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Cationic microgel emulsion with a high solid content by a multistep addition method in inverse microemulsion polymerization
Author(s) -
Li Guanghui,
Zhang Guicai,
Wang Lei,
Ge Jijiang
Publication year - 2014
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.40585
Subject(s) - cationic polymerization , microemulsion , emulsion polymerization , polymerization , monomer , materials science , polymer chemistry , chemical engineering , viscosity , emulsion , polyacrylamide , solution polymerization , pulmonary surfactant , chemistry , polymer , composite material , engineering
The multistep addition of a monomer and initiator was developed to successfully synthesize cationic polyacrylamide microgels with solid contents (SCs) greater than 35% and cationic monomer concentrations of 0–40 mol % by inverse microemulsion polymerization. Two feed methods, three‐step nonuniform addition and five‐step uniform addition, were implemented to obtain microgel emulsions with 37% SC. The former addition method was designed according to the solubilization limit of the microemulsion before step polymerization, and that of the latter was a constant based on the remaining surfactant weight in the reactor. The product properties in the intermediate processes of these two methods were compared by dynamic light scattering and viscosity measurement. The results show that the products here were translucent microemulsions instead of milky ones when they were synthesized by a semicontinuous polymerization. Also, the particle sizes of these two methods were almost the same; this indicated that the oscillation phenomenon in continuous polymerization at a high SC was avoided. With the former feed method, the risk and operation cost in the synthesis process could be cut down greatly. Moreover, the viscosity of the cationic microgel emulsion conformed to the Krieger–Dougherty equation with a greater value of intrinsic viscosity than that of a hard‐sphere system because of an electroviscous effect. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131 , 40585.