基于硅烷增强的绿色轮胎用功能性橡胶复合材料:最新技术

Jeevanandham Neethirajan, Arshad Rahman Parathodika, Guo-Hua Hu, Kinsuk Naskar
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引用次数: 1

摘要

二氧化硅是继炭黑之后橡胶工业最重要的、性价比最高的补强填料。由于二氧化硅表面存在极性官能团,非极性弹性体的二氧化硅增强机理变得复杂。二氧化硅的极性性质通过形成氢键导致填料之间的相互作用。因此,相当大的非分散二氧化硅团簇保留在非极性橡胶基体中。为了避免这些强的填料-填料相互作用并改善橡胶/二氧化硅相容性,需要对二氧化硅表面进行改性。这可以使用具有能够连接橡胶和二氧化硅的官能团的偶联剂来完成。人们发现,当二氧化硅/硅烷偶联剂存在时,轮胎胎面魔术三角中的滚动阻力和湿抓地力等关键性能比炭黑配方更好地平衡,使系统更接近绿色轮胎的目标。本文综述了橡胶配方开发和化学方面为充分挖掘汽车轮胎用硅烷/硅烷增强材料的潜力所做的努力。重点介绍了复合成分、工艺技术、功能化弹性体、新型硅烷和硅烷的变体如何增强魔三角和硅烷-硅烷反应机理。此外,还重点介绍了硅烷化的动力学和硅烷化程度的测量。展望了该领域未来的研究方向。希望这篇综述能够促进未来二氧化硅/硅烷科学技术的发展,以满足学术和工业的需求。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Functional rubber composites based on silica-silane reinforcement for green tire application: the state of the art

Silica is the rubber industry’s most essential and cost-effective reinforcing filler after carbon black. The silica reinforcement mechanism with a non-polar elastomer is complicated by the presence of polar functional groups on the silica surface. This polar nature of silica causes filler-to-filler interaction by forming hydrogen bonds. Therefore, sizeable non-dispersed silica clusters remain in a non-polar rubber matrix. To avoid these strong filler-filler interactions and improve rubber/silica compatibility, the silica surface needs to be modified. This can be done using a coupling agent which has functional groups capable of linking both the rubber and silica. It has been discovered that when silica/silane coupling agents are present, the critical properties like rolling resistance and wet grip in the magic triangle of tire tread balance out better than carbon black formulations, bringing the system closer to the green tire goal. In this review article, the efforts made by both the rubber formulation development and chemistry to fully exploit the potential of silica/silane reinforcement for automotive tires are retrospected. Highlights on how compounding ingredients, process technology, functionalized elastomer, novel silanes, and the variant of silicas can enhance the magic triangle and silica-silane reaction mechanism are provided. In addition, the kinetics of silanization and measurements for the degree of silanization is also highlighted. Future research directions in this area are also touched upon. Hopefully, this review can stimulate future silica/silane scientific and technology developments for both academic and industrial-oriented requirements.

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