Abstract: Dye-containing polymers wherein the dyes are organic in nature are incorporated into glasses produced by a sol-gel technique. The glasses may be inorganic or organic-modified metal oxide heteropolycondensates. The dye-containing polymers are covalently bonded to the glass through a linking group. The products of this invention can be used to make optically clear colored films which can be employed in the imaging, optical, solar heat energy and related arts.

Abstract: A block copolymer comprising a monoalkenylaromatic hydrocarbon block and a hydrogenated conjugated diene hydrocarbon block in which groups ##STR1## R being an organic radical, are grafted at the aromatic groups, and preparation thereof by reacting the block copolymer with an azide ##STR2##

Abstract: Process for the imidization of vinyl-aromatic copolymers containing maleic anhydride, using as an imidizing agent an amide, the imidization being conducted in an anhydrous state and in the presence of a catalyst.

Abstract: A material that includes an organic polymer capable of being rendered electrically conductive by electrochemical oxidation or reduction, and a redox compound ionically or covalently bonded to the polymer. The redox potential of the redox compound is more positive than the redox potential of the polymer when the polymer is electrically conductive in the oxidized state and more negative than the redox potential of the polymer when the polymer is electrically conductive in the reduced state.

Abstract: This invention relates to a p-methyl styrene polymer represented by the following formula: ##STR1## Z denotes a group such as a functional group. Poly p-methylstyrene (PPMS) is lithiated by reaction with n-butyllithium. The lithiated PPMS is used to prepare polymers containing functional groups. As an example, a solution of PPMS (MW 260,000), 1.0 g in 20 ml of cyclohexane, was reacted with n-butyllithium, 8.5 mmol, and tetramethylethylenediamine, 8.7 mmol, for 20 hours to obtain a precipitate. The precipitate was dissolved in THF, and CO.sub.2 was blown into the solution. The solution was washed with an aqueous solution of HCl and dropped into methanol to obtain a solid polymer having carboxyl group functionality.

Abstract: A process for producing a modified conjugated diene polymer which comprises the steps of (I) polymerizing a conjugated diene in an inert organic solvent in the presence of a catalyst comprising (a) a lanthanum series rare earth element compound, (b) an organoaluminum compound represented by the general formula, Alr.sup.1 R.sup.2 R.sup.3 (wherein R.sup.1, R.sup.2 and R.sup.3 which may be same or different, are hydrogen atoms or hydrocarbon groups of 1 to 8 carbon atoms and at least one of R.sup.1, R.sup.2 and R.sup.3 is said hydrocarbon group) and, if necessary, at least one member selected from the group consisting of (c) a Lewis acid and/or (d) a Lewis base, and then (II) modifying the resulting reactive polymer with a modifying compound selected from the group consisting of the following components (e), (f) and (g): (e) an organometal halide compound represented by the general formula, R.sub.n .sup.4 MX.sub.4-n (wherein R.sup.

Abstract: A carbonyl groups containing macromolecular material which is suitable for use as a sorbent for ammonia, urea or amino compounds. It contains structural units having 3 or more, optionally hydrated vicinal carbonyl groups, preferably keto groups, the C-atoms of which may form part of a ring structure. Particularly, the ring structure contains 5-7 C-atoms, and at least 2 ring atoms may form part of an aromatic ring system. The starting material used may be made of a polymer of the same type as that used in the manufacture of ion exchange resins. The carbonyl group containing unit may form part of an independent compound, e.g., ninhydrin which may be physically bonded to the macromolecular material, but is preferably covalently bonded thereto.

Abstract: A fluoroelastomer composition curable in reactive admixture with an acid acceptor that includes an elastomeric gum consisting essentially of vinylidene fluoride, tetrafluoroethylene, and copolymerizable hydrocarbon olefin and a combination of(A) polyhydroxy compound, and(B) organo-onium compound, and process of curing the elastomeric copolymer with an admixture of (A) and (B) and an acid acceptor, and the resulting shaped or formed, cured articles are described.

Abstract: There is disclosed an improved method for open steam curing of mineral-loaded elastomers. It has been discovered that use of a vulcanization agent comprising a mixture of an alkyl phenol disulfide and a guanidine compound provides a synergistic curing system that is superior over the use of either component alone. The improved curing system of the present invention is particularly suited for the open steam curing of mineral-loaded chlorobutyl compounds. The cure system may be used in addition to zinc oxide and results in excellent states of cure as determined by tensile elongation and hardness measurements.

Abstract: Halocarbons are readily bonded to a variety of substrates, including metals, polyolefins, styrenics, polyamides and thermoplastic polyesters, by treating the surface(s) to be bonded with a neoalkoxy zirconate compound. The articles produced by the aforesaid process resist delamination. Applicable fluorinated compounds include fluorinated polymers such as Teflon. The specific zirconate compound preferred is dependent on the particular substrate and the halogenated organic compound to be bonded. Preferred are organo-zirconates having the formula: ##STR1## wherein R, R.sup.1 and R.sup.2 are each monovalent hydrocarbon groups or substantive derivatives thereof; the A groups are independently selected from diester phosphates, diester pyrophosphates, oxyalkylamino, oxyalkylarylamino, or sulfonyl groups; B is an R'.sub.2 C group or a carbonyl group; R' is a hydrogen group or an alkyl group having from 1 to 6 carbon atoms; and n is 1 or 2.

Abstract: The present invention relates to an impact resistant polymeric composition comprising a polyester and a thermally stable modified selectively hydrogenated high 1,2 content block copolymer wherein at least one graftable functional molecule is grafted to the block copolymer in the vinylarene block.

Abstract: Superior vulcanization agents for rubber are prepared by reacting sulfur with an olefin at 140.degree.-160.degree. C. in an aqueous reaction media in the presence of a basic catalyst and a dispersing agent.

Abstract: This invention relates to a process for polymerizing acrylic monomers and possibly non-acrylic co-monomers by means of polymerization-initiating agents of the formula:R--M (I)in which M represents a metal selected among the alkaline and alkaline-earth metals and R represents an alkyl radical, which may have a straight or branched chain and contains 2 to 6 carbon atoms, or an aryl radical.The polymerization or copolymerization is effected in the presence of an additive consisting of a salt of an alkaline or alkaline-earth metal and of a mineral acid, such as lithium chloride.

Abstract: Reaction products of sulfur with an unsaturated reactant selected from d-limonene, 5-ethylidene-2-norbornene, styrene, and dicyclopentadiene, reacted at a temperature above the melting point of sulfur and below 159.degree. C. until chemically combined, then further reacted above the melting point of sulfur until solidified. The resulting products serve as vulcanizing agents when compounded with rubber. The unvulcanized rubber compounds exhibit less blooming and better adhesion to a variety of substrates than rubber compositions compounded with soluble or insoluble sulfur. Vulcanizates containing the present compositions and a method for increasing the adhesion of rubber to a substrate during a vulcanization process are also disclosed.

Abstract: Polycarbon sulphide derivatives comprise units (R.sub.x CS.sub.m).sub.n in whichR represents hydrogen, an alkali metal or a transition metal,x is the degree to which R is present in the carbon-sulphur structure,m is the degree of substitution with sulphur andn is the number of units in the polymer chain.As shown by the single FIGURE of the drawing, the insertion of R is reversible.

Abstract: Reaction products of sulfur with an unsaturated reactant selected from d-limonene, 5-ethylidene-2-norbornene, styrene, and dicyclopentadiene, reacted at a temperature above the melting point of sulfur and below 159.degree. C. until chemically combined, then further reacted above the melting point of sulfur until solidified. The resulting products serve as vulcanizing agents when compounded with rubber. The unvulcanized rubber compounds exhibit less blooming and better adhesion to a variety of substrates than rubber compositions compounded with soluble or insoluble sulfur. Vulcanizates containing the present compositions and a method for increasing the adhesion of rubber to a substrate during a vulcanization process are also disclosed.

Abstract: Vulcanizable fluoroelastomer compositions having as base a copolymer of vinylidene fluoride (from 40 to 84 mol %) with perfluoropropene (15 to 30 mol %) and with tetrafluoroethylene (0.30 mol %) and containing a vulcanizing agent of the polyhydroxy compound type, an accelerator of the aminophosphinic compound type, metal oxides and/or hydroxides of basic character and an alkyl, cycloalkyl or aryl compound from the group of phosphoric esters, aminophosphoric esters, sulfoxides and sulfones.

Abstract: Glutarimide polymers having an acid and anhydride content lower than the acid and/or anhydride content normally present in the glutarimide polymers. Blends of the reduced acid and anhydride glutarimide polymers with thermoplastic materials are disclosed. A process for altering the properties oif imide polymers by reducing or substantially removing acid and anhydride levels normally present in the imide polymer is also disclosed.

Abstract: Improved acrylic acid absorbency resins are made utilizing a chain transfer agent during the polymerization process.

Abstract: A process for improving the extrudability of a vinylidene chloride interpolymer pellet. A vinylidene chloride interpolymer pellet displaying a first endotherm, as determined by differential scanning calorimetry according to American Society of Testing and Materials Test Method D-3417, below 75.degree. Celsius is exposed to a temperature above about 55.degree. Celsius for a length of time sufficient to raise said first endotherm to 75.degree. Celsius or above. Pellets treated in such a manner possess improved extrudability.

Abstract: A thermoplastic molding composition which comprises a blend of:(A) a copolymer having recurring units of a monoalkenyl aromatic monomer and recurring units of an .alpha.,.beta.-ethylenically unsaturated dicarboxylic anhydride N-substituted imide, and(B) a hydrogenated elastomeric block copolymer having at least one substantially completely hydrogenated diene polymer mid block and at least two monoalkenyl arene polymer end blocks in which at least a portion of the arene groups contained in the end blocks are substituted with at least one substituent selected from the group consisting of nitro, cyano and trifluoromethanesulfonyl.

Abstract: The bond strength between a sulphur-vulcanizable rubber and a metal, especially brass, is increased by using as bonding promoter a compound having the formula[.sup.- O.sub.2 C CH.sub.2 S--B--S CH.sub.2 CO.sub.2.sup.- ]M.sup.++or a hydrate thereof, where B represents a divalent organic radical and M represents cobalt or nickel.

Abstract: A method for the preparation of a graft polymer membrane comprising an inactive polymer film having TFS as a graft chain. The inactive polymer film is irradiated with ionizing radiation, and the resulting irradiated film is graft-polymerized by contacting said film with TFS.This product may then be sulfonated to provide a cation exchange membrane; or the obtained graft polymer may be haloalkylated, and quarternary aminated to provide an anion exchange membrane; or the graft polymer membrane may be used to prepare a weakly acidic cation exchange membrane by substituting at least part of the benzene rings of the graft polymer by one of the groups among hydroxyl groups, carboxylic acid groups, phosphoric acid groups and phosphorous acid groups.The polymeric membrane products are also disclosed and claimed.

Abstract: There are disclosed polymerizable thioester synergists which have utility in enhancing the antioxidative activity of phenolic and amine stabilizers. The invention is also concerned with the thioesters themselves, their use in oxidizable organics, their combination with polymerizable and/or conventional antioxidants, and with polymers which contain these thioesters as physical admixtures or segmeric units of the polymer.

Abstract: A cure system for halogen-containing polymers that comprises a thiourea derivative, a thiuram sulfide and an inorganic base yields stable cross-linked products with useful properties when incorporated into normal vulcanization procedures.

Abstract: A polymer having a fluorine-containing end group which is produced by polymerizing a monomer capable of radical polymerization in the presence of a fluorine-containing thiol; a vinyl ester polymer having a fluorine-containing end group which is produced by polymerizing vinyl ester in the presence of a fluorine-containing thiol; and vinyl alcohol polymer having a fluorine-containing end group which is produced by saponifying the said vinyl ester polymer; and processes for producing the same are provided.The polymers of this invention are superior in water repellency, oil repellency, heat resistance, chemical resistance, and surface activity which are characteristic of fluorocarbon compounds, and are expected to find use in various application areas.

Abstract: Additives for rubber compositions, giving vulcanizates having improved retention of optimum physical properties, are polymeric trithiocarbonates having a structure comprising repeating units of the formula ##STR1## where R is an organic bridging group, e.g. an alkylene group.

Abstract: A cis-1,4-polyisoprene rubber composition capable of giving a vulcanizate having improved strength, said composition comprising (1) a synthetic cis-1,4-polyisoprene rubber having epoxy groups, (2) a compound having at least two primary amino groups, and (3) a sulfur vulcanization system.

Abstract: A continuous process for sulfonating elastomeric polymers to form neutralized sulfonated elastomeric polymers with improved physical properties includes the steps of; (a) contacting a cement of an elastomeric polymer with a sulfonating agent in a staged reaction vessel for a sufficient period of time at a temperature of about -50.degree. C. to about +100.degree. C. to form an unneutralized sulfonated elastomeric polymer; (b) continuously transferring the cement of the unneutralized sulfonated elastomeric polymer to a neutralization vessel; (c) continuously adding a quenching agent and neutralizing agent to the cement of the unneutralized sulfonated elastomeric polymer in a staged neutralization vessel wherein the sulfonated cement is quenched and the neutralization agent reacts with the unneutralized sulfonated polymer to form the neutralized sulfonated elastomeric polymer; and (d) isolating said neutralized sulfonated elastomeric polymer.

Abstract: A sulfur-curable rubber skim stock which upon curing exhibits improved adhesion to brass-plated steel under high humidity, heat aging conditions is provided. The sulfur-curable rubber skim stock comprises natural rubber or a blend of natural rubber and synthetic rubber, carbon black, an organo-cobalt compound, sulfur and a small amount of dithiodipropionic acid. The skim stock can be utilized in various applications where brass-plated steel reinforcement is desirable including tires, conveyor belts, hoses and the like.

Abstract: A surface modifying composition for vulcanized rubber comprises a halogen-releasable halogenoid and a waxy substance having a melting point of not more than 100.degree. C. and is non-solvent type. In the surface modification of vulcanized rubber, the surface coated with the surface modifying composition is heated at 60.degree.-150.degree. C.

Abstract: Compositions of vulcanizeable diene rubber, a cross-linking agent, a vulcanization accelerator and a vulcanization system alterative are disclosed, which have improved properties of scorch delay, cure rate and reversion resistance. The alterative is a compound of the formula ##STR1## where R.sub.1 and R.sub.2 are the same or different radicals selected from alkyl of 1-12 carbon atoms, phenyl, cycloalkyl of 3-8 carbon atoms and alkyaryl and aralkyl of 7-12 carbon atoms, and R.sub.3 is selected from the same as R.sub.1 and R.sub.2, optionally substituted with one or more halogen, nitro, alkoxy, carboalkoxy, acyl, acyloxy, amido, cyano, thio or sulfonyl substituents.

Abstract: Compositions that cure when heated comprise(A) an epoxide resin and(B) an effective amount of(i) a diaryliodosyl salt of formula ##STR1## where R.sup.1 and R.sup.2, which may be the same or different, each represents a monovalent aromatic radical of from 4 to 25 carbon atoms, such as a substituted or unsubstituted phenyl group,M represents a metal or metalloid atom, such as phosphorus or boron,X represents a halogen atom, particularly chlorine or fluorine, andn is 4, 5, or 6, and is greater by one than the valency of M or MX.sub.n.sup.- represents pentafluorohydroxoantimonate, and(ii) a catalyst for the diaryliodosyl salt which is a salt or complex of a d-block transition metal, a stannous salt, an organic peroxide, or an .alpha.-hydroxy compound.Typically, the epoxide resin (A) is a bisphenol A diglycidyl ether, the salt (i) is diphenyliodosyl tetrafluoroborate or hexafluorophosphate, and the catalyst (ii) is cupric acetylacetonate or benzpinacol.

Abstract: Poly(arylene sulfide) compositions and process comprising producing poly(arylene sulfide) in the presence of a thermoplastic elastomeric hydrogenated conjugated diene/monovinyl arene block copolymer present in an amount sufficient to improve the physical properties of the composition.

Abstract: Polymers which have two or more stable, reversibly interconvertible oxidation states with half-wave potentials E.sub.1/2 of from -1.5 to +1 V, and which are obtained when a polymer having a reactive side group is reacted with a 1,9-substituted phenalene, are useful for producing electrically conductive systems, in the electrical industry, and for converting and fixing radiation, for producing electric switches, as electrochromic displays, for providing an antistatic finish on plastics and as reversible redox systems.

Abstract: Vulcanisable, elastomeric chloroprene-sulphur copolymers having viscosities of from 60 to 35 MU, strengths of >20 MPa and sulphur contents of from about 0.5 to 0.7%, by weight, in the batch are obtained by polymerising chloroprene in the presence of from 0.10 to 0.35%, by weight, of sulphur to form a latex I, polymerising chloroprene in the presence of from 0.50 to 1.00% by weight, of sulphur to form a latex II, mixing latices I and II in a ratio of from 4:1 to 1:4 (based in each case on solids), optionally together with other sulphur-modified polychloroprene latices, the mixture is peptised and worked-up to form the solid rubber, the percentages quoted being based on the quantity of monomer.

Abstract: Polystyrene and styrene copolymers are simultaneously crosslinked and sulfonated in a homogeneous reaction mixture by incorporation of from 0.1 to 5 mole percent of specific crosslinking reagents in the polymer sulfonating solution. The crosslinking reagents are selected aryl compounds having at least two --CH.sub.2 X radicals where X is hydroxyl, chlorine or bromine.

Abstract: A method of improving the handling of low molecular weight EPM or EPDM polymers which includes reacting the low molecular weight polymer with a monomer capable of providing quaternary salt forming groups and then cross linking the resulting polymer with a difunctional cross linking agent whereby the polymer takes on the characteristics of a high molecular weight polymer but which can be returned to the characteristics of a low molecular weight polymer upon exposure to elevated temperature.

Abstract: Improved tack, green strength or non-black filler interaction capability are realized in a treated diene rubber. The method of treating diene rubber to achieve the improvements is shown, together with a composition in which maleamic acid or derivatives of maleamic acid are combined with sulfur or an organic sulfur compound capable of generating a thiyl radical.

Abstract: Substantially linear, synthetic, water-soluble or water-dispersible cationic interpolymeric surfactants which are particularly useful for reducing the surface tension of an aqueous medium; such surfactants having a critical micelle concentration of from 0.01 to about 10 percent in water at 25.degree. C.

Abstract: The invention relates to a process for preparing products containing polymer chains in which a linear prepolymer or polymer contains at least one free acid group at each chain and is reacted with an alkoxide of a metal having a valence of more than 2, such as zirconium, titanium or cerium, possibly in the presence of a non polar solvent, the alkoxide of the metal having a valence of more than 2 being used in such a quantity that the alkoxide functions are in excess with respect to the stoichiometric amount of the acid functions carried by said linear prepolymer or polymer, the reaction mixture being stirred in the presence of humidity until a product is obtained wherein the hydrogen atoms of the free acid end groups of the prepolymer or polymer are substituted by an atom of the metal (M) which is itself linked to another atom of said metal by M-O-M linkages. The invention relates also to the products containing a prepolymer or polymer .alpha.,.omega.

Abstract: A process for reducing doped polyacetylene crosslinking and embrittlement comprises treating the polyacetylene with a material selected from the class consisting of (a) hindered phenols; (b) alkyl ethers of hydroquinone, wherein the alkyl group has from 1 to about 12 carbon atoms; and (c) dialkyl thiodipropionates wherein each of said alkyl groups has from 1 to about 18 carbon atoms and each alkyl group may be the same or different. A doped polyacetylene composition exhibiting enhanced resistance to polyacetylene crosslinking and embrittlement contains a doped polyacetylene and a material, as defined above, associated with said doped polyacetylene.

Abstract: Coating compositions capable of liquid application to substrates consist essentially of a curable film forming polyol-containing component and an organic reactive diluent. The reactive diluent is an organic compound containing a primary or secondary hydroxyl group and further characterized by having a retained solids value of greater than about 80 percent, a hydroxyl equivalent weight of from about 180 to about 800, and a liquid viscosity of less than about 10 poise at 60.degree. C. The coating compositions can be formulated to contain little or no volatile organic solvent and/or water.

Abstract: A novel chelate polymer having the formula: ##STR1## wherein R is a 2-thiazolyl or 2-benzothiazolyl group, is produced by reacting polymaleimide, formaldehyde, and m-aminobenzoic acid in the presence of a solvent, then coupling the resultant reaction product with a diazotized compound of 2-aminothiazole or 2-aminobenzothiazole. The novel polymers thus produced are useful as metal indicators or pH indicators.

Abstract: Polymers having a substantially completely fluorinated surface of low surface energy and substantially free of oxygen and having a thickness up to about 200 Angstroms, the remainder of the polymer comprising a non-fluorinated polymer.

Abstract: A process for polymerizing cycloalkenes into polyalkenamers is described wherein trisubstituted silyl groups are attached to the cycloalkenes. The silyl groups thus attached do not act as a poison to the polymerization process. Trimethylsilyl group can be substituted by other desired functional groups after the polymerization.

Abstract: A novel rubber compound which comprises 100 parts by weight of a rubber component (I), 0.1-15 parts by weight of an amine salt of carboxylic acid (II) and 0-7 parts by weight of sulfur (III), said rubber component (I) consisting of 40-100% by weight of an elastomeric copolymer (A) and 60-0% by weight of a vulcanizable rubber (B); said elastomeric copolymer (A) being composed of a C.sub.4 or C.sub.5 conjugated diene, styrene and a glycidyl group-containing monomer; the amount of said conjugated diene, the total amount of said conjugated diene and said styrene and the amount of said glycidyl group-containing monomer being 50% by weight or more, 80-99.5% by weight and 0.5-20% by weight, respectively, based on the weight of said elastomeric copolymer (A); and the content of said glycidyl group-containing monomer in said rubber component (I) being 0.

Abstract: Method for converting pendant functional groups, particularly upon perfluorocarbon copolymeric cationic exchange materials, to sulfonyl fluoride pendant functional groups. The method comprises a catalyzed reaction between the perfluorocarbon functional group and SF.sub.4 under pressure at relatively mild reaction temperatures.

Abstract: A vulcanization system consisting of(a) 20-50 parts by weight of sulphur or 20-50 parts by weight of a sulphur donor,(b) 20-50 parts by weight of an accelerator of the mercapto or sulphenamide group,(c) 0-10 parts by weight of a conventional accelerator additive, and(d) 20-50 parts by weight of a compound corresponding to the general formula (i): ##STR1## wherein R.sub.1 to R.sub.5 are identical or different and denote hydrogen, halogen, nitro, cyano, CF.sub.3, CCl.sub.3, carboxyl, an alkoxy group containing 1-4 C-atoms in the alkyl part, or a C.sub.1 -C.sub.4 alkyl group but the groups R.sub.1 -R.sub.5 must not all be hydrogen;x represents 1-4, preferably 2-3,y represents 0 or 1, andZ denotes divalent groups such as ##STR2## C.sub.1 -C.sub.12 alkylene, C.sub.4 -C.sub.12 cycloalkylene, C.sub.6 -C.sub.10 arylene or C.sub.8 -C.sub.12 arylalkylene, andR.sub.6 denotes the group corresponding to the formula: ##STR3## wherein R.sub.1 -R.sub.5 have the meaning indicated above and may all be hydrogen;C.sub.1 -C.sub.

Abstract: An alkali metal acrylate polymer obtained by suspending an aqueous solution of acrylic acid and an alkali metal acrylate in an alicyclic or aliphatic hydrocarbon solvent containing a surfactant having an HLB value of 8-12 and subjecting the suspension to inverse suspension polymerization in the presence of a water-soluble radical polymerization initiator has a much higher water-absorbency and particularly salt solution-absorbency than known ones. If said polymer is crosslinked with a crosslinking agent, its stability in the fluid-absorbed state for a long period of time is improved and the absorption rate when absorbing water is also improved.