Zhan Zhiming, He Hezhi, Zhu Zhiwen, Xue Bin, Wang Guozhen, Chen Ming, Xiong Chengtian
National Engineering Research Center of Novel Equipment for Polymer Processing, Guangdong Provincial Key Laboratory of Technique and Equipment for Macromolecular Advanced Manufacturing, South China University of Technology South China University of Technology, Guangzhou 510640, China.
Key Laboratory of Polymer Processing Engineering, Ministry of Education, South China University of Technology, Guangzhou 510640, China.
Materials (Basel). 2019 Jul 24;12(15):2352. doi: 10.3390/ma12152352.
In this study, the in-situ compatibilization reaction between recycled acrylonitrile-butadiene-styrene copolymer (rABS) and functional styrene-ethylene-butylene-styrene block maleic anhydride (SEBS-g-MAH) was confirmed, which contributed to the toughening phenomenon of rABS, especially the notched impact strength. As mechanical test that manifested, the rABS/SEBS-g-MAH blends are stronger and more ductile than the rABS/SEBS blends. Prominently, the former has great advantage over the latter in terms of improving the impact performance. Scanning electron microscope (SEM) images showed that the compatible segments that were generated by reaction not only improve the interface adhesion of rABS/SEBS-g-MAH blends but also promote the evolution of co-continuous structures, which can be evidently observed after etching. Furthermore, the SEM micrographs of tensile fracture surfaces indicated that the formation of the co-continuous phase and the improvement of interface adhesion are the most profound reasons for the excellent tensile properties of the rABS/SEBS-g-MAH blends. The impact fracture surface revealed that two-phase interface affects crack propagation and shear yielding absorbs more impact energy than simple interface debonding does at higher deformation rates. Meanwhile, rheological analysis demonstrated that the complex viscosity of the rABS/SEBS-g-MAH (80/20 wt%) blend with a co-continuous structure exhibits a maximum positive deviation at low frequencies from the theoretical value calculated using the rule of logarithmic sum, which indicated a connection between co-continuous structure and complex viscosity. In addition, the storage modulus vs. loss modulus curves of the blends revealed that the viscoelastic behavior of rABS/SEBS-g-MAH blends is very similar to that of rABS.
在本研究中,证实了回收丙烯腈-丁二烯-苯乙烯共聚物(rABS)与功能性苯乙烯-乙烯-丁烯-苯乙烯嵌段马来酸酐(SEBS-g-MAH)之间的原位增容反应,这促成了rABS的增韧现象,尤其是缺口冲击强度。如力学测试所示,rABS/SEBS-g-MAH共混物比rABS/SEBS共混物更强且更具韧性。显著的是,前者在改善冲击性能方面比后者具有很大优势。扫描电子显微镜(SEM)图像显示,反应生成的相容链段不仅改善了rABS/SEBS-g-MAH共混物的界面粘附性,还促进了双连续结构的演变,蚀刻后可明显观察到这一点。此外,拉伸断口表面的SEM显微照片表明,双连续相的形成和界面粘附性的改善是rABS/SEBS-g-MAH共混物优异拉伸性能的最主要原因。冲击断口表面显示,两相界面影响裂纹扩展,在较高变形速率下,剪切屈服比简单的界面脱粘吸收更多的冲击能量。同时,流变学分析表明,具有双连续结构的rABS/SEBS-g-MAH(80/20 wt%)共混物的复数粘度在低频下相对于使用对数和规则计算的理论值呈现最大正偏差,这表明双连续结构与复数粘度之间存在联系。此外,共混物的储能模量与损耗模量曲线表明,rABS/SEBS-g-MAH共混物的粘弹性行为与rABS非常相似。