• Title/Summary/Keyword: 전해석

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Study of the Electrolytic Reduction of Uranium Oxide in LiCl-Li$_{2}$O Molten Salts with an Integrated Cathode Assembly

  • Park Sung-Bin;Seo Chung-seok;Kang Dae-Seung;Kwon Seon-Gil;Park Seong-Won
    • Journal of Nuclear Fuel Cycle and Waste Technology(JNFCWT)
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    • v.3 no.2
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    • pp.105-112
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    • 2005
  • The electrolytic reduction of uranium oxide in a LiCl-Li$_{2}$O molten salt system has been studied in a 10 g U$_{3}$O$_{8}$ /batch-scale experimental apparatus with an integrated cathode assembly at 650$^{\circ}C$. The integrated cathode assembly consists of an electric conductor, the uranium oxide to be reduced and the membrane for loading the uranium oxide. From the cyclic voltammograms for the LiCl-3 wt$\%$ Li$_{2}$O system and the U$_{3}$O$_{8}$-LiCl-3 wt$\%$ Li$_{2}$O system according to the materials of the membrane in the cathode assembly, the mechanisms of the predominant reduction reactions in the electrolytic reactor cell were to be understood; direct and indirect electrolytic reduction of uranium oxide. Direct and indirect electrolytic reductions have been performed with the integrated cathode assembly. Using the 325-mesh stainless steel screen the uranium oxide failed to be reduced to uranium metal by a direct and indirect electrolytic reduction because of a low current efficiency and with the porous magnesia membrane the uranium oxide was reduced successfully to uranium metal by an indirect electrolytic reduction because of a high current efficiency.

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Surfactant recycling using micellar enhanced ultrafiltration

  • 양중석;백기태;양지원
    • Proceedings of the Korean Society of Soil and Groundwater Environment Conference
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    • 2004.04a
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    • pp.177-180
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    • 2004
  • 계면활성제를 이용한 오염된 토양을 복원하는데 있어 계면활성제의 회수하는 방법의 하나로 한외여과 방식의 타당성을 검토하였다. 계면활성제의 종류, 전해질과 첨가제로서의 알코올 및 휴믹 물질과 점토질에 의한 상대 플럭스의 변화와 투과액의 계면활성제의 농도 변화를 살펴보았다. 계면활성제의 경우 임계미셀농도 낮을수록 투과액의 농도가 낮았으며, 기타 첨가물은 농도에 비례하여 상대 플럭스가 감소하는 경향을 보였다.

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MnO2 deposition on surface of Nickel mesh as cathode of Al-air battery (알루미늄 공기전지용 캐소드로서 니켈메쉬 표면에 이산화망간 도금)

  • O, Gi-Seok;Choe, Jin-Seop
    • Proceedings of the Korean Institute of Surface Engineering Conference
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    • 2015.05a
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    • pp.152-153
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    • 2015
  • 알루미늄 공기전지의 환원전극으로 많은 재료들이 쓰이고 있지만 그중에서도 니켈은 값이 싸며 전기 전도도가 높아 많이 쓰이고 있다. 니켈 메쉬표면에 이산화망간을 촉매로써 처리하지만 이산화망간 용액을 적시고 말리는 기존방법에서는 균일하게 처리가 되지 않고 공기가 통하지 않는 경우도 있기 때문에 보다 균일한 처리를 위해 전해도금을 연구하였다.

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Properties Change of Electroplated Permalloy Thin Films by Organic Additives (유기첨가제에 의한 전기도금 퍼말로이 박막의 물성변화)

  • Bang, Won-Bae;Bae, Jong-Hak;Hong, Ki-Min;Chung, Jin-Seok;Ko, Young-Dong;Lee, Hee-Bok
    • Journal of the Korean Magnetics Society
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    • v.17 no.3
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    • pp.133-136
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    • 2007
  • We investigated the changes of the magnetic properties in electroplated Permalloy thin films by a few organic additives added to the plating electrolytes. Under identical electroplating conditions, the crystalline orientations and the surface roughness of the plated thin films were different from those prepared with a pure electrolyte. These property changes reduced the coercivity and increased the magnetoimpedance ratio (MIR) up to 20%.

Electrochemical Studies of o-Cresolphthalexon at Mercury Electrode in Alkaline Media (염기성용액 중의 수은전극에서 o-Cresolphthalexon의 전기화학적 연구)

  • Chong-Min Pak;Sam-Woo Kang;Lee-Mi Do;Tae Yoon Eom;Ki-Suk Jung
    • Journal of the Korean Chemical Society
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    • v.35 no.2
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    • pp.158-164
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    • 1991
  • The reduction mechanism at a mercury electrode of o-cresolphthalexon(OCP) in strongly alkaline supporting electrolytes has been investigated by several electrochemical techniques. The radical formed after first one electron reduction uptake, dimerizes. The result of cyclic voltammetric investigation demonstrated the reversible nature of the electron transfer and standard rate constant was $3.27{\times}10^{-2}$ cm/sec. The apparent irreversible behavior of the second wave is a result of the existence of a fast protonation following the second electron transfer. At low concentration of OCP(< $1{\times}10^{-4}$M), cathodic current were remarkably adsorptive properties. Prolonged electrolysis was carried out at controlled potential of -1.85V, original violet color of the solution becames progressively weaker, and then colorless solution. The final product of an exhaustive electrolysis is electro-inactive. The appearence of four steps may be explained by the fact that the reduction of OCP elucidated ECEC mechanism.

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Patent Analysis for Pyroprocessing of Spent Nuclear Fuels (사용후핵연료 파이로처리기술의 특허 동향 분석)

  • Yoo, Jae-Hyung;Kim, Jung-Kuk;Lee, Han-Soo;Seo, In-Seok;Kim, Eun-Ka
    • Journal of Nuclear Fuel Cycle and Waste Technology(JNFCWT)
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    • v.9 no.4
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    • pp.247-258
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    • 2011
  • Analysis of foreign and domestic patents for pyroprocessing technology of spent nuclear fuels was carried out in this study. The current status of pyroprocessing technology development in such countries as Korea, USA, Japan and EU was analyzed by classifying the patents for 1975 through 2009 according to registration country, assignee, calendar year and technology area. The major assignees' activity indices were compared in order to find out whether there is any concentrated area of technical details. Technology competitiveness of the countries was also investigated from the information of patent citation number and family size. Furthermore, some essential unit technologies required for the commercialization of pyroprocessing were derived and examined in the aspect of the state of art as well as the trend of technology development.

Study on the Effect of (Dodecyldimethylammonio)propanesulfonate Zwitterionic Surfactant on Cu Electrodeposition (구리전해도금에서 양쪽이온성 계면활성제인 (Dodecyldimethylammonio)propanesulfonate의 영향 연구)

  • Shin, Yeong Min;Kim, In Ui;Bang, Daesuk;Cho, Sung Ki
    • Journal of the Korean Electrochemical Society
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    • v.24 no.3
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    • pp.35-41
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    • 2021
  • In this study, the effect of zwitterionic surfactant on Cu electrodeposition was investigated through cyclic voltammetry. With the addition of (dodecyldimethylammonio)propanesulfonate (DDAPS) as a representative zwitterionic surfactant in the electrolyte for Cu electrodeposition, the electrochemical Cu2+ reduction was inhibited on Cu and glassy carbon electrodes. Its inhibition effect was similar to that of cationic surfactant rather than anionic surfactant. Moreover, DDAPS interacted with chloride ion and exhibited the mass transfer-dependent inhibition behavior, which indicates that its inhibition function is associated with the formation of its surface aggregates on anion-covered Cu surface. In addition, adsorbed DDAPS slightly reduced the surface roughness of Cu electrodeposits. These characteristics were similar to those of cationic surfactant, but less obvious. It means the effect of DDAPS on Cu electrodeposition originates from the cationic head group which is shield by anionic head group.

Study on the Manufacture of High-purity Vanadium Pentoxide for VRFB Using Chelating Agents (킬레이트제를 활용한 VRFB용 고순도 오산화바나듐 제조 연구)

  • Kim, Sun Kyung;Kwon, Sukcheol;Kim, Hee Seo;Suh, Yong Jae;Yoo, Jeong Hyun;Chang, Hankwon;Jeon, Ho-SeoK;Park, In-Su
    • Resources Recycling
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    • v.31 no.2
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    • pp.20-32
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    • 2022
  • This study implemented a chelating agent (Ethylenediaminetetraacetic acid, EDTA) in purification to obtain high-purity vanadium pentoxide (V2O5) for use in VRFB (Vanadium Redox Flow Battery). V2O5 (powder) was produced through the precipitation recovery of ammonium metavanadate (NH4VO3) from a vanadium solution, which was prepared using a low-purity vanadium raw material. The initial purity of the powder was estimated to be 99.7%. However, the use of a chelating agent improved its purity up to 99.9% or higher. It was conjectured that the added chelating agent reacted with the impurity ions to form a complex, stabilizing them. This improved the selectivity for vanadium in the recovery process. However, the prepared V2O5 powder exhibited higher contents of K, Mn, Fe, Na, and Al than those in the standard counterparts, thus necessitating additional research on its impurity separation. Furthermore, the vanadium electrolyte was prepared using the high-purity V2O5 powder in a newly developed direct electrolytic process. Its analytical properties were compared with those of commercial electrolytes. Owing to the high concentration of the K, Ca, Na, Al, Mg, and Si impurities in the produced vanadium electrolyte, the purity was analyzed to be 99.97%, lower than those (99.98%) of its commercial counterparts. Thus, further research on optimizing the high-purity V2O5 powder and electrolyte manufacturing processes may yield a process capable of commercialization.