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具有纳米结构的天然橡胶的熵弹性和能量弹性。

Entropic and Energetic Elasticities of Natural Rubber with a Nanomatrix Structure.

机构信息

Department of Chemical Science and Engineering, National Institute of Technology, Tokyo College, 1220-2, Kunugida-cho, Hachioji, Tokyo 193-0997, Japan.

Department of Materials Science and Technology, Nagaoka University of Technology, 1603-1, Kamitomioka-cho, Nagaoka, Niigata 940-2188, Japan.

出版信息

Langmuir. 2020 Sep 29;36(38):11341-11348. doi: 10.1021/acs.langmuir.0c02111. Epub 2020 Sep 14.

Abstract

The entropic and energetic elasticities of natural rubber with a nanomatrix structure are investigated by measuring the viscoelastic properties of deproteinized natural rubber (DPNR)--polystyrene (PS). A nanomatrix structure is formed by graft copolymerization of styrene onto the surface of natural rubber particles, followed by coagulation. The morphology of the nanomatrix structure is observed with transmission electron microscopy. Natural rubber particles with about 1 μm diameter are well dispersed in a nanomatrix of PS. The horizontal shift factor () and vertical shift factor () are determined by superposition to create a master curve according to the time-temperature superposition principle. The positive slope of DPNR appears in the plot of versus temperature, suggesting that entropic elasticity occurs. In contrast, the slopes of DPNR--PS are negative at lower temperatures but positive at higher temperatures. The negative slope, which suggests entropic elasticity, may be attributed to the formation of a nanomatrix structure. Natural rubber with a nanomatrix structure realizes both energetic elasticity and entropic elasticity.

摘要

通过测量去蛋白天然橡胶(DPNR)-聚苯乙烯(PS)的黏弹性,研究了具有纳米矩阵结构的天然橡胶的熵弹性和能量弹性。通过苯乙烯接枝到天然橡胶颗粒表面,然后再进行凝聚,形成纳米矩阵结构。用透射电子显微镜观察纳米矩阵结构的形态。直径约 1μm 的天然橡胶颗粒在 PS 的纳米矩阵中得到了很好的分散。根据时温叠加原理,通过叠加确定水平移动因子()和垂直移动因子(),以创建主曲线。DPNR 中出现的正斜率表明存在熵弹性。相比之下,在较低温度下,DPNR-PS 的斜率为负,但在较高温度下为正。负斜率表明熵弹性可能归因于纳米矩阵结构的形成。具有纳米矩阵结构的天然橡胶实现了能量弹性和熵弹性。

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