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首页> 外文期刊>Journal of Applied Polymer Science >Solid-state C-13-NMR studies of changes in crosslinked carbon structure of natural rubber during heating under air and nitrogen environments
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Solid-state C-13-NMR studies of changes in crosslinked carbon structure of natural rubber during heating under air and nitrogen environments

机译:固态C-13-NMR研究在空气和氮气环境下加热过程中天然橡胶的交联碳结构的变化

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摘要

The chemical changes that occur in thermal degradation of sulfur-cured natural rubber were investigated using C-13-NMR analysis. The crosslinked carbons formed during the vulcanization process appear in the NMR spectra as peaks representing the various structures formed. Samples of vulcanized rubber were heat-aged at 100 and 150 degrees C under both air (oxidative) and nitrogen (inert) environments to assess both temperature and oxidative effects. Changes were observed by measuring peak areas under the crosslinked carbon peaks. A- and B-type cis monolinkages were found to decompose much faster by oxidative factors at both 100 and 150 degrees C than under nitrogen at either temperature. The polylinkages, however, showed the opposite result of thermal degradation predominating over oxidative factors. Cis-trans isomerization of the main chain carbons was observed at the higher temperature while absent at 100 degrees C. (C) 1998 John Wiley & Sons, Inc. J Appl Polym Sci 70: 1371-1383, 1998. [References: 28]
机译:使用C-13-NMR分析研究了硫磺硫化天然橡胶热降解过程中发生的化学变化。在硫化过程中形成的交联碳在NMR光谱中显示为代表所形成的各种结构的峰。在空气(氧化)和氮气(惰性)环境下,将硫化橡胶样品分别在100和150摄氏度下热老化,以评估温度和氧化作用。通过测量交联的碳峰下的峰面积观察到变化。发现在100和150摄氏度下,A型和B型顺式单键在100和150摄氏度下的氧化因子分解速度都比在任何温度下在氮气下快得多。然而,多键显示出相反的结果,即热降解高于氧化因子。在较高的温度下观察到主链碳的顺反异构化,而在100摄氏度下则不存在。(C)1998 John Wiley&Sons,Inc. J Appl Polym Sci 70:1371-1383,1998. [参考文献:28]

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