Thermophoresis at a charged surface: the role of hydrodynamic slip
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منابع مشابه
Thermophoresis at a charged surface: the role of hydrodynamic slip.
By matching boundary layer hydrodynamics with slippage to the force-free flow at larger distances, we obtain the thermophoretic mobility of charged particles as a function of the Navier slip length b. A moderate value of b augments Ruckenstein's result by a term 2b/λ, where λ is the Debye length. If b exceeds the particle size a, the enhancement coefficient a/λ is independent of b but proportio...
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Equilibrium and nonequilibrium molecular dynamics simulations were conducted in order to evaluate the hypothesis that the hydrodynamic slip length is a surface property. The system under investigation was water confined between two graphite layers to form nanochannels of different sizes (3-8 nm). The water-carbon interaction potential was calibrated by matching wettability experiments of graphi...
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Thermally induced particle flow in a charged colloidal suspension is studied in a fluid-mechanical approach. The force density acting on the charged boundary layer is derived in detail. From Stokes' equation with no-slip boundary conditions at the particle surface, we obtain the particle drift velocity and the thermophoretic transport coefficients. The results are discussed in view of previous ...
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Observation of slip flow in thermophoresis.
Two differing theories aim to describe fluidic thermophoresis, the movement of particles along a temperature gradient. While thermodynamic approaches rely on local equilibrium, hydrodynamic descriptions assume a quasi-slip-flow boundary condition at the particle's surface. Evidence for slip flow is presented for the case of thermal gradients exceeding (aS_(T)(-1) with particle radius a and Sore...
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ژورنال
عنوان ژورنال: Journal of Physics: Condensed Matter
سال: 2008
ISSN: 0953-8984,1361-648X
DOI: 10.1088/0953-8984/21/3/035103