Acrylonitrile butadiene styrene terpolymer

Property Polystyrene (PS) Poly(styrene-i) (j-acrjio-nitrile ) (SAN) Glass-fil led PS High impact PS HIPS Acrylonitrile— butadiene—styrene terpolymer (ABS) Type 1 Type 2 Standard ABS Super ABS... [Pg.503]

NOVODUR P2 HAT BAYER General purpose acrylonitrile-butadiene-styrene terpolymer... [Pg.324]

Sullvac Acrylonitrile butadiene styrene terpolymer O Sullivan Rubber Corp. [Pg.683]

ABS Acrylonitrile-butadiene-styrene terpolymer CA Cellulose acetate... [Pg.728]

Polycarbonate is blended with a number of polymers including PET, PBT, acrylonitrile-butadiene-styrene terpolymer (ABS) rubber, and styrene-maleic anhydride (SMA) copolymer. The blends have lower costs compared to polycarbonate and, in addition, show some property improvement. PET and PBT impart better chemical resistance and processability, ABS imparts improved processability, and SMA imparts better retention of properties on aging at high temperature. Poly(phenylene oxide) blended with high-impact polystyrene (HIPS) (polybutadiene-gra/f-polystyrene) has improved toughness and processability. The impact strength of polyamides is improved by blending with an ethylene copolymer or ABS rubber. [Pg.143]

Most acrylonitrile-butadiene styrene terpolymer (ABS) is produced as a graft of SAN onto a butadiene polymer backbone. This graft copolymer may be blended with more SAN or acrylonitrile elastomer (NBR) to improve its properties. ABS is more ductile than SAN. The Tt and the heat deflection temperature of ABS vary with the composition, and ABS may have one set of values for the PBD domains and another set for the SAN matrix. The permeabilities of ABS to oxygen, nitrogen, and carbon dioxide are much less than those of hope. [Pg.149]

B.M. Rao, P.R. Rao, and B. Sreenivasulu, Grafting of maleic anhydride onto acrylonitrile-butadiene-styrene terpolymer Synthesis and characterization, Polym.-Plast. Technol. Eng., 38(5) 967-977, November 1999. [Pg.259]

R. Qi, J. Qian, and C. Zhou, Modification of acrylonitrile-butadiene-styrene terpolymer by grafting with maleic anhydride in the melt. I. Preparation and characterization, J. Appl. Polym. Sci., 90(5) 1249-1254, October 2003. [Pg.259]

R. Qi, Z. Chen, and C. Zhou, Solvothermal preparation of maleic anhydride grafted onto acrylonitrile-butadiene-styrene terpolymer (ABS), Polymer, 46(12) 4098-4104, May 2005. [Pg.259]

C. Deacon and C.A. Wilkie, Graft copolymerization of acrylic acid on to acrylonitrile-butadiene-styrene terpolymer and thermal analysis of the copolymers, Eur. Polym. J., 32(4) 451-455, April 1996. [Pg.259]

Z. Zhou, N. Liu, and H. Huang, Reactivity of acrylonitrile-butadiene-styrene terpolymer grafted with long-chain unsaturated carboxylic acids, Polymer, 45(21) 7109-7116, September 2004. [Pg.259]

Z.F. Zhou, H. Huang, and N.C. Liu, Kinetics and mechanism of grafting of undecylenic acid onto acrylonitrile-butadiene-styrene terpolymer,. Polym. Sci., Part A Polym. Chetti., 39(4) 486-494, February 2001. [Pg.259]

G.T.K. Fey, D.C. Lee, and Y.Y. Lin, High-capacity carbons prepared from acrylonitrile-butadiene-styrene terpolymer for use as an anode material in lithium-ion batteries, J. Power Sources, 119-121 39-44, June 2003. [Pg.264]

M.-H. Yang, The thermal degradation of acrylonitrile-butadiene-styrene terpolymer under various gas conditions, Polym. Test., 19(1) 105-110, February 2000. [Pg.266]

Chemical processes are far more varied and may involve either the formation of radicals or ions along a polymeric backbone. Both cationic processes3 as well as radical processes have been widely used for graft copolymerization of vinyl monomers onto various polymers. Radical graft copolymerization has been reported for many polymers including styrene-butadiene block copolymers, and acrylonitrile-butadiene-styrene terpolymer, ABS.3 7 9... [Pg.109]

ID IQ 2D 2D-NMR 2h2o 2Q 3Q 9BEN A1 ABS AC ACM ACN AFM Al-CSM ALMA-i5 Al-m-EPDM AN AO APT ASTM ATR ATR-IR B/S BABA Two-dimensional Single-quantum One-dimensional Deuteron solid-state NMR Deuterated water Double-quantum Triple-quantum 9 borobicyclo [3, 3, 1] nonane Amide 1 Acrylonitrile-butadiene-styrene terpolymer Accelerator Acrylate rubber Acrylonitrile Atomic Force Microscopy Aluminium salt of chlorosulfonate polyethylene Allyl-rf5 methacrylate Aluminium salt of maleated EPDM Acrylonitrile 1-Allyl oxyoctane Attached Proton Test American Standards for Testing and Materials Attenuated total reflectance spectroscopy Attenuated total reflectance-IR spectroscopy Butadiene/styrene Back-to-back... [Pg.597]

N,N -bis-l,4-(l,4-dimethylpentyl)-p-phenylendiamine acrylonitrile butadiene styrene terpolymer atomic force microscopy atactic... [Pg.3]

Various patents on the homopolymerization of BD in the presence of styrene are available [581-590]. According to these patents, St is used as a solvent in which BD is selectively polymerized by the application of NdV/DIBAH/EASC. At the end of the polymerization a solution of BR in St is obtained. In subsequent reaction steps the unreacted styrene monomer is either polymerized radically, or acrylonitrile is added prior to radical initiation. During the subsequent radical polymerization styrene or styrene/acrylonitrile, respectively, are polymerized and ris-l,4-BR is grafted and partially crosslinked. In this way BR modified (or impact modified) thermoplast blends are obtained. In these blends BR particles are dispersed either in poly(styrene) (yielding HIPS = high impact poly(styrene) or in styrene-acrylonitrile-copolymers (yielding ABS = acrylonitrile/butadiene/ styrene-terpolymers). In comparison with the classical bulk processes for HIPS and ABS, this new technology allows for considerable cost reductions... [Pg.98]

During weathering, phenolic antioxidants are photooxidized into hydroperoxycy-clohexadienones, such as 59 (Pospisil, 1993 Pospisil, 1980). The presence of peroxidic moieties in 57 and 59 renders them thermolabile at temperatures exceeding 100 °C and photolysable under solar UV radiation. Both processes account for homolysis of the peroxidic moieties. As a result, the oxidative degradation of the polymeric matrix is accelerated by formed free-radical fragments (tests were performed with atactic polypropylene and acrylonitrile-butadiene-styrene terpolymer (ABS) (PospiSil, 1981 PospiSil, 1980). Low-molecular-weight products of homolysis, such as 60 to 63 are formed in low amounts. [Pg.69]

Cycolac Acrylonitrile-butadiene-styrene terpolymer ABS Borg-Wamer... [Pg.941]

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