Rheological behavior of polyolefins during UV irradiation at high temperature as a coupled degradative process

被引:22
作者
Marek, Adam A. [1 ,2 ]
Verney, Vincent [1 ,3 ]
机构
[1] Univ Clermont Ferrand, Univ Clermont Auvergne, Inst Chim Clermont Ferrand, F-63000 Clermont Ferrand, France
[2] Silesian Tech Univ, Dept Organ Chem Technol & Petrochem, PL-44100 Gliwice, Poland
[3] CNRS, ICCF, UMR 6296, F-63178 Aubiere, France
关键词
Photo-rheology; Polyolefins; Cole-Cole plots; UV irradiation; UV LED; PEROXIDE-PROMOTED DEGRADATION; REACTIVE EXTRUSION; CROSS-LINKING; POLYPROPYLENE; POLYETHYLENE; PHOTODEGRADATION; EXTRUDER; BLEND;
D O I
10.1016/j.eurpolymj.2015.09.003
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 photo-rheology method was applied to determinate the differences in the rheological behavior of selected polyolefins (PP, HDPE and LDPE) over a range of temperatures, higher than melting temperatures (160-200 degrees C) and during UV irradiation as a coupled degradative conditions in air atmosphere. Both, UV mercury lamp and UV LED were used as irradiation source. Multiwave experiments were performed and viscoelastic data were plotted in the complex plane to obtain Cole-Cole plots at different conditions. It helped to assess the molecular evolution of the examined materials. The competition between chain scissions and chain recombination (crosslinking) was observed. Chain scission reactions occurred in PP and for HDPE and LDPE crosslinking reactions predominated, especially over 180 degrees C. UV irradiation intensified these effects. In the case of HDPE chain scission reactions were also observed especially below 180 degrees C in processes performed without UV. At higher temperature and under UV irradiation crosslinking reactions and increase of viscosity began to dominate. Despite different energy and emission spectra of irradiation sources, the similar effects were observed. (C) 2015 Elsevier Ltd. All rights reserved.
引用
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页码:1 / 11
页数:11
相关论文
共 36 条
[21]   Phase behavior and its viscoelastic responses of poly(methyl methacrylate) and poly(styrene-co-maleic anhydride) blend systems [J].
Li, RM ;
Yu, W ;
Zhou, CX .
POLYMER BULLETIN, 2006, 56 (4-5) :455-466
[22]   Examination of the possibility of recycling and utilizing recycled polyethylene and polypropylene [J].
Meran, Cemal ;
Ozturk, Orkun ;
Yuksel, Mehmet .
MATERIALS & DESIGN, 2008, 29 (03) :701-705
[23]  
Mudgal, 2011, PLASTIC WASTE ENV RE
[24]   A comparison of rheology and FTIR in the study of polypropylene and polystyrene photodegradation [J].
Myllari, Ville ;
Ruoko, Tero-Petri ;
Syrjala, Seppo .
JOURNAL OF APPLIED POLYMER SCIENCE, 2015, 132 (28)
[25]   Photoinitiated grafting of maleic anhydride onto polypropylene [J].
Pan, B ;
Viswanathan, K ;
Hoyle, CE ;
Moore, RB .
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 2004, 42 (08) :1953-1962
[26]  
Qu BJ, 2000, J POLYM SCI POL CHEM, V38, P999, DOI 10.1002/(SICI)1099-0518(20000315)38:6<999::AID-POLA9>3.0.CO
[27]  
2-1
[28]   The role of physical structure and morphology in the photodegradation behaviour of polypropylene [J].
Rabello, MS ;
White, JR .
POLYMER DEGRADATION AND STABILITY, 1997, 56 (01) :55-73
[29]   MELTING BEHAVIOR OF CONTROLLED RHEOLOGY POLYPROPYLENE [J].
RYU, SH ;
GOGOS, CG ;
XANTHOS, M .
POLYMER, 1991, 32 (13) :2449-2455
[30]  
Tamboli SM, 2004, INDIAN J CHEM TECHN, V11, P853