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Phase rearrangement in two‐stage emulsion polymers of butyl acrylate and styrene: Mechanical properties
Author(s) -
O'Connor Kevin M.,
Tsaur ShengLiang
Publication year - 1987
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.1987.070330614
Subject(s) - materials science , emulsion polymerization , styrene , butyl acrylate , polystyrene , polymer chemistry , differential scanning calorimetry , polymer , acrylate , chemical engineering , coalescence (physics) , emulsion , copolymer , particle size , composite material , physics , astrobiology , engineering , thermodynamics
The mechanical and thermal properties of films from a series of two‐stage emulsion polymers were investigated. The emulsion polymers were made by polymerizng styrene in the presence of a preformed poly(butyl acrylate‐co‐divinyl benzene) seed latex. The effects of seed particle size, seed particle crosslinking via the amount of divinyl benzene, styrene/butyl acrylate ratio, and thermal history on the film properties were studied. Latex particles were characterized by light scattering and film formation behavior. Dried films were characterized by differential scanning calorimetry, dynamic mechanical analysis, and stress‐strain behavior. Although evidence was obtained for nearly complete phase separation between the polystyrene (PS) and poly(butyl acrylate) (PBA) phases, the site of styrene polymerization and thus the PS phase morphology is influenced by seed particle size, seed crosslinking, and S/BA ratio. The morphology of as‐dried films consists of finely dispersed PS domains in a continuous PBA matrix. Thermal annealing above the PS T g causes coalescence of the PS domains, resulting in significantly improved mechanical properties. The extent of PS phase coalescence is also influenced by the level of seed crosslinking.