Biobased Poly(lactide)/ethylene-co-vinyl Acetate Thermoplastic Vulcanizates: Morphology Evolution, Superior Properties, and Partial Degradability

被引:73
作者
Ma, Piming [1 ]
Xu, Pengwu [1 ]
Zhai, Yinghao [2 ]
Dong, Weifu [1 ]
Zhang, Yong [2 ]
Chen, Mingqing [1 ]
机构
[1] Jiangnan Univ, Sch Chem & Mat Engn, Minist Educ, Key Lab Food Colloids & Biotechnol, Wuxi 214122, Peoples R China
[2] Shanghai Jiao Tong Univ, Sch Chem & Chem Engn, Shanghai 200240, Peoples R China
来源
ACS SUSTAINABLE CHEMISTRY & ENGINEERING | 2015年 / 3卷 / 09期
基金
中国国家自然科学基金;
关键词
Thermoplastic vulcanizate; Dynamic cross-link; Morphology; Property; Degradation; POLY(LACTIC ACID); DYNAMIC VULCANIZATION; BLENDS; RUBBER; PHASE; COMPATIBILIZATION; DEGRADATION; PERFORMANCE; CONTINUITY; PEROXIDE;
D O I
10.1021/acssuschemeng.5b00462
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Partially biobased thermoplastic vulcanizates (TPV) with novel morphology, superior properties and partial degradability were prepared by dynamic cross-link of saturated poly(lactide) and ethylene-co-vinyl acetate (PLA/EVA) blends using 2,5-dimethyl-2,5-di(tert-butylperoxy)hexane (AD) as a free radical initiator. EVA showed higher reactivity with free radicals in comparison with PLA, leading to much higher gel content of the EVA phase (G(f-EvA)) than that of the PLA phase (G(f-PLA)). However, the G(f-PLA) increased more steeply at AD content larger than 1 wt % where the reaction of EVA approached to a saturation point. The competing reaction changed the viscosity ratio of the two components (eta(PLA)/eta(EVA)) that resulted in a novel morphology evolution of the TPV, i.e., from sea-island-type morphology to phase inversion via a dual-continuous network-like transition and finally cocontinuity again with increasing the AD content. The cross-link and phase inversion considerably enhanced the melt viscosity (eta*), elasticity (G') and the solid-like behavior of the PLA/EVA-based TPV. Meanwhile, superior tensile strength (sigma(t) = 21 MPa), low tensile set (T-s = 30%), moderate elongation (epsilon(b) = 200%) and suitable stiffness (E' = 350 MPa, 25 degrees C) were successfully achieved by tailoring the cross-link structure and phase morphology. In addition, the TPV are partially degradable in aqueous alkali. A degradation rate of approximately 5 wt % was achieved within 10 weeks at 25 degrees C and the degradation mechanism was investigated from both molecular and macroscopic levels. Therefore, this work provides a new type of partially biobased and degradable materials for substitution of traditional TPV.
引用
收藏
页码:2211 / 2219
页数:9
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