期刊文献+

聚乳酸/纳米SiO_2复合纤维的制备及力学性能 被引量:8

Preparation and Mechanical Property of PLA/SiO_2 Composite Fibers
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摘要 首先用硅烷偶联剂(GPS)对纳米SiO2进行接枝改性,利用粒径分析仪、FTIR和沉降实验对改性前后纳米SiO2的粒径大小、结构和溶剂稳定性的变化进行了表征;然后将改性前后的纳米SiO2分别与聚乳酸(PLA)在双螺杆挤出机中熔融混合,利用牵伸卷绕装置制备了PLA/SiO2和PLA/M-SiO2(改性后SiO2)复合纤维。利用视频显微镜和单纱强力仪研究了不同纳米SiO2含量对PLA/SiO2和PLA/M-SiO2复合纤维结构形貌和力学性能的影响,以及不同牵伸倍数对PLA/M-SiO2复合纤维结构形貌和力学性能的影响。结果表明M-SiO2粒径明显减小,且硅烷偶联剂结构中的有机官能团与SiO2表面硅羟基发生反应,减少了其表面Si-OH的量,使得M-SiO2表现出良好的溶剂稳定性和分散性;PLA/M-SiO2复合纤维的力学性能较PLA/SiO2复合纤维得到了明显的改善;当改性纳米SiO2含量为1%时复合纤维强度最好;当牵伸倍数为3时复合纤维强度最好。 The modified nano-SiO2(M-SiO2)was prepared using silane coupling agent to graft and modify nanoSiO2.The particle size,structure and solvent stability of nano-SiO2 before and after modification were characterized by particle size analyzer,FTIR and settlement experiment,respectively.Then the PLA/SiO2 and PLA/M-SiO2 composite fibers were prepared using twin-screw extruder with molten mixing and followed by a draft collecting process.The effects of different SiO2 amounts on structural morphologies and mechanical properties of PLA/SiO2 and PLA/M-SiO2 composite fibers,and different drafting ratios on structural morphologies and mechanical properties of PLA/M-SiO2 composite fibers were studied by optical microscopy and signal-yarn strength tester.The results indicate that the organic modification decrease the particle size of nano SiO2.The M-SiO2 possesses excellent solvent stability and dispersion,attributed to the chemical reaction between organic functional groups of silane coupling agent and hydroxyl groups of nano silica surface.Compared to the PLA/SiO2 composite fibers,the mechanical properties of PLA/M-SiO2 composite fibers have notable improvements.The PLA/M-SiO2 composite fibers reach the maximum strength of the fiber,when the M-SiO2 amount and drafting ratio is 1% and 3times,respectively.
出处 《材料导报》 EI CAS CSCD 北大核心 2015年第2期96-100,共5页 Materials Reports
基金 中国博士后科学研究基金(2014M560391) 国家自然科学基金(51006046) 国家863高技术研究发展计划项目(2012AA030313)
关键词 纳米SIO2 硅烷偶联剂改性 聚乳酸 复合纤维 力学性能 nano-SiO2 silane coupling agent modification polylactic acid composite fibers mechanical property
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参考文献11

  • 1Li D D,Shentu B Q, Weng Z X. Preparation and properties of polylactide/poly ( ethylene~co~octene)/nano~Si〇2 ternary composites[J]. J Macromol Sci: Phys,2012,51(9) : 1766.
  • 2马云霞,王标兵,张淑娴,李庆蛟,王玉龙.聚乳酸/纳米银负载二氧化硅共混物的动态流变性能[J].塑料,2012,41(6):72-74. 被引量:5
  • 3Huang T C,Yeh J M, Yang J C. Effect of silica size on the thermal,mechanical and biodegradable properties of polylac-tide/silica composite material prepared by melt blending[J]. Adv Mater Res,2010,123-125:1215.
  • 4王劭妤,石坚,郑来云.碳纳米管/PLA复合材料制备及性能[J].复合材料学报,2012,29(6):50-54. 被引量:16
  • 5Nekhamanurak B, Patanathabutr P, Hongsriphan N. Surface modified CaC〇3 nanoparticles with silica via sol-gel process using in poly (lactic acid) nanocomposite [ J J. Adv Mater Res, 2012,488-489 : 520.
  • 6张玲,杨建民,冯超伟,李春忠.表面复合纳米SiO_2和碳纳米管玻璃纤维增强尼龙6的结构与性能[J].高分子学报,2010,20(11):1333-1339. 被引量:25
  • 7Zhuang W, Liu J, Zhang J H,et al. Preparation, characterization, and properties of TiC^/PLA nanocomposites by in situ polymerization[J]. Polym Compos,2009,30(8) : 1074.
  • 8Joubert M, Delaite C, Bourgeat-Lami E. Ring-opening polymerization of caprolactone and L-lactide from silica nanoparticles surface[J]. J Polym Sci Part A: Polym Chem,2004, 42(8):1976.
  • 9Carrot G? Rutot-houze D, Pottier A, et al. Surface-initiated ring-opening polymerization: A versatile method for nanoparticle ordering[J], Macromolecules,2002,35(22) :8400.
  • 10Yan S F,Yin J B,Yang Y,et al. Surface-grafted silica linked with L-lacticacid oligomer: A novel nanofiller to improve the performance of biodegradable poly (L-lactide)[J]. Polymer,2007,48(6) :1688.

二级参考文献42

  • 1吴亮,吴德峰,张明,吴兰峰.聚乳酸/蒙脱土纳米复合材料的流变行为[J].中国塑料,2006,20(11):53-57. 被引量:6
  • 2Laura D M, Keskkula H, Barlow J W, Paul D R. Polymer,2002,43:4673 - 4687.
  • 3Shen Z Q, Bateman S, Wu D Y, Mcmahon P, Dell' Olio M, Gotama J. Compos Sei Technol,2009 ,69 :239 -244.
  • 4Fornes T D,Paul D R. Polymer,2003,44:4993 - 5013.
  • 5O' Connor I, Hayden H, Coleman J N, Gun' ko Y K. Sma11,2009,5:466 - 469.
  • 6O' Connor l,Handen H,O' Connor S,Coleman J N,Gun' ko Y K. J Phy Chem C ,2009,113:20184 -20192.
  • 7Wang F,Wang G C,Yang S,Li C Z. Langmuir,2008 ,24 :5825 -5831.
  • 8Tang Z Y, Wang Y, Podsiadlo P, Kotov N A. Adv Mater,2006,18,3203 - 3224.
  • 9Meng H, Sui G X, Fang P F, Yang R. Polymer, 2008,49:610 - 620.
  • 10Xie S B,Zhang S M,Liu H J,Chen G M,Feug M,Qin H L,Wang F S,Yang M S. Polymer,2005,46:5417 -5427.

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