization or copolymerization of alpha olefins. The non-phthalate compounds may be used in the preparation of the solid catalyst component, thus serving as “internal electron donors”, or employed during or prior to polymerization as “external electron donors,” and therefore they can be used to prepare phthalate-free polyolefins.

Abstract: The present invention relates to a process of producing an ethylene polymer composition in multiple stages, of which the first stage is preferably a slurry polymerization stage, in the presence of a catalyst system, comprising: a) a solid catalyst precursor, comprising a transition metal selected from titanium and vanadium; magnesium; a halide, optionally an electron donor; and a solid particulate material comprising an inorganic oxide, and wherein the median particle diameter, D50, of the solid catalyst precursor, based upon the total volume of solid catalyst precursor, is from 1 to 13 micrometers; and b) an organoaluminium compound.

Abstract: A process for making a radial multi-block copolymer, comprising: (a) anionically polymerizing styrene monomer A1, at least one monovinylarene monomer A2 other than styrene and at least one conjugated diene monomer B using a lithium-based initiator to form block copolymer chains; (b) adding a metal alkyl compound other than the lithium-based initiator after initiating anionic polymerization in step (a), wherein the molar ratio of the metal alkyl compound to lithium is greater than about 2.0; and (c) adding a coupling agent having more than two functional groups to form the radial multi-block copolymer, wherein the radial multi-block copolymer comprises a residue Z derived from the coupling agent and block copolymer chains from step (b) coupled to the residue Z.

Abstract: This invention relates to a process for polymerizing olefins in which the amount of trimethylaluminum in a methylalumoxane solution is adjusted to be from 1 to 25 mol %, prior to use as an activator, where the mol % trimethylaluminum is determined by 1H NMR of the solution prior to combination with any support. This invention also relates to a process for polymerizing olefins in which the amount of an unknown species present in a methylalumoxane solution is adjusted to be from 0.10 to 0.65 integration units prior to use as an activator, where the amount of the unknown species is determined by the 1H NMR spectra of the solution performed prior to combination with any support. Preferably, the methylalumoxane solution is present in a catalyst system also comprising a metallocene transition metal compound.

Abstract: The present invention concerns heterophasic propylene copolymers, comprising a propylene homopolymer (PPH) and an ethylene-propylene rubber (EPR), having a broad molecular weight distribution and a well-defined total ethylene content and a specific ratio of the intrinsic viscosities of the ethylene-propylene rubber (EPR) and the propylene homopolymer (PPH), ?EPR/?PPH. The invention further concerns the process to produce such heterophasic propylene copolymers. The heterophasic propylene copolymers of the present invention are particularly suited for corrugated sheet and cast film applications.

Abstract: Disclosed is a method for preparing a vinyl aromatic hydrocarbon-conjugated diene block copolymer using a coupling reaction with improved ion stability. The method comprises (a) polymerizing a vinyl aromatic hydrocarbon monomer in a hydrocarbon solvent with an organic lithium compound as a polymerization initiator to prepare a first mix solution comprising a vinyl aromatic hydrocarbon block; and (b) adding a conjugated diene monomer to the first mix solution of step (a) to form a conjugated diene block on an end of the vinyl aromatic hydrocarbon block and to thereby prepare a second mix solution comprising a vinyl aromatic hydrocarbon block-conjugated diene block, wherein the method further comprises (c) adding a Lewis acid to the first mix solution before, during or after polymerization of the vinyl aromatic hydrocarbon monomer of step (a).

Abstract: The present invention relates to a process of producing an ethylene polymer composition in multiple stages of which the first stage is a slurry polymerization stage, in the presence of a catalyst system comprising a) a solid catalyst precursor comprising a transition metal selected from titanium and vanadium; magnesium, a halide, optionally an electron donor, and a solid particulate material comprising an inorganic oxide, wherein the median particle diameter of the solid catalyst precursor based upon the total volume of solid catalyst precursor, D50, is from 1 to 13 micrometers; and b) an organoaluminium compound.

Abstract: A propylene block copolymer comprising 60 to 85% by weight of a propylene polymer component and 15 to 40% by weight of an ethylene-propylene copolymer component, and satisfying the following requirements (I) to (V): (I) the above propylene polymer component has a melting temperature of 160° C. or higher measured according to DSC; (II) the above ethylene-propylene copolymer component has an ethylene content of 40 to 60% by weight measured according to a 13C-NMR spectrum; (III) the above ethylene-propylene copolymer component has a crystallization peak between 90 to 105° C. in its DSC measurement, and the above crystallization peak is 2 to 10 J in its heat of crystallization, per 1 g of the above ethylene-propylene copolymer component; (IV) the above ethylene-propylene copolymer component has a glass transition temperature of ?50° C.

Abstract: According to an aspect of the present invention, a method is provided in which a double diphenylethylene compound is reacted with a polymer that contains a carbocationically terminated chain thereby providing a 1,1-diphenylene end-functionalized chain. Subsequently, an alkylating agent is reacted with the 1,1-diphenylene end-functionalized chain, thereby providing an alkylated 1,1-diphenylene end-functionalized chain. In some embodiments, the method further comprises (a) optionally combining a 1,1-diphenylorganolithium compound with the alkylated 1,1-diphenylene end-functionalized polymer followed by (b) reacting an organolithium compound with the alkylated 1,1-diphenylene end-functionalized polymer. This provides an anionically terminated polymer, which can be used, for example, in subsequent anionic polymerization and coupling reactions.

Abstract: Disclosed are propylene impact copolymer compositions, articles thereof, and processes for producing same. Polymerization with an improved catalyst composition provides a propylene impact copolymer with high melt flow and low volatiles content.

Abstract: A process for the preparation of a functionalized, coupled or starred block copolymer which is usable in a sulphur-cross-linkable rubber composition of reduced hysteresis in the cross-linked state, one at least of said blocks consisting of a polyisoprene and at least one other block consisting of a diene elastomer other than a polyisoprene the molar ratio of units originating from one or more conjugated dienes of which is greater than 15%.

Abstract: A novel method of preparing carboxyl-terminated polymers. A monomer is mixed with an organolithium initiator in a hydrocarbon solvent so as to anionically polymerize linear living polymer lithium chains. A trialkyl aluminum compound is also mixed so as to form polymer lithium: aluminate complexes in equilibrium with the linear living polymer lithium chains. When a cyclic anhydride terminator is mixed, the cyclic anhydride terminator preferentially reacts with the C—Li center on a living polymer lithium chain rather than with the C—Al—Li center on a polymer lithium: aluminate complex.

Abstract: A powder system for use in solid freeform fabrication. The powder system includes at least one polymer having reactive properties and fusible properties. The at least one polymer is reactive with a liquid binder and is fusible at a temperature above the melting point or glass transition temperature of the at least one polymer. The at least one polymer may be a single co-polymer having at least one reactive portion and at least one fusible portion or may be a mixture of polymers including at least one reactive polymer and at least one fusible polymer. A method of forming an object by solid freeform fabrication is also disclosed.

Abstract: The present invention provides a hot-melt adhesive composition comprising a blend of: a reactive filler comprising an aluminum compound, a magnesium compound, a calcium compound, a barium compound or a mixture thereof; and, a grafted polyolefin having a functional group for reaction with the reactive filler. Such a hot-melt adhesive is particularly useful for bonding a polyolefin-based substrate to dissimilar materials such as metals, wood, ceramics and thermoset plastics.

Abstract: A preparation process for a copolymer having two blocks usable in a sulphur-cross-linkable rubber composition of reduced hysteresis in the cross-linked state, such a block copolymer in which one of the blocks is a polyisoprene and the other a diene elastomer other than a polyisoprene, and this rubber composition for tire treads. A process for the preparation of this copolymer involves copolymerizing one or more monomers including a conjugated diene other than isoprene using a catalytic system including at least one hydrocarbon solvent, a compound A of a metal of group IIIA, a compound B of an alkaline-earth metal and a polymeric initiator C having a C—Li bond which is constituted of a monolithiated polyisoprene intended to form the polyisoprene block, the number-average molecular weight Mn1 of the polyisoprene block being between 2,500 and 20,000 g/mol.

Abstract: This invention provides the following: an amphiphilic functional substance with lipophilicity, affinity for supercritical CO2, and if necessary hydrophilicity comprising an oligoolefin chain and a perfluoroalkyl group(s) at a single end thereof or at both ends thereof with or without the intervention of a poly(oxyalkylene) chain, which enables the utilization of supercritical CO2 as a reaction medium; a photopolymerizable functional substance comprising an oligoolefin chain and a reversible photopolymerization/dissociation group(s) at a single end thereof or at both ends thereof and a functional substance comprising a photo- and/or thermodissociable polymer obtained by photopolymerization of the aforementioned photopolymerizable functional substance, which can be utilized as recycle polymers; a hydrolyzable functional substance comprising a polymer obtained by chain-elongating plural oligoolefin chains through ester linkages, which can be utilized as a recycle polymer; and a functional substance capable of fo

Abstract: A biaxially oriented polyolefin multilayer film containing: (a) a core layer containing (i) greater than about 0% by weight to about 50% by weight of an isotactic polypropylene-containing impact copolymer, (ii) about 10% by weight to 70% by weight of an alpha olefin/polypropylene copolymer-containing thermoplastic olefin and (iii) about 10% by weight to 70% by weight of an isotactic propylene homopolymer; and (b) at least one polyolefin skin layer adjacent to the core layer is disclosed.

Abstract: A syndiotactic styrenic polymer having a narrow molecular weight distribution which is a (co)polymer comprising at least one structural unit represented by the following Formula (1): wherein C1 of a phenyl group thereof has a tacticity of 30% or more in terms of a racemic pentad determined by 13C-NMR, and Ra and m are as defined in the specification. The disclosure is also directed to a block copolymer comprising the above polymer as one segment, to a block graft polymer prepared by modifying one block of the above polymer with a nitrogen-containing aromatic polymer, and to a process for preparing a syndiotactic styrenic polymer in which a styrenic monomer is polymerized in the presence of a catalyst comprising a reaction product of a transition metal compound and at least one co-catalyst selected from organic aluminunoxy compounds.

Abstract: The invention relates to absorptive, crosslinked polymers which are based on partly neutralized, monoethylenically unsaturated monomers carrying acid groups, and have improved properties, in particular in respect of their capacity for transportation of liquids in the swollen state, and which have been after-crosslinked on their surface at temperatures of at least 150° C. with a combination of polyol as after-crosslinking compound and a cation in the form of an aqueous solution.

Abstract: A process for forming a copolymer comprising the steps of (i) preparing a living polymer segment by using anionic polymerization techniques, (ii) modifying the living polymer by reacting it with an alkyl metal halide to form an organometallic polymeric intermediate, and (iii) preparing a second polymer segment from the organometallic polymeric intermediate by combining the intermediate, conjugated diene monomer, and a coordination catalyst that will polymerize the conjugated diene monomer.

Abstract: In a process for the anionic polymerization of vinylaromatic monomers or dienes in the presence of a lithium organyl or lithium alcoholate and a magnesium and/or an aluminum compound, a sterically hindered phenol or amine is added.

Abstract: Disclosed are a propylene polymer having a high crystallinity of a boiled heptane-insoluble component contained therein, a high stereoregularity and an extremely long mesochain (continuous propylene units wherein directions of {acute over (&agr;)}-methyl carbons are the same as each other), and a process for preparing said polymer. Further disclosed is a propylene polymer composition comprising the above propylene polymer and at least one stabilizer selected from a phenol type stabilizer, an organophosphite type stabilizer, a thioether type stabilizer, a hindered amine type stabilizer a metallic salt of higher aliphatic acid. The propylene block polymer of the invention is well-balanced between rigidity, heat resistance and moisture resistance, and can be favorably used for sheet, filament, injection molded product, blow molded product, etc.

Abstract: Disclosed are a propylene polymer having a high crystallinity of a boiled heptane-insoluble component contained therein, a high stereoregularity and an extremely long mesochain (continuous propylene units wherein directions of &agr;-methyl carbons are the same as each other), and a process for preparing said polymer. Also disclosed are a propylene block copolymer containing a crystalline polypropylene portion having a high crystallinity of a boiled heptane-insoluble component contained therein, a high stereoregularity and an extremely long mesochain, and a process for preparing said copolymer. Further disclosed is a propylene polymer composition comprising the above propylene polymer or propylene block copolymer and at least one stabilizer selected from a phenol type stabilizer, an organophosphite type stabilizer, a thioether type stabilizer, a hindered amine type stabilizer and a metallic salt of higher aliphatic acid.

Abstract: A process prepares impact-modified thermoplastic molding compositions which comprise a soft phase made from a rubber dispersed in a hard matrix composed of vinylaromatic monomers, where the hard matrix is prepared by anionic polymerization in the presence of a metal alkyl compound or a metal aryl compound of an element of the second or third main group, or of the second subgroup, of the Periodic Table.

Abstract: The present invention intends to provide an ethylene/&agr;-olefin copolymer of specific structure, exhibiting excellent performance as a lubricant oil additive, capable of having various functional groups in high ratio, and serviceable as raw material for various solubilizing agents. The ethylene/&agr;-olefin copolymer of the present invention is composed of ethylene and an &agr;-olefin having 3 to 10 carbon atoms, and characterized by specific characteristics.

Abstract: An anionically polymerized impact-modified polystyrene has a yield stress of at least 24 MPa, measured at 23° C. to DIN 53455 and a hole impact strength of at least 11 kJ/m2, measured at 23° C. to DIN 53753, measured in each case on a specimen produced to ISO 3167. A preparation process is described.

Abstract: The present invention relates to a continuous method of preparing a block-graft or star-shaped copolymer. This method involves providing a living polymer, mixing the living polymer with a first monomer under conditions effective to produce a block copolymer, wherein the first monomer includes a polymerization site and a polymerization initiation site, and mixing the block copolymer with a second monomer under conditions effective to produce a block-graft or star-shaped copolymer. The present invention also relates to a continuous method of preparing a graft or graft-block copolymer.

Abstract: A process comprising contacting ethylene and at least one alpha-olefin comonomer having with a transition metal based catalyst system in two fluidized bed reactors connected in series, in the gas phase, under polymerization conditions, with the proviso that a hydrocarbyl aluminum cocatalyst is introduced into the first reactor and a different hydrocarbyl aluminum cocatalyst or no cocatalyst is introduced into the second reactor.

Abstract: A composition for the detackification and clarification of acid and alkaline paint and lacquer waste waters and paint spray booth wastes, comprising:an inorganic-organic and/or organic adduct alloy polymer composition having the formula:A.multidot.B.sup.+ .multidot.D.sup.+wherein: A=[(SiO.sub.2 /Me.sup.I.sub.2 O).sub.u Me.sup.II.sub.m Me.sub.m.sup.III(OH).sbsp.p.sup.(SO.sbsp.4.sup.).sbsp.y.sup.(Aci) (2m+3n)-p-2y].sub.rwhere r=1 to 98% bw; u=0 to 10% bw; ##STR1## where: x=0 to 98% bw; Z is a divalent substituted or unsubstituted aliphatic, cycloaliphatic, heterocyclic or aromatic radicalD.sup.+ =(PQAM).sub.wwherew=2 to 98% b.w. of polyquaternized polymer (PQAM)Me.sub.m.sup.II is selected from the divalent cationic group comprising: Mg, Zn, Ca, and Fe.sup.2+m=0 to 5Me.sub.n.sup.III is a tri-or more valent metal selected from the group comprising: Fe, Al, and Al--Zn complexes;n=1 to 20Aci is selected from the monovalent anionic group comprising Cl.sup.-, Br.sup.-, I.sup.-, NO.sub.3 --, H.sub.2 PO.sub.4 --, CH.

Abstract: The present invention is directed to a process of atom (or group) transfer radical polymerization for the synthesis of novel homopolymer or a block or graft copolymer, optionally containing at least one polar group, with well defined molecular architecture and narrow polydispersity index, in the presence of an initiating system comprising (i) an initiator having a radically transferrable atom or group, (ii) a transition metal compound, and (iii) a ligand; the present invention is also directed to the synthesis of a macromolecule having at least two halogen groups which can be used as a macroinitiator component (i) to subsequently form a block or graft copolymer by an atom or group transfer radical polymerization process; the present invention is also directed to a process of atom or group transfer radical polymerization for the synthesis of a branched or hyperbranched polymer; in addition, the present invention is directed to a process of atom or group transfer radical polymerization for the synthesis of a ma

Abstract: A viscosity modifier comprising a low molecular weight block copolymer including A blocks and B blocks, wherein the A blocks comprise at least about 93 wt. % polyethylene and the B blocks comprise a copolymer of between about 40 wt. % to 75 wt. % ethylene and at least one other .alpha.-olefin; wherein the resulting block copolymer has an average ethylene content of between about 60 wt. % to 80 wt. %.

Abstract: Disclosed is a graft copolymer (A+B) of a styrene-based monomer (A) and a terminal styrene derivative-modified olefin-based macromer (B) of formula (1), having a high degree of syndiotacticity for the stereospecificity of the chains derived from the styrene-based monomer: ##STR1## R is H or alkyl; X is H, halogen, or a substituent having one or more of C, Sn and Si; n is 1 to 4; m is 0 or a natural number; Z is a chain moiety derived from an olefin-based monomer. The copolymer is prepared by copolymerizing (A) and (B) in the presence of a catalyst comprising (a) a transition metal compound, (b) (i) a specific oxygen-containing compound and/or (ii) a compound capable of reacting with the compound (a) to form an ionic complex, and optionally (c) an alkylating agent.

Abstract: Blends of olefin polymers and syndiotactic vinyl polymers are produced by the catalytic polymerization of olefins and aromatic vinyl compounds or methacrylate esters as vinyl compounds in inert diluents in the presence of a catalyst mixture of transition metal compounds, metalloxane compounds and metal alkyl compounds.The blends have a finely dispersed distribution of the blending components and are suitable for the production of films, sheets, fibers, panels, coatings, pipes, hollow objects, injection molded products and foams.

Abstract: Homopolymers or copolymers obtained by a multistage process of olefins having the formula CH.sub.2 .dbd.CHR, in which R is hydrogen or R has from 1 to 10 carbon atoms and is an alkyl, cycloalkyl or aryl group, the process comprising:(A) a first stage of polymerization in which one or more of the olefins are polymerized in the presence of a titanium or vanadium catalyst;(B) a treatment stage in which the product obtained in the first stage of polymerization (A) is brought into contact with a compound capable of deactivating the catalyst present in the stage (A); and also brought into contact with a compound of a transition metal M selected from the group consisting of Ti, Zr, V, or Hf containing at least one M-.pi. bond and optionally with an alkyl-Al compound; and(C) a second stage of polymerization in which one or more of the olefins are polymerized, in one or more reactors, in the presence of the product obtained in treatment stage (B).

Abstract: The invention relates to a high-molecular-weight reactor blend comprising a high-molecular weight polypropylene and a high-molecular weight ethylene-propylene copolymer and having an ethylene content in the range from 0.1 to 2% by weight based on the total amount of blend, a melt flow index MFR (230/5) of .ltoreq.5 dg/min and a molecular weight distribution M.sub.w /M.sub.n in the range from 6 to 20.

Abstract: An isobutylene-based polymer as a polymer of cationically polymerizable monomers principally composed of isobutylene or a combination of isobutylene and a styrene-series monomer, generates a molded article with outstanding properties, the isobutylene-based polymer characteristically satisfying the following provisions;1. the isobutylene-based polymer has a substantially continuos molecular weight distribution on a gel-permeation chromatogram;2. the molecular weight at the highest peak on a gel-permeation chromatogram is within a range of 10,000 to 500,000; and3. the length (a) of the elution time in the lower molecular region of the mountain from the highest peak and the length (b) of the elution time in the higher molecular region of the mountain from the highest peak on a gel-permeation chromatogram, satisfy the provision represented by the formula (b)/(a).gtoreq.1.3.

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: There are disclosed a graft copolymer formed by grafting a styrenic monomer onto a high polymer having double bonds in the side chain to constitute highly syndiotactic polystyrenic chain as the graft component, the graft copolymer having a content of graft component of 0.005 to 99% by weight and a reduced viscosity of 0.01 to 30 dl/g as measured at a concentration of 0.05 g/dl in 1,2,4-trichlorobenzene at 135.degree. C. or a melt index of 0.001 to 500 g/10 minutes as measured at 300.degree. C. under a load of 2.16 kg; a process for efficiently producing the above graft copolymer using a catalyst comprising specific components; and a resin composition comprising the above graft copolymer, a highly syndiotactic styrenic polymer or other thermoplastic resin and, when necessary, an inorganic or organic filler. The above graft copolymer and resin composition are excellent in resistance to heat and chemicals, electrical properties, moldability, compatibility, impact resistance, etc.

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 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: A composition for the detackification and clarification of acid and alkaline paint and lacquer waste waters and paint spray booth wastes, comprising:an inorganic-organic and/or organic adduct alloy polymer composition having the formula:A.multidot.B.sup.+ .multidot.D.sup.+wherein:A=[(SiO.sub.2 /Me.sup.I.sub.2 O).sub.u Me.sup.II.sub.m Me.sub.m.sup.III(OH) p.sup.(SO 4.sup.) y.sup.(Aci) (2m+3n)-p-2y].sub.4wherer=1 to 98% bw;u=0 to 10% bw; ##STR1## where: x=0 to 98% bw; Z is a divalent substituted or unsubstituted aliphatic, cycloaliphatic, heterocyclic or aromatic radicalD.sup.+ (PQAM).sub.wwherew=2 to 98% b.w. of polyquaternized polymer (PQAM)Me.sub.m.sup.II is selected from the divalent cationic group comprising: Mg, Zn, Ca, and Fe.sup.2+m=0 to 5Me.sub.n.sup.III is a tri-or more valent metal selected from the group comprising: Fe, Al, and Al-Zn complexes;n=1 to 20Aci is selected from the monovalent anionic group comprising Cl.sup.-, Br.sup.-, I.sup.-, NO.sub.3 --, H.sub.2 PO.sub.4 --, CH.sub.3 COO.sup.-, OH.

Abstract: It is sometimes advantageous to disperse crystalline polymers throughout rubbery elastomers. For instance, the cold flow characteristics and green strength of polydiene rubbers can be improved by dispersing syndiotactic-1,2-polybutadiene therein. This invention discloses a process for preparing a highly dispersed blend of a crystalline polymer in a rubbery elastomer which comprises (1) polymerizing at least one diene monomer in an organic solvent under solution polymerization conditions to form a polymer cement of the rubbery elastomer in the organic solvent, (2) polymerizing additional monomers in the polymer cement into the crystalline polymer to form a rubbery cement having the crystalline polymer dispersed therein, and (3) recovering the highly dispersed blend of the crystalline polymer in the rubbery elastomer from the organic solvent in the rubber cement.

Abstract: An elastomeric polymer composition that exhibits improved processability and green strength comprises: from about 95 to about 70 parts by weight of one rubbery polymer selected from the group consisting of butyl rubber, chlorinated butyl rubber and brominated butyl rubber and from about 5 to about 30 parts by weight of a block copolymer having an elastomeric polyisobutylene midblock and two plastomeric endblocks of polymerized monovinylidene aromatic monomers and star-shaped block copolymers having from three to six arms wherein the inner elastomeric blocks are polyisobutylene and the outer plastomeric blocs are polymerized monovinylidene aromatic monmers for a total of 100 parts by weight of the rubbery polymer and the block copolymer. Vulcanizates of the composition that exhibit reduced permeability to gases and improved tear strength are provided together with a process for their production.

Abstract: Propylene is copolymerized with ethylene in solvent-free polymerization in two steps where a resinous polymer is produced in the first step and a rubbery polymer is produced in the second step over a Ziegler catalyst whose solid catalyst component has undergone preliminary polymerization of an .alpha.-olefin in the absence of an organoaluminum compound. The solid catalyst components is specified. Less sticky polymer powder is obtainable.

Abstract: There is provided a process for producing a styrenic graft copolymer which comprises coplymerizing a styrenic monomer and a styrenic monomer having a hydrocarbon radical with an unsaturated bond in the presence of a catalyst comprising as primary ingredient (A) a transition metal compound and (B) a contact product of an organoaluminum compound and a condensation agent or (C) a compound which produces an ionic complex by reacting with the above-mentioned transition metal compound and subsequently graft polymerizing an ethylenically unsaturated monomer onto the resultant styrenic copolymer.The above-described styrenic graft copolymer is greatly improved in terms of compatibility, adhesivity, coatability and wettability while preserving heat resistance and chemical resistance thereof, and thus effective as a variety of constructional materials and compatibilizing agents.

Abstract: Disclosed is a process for producing a styrene polymer composition, which comprises polymerizing styrene monomer using a catalyst comprising (A) aluminoxane and (B) a compound of the group IV B transition metal in the periodic table, in the presence of rubber-like elastomer.The resin composition obtained thereby is superior in heat resistance, and impact strength, and utilized as the starting material for various moldings.

Abstract: Elastomeric polymers comprising polymerized alpha-olefins or conjugated alkadienes are produced by cationic polymerization in the presence of titanium tetrachloride and an electron pair donor selected from pyridine or a non-hindered alkylpyridine. The polymers have very narrow, mono-modal molecular weight distributions such a achived by anionic polymerization. Polymerization of each monomer is terminated prior to broadening of the molecular weight distribution which significantly detracts from polymer properties.

Abstract: A crystalline block copolymer containing at least a triblock or at least a radial structure and a process for producing the same, wherein at least one block comprising a vinyl aromatic compound having a glass transition temperature (Tg) of not lower than 50.degree. C., at least one block comprising a conjugated diene polymer having a 1,4-trans linkage content, a Tg not higher than 10.degree. C. and crystallinity at 25.degree. C. and in which the crystalline block copolymer optionally which contains the radial structure further comprises a coupling agent. The polymer or the composition containing the same can be utilized for fixing materials of affected portions for medical purposes, protector materials for various sports, films, laminates, toys, artificial flowers, heat-sensitive sensors, coupling devices, insulating materials, framework materials, etc.

Abstract: Block copolymers compose a polyisobutylene rubbery soft segment of M.sub.n of about 5,000 to above 500,000 and glassy hard segments of M.sub.n of about 5,000 or higher and usually about 10,000 to 35,000 or more, are made by preparing a living polymer block of the polyisobutylene and then polymerizing on said living polyisobutylene block the glassy hard segments by adding thereto an electron donor having a donor number of 15 to 50 and then adding and polymerizing the monomers for the glassy hard segments. The monomers for the glassy hard segments are styrene and its derivatives and indene and its derivatives and mixtures thereof.