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Solute Concentration Distribution in the Vicinity of Solid-Liquid Interface under the Imposition of a Time-Varying Force

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Title: Solute Concentration Distribution in the Vicinity of Solid-Liquid Interface under the Imposition of a Time-Varying Force
Authors: Xu, Guangye Browse this author
Iwai, Kazuhiko Browse this author →KAKEN DB
Keywords: solute concentration distribution
time-varying electromagnetic force
mass transfer
circulating micro-scale flow
Issue Date: 15-Jul-2022
Publisher: 一般社団法人 日本鉄鋼協会
Journal Title: ISIJ international
Volume: 62
Issue: 7
Start Page: 1389
End Page: 1395
Publisher DOI: 10.2355/isijinternational.ISIJINT-2021-177
Abstract: Mass transfer is often the rate determining step for solid-liquid reaction, such as an electroplating process in automotive industry and a refining process in metallurgical industry. The decrease of concentration boundary layer thickness through the excitation of convection is adapted to enhance the solid-liquid chemical reaction rate. Therefore, traditional methods excite a macro-scale flow in the bulk liquid. Because the concentration boundary layer exists in the velocity boundary layer, the traditional methods have the limitation in enhancing mass transfer rate. Therefore, a new method was proposed, which imposes force directly near the solid-liquid interface. In the past research, force, with or without an oscillating component was imposed near the solid-liquid interface during the dissolution of a Cu anode into a Cu2+ aqueous solution. The increase of Cu2+ concentration under the force imposition with oscillating component was suppressed compared to that by imposing the force without oscillating component just above the center of the anode. This research evaluated the dissolved Cu2+ concentration distribution and the liquid flow pattern in the whole vicinity of the solid-liquid interface under the force imposition with or without oscillation component. The results indicated that by imposing the force with oscillating component, the increase of the Cu2+ concentration was suppressed in the whole vicinity of the solid-liquid interface, and the Cu2+ concentration distributed more uniformly near the solid-liquid interface. This might be because of the excitation of circulating micro-scale flows near the side parts of the anode surface.
Type: article
URI: http://hdl.handle.net/2115/86581
Appears in Collections:工学院・工学研究院 (Graduate School of Engineering / Faculty of Engineering) > 雑誌発表論文等 (Peer-reviewed Journal Articles, etc)

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