2.
    发明专利
    未知

    公开(公告)号:NO133842C

    公开(公告)日:1976-07-07

    申请号:NO15853365

    申请日:1965-06-16

    Abstract: Solutions of a polymer of at least one a ,b -olefinically unsaturated nitrile monomer and a polyalkenyl monomer in a polar solvent are useful in making films. Preferably the nitrile monomer is acrylonitrile, methacrylonitrile, a -chloroacrylonitrile, crotononitrile or vinylidene cyanide. The polyakenyl monomer preferably contains at least two CH2=C= groups separated by at least one other group, e.g. allyl or methallyl esters of unsaturated carboxylic acids, polyacrylates, -methacrylates or -maleates, divinyl or di(meth)allyl ether, diallyl or triallyl compounds, dienes (non-conjugated), divinyl or trivinyl compounds, diisopropenylbenzene, tetra-allyl or -vinyl compounds, diallyl vinyl silane, tri(meth)acryloyl-perhydrotriazine, bisacrylamides, (meth)allyl-substituted methacrylamide and poly-allyl or -vinyl ethers of polyhydroxy compounds; these monomers are preferably used in proportions of 0.05-5 parts by weight per 100 parts of nitrile monomer. If desired, up to 5 to 15% by weight of the nitrile monomer can be replaced by one or more mono-alkenyl monomers copolymerizable therewith. Preferred solvents include a dimethyl formamide - ethylene carbonate mixture, and nitro-ethane. Also listed are other amides, thio-amides, cyano-amides, methyl pyrrolidone, butyrolactone, tetramethyloxamide, lactams, tetracyanopentane, dimethylcyanamide, N-formyl compounds, sulphones, nitromethane, ethylene cyanohydrin, nitriles, dimethylaminophosphine oxide and tetramethyl-methane-phosphonamide. Instead of the organic solvents, inorganic salt solution systems may be used. Aqueous solutions of (substituted) guanidine thiocyanate are also suitable as solvents. The film-forming polymers may be prepared by batch, bulk, solution or suspension polymerization techniques but preferably are made in an aqueous medium in the presence of a redox catalyst composed of a water-soluble peroxygen compound, e.g. a persulphate, and an oxidizable sulphur compound, e.g. sodium meta-bisulphite, as promoter. A mercaptan may also be present. Preferably the co-polymers are made in two steps, the first step comprising the co-polymerization of a portion of the a ,b -olefinically unsaturated nitrile and all of the polyalkenyl monomer to high conversion, the second step comprising polymerizing (e.g. to 70-100% conversion) the remainder of the nitrile monomer, which may be added all at once or in increments, on to or in the presence of the polymer "seed" thus formed in the first step. Emulsifiers, surface-active agents or dispersing agents may be used throughout both the seed step and the main polymerization step. Examples illustrate solutions, and preparation, of copolymers of acrylonitrile with butanediol divinyl ether, tetramethylene diacrylate or divinyl benzene, and a copolymer of methacrylonitrile with tetramethylene diacrylate.

    3.
    发明专利
    未知

    公开(公告)号:DK142953B

    公开(公告)日:1981-03-02

    申请号:DK543371

    申请日:1971-11-05

    Inventor: COFFEY G P BALL L E

    Abstract: 1360685 Graft polymers STANDARD OIL CO 21 Oct 1971 [13 Nov 1970] 48958/71 Heading C3G A graft polymer is produced by polymerization of (A) from 70 to 85% by weight of an olefinically unsaturated nitrile, (B) 2 to 13% of an alpha-olefin of structure wherein R 1 and R 11 are C 1 to C 7 -alkyl groups, (C) 2 to 30% of a monomer selected from a vinyl ester, acrylate ester, an acrylamide or a methacrylate ester, and (D) up to 17% of a vinyl or vinylidene aromatic monomer, wherein the combined amount of (A)+(B)+(C)+(D) is 100%, in the presence of from 1 to 30 parts by weight per 100 parts of (A) + (B) + (C)+(D) of (E) a rubbery polymer of 50 to 100% by weight of polymerized conjugated diene monomer and 50 to 0% of a polymerized vinyl or vinylidene aromatic monomer. In the examples, graft polymers are prepared in aqueous emulsion from (a) butadiene-styrene rubber or polybutadiene, acrylonitrile, isobutylene, styrene and methyl acrylate, N-t-octyl acrylamide, N-t-butyl acrylamide or vinyl acetate and (b) polybutadiene, acrylonitrile, diisobutylene, styrene and methyl acrylate.

    4.
    发明专利
    未知

    公开(公告)号:SE7709434L

    公开(公告)日:1978-02-24

    申请号:SE7709434

    申请日:1977-08-22

    Abstract: Process for preparing low molecular weight, light weight and high molecular weight xylene-formaldehyde thermoplastic polymers, comprising reacting formaldehyde or a formaldehyde producing material with xylene in the presence of an acid catalyst at an elevated temperature in a closed reactor of the which excludes air during the reaction. (Machine-translation by Google Translate, not legally binding)

    5.
    发明专利
    未知

    公开(公告)号:SE7701568L

    公开(公告)日:1977-08-14

    申请号:SE7701568

    申请日:1977-02-11

    Abstract: Polymeric compositions having good impact resistance, low permeability to gases, and high-softening temperatures which are composed of a conjugated diene monomer, such as butadiene, an olefinically unsaturated nitrile, such as acrylonitrile, an alpha-olefin, such as isobutylene, and indene are described.

    XYLENE-FORMALDEHYDE RESINS AND COMPOSITIONS

    公开(公告)号:AU508354B2

    公开(公告)日:1980-03-20

    申请号:AU2777677

    申请日:1977-08-10

    Abstract: Process for preparing low molecular weight, light weight and high molecular weight xylene-formaldehyde thermoplastic polymers, comprising reacting formaldehyde or a formaldehyde producing material with xylene in the presence of an acid catalyst at an elevated temperature in a closed reactor of the which excludes air during the reaction. (Machine-translation by Google Translate, not legally binding)

    8.
    发明专利
    未知

    公开(公告)号:NO133842B

    公开(公告)日:1976-03-29

    申请号:NO15853365

    申请日:1965-06-16

    Abstract: Solutions of a polymer of at least one a ,b -olefinically unsaturated nitrile monomer and a polyalkenyl monomer in a polar solvent are useful in making films. Preferably the nitrile monomer is acrylonitrile, methacrylonitrile, a -chloroacrylonitrile, crotononitrile or vinylidene cyanide. The polyakenyl monomer preferably contains at least two CH2=C= groups separated by at least one other group, e.g. allyl or methallyl esters of unsaturated carboxylic acids, polyacrylates, -methacrylates or -maleates, divinyl or di(meth)allyl ether, diallyl or triallyl compounds, dienes (non-conjugated), divinyl or trivinyl compounds, diisopropenylbenzene, tetra-allyl or -vinyl compounds, diallyl vinyl silane, tri(meth)acryloyl-perhydrotriazine, bisacrylamides, (meth)allyl-substituted methacrylamide and poly-allyl or -vinyl ethers of polyhydroxy compounds; these monomers are preferably used in proportions of 0.05-5 parts by weight per 100 parts of nitrile monomer. If desired, up to 5 to 15% by weight of the nitrile monomer can be replaced by one or more mono-alkenyl monomers copolymerizable therewith. Preferred solvents include a dimethyl formamide - ethylene carbonate mixture, and nitro-ethane. Also listed are other amides, thio-amides, cyano-amides, methyl pyrrolidone, butyrolactone, tetramethyloxamide, lactams, tetracyanopentane, dimethylcyanamide, N-formyl compounds, sulphones, nitromethane, ethylene cyanohydrin, nitriles, dimethylaminophosphine oxide and tetramethyl-methane-phosphonamide. Instead of the organic solvents, inorganic salt solution systems may be used. Aqueous solutions of (substituted) guanidine thiocyanate are also suitable as solvents. The film-forming polymers may be prepared by batch, bulk, solution or suspension polymerization techniques but preferably are made in an aqueous medium in the presence of a redox catalyst composed of a water-soluble peroxygen compound, e.g. a persulphate, and an oxidizable sulphur compound, e.g. sodium meta-bisulphite, as promoter. A mercaptan may also be present. Preferably the co-polymers are made in two steps, the first step comprising the co-polymerization of a portion of the a ,b -olefinically unsaturated nitrile and all of the polyalkenyl monomer to high conversion, the second step comprising polymerizing (e.g. to 70-100% conversion) the remainder of the nitrile monomer, which may be added all at once or in increments, on to or in the presence of the polymer "seed" thus formed in the first step. Emulsifiers, surface-active agents or dispersing agents may be used throughout both the seed step and the main polymerization step. Examples illustrate solutions, and preparation, of copolymers of acrylonitrile with butanediol divinyl ether, tetramethylene diacrylate or divinyl benzene, and a copolymer of methacrylonitrile with tetramethylene diacrylate.

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