材料科学
天然橡胶
小角X射线散射
碳纳米管
纳米复合材料
硫化
复合材料
异戊二烯
成核
变形(气象学)
纳米管
散射
聚合物
化学
光学
物理
有机化学
共聚物
作者
Xuan Fu,Zhengtian Xie,Lai-Yun Wei,Cheng Huang,Ming‐Chao Luo,Guangsu Huang
摘要
Abstract Enhanced strain‐induced crystallization (SIC) behavior in isoprene rubber/multiwall carbon nanotube (IR/MWCNT) nanocomposites was analyzed in terms of structural orientation during uniaxial deformation. In situ synchrotron wide‐angle X‐ray diffraction and small‐angle X‐ray scattering (SAXS) reveal the molecular orientation in IR/MWCNT composites at different scales. The inclusion of MWCNTs leads to a decrease in the molecular orientation at small strain due to the promotion of SIC. Meanwhile, the presence of MWCNTs induces a large‐scale orientation within the vulcanized rubber network based on SAXS results. Considering the heterogeneous nature of the vulcanized network, the nucleation process during SIC is discussed from the viewpoint of thermodynamics. The oriented large‐scale structure in IR/MWCNT composites is composed of local rubber chains stretched up MWCNTs, from which the additional nuclei are induced. By forming a bound rubber layer around MWCNTs through attractive interactions, MWCNTs can amplify the local strain of rubber segments and form a highly oriented large‐scale structure, but without altering the overall molecular orientation level. The evolution of detailed structural orientation in MWCNT‐filled rubber composites during deformation is revealed for the first time. © 2017 Society of Chemical Industry
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