Abstract: Polyvinyl halide resin absent allylic halogen is disclosed. Another polyvinyl halide resin absent allylic halogen, allylic branching and unsaturation is also disclosed. The compositions of this invention are prepared by contacting any polyvinyl halide resin with a hydrogen-substituting compound that has a selective affinity for the allylic halogens.

Abstract: The present invention provides a process for the production of polymers with an optical position in diagram where refraction index n.sub.D is plotted against optical dispension v.sub.D expedient for an optical use by metathetic counterion exchange, wherein, in a polymer of the general formula: ##STR1## R.sub.1 and R.sub.2, which can be the same or different, are divalent organic radicals, R.sub.3 and R.sub.4, which can be the same or different, are monovalent organic radicals, n is a whole number greater than 2 and y is 0 or 1. R.sub.1, R.sub.2, R.sub.3, R.sub.4, y and n are so chosen that together they form a polymeric basic structure which promotes glass formation and prevents crystallisation, and X.sup.- is a halogen atom. The halogen ion is replaced by an equivalent of a mono- or polyvalent organic or inorganic counterion different from the halogen ion and suitable for the adjustment of the desired solid body properties.

Abstract: A process is provided to functionalize hydrogenated block copolymers of vinyl aromatics and conjugated diolefin in a melt phase. The functionality is predominantly grafted to vinyl aromatic blocks by this process. The process is preferably performed in an extruder.

Abstract: A process for making polymers of conjugated dienes which contain hydroxyl groups, including highly reactive primary hydroxyl groups, in the diene blocks which comprises(a) making a precursor polymer by polymerizing at least one conjugated diene which leaves 1,2 disubstituted, 1,1 disubstituted, 1,1,2 trisubstituted or tetrasubstituted olefinic unsaturation in the polymer,(b) optionally partially hydrogenating said precursor polymer,(c) epoxidizing said precursor polymer such that epoxy groups form at said substituted sites and the amount of epoxy functionality in the polymer is from at least 0.1 Meq/g polymer, and(d) reacting the epoxidized polymer with an alcohol having one unprotected hydroxyl group in a solvent in the presence of a Lewis acid selected from the group consisting of MX.sub.n where M is selected from the group consisting of boron, aluminum, iron and tin, and X is a halogen, and organic complexes of such acids.A diene polymer containing 0.

Abstract: Polymeric hydrocarbons having reactive borane groups at chain ends or in the polymer chain are described. These types of polymers can be used as intermediate materials for preparing a broad range of polymers which have functional groups located at both ends of the polymer chain (telechelic polymers). The process of preparing the borane-containing polymers involves metathesis degradation of the polymer at the double bond locations in the backbone and simultaneous functionalization of the broken chain ends by borane monomers. Depending on the nature of the borane monomer, the location of boron atoms can be controlled to be at either the chain ends (telechelic) or in the polymer backbone. The concentration of boron in the resulting polymer is related to the reaction time and the mole ratio between borane monomer and the double bonds in the starting hydrocarbon polymer. In turn, the borane groups are interconvertible to various functional groups, such as OH, NH.sub.2, and halides, under mild reaction conditions.

Abstract: A process for making polymers of conjugated dienes which contain hydroxyl groups, including highly reactive primary hydroxyl groups, in the diene blocks which comprises(a) making a precursor polymer by polymerizing at least one conjugated diene which leaves 1,2 disubstituted, 1,1 disubstituted, 1,1,2 trisubstituted or tetrasubstituted olefinic unsaturation in the polymer,(b) optionally partially hydrogenating said precursor polymer,(c) epoxidizing said precursor polymer such that epoxy groups form at said substituted sites and the amount of epoxy functionality in the polymer is from at least 0.1 Meq/g polymer, and(d) reacting the epoxidized polymer with an alcohol having one unprotected hydroxyl group in a solvent in the presence of a Lewis acid selected from the group consisting of MX.sub.n where M is selected from the group consisting of boron, aluminum, iron and tin, and X is a halogen, and organic complexes of such acids.A diene polymer containing 0.

Abstract: Succinimides, succinic esters, and succinic ester-amides are formed by (A) reacting (i) at least one substantially aliphatic polymer of at least one lower olefin, and (ii) an acidic reactant or a mixture of two or more acidic reactants represented by the general formulaR--CO--CH.dbd.

Abstract: Visible gels are formed by mixing an inorganic crosslinking agent with a low viscosity aqueous solution having a low polyacrylamide content. The visible gels are employed to reduce the water/hydrocarbon permeability ratio of subterranean formations.

Abstract: A room-temperature curable resin composition comprising (a) an acrylic polymer having a plurality of alicyclic epoxide functions, and (b) an amount effective to initiate the curing reaction at room-temperature of the acrylic polymer (a) of a proton-donating cation polymerization initiator. The composition finds its uses in coating compositions, sealants, potting and casting compositions.

Abstract: Novel dipropargyl ether of alpha, alpha'-bis(4-hydroxyphenyl)-para-diisopropylbenzene is useful in preparing resins having desirable properties as laminates and the like.

Abstract: Novel halostyrene telechelic polymers having from 2 to about 6 terminal halogens, halostyrene-polyether, block copolymers having ABA type structures in star type structures, depending on the number of halogen terminii in the starting halostyrene block, and a process for their formation is described. The halostyrene polymers are formed by the initiator transfer agent or inifer polymerization method; while the polyether block is polymerized by silver catalysis of monomers such as tetrahydrofuran. The polymers and copolymers have good flame resistance.

Abstract: The present invention is directed to a process for synthesizing hydroxylated plasma-polymerized films, as well as the hydroxylated plasma-polymerized films produced by the process of the invention. In addition, the present invention is directed to the use of hydroxylated plasma-polymerized films produced by the process of the invention for enhancing the compatibility and/or implantability of biomedical implants and/or devices.

Abstract: A process for preparing a functionalized petroleum resin which comprises the steps of: dissolving a petroleum resin having a norbornene moiety with a double bond in a solvent to form a solution; adding to the solution a borane compound having the formula: ##STR1## wherein R.sub.1 and R.sub.2 are alkyl or cycloalkyl groups having about 1 to about 10 carbonations; reacting said petroleum resin with said borane compound at about room temperature for a sufficient period of time to form a borane intermediate; and reacting said borane intermediate with a chemical agent to convert said borane intermediate into said functionalized petroleum resin.

Abstract: A linear addition polymer having sidegroups which may be coupled to it or not through a spacer and have a molecular hyperpolarizability .beta. of at least 10.sup.-38 m.sup.4 /V, characterized in that the recurring units of the polymer correspond to the formula ##STR1## wherein X represents a hydrogen atom or a lower alkyl group and m=1 or optionally 0, wherewhen m=1Y represents a ##STR2## group and R has the meaning of a) a hyperpolarizable group having a molecular hyperpolarizability .beta. of at least 10.sup.-38 m.sup.4 /V, in the presence or not of a spacer, and optionally along withb) a mesogenic group in the presence or not of a spacer, and/orc) a hydrogen atom or a substituted or unsubstituted organic group having not more than 30 carbon atoms, andwhen m=0Y represents a--CN, a substituted or unsubstituted phenyl group or a group of the formula --OR.sub.1 or --CH.sub.2 OR.sub.1, wherein R.sub.

Abstract: A linear addition polymer having sidegroups which may be coupled to it or not through a spacer and have a molecular hyperpolarizability .beta. of at least 10.sup.-38 m.sup.4 /V, characterized in that the recurring units of the polymer correspond to the formula ##STR1## wherein X represents a hydrogen atom or a lower alkyl group and m=1 or optionally 0, wherewhen m-1Y represents a ##STR2## group and R has the meaning of (a) a hyperpolarizable group having a molecular hyperpolarizability .beta. of at least 10.sup.-38 m.sup.4 /V, in the presence or not of a spacer, and optionally along with(b) a mesogenic group in the presence or not of a spacer, and/or(c) a hydrogen atom or a substituted or unsubstituted organic group having not more than 30 carbon atoms, andwhen m=0Y represents a --CN, a substituted or unsubstituted phenyl group or a group of the formula --OR.sub.1 or --CH.sub.2 OR.sub.1, wherein R.sub.

Abstract: C.sub.5 -C.sub.9 lactone based adduct materials are made by reacting a C.sub.5 -C.sub.9 lactone with a polyamine, a polyol or an amino alcohol to form a lactone adduct intermediate, and thereafter reacting the intermediate with a hydrocarbyl substituted C.sub.4 -C.sub.10 monounsaturated dicarboxylic acid producing material, e.g., a polyisobutenyl succinimide, which, in turn, preferably was made by reacting a polymer of a C.sub.2 to C.sub.10 monoolefin, preferably polyisobutylene, having a molecular weight of about 300 to 10,000 with a C.sub.4 to C.sub.10 monounsaturated acid, anhydride or ester, preferably maleic anhydride, such that there are 0.7 to 2.0 dicarboxylic acid producing moieties per molecule of said olefin polymer used in the reaction mixture. The resulting adduct material are useful per se, as oil soluble dispersant additives, and are useful in fuel and lubricating oil compositions including concentrates containing the additives.

Abstract: Stable boron resins of high selective absorbent power and their production process. Said boron resins consist of a polyacrylic matrix functionalized with quaternary ammonium groups, an epoxy group and phenylboric groups in accordance with general formula (I): ##STR1## in which P , R.sub.1, R.sub.2, R.sub.3, R.sub.4 and X.sup.- are as defined in the text.The resins are prepared by reacting an amine resin with an epihalohydrin and condensing the reaction product with a suitable boroxin.The resins of formula (I) can be used for separating sugars, in particular for purifying lactulose. They have greater selective power than currently known boron resins.

Abstract: Stable boron resins of high selective absorbent power and their production process. Said boron resins consist of a polyacrylic matrix functionalized with quaternary groups, an epoxy group and phenylboric groups in accordance with general formula (I): ##STR1## in which P, R, R.sub.1, R.sub.2, R.sub.3, Y and X.sup.- are as defined in the text.The resin is prepared by condensing an acrylic resin with an epihalohydrin and then with a halide or hydroxide of an oxiphenyl-aminophenyl- or thiophenyl-boroxin or their alkyl derivatives.Compared with similar currently known resins, the resins of formula (I) have improved selectivity in sugar separation. They can be used for purifying lactulose.

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: 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: Radiation sensitive material suitable for the production of radiation sensitive plates for lithographic printing plate manufacture is based on a polymer including a plurality of structural units represented by the formula: ##STR1## in which, R represents H or CH.sub.3 ; each R.sub.1, which may be the same or different represents H or alkyl; R.sub.2 represents a single bond or a substituted or unsubstituted divalent radical; Ar represents a substituted or unsubstituted divalent radical derived from an aromatic or heteroaromatic compound; X represents O, S or NH; A represents an anion; Y represents a carbonyl oxy or aromatic radical; and n is an integer equal to or greater than 1.

Abstract: A thermoplastic polymer having good tensile strength at elevated temperatures is obtained by modifying a block copolymer composed of a conjugated diene compound and an alkenyl arene compound. The block copolymer is first selectively hydrogenated and thereafter modified by grafting silicon or boron containing functional groups primarily in the alkenyl arene block via metalation. Each silicon containing functional group preferably contains at least two functional groups which allow crosslinking by condensation reactions.

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: 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: The present invention relates to a process for the preparation of functional alpha-olefin homo- and copolymers by polymerization through a borane monomer intermediate.Borane monomers, derived from mono-hydroboration of appropriate dienes with dialkyl borane, have been found to be stable to Ziegler-Natta catalysts. In turn, the borane homo- and copolymers are easily converted to a variety of other functionalities; e.g., alcohols, aldehydes, amines, etc.

Abstract: The present invention relates to a process for the preparation of functional alpha-olefin homo- and copolymers by polymerization through a borane monomer intermediate.Borane monomers, derived from mono-hydroboration of appropriate dienes with dialkyl borane, have been found to be stable to Ziegler-Natta catalysts. In turn, the borane homo- and copolymers are easily converted to a variety of other functionalities; e.g., alcohols, aldehydes, amines, etc.

Abstract: Block polymer compositions are provided which are useful as positive or negative resists utilizing aryl onium salts in combination with silicone-organic block polymers, such as polydimethylsiloxane-poly-t-butylmethacrylate block polymers. A silicone prepolymer is used in combination with certain polymerizable vinyl monomers such as t-butylmethacrylate. The silicone prepolymer has chemically combined pinacolate groups in the backbone or terminal positions which are capable of generating free-radicals upon thermolysis.

Abstract: The aerobically hardenable compositions which comprise polymerizable systems containing components having some degree of ethylenic unsaturation and an oxygen-stable polymerization initiator of at least one organo-boron compound containing at least a major portion of boron to carbon bonds and possibly some boron to hydrogen bonds in the molecule and the boron containing radials are bound to an organic polymer matrix which is oxygen stable, the compositions being useful as casting resins, fillers and adhesives.

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 nitrol, cyano and trifluromethanesulfonyl.

Abstract: Vulcanizable fluoroelastomer compositions based on vinylidene fluoride, comprising, as a vulcanizing system, a polyhydroxyl aromatic compound, a divalent metal compound of basic nature, and an accelerator consisting of a salt of ammonium or of phosphonium or of quaternary amino-phosphonium in which the anion is a complex of a Cd or Zn or Ni or Pb halide.

Abstract: An adhesive composition, particularly useful for laminating carboxylate-containing films, comprises an aqueous dispersion of a film-forming vinylidene chloride copolymer wherein the vinylidene chloride copolymer includes on a comonomer weight basis:(a) from about 45 to about 90 percent vinylidene chloride,(b) from about 5 to about 25 percent of a polar comonomer having one or more hydroxyl groups, and(c) from about 0 to about 30 percent of a plasticizing monomer for vinylidene chloridein combination with:(d) a cross-linking agent dissolved in the continuous aqueous phase of the vinylidene chloride copolymer.

Abstract: A method for increasing the porosity of a cross-linked copolymer composed essentially of at least one monovinyl aromatic compound selected from the group consisting of styrene, vinyl toluene and ethyl vinyl benzene, at least one polyvinyl aromatic compound selected from the group consisting of divinyl benzene, trivinyl benzene, divinyl toluene and divinyl xylene, and an aliphatic vinyl compound, wherein the proportion of the polyvinyl aromatic compound relative to the total vinyl compounds is from 8 to 80% by weight, and the proportion of the aliphatic vinyl compound relative to the total vinyl compounds is from 0 to 20% by weight, which method comprises treating particles of said copolymer with a Lewis acid catalyst in an amount of from 0.05 to 1 part by weight relative to 1 part by weight of the copolymer particles, in the presence of an organic solvent.

Abstract: Stable boron resins of high selective absorbent power and a relative production process; said boron resins are constituted by a polyacrylic matrix bifunctionalized with quaternary ammonium groups and with alkylphenylboric groups in accordance with general formula (I) ##STR1## in which .circle.P , R, R.sup.1, R.sup.2, R.sup.3, X are as defined in the text.The resin (I) is prepared by condensing an amino resin with halophenylboroxine or with haloalkylphenylboroxine.The resin of formula (I) can be used for purifying lactulose.

Abstract: A process for preparing aromatic-moiety-containing polymers having modified physical properties is disclosed. Briefly, the process comprises reacting in the presence of a Friedel-Crafts catalyst: (a) a suitable aromatic-moiety containing polymer resin and (b) a homopolymer of .omega.-halo-.alpha.-olefins, or co- or terpolymer of .omega.-halo-.alpha.-olefins with other .alpha.-olefins and/or ethylene.

Abstract: A method for modifying a rubber having an unsaturated carbon bond which comprises reacting the rubber with an organic compound represented by the general formula ##STR1## wherein --R represents a hydrocarbon group, and --X is --H, --CN or ##STR2## in which --Y represents an organic atomic grouping, in the presence of a Lewis acid to introduce an ester group. Optionally, the ester group introduced is converted into a carboxyl group by chemically treating the reaction product.

Abstract: Stable boron resins of high selective absorbent power and a relative production process; said boron resins are constituted by a polyacrylic matrix bifunctionalized with quaternary ammonium groups and with alkylphenylboric groups in accordance with general formula (I) ##STR1## in which P , R, R.sup.1, R.sup.2, R.sup.3, X are as defined in the text. The resin (I) is prepared by condensing an amino resin with halophenylboroxine or with haloalkylphenylboroxine.The resin of formula (I) can be used for purifying lactulose.

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: Improved thermally-curable adhesive compositions for bonding articles of poly(butylene terephthalate) together or to other articles are disclosed. The adhesive compositions comprise at least one epoxidic prepolymer having two or more epoxy groups, an aromatic halonium complex salt thermal initiator dissolved in a compatibilizing non-epoxidic organic liquid, a copper carboxylate salt cocatalyst, a polyhydric alcohol, and optionally, silica filler. The adhesive compositions when heated, cure to form an adhesive bond between articles of poly(butylene terephthalate) which exhibits a vastly improved bond strength over presently available epoxy adhesive materials.

Abstract: There is disclosed a process for the functionalization of polymeric resins, wherein a halo-methylated resin, with a crosslink density of at least 4 percent is reacted with an alkyllithium wherein the alkyl radical is 1 to 12 carbon atoms; followed by a reaction to produce a polymeric material having a desired pendant functionality. Materials produced from the process of this invention have utility as intermediates in the production of polymer-bound catalysts and exchange resins.

Abstract: A process for preparing aromatic-moiety-containing polymers having modified physical properties is disclosed. Briefly, the process comprises reacting in the presence of a Friedel-Crafts catalyst: (a) a suitable aromatic-moiety containing polymer resin and (b) a homopolymer of .omega.-halo-.alpha.-olefins, or co- or terpolymer of .omega.-halo-.alpha.-olefins with other .alpha.-olefins and/or ethylene.

Abstract: A method for preparing essentially color-free, stabilized polymers of conjugated dienes or vinyl aromatic hydrocarbons or copolymers of conjugated dienes and vinyl aromatic hydrocarbons involves a first stage in which a living polymer of a conjugated diene or vinyl aromatic hydrocarbon or copolymer of a conjugated diene and a vinyl aromatic hydrocarbon is prepared by anionically polymerizing the conjugated diene or vinyl aromatic hydrocarbon, or copolymerizing the conjugated diene and the vinyl aromatic hydrocarbon using a lithium-based catalyst and an inert hydrocarbon diluent. Then, the living polymer or copolymer is terminated by the addition of a suitable terminating agent. Following the termination procedure, boric acid is added to the polymer of copolymer in a sufficient amount to prevent or substantially reduce color formation. Then, stabilizing agents are added to the polymer or copolymer and the polymer or copolymer is recovered from the diluent.

Abstract: A process for preparing a fluorinated polymer having carboxylic ester groups from a corresponding polymer having carboxylic acid groups is disclosed, wherein the polymer having carboxylic acid groups is treated with a selected ortho ester, acetal, ketal, borate ester or sulfite ester. The process is useful for assuring that all of the carboxylate groups of a polymer are in the ester form before an extrusion or lamination procedure, both of which are performed with heat and pressure, so as to preclude decarboxylation of free carboxylic acid groups during such procedure.

Abstract: This invention relates to solid nonionic cross-linked resins containing amine or phosphine borane adducts capable of being used as reducing agents for metal ions, aldehydes, ketones, alkenes and the like.

Abstract: An improved process for curing a polyepoxide composition with a polycarboxylic acid or polycarboxylic acid anhydride is described wherein the addition of a diphenyliodonium salt accelerator provides for shortened curing reaction times at lower reaction temperatures or at room temperatures if the composition is exposed to a source of ultraviolet radiation.

Abstract: Certain aryloxyphosphonium salts have been found to be effective as curing agents for various cationically polymerizable organic materials, such as epoxy resins, when incorporated into such materials. The materials are found to be moisture curable coating compositions.

Abstract: Concentrates containing from 0.5% to 20% by weight of an alkali metal borohydride, balance essentially inert dry resinous polymer are added to plastics in amounts effective to reduce traces impurities and thereby result in improved heat and light stability.

Abstract: This invention relates to solid nonionic crosslinked resins containing amine or phosphine borane adducts capable of being used as reducing agents for metal ions, aldehydes, ketones, alkenes and the like.

Abstract: A range of titano-borate glass compositions e.g. for use as cross linking agents in the preparation of polycarboxylic acid cements. The glass may contain one or more further metal oxides, for example calcium and/or zinc, and typically comprises 25-40 mole % calcium, 45-65 mole % boric oxide and up to 15 mole % titanium dioxide. The specification also describes the preparation of polycarboxylic acid, typically polyacrylic acid, cements incorporating the glasses.

Abstract: The invention provides a method of treating hydrogels formed from the polymerization of monomers having reactive olefinic double bonds by contacting them with reactive thiol compounds. In a preferred embodiment where the hydrogel structure includes a cis-glycol containing unit, a suitable thiol is used in conjunction with a borate buffer. The present invention also provides materials that are treated with the above thiol compounds.

Abstract: A glass composition for effecting crosslinking of a polycarboxylic acid cement and cement compositions formed therefrom. The glass is of the aluminoborate type and comprises 40 to 75 mole % boric oxide, not more than 60 mole % zinc oxide, not more than 50 mole % calcium oxide and not more than 20 mole % alumina. Cements formed from the glasses have a wide range of applications including structural cements, dental filler and orthopaedic cements.