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Acrylate Polyacrylate specific

The combination of durability and clarity and the ability to tailor molecules relatively easily to specific applications have made acryflc esters prime candidates for numerous and diverse applications. At normal temperatures the polyacrylates are soft polymers and therefore tend to find use in applications that require flexibility or extensibility. However, the ease of copolymerizing the softer acrylates with the harder methacrylates, styrene, acrylonitrile, and vinyl acetate, allows the manufacture of products that range from soft mbbers to hard nonfilm-forming polymers. [Pg.171]

One is still however left with the problem of why, since poly(methyl acrylate) contains the highest carbonyl group concentration of all polyacrylates, does it show an unfavourable heat of mixing The answer lies in the neglection of contributions from dispersive forces. If one assumed that the dispersive and specific contributions could be separated. [Pg.155]

The above criteria were employed to select several commercially supplied Class PS elastomers for laboratory screening by employing selected tests taken from National Bureau of Standards NBSIR 77-1437(j4) and ANSI/ASTM D-3667-78 specifications for "Rubber Seals Used in Flat-Plate Solar Collectors". Four silicone, three EPDM, two fluorocarbon, three epichlorohydrin, one ethylene-acrylic, one polyacrylic, one chlorosulfonated polyethylene, one bromobutyl and two butyl rubbers were studied in these screening tests. These materials are identified in Table I and those compositions which were revealed by their manufacturers are shown in Table II. Undoubtedly some materials which should have been included were omitted however, we hope that this sampling will provide an indication of the applicability of a wide range of materials for use as sealants in thermal solar collectors. [Pg.48]

Some specific recent applications of the chromatography-mass spectrometry technique to various types of polymers include the following PE [130, 131], poly(l-octene), poly(l-decene), poly(l-dodecene) and 1-octene-l-decene-l-dodecene terpolymer [132], chlorinated polyethylene [133], polyolefins [134,135], acrylic acid, methacrylic acid copolymers [136, 137], polyacrylate [138], styrene-butadiene and other rubbers [139-141], nitrile rubber [142], natural rubbers [143,144], chlorinated natural rubber [145,146], polychloroprene [147], PVC [148-150], silicones [151,152], polycarbonates (PC) [153], styrene-isoprene copolymers [154], substituted PS [155], polypropylene carbonate [156], ethylene-vinyl acetate copolymer [157], Nylon 6,6 [158], polyisopropenyl cyclohexane-a-methylstyrene copolymers [195], cresol-novolac epoxy resins [160], polymeric flame retardants [161], poly(4-N-alkylstyrenes) [162], pol)winyl pyrrolidone [31,163], vinyl pyrrolidone-methacryloxysilicone copolymers [164], polybutylcyanoacrylate [165], polysulfide copolymers [1669], poly(diethyl-2-methacryloxy) ethyl phosphate [167, 168], ethane-carbon monoxide copolymers [169], polyetherimide [170], and bisphenol-A [171]. [Pg.125]

This process exploits an imusual effect of the difference in solubility of acrylic acid monomer and polyacrylic acid in specific solvents. When products based on the process were first developed [4] and made commercially available, benzene was used as the polymerisation medium. The polymerisation reaction is initiated in a system containing a mixture of acrylic acid monomer and a cross-linking monomer (typically a multi-allyl ether derivative of sucrose or pentaeryrthritol) and, as the polymer network grows, the solubility in the solvent decreases until precipitation of the polymer network occurs in the form of a small particle size powder. The use of a cross-linking monomer results in a 3D network of... [Pg.39]

The carboxylic polyacrylates are effective as laminating adhesives for both flexible and rigid surfaces. The particular carboxylic acrylate used for a given laminating application is determined by the characteristics of the surfaces to be adhered, whether adhesive or cohesive bond failure is desired, the bond strength required of the adhesive, and many other factors. These may include stiffness, friability, extensibility, clarity, cold flow, moisture resistance, solvent or chemical resistance, heat and light insensitivity, radiation resistance, compatibility with resins and other polymeric materials or pigments, and vulcanizability. The carboxylic polyacrylates may be varied to meet the adhesive requirements of a specific application by ... [Pg.278]


See other pages where Acrylate Polyacrylate specific is mentioned: [Pg.97]    [Pg.323]    [Pg.38]    [Pg.156]    [Pg.157]    [Pg.857]    [Pg.263]    [Pg.323]    [Pg.1236]    [Pg.390]    [Pg.187]    [Pg.156]    [Pg.586]    [Pg.507]    [Pg.549]    [Pg.63]    [Pg.314]    [Pg.135]    [Pg.2198]    [Pg.63]    [Pg.109]    [Pg.478]    [Pg.395]    [Pg.114]    [Pg.189]    [Pg.1305]    [Pg.16]    [Pg.43]    [Pg.66]    [Pg.157]    [Pg.177]    [Pg.265]    [Pg.37]    [Pg.1714]    [Pg.31]    [Pg.200]   


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