Shear-degradation of grease and base oil availability in starved EHL lubrication

Author(s):  
J-S. Mérieux ◽  
S. Hurley ◽  
A.A. Lubrecht ◽  
P.M. Cann
Lubricants ◽  
2020 ◽  
Vol 8 (2) ◽  
pp. 12
Author(s):  
Tomas Zapletal ◽  
Petr Sperka ◽  
Ivan Krupka ◽  
Martin Hartl

This paper deals with an experimental study of film thickness and friction of commercial-grade grease and its base oil in a highly loaded contact. In-situ measurements were conducted for two surface textures on a ball-on-disc optical tribometer at the border of mixed lubrication. At high speeds, the film thickness and the friction of grease correspond with the base oil, while, the thickener enters the contact area and locally affects the film thickness and friction at low speeds. It was found out that the thickener starts to enter the contact area approximately at the same speed when the base oil friction increases on Stribeck curve but without direct solid to solid contact. It indicates that both effects can have the same origin. Change of lubricant flow in contact inlet area was discussed as a possible explanation.


2020 ◽  
Vol 69 (1) ◽  
Author(s):  
Jie Zhang ◽  
Mao Ueda ◽  
Sophie Campen ◽  
Hugh Spikes

AbstractThe frictional properties of ZDDP tribofilms at low entrainment speeds in boundary lubrication conditions have been studied in both rolling/sliding and pure sliding contacts. It has been found that the boundary friction coefficients of these tribofilms depend on the alkyl structure of the ZDDPs. For primary ZDDPs, those with linear alkyl chains give lower friction those with branched alkyl chain ZDDPs, and a cyclohexylmethyl-based ZDDP gives markedly higher friction than non-cyclic ones. Depending on alkyl structure, boundary friction coefficient in rolling-sliding conditions can range from 0.09 to 0.14. These differences persist over long duration tests lasting up to 120 h. For secondary ZDDPs, boundary friction appears to depend less strongly on alkyl structure and in rolling-sliding conditions stabilises at ca 0.115 for the three ZDDPs studied. Experiments in which the ZDDP-containing lubricant is changed after tribofilm formation by a different ZDDP solution or a base oil indicate that the characteristic friction of the initial ZDDP tribofilm is lost almost as soon as rubbing commences in the new lubricant. The boundary friction rapidly stabilises at the characteristic boundary friction of the replacement ZDDP, or in the case of base oil, a value of ca 0.115 which is believed to represent the shear strength of the bare polyphosphate surface. The single exception is when a solution containing a cyclohexylethyl-based ZDDP is replaced by base oil, where the boundary friction coefficient remains at the high value characteristic of this ZDDP despite the fact that rubbing in base oil removes about 20 nm of the tribofilm. XPS analysis of the residual tribofilm reveals that this originates from presence of a considerable proportion of C-O bonds at the exposed tribofilm surface, indicating that not all of the alkoxy groups are lost from the polyphosphate during tribofilm formation. Very slow speed rubbing tests at low temperature show that the ZDDP solutions give boundary friction values that vary with alkyl group structure in a similar fashion to rolling-sliding MTM tests. These variations in friction occur immediately on rubbing, before any measurable tribofilm can develop. This study suggest that ZDDPs control boundary friction by adsorbing on rubbing steel or tribofilm surfaces in a fashion similar to organic friction modifiers. However it is believed that, for primary ZDDPs, residual alkoxy groups still chemically bonded to the phosphorus atoms of newly-formed polyphosphate/phosphate tribofilm may also contribute to boundary friction. This understanding will contribute to the design of low friction, fuel efficient crankcase engine oils. Graphical Abstract


2015 ◽  
Vol 642 ◽  
pp. 8-12
Author(s):  
William W.F. Chong ◽  
Miguel de La Cruz

The paper introduces an alternative approach to predict boundary friction for rough surfaces at micros-scale through the empirical integration of asperity-like nanoscale friction measurements. The nanoscale friction is measured using an atomic force microscope (AFM) tip sliding on a steel plate, confining the test lubricant, i.e. base oil for the fully formulated SAE grade 10w40. The approach, based on the Greenwood and Tripp’s friction model, is combined with the modified Elrod’s cavitation algorithm in order to predict the friction generated by a slider-bearing test rig. The numerical simulation results, using an improved boundary friction model, showed good agreement with the measured friction data.


e-Polymers ◽  
2011 ◽  
Vol 11 (1) ◽  
Author(s):  
Ming Duan ◽  
Shenwen Fang ◽  
Liehui Zhang ◽  
Fuxiao Wang ◽  
Peng Zhang ◽  
...  

AbstractAn experimental study of the flow-induced scission behaviour of four star hydrolyzed polyacrylamides (HPMA) with different arms during planar elongational flow in a cross-slot flow cell is described. The results showed that the shear stability of linear HPAM in distilled water was not essentially different from star HPAM. Polymer scission was not observed in either system in a shear rate range from 20,000 to 100,000s-1, which can be attributed to the strong polyelectrolyte behaviour of HPAM in distilled water. However, at the same shear rate, the star HPAMs exhibited superior shear stability in comparison to the linear HPAMs in aqueous solutions containing NaCl (CNaCl=0.2-1.0%wt) and, in particular, the initial reduction rate of relative viscosity (R) decreased with the degree of branching of the HPAMs. In addition, it was found that the R of five HPAMs in NaCl aqueous solutions exhibited an exponential dependence on shear rate, in which the coefficient C1 can be used to quantitatively evaluate shear stability. In star HPAM NaCl aqueous solutions, the increase of R with shear rate is very likely due to the decrease of the hydrodynamic radius (Rh) of these HPAMs, while the increase of R with NaCl concentrations can be attributed to the relatively low viscosity of these polymers at high NaCl concentrations.


2016 ◽  
Vol 93 ◽  
pp. 502-510 ◽  
Author(s):  
C. Mary ◽  
D. Philippon ◽  
N. Devaux ◽  
N. Fillot ◽  
D. Laurent ◽  
...  
Keyword(s):  
Base Oil ◽  

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