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Visually Based Characterization of the Incipient Particle Motion in Regular Substrates: From Laminar to Turbulent Conditions
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Beyond the no-slip boundary condition.

Howard Brenner1

  • 1Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139-4307, USA. hbrenner@mit.edu

Physical Review. E, Statistical, Nonlinear, and Soft Matter Physics
|December 21, 2011
PubMed
Summary
This summary is machine-generated.

This study proposes a new macroscopic method for fluid slip boundary conditions, suggesting the energy equation governs slip. The derived relation accurately predicts gas and liquid creep behavior at solid surfaces.

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Area of Science:

  • Fluid dynamics
  • Physical chemistry
  • Surface science

Background:

  • Determining the correct fluid slip boundary condition at solid interfaces is crucial for accurate fluid flow modeling.
  • Existing models often rely on the momentum equation, but its applicability to slip phenomena is debated.

Purpose of the Study:

  • To develop a simple macroscopic approach for fluid slip boundary conditions.
  • To identify whether the energy or momentum equation dictates the fluid-mechanical boundary condition for slip.

Main Methods:

  • A macroscopic theoretical framework was developed, focusing on the energy equation.
  • A constitutive relation for slip velocity was derived based on near-equilibrium linear thermodynamics.

Main Results:

  • The study proposes that the energy equation, not the momentum equation, determines the slip boundary condition.
  • A general constitutive relation for slip velocity was derived: (v(m))(slip)=-α∂lnρ/∂s|(wall).
  • This relation successfully explains experimental data for thermal and pressure-driven creep in gases and liquids.

Conclusions:

  • The energy equation provides a more accurate basis for fluid slip boundary conditions.
  • The derived constitutive relation offers a unified explanation for various creep phenomena at solid-fluid interfaces.
  • This work advances the understanding of fluid behavior at the nanoscale and microscale.