Manfred Jungk

Energy efficient siloxane lubricants utilizing temporary shear-thinning

This study investigates the rheologic properties, elastohydrodynamic film, and friction coefficients of several siloxane-based lubricants to assess their shear stability and their potential for energy efficient lubrication. Several siloxane-based polymers with alkyl, aryl, and alkyl-aryl branches were synthesized in order to examine the relationship between their molecular structures and tribological performance. Nuclear magnetic resonance spectroscopy and gel permeation chromatography were used to characterize the molecular structures and masses, respectively. Density, viscosity, elastohydrodynamic film thickness, and friction measurements were measured from 303 to 398 K. Film thickness and friction measurements were made at loads and speeds that cover the boundary, mixed, and full film lubrication regimes. These results illustrate that the shear characteristics of siloxane lubricants vary significantly with polymer length as well as branch structure and content. The findings provide quantitative insight into the features of siloxane molecular structure conducive to optimum film formation with minimum wear and elastohydrodynamic friction to enhance energy efficiency.

Correlation of Polysiloxane Molecular Structure to Shear-Thinning Power-Law Exponent Using Elastohydrodynamic Film Thickness Measurements

Siloxane-based polymers (polysiloxanes) are susceptible to temporary shear-thinning that manifests as a reduction of elastohydrodynamic film thickness with increasing entrainment speed or effective shear rate. The departure from Newtonian film thickness can be predicted with the power-law exponent ns, an indicator of the severity of shear-thinning in a polymeric fluid that is influenced by the macromolecular structure. In this paper, a combination of extant rheological and tribological models is applied to determine the power-law exponent of several polysiloxanes using film thickness measurements. Film thickness data at several temperatures and slide-to-roll ratios are used to validate the methodology for several siloxane-based polymers with alkyl and aryl branches.

Erratum to: Traction Characteristics of Siloxanes with Aryl and Cyclohexyl Branches

The molecular structures, rheological properties, and friction coefficients of several new siloxane-based polymers were studied to explore their traction characteristics. The molecular structures including branch content were established by nuclear magnetic resonance spectroscopy, while the molecular mass distributions were determined by gel permeation chromatography. Density, viscosity, elastohydrodynamic film formation, and friction were investigated over a temperature range of 303–398 K. Film thickness and friction measurements were studied under the conditions that are representative of boundary, mixed, and full-film lubrication regimes, aiming at maximizing traction performance and temperature stability by simultaneous optimization of the size and content of ringshaped branch structures. This study provides quantitative insight into the effect of siloxane molecular structure on the tribological performance for traction drive applications such as continuously variable transmissions.