边界条件下的全氟聚烷基醚润滑剂:铁催化的润滑剂降解

D. J. Carré
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引用次数: 11

摘要

全氟聚烷基醚(PFPAE)油和油基润滑脂在边界润滑条件下表现出明显的降解。在没有明显氧气浓度的情况下,如在航天器轨道环境中,降解机制包括两个步骤:(1)PFPAE分子与新暴露的铁的初始反应形成刘易斯酸FeF3,然后(2)FeF3与未反应的PFPAE分子反应,导致醚酸键的断裂。其结果是在低于热分解开始的温度下发生自催化降解。这一机制假设得到了以下实验结果的支持:(1)PFPAE与FeF3反应产生的氟化酮和酸氟醚裂解产物比母体PFPAE分子反应性更强,分子量更低,因此润滑能力更差。(2)在边界润滑条件下,在磨损试验部件的磨损轨迹中形成FeFx化合物。根据这些实验结果,可以预测PFPAE油在高温(约350°C)和新暴露的金属表面(即边界润滑条件)下的性能较差。这一预测通过磨损试验得到证实,在磨损试验中,PFPAE的性能与添加了环烷酸铅或二烷基二硫代氨基甲酸锑的商业石油基和合成碳氢化合物润滑剂的性能进行了比较。试验结果证实了一个众所周知的事实,即在边界润滑条件下,抗磨添加剂对延长磨损寿命非常重要。此外,结果表明,与其他测试润滑油相比,PFPAE润滑油没有表现出足够的润滑性能。PFPAE的降解机制和目前还没有可溶的抗磨添加剂这两个事实都意味着PFPAE润滑剂目前不适合存在边界润滑条件的应用,特别是涉及高负荷的应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Perfluoropolyalkylether lubricants under boundary conditions: Iron catalysis of lubricant degradation
Perfluoropolyalkylether (PFPAE) oils and oil-based greases exhibit signifcant degradation under boundary lubrication conditions. In the absence of significant concentrations of oxygen, as in the case of spacecraft orbital environments, the degradation mechanism consists of two steps: (1) the initial reaction of the PFPAE molecules with freshly exposed iron to form the Lewis acid, FeF3, followed by (2) the reaction of the FeF3 with unreacted PFPAE molecules, which results in the cleavage of the etherate linkages. The result is an autocatalytic degradation that takes place at temperatures below the onset of thermal decomposition. This mechanistic hypothesis is supported by the following experimental results: (1) The reaction of PFPAE with FeF3 has been shown to give rise to fluorinated-ketone and acid fluoride ether-cleavage products that are more reactive than the parent PFPAE molecules and have lower molecular weights and thus poorer lubricating ability. (2) FeFx compounds are formed in the wear tracks of wear-test components under boundary lubrication conditions. On the basis of these experimental results, poor performance can be predicted for PFPAE oils under conditions in which high temperatures (approximately 350 °C) and freshly exposed metal surfaces are present (i.e., the conditions of boundary lubrication). This prediction is corroborated through wear tests in which the performance of PFPAE is compared to the performance of commercial petroleum-based and synthetic- hydrocarbon lubricants to which lead naphthenate or antimony dialkyldithiocarbamate have been added. The test results confirm the well-known fact that the antiwear additives are very important to prolonged wear life under boundary lubrication conditions. In addition, the results show that, compared to the other lubricants tested, the PFPAE lubricants do not demonstrate adequate lubrication pevormance. Both the PFPAE degradation mechanism and the fact that soluble antiwear additives are not currently available imply that PFPAE lubricants are not currently suitable for applications in which boundary lubrication conditions exist, especially when high loads are involved.
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