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首页> 外文期刊>Journal of Macromolecular Science. Physics >Effects of carbon black on chain mobility and dynamic mechanical properties of solution polymerized styrene-butadiene rubber
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Effects of carbon black on chain mobility and dynamic mechanical properties of solution polymerized styrene-butadiene rubber

机译:炭黑对固溶丁苯橡胶链迁移率和动态力学性能的影响

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摘要

The structure of the bound rubber, the 1H NMR (nuclear magnetic resonance) relaxation time, and the crosslink density of the physical network and the glass transition, were studied for solution polymerized styrene-butadiene rubber (SSBR) filled by carbon black, to investigate the effects of carbon black on the chain mobility and dynamic mechanical properties. It was found by ~1H NMR analysis that the rubber chains were adsorbed on the surface of carbon black to form physical crosslinks and restrict the mobility of the chains, especially for some high-mobility units such as chain ends. It was calculated, according to the molecular weight between adjacent crosslinks, that the main motion units of the tightly adsorbed chains appeared to be similar in size to the chain segments. The glass transition temperature (T _g) obtained by differential scanning calorimetry (DSC) could not be used to judge the effect of carbon black on chain mobility, while the appearance and change of the loss-tangent (tan) peak at high temperature in dynamic mechanical thermal spectrometry (DMTS) test showed that there were three chain states: free chains, loosely adsorbed chains, and tightly adsorbed chains. The dynamic rheology test showed that the unfilled SSBR compound had the rheological characteristics of entangled chain networks; however the nonlinear viscoelasticities of the filled SSBR were related to the gradual disentanglement of adsorbed chains and free chains. The peaks in tan δ vs. temperature curves implied that the motion unit size decreased with the increase of bound rubber content, and the modulus vs. temperature curve showed an apparently lower mobility of adsorbed chains than that of free chains through the very low dependence of modulus on temperature for the highly filled compounds. The extremely high tensile modulus of the vulcanizate with 63.6% carbon black at room temperature also implied that the adsorbed chains were in the glass state due to their restriction by the carbon black.
机译:研究了用炭黑填充的溶液聚合的丁苯橡胶(SSBR)的结合橡胶的结构,1H NMR(核磁共振)弛豫时间以及物理网络的交联密度和玻璃化转变,以研究炭黑对链迁移率和动态力学性能的影响。通过〜1 H NMR分析发现,橡胶链吸附在炭黑的表面上以形成物理交联并限制链的迁移,特别是对于某些高迁移率的单元,例如链端。根据相邻交联之间的分子量,可以计算出紧密吸附的链的主要运动单元的大小似乎与链段相似。通过差示扫描量热法(DSC)获得的玻璃化转变温度(T _g)不能用于判断炭黑对链迁移率的影响,而动态高温下损耗角正切(tan)峰的出现和变化机械热光谱法(DMTS)测试表明,存在三种链状状态:自由链,松散吸附的链和紧密吸附的链。动态流变测试表明,未填充的SSBR化合物具有缠结链网络的流变特性;然而,填充的SSBR的非线性粘弹性与吸附链和自由链的逐渐解缠有关。 tanδ与温度的关系曲线的峰值表明,运动单元的尺寸随结合橡胶含量的增加而减小,并且模量与温度的关系曲线显示,由于对链的依赖性极低,吸附链的迁移率明显低于自由链。高填充化合物的温度模量。室温下具有63.6%炭黑的硫化橡胶的极高拉伸模量也暗示了吸附链由于受到炭黑的限制而处于玻璃态。

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