Abstract

In recent years, substantial advancements have been achieved in augmenting the energy efficiency of hydraulic fluids through the integration of polymers. This study employs a multiscale approach, encompassing an analysis of polymer coil size evolution and flow field characteristics, with the aim of investigating the behavior of both dipole and non-dipole polymers within the host solvent. The ultimate goal is to establish a comprehensive understanding of the correlation between atomic properties of additives and the macroscopic properties of the polymer solution.To achieve this, the study employs an atomistic-continuum hybrid model that combines Brownian Dynamics and Lattice Boltzmann techniques within the bead-spring concept framework. Four chains, each comprising 64 particles, are subjected to varying shear rates. The primary focus centers on the examination of alterations in the radius of gyration and the velocity field within the polymer solution. Notably, the inclusion of dipole-dipole interactions exerts a profound influence on the configuration of the polymers. The results illuminate that non-dipole polymers display a more pronounced coupling with bulk flow hydrodynamics, leading to the confinement of particle motion in directions perpendicular to the primary stream. In contrast, dipole polymers experience a slower increase in coil size when compared to their non-dipole counterparts. These findings furnish valuable insights for the enhancement of energy-efficient hydraulic fluids and contribute to a fundamental comprehension of polymer behavior in lubricants, charting the course for the development of advanced hydraulic fluids in the future.

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