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From heterocoagulated colloids to core-shell particles
被引:33
|作者:
Li, H
[1
]
Han, J
[1
]
Panioukhine, A
[1
]
Kumacheva, E
[1
]
机构:
[1] Univ Toronto, Dept Chem, Toronto, ON M5S 3H6, Canada
基金:
加拿大自然科学与工程研究理事会;
关键词:
polymer colloids;
heterocoagulation;
core-shell particles;
conductive polymers;
silica;
titanyl sulfate;
spreading;
D O I:
10.1006/jcis.2002.8632
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
Heterocoagulation of large and small oppositely charged colloid particles, accompanied by spreading of small beads over the surface of large spheres, offers a promising alternative to synthesis of core-shell particles via interfacial polymerization. In this paper, conditions required for complete spreading of the shell-forming polymer over the surface of the core-forming material (CFM) are predicted in terms of a critical distance, x(cr), between the small particles on the surface of the CFM. The theoretical value of x(cr) is tested in experiments conducted for polypyrrole/polyacrylic and silica-titanyl sulfate/polyacrylic heterocoagulate units. (C) 2002 Elsevier Science (USA).
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页码:119 / 128
页数:10
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