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聚己内酯在应变下结晶的聚氯乙烯共混物中的取向:应变速率的作用

Orientation of Poly(-caprolactone) in Its Poly(vinyl chloride) Blends Crystallized under Strain: The Role of Strain Rate.

作者信息

Wan Ruru, Sun Xiaoli, Ren Zhongjie, Li Huihui, Yan Shouke

机构信息

State Key Laboratory of Chemical Resource Engineering, Beijing University of Chemical Technology, Beijing 100029, China.

Key Laboratory of Rubber-Plastics, Qingdao University of Science & Technology, Qingdao 266042, China.

出版信息

Materials (Basel). 2020 Dec 11;13(24):5655. doi: 10.3390/ma13245655.

Abstract

The blends of high and low molecular weights poly(ε-caprolactone) (PCL) with poly(vinyl chloride (PVC) were prepared. The samples before and after the crystallization of PCL were uniaxially stretched to different draw ratios. The orientation features of PCL in a stretched crystalline PCL/PVC blend and crystallized from the amorphous PCL/PVC blends under varied strains were studied by wide-angle X-ray diffraction (WAXD) diffraction. It was found that a uniaxial stretching of crystalline PCL/PVC blend with high molecular weight PCL results in the -axis orientation along the stretching direction, as is usually done for the PCL bulk sample. For the stretched amorphous PCL/PVC blend samples, the crystallization of high molecular weight PCL in the blends under a draw ratio of λ = 3 with a strain rate of 6 mm/min leads to a ring-fiber orientation. In the samples with draw ratios of λ = 4 and 5, the uniaxial orientation of -, -, and -axes along the strain direction coexist after crystallization of high molecular weight PCL. With a draw ratio of λ = 6, mainly the -axis orientation of high molecular weight PCL is identified. For the low molecular weight PCL, on the contrary, the ring-fiber and -axis orientations coexist under a draw ratio of λ = 3. The -axis orientation decreases with the increase of draw ratio. When the λ reaches 5, only a poorly oriented ring-fiber pattern has been recognized. These results are different from the similar samples stretched at a higher strain rate as reported in the literatures and demonstrate the important role of strain rate on the crystallization behavior of PCL in its blend with PVC under strain.

摘要

制备了高分子量和低分子量聚(ε-己内酯)(PCL)与聚氯乙烯(PVC)的共混物。将PCL结晶前后的样品单轴拉伸至不同的拉伸比。通过广角X射线衍射(WAXD)研究了在不同应变下,拉伸结晶的PCL/PVC共混物中PCL以及从非晶态PCL/PVC共混物中结晶的PCL的取向特征。结果发现,含有高分子量PCL的结晶PCL/PVC共混物单轴拉伸会导致沿拉伸方向的c轴取向,这与通常对PCL本体样品所做的情况相同。对于拉伸的非晶态PCL/PVC共混物样品,在拉伸比λ = 3、应变速率为6 mm/min的条件下,共混物中高分子量PCL的结晶会导致环形纤维取向。在拉伸比为λ = 4和5的样品中,高分子量PCL结晶后,a、b和c轴沿应变方向的单轴取向共存。当拉伸比为λ = 6时,主要识别出高分子量PCL的c轴取向。相反,对于低分子量PCL,在拉伸比λ = 3时,环形纤维取向和c轴取向共存。c轴取向随着拉伸比的增加而降低。当λ达到5时,仅识别出取向较差的环形纤维图案。这些结果与文献中报道的以较高应变速率拉伸的类似样品不同,证明了应变速率对PCL与PVC共混物在应变下结晶行为的重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c35/7763942/63d5878cdbbf/materials-13-05655-g001.jpg

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