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Complexation of poly(dimethylsiloxane)/poly(methyl methacrylate‐ co ‐butyl acrylate‐ co ‐methacrylic acid) latex with poly(dimethylsiloxane)/poly(vinyl acetate‐ co ‐butyl acrylate) latex
Author(s) -
Yang Mingjiao,
Dan Yi
Publication year - 2004
Publication title -
journal of applied polymer science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.575
H-Index - 166
eISSN - 1097-4628
pISSN - 0021-8995
DOI - 10.1002/app.20212
Subject(s) - materials science , polymer chemistry , copolymer , methyl methacrylate , butyl acrylate , emulsion polymerization , vinyl acetate , methacrylic acid , acrylate , methacrylate , ultimate tensile strength , polymer , composite material
Two latices—the poly(dimethylsiloxane) (PDMS)/poly(methyl methacrylate‐ co ‐butyl acrylate‐ co ‐methacrylic acid) system (PA latex) and the PDMS/poly(vinyl acetate‐ co ‐butyl acrylate) system (PB latex)—were prepared by seeded emulsion polymerization, and PA/PB complex latices were obtained through the interparticle complexation of the PA latex with the PB latex. In addition, for the further study of the interparticle complexation of the PA latex with the PB latex, copolymer latices [PDMS/methyl methacrylate‐ co ‐butyl acrylate‐ co ‐vinyl acetate‐ co ‐methacrylic acid) (PC)] were prepared according to the monomer recipe of the complex latices and the polymerization process of the component latices. The properties of the obtained polymer latices and complex latices were investigated with surface‐tension, contact‐angle, and viscosity measurements. The mechanical properties of the coatings obtained from the latices were investigated with tensile‐strength measurements. The results showed that, in comparison with the two component latices (PA latex and PB latex) and the corresponding copolymer latices (PC latices), the PA/PB complex latices had lower surface tension, lower viscosities, and better wettability to different substrates. The tensile strengths of the coatings obtained from the complex latices were higher than the tensile strengths of the coatings from the two component latices and copolymer latices. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 92: 2522–2527, 2004

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