Enhancement of cellulose acetate degradation under accelerated weathering by plasticization with eco-friendly plasticizers

被引:59
|
作者
Quintana, Robert [1 ,2 ,3 ]
Persenaire, Olivier [1 ,2 ]
Lemmouchi, Yahia [4 ]
Sampson, John [4 ]
Martin, Stuart [4 ]
Bonnaud, Leila [1 ,2 ]
Dubois, Philippe [1 ,2 ]
机构
[1] Mat Nova Asbl, B-7000 Mons, Belgium
[2] Univ Mons UMONS, B-7000 Mons, Belgium
[3] ASTAR, Inst Mat Res & Engn, Singapore 117602, Singapore
[4] British Amer Tobacco, Grp R&D Ctr, Southampton SO15 8TL, Hants, England
关键词
Cellulose acetate; Degradation; Weathering; Plasticization; Blend; MECHANICAL-PROPERTIES; BIODEGRADATION;
D O I
10.1016/j.polymdegradstab.2013.06.032
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Cellulose acetate (CA) with a degree of substitution (DS) of 2.5 has been plasticized using eco-friendly plasticizers such as triacetin, tripropionin, triethyl citrate, tributyl citrate, tributyl 2-acetyl citrate and poly(ethylene glycol) of low molecular weight. Thermo-mechanical properties and hydrophilicity of the modified CA have been measured and correlated with the content and nature of the plasticizer used and compared with unplasticized CA. The increase in toughening and the change in the hydrophilicity by the plasticization were evaluated in terms of aging and weathering stability under accelerated conditions. Samples were exposed to UV-degradation with water spray periods. The treated samples were removed periodically and characterized by several analytical techniques. The results are discussed with particular emphasis toward the effects of plasticization on enhancement of the degradation rate of CA. The plasticization of CA triggered an increase of the weight loss between 50 and 90%, where low molecular weight plasticizers were shown to be more effective. A right balance between hydrophilicity and plasticization efficiency (reduction of T-g) is needed to increase the degradation rate of CA. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1556 / 1562
页数:7
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