聚合物非线性粘弹性的链各向异性效应

Junhao Wu, Suguru Saitoh, S. Fujii, S. Kawahara, Yoshinobu Isono
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引用次数: 2

摘要

对聚丁二烯试样进行了剪切动模量的测定,首先进行了部分交联,然后进行了大范围的二次交联。以这种方式制备的聚合物有望保持各向异性链构型。聚合物在G′和tanδ上表现出与未变形交联聚合物不同的行为。前者的G′值较低,而tanδ值较高。随延伸程度的增加,偏差变大。可以得出结论,链各向异性确实是聚合物非线性粘弹性的根源之一。它降低了能量储存项,提高了能量损失项。
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Chain Anisotropy Effect on Polymer Nonlinear Viscoelasticity
Measurements of shear dynamic modulus have been made on the polybutadiene samples firstly cross-linked partly followed by the second cross-linking in large extension. The polymers prepared in this manner were expected to keep anisotropic chain configuration. The polymers showed different behaviors in G′ and tanδ from those cross-linked at no deformation. The former polymers showed lower values of G′ and higher values of tanδ than the latter polymers. The deviations became large with increase in degree of extension. It may be concluded that chain anisotropy is really one of the origins for nonlinear viscoelasticity of polymers. It lowers the energy storage term and raises the energy loss term.
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