Many Tribology Group publications are Open Access thanks to funding from the EPSRC.

Citation

BibTex format

@article{Ayestaran:2021:10.1038/s42004-021-00615-x,
author = {Ayestaran, Latorre C and Moore, J and Remias, J and Spikes, H and Dini, D and Ewen, J},
doi = {10.1038/s42004-021-00615-x},
journal = {Communications Chemistry},
pages = {1--11},
title = {Mechanochemistry of phosphate esters confined between sliding iron surfaces},
url = {http://dx.doi.org/10.1038/s42004-021-00615-x},
volume = {4},
year = {2021}
}

RIS format (EndNote, RefMan)

TY  - JOUR
AB - The molecular structure of lubricant additives controls not only their adsorption and dissociation behaviour at the nanoscale, but also their ability to reduce friction and wear at the macroscale. Here, we show using nonequilibrium molecular dynamics simulations with a reactive force field that tri(s-butyl)phosphate dissociates much faster than tri(n-butyl)phosphate when heated and compressed between sliding iron surfaces. For both molecules, dissociative chemisorption proceeds through cleavage of carbon−oxygen bonds. The dissociation rate increases exponentially with temperature and stress. When the rate−temperature−stress data are fitted with the Bell model, both molecules have similar activation energies and activation volumes and the higher reactivity of tri(s-butyl)phosphate is due to a larger pre-exponential factor. These observations are consistent with experiments using the antiwear additive zinc dialkyldithiophosphate. This study represents a crucial step towards the virtual screening of lubricant additives with different substituents to optimise tribological performance.
AU - Ayestaran,Latorre C
AU - Moore,J
AU - Remias,J
AU - Spikes,H
AU - Dini,D
AU - Ewen,J
DO - 10.1038/s42004-021-00615-x
EP - 11
PY - 2021///
SN - 2399-3669
SP - 1
TI - Mechanochemistry of phosphate esters confined between sliding iron surfaces
T2 - Communications Chemistry
UR - http://dx.doi.org/10.1038/s42004-021-00615-x
UR - https://www.nature.com/articles/s42004-021-00615-x
UR - http://hdl.handle.net/10044/1/92997
VL - 4
ER -