In Situ Polymerization, Thermal, Damping, and Mechanical Properties of Multiwalled Carbon Nanotubes/Polyisobutylene-Based Polyurethane Nanocomposites

被引:9
|
作者
Li, Yuqi [1 ,2 ]
Hu, KaiFang [3 ]
Jiao, Hongyu [3 ]
Liu, Xiulan [3 ]
Wang, Qihua [1 ]
Pan, Guangqin [3 ]
Zhang, Xinrui [1 ]
Wang, Tingmei [1 ]
机构
[1] Chinese Acad Sci, Lanzhou Inst Chem Phys, State Key Lab Solid Lubricat, Lanzhou 730000, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100039, Peoples R China
[3] Res Inst Lanzhou Petrochem Co, Lanzhou Inst Chem Ind, Lanzhou 730000, Peoples R China
基金
美国国家科学基金会;
关键词
NANOTUBES; COMPOSITES; STABILITY;
D O I
10.1002/pc.22930
中图分类号
TB33 [复合材料];
学科分类号
摘要
Despite the development of strong, durable, and cost efficient polyisobutylene-based polyurethane (PIB-based PU) materials has yet to be achieved. The well dispersion and maximum interfacial interaction between the nanofiller and the PIB-based PU at low loading have been scarcely studied. Here, the preparation of PIB-based PU nanocomposites with Multiwalled carbon nanotubes (MWCNTs) using a simple in situ polymerization method is reported. The thermogravimetric analysis tests show that MWCNTs significantly improved the thermal stability of MWCNTs/PIB-based PU nanocomposites. Compare to the pure PIB-based PU the onset temperature of degradation for the nanocomposite was about 20 degrees C higher at 0.7 wt% MWCNTs loading. Efficient load transfer is found between the nanofiller MWCNTs and PIB-based PU and the mechanical properties of the MWCNTs/PIB-based PU nanocomposite with well dispersion are improved. A 63% improvement of Young's modulus and slightly increased of tensile strength are achieved by addition of only 0.7 wt% of MWCNTs. The experimentally determined Young's modulus is in well agreement with the theoretical simulation. It is worth noting that the PIB-based PU and MWCNTs/PIB-based PU nanocomposites exhibit excellent damping properties (tan >0.3) from -45 degrees C to 8 degrees C. POLYM. COMPOS., 36:198-203, 2015. (c) 2014 Society of Plastics Engineers
引用
收藏
页码:198 / 203
页数:6
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