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Scientific and Technical Aerospace Reports Volume 39 April 6, 2001

Scientific and Technical Aerospace Reports Volume 39 April 6, 2001

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<strong>2001</strong>0024999 Case Western Reserve Univ., Dept. of Mechanical <strong>and</strong> <strong>Aerospace</strong> Engineering, Clevel<strong>and</strong>, OH USA<br />

Gas-Evolving Effect on Mass Transfer in Rotating Electrochemical Cells Under Microgravity<br />

Kamotani, Y., Case Western Reserve Univ., USA; Proceedings of the Fifth Microgravity Fluid Physics <strong>and</strong> Transport Phenomena<br />

Conference; December 2000, pp. 1478-1487; In English; See also <strong>2001</strong>0024890; No Copyright; Avail: CASI; A02, Hardcopy;<br />

A10, Microfiche<br />

On earth, gas evolution in electrochemical reactors occurs widely in the electrochemical industry. In water electrolysis <strong>and</strong><br />

electrochemical machining <strong>and</strong> electrosynthesis, the gas bubbles agitate the electrolytic cells <strong>and</strong> enhance the mass transfer,<br />

thereby improving the yield of the electrochemical cells. In fact, there are relatively few major electrochemical processes in which<br />

evolved gases do not appear. Therefore, the design of life support systems in space requires sufficient electrochemical information<br />

related to the behavior of bubbles generated on an electrode. For example, the processes of carbon dioxide removal, oxygen generation,<br />

water reclamation <strong>and</strong> human waste treatment in spaceflight involve gas generation in the systems. Although much research<br />

work has been done on electrolytic gas evolution in the presence of gravity or forced flow, much less work is available on electrolytic<br />

gas evolution in microgravity. In the absence of gravity the conventional electrochemical cells would be inefficient as the<br />

generated bubbles tend to stay near the electrodes. In the present work we propose rotating electrochemical cells as a means of<br />

enhancing the mass transfer significantly <strong>and</strong> removing the generated gas bubbles effectively in microgravity. Moreover, the<br />

design of electrochemical cells becomes relatively compact because it does not require additional pumps <strong>and</strong> separators to process<br />

the bubble-electrolyte flow. The subject of gas evolution in rotating electrochemical cells has never been investigated. Most studies<br />

of gas bubbles in electrolytic cells were performed in the presence of natural convection or forced convection. Forced convection<br />

can be used to remove gas bubbles from the electrodes of an electrochemical system in microgravity but the bubbles still need<br />

to be removed from the electrolyte somehow. by rotating the cells one can remove the bubbles from the electrodes <strong>and</strong> the electrolyte.<br />

The main objective of the proposed work is to gain basic knowledge of bubble behavior <strong>and</strong> its effect on mass transfer in<br />

rotating electrochemical cells under microgravity as well as normal gravity conditions. The mass transfer rates <strong>and</strong> various bubble<br />

layer characteristics will be measured <strong>and</strong> analyzed under various conditions in rotating electrochemical cells in normal gravity<br />

as well as during parabolic flights. Based on the results, a theoretical model will be constructed to predict the bubble-induced convection<br />

in rotating electrochemical cells. The test section, such is shown, consists of two horizontal electrode disks, which serve<br />

as cathode (top) <strong>and</strong> anode (bottom), <strong>and</strong> a vertical annular Lexan side wall. The anode is made of copper. The cathode is divided<br />

into eight ring-shaped sections. The reason for the sectioned cathode is to measure local mass transfer rate. With this arrangement<br />

only hydrogen bubbles are generated from the top cathode. The generated bubbles move toward the center along the top wall. A<br />

tube is attached to the top plate at the center to remove the bubbles. The gap between the electrodes is variable. A cupric sulfatesulfuric<br />

acid solution (CuSO4 - H2SO4 - H2O) is used as the test fluid. The test section is placed in a rotating system. The bubble<br />

layer along the cathode surface is illuminated by a laser light sheet <strong>and</strong> a video camera records the bubbles. The bubbles move<br />

in the radially inward direction as well as in the azimuthal direction due to Coriolis force. The camera <strong>and</strong> laser light source are<br />

placed on the rotating frame. to minimize the impact of high-g on the equipment, they are placed near the center of the rotating<br />

frame. Mirrors <strong>and</strong> a fiber optic cable are used to illuminate <strong>and</strong> take pictures of the inner test section. From this measurement<br />

we will determine the bubble layer thickness distribution <strong>and</strong> the bubble velocities (radial components) <strong>and</strong> sizes at various locations.<br />

The mass transfer rate will be determined from the amount of electrodeposited copper on each sectioned platinum cathode<br />

using the anode dissolution method. Applied current density in the present experiment is a combination of the partial current density<br />

consumed by hydrogen gas generation <strong>and</strong> that for copper electrodeposition on each sectioned cathode. In the anode dissolution<br />

method the electrolytic cell is charged, with the polarity reversed, at a constant current density to dissolve the electrodeposited<br />

copper on the platinum anode. The passivation of the cell occurs when the deposited copper is completely depleted on the anode.<br />

The amount of electrodeposited copper on each sectioned platinum can then be calculated from the current density <strong>and</strong> the time<br />

to passivate. The local mass transfer rate <strong>and</strong> partial current density for copper deposition is determined from the amount of deposition.<br />

After the data analysis, we will construct a theoretical model to predict the average mass transfer coefficient, or the average<br />

Sherwood number, as a function of the important dimensionless parameters. It is known that generally there are three different<br />

mass transfer mechanisms acting at gas evolving electrodes with an intensity depending on the operating conditions: (i) bubble-induced<br />

microconvection owing to periodic microflows in the vicinity of gas bubbles adhering to <strong>and</strong> detaching from the electrode<br />

surface, (ii) bubble-induced macroconvection owing to buoyancy flow of a gas-liquid dispersion along the electrode, the flow is<br />

caused by the density difference between the dispersion <strong>and</strong> that of the (nearly) bubble-free liquid, <strong>and</strong> (iii) single-phase free convection<br />

owing to density gradients in the liquid phase near the electrode surface. We will take basically the same approach in<br />

constructing our model. In the present work, since the solutal boundary layer is relatively thin, we have basically the microconvection<br />

<strong>and</strong> the bubble-induced macroconvection.<br />

Author (revised)<br />

Gas Evolution; Electrochemical Cells; Mass Transfer; Microgravity; Bubbles; Rotation<br />

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