journal article·2007-06

Synthesis, characterization, and antibacterial activities of novel N-halamine copolymers

Ying Chen, Li Wang, Haojie Yu, Quan Shi, Xiaochen Dong

Journal of Materials Science· Volume 42· Issue 11
Publisher page

Abstract

The synthesis and antibacterial properties of N-halamine copolymers are reported in this paper. 3-(4′-vinylbenzyl)-5,5-dimethylhydantoin (VBDMH) monomer and its copolymers with n-butyl methacrylate (BMA) were prepared under mild conditions. The effects of monomer feeds on the composition of the final copolymers and reaction conversion were investigated. It was found that VBDMH had higher reactivities than BMA in the copolymerization reactions and the reactivity ratios of VBDMH and BMA were calculated to be 8.91 and 0.42, respectively, according to the Fineman–Ross equation in the preparation of PBMA-co-VBDMH. Two chlorination methods were applied and compared in the process of polymers chlorination. After chlorination by tert-butyl hypochlorite, the polymers provided powerful antibacterial activities against Escherichia coli (E. coli). The surface morphologies of the chlorinated polymer films used in antibacterial assessment were observed by scanning electron microscope. The copolymers before and after chlorination were characterized with fourier transform infrared (FTIR) and 1H-nuclear magnetic resonance (1H-NMR). Their thermal properties were analyzed with thermogravimetric analysis (TGA) studies.
Source: openaire · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Antimicrobial agents and applications · Phenothiazines and Benzothiazines Synthesis and Activities · Click Chemistry and Applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

References (17)

Show source-provided references
1. Lin J, Winkelmann C, Worley SD, Kim J, Wei C-I, Cho U, Broughton RM, Santiago JI, Williams JF (2002) J Appl Polym Sci 85(1):17710.1002/app.10588 ↗
2. Chen Y, Wang L, Jiang S, Yu HJ (2003) J Polym Mater 20(3):279
3. Jiang S, Wang L, Yu HJ, Chen Y (2005) React Funct Polym 62:20910.1016/j.reactfunctpolym.2004.11.002 ↗
4. Worley SD, Sun G (1996) Trends Polym Sci 4(11):364
5. Sun G, Chen TY, Habercom MS, Wheatley WB, Worley SD (1996) Water Res Bull 32:79310.1111/j.1752-1688.1996.tb03476.x ↗
6. Sun G, Chen TY, Worley SD (1996) Polymer 37:375310.1016/0032-3861(96)00194-2 ↗
7. Worley SD, Sun G (1996) Polym Mater Encyclopedia 1:550
8. Eknoian MW, Putman JH, Worley SD (1998) Ind Eng Chem Res 37:287310.1021/ie970943d ↗
9. Sun G, Xu X (1998) Textile Chem Colorist 30(6):26
10. Sun YY, Sun G (2001) J Polym Sci 39:334810.1002/pola.1317 ↗
11. Sun YY, Sun G (2001) J Appl Polym Sci 80:246010.1002/app.1353 ↗
12. Sun YY, Sun G (2002) Macromolecules 35:890910.1021/ma020691e ↗
13. Baumgarten HE (1973) Organic syntheses, vol. 5. John Wiley and Sons, New York, p 183
14. Fineman M, Ross SD (1950) J Polym Sci 5:25910.1002/pol.1950.120050210 ↗
15. Hawkins WJ (1984) Polymer degradation and stabilization. Springer-Verlag, Berlin10.1007/978-3-642-69376-2 ↗
16. Xue GB (1986) Practical sterilization study, 2 edn. The People’s Military Medical Publishing Company, Shanghai, p 45
17. Chen YJ, Worley SD, Kim J, Wei CI, Chen TY, Suess J, Kawai H, Williams JF (2003) Ind Eng Chem Res 42:571510.1021/ie0303303 ↗