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聚碳酸酯/丙烯腈-丁二烯-苯乙烯共混物松弛行为的流变学研究

Rheological Investigation of Relaxation Behavior of Polycarbonate/Acrylonitrile-Butadiene-Styrene Blends.

作者信息

Seo Jae Sik, Jeon Ho Tak, Han Tae Hee

机构信息

Department of Organic and Nano Engineering, Hanyang University, Seoul 04763, Korea.

Interior System Plastic Materials Development Team, Material Development Center, Hyundai Motor Company, Hwaseong 18280, Korea.

出版信息

Polymers (Basel). 2020 Aug 25;12(9):1916. doi: 10.3390/polym12091916.

DOI:10.3390/polym12091916
PMID:32854352
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7563493/
Abstract

The rheological properties of polycarbonate/acrylonitrile-butadiene-styrene (PC/ABS) blends with various blend ratios are investigated at different temperatures to determine the shear dependent chain motions in a heterogeneous blend system. At low frequency levels under 0.1 rad/s, the viscosity of the material with a blend ratio of 3:7 (PC:ABS) is higher than that of pure ABS polymer. As the temperature increases, the viscosities of ABS-rich blends increase rather than decrease, whereas PC-rich blends exhibit decrease in viscosity. Results from the time sweep measurements indicate that ordered structures of PC and the formation and breakdown of internal network structures of ABS polymer occur simultaneously in the blend systems. Newly designed sequence test results show that the internal structures formed between PC and ABS polymers are dominant at low shear conditions for the blend ratio of 3:7 and effects of structural change and the presence of polybutadiene (PBD) become dominant at high shear conditions for pure ABS. The results of yield stress and relaxation time for PC/ABS blends support this phenomenon. The specimen with a blend ratio of 3:7 exhibited the highest value of yield stress at high temperature among others, which implies that the internal structure become stronger at higher temperature. The heterogeneity of ABS-rich blends increases whereas that of PC-rich blends decreases as temperature increases.

摘要

研究了不同共混比例的聚碳酸酯/丙烯腈-丁二烯-苯乙烯(PC/ABS)共混物在不同温度下的流变性能,以确定非均相共混体系中依赖剪切的链运动。在低于0.1 rad/s的低频水平下,共混比例为3:7(PC:ABS)的材料粘度高于纯ABS聚合物。随着温度升高,富含ABS的共混物粘度增加而非降低,而富含PC的共混物粘度则降低。时间扫描测量结果表明,共混体系中PC的有序结构以及ABS聚合物内部网络结构的形成和破坏同时发生。新设计的序列测试结果表明,对于3:7的共混比例,PC与ABS聚合物之间形成的内部结构在低剪切条件下占主导地位,而对于纯ABS,结构变化和聚丁二烯(PBD)的存在的影响在高剪切条件下占主导地位。PC/ABS共混物的屈服应力和松弛时间结果支持了这一现象。共混比例为3:7的试样在高温下的屈服应力值高于其他试样,这意味着内部结构在较高温度下变得更强。随着温度升高,富含ABS的共混物的非均质性增加,而富含PC的共混物的非均质性降低。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec2c/7563493/2c889f87ca77/polymers-12-01916-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec2c/7563493/af2ba511193f/polymers-12-01916-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec2c/7563493/449f35f0f2ff/polymers-12-01916-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec2c/7563493/f981c3f2ee0c/polymers-12-01916-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec2c/7563493/8ea7c8000e2f/polymers-12-01916-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec2c/7563493/74f9998e6fdc/polymers-12-01916-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec2c/7563493/543a09739e25/polymers-12-01916-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec2c/7563493/2d6d99da85f2/polymers-12-01916-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec2c/7563493/2c889f87ca77/polymers-12-01916-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec2c/7563493/af2ba511193f/polymers-12-01916-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec2c/7563493/449f35f0f2ff/polymers-12-01916-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec2c/7563493/f981c3f2ee0c/polymers-12-01916-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec2c/7563493/8ea7c8000e2f/polymers-12-01916-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec2c/7563493/74f9998e6fdc/polymers-12-01916-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec2c/7563493/543a09739e25/polymers-12-01916-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec2c/7563493/2d6d99da85f2/polymers-12-01916-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec2c/7563493/2c889f87ca77/polymers-12-01916-g008.jpg

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