Toughening of Polycarbonate through Reactive Melt Blending:Effect of Hydroxyl Content and Viscosity of Hydroxyl-terminated Polydimethysiloxane

Shuang-mei Zhang Hui-xian Zhang Wei-yi Zhang Zhi-qiang Wu Feng Chen Qiang Fu

Citation:  Shuang-mei Zhang, Hui-xian Zhang, Wei-yi Zhang, Zhi-qiang Wu, Feng Chen, Qiang Fu. Toughening of Polycarbonate through Reactive Melt Blending:Effect of Hydroxyl Content and Viscosity of Hydroxyl-terminated Polydimethysiloxane[J]. Chinese Journal of Polymer Science, 2014, 32(7): 823-833. doi: 10.1007/s10118-014-1474-1 shu

Toughening of Polycarbonate through Reactive Melt Blending:Effect of Hydroxyl Content and Viscosity of Hydroxyl-terminated Polydimethysiloxane

    通讯作者: Qiang Fu,
  • 基金项目:

    This work was financially supported by the National Natural Science Foundation of China (Nos. 21034005 and 51121001).

摘要: In this study, four hydroxyl-terminated polydimethylsiloxanes (PDMSOH) with different viscosities and hydroxyl contents were used to improve the toughness of polycarbonate (PC) through reactive melt blending. A largely improved toughness of PC has been achieved, and the low temperature toughness of PC/PDMSOH blends could overtake that of PC homopolymer in much higher temperatures (e.g. -10 ℃versus 23 ℃). Moreover, it was found that the more the hydroxyl content, the less the PDMSOH was needed to reach the highest toughness, suggesting that equivalent molar ratio between the carbonyl group content of PC and the hydroxyl group content of PDMSOH was required for the toughening of PC. Ultraviolet spectrophotometry was used to analyze the possible reaction between PC and PDMSOH. Contact angle was measured to assess the change of interfacial interaction between PC and PDMSOH as change of viscosity and hydroxyl content. The formation of PC-co-PDMSOH copolymer was believed to be the key for the toughening effect. This work gives a profound recommendation of the optimum kind and dosage of PDMSOH which should be used to improve the toughness of PC and will find immediate industrial applications.

English


    1. [1]

      LeGrand, D.G. and Bendler, J.T., Handbook of polycarbonate science and technology Marcel Dekker Inc., New York, 2000

    2. [2]

      Alegria, A., Mitxelena, O. and Colmenero, J., Macromolecules, 2006, 39(7): 2691

    3. [3]

      Chen, L., Zhang, X., Li, H., Li, B., Wang, K., Zhang, Q. and Fu, Q., Chinese J. Polym. Sci., 2011, 29(1): 125

    4. [4]

      Yuan, D. and Cai, X., Chinese J. Polym. Sci., 2013, 31(10): 1352

    5. [5]

      Zhou, W. and Osby, J., Polymer, 2010, 51(9): 1990

    6. [6]

      Kumar, S. and Maiti, S., Polym. Plast. Technol., 2007, 46(4): 427

    7. [7]

      Kim, S.R. and Kim, D.J., J. Appl. Polym. Sci., 2008, 109(6): 3439

    8. [8]

      Nodera, A. and Kanai, T., J. Appl. Polym. Sci., 2006, 100(1): 565

    9. [9]

      Nodera, A. and Kanai, T., J. Appl. Polym. Sci., 2006, 102(2): 1697

    10. [10]

      Knauss, D., Yamamoto, T., Yoon, T. and McGrath, J., Proceedings Am. Chem. Soc. Divis. Polym. Mater. Sci. Eng., 1995, 721995: 232

    11. [11]

      Chen, X., Lee, H.F. and Gardella Jr, J.A., Macromolecules, 1993, 26(17): 4601

    12. [12]

      Vaughn, H.A., J. Polym. Sci. Polym. Lett., 1969, 7(8): 569

    13. [13]

      van Aert, H.A. M., Nelissen, L., Lemstra, P.J. and Brunelle, D.J., Polymer, 2001, 42(5): 1781

    14. [14]

      Niznik, G. and LeGrand, D., J. Polym. Sci.: Polym. Sympo., 1977, 60: 97

    15. [15]

      McDermott, P.J., Krafft, T.E. and Rich, J.D., J. Polym. Sci. Part A: Polym. Chem., 1991, 29(12): 1681

    16. [16]

      Kim, Y.S., Yang, J., Wang, S., Banthia, A.K. and McGrath, J.E., Polymer, 2002, 43(25): 7207

    17. [17]

      Evans, T.L. and Carpenter, J.C., Makromol. Chem. Macromol. Sympo., 1991, 42/43(1): 177

    18. [18]

      Cella, J. and Rubinsztajn, S., Macromolecules, 2008, 41(19): 6965

    19. [19]

      Niznek G.E. and LeGrand D.G., J. Polym. Sci. Polym. Sympo., 1977, 60: 97

    20. [20]

      Hawkins, C.M. and Gallucci, R.R., 1991, U.S. Pat., 4.994.532

    21. [21]

      Peters, E.N., 1993, U.S. Pat., 5.194.524

    22. [22]

      Archey, R.L., Mason, J.P. and Vescio, L.J., 1999, U.S. Pat., 5.986.019

    23. [23]

      Konig, A., Ebert, W. and Kohler, W., 2000, U.S. Pat., 6.066.700

    24. [24]

      Wouters, G.J., 2002, U.S. Pat., 6.372.847

    25. [25]

      Wildes, G., Keskkula, H. and Paul, D., Polymer, 1999, 40(25): 7089

    26. [26]

      Loyens, W. and Groeninckx, G., Polymer, 2002, 43(21): 5679

    27. [27]

      Bai, H., Wang, Y., Song, B., Huang, T. and Han, L., J. Polym. Sci. Part B: Polym. Phys., 2009, 47(1): 46

    28. [28]

      Wu, Q., Xue, Z., Qi, Z. and Wang, F., Polymer, 2000, 41(6): 2029

    29. [29]

      Wang, J., Montville, D. and Gonsalves, K., J. Appl. Polym. Sci., 1999, 72(14): 1851

    30. [30]

      Smith, R.C. and Protasiewicz, J.D., J. Am. Chem. Soc., 2004, 126(8): 2268

    31. [31]

      Schlereth, D.D. and Karyakin, A.A., J. Electroanal. Chem., 1995, 395(1): 221

    32. [32]

      Migahed, M.D. and Zidan, H.M., Curr. Appl. Phys. 2006, 6(1): 91

    33. [33]

      Xue, Y., Liu, Y., Lu, F., Qu, J., Chen, H. and Dai, L., J. Phys. Chem. Lett., 2012, 3(12): 1607

    34. [34]

      Wu, S., J. Macromol. Sci. C., 1974, 10(1): 1

    35. [35]

      Wu, S., Polymer interface and adhesion, Marcel Dekker Inc., New York, 1982

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  • 发布日期:  2014-07-05
  • 收稿日期:  2014-02-24
  • 修回日期:  2014-04-21
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