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X-ray absorption near edge structure spectroscopy (XANES) analysis has been routinely used to study the complex chemical interactions between additives in engine oil and metallic surfaces during high-temperature and pressure reciprocating wear conditions. XANES analysis provides detailed chemical and structural information on the resultant antiwear and tribo films formed on metallic surfaces. The following review will illustrate how XANES analysis on the macro scale can provide the information required to elucidate complex film formation mechanisms, then describes the use of emerging XANES spectromicroscopy to such systems, and concludes by showing the complementary nature of the macro and micro scale spatially resolved XANES analysis; Professor Bancroft has utilized the combination of these to stay at the forefront of XANES research in the field of tribology and in spectroscopy science in general.Key words: tribology, XANES, X-ray absorption near edge structure spectroscopy, metals, thiophosphates, spectromicroscopy, tribochemistry.

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The chemical interaction of two kinds of dispersants (bis-succinimide dispersant and borated bis-succinimide dispersant) with four kinds of antiwear (AW) and extreme pressure (EP) additives (zinc dialkyldithiophosphate, dialkyldithiophosphate ester, diphenylphosphate ester and dialkyldithiocarbamate) has been investigated under different contact pressures. The chemical compositions of the tribofilms have been studied by B, N, P and S X-ray absorption near edge structure (XANES) spectroscopy. The N K-edge XANES analysis has been used to follow the reaction pathway of amine and imide functional groups in the dispersants and their interactions with EP and AW additives. It has been found that AW additives react with amine to form amine phosphate at low load. However, at high load, there is a good evidence for the formation of a nitrate phase in the tribofilms, the first direct observation of oxidative dispersant loss in the rubbing contact. On the other hand, EP additives behave differently and in general are less reactive. The B K-edge XANES has been employed to follow the interaction of borated dispersant with the EP and AW additive. In general, boron originally in the trigonal coordination, is converted to a tetrahedral coordination form in the process of tribofilm formation.

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X-ray absorption near-edge structure (XANES) spectroscopy at macro-scale (mm 2 ) and X-ray photoelectron emissions microscopy (X-PEEM) at micro-scale (lm 2 ) have been used to investigate the chemistry and spatial distributions of chemical species in tribochemical films generated from ashless thiophosphate oil additives on steel. Two different ashless thiophosphate additives were used: a triaryl monothiophosphate (MTP) and a dialkyldithiophosphate (DTP). Atomic force microscopy (AFM) and secondary electron microscopy (SEM) were also used to investigate the thickness and the topography of the tribofilms. Macro-scale XANES analysis showed that both ashless thiophosphates reacted with the steel surface to produce short to medium chain polyphosphates as the main constituent and sulfur species as minor component. From the PEEM experiment, it was found that the DTP tribofilm was microchemically heterogeneous, with areas of varying degrees of polyphosphate chain length. Conversely, MTP formed a tribofilm microchemically homogeneous, with areas comprised of only short chain polyphosphates. From, the different areas of polyphosphate chain length within the DTP tribofilm, colour-coded polyphosphate distribution map was generated. AFM, X-PEEM and SEM revealed that the DTP film was thicker and was composed of AW pads that were wider in area than MTP. This resulted in a smaller wear scar width (WSW) value for DTP. This is the first time that all these analytical techniques have been combined to better understand the nature of the tribofilms from ashless additives. We have concluded that an ideal AW film is comprised of a thick film with pad-like structures that are wider in area and microchemically heterogeneous, with areas of varying polyphosphate chain length.

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