• Title/Summary/Keyword: 수용액 화학

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A Study on the Synthesis of Aluminum Citrate from Aluminum Chloride Solutions (염화(鹽化)알루미늄 수용액(水溶液)으로부터 Aluminum Citrate의 합성(合成) 연구(硏究))

  • Lee, Hwa-Young
    • Resources Recycling
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    • v.18 no.6
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    • pp.18-23
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    • 2009
  • An investigation on the synthesis of aluminum citrate, one of the aluminum organic compounds, has been performed using aluminum chloride solutions as a starting material. For the synthesis of aluminum citrate, citric acid was added to aluminum solutions with the mole ratio of citric acid to aluminum to be 2.5 and aluminum citrate synthesized was also characterized in terms of chemical analysis, X-ray diffraction, particle size measurement and SEM analysis. As a result, it was found that the ratio of ethanol/Al solution more than 4.0 was required for the synthesis of aluminum citrate from aluminum solutions. Furthermore, the pH should be controlled to be more than 7.0 in order to obtain the recovery of aluminum citrate higher than 97%. From the chemical analysis of aluminum citrate synthesized in this work, the content of $NH_4$, Al and C was found to be 17.0, 4.01 and 25.7%, respectively. Accordingly, the aluminum citrate synthesized from aluminum solutions was confirmed to be $(NH_4)_5Al(C_6H_4O_7)_2{\cdot}2H_2O$.

토양 특성에 따른 Trichloroethylene (TCE:) 흡착능 비교

  • 정현정;이민희
    • Proceedings of the Korean Society of Soil and Groundwater Environment Conference
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    • 2002.09a
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    • pp.362-365
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    • 2002
  • 토양의 물리/화학적 특성에 따른 토양의 유기오염물 흡착능 변화를 규명하기 위하여, 토양 내 clay 함량 및 유기물 함량변화, 수용액 내 TCE 농도변화에 따른 TCE 의 토양내 흡착량 변화를 측정하였다. 수용액의 pH와 실내온도는 일정하게 유지시켰으며 clay는 표면적이 다른 Ca-montmorillonite, Na-montmorillonite, kaolin을 이용하였고, 유기물질로는 활성탄을 사용하였다. 일정한 토양성분과 실제토양에 대해 수용액 내 TCE의 농도를 변화시켜 농도변화에 따른 흡착량 변화를 측정하였다. 실험결과 유기물과 점토함량의 증가에 따라 흡착량은 모두 증가하였으나 활성탄에 의한 TCE 흡착량이 점토에 비해 매우 높았으므로 유기물에 의한 TCE 흡착영향이 점토에 의한 흡착 영향보다 큰 것으로 나타났다. TCE 농도변화에 따른 흡착결과는 실제토양과 모사토양에서 모두 농도가 증가함에 따라 흡착 증가율이 증가하다가 감소하는 Langmuir isotherm 형태를 보여 주었다.

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Electrochemical Reduction of Nitrate Ion in an Aqueous Solution (수용액에서 질산성 질소의 전기화학적 환원거동)

  • Park, J.K.;Jeon, C.J.;Lee, C.K.
    • Proceedings of the Korean Institute of Resources Recycling Conference
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    • 2003.10a
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    • pp.246-251
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    • 2003
  • 전기분해법을 이용하여 수용액 중의 질산성 질소의 환원거동에 대한 연구를 통하여 수용액중의 질산 함량을 제어하는 연구를 수행하였다. 촉매전극을 채택한 복극전해조에서 30분의 조업에 질산 100ppm 이하의 저농도 용액은 70%, 300ppm 이상의 고농도의 경우는 90%까지 질소를 용이하게 제거할 수 있었다. 초기 질소농도가 증가하면서 한계전류밀도도 크게 증가하였으며, pH가 감소할수록 환원전류가 증가하였다. 그리고 수용액의 pH는 질소 환원반응기구에 큰 영향을 주는 것으로 판명되었으며, 산성에서는 질소형태로 중성 혹은 염기성에서는 암모니아 형태로 환원되는 것으로 추정된다.

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Analysis of Chemistry Textbook Content and Teachers' Recognitions about Ionization and Ionization constant of Strong Acid (강산의 이온화도와 이온화 상수에 대한 화학 교과서 내용 및 교사들의 인식 분석)

  • Paik, Seoung-Hey;Go, Hyung-Suk;Jeon, Min-Cheol
    • Journal of the Korean Chemical Society
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    • v.57 no.2
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    • pp.279-288
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    • 2013
  • In this study, we analyzed the values of ionization and ionization constants in the chemistry textbooks developed during 1945-2009 year. The chemistry teachers compared strength of strong acids in aqueous solution by questionnaire. In the questionnaire, we searched chemistry teachers' cognitions about the discordance reason of ionization constant formulation and the values in the textbooks. The subjects were 46 chemistry teachers. As results, the teachers compared the strength of strong acids in aqueous solution based on the ionization and ionization constant values in the textbooks. They didn't notice the problem of discordance of ionization constant formulation and the values in the textbooks. Even though they recognized the problem, they could not find the solution, and thought the problem arrived by experiment error or measurement error.

Iron Ion Contamination and Acid Washing Effect of Polymer Membrane and Electrode in Polymer Electrolyte Fuel Cell (고분자전해질 연료전지에서 고분자 막과 전극의 철 이온 오염 및 산 세척 효과)

  • Yoo, Donggeun;Park, Minjeong;Oh, Sohyeong;Park, Kwon-Pil
    • Korean Chemical Engineering Research
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    • v.60 no.1
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    • pp.20-24
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    • 2022
  • In the process of long-term use of PEMFC (Proton Exchange Membrane Fuel Cells), chemical degradation of membrane electrode assembly (MEA) occurs due to corrosion of stack elements and contamination of supply gas. In this study, we investigated whether chemically degraded MEA can be recovered by acid washing. The performance was measured and compared in a PEMFC cell after contamination with iron ions and washing with an aqueous sulfuric acid solution. The performance was reduced by about 25% by 0.5 ppm iron ion contamination, and 97.1% performance recovery was possible by washing of 0.15 M sulfuric acid. The membrane resistance was increased due to iron ion contamination of the polymer membrane, and the ionic conductivity was restored by washing the iron ions from the membrane while minimizing the loss of the electrode catalyst by washing with a low-concentration sulfuric acid aqueous solution. The possibility of solving the decrease in durability caused by chemical contamination of PEMFC MEA by the acid washing was confirmed.

Selective determination of mercury (II) ion in aqueous solution by chemiluminescence method (화학발광법에 의한 수용액 중의 선택적 수은(II) 이온 정량)

  • Kim, Kyung-Min;Jang, Taek-Gyun;Kim, Young-Ho;Oh, Sang-Huyb;Lee, Sang-Hak
    • Analytical Science and Technology
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    • v.24 no.4
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    • pp.243-248
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    • 2011
  • A selective determination method of mercury (II) ion in aqueous solution by luminol-based chemiluminescence system (luminol CL system) has been developed. Determination of metal ions such as copper (II), iron (III), chromium (III) ion in solution by the luminol CL system using its catalytic role in the reaction of luminol and hydrogen peroxide has been reported by several groups. In this study, the catalytic activity of mercury (II) ion in the reaction of luminol and hydrogen peroxide was observed by the enhanced CL intensity of the luminol CL system. Based on this phenomenon, experimental conditions of the luminol CL system were investigated and optimized to determine mercury (II) ion in aqueous solution. While mercury (II) ion in mixed sample solution containing mercury (I) and (II) ions highly enhanced the CL intensity of the luminol CL system, the mercury (I) ion could not enhanced the CL intensity. Thus selective determination of the mercury (II) ions in a mixture containing mercury (I) and (II) ions could be achieved. Each concentration of mercury (I) and (II) ions in aqueous solution can be obtained from the results of the CL method that give the concentration of only mercury (II) ion and the inductively coupled plasma (ICP) method that give the total concentration of mercury ions. On the optimized conditions, the calibration curve of mercury (II) ion was linear over the range from $1.25{\times}10^{-5}$ to $2.50{\times}10^{-3}M$ with correlation coefficient of 0.991. The detection limit of mercury (II) ion in aqueous solution was calculated to be $1.25{\times}10^{-7}M$.