Polyacrylates poly

Polyacrylics" Poly(acrylic acid)" Poly(methacrylic acid) 1... 

Synonyms Acrylic acid homopolymer Acrylic acid polymer Acrylic acid, polymers Acrylic acid resin Acrylic polymer Acrylic polymer resins Acrylic resin Atactic poly(acrylic acid) PAA Polyacrylate Poly (acrylic acid) 2-Propenoic acid, homopolymer Propenoic acid polymer Propenoic acid, polymers, homopolymer IMinition Polymer of acrylic acid En rirical (CjHjOj),... 

Correia etal. also reported the surface tension [8] and temperature-dependent behavior [9] of a side-chain liquid crystalline polyacrylate (poly( 3-[4-(4-... 

Gelovoy, A., Cheung, M.R and Zimbo, M. (1989) Molecular weight degradation of polyacrylate during processing of polyacrylate/poly(phenylene sulfide) blends, Polym. Comm., 30,, 322—324. 

D. Klempner and H. L. Frisch, Thermal Analysis of Polyacrylate Poly(urethane urea) Interpenetrating Polymer Networks, J. Polym. Sci. Part B 8(7), 525 (1970). PU/poly-acrylate lENs. 

Most work has been with free-radical systems but other chemistries can be used. Begishev etal. studied frontal anionic polymerization of e-caprolactam [18, 19], and epoxy chemistry has been used as well [20-23]. Mariani ctal. demonstrated frontal ring-opening metathesis polymerization [17]. Fiori et al. produced polyacrylate-poly(dicydopentadiene) networks frontally [24], and Pojman etal. studied epoxy-acrylate binary systems [25]. Polyurethanes have been prepared frontally [13,14, 26]. Frontal atom transfer radical polymerization has been achieved [16] as well as FP with thiol-ene systems [27]. Recent work has been done using FP to prepare microporous polymers [28-30], polyurethane-nanosilica hybrid nanocomposites [31], and segmented polyurethanes [32]. 

Pressure-Sensitive Adhesives, e.g., natural and synthetic rubbers in conjunction with modified natural resins and/or synthetic resins also polyacrylates, poly(vinyl ethers). Uses nonspecific adhesion to virtually any surfaces, more particularly for the permanently tacky coating of tapes, films, and labels. 

As a result, viscosity modification, through the use of various soluble polymeric thickeners, represented the first attempt to modify the liquid properties of cyanoacrylates. Thickeners and fillers must be compatible with the cyanoacrylates and must not set off the easily triggered anionic cure. Polymers which have been used to increase the base viscosity of the monomers include polymethacrylates (the most common), poly acrylates, poly cyanoacrylates, poly vinylacetates, baked polyacrylics, poly lactic acid, cellulose nitrates and other esters such... 

Interest in superabsorbent polymers dates back to the 1960 s. Interest in synthetic absorbent polymers was increasing,and swellable polymers of most known water soluble monomers were prepared. Crosslinked poly(acrylamide), poly(N-vinyl-2-pyrrolidone), polyacrylates, poly(vinylalcohol) and poly(ethylene oxide) were evaluated as absorbents, as were the myriad copolymers and terpolymers possibly derived from combinations of the water soluble monomers under an enormous number of conditions. A variety of applications for them were also reported, including a claim for the use of swellable polymers as part of an absorbent article such as a diaper [1]. 

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