Wan Ruru, Sun Xiaoli, Ren Zhongjie, Li Huihui, Yan Shouke
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.
Materials (Basel). 2020 Dec 11;13(24):5655. doi: 10.3390/ma13245655.
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.
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。