期刊文献+

十六烷基膦酸表面修饰纳米镍粉及其复合材料的制备和性能

Preparation and Properties of Surface Modified Nano-Ni Particles with n-Hexadecylphosphonic and Its Composites
下载PDF
导出
摘要 以十六烷基膦酸作为修饰剂,对纳米镍粉进行表面改性处理,通过溶液共混的方法制备改性镍粉与聚丙烯的聚合物基复合材料。利用X射线光电子能谱( XPS)、 X射线衍射( XRD)及透射电子显微镜( TEM)等测试手段研究改性镍粉的表面形态;利用扫描电子显微镜( SEM)研究复合材料断面形貌;利用介电频谱分析系统对复合材料的介电常数和介电损耗等进行了测试。结果表明,纳米镍粉表面形成厚度为2~4 nm的十六烷基膦酸包覆层,使纳米镍粉由亲水性变为亲油性;聚丙烯基复合材料中,改性镍粉均匀分散;复合材料的介电常数在镍填充量为40%时,可以达到纯聚丙烯的近10倍。 Through the modification of nano-Ni particles with n-hexadecylphosphonic acid( HDPA) as surface modifier, Ni/HDPA hybrid particles were prepared. Composite of polypropylene( PP) and Ni/HDPA was pre-pared by solution blending. The dispersion of Ni in PP, the compatibility and stability of Ni and PP, the die-lectric performance of composite were discussed. The X-ray photoelectron spectroscopy( XPS) , X-ray diffrac-tion( XRD) and transmission electron microscope( TEM) results showed the surface morphology of Ni/HDPA, while the fracture surface morphology and the dielectric properties of composite were demonstrated by scanning electron microscope ( SEM) and the dielectric spectrum analysis system. It is found that a coverage layer, which is 2-4 nm thick, of n-hexadecylphosphonic can be formed on the surface of nano-Ni. In the presence of the coverage layer, nano-Ni was changed from hydrophilicity into lipophilicity, in results of which the Ni/HDPA disperses well in the PP matrix. At the Ni/HDPA volume fraction of 40%, permittivity of composite can be as high as 10 times of pure PP.
作者 尚光远 李明
出处 《高等学校化学学报》 SCIE EI CAS CSCD 北大核心 2014年第2期427-432,共6页 Chemical Journal of Chinese Universities
关键词 纳米镍 十六烷基膦酸 表面修饰 聚合物基复合材料 Nano-Ni n-Hexadecylphosphonic acid Surface modification Polymer matrix composite
  • 相关文献

参考文献32

  • 1Zavyalov A A;Pivkina A N;Schoonman J.查看详情[J],{H}Solid State Ionicis2002415-419.
  • 2李芝华,李珍,林伟.不同质子酸掺杂对银/聚苯胺纳米复合材料结构和导电性的影响[J].高分子学报,2013,23(7):827-831. 被引量:8
  • 3李军波,李桂珍,韩晨,杜德光,肖理慧,张军凯,周惠云.聚甲基丙烯酸单层保护金纳米粒子的制备及pH响应性聚集[J].高分子学报,2012,22(11):1243-1247. 被引量:1
  • 4Fadeev A Y;McCarthy T J.查看详情[J],{H}LANGMUIR20007268-7274.
  • 5Hotchkiss P J;Jones S C;Paniagua S A;Sharma A Kippelen B Armstrong N R Marder S R.查看详情[J],Accounts of Chemical Re-search2012(3):337-346.
  • 6Hauffman T;Lokeren L V;Willem R;Hubin A Terryn H.查看详情[J],{H}LANGMUIR20123167-3173.
  • 7Polaske N W;Lin H C;Tang A;Mayukh M Oquendo L E Green J T Ratcliff E L Armstrong N R Saavedra S S McGrath D V.查看详情[J],{H}LANGMUIR201114900-14909.
  • 8Acton O;Ting G G;Shamberger P J;Ohuchi F S Ma H Jen A K Y.查看详情[J],Applied Materials&Interfaces2010(2):511-520.
  • 9Rao B V.查看详情[J],{H}Journal of Thermal Analysis and Calorimetry2010577-587.
  • 10Ilia G;Drehe M;Vlase T;Vlase G Macarie L Doca N.查看详情[J],{H}Journal of Thermal Analysis and Calorimetry2010917-923.

二级参考文献42

  • 1李新贵,孙晋,黄美荣.聚苯胺/金属纳米粒子复合物的制备及性能[J].化学进展,2007,19(5):787-795. 被引量:14
  • 2Zhang K, Cutler J I, Zhang J, Zheng D, Auyeung E, Mirkin C A. J Am Chern Soc ,2010,131 : 15151 - 15153.
  • 3Oren R, Liang Z, Barnard J, Warren S C, Wiesner U, Huck W. J Am Chern Soc ,2009,131 : 1670 - 1671.
  • 4Yavuz M , Jensen G, Penaloza D, Seery T , Pendergraph S, R usling J , Sotzing G. Langmuir, 2009 ,25 : 13120 - 13124.
  • 5Grimm A, Nowak C, Hoffmann J, Schartl W. Macromolecules ,2009,42 :6231 - 6238.
  • 6Shan J, Tenhu H. Chern Commun ,2007,44 :4580 - 4598.
  • 7Liang M T, Lin I C, Whittaker M R, Minchin R F, Monteiro M J, Toth I. ACS Nano,2010,4 :403 - 413.
  • 8Gehan H, Fil1aud L, Chehimi M M, Aubard J, Hohenau A, Felidj N, Mangeney C. ACS Nano ,2010,4: 6491 - 6500.
  • 9Sardar R, Bjorge N S , Shumaker-Patry J S. Macromolecules, 2008 ,41 : 4347 - 4352.
  • 10Chakraborty S, Bishnoi S W .Perez-Luna V H. J Phys Chern C ,2010,114 :5947 - 5955.

共引文献7

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