Wetting Solution and Electrical Double Layer Contributions to Bulk Electrical Conductivity of Sand-Clay Mixtures

2008 ◽  
Vol 7 (3) ◽  
pp. 972-980 ◽  
Author(s):  
M. A. Mojid ◽  
H. Cho
Keyword(s):  
Electrical Conductivity ◽  
Double Layer ◽  
Electrical Double Layer ◽  
Bulk Electrical Conductivity

Effect of Electrical Double Layer on Electrical Conductivity and Pressure Drop in Pressure-Driven Micro-Channel Flow

2006 ◽  
Author(s):  
Bochuan Lin ◽  
Heng Ban
Keyword(s):  
Electrical Conductivity ◽  
Pressure Drop ◽  
Channel Flow ◽  
Double Layer ◽  
Electrical Double Layer ◽  
Debye Length ◽  
Channel Width ◽  
Micro Channel ◽  
Order Of Magnitude ◽  
Pressure Driven

The effect of electrical double layer (EDL) on micro-channel flow has been studied widely. Most research focused on flows with typical channel width or pipe diameter much greater than the thickness of EDL (Debye length). In such cases, the influence of EDL on the overall electrical conductivity is small, and a constant bulk electrical conductivity is often used in calculations. In our study of pressure-driven micropipette injection flow, the pipe size is on the same order of magnitude as the Debye length. To elucidate the effect of overlapping EDL the flow inside a micro-channel was analyzed. The governing equations for the flow, the Poisson equation for the electric potential, and the charge continuity equation for the net charge were solved analytically. The effect of overlapping EDL on the electrical conductivity and velocity distribution in the micro-channel and the pressure drop were quantified. The results showed that, the average conductivity of electrolyte solution inside the channel increased significantly, dependent on the channel width. With the modified mean electrical conductivity, the pressure drop for the pressure-driven flow was smaller than that without considering the influence of EDL on conductivity.

Modeling the Electrical Double Layer to Understand the Reaction Environment in a CO2 Electrocatalytic System

2019 ◽  
Author(s):  
Divya Bohra ◽  
Jehanzeb Chaudhry ◽  
Thomas Burdyny ◽  
Evgeny Pidko ◽  
wilson smith
Keyword(s):  
Electric Field ◽  
Double Layer ◽  
Electrical Double Layer ◽  
Surface Reaction ◽  
Catalyst Surface ◽  
Local Reaction ◽  
Reaction Diffusion ◽  
Alkali Metal Cations ◽  
Applied Potential ◽  
Critical Aspect

<p>The environment of a CO<sub>2</sub> electroreduction (CO<sub>2</sub>ER) catalyst is intimately coupled with the surface reaction energetics and is therefore a critical aspect of the overall system performance. The immediate reaction environment of the electrocatalyst constitutes the electrical double layer (EDL) which extends a few nanometers into the electrolyte and screens the surface charge density. In this study, we resolve the species concentrations and potential profiles in the EDL of a CO<sub>2</sub>ER system by self-consistently solving the migration, diffusion and reaction phenomena using the generalized modified Poisson-Nernst-Planck (GMPNP) equations which include the effect of volume exclusion due to the solvated size of solution species. We demonstrate that the concentration of solvated cations builds at the outer Helmholtz plane (OHP) with increasing applied potential until the steric limit is reached. The formation of the EDL is expected to have important consequences for the transport of the CO<sub>2</sub> molecule to the catalyst surface. The electric field in the EDL diminishes the pH in the first 5 nm from the OHP, with an accumulation of protons and a concomitant depletion of hydroxide ions. This is a considerable departure from the results obtained using reaction-diffusion models where migration is ignored. Finally, we use the GMPNP model to compare the nature of the EDL for different alkali metal cations to show the effect of solvated size and polarization of water on the resultant electric field. Our results establish the significance of the EDL and electrostatic forces in defining the local reaction environment of CO<sub>2</sub> electrocatalysts.</p>

Electrical Double Layer Formation on Glassy Carbon in Aqueous Solution

2021 ◽  
pp. 138416
Author(s):  
Sofia B. Davey ◽  
Amanda P. Cameron ◽  
Kenneth G. Latham ◽  
Scott W. Donne
Keyword(s):  
Aqueous Solution ◽  
Double Layer ◽  
Glassy Carbon ◽  
Electrical Double Layer ◽  
Layer Formation

Enzyme Immobilization Behavior on the Surface of Hydroxyapatite Capsules under Alkaline Condition

2018 ◽  
Vol 782 ◽  
pp. 21-26
Author(s):  
Takeshi Yabutsuka ◽  
Masaya Yamamoto ◽  
Shigeomi Takai ◽  
Takeshi Yao
Keyword(s):  
Enzyme Immobilization ◽  
Double Layer ◽  
Isoelectric Point ◽  
Electrical Double Layer ◽  
Alkaline Condition ◽  
Bicarbonate Buffer

We prepared hydroxyapatite (HA) capsules encapsulating maghemite particles. In order to evaluate enzyme immobilization behavior of the HA capsules under alkaline condition, we immobilized five kinds of enzymes with different isoelectric point in carbonate/bicarbonate buffer (CBB, pH 10.0). When the enzymes in CBB were moderately charged, immobilization efficiency on the HA capsules showed the highest value. It was suggested that immobilization efficiency was affected according to both pI of enzyme and pH of the surrounding solution and that enzyme immobilized on the HA capsules by not only electrical double layer interactions but also ion interaction and other interactions.

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