Statistical Thermodynamic Theory for Non-Equilibrium, Quasi-Equilibrium, and Equilibrium Electrochemical Reactions

2013 ◽  
Vol 160 (8) ◽  
pp. H420-H429 ◽  
Author(s):  
Heui-Seol Roh
2021 ◽  
Vol 23 (14) ◽  
pp. 8705-8716
Author(s):  
Seishi Shimizu ◽  
Nobuyuki Matubayasi

Enhanced surfactant association by solutes drives cooperative solubilization according to the universal statistical thermodynamic theory.


2007 ◽  
Vol 579 ◽  
pp. 173-226 ◽  
Author(s):  
B. ZALTZMAN ◽  
I. RUBINSTEIN

Electric conduction from an electrolyte solution into a charge selective solid, such as ion exchange membrane or electrode, becomes unstable when the electrolyte concentration near the interface approaches zero owing to diffusion limitation. The sequence of events leading to instability is as follows: upon the decrease of the interface concentration, the electric double layer at the interface transforms from its common quasi-equilibrium structure to a different, non-equilibrium one. The key feature of this new structure is an extended space charge added to the usual one of the quasi-equilibrium electric double layer. The non-equilibrium electro-osmotic slip related to this extended space charge renders the quiescent conductance unstable. A unified asymptotic picture of the electric double-layer undercurrent, encompassing all regimes from quasi-equilibrium to the extreme non-equilibrium one, is developed and employed for derivation of a universal electro-osmotic slip formula. This formula is used for a linear stability study of quiescent electric conduction, yielding the precise parameter range of instability, compared with that in the full electroconvective formulation. The physical mechanism of instability is traced both kinematically, in terms of non-equilibrium electro-osmotic slip, and dynamically, in terms of forces acting in the electric double layer.


2007 ◽  
Vol 62 (18-20) ◽  
pp. 5160-5166 ◽  
Author(s):  
Benito Serrano ◽  
Miguel Salaices ◽  
Aaron Ortiz ◽  
Hugo I. de Lasa

2020 ◽  
Vol 22 (48) ◽  
pp. 28304-28316
Author(s):  
Seishi Shimizu ◽  
Nobuyuki Matubayasi

Adsorbate–adsorbate interaction can be determined directly from an adsorption isotherm via a rigorous statistical thermodynamic theory.


1993 ◽  
Vol 98 (6) ◽  
pp. 5006-5018 ◽  
Author(s):  
M. A. Carignano ◽  
I. Szleifer

Author(s):  
Kohei Ito ◽  
Ryohei Muramoto ◽  
Isamu Shiozawa ◽  
Yasushi Kakimoto ◽  
Takashi Masuoka

By the development of micro-fabrication technology, much smaller-size electronic devices will be soon available. In such a smaller device, a non-equilibrium state might appear in metal and/or semiconductor. In this case, it is difficult to estimate the device performance by the macroscopic transport equations that assume quasi-equilibrium distribution. We are developing a numerical simulation based on Boltzmann transport equation (BTE), which can analyze thermal and electric phenomena even when the state is far from equilibrium. In this study, we show a new formulation of BTE for free electron in metal and its calculation result: the thermoelectric power obtained agreed with that of experimental value: the heat flux derived by the non-equilibrium distribution was two-orders small than that estimated by thermal conductivity.


1949 ◽  
Vol 22 (2) ◽  
pp. 320-332
Author(s):  
Geoffrey Gee

Abstract Experimental data are reported on the effects of vulcanization, extension, and temperature on the swelling of rubber. Although in qualitative agreement with a simple equation derived from a statistical theory of polymer solutions, these reveal quantitative discrepancies which are important in discussions of two-phase equilibria.


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