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Frontiers of Chemical Science and Engineering

ISSN 2095-0179

ISSN 2095-0187(Online)

CN 11-5981/TQ

Postal Subscription Code 80-969

2018 Impact Factor: 2.809

Front. Chem. Sci. Eng.    2008, Vol. 2 Issue (3) : 231-235    https://doi.org/10.1007/s11705-008-0055-7
Preparation and sedimentation behavior of conductive polymeric nanoparticles
WANG Jixiao, LIU Rui, ZHANG Xiaoyan, ZHOU Zhibin, WANG Zhi, WANG Shichang
State Key Laboratory of Chemical Engineering, Chemical Engineering Research Center, School of Chemical Engineering and Technology, Tianjin University;
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Abstract A facile route to prepare Fe3O4/polypyrrole (PPY) core-shell magnetic nanoparticles was developed. Fe3O4 nanoparticles were first prepared by a chemical co-precipitation method, and then Fe3O4/PPY core-shell magnetic composite nanoparticles were prepared by in-situ polymerization of pyrrole in the presence of Fe3O4 nanoparticles. The obtained nanoparticles were characterized by scanning electronic microscopy (SEM), transmission electronic microscopy (TEM) and laser particle size analyzer. The images indicate that the size of Fe3O4 particles is about 10 nanometers, and the particles are completely covered by PPY. The Fe3O4/PPY core-shell magnetic composite nanoparticles are about 100 nanometers and there are several Fe3O4 particles in one composite nanoparticle. The yield of the composite nanoparticles was about 50%. The sedimentation behavior of Fe3O4/PPY core-shell magnetic nanoparticles in electrolyte and soluble polymer solutions was characterized. The experimental results indicate that the sedimentation of particles can be controlled by adjusting electrolyte concentration, solvable polymers and by applying a foreign field. This result is useful in preparing gradient materials and improving the stability of suspensions.
Issue Date: 05 September 2008
 Cite this article:   
LIU Rui,WANG Jixiao,WANG Zhi, et al. Preparation and sedimentation behavior of conductive polymeric nanoparticles[J]. Front. Chem. Sci. Eng., 2008, 2(3): 231-235.
 URL:  
https://academic.hep.com.cn/fcse/EN/10.1007/s11705-008-0055-7
https://academic.hep.com.cn/fcse/EN/Y2008/V2/I3/231
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