• Transactions of the Korean hydrogen and new energy society
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• v.23 no.4
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• pp.390-396
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• 2012

In order to understand the nature of dendritic zinc growth, electrochemical zinc redox reaction on nickel plate was investigated in aqueous solutions containing different concentrations, 0.2, 0.1 and 0.02 $mol{\cdot}dm^{-3}$ (M), of zinc sulfate ($ZnSO_4$) or zinc chloride ($ZnCl_2$). Zinc ion was efficiently reduced and oxidized on nickel in the high-concentration (0.2 M) solution, whereas relatively poor efficiency was obtained from the other low-concentration solutions (0,1 and 0.02 M). Cyclic voltammetry (CV) analysis revealed that the 0.2 M electrolyte solution decomposes at more positive potentials than the 0.1 and the 0.02 M solutions. These results suggested that the concentration of electrolyte solution and anion would be an important factor that suppresses the reaction of the zinc dendrite formation. Scanning Electron Microscopy (SEM) data revealed that the shape of dendritic zinc and its growing behavior were also influenced by electrolyte concentration.

• Journal of the Korean Electrochemical Society
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• v.2 no.4
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• pp.232-236
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• 1999

A solar cell based on dye-sensitized photoelectric conversion was studied by electrochemical and spec-trofluorometric methods for the purposes of enhancing its efficiency and stability of $TiO_2$ solar cells. Nanocrystalline $TiO_2$ was used to prepare photoelectrodes, and photosensitizing dyes such as malachite green oxalate, basic blue3, rhodamine B, and bromocresol purple were chosen as sensitizers. Electrochemical oxidation potentials and absorption and emission wavelengths of dyes were used to determine energy levels of the dyes. By comparing excited energy levels of the dyes with the conduction band edge potential $(E_{c,s})\;of\;TiO_2$ calculated by using the flat-band potential $(E_{fb})\;of\;TiO_2$, properties of a dye required to fabricate a high efficient photosensitizing solar cell with high short-circuit current $(J_{sc})$ were suggested. Enhanced stability of photocurrent was obtained by coating a $TiO_2|ITO$ electrode with Polypyrrole that Possibly Prevented the recombination between the conduction band electrons and oxidized dyes and suppressed the direct electrode redox reactions of dyes on ITO.

• Economic and Environmental Geology
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• v.49 no.3
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• pp.167-179
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• 2016

Water quality of Oseepchun, Dogye area, was investigated quantitatively for its origin and hydrogeochemistry in relation to the influence of groundwater. Groundwater appears to be the principal source of Oseepchun from the water-quality monitoring data including redox potentials, composition of dissolved ions and their correlations, hydrogen and oxygen stable isotopic ratios, and the distribution and occurrence of contaminants. Water-quality type of the surface water was grouped by the water-rock interactions as $Ca-HCO_3$ type originated from carbonated bed-rocks in the Joseon Supergroup, (Ca, Mg)-$SO_4$ type related with dissolution of surfide minerals in coal beds of Pyeongan Supergroup, and (Ca, Mg)-($HCO_3$, $SO_4$) type of the mixed one. Locally water pollution occurs by high $SO_4$ from mine drainage and $NO_3$ from waste-treatment facility. Intensive precipitation in summer has no effect on the water type of Oseepchun, but increases the inflow of nitrate and chloride originated from land surface. Results of this study direct that groundwater-surface water interaction is intimate, and thus surface-water resource management should begin with groundwater characterization.

• Korean Journal of Soil Science and Fertilizer
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• v.44 no.6
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• pp.1220-1225
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• 2011

Anaerobic decomposition of organic materials in flooded rice fields produces methane ($CH_4$) gas, which escapes to the atmosphere primarily by transport through organs of the rice plants such as arenchyma etc., Although the annual amount of methane emitted from a given area is influenced by cultivation periods of rice and organic/inorganic amendments etc., soil type also affects methane emission from paddy soil during a rice cultivation. A field experiment was conducted to evaluate effects of soil type on $CH_4$ emission in two paddy soils. One is a red-yellow soil classified as a Hwadong series (fine, mixed, mesic family of Aquic Hapludalfs), and the other is a gley soil classified as a Shinheung series (fine loamy, mixed, nonacid, mesic family of Aeric Fluvaquentic Endoaquepts). During a flooded periods, redox potentials of red-yellow soil were significantly higher than gley soil. $CH_4$ emission in red-yellow soil ($0.21kg\;ha^{-1}\;day^{-1}$) was lower than that in gley soil ($5.25kg\;ha^{-1}\;day^{-1}$). In the condition of different soil types, $CH_4$ emissions were mainly influenced by the content of total free metal oxides in paddy soil. The results strongly imply that iron- or manganese-oxides of well ordered crystalline forms in soil such as goethite and hematite influenced on a $CH_4$ emission, which is crucial role as a $CH_4$ oxidizers in paddy soil during a rice cultivation.

• Resources Recycling
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• v.30 no.3
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• pp.30-40
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• 2021

The present study investigates the bioleaching efficiencies of arsenic via contact and non-contact mechanisms. The attachment of Acidithiobacillus ferrooxidans was restricted by a partition system comprising a semi-permeable membrane with a molecular weight cutoff of 12-14 kDa. The results were compared for two arsenic concentrations in the system (1.0% and 0.5% w/v) to maintain a homogeneous system. The overall bacterial performance was monitored by comparing total arsenic and iron concentrations, Fe ion speciation, pH, and solution redox potentials in flask bioleaching experiments over a period of 10 d. Our results indicated that bacterial attachment could increase arsenic extraction efficiency from 20.0% to 44.9% at 1.0 % solid concentrations. These findings suggest that the bacterial contact mechanism greatly influences arsenic bioleaching from mine tailings. Therefore, systems involving two-step or non-contact bioleaching are less effective than those involving one-step or contact bioleaching for the efficient extraction of arsenic from mine tailings.

• Clean Technology
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• v.25 no.1
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• pp.46-55
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• 2019

CdS and CdZnS/ZnO materials were prepared using precipitation method and used as photocatalysts for the photocatalytic degradation of rhodamine B (RhB) under visible light irradiation. The prepared photocatalysts were also characterized by XRD and UV-vis DRS. The results indicated that the photocatalysts with intended crystalline structures were successfully obtained and both the CdS and CdZnS/ZnO can absorb visible light as well as UV. The photocatalytic activities were examined with the addition of scavenger for various active chemical species and the difference of reaction mechanisms over the catalysts were discussed. The $CH_3OH$, KI and p-benzoquinone were used as scavengers for ${\cdot}OH$ radical, photogenerated positive hole and ${\cdot}O_2{^-}$ radical, respectively. The CdS and CdZnS/ZnO showed different photocatalytic degradation mechanisms of RhB. It can be postulated that ${\cdot}O_2{^-}$ radical is the main active species for the reaction over CdS photocatalyst, while the photogenerated positive hole for CdZnS/ZnO photocatalyst. As a result, the predominant reaction pathways over CdS and CdZnS/ZnO photocatalysts were found to be the dealkylation of chromophore skeleton and the cleavage of the conjugated chromophore structure, respectively. The above results may be mainly ascribed to the difference of band edge potential of conduction and valence bands in CdS, CdZnS and ZnO semiconductors and the redox potentials for formation of active chemical species.