• Title/Summary/Keyword: MEO process

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Recovery of Silver from the Spent Solution Generated from Electrochemical Oxidation of Radioactive Wastes (放射性 폐기물의 전기화학적 분해 폐액으로부터 銀의 回收)

  • 문제권;정종훈;오원진;이일희
    • Resources Recycling
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    • v.10 no.5
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    • pp.22-28
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    • 2001
  • Recovery of silver in the spent solution generated from MEO(Mediated Electrochemical Oxidation) process, which is a process to decompose radioactive organic mixed wastes at low temperature, was performed using chemical method. Silver nitrate in 5M nitric acid solution could be completely recovered as AgCl by using 1% excess of the stoichiometric HCl equivalents. Then, AgCl was transformed to Ag metal by reduction reaction with hydrogen peroxide under alkaline media. The optimum pH for the reduction to silver metal was found to be in the range of 12.8∼13.0.

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Continuous Mediated Electrochemical Oxidation of Ethylene Glycol by Co(III)/Co(II) and Fe(III)/Fe(II) Redox Systems (Co(III)/Co(II) 및 Fe(III)/Fe(II) 산화환원계에 의한 에텔렌글리콜의 연속 매개전해 산화)

  • Kim, Ik-Seong;Park, Seung-Cho
    • Applied Chemistry for Engineering
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    • v.16 no.5
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    • pp.635-640
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    • 2005
  • Mediated electrochemical oxidation (MEO) is an aqueous process which oxidizes organics electrochemicallly at low temperatures and pressures. The useful process can be used to treat mixed wastes containing hazardous organics. This paper have studied MEO of ethylene glycol (EG) in nitric acids by Fe(III)/Fe(II) and Co(III)/Co(II) system. It investigated current density, supporting electrolyte concentration, hydraulic retention time, removal efficiency of EG by MEO. Removal efficiency of EG by MEO was superior in Co(III)/Co(II) redox system than Fe(III)/Fe(II) redox system, where MEO removal efficiency was 100 percent. In case of EG, the reactions were fast and good yields of carbon dioxide formation was observed.

The Removal of NOx by Mediated Electrochemical Oxidation Using Ag(II) As a Mediator (Ag(II)를 매개체로 사용하는 전기화학적 매개산화에 의한 NOx 제거)

  • Lee, Min-Woo;Park, So-Jin;Lee, Kune-Woo;Choi, Wang-Kyu
    • Journal of Nuclear Fuel Cycle and Waste Technology(JNFCWT)
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    • v.9 no.3
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    • pp.121-129
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    • 2011
  • The effects of the applied current density, the $AgNO_3$ concentration, the scrubbing liquid flow rate and the NO-air mixed gas flow rate on the NO removal efficiency were investigated by using $Ag^{2+}$ mediated electrochemical oxidation (MEO). Results showed that the NO removal efficiency increased with increasing the applied current density. The effect of the $AgNO_3$ concentration on the NO removal efficiency was negligibly small in the concentration of $AgNO_3$ above 0.1 M. When the scrubbing liquid flow rate increased, the NO removal efficiency was gradually increased. On the other hands, the NO removal efficiency decreased with increasing the NO-air mixed gas flow rate. As a result of the treatment of NO-air mixed gas by using the MEO process with the optimum operating condition and the chemical absorption process using 3 M $HNO_3$ solution as a scrubbing liquid, the removal efficiency of NO and $NO_x$ was achieved as 95% and 63%, respectively.

Removal of Heavy Metal Ions by Electrocoagulation for Continuous Use of Fe2+/Fe3+-Mediated Electrochemical Oxidation Solutions

  • Jung, Youn-Su;Pyo, Myoung-Ho
    • Bulletin of the Korean Chemical Society
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    • v.29 no.5
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    • pp.974-978
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    • 2008
  • Removal of heavy metal ions ($Cd^{2+}$ and $Zn^{2+}$) by electrocoagulation (ECG) was investigated in an acidic condition, which is necessary for re-using or discharging the mediated electrochemical oxidation (MEO) media. Effects of various parameters such as electrolytes, current densities, and electrode materials were examined for a metal-contaminated MEO system using $Fe^{2+}/Fe^{3+}$ pairs as a mediator. It was found that ECG with Al electrodes is greatly affected by the presence of $Fe^{2+}$. [$Cd^{2+}$] and [$Zn^{2+}$] remain constant until [$Fe^{2+}$] reaches a certain concentration level (ca. 10 mM). This preferential removal of $Fe^{2+}$ during ECG with Al electrodes is not alleviated by controlling current densities, potential programs, and solution mixing. ECG with Fe electrodes, on the other hand, resulted in relatively fast removal of $Cd^{2+}$ and $Zn^{2+}$ under coexistence of $Fe^{2+}$, indicative of the different role between $Fe^{n+}$ generated from an electrode and $Fe^{2+}$ initially present in a solution. When ECG was performed with Fe electrodes until [$Fe^{n+}$] became the same as the concentration of initially present $Fe^{2+}$, [$Cd^{2+}$] and [$Zn^{2+}$] were reduced to one-tenth of the initial concentrations, suggesting the possibility of a continuous use of the medium for a subsequent MEO process.

Destruction of Spent Organic ion Exchange Resins by Ag(II)-Mediated Electrochemical Oxidation (Ag(II)매개산화에 의한 폐 유기이온교환수지의 분해)

  • Choi Wang-Kyu;Nam Hyeog;Park Sang-Yoon;Lee Kune-Woo;Oh Won-Zin
    • Journal of the Korean Electrochemical Society
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    • v.2 no.4
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    • pp.183-189
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    • 1999
  • A study on the destruction of organic cation and anion exchange resins by electro-generated Ag(II) as a mediator was carried out to develop the ambient-temperature aqueous process, known as Ag(II)-mediated electro-chemical oxidation (MEO) process, for the treatment of a large quantity of spent organic ion exchange resins as the low and Intermediated-level radioactive wastes arising from the operation, maintenance and repairs of nuclear facilities. The effects of controllable process parameters such as applied current density, temperature, and nitric acid concentration on the MEO of organic ion exchange resins were investigated. The cation exchange resin was completely decomposed to $CO_2$. The current efficiency increased with a decrease in applied current density while nitric acid concentration and temperature on the MEO of cation exchange resin did not affect the MEO. On the other hand, anion exchange resins were decomposed to CO and $CO_2$. The ultimate conversion to CO was about $10\%$ regardless of temperature. The destruction efficiencies to $CO_2$ were dependent upon temperature and the effective destruction of anion exchange resin could be obtained above $60^{\circ}C$.

Recovery of Silver and Nitric Acid in the Liquid Waste Resulted from the Mediated Electrochemical Oxidation Process (전기화학적 매개산화공정 폐액에서 은 및 질산의 회수)

  • 최왕규;김영민;이근우;박상윤;오원진
    • Resources Recycling
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    • v.7 no.3
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    • pp.17-26
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    • 1998
  • A study on the recovery of silver and nitric acid in the liquid waste resulted from the mediated electrochemical oxidation(MEO) process was conducted. The removal of silver in the concentrated nitric acid solutions was carried out by the electrodeposition. The removal efficiency more than 98% could be obtained in nitric acid concentrations less than 3 M with the current efficiency of nearly 100%. The experimonts on the evaporation for the recovery of nitric acid were performed as well. At the evaporation factor of 25., the degree of nitric acid recovery in 3.5 M nitric acid solution containing 0.5 to 1.0 mol% NaNO, was 80~90% resulting in 2.8~3.1 M nitric acid. The design factors and operating conditions of the distillation tower were analyzed by using MEH model derived by Maphtali-Sandholm with the throughput of 4 kg/hr for the enrichment of dilute nitric acid solution recovered by evaporation to reuse in the MEO process. The distillation column composed of eleven theoretical stages having the overall tray efficiency of 70% are needed to obtain 1.03 kg/h of 12M nitric acid and 2.97 kg/h of water with feed being introduced to the column at tray 6 from the bottom at the reflux ratio of 0.25, the reboiler with the heat load of 2.7 kW, and the condenser with the cooling load of 0.5 kW.

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A Study of the Royal Lady's Dress in Late Joseon Dynasty According to the King's Wedding Process (가례시 절차에 따르는 조선후기의 왕실여성 복식연구)

  • Kim, Soh-Hyeon
    • Journal of the Korean Society of Costume
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    • v.59 no.3
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    • pp.96-108
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    • 2009
  • This study is made on the royal lady's dress In late Joseon dynasty according to the King Heon-jong and Lady Kyung-bin's Wedding Diary in the year of Jung-mi(1847) and summarised as follows: Girls' full dress was a set of a red skirt, a violet undo. jacket, and a light yellow jacket and a green Gyeon-ma-gi(a kind of top jacket) with he. hair Saeng-meo-ri hanging Do-tu-rak-daeng-gi(a kind of hair ribbon). At the big ceremony, girls wore a green Dang-ui instead of Gyeon-ma-gi. A girl picked up as a royal concubine wore a green Won-sam, which was decorated with gilt letters meaning longevity, patched emblems of gilt letter meaning longevity on the breast and on the back, belted with Bong-dae(a red sash with gilt phoenexes), like a princess's full dress. At the Kyung-bin's installation of Crown Princess and her first greeting ceremony with royal elders, she wore a green Won-sam as a formal dress, which had an embroidered emblem of phoenix, the belt with crystal ornaments, Pae-ok(佩玉), Kyu(圭) of blue jade, Shou(綬) with an phoenix. At a Dong-wrae-yun(drinking ceremony after bride and bridegroom's bowing to each other), she wore the embroidered red Jang-sam as a formal dress. Kyung-bin wore a purple Won-sam with Bong-dae as a full dress for a royal feast. According to the occasions, the same dress was differentiated with ornaments and rotors. Ji-keum-bal was an attire for ordinary ceremony. The attire was equipped with a woven gold green Dang-ui with an emblem of phoenix, a blue gilt underskirt and a red gilt overskirt. No-ui was worn as outdoor clothes. Jang-sam was worn by various classes, so it was differentiated with materials and names according to her class.

Diffusion Coefficient of Ag(I) ion in the Concentrated Nitric Acid Solution (고농도 질산용액에서 Ag(I) 이온의 확산계수 측정)

  • Park Sang Yoon;Choi Wang Kyu;Lee Kune Woo;Moon Jei Kwon;Oh Won Zin
    • Journal of the Korean Electrochemical Society
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    • v.2 no.2
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    • pp.93-97
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    • 1999
  • From the anodic peak currents of cyclic voltammograms for Ag(I)/Ag(II) couple obtained with the variation of nitric acid concentration, Ag(I) concentration and solution temperature at a Pt electrode in concentrated nitric acid solutions, the diffusion coefficients of Ag(I) ion were evaluated to estimate the limiting current density of Ag(II)-mediated electrochemical oxidation (MEO) process, which has been effectively used for the complete destruction of hazardous organic materials. The results showed that, due to the water decomposition reaction which occurred simultaneously with the Ag(I) ion oxidation, background subtractions for the cyclic voltammograms were required to estimate the correct peak currents. The empirical relationship for the diffusion coefficient of Ag(I) was suggested as a function of solution viscosity and temperature.