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Acrylonitrile-butyl acrylate copolymer

Brar and Sunita [58] described a method for the analysis of acrylonitrile-butyl acrylate (A/B) copolymers of different monomer compositions. Copolymer compositions were determined by elemental analyses and comonomers reactivity ratios were determined using a non-linear least squares errors-in-variables model. Terminal and penultimate reactivity ratios were calculated using the observed distribution determined from C( H)-NMR spectra. The triad sequence distribution was used to calculate diad concentrations, conditional probability parameters, number-average sequence lengths and block character of the copolymers. The observed triad sequence concentrations determined from C( H)-NMR spectra agreed well with those calculated from reactivity ratios. [Pg.177]

Regions of Methyl and Methylene Carbons of a 1-Butene-Propylene Copolymer [Pg.178]

Carbon Comonomer sequences Chemical shift differences, ppm [Pg.178]

Reprinted by permission of A. Aoki, T. Hayashi and T. Asakura, Macromolecules, 1992, 25, 1, 155. [Pg.178]

Yamada and co-workers [59] pointed out that spectroscopic methods such as IR spectroscopy and NMR spectroscopy previously used in sequencing studies on ethylene-propylene-diene and hydrogenated acrylonitrile butadiene rubbers often encountered the same difficulties experienced with the analysis of vulcanised rubbers, i.e., their insolubility. [Pg.180]


Tallow Tallow alcohol Tosylamide/formaldehyde resin VA/crotonates copolymer Vinyl acetate/butyl acrylate copolymer Vinyl acetate/crotonic acid copolymer Vinylidene chloride/acrylonitrile copolymer Vinylidene chloride/methyl acrylate copolymer Vinylidene chloride/vinyl chloride copolymer Zinc laurate paper/paperboard, dry food-contact Acrylamides copolymer Acrylates copolymer Alkenyl succinic anhydride Ammonium maleic anhydride/diisobutylene copolymer Ammonium nitrate... [Pg.5505]

Figure 5.10 C( F1)-NMR spectrum of acrylonitrile-w-butyl acrylate copolymer in CDCl3-DMSO-Dg mixture. Reproduced with permission from A.S. Brar and A. Sunita, Polymer, 1993, 34, 3391. 1993, Elsevier... Figure 5.10 C( F1)-NMR spectrum of acrylonitrile-w-butyl acrylate copolymer in CDCl3-DMSO-Dg mixture. Reproduced with permission from A.S. Brar and A. Sunita, Polymer, 1993, 34, 3391. 1993, Elsevier...
Studies of the particle—epoxy interface and particle composition have been helphil in understanding the mbber-particle formation in epoxy resins (306). Based on extensive dynamic mechanical studies of epoxy resin cure, a mechanism was proposed for the development of a heterophase morphology in mbber-modifted epoxy resins (307). Other functionalized mbbers, such as amine-terminated butadiene—acrylonitrile copolymers (308) and -butyl acrylate—acryhc acid copolymers (309), have been used for toughening epoxy resins. [Pg.422]

Acrylan-Rubber Butyl acrylate-acrylonitrile copolymer Monomer Corp... [Pg.657]

ASA structural latexes have been synthesized in a two stage seeded emulsion polymerization. In the first stage, partially crosslinked poly(n-butyl acrylate) and poly( -butyl acrylate-sfaf-2-ethylhexyl acrylate) rubber cores are synthesized. In the second stage, a hard styrene acrylonitrile copolymer (SAN) shell is grafted onto the rubber seeds (16). [Pg.333]

J.A. Herbig and 1.0. Salyer, Binary blends of styrene/acrylonitrile copolymer and butyl acrylate/acry-lonitrile copolymer and methods for preparing the same, US Patent 3118855, assigned to Monsanto Chemicals, January 21,1964. [Pg.345]

Copolymers of acrylonitrile and methyl acrylate and terpolymers of acrylonitrile, styrene, and methyl methacrylate are used as bamer polymers. Acrylonitrile copolymers and multipolymers containing butyl acrylate, ethyl aciylate, 2-ethylhexyl acrylate, hydroxyethyl acrylate, methyl methaciylate. vinyl acetate, vinyl ethers, and vinylidene chlonde are also used in bamer films, laminates, and coatings. Environmentally degradable polymers useful in packaging are prepared from polymerization of acrylonitrile with styrene and methyl vinyl ketone. [Pg.21]

ABA ABS ABS-PC ABS-PVC ACM ACS AES AMMA AN APET APP ASA BR BS CA CAB CAP CN CP CPE CPET CPP CPVC CR CTA DAM DAP DMT ECTFE EEA EMA EMAA EMAC EMPP EnBA EP EPM ESI EVA(C) EVOH FEP HDI HDPE HIPS HMDI IPI LDPE LLDPE MBS Acrylonitrile-butadiene-acrylate Acrylonitrile-butadiene-styrene copolymer Acrylonitrile-butadiene-styrene-polycarbonate alloy Acrylonitrile-butadiene-styrene-poly(vinyl chloride) alloy Acrylic acid ester rubber Acrylonitrile-chlorinated pe-styrene Acrylonitrile-ethylene-propylene-styrene Acrylonitrile-methyl methacrylate Acrylonitrile Amorphous polyethylene terephthalate Atactic polypropylene Acrylic-styrene-acrylonitrile Butadiene rubber Butadiene styrene rubber Cellulose acetate Cellulose acetate-butyrate Cellulose acetate-propionate Cellulose nitrate Cellulose propionate Chlorinated polyethylene Crystalline polyethylene terephthalate Cast polypropylene Chlorinated polyvinyl chloride Chloroprene rubber Cellulose triacetate Diallyl maleate Diallyl phthalate Terephthalic acid, dimethyl ester Ethylene-chlorotrifluoroethylene copolymer Ethylene-ethyl acrylate Ethylene-methyl acrylate Ethylene methacrylic acid Ethylene-methyl acrylate copolymer Elastomer modified polypropylene Ethylene normal butyl acrylate Epoxy resin, also ethylene-propylene Ethylene-propylene rubber Ethylene-styrene copolymers Polyethylene-vinyl acetate Polyethylene-vinyl alcohol copolymers Fluorinated ethylene-propylene copolymers Hexamethylene diisocyanate High-density polyethylene High-impact polystyrene Diisocyanato dicyclohexylmethane Isophorone diisocyanate Low-density polyethylene Linear low-density polyethylene Methacrylate-butadiene-styrene... [Pg.958]

Effect of Molecular Structure. Table III shows the effects of the molecular structure of the liquid polymer on the fracture energy of toughened systems. The CTIN is a carboxyl terminated isoprene-acrylonitrile copolymer CTBS is a carboxyl terminated butadiene and styrene copolymer, and CTA is a copolymer of ethyl acrylate-butyl acrylate. [Pg.334]

Mercapto-terminated block copolymers and block terpolymers prepared by Tsuji [4] such as poly(acrylonitrile-b-butyl acrylate) and poly(acrylonitrile-b-butyl acrylate-b-ethyl acrylate), respectively, used the RAFT chain transfer agent cumyl dithiobenzoate. The block copolymer had a M of48,600 daltons. [Pg.590]

Liquid polymers are useful as tackifiers for rubbers, 72) and acrylic coatings. The most interesting are hydroxytelechelic polybutadienes, especially liquid butadiene-acrylonitrile (85/15) copolymers (trademark CN-15, ARCO). This product, known since 1971 as a tackifier, has the following characteristics viscosity 493 poises at 30 °C, tv[n = 4400, hydroxyl number/chain = 2.5. The incorporation of 5% of CN-15 in ethylene-propylene rubber (EPT Nordel 1070) increases its tack considerably 173) close to that of natural rubber or butyl rubbers (Table 4.1). [Pg.209]

Samples tested were styrene copolymers of methacrylates, acrylates, vinyl acetate, and acrylonitrile, in addition to ethyl methacrylate-butyl methacrylate copolymers. These samples were dissolved in the initial mobile phase and the injection volume was 0.05-0.2 mL. These samples were prepared by solution polymerization at low conversion and have rather narrow CCD. These samples are random (statistical) copolymers. [Pg.215]

The paint studied is a typical automotive thermosetting enamel which consists of an epoxy functional acrylic copolymer and butylated melamine crosslinking agent. The acrylic copolymer is composed of methyl methacrylate, n-butyl methacrylate, n-butyl acrylate, styrene, acrylonitrile, 2-ethyl hexyl acrylate and 2-hydroxyethyl methacrylate. Carbon black was used as the pigment. [Pg.412]

In ASA terpolymer acrylic acid brings more flexibility and the material has very good mechanical properties and weather resistance. For these reasons ASA is extensively used in automotive industry and in the fabrication of various appliances. Even more frequently than acrylic acid itself, various acrylates are used in copolymers. Among these can be mentioned the copolymers of acrylic acid esters with methacrylic acid esters such as poly(methyl methacrylate-co-methyl acrylate), poly(methyl methacrylate-co-ethyl acrylate), poly(methyl methacrylate-co-butyl acrylate), poly(ethyl methacrylate-co-ethyl acrylate), poly(acrylonitrile-co-methyl acrylate), poly(alkyl acrylate-co-methyl methacrylates), and poly(alkyl acrylate-co-hydroxyethyl methacrylates) where alkyl can be methyl, ethyl, butyl, etc. Some literature information regarding thermal decomposition of copolymers including acrylic acid and acrylic acid esters is given in Table 6.7.8 [6],... [Pg.358]

A random copolymer of styrene and acrylonitrile exhibited a 20 C higher use temperature than that of polystyrene a random copolymer of styrene with butyl acrylate was more flexible than the styrene homopolymer. [Pg.220]


See other pages where Acrylonitrile-butyl acrylate copolymer is mentioned: [Pg.177]    [Pg.177]    [Pg.497]    [Pg.121]    [Pg.246]    [Pg.90]    [Pg.415]    [Pg.253]    [Pg.473]    [Pg.196]    [Pg.509]    [Pg.417]    [Pg.422]    [Pg.489]    [Pg.192]    [Pg.509]    [Pg.212]    [Pg.284]    [Pg.2533]    [Pg.417]    [Pg.422]    [Pg.42]    [Pg.153]    [Pg.415]    [Pg.220]    [Pg.509]   


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Acrylic copolymers

Acrylonitrile copolymers

Acrylonitrile-butyl Acrylate

Butyl Acrylate

Copolymer acrylate

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