Microstructure studies of isotactic polypropylene under natural weathering by positron annihilation lifetime spectroscopy

被引:14
|
作者
Ni, Kai [1 ]
Zhu, Jingjun [2 ]
Liao, Xia [1 ]
Lv, Yadong [1 ]
Wu, Lingyun [1 ]
Zhang, Qiongwen [1 ]
An, Zhu [2 ]
Yang, Qi [1 ]
Huang, Yajiang [1 ]
Li, Guangxian [1 ]
机构
[1] Sichuan Univ, State Key Lab Polymer Mat Engn, Coll Polymer Sci & Engn, Chengdu 610065, Sichuan, Peoples R China
[2] Sichuan Univ, Key Lab Radiat Phys & Technol, Minist Educ, Inst Nucl Sci & Technol, Chengdu 610064, Sichuan, Peoples R China
基金
中国国家自然科学基金;
关键词
Polypropylene; Natural weathering; Microstructure; Molecular mobility; Positron annihilation lifetime spectroscopy; FREE-VOLUME; ENVIRONMENTAL DEGRADATION; DENSITY POLYETHYLENE; IRON CARBOXYLATES; AMORPHOUS REGIONS; CRYSTALLIZATION; PHOTOOXIDATION; BEHAVIOR; PHOTODEGRADABILITY; POLYCARBONATE;
D O I
10.1007/s10965-015-0753-z
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The microstructure evolution of isotactic polypropylene (PP) exposed to subtropical humid climate of Guangzhou of China, were investigated by gel permeation chromatography, Fourier transform infrared spectroscopy, differential scanning calorimeter, dynamic mechanical analysis and positron annihilation lifetime spectroscopy. Positron data showed that the free volume of PP matrix decreased with involving a shrinking of the free volume hole sizes as the extent of weathering degradation of PP aggravated. The shrinkage of free volume hole sizes may be traced to the loss of mobility of molecules of PP matrix. The increase of the glass transition temperature substantiated undoubtedly the decrease of molecular mobility of PP chains. The increase in crystallinity might increase the amount of rigid amorphous fraction of PP matrix, which induced the loss of molecular mobility. Furthermore, the decrease of ortho-positronium formation ought to be correlated to the increase in crystallinity and the increasing amount of scavenchers which were in this work represented by the carbonyl groups.
引用
收藏
页数:9
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