Suspension Polymerization of Thermally Expandable Microcapsules with Core-Shell Structure Using the SPG Emulsification Technique: Influence of Crosslinking Agents and Stabilizers

被引:9
|
作者
Bu, Ji Hyun [1 ]
Kim, Yeongseon [1 ]
Ha, Jin Uk [2 ]
Shim, Sang Eun [1 ]
机构
[1] Inha Univ, Dept Chem Engn, Inchon 402751, South Korea
[2] Korea Automot Technol Inst, Enviromental Mat & Components R&D Ctr, Chungnam 330912, South Korea
关键词
SPG emulsification; suspension polymerization; microcapsule; crosslinking agent; stabilizer; MEMBRANE EMULSIFICATION; MICROSPHERES; MORPHOLOGY;
D O I
10.7317/pk.2015.39.1.78
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
With aiming to prepare microcapsules having a particle size of 30-50 mu m, thermally expandable capsules with relatively uniform particle sizes consisting of a n-octane/poly(acrylonitrile-co-methyl methaciylate) core/shell structure were synthesized using SPG membrane emulsification and suspension polymerization. Four steric stabilizers and five crosslinking agents were employed. When poly(vinyl alcohol) as a stabilizer was used, the prepared capsules showed a smooth and regular morphology and the liquid hydrocarbon (n-octane) was well encapsulated in the core. When 1,4-butnaediol methaciylate (BDDMA) was used as a crosslinker, the uniform capsules with the average diameter of 36.8 mu m were synthesized. The capsules prepared with 0.05 mol% BDDMA showed the best encapsulation efficiency.
引用
收藏
页码:78 / 87
页数:10
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