期刊文献+

UHMWPE/HDPE/PA1012复合材料的制备及性能研究 被引量:3

Preparation and Performance Research of UHMWPE/HDPE/PA1012 Composites
下载PDF
导出
摘要 以高密度聚乙烯接枝马来酸酐(HDPE-g-MAH)为相容剂,在双螺杆挤出机上通过原位增容反应制备了超高摩尔质量聚乙烯(UHMWPE)/HDPE/尼龙1012(PA1012)复合材料。固定配比PE(HDPE∶UHMWPE)∶PA1012∶HDPE-g-MAH=50∶50∶7,考察HDPE与UHMWPE的比例对复合材料性能的影响。研究发现随着UHMWPE含量的增加,共混物的拉伸强度逐渐增加,断裂伸长率逐渐减小。维卡软化温度在HDPE∶UHMWPE=60∶40时达到最小值,仅为141℃,高于或低于此配比,维卡软化温度有所提高。复合材料的耐磨性则呈现出先减小后增加的趋势;通过SEM对复合材料的微观形态、结构进行表征,发现随着HDPE与UHMWPE配比的变化,复合材料的基体与分散相发生了反转,从而引起了复合材料性能的改变。 The ultra-high molecular weight polyethylene (UHMWPE) /high density polyethylene (HDPE) /nylon 1012 (PA1012) composites were prepared by in situ reactive compatibilization in a twinscrew extruder with HDPE graft maleic anhydride (HDPE-g-MAH) as the compatilizer. With the fixed proportion of PE (HDPE/UHMWPE) : PA1012 : HDPE-g-MAH of 50 : 50 : 7, the effect of the ratio variation of HDPE to UHMWPE on the composites' properties was researched. The results showed that with the increase of UHMWPE content, the tensile strength of the blend increases gradually and the elongation at break decreases gradually. The Vicat softening temperature of the composites reached the minimum value of only 141 ℃ when the ratio of HDPE to UHMWPE is 60 : 40. The abrasion resistance of the composites shows the trend of reducing first and increasing then, The microscopic morphology and structure of the composites were characterized by scanning electron microscope. And the results indicate that with the changing ratio of HDPE to UHMWPE, the matrix and the dispersed phase of the composites inverses, leading to the changes of composites performance.
出处 《塑料工业》 CAS CSCD 北大核心 2016年第10期14-17,29,共5页 China Plastics Industry
关键词 耐热性能 相转变 超高摩尔质量聚乙烯/高密度聚乙烯/尼龙1012复合材料 微观结构 Heat Resistance Phase Inversion Uhra-high Molecular Weight Polyethylene/High DensityPolyethylene/Nylon 1012 Composites Microstructure
  • 相关文献

参考文献8

二级参考文献51

  • 1陈寿羲,金永泽.超高分子量聚乙烯的结晶形态[J].高分子材料科学与工程,1993,9(2):81-85. 被引量:10
  • 2杨燕.汽车塑料应用日益深化[J].北京汽车,2004(4):24-29. 被引量:6
  • 3张师军,王小兰.中国石化汽车塑料开发现状及前景[J].中国石化,2004(9):62-63. 被引量:2
  • 4[1]Utracki L A.Polym Eng and Sci,1995,35:2~17
  • 5[2]Campoy I,Arribas J M,Zaporta M A M,Marco C,Gomez M A,Fatou J F.Eur Polym J,1995,31:475~480
  • 6[3]Beltrame P L,Castelli A,Di Pasquantonio M,Canetti M,Seves A.J Appl Polym Sci,1996,60:579~590
  • 7[4]Bidaux J E,Smith G D,Bernet N,Manson J A D,Hilborn J.Polymer,1996,37:1129~1136
  • 8[5]Marco C,Ellis G,Gomez M A,Fatou J G,Arribas M,CampoyI,Fontech A.J Appl Polym Sci,1997,65:2665~1677
  • 9[6]Tjong S C.J Materials Sci,1997,32:4613~4617
  • 10[7]Heino M,Hietaoja P,Seppala J,Harmia T,Friedrich K.J Appl Polym Sci,1997,66:2209~2220

共引文献83

同被引文献18

引证文献3

二级引证文献3

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