Synthesis and characterization of model carboxylated latexes for studies of film formation from latex blends

Citation
Js. Tang et al., Synthesis and characterization of model carboxylated latexes for studies of film formation from latex blends, J APPL POLY, 77(3), 2000, pp. 644-659
Citations number
20
Categorie Soggetti
Organic Chemistry/Polymer Science","Material Science & Engineering
Journal title
JOURNAL OF APPLIED POLYMER SCIENCE
ISSN journal
00218995 → ACNP
Volume
77
Issue
3
Year of publication
2000
Pages
644 - 659
Database
ISI
SICI code
0021-8995(20000718)77:3<644:SACOMC>2.0.ZU;2-R
Abstract
Poly(n-butyl methacylate-co-n-butyl acylate) [P(BMA/BA)] soft latexes (carb oxylated and noncarboxylated) were synthesized using a semicontinuous emuls ion polymerization process that was designed on the basis of a theoretical calculation to determine the suitable surfactant [i.e., sodium dodecyl sulf ate (SDS)], monomer, and water feed rates to maintain a constant particle n umber throughout the polymerization (guaranteeing monodispersity in the par ticle size), to obtain a homogeneous copolymer composition, and to independ ently control the particle size and carboxyl group concentration. The exper imental results support the theoretical calculation. The surface coverage o f the carboxyl groups present on the soft latex particles ranges from 7.6 t o 21.9% for a series of latexes with particle sizes around 120 nm. Tn anoth er series of latexes, the particle size was varied over a range from 120 to 450 nm. Monodisperse carboxylated polystyrene hard latexes were synthesize d by shot growth (batch) and semicontinuous processes. The shot growth meth od is somewhat inflexible in providing more choices in surfactant, particle size, and surface carboxyl coverage. A semicontinuous process designed usi ng a similar method used for the synthesis of P(BMA/BA) latexes successfull y eliminated the drawbacks of the shot growth process. In this way, the cha nges in the surface carboxyl coverage (varies from 0 to 77.2% ) was indepen dent of the particle size, which was precisely controlled by the amount of styrene fed under suitable styrene and SDS feed rates. (C) 2000 John Wiley & Sons, Inc.