Elucidating tribochemical reaction mechanisms: insights into tribofilm formation from hydrocarbon adsorbates coupled with tribochemical substrate wear†

Yu-Sheng Li, Fakhrul H. Bhuiyan, Jongcheol Lee, Ashlie Martini and Seong H. Kim
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Abstract

Tribochemical reactions, chemical processes that occur by frictional shear at sliding interfaces, lead to tribofilm formation or substrate wear that directly affect the efficiency of machinery. Here, we report tribofilm growth through tribopolymerization and tribochemical wear of a silica surface due to reactions with organic precursors methylcyclopentane, cyclohexane, cyclohexene, and α-pinene. The activation volume determined from the stress dependence of reaction yield is correlated to the chemical reactivity of the precursor molecules. The molecules with higher tribochemical reactivity exhibited smaller activation volume, implying that less mechanical energy was required to initiate tribochemical reactions. Nudged elastic band calculations for the hypothetical pathways for the observed tribochemical reactions suggested that the smaller activation volume could be related to smaller thermal activation energy at the rate-limiting step. The tribofilm formation yield was found to increase with load whereas the load dependence of tribochemical wear was negligible. The environment dependence of the sliding processes was also analyzed. Results showed that, compared to a dry N2 environment, the tribopolymerization reaction yield increased in dry air but decreased in N2 with 40% relative humidity, while the wear rate remained unchanged. This finding suggested that during sliding, the reactive sites exposed at the worn surface could be re-oxidized by even trace amounts of oxygen or water vapor in the environment. This analysis of tribofilm yield and substrate wear in various environments showed that ambient gas can change the tribochemical reactivities of the reactant, which leads to different load dependencies of tribopolymerization and tribochemical wear.

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阐明摩擦化学反应机制:深入了解碳氢化合物吸附物与摩擦化学基体磨损相结合形成的三膜†。
摩擦化学反应是在滑动界面上通过摩擦剪切发生的化学过程,会导致三膜形成或基体磨损,直接影响机械的效率。在此,我们报告了有机前体甲基环戊烷、环己烷、环己烯和α-蒎烯与二氧化硅表面的摩擦聚合反应和摩擦化学磨损导致的三膜生长。根据反应产率的应力相关性确定的活化体积与前体分子的化学反应活性相关。摩擦化学反应活性较高的分子表现出较小的活化体积,这意味着启动摩擦化学反应所需的机械能较少。对所观察到的摩擦化学反应的假设途径进行的弹性带计算表明,活化体积较小可能与限速步骤的热活化能较小有关。研究发现,三膜形成率随载荷的增加而增加,而摩擦化学磨损与载荷的关系可以忽略不计。此外,还分析了滑动过程的环境依赖性。结果表明,与干燥的 N2 环境相比,摩擦聚合反应产率在干燥空气中增加,但在相对湿度为 40% 的 N2 环境中降低,而磨损率保持不变。这一发现表明,在滑动过程中,即使环境中存在微量的氧气或水蒸气,磨损表面上暴露的反应位点也会被重新氧化。对不同环境下三膜产量和基体磨损的分析表明,环境气体会改变反应物的摩擦化学反应活性,从而导致摩擦聚合和摩擦化学磨损的负荷依赖性不同。
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Back cover Vortex mediated fabrication of 2D antimonene sheets from antimony powder† Mechanical approach for creating different molecular adducts and regulating salt polymorphs: a case study of the anti-inflammatory medication ensifentrine† Exploring mass transfer as a parameter in mechanochemical processes† Back cover
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