• Journal of the Korean Ceramic Society
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• v.12 no.4
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• pp.37-42
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• 1975

철(II)이온을 안정화 하기위하여, 2산화 규소와, 구상, 입방체상 및 침상의 서로 다른형태의 산화 제2철로부터 규산철을 합성하였다. 메타놀증기로 포화시킨 질소까스를 튜브로에 도입시켜 얻은 환원성 분위기속에서, 114$0^{\circ}C$에서 11$65^{\circ}C$의 온도범위에서, 가스유속을 0.13 및 0.25l/min. 로서, 환원시간 4-150분동안 교상반응을 진행하였다. 반응생성의 동태를 오르자트 가스분석으로 검토하였으며, 생성물의 확인은 X-선 회절시험 및 감량정량에 의하였으며, 결과는 다음과 같다. 1 : 1.1의 몰비로 혼합한 산화제2철과 2산화 규소의 경우, 가스유속이 0.13l/min일 때, 규산철 합성반응시간은 구상, 입방체상 및 침상산화철에 있어서 각기 8-27분, 10-16분 및 6-7분으로 구상의 경우가 범위가 가장 넓었다. 또한, 반응속도는 산화제2철의 표면적의 평방근에 비례하였고 반응시간의 평방근에 역비례하였다.

• Proceedings of the Korean Institute of Surface Engineering Conference
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• 2017.05a
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• pp.150.1-150.1
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• 2017

구조용 합금 중 가장 우수한 비강도를 나타내는 마그네슘 및 마그네슘 합금은 최근 자동차, 항공, 기계 및 전자산업 등 다양한 산업분야에서 이용되고 있다. 하지만 마그네슘 합금은 반응성이 매우 커서 쉽게 부식되는 단점이 있다. 따라서 최근 내식성 향상을 위한 표면처리 기술에 대한 연구의 필요성이 증대되고 있으며, 그 중 플라즈마 전해산화법(Plasma electrolytic oxidation)은 양극산화반응을 이용하여 고내식성, 고경도의 산화피막을 금속 표면에 형성시키는 방법으로 많은 연구가 진행되고 있다. 본 연구에서는 탄산이온이 포함된 수용액에서 수산화나트륨의 농도가 AZ31 마그네슘 합금의 플라즈마전해산화 피막형성에 미치는 영향에 대해 알아보았다. 다양한 농도의 수산화나트륨 용액에서 DC 전류를 인가하여 플라즈마전해산화 피막을 형성하였다. 탄산 이온이 포함된 수용액에서 수산화나트륨의 농도가 높아질수록 플라즈마 전해산화 피막의 형성전압은 낮아지며, 초기 피막 형성전압 상승 속도 또한 빠르게 증가하며 피막 형성전압 등락의 폭은 감소하는 것으로 나타났다.

• Journal of the Korean Chemical Society
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• v.31 no.2
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• pp.178-183
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• 1987

The kinetics of the reaction of $[Mo_3O_4(H_2O)_9]^{4+}$ with $VO_2^+$have been studied at $25^{\circ}C$ by spectrophotometric method. With$VO_2^+$ in excess, the $[Mo_3O_4(H_2O)_9]^{4+}$ reaction can be expressed as $Mo^{IV}_3+6V^V{\rightleftarrows}3Mo^{IV}+6V^IV}$. Observed rate constants for the reaction are dependent on [$H^+$] and [$VO_2^+$]. Mechanism for the redox of $[Mo_3O_4(H_2O)_9]^{4+}$and $VO_2^+$ is proposed and discussed.

• Proceedings of the Korean Nuclear Society Conference
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• 1998.05b
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• pp.231-236
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• 1998

원자력 발전소의 핵연료 피복관 재료로 사용되고 있는 Zr합금의 부식특성에 미치는 Sn의 영향을 조사하기 위해 Sn 함량을 0.5, 0.8, 1.5, 2.0wt.%로 조절한 Zr-xSn 2원계 합금과 Zr-0.4Nb-xSn 3원계 합금을 제조하여 36$0^{\circ}C$ 물 분위기의 mini-autoclave에서 부식실험을 수행하였다. 2원계 합금에서 Sn이 0.5, 0.8, 1.5wt.% 첨가된 합금에서는 15일에서 속도천이가 발생한 후 급격한 부식 가속 현상이 나타났으나, 2.0wt.%가 첨가된 합금에서는 100일까지 부식 실험에서도 천이 현상을 보이지 않는 매우 높은 부식 저항성을 보였다. 그러나 3원계 합금에서는 2원계 합금과는 달리 40일 시험에서도 모든 합금들이 속도 천이 현상을 보이지 않고 천이전 영역에서의 부식 거동을 보이며, Sn 함량 변화에 따른 부식 속도의 차이를 감지할 수 없었다. 이러한 경향은 2원계 합금과 3원계 합금에서 Sn의 고용도 차, 미량 첨가된 Nb의 영향 및 석출물의 특성과 관련이 있는 것으로 사료된다. 또한 수소 흡수율면에서도 Sn 함량 변화에 따라 부식 거동과 비슷한 경향을 보이면서 2.0wt.%에서 가장 낮은 수소흡수율을 보였다 천이전 영역에서 산화막 구조 관찰 결과 천이전 영역의 모든 산화막에서 보호적 성질을 나타내는 tetragonal-ZrO$_2$가 관찰되었는데, tetragonal-ZrO$_2$의 분율은 Sn 함량에 따라 거의 같게 나타났다.

• Korean Journal of Food Science and Technology
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• v.17 no.2
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• pp.71-74
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• 1985

In the present study, a tentative mechanism for the decomposition of the hydroperoxide formed during the thermal oxidation of an edible soybean oil was proposed. The soybean oil was thermally oxidized at $120^{\circ}C$ for 7 hrs with air injection at a rate of 120 ml/min. Through kinetic studies of the decomposition process based on the tentative mechanism and the actual experimental data obtained from the hydroperoxide decomposition at 100, 120, 150 and $180^{\circ}C$, it was found that the reaction order of the hydroperoxide decomposition in these conditions was of first order. It was also estimated that the dissociation energy for the hydroperoxide in the same conditions was 15.876 kcal/g. mol.

• Journal of Korean Society of Environmental Engineers
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• v.31 no.10
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• pp.831-838
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• 2009

In order to evaluate a removal characteristic of diclofenac, ibuprofen and naproxen by oxidizing agents, $Cl_2,\;O_3$ and $O_3/H_2O_2$ are used as oxidants in this study. In case of that $Cl_2$ is used for oxidizing pharmaceuticals, ibuprofen is not removed entirely at $Cl_2$ dose range of 0.5~5.0 mg/L for 60 minutes, however, removal tendency of diclofenac and naproxen are so obviously at $Cl_2$ dose higher than 0.5 mg/L. In addition, as $Cl_2$ dose and contact time are increased, the removal rate of diclofenac and naproxen is enhanced. When $O_3$ is used as oxidizing agent, ibuprofen is not eliminated at $O_3$ dose range of 0.2~5.0 mg/L. On the contrary, 72~100% of diclofenac and 49~100% of naproxen are removed at $O_3$ dose of 0.2~5.0 mg/L. From experiments using $O_3/H_2O_2$ as an oxidant, we can find that $O_3/H_2O_2$ is much more effective than $O_3$ only for removal of diclofenac and naproxen. Moreover, the efficiency is raised according to increase of $H_2O_2$ dose, however, experiments using $O_3/H_2O_2$ show that oxidation of pharmaceuticals is less effective as $H_2O_2$ to $O_3$ ratio increased to above approximately 1.0. On reaction rate constant and half-life of diclofenac, ibuprofen and naproxen depending on $Cl_2$, $O_3$ and $O_3/H_2O_2$ dose, an oxidation of pharmaceuticals by $Cl_2$ and $O_3$ particularly has a comparatively high reaction rate constant and short half-life comparing $O_3/H_2O_2$. From above results, we can fine that diclofenac and naproxen can be easily eliminated in oxidation processes.

• Journal of the Korean Society of Propulsion Engineers
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• v.24 no.3
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• pp.12-17
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• 2020

The mechanical properties of the propellant with yellow iron oxide were slightly increased compared to the propellant with red iron oxide. The propellant with yellow iron oxide used two types of AP. As the ratio of small particles of AP increased, the burning rate increased. The propellant may be applied to the propellant under operating conditions of 17.5 mm/sec or less having a pressure index of 0.5. The burning rate downs in the mixer scale-up. The stress at maximum load of propellant decreased and the strain at maximum load increased in the mixer scale-up. The yellow iron oxide did not affect the adhesive force between the insulation/liner/propellant.

• Korean Journal of Food Science and Technology
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• v.39 no.2
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• pp.133-137
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• 2007

The 2,2-diphenyl picrylhydrazyl (DPPH) method, which can be used to predict the oxidative stability of edible oils, was previously reported by our research group. Not only free radical scavenging antioxidants but also radicals from oxidized oils are capable of reacting with DPPH radicals, thereby reducing the absorbance of DPPH. In this study, the optimum sample size of edible oils for the DPPH method was determined, and the oxidation of the edible oils was monitored via DPPH, coupled with other conventional methods. The optimum sample size was determined as 1.5 g using soybean oil. Soybean, corn, virgin olive, and refined olive oils were thermally oxidized for 3 hr at $180^{\circ}C$ and analyzed via DPPH, conjugated dienoic acid (CDA) value, and p-anisidine value (p-AV) protocols. Soybean and corn oils were found to be more sensitive to thermal oxidation than virgin and refined olive oils, on the basis of the CDA value and p-AV measurements. The DPPH method can indicate the inherent radical scavenging activity of unoxidized samples, the time required for the depletion of antioxidants, and the rate of degradation of the antioxidants. The soybean and corn oils evidenced higher levels of free radical scavenging compounds, required more time for the consumption of inherent antioxidants, and also manifested steeper antioxidant degradation rates than olive oils, based on the results of DPPH analysis. The DPPH method, accompanied by other conventional methods, may prove useful in predicting the degree of oxidation of vegetable oils.

• Journal of the Korean Chemical Society
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• v.39 no.1
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• pp.29-34
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• 1995

The rates for the oxidation reaction of l-ascorbic acid by Cu(Ⅱ)-polyamine complexes were measured by Onish's method at the pH 4.6. The oxidation process of l-ascorbic acid is proposed to occur by the inner-sphere mechanism that involves the formation of a Cu(Ⅱ)-ascorbic acid complex and electron transfer at the rate-determining step.

• Resources Recycling
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• v.13 no.1
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• pp.28-38
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• 2004

The characteristics of cyanide decomposition in aqueous phase by electric oxidization have been explored in an effort to develop a process to recycle waste water. Considering current efficiency and voltage, the free cyanide decomposition experiment by electric oxidization indicated that 5 V of voltage and copper catalytic Cu/CN mole ratio 0.05 was the most appropriate condition, where current efficiency was 26%, and decomposition speed was 5.6 mM/min. High voltage and excess copper addition increased decomposition speed a little bit but not current efficiency. The experiment of free cyanide density change proves that high density cyanide is preferred because speed and current efficiency increase with density. Also, the overall decomposition reaction could be represented by the first order with respcect to cyanide with the rate constant of $1.6∼7.3${\times}$10^{-3}$ $min^{-1}$ The mass transfer coefficient of electric oxidization of cyanide came out as $2.42${\times}$10^{-5}$ $min^{-1}$ Furthermore, the Damkohler number was calculated as 5.7 in case of 7 V and it was found that the mass transfer stage was the rate determining step.