期刊文献+

熔体自由基反应法制备聚丙烯/碳纳米管复合材料

Preparing Polypropylene/Carbon Nanotubes Nanocomposites by Melt Radical Grafting Reaction
在线阅读 下载PDF
导出
摘要 以2,5-二甲基-2,5-双(叔丁基过氧基)己烷(DHBP)在聚丙烯体系中引发形成自由基,以二硫化四甲基秋兰姆(TMTD)调控自由基反应,通过熔融共混一步法制备了共价接枝的聚丙烯/碳纳米管(PP/CNTs)复合材料。通过拉曼光谱和透射电子显微镜证明发生了共价接枝反应,并研究了PP/CNTs的结晶性能、热性能与力学性能。结果表明,发生共价接枝的PP/CNTs与未接枝的PP/CNTs及PP相比,其结晶温度分别提高了2.6和12.0℃,热分解温度T5%分别提高了6.4和34.8℃,其拉伸强度和拉伸模量略有提高,冲击强度分别提高了56.7%和58.1%。 We report a facile melt radical grafting reaction method to fabricate covalent grafted polypropylene(PP)/carbon nanotubes(CNTs) nanocomposites using 2,5-dimethyl-2,5(tert-butylperoxy) hexane peroxide(DHBP) to induce the radical and using tetramethylthiuram(TMTD) to control radical grafting reaction.The covalent grafting reaction was characterized by Raman spectroscopy and TEM.The crystallization,thermal and mechanical properties of the composites were studied.Compared with noncovalent grafted PP/CNTs composites and PP,the covalent grafted nanocomposites showed increased crystallization temperatures(2.6 and 12.0 ℃,respectively) and thermal decomposition temperatures(6.4 and 34.8 ℃,respectively),an increased tensile strength and tensile modulus to a little extent,and increased notched impact strength by 56.7% and 58.1%,respectively.
出处 《应用化学》 CAS CSCD 北大核心 2013年第4期413-419,共7页 Chinese Journal of Applied Chemistry
基金 国家自然基金资助项目(50873099)
关键词 聚丙烯 碳纳米管 纳米复合材料 自由基接枝 polypropylene carbon nanotubes nanocomposites radical grafting
  • 相关文献

参考文献20

  • 1Ago H, Pertritsch K, Shaffer M S P, et al. Composites of Carbon Nanotubes and Conjugated Polymers for Photovoltaic Devices[J]. Adv Mater, 1999,11 (15) : 1281-1285.
  • 2Lefenfeld M, Blanchet G, RogersJ. High-Performance Contacts in Plastic Transistors and Logic Gates that Use Printed Electrodes of DNNSA-PANI Doped with Single-Walled Carbon Nanotubes[J]. Adv Mater ,2003,15(14) : 1188-1191.
  • 3Bhattacharyya A R,Potschke P , Abdel-Goad M ,et al. Effect of Encapsulated SWNT on the Mechanical Properties of Melt Mixed PA12/SWNT Composites[J]. Chem Phys Lett,2004,392(1/3) :28-33.
  • 4Tasis D, Tagmatarchis N ,Bianco A,et al. Chemistry of Carbon Nanotubes[J]. Chem Rev ,2006 ,106(3) : 1105-1136.
  • 5Xia H, Wang Q, Li K, et al. Preparation of Polypropylene/Carbon Nanotube Composite Powder with a Solid-State Mechanochemical Pulverization Process[J].J Appi Polym Sci,2004 ,93( 1) :378-386.
  • 6Mcintosh D, Khabashesku V N, Barrera E V. Nanocomposite Fiber Systems Processed from Fluorinated Single-walled Carbon Nanotubes and a Polypropylene Matrix[J]. Chem Mater,2006,18(19) :45614569.
  • 7Mcintosh D, Khabashesku V N, Barrera E V. Benzoyl Peroxide Initiated in situ Functionalization, Processing, and Mechanical Properties of Single-walled Carbon Nanotube-polypropylene Composite Fibers[J].J Phys Chem C, 2007, 111(2) :1592-1600.
  • 8Farzi G, Akbar S, Beyou E, et al. Effect of Radical Grafting of Tetramethylpentadecane and Polypropylene on Carbon N anotubes' Dispersibility in Various Solvents and Polypropylene Matrix[J]. Polymer, 2009 ,50 ( 25) : 590 1-5908.
  • 9Zhang ZJ , Wan D, Xing H P , et al. A New Grafting Monomer for Synthesizing Long Chain Branched Polypropylene Through Melt Radical Reaction[J]. Polymer ,2012,53(1) :121-129.
  • 10Zhang ZJ, WanD, An YJ, et al. Controlling the Evolution of Polypropylene Microstructure During Melt Free Radical Modification Using Zinc Dithiocarbamate with Different N-Substituted Groups[J]. Polym Degrad Stab ,2011 ,96( 4) :653- 659.

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