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Microemulsion Radical Polymerization of Alkyl Acrylates
Author(s) -
Capek I.,
Juraničová V.,
Bartoň J.,
Asua J. M.,
Ito K.
Publication year - 1997
Publication title -
polymer international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.592
H-Index - 105
eISSN - 1097-0126
pISSN - 0959-8103
DOI - 10.1002/(sici)1097-0126(199705)43:1<1::aid-pi751>3.0.co;2-i
Subject(s) - polymerization , monomer , polymer chemistry , radical polymerization , microemulsion , bulk polymerization , solution polymerization , alkyl , chemistry , materials science , polymer , organic chemistry , pulmonary surfactant , biochemistry
The oil/water microemulsion polymerizations of alkyl (methyl (MA), ethyl (EA), butyl (BA), hexyl (HA) and 2‐ethylhexyl (EHA)) acrylates initiated by a water‐soluble (ammonium peroxodisulphate (APS)) initiator were investigated. The rate of polymerization versus conversion curve shows two inconstant intervals. The maximum rate of polymerization of MA, EA, BA and EHA is found to be proportional to the 0·53, 0·17, 0·46 and 0·59 powers of the APS concentration and to the first power of the monomer (MA, BA and EHA) concentration. Homogeneous (solution) radical polymerization is operative in the MA, BA and EHA systems. The strong rate dependence on the EA monomer concentration is assumed to be caused by both the polymerization within the micelle core and the gel effect. The particle size was observed to increase with conversion in the EA and BA runs and to decrease in the EHA and HA runs. The number of particles increased with conversion during the whole polymerization. The polymer particles grow by recruiting monomer and emulsifier from the free monomer‐swollen micelles and dead particles. © 1997 SCI.