The Synthesis and Properties of Emulsion Copolymerization of Styrene with N-Substituted Phenyl Maleimide

Article Preview

Abstract:

The synthesis and characterization of copolymer emulsions of styrene with two types of N-substituted phenyl maleimide (N-p-Methyl–MPhMI and N-m-Methyl–MPhMI) were investigated and researched in this thesis, by varying the mole fraction of N-substituted phenyl maleimide and using a seed emulsion polymerization process. The emulsion was steady with high yield, low intrinsic viscosity, and high solid content (40%). In this thesis, we studied that the substituted position on the benzene ring of the N - substituted phenyl maleimide has significant influence on emulsion properties and thermal properties of copolymer emulsion copolymer. The result shows that: the polarity of N-p-MPhMI is higher than N-m-MPhMI, which can significantly improve the yield, and reduces the emulsion gel rate. N-p-MPhMI is more electronegative than N-m-MPhMI, and N-p-MPhMI-St copolymer emulsion has high zero shear viscosity and low surface tension than N-m-MPhMI-St. And N-m-MPhMI-St copolymer emulsion decreased the viscosity of Pst homopolymer emulsion. However, N-p-MPhMI-St copolymer emulsion rheology curve changes into pseudoplastic fluid. The addition of the N-substituted phenyl maleimide can improve the heat resistance of polystyrene, and N-p-methylphenyl maleimide with styrene copolymer can increase the glass transition temperature of copolymer more remarkably than copolymer N- m-tolylmaleimide with styrene can do.

You might also be interested in these eBooks

Info:

Periodical:

Advanced Materials Research (Volumes 1025-1026)

Pages:

683-687

Citation:

Online since:

September 2014

Authors:

Export:

Price:

Permissions CCC:

Permissions PLS:

Сopyright:

© 2014 Trans Tech Publications Ltd. All Rights Reserved

Share:

Citation:

* - Corresponding Author

[1] T.I. Otsu, A. Kikazu Matsumoto, and T. Kubots: Polymer Bulletin Vol. 23, No. 1(1990), p.43.

Google Scholar

[2] T.I. Otsu, Akikazu Matsumoto, and A. Tatsumi: Polymer Bulletin Vol. 24, No. 5 (1990), p.467.

Google Scholar

[3] A. Matsumoto, T. Kubota and T. Iotsu: Macromolecules, Vol. 23, No. 21 (1990), p.4508.

Google Scholar

[4] A. Matsumoto, Y. Oki and T.I. Otsu: Macromolecules, Vol. 25, No. 12 (1992), p.3323.

Google Scholar

[5] V. Choudhar y, A. Mishra: J. Appl. Polymer Sci. Vol. 62, No. 4 (1996), p.707.

Google Scholar

[6] V. Anand and V. Choudhary: M acromolecular Chem. Phys. Vol. 202, No. 6 (2001), p.943.

Google Scholar

[7] Y. Yuan, S. Siegmann and M. Narkis: J. Appl. Polymer Sci. Vol. 61, No. 6 (1996), p.1049.

Google Scholar

[8] Y. Liting, L.Y. hong and L.Y. fang: J. Appl. Polymer Sci. Vol. 91, No. 2 (2004), p.867.

Google Scholar

[9] Y. Qin, C. Zhengguo, S. Jing and Z. Meng: J. Funct. Polymer Vol. 21, No. 3 (2008), p.70.

Google Scholar

[10] Y. Qin, C. Zhengguo and S. Jing: J. Colloid and polymer Vol. 24, No. 3 (2006), p.18.

Google Scholar