DIALLYL CHLORIDE COPOLYMER

Another use is of minor proportions of polyfunctional aUyl esters, eg, diallyl maleate, triallyl cyanurate, and triaUji isocyanurate, for cross-linking or curing preformed vinyl-type polymers such as polyethylene and vinyl chloride copolymers. These reactions are examples of graft copolymerization in which specific added peroxides or high energy radiation achieve optimum cross-linking (see Copolymers). [Pg.80]

Use of diallyl phthalate and diallyl maleate copolymers with vinyl chloride as rubbery sealants [135]. [Pg.327]

Synonyms Acrylamide-diallyidimethyl ammonium chloride Acrylamide/dimethyl-diallyl ammonium chloride copolymer Diallyidimethyl ammonium chloride with acrylamide N,N-Dimethyl-N-2-propenyl-2-propen-1-aminium chloride, polymer with 2-propenamide Poly (acrylamide-co-diallyidimethyl ammonium chloride) 2-... [Pg.2373]

Fig. 1. Functional monomers used in acrylamide copolymers. Methacrylamidopropyltrim ethyl ammonium chloride [51410-72-1] (1), acryloyloxyethyltrimethylammonium chioride [44992-01-0] (2), methacryloyloxyethyltrimethylammonium chloride [50339-78-1] (3), /V,/V-dimethy1aminoethy1 methacrylate [2867-47-2] (4), /V,/V-dimethylaminopropy1 acryl amide [3845-76-9] (5), diallyl dimethyl amm onium chloride...

Copolymers of diallyl dimethyl ammonium chloride [7398-69-8] with acrylamide have been used in electroconductive coatings (155). Copolymers with acrylamide made in activated aqueous persulfate solution have flocculating activity increasing with molecular weight (156). DADM ammonium chloride can be grafted with cellulose from concentrated aqueous solution catalysis is by ammonium persulfate (157). Diallyl didodecylammonium bromide [96499-24-0] has been used for preparation of polymerized vesicles (158). [Pg.88]

The extent of hydrolysis of the copolymers was determined by conductometric titration. The increase in carboxylate content was determined by difference, before and after hydrolysis. (The AMPS content of the polymers, where measured, was determined by colloid titration with poly [diallyl dimethyl ammonium chloride].)... [Pg.109]

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]

Although they lack commercial importance, many other poly(vinyl acetal)s have been synthesized. These include acetals made from vinyl acetate copolymerized with ethylene (43—46), propylene (47), isobutylene (47), acrylonitrile (48), acrolein (49), acrylates (50,47), allyl ether (51), divinyl ether (52), maleates (53,54), vinyl chloride (55), diallyl phthalate (56), and starch (graft copolymer) (47). [Pg.450]

FIG. 7 Ionic strength (7) dependence of the protein global charge at the onset of complexation (Zpr)c in bovine serum albumin and polyelectrolyte mixtures (type 1 titrations). PMAPTAC poly(acrylamidopropyl trimethylammonium) chloride PAMPS poly(acrylamido methylpropylsulfonate) PAMPS(8) copolymer of AMPS and 20 mol% acrylamide PDADMAC poly(diallyl dimethylammonium) chloride. (Reprinted with permission from Ref. 22. Copyright 1998 American Chemical Society.)... [Pg.698]

Creme rinses and most hair conditioners are basically compositions containing cationic surfactant in combination with long chain fatty alcohol or other lipid components. Distearyldimonium chloride, cetrimonium chloride, stearalkonium chloride, and behentrimonium methosulfate are typical cationic surfactants used in many of today s hair conditioning products. Amines like dimethyl stearamine or stearamidopropyl dimethylamine are other functional cationics used in these products. Cationic polymers such as Polyquaternium-10 (quaternized ceUulosic) and Polyquatemium-7 (copolymer of diallyl dimethyl ammonium chloride and acrylamide) are also used (more in shampoos than in hair conditioners) however, care must be taken to avoid buildup on hair when formulating with cationic polymers. See the section on Cationic Polymers and Their Interactions with Hair in Chapter 7. [Pg.204]

Cationic polymers such as polymer JR (polyquaternium-10), a quater-nized cellulosic ingredient [6] cationic guar, a quaternized polymer of galactose Merquat polymers (polyquaternium-6 and -7) copolymers of dimethyl diallyl ammonium chloride and acrylamide [7] and Gafquat polymers (polyquaternium-11) (copolymer of polyvinyl pyrrolidone and dimethy-laminoethyl methacrylate) [8] have all been used and are currently used in conditioning shampoos, setting lotions, or mousses. [Pg.208]

A limitation is, however, encountered with Noryl resins indeed, because PS is a very brittle material, their impact strength decreases when the percentage of PS is raised [37]. To circumvent this problem, rubbers are added to Noryl resins to increase the toughness [39]. Thanks to the exceptional blending properties of PPO , numerous mixed materials have been developed, for instance, with diallyl phthalates, polysulfone, acrylates, coumarone-indene, or polyvinyl chloride (PVC) [39]. It has also been shown that PPO could be blended with styrene-butadiene block copolymers, hence allowing to expand the temperature of use of the resulting materials [40]. Accordingly, the combination of various... [Pg.103]

Propanone oxime. See Acetone oxime Propathene. See Polypropylene Propenamide 2-Propenamide. See Acrylamide 2-Propenamide, N-(3-(dimethylamino) propyl)-2-methyl-. See Dimethyl amlnopropylmethacrylamide 2-Propenamide, homopolymer. See Polyacrylamide Propenamide, polymer with propenoic acid, butenoic acid, and/or alkyl propenoates. SeeAcrylates/acrylamlde copolymer 2-Propen-1-aminium, N,N-dimethyl-N-2-propenyl-, chloride. See Dimethyl diallyl ammonium chloride Propeneacid. See Acrylic acid 1-Propene, homopolymer. See Polypropylene... [Pg.1319]

Diallyl dimethyl ammonium chloride. See Dimethyl diallyl ammonium chloride Diallyidimethyl ammonium chloride with acrylamide. See Polyquatemium-7 Diallyidimonium chloride/hydroxyethylcellulose copolymer. See Polyquatemium-4 Diallyl disulfide. See Allyl disulfide Diallyl ester acetic acid. See Diacetone acrylamide Diallyl fumarate CAS 2807-54-7... [Pg.1200]

Chemical Description Copolymer of sodium acrylate and dimethyl diallyl ammonium chloride... [Pg.650]

The free radical polymerizations of 3-[(2-Acrylamido-2-mefliyl propyl)dimethylammonio]-l-propanesulfonate with acrylamide and/or acrylic acid, and 3-(i Tj -diallyl-i /-methylammonio)-l-propanesulfonate with A, iV diailyl-i, iV-dimethyl ammonium chloride or AT,A/-diallyl-iV,-methyl amine have been studied. Reactivity ratios indicate random incorporation of comonomers. Molecular weights range from 3.0 x 10 to 15.1 x 10 g mol for the acrylamido-based copolymers and from 2.2 x 10 to 6.0 x 10 g mol for the cyclocopolymers. Second virial coefficients and viscosities decrease as sulfobetaine content increa s for each of the copolymers. A transition from polyelectrolyte to polyampholyte behavior is observed with added NaCl for those copolymers with sulfobetaine monomer incorporation greater than 40 mol%... [Pg.12]

Kriz J, Dybal J, Dautzenberg H (2001) Cooperative interactions of unlike macromolecules 3. NMR and theoretical study of the electrostatic coupling of sodium polyphosphates with diallyl(dimethyl)ammonium chloride-acrylamide copolymers. J Phys Chem A 105 7486-7493. doi 10.1021/jp010185b... [Pg.90]

Gartner HA. Process for the production of high molecular weight copolymers of diallyl dimethyl ammonium chloride and acrylamide in an aqueous dispersed phase. European patent 363024. 1988. [Pg.393]

Chem. Descrip. Diallyl dimethyl ammonium chloride/acrylamide copolymer and acrylamidopropyltrimonium chloride/acrylamide copolymer aq. blend Ionic Nature Cationic Chem. Analysis 18% solids CAS 26590-05-6... [Pg.1161]

Dimethyl diallyl ammonium chloride deposit control agent Styrene/MA copolymer, suHbnated deposit control agent, boiler water treatment Versa-TL 4... [Pg.2576]

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