• Resources Recycling
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• v.18 no.3
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• pp.62-68
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• 2009

Continuous operation for 24h was carried out to establish the optimum condition at the magnesium fused salt electrolysis using a self made 150 ampere mono-polar type cell. An electrolyte composition of $MgCl_2$ 25%, NaCl 55%, $CaCl_2$ 19%, $CaF_2$ 1% was electrolyzed with applied voltage 7V, cathode current density $0.7-0.75A/cm^2$, electrode distance 6cm at $720{\sim}740^{\circ}C$ for 24 hours. Changes of applied current, composition of the electrolyte, current efficiency were investigated. Through the experiments, there were not any operating troubles with the self-made electrolytic cell. Purity of the electrolyzed magnesium metal was above 99%, and 89% of current efficiency was achieved. Some basic data for scale-up of the magnesium electrolysis equipment which would be necessary for commercialization were obtained.

• Journal of the Korean Applied Science and Technology
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• v.29 no.2
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• pp.193-198
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• 2012

The following results are from the test of semi-gel electrolyte to store energy efficiently and use advanced VRLA batteries by photovoltaic and wind power generation. Semi-Gel electrolyte with Silica 5% became Gel after 1 and half hour. It shows it is the most suitable time that the electrolyte can be absorbed into the separator and active material of plate to be gel. The test also says that semi-gel electrolyte shows the much better performance for low-rate discharge and the liquid electrolyte is good for high-rate discharge because the reaction rate of gel electrolyte is slower than liquid one for high-rate discharge performance. The test with DOD10% and DOD100% says that 5% silica electrolyte shows much better performance for life efficiency than liquid one. Because semi-gel electrolyte increase the efficiency of gas recombination at the chemical reaction of VRLA battery and it makes minimizing the reduction of electrolyte. Using the 5% silica electrolyte in order to improve the stroage efficiency and life performance for photovoltic and wind power generation, it causes improving by 4.8% for DOD100% and 20% for DOD10%.

• Resources Recycling
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• v.16 no.1 s.75
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• pp.54-58
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• 2007

In the continuous flow reductive treatment for recovery of silver from actual photographic wastewater, the effects of electrolysis time, applied potential, and the concentration of silver ion on the process have been examined. The efficiency of silver recovery for diluted photographic wastewater was increased with applied potential and reached its maximum at 6 V. However, the recovery of silver was shown to be decreased with potential above this. When the wastewater was undiluted, the efficiency of silver recovery was observed to rise as the applied potential became lower under the experimental conditions.

• Journal of the Korean institute of surface engineering
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• v.19 no.2
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• pp.59-64
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• 1986

Pulse current was empolyed to the chromium electroplating bath of self-regulating high speed in the following range of conditions; 10-80$^{\circ}C$, 0-400A/$dm^2$, 10-100KHz. The current efficiency was compared with that of a conventional direct current plating in respect of current density and electrode interdistance. The effect of pulse current was found to increase the current efficiency at least 10-20 percent more than the conventional direct current plating in the high current density more than 100A/$dm^2$ and at 3-4mm of electrode interdistance. The surface appearance was also studied and known to be of great influenced by pulse frequency.

• Journal of the Korean Electrochemical Society
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• v.20 no.1
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• pp.13-17
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• 2017

In this study, we studied the organic electrolyte application to electrochemical capacitor for high operation voltage. For high operating voltage, 5 wt % of gamma butyroloctone (GBL) was added in the bare electrolyte. During the cycle performance, stable SEI layers were formed by reductive decomposition of additive GBL. As a result, columbic efficient of 1M $SBPBF_4$ in EC:DMC(1:1) with GBL composite was enhanced to 70% after the 2000th cycle at voltage range 0-3.5 V. Additionally, SEI layer protected the surface of electrode and prevent the side-reaction between electrolyte to electrode.

• Proceedings of the Korean Radioactive Waste Society Conference
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• 2009.11a
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• pp.346-346
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• 2009

산화물 형태 사용후핵연료의 효율적 처분 혹은 재활용을 위한 연구 가운데, 고온의 LiCl 용융염 중에서 전해환원하여 금속으로 환원시킨 후, 환원된 금속을 고온의 LiCl-KCl 용융염에서 전해정련하는 연구가 국내외적으로 활발하게 진행되고 있다. 전해환원을 위해 일정 농도 $Li_2O$가 LiCl 용융염에 첨가되며 $Li_2O$ 농도가 높으면 반응 재질의 부식성이 크게 증가하므로 일반적으로 우라늄 산화물은 1wt% 이하의 $Li_2O$ 농도에서 전해환원 된다. 우라늄 산화물의 전해환원 전위는 $Li_2O$의 전해환원 전위 보다 표준 상태를 기준으로 공정온도인 650 $^{\circ}C$ 에서 약 70 mV 정도 낮기 때문에 전해환원 과정에서 $Li_2O$ 의 환원으로 Li 금속이 생성될 가능성이 있으며 우라늄 산화물은 대부분 직접 전해환원 되지만 일부 Li에 의해 화학적으로 환원되기도 한다. 전해환원 공정에서 환원되지 않은 희토류 산화물은 전해정련 공정에서 $UCl_3$와 반응하여 $UO_2$를 생성시켜 공정 효율을 떨어뜨린다. 따라서 전해환원 공정에서 가능하연 최대한 희토류 산화물을 금속으로 환원시키는 조건을 찾아내는 것이 바람직하고 이를 위해서 우선 전해환원 공정에서 희토류 산화물의 화학적 거동의 이해가 요구된다. 본 연구에서 열역학적 검토를 통하여 희토류 산화물의 환원 조건을 조사한 결과 희토류 산화물은 매운 낮은 $Li_2O$ 농도에서 Li에 의해 환원되고, 1wt% 이하의 $Li_2O$ 농도에서는 Sc와 Lu의 산화물이 $Li_2O$와 복합산화물을 형성하고 이들 복합산화물은 Li에 의해 환원되지 않는 것으로 나타났다. 또한 희토류 원소 별로 희토류 원소 산화물의 Li에 의한 환원 조건으로서 평형상태에서의 $Li_2O$ 농도 즉 환원 임계 $Li_2O$ 농도를 실험적으로 측정하였으며 1wt% $Li_2O$ 농도 이하에서 열역학적 해석과 동일하게 Sc와 Lu만이 복합산화물을 형성하여 Li에 의해 직접환원 되지 않는 것으로 관찰되었다.

• Resources Recycling
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• v.31 no.3
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• pp.81-87
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• 2022

Energy consumption per unit weight of metal (kwh/kg of metal) is one of the most important economic indicators in the process of molten salt electrolysis. It is related to the heat loss of salt bath and the current efficiency of the process. The current efficiency is highly dependent on electrolysis temperature. On the other hand, the temperature of salt bath may increase significantly due to the difference (larger energy input than consumption) in heat balance at the beginning of electrolysis, which may cause different electrolysis temperature from an initially targeted value. This results in a bad effect on current efficiency. Therefore, it will be helpful to the reduction of energy consumption to compare the calculated and measured values of the temperature change of salt bath through the heat balance review at the early stage of electrolysis and to evaluate the energy loss to outside. In this study, based on the authors' experimental data, the heat balance was reviewed at the beginning of the electrolysis, and it was possible to evaluate the energy loss to the outside and the increase of the temperature of the salt bath quantitatively. Through such a method, heat loss reduction plan can be derived and current efficiency can be improved so that energy consumption can be reduced.

• Proceedings of the Korean Institute of Electrical and Electronic Material Engineers Conference
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• 2009.11a
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• pp.269-269
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• 2009

염료감응형 태양전지는 다공질 $TiO_2$ 전극막, 광감응형 염료, 전해질로 구성된 전기화학적 원리를 이용한 태양전지이다. 전해질은 전자가 빠져나간 염료에 전자를 공급하고 $PtCl_4$로부터 전자를 공급받아 산화/환원 반응을 한다. $PtCl_4$는 하부 기판에서 전자를 전해질에 제공한다. 본 연구에서는 Sealant를 이용하여 전해질의 면적이 효율에 어떤 영향을 미치는지 관찰하였다. AM 1.5 (100 $mW/cm^2$)하에서의 광 에너지로 측정한 효율은 전해질 면적이 1 $cm^2$ 일 때 가장 높은 4.46%의 효율이 나타났다.

• Proceedings of the Korea Society for Energy Engineering kosee Conference
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• 1999.05a
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• pp.177-182
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• 1999

감압증발의 효율을 향상시키기 위한 방법으로 액주내의 기포생성에 의한 자기 미립화를 수반하는 과열액분류의 증발을 분사 감압증발이라고 하며, 특히 적절한 방법으로 액체내에 기포핵을 공급하는 경우에는 매우 좋은 증발성능이 얻어 진다는 것이 보고되어 있다. 따라서 본 연구에서는 온배수를 감압증발시켜 저온저압의 증기를 제조하여 MVR로부터 승온승압에 의해 고온의 증기를 얻기위한 것이 연구의 목적이므로, 증발효율향상을 위해 기포핵 공급용 전해전류장치를 설치하고, 감압증발용의 노즐을 원통형 튜브로 대체하기위해 튜브형 노즐로 부터 과열액을 급격히 감압시켜 자기미립화에 의한 증발을 유도하여 전해전류가 증발효율에 미치는 영향을 실험적으로 연구하고자 작동액체로써 물을 사용하고, 액체온도, 액체유량, 과열도 및 기포핵 공급용의 전해전류량을 변화시켜 실험을 수행하였다.(중략)

• Clean Technology
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• v.18 no.4
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• pp.446-450
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• 2012

Strong alkaline electrolyzed water which is produced in cathode by electrolyzing the solution where electrolytes (NaCl, $K_2CO_3$ etc.) are added in diaphragm electrolytic cell, is eco-friendly and has cleaning effects. So, it is viewed as a substitution of chemical cleaner. In addition, strong alkaline electrolyzed water is being used by some Japanese automobile and precision parts manufacturing industries. When strong alkaline electrolyzed water is produced by using diaphragm electrolytic cell, it is necessarily produced at the anode side. Since strong acidic electrolyzed water produced is discarded when its utilization cannot be found, production efficiency of electrolyzed water is consequently decreased. Also, there is a weakness electrolytic efficiency is decreasing due to the pollution of diaphragm. In order to overcome this, non-diaphragm all-in-one electrolytic cell integrated with electrode reaction chamber and dilution chamber was applied. Strong alkaline electrolyzed water was produced for different composition of electrolytes, and their properties and characteristics were identified. In comparing the properties between strong alkaline electrolyzed water produced in diaphragm electrolytic cell and that produced in all-in-one electrolytic cell, the differences in ORP and chlorine concentration were found. In emulsification test to confirm surface-active capability, similar results were obtained and strong alkaline electrolyzed water produced in non-diaphragm all-in-one electrolytic cell was identified to be useable as a cleaner like strong alkaline electrolyzed water produced in diaphragm electrolytic cell. Strong alkaline electrolyzed water produced in non-diaphragm all-in-one electrolytic cell is thought to have sterilizing power because it has active chlorine which is different from strong alkaline electrolyzed water produced in diaphragm electrolytic cell.