期刊文献+

Synthesis and Characterization of Temperature-sensitive Cellulose-graftPoly(N-isopropylacrylamide) Copolymers 被引量:7

Synthesis and Characterization of Temperature-sensitive Cellulose-graftPoly(N-isopropylacrylamide) Copolymers
原文传递
导出
摘要 A new series of cellulose-graft-poly(N-isopropylacrylamide) (cellulose-g-PNIPAM) copolymers were prepared by atom transfer radical polymerization (ATRP) of N-isopropylacrylamide monomers from a cellulose-based macro-initiator, which was homogeneously synthesized in an ionic liquid 1-allyl-3-methylimidazolium chloride (AmimC1). The composition of cellulose-g-PNIPAM copolymers could be adjusted by altering the feeding ratio and reaction time. The resultant copolymers with relatively high content of PNIPAM segments (molar substitution of PNIPAM ≥ 18.3) were soluble in water at room temperature. Aqueous solutions of cellulose-g-PNIPAM copolymers exhibited clear temperature-sensitive behavior, and their sol-to-gel phase transition properties were investigated by dynamic light scattering (DLS) and UV measurements. Compared with pure PNIPAM, the cellulose-g-PNIPAM copolymers possessed higher lower critical solution temperatures (LCST) in a range from 36.9 ℃ to 40.8 ℃, which are close to normal human body temperature, and could be tuned by adjusting the content of PNIPAM segments in copolymers. Spherical structure of cellulose-g-PNIPAM copolymers formed at temperatures above LCST and its morphology was observed by TEM and SEM. These novel cellulose-g-PNIPAM copolymers may be attractive substrates for some biomedical applications, such as drug release and tissue engineering. A new series of cellulose-graft-poly(N-isopropylacrylamide) (cellulose-g-PNIPAM) copolymers were prepared by atom transfer radical polymerization (ATRP) of N-isopropylacrylamide monomers from a cellulose-based macro-initiator, which was homogeneously synthesized in an ionic liquid 1-allyl-3-methylimidazolium chloride (AmimC1). The composition of cellulose-g-PNIPAM copolymers could be adjusted by altering the feeding ratio and reaction time. The resultant copolymers with relatively high content of PNIPAM segments (molar substitution of PNIPAM ≥ 18.3) were soluble in water at room temperature. Aqueous solutions of cellulose-g-PNIPAM copolymers exhibited clear temperature-sensitive behavior, and their sol-to-gel phase transition properties were investigated by dynamic light scattering (DLS) and UV measurements. Compared with pure PNIPAM, the cellulose-g-PNIPAM copolymers possessed higher lower critical solution temperatures (LCST) in a range from 36.9 ℃ to 40.8 ℃, which are close to normal human body temperature, and could be tuned by adjusting the content of PNIPAM segments in copolymers. Spherical structure of cellulose-g-PNIPAM copolymers formed at temperatures above LCST and its morphology was observed by TEM and SEM. These novel cellulose-g-PNIPAM copolymers may be attractive substrates for some biomedical applications, such as drug release and tissue engineering.
出处 《Chinese Journal of Polymer Science》 SCIE CAS CSCD 2015年第12期1640-1649,共10页 高分子科学(英文版)
基金 financially supported by the National Natural Science Foundation of China(No.51425307)
关键词 Cellulose-g-PNIPAM ATRP TEMPERATURE-SENSITIVE Water soluble. Cellulose-g-PNIPAM ATRP Temperature-sensitive Water soluble.
作者简介 Corresponding authors: Jun Zhang (张军), E-mail: jzhang@iccas.ac.cnZhi-hua Gan (甘志军), E-mail: zhgan@mail.buct.edu.cn
  • 相关文献

参考文献1

二级参考文献29

  • 1Huang, X., Sevimli, S.I. and Bulmus, V., Eur. Polym. J., 2013, 49: 2895.
  • 2Wang, J., Yao, Y., Ji, B., Huang, W. and Yan, D., Chinese J. Polym. Sci., 2011, 29(2): 241.
  • 3Deng, J.N., Wang, W.B., Zheng, Z.H., Ding, X.B. and Peng, Y.X., Chinese J. Polym. Sci., 2014, 32(7): 817.
  • 4Bagheri, M. and Bigdeli, E., J. Polym. Res., 2013, 20: 84.
  • 5Stefani, M., Coudane, J. and Vert, M., Polym. Degrad. Stab., 2006, 91: 2554.
  • 6Bencini, M., Ranucci, E., Ferruti, P., Manfredi, A., Trotta, F. and Cavalli, R., J. Polym. Sci., Part A: Polym. Chem., 2008, 46: 1607.
  • 7Zou, T., Li, S.L., Zhang, X.Z., Wu, X.J. and Cheng, S.X., J. Polym. Sci., Part A: Polym. Chem., 2007, 45: 5256.
  • 8Hawker, C.J. and Wooley, K.L., Science, 2005, 309: 1200.
  • 9Gohy, J.F., Willet, N., Varshney, S., Zhang, J. and Jér?me, R., Angew. Chem. Int. Ed., 2001, 40: 3214.
  • 10Mitsukami, Y., Hashidzume, A., Yusa, S., Morishima, Y. and Lowe, A.B., Polymer, 2006, 47: 4333.

共引文献3

同被引文献39

引证文献7

二级引证文献13

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部