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2-hydroxyl propyl acrylate

Physical Constant 2-hydroxyl Ethyl Acrylate 2-hydroxyl Propyl Acrylate 2-hydroxyl Ethyl Methacrylate 2-hydroxyl Propyl Methacrylate Glycidyl Acrylate, Glycidyl Methacrylate... [Pg.437]

Common comonomers are those that place carboxylic, sulfonate, phosphite, polyethylene glycol, or hydrophobic groups along the backbone. They include maleic anhydride (subsequently hydrolyzed), sodium 2-acrylamido tert-butylsulfonic acid (Na-ATBS), sodium styrene sulfonate, l-allyloxy-2-hydroxypropyl sulfonate, l-allyloxy-2-hydroxypropyl phosphite, vinyl phosphonic acid, vinyl acrylate, polyethoxy acrylate, ethyl acrylate, methyl vinyl ether, and hydroxyl propyl acrylate [2,47-50]. [Pg.388]

Hydroxyl ethyl acrylate 2 hydroxy propyl methacrylate... [Pg.27]

ZnO-Acrylic nanocomposites are prepared by adding various amounts of 3-(trimethoxysilyl) propyl methacrylate (TPMA)-modified ZnO nanoparticles in 2 ml ethanol blended with methyl methacrylate (0.90 g), hydroxyl ethyl methacrylate (1.95 g), and trimethylolpropane triacrylate (1.77... [Pg.284]

Frequently, hydroxyl functional monomers are used as part of the copolymer with the hydroxy group providing the site for crosslinking with, for example, an amino crosslinker, when the coating is stoved. Two hydroxy functional types have been shown. Hydroxyl ethyl has a terminal (primary) hydroxyl group which is more reactive than the secondary hydroxy group on the hydroxy propyl chain. It is thus possible to get more rapid cure response by incorporation of hydroxy ethyl rather than hydroxy propyl functionality in the acrylic copolymer. This, however, may not always be advantageous as frequently rapid cure can lead to poor adhesion. [Pg.442]


See other pages where 2-hydroxyl propyl acrylate is mentioned: [Pg.170]    [Pg.85]    [Pg.153]    [Pg.214]    [Pg.67]    [Pg.692]    [Pg.210]   
See also in sourсe #XX -- [ Pg.437 ]




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Propyl acrylate

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