• Applied Chemistry for Engineering
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• v.31 no.3
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• pp.258-266
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• 2020

The chemical fixation of CO₂ into cyclic carbonates is considered to be one of the most promising way to alleviate global warming and produce fine chemicals. In this work, the catalytic applicability of metal-organic frameworks (MOFs) as porous crystalline materials for the synthesis of five-membered cyclic carbonate from CO₂ and epoxides was reviewed. In addition, we have briefly classified the materials based on their different structural features and compositions. The studies revealed that MOFs exhibited good catalytic performance towards cyclic carbonate synthesis because of the synergistic effect between the acid sites of MOFs and nucleophile. Moreover, the effect of structure of designed MOFs and mechanism for the cycloaddition of CO₂ were suggested.

• Analytical Science and Technology
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• v.12 no.4
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• pp.279-283
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• 1999

The purpose of this study was to optimize carbonate suspension counting method for the measurements of high level activity of $^{14}C$ in a reactor stack effluent gases. Although it is less sensitive method, the carbonate suspension counting method has been found to be a suitable technique for the $^{14}C$ monitoring of samples with small amount but with high specific activity and to be relatively simple and fast.

• The Sea:JOURNAL OF THE KOREAN SOCIETY OF OCEANOGRAPHY
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• v.14 no.3
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• pp.171-180
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• 2009

Based on the constituent analysis of sediments near Dok Island, the origin and sedimentary facies were Investigated. The sediments are mainly from originated from volcanic and volcaniclastic rock fragments derived from Dok Island and carbonate sediments formed by a variety of shallow-dwelling organisms that secreted calcareous skeletons. Carbonate producers include mollusks (bivalves and gastropods), encrusting & branching bryozoans, encrusting & segmented red algae, worm tubes, barnacles, diatoms, sponge spicules and echinoderm fragments. The distribution and relative amount of these constituents are basically dependent upon water depth and grain size even though local variations can be observed within the same depth interval. Five sedimentary facies can be divided: nearshore facies (<20 m), neritic facies ($20{\sim}100m$), upper transitional facies ($100{\sim}200m$), lower transitional facies ($200{\sim}700m$), and hemipelagic facies (>700 m). The sediments that were sampled below the water depth of 2,000 m still contain a significant amount of carbonates (ca. $10{\sim}20%$), implying that the carbonate compensation depth in the East Sea may well exceed this water depth.

• Resources Recycling
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• v.15 no.3 s.71
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• pp.74-80
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• 2006

In this article, we would like to investigate a durability characterization of cement mortar with inert filler, which is ground calcium carbonate(GCC). The kinds of techniques to evaluate cement mortar are chloride ion ingress, carbonation and sulfate attack. For the experimental result of the resistance of chloride ion ingress, carbonation and sulfate attack, as the addition of GCC makes decreasing the permeability by micro-filler effect, the specimens of $5{\sim}15%$ ratio of replacement are superior to the GCC0 mortar specimen with respect to durability of cement matrix in this scope.

• 한국신재생에너지학회:학술대회논문집
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• 2010.06a
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• pp.130.2-130.2
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• 2010

한전 전력연구원에서는 2009년 12월부터 125 kW급 용융탄산염 연료전지 발전시스템의 성능평가를 위한 운전이 진행되고 있다. 현재 진행 중인 "250 kW급 열병합 용융탄산염 연료전지 Proto Type개발" 과제의 최종시작품인 250 kW급 발전시스템은 125 kW급 MCFC 스택 2기로 설계되어, 125 kW급 시스템의 시험운전은 매우 중요한 기술적 성과가 될 것이다. 현재 125 kW급 MCFC 스택은 10,000 $cm^2$의 유효전극면적을 갖는 단위전지들로 구성되었으며, 적층 스택의 온도 및 농도분포의 최적화를 위해 내부 매니폴드 및 Co-flow Type 열교환기 기반의 분리판을 개발 적용하였다. 연료극의 전극 구성은 Ni-Al alloy로, 공기극의 전극 구성은 Lithiated-NiO로 이루어졌다. 그리고 매트릭스는 ${\alpha}-LiAlO_2$로 제작되었고, 전해질은 Li과 K Carbonate가 68 : 32 비율로 섞인 용융염을 사용하였다. 본 125 kW급 용융탄산염 연료전지 시스템의 운전평가는 고적층 스택의 온도 및 농도 분포를 확인하고, 최적화된 스택 운전 조건을 도출하는 것을 그 목적으로 하고 있다. 125kW급 스택 1기의 규모의 주변기기 시스템은 외부개질기, 촉매연소기, 이젝터, 고온순환 블로어 및 공기블로어 등으로 이루어져 있다. 고온형 연료전지 시스템에서 연료극과 공기극의 균일한 온도 및 압력 확보는 매우 중요하며, 이를 위하여 외부개질기 및 촉매연소기 연동을 통한 온도편차를 최소화하고, 기존 고온용 순환 블로어 대신 이젝터를 개발 도입하여 압력균형을 조절하였다. 125kW급 MCFC 시스템은 2009년 12월부터 전처리 운전을 시작하여 2010년 1월 말부터 PCS로 전기를 생산하고 있다. 평균전압 0.83V에서 100kW의 출력을 기록하였으며, 피크부하 120 kW, 누적출력량 30 MWh를 초과달성하였다.

• Journal of the Korean Crystal Growth and Crystal Technology
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• v.20 no.6
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• pp.283-288
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• 2010

Nanosized NiO powder was prepared by mixing an acid nickel salt and a base nickel salt and their reduction behavior was studied. Ni formate was employed as an acid salt and nickel hydroxide and basic nickel carbonate as base salts. One equivalent acid salt was mixed with 9 equivalent base salt. The mixture of the formate and the carbonate produced ~100 run spherical NiO powder by heat treatment at $750^{\circ}C$/2 h, but the mixture of the formate and the hydroxide gave rise to ~100 nm pseudo spherical NiO powder by heat treatment at $600^{\circ}C$/2 h and grew fast to give pseudo cubic crystals of 100~600 run by heat treatment at $750^{\circ}C$/2 h. Reduction by hydrogen gas proceeded much faster for the one with the hydroxide than that with the carbonate to give porous body with well grown necks. Their behavior was studied by analysis of TG/DSC, XRD, and SEM.

• Journal of Nuclear Fuel Cycle and Waste Technology(JNFCWT)
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• v.11 no.2
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• pp.85-93
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• 2013

This study has been carried out to elucidate the characteristics of the dissolution for Thermal Decomposed Solid Waste of uranium-bearing sludge (TDSW), the removal of impurities by an alkalization in a nitric acid dissolving solution of TDSW, and the selective removal (/recovery) of uranium by an acidification in an carbonate alkali solution, respectively. TDSW generated by thermal decomposition of U-bearing sludge which was produced in the uranium conversion plant operation, was stored in KAERI as a solid-powder type. It is found that the dissolution of TDSW is more effective in nitric acid dissolution than oxidative-dissolution with carbonate. At 1 M nitric acid solution, TDSW was undissolved about 30wt% as a solid residue, and uranium contained in TDSW was dissolved more than 99%. In order to the alkalization for the nitric acid dissolving solution of TDSW, carbonate alkalization is more effective with respect to remove the impurities. At the carbonate alkali solution controlled to about 9 of pH, Al, Ca, Fe and Zn co-dissolved with U in dissolution step was removed about $98{\pm}1%$. On the other hand, U could be recovered more than 99% by an acidification at pH about 3 in a carbonate alkali solution, which was nearly removed the impurities, adding 0.5M $H_2O_2$. It was found that uranium could be selectively recovered (/removed) from TDSW.

• Proceedings of the Korea Society for Energy Engineering kosee Conference
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• 1998.05a
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• pp.243-251
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• 1998

내부개질형 용융탄산염 연료전지는 일반적인 연료전지가 갖는 고효율, 저공해, 모듈화 가능성 등의 장점 이외에도, 스택의 반응열을 열교환 없이 직접 개질반응에 이용하는 내부개질 특성 때문에 발전 설비의 단순화에 따른 추가 열효율의 상승이라는 장점을 갖는다. 또한 외부개질 용융탄산염 연료전지가 중앙집중식 대형 발전에 적합한 것과는 달리 내부개질형은 수십 MW 이하의 분산배치형 혹은 현장설치형에 더욱 적합하다는 특징이 있다. (중략)

• Transactions of the Korean Society of Mechanical Engineers B
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• v.38 no.2
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• pp.121-128
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• 2014

This study aims to develop a simulation bed for the mechanical balance of plants of high temperature fuel cells such as molten carbonate fuel cells. For using fuel cells in transportation, the optimization of the balance of plants should be considered. In this study, the dynamic model of a molten carbonate fuel cell and the model's responses to inlet gas composition, pressure, flow rate, and stack temperature were analyzed. On/off simulation was performed for testing the dynamic model's feasibility. The simulation results are in reasonable agreement with the experimental results from published literatures.

• Applied Chemistry for Engineering
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• v.10 no.5
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• pp.754-760
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• 1999

The properties of the catalyst for a direct internal reforming type molten carbonate fuel cell were examined by ICP, BET, CHN, EDS, and $H_2$ chemisorption. Potassium and lithium, the components of carbonate electrolyte, were transported to the catalyst during the operation of fuel cell, and the amounts of the deposited alkali elements were reduced in the order of inlet, outlet, and the middle. From the direct correlation between the amount of alkali and the physical properties such as BET surface area and Ni dispersion, and from the observation of the lump of the alkali species on the poisoned catalyst, it was confirmed that the physical blocking of the catalyst by alkali deposition was the main reason for the deactivation. Although the amount of alkali species was greater at the inlet than at the oulet, the catalyst sampled from the outlet had lower activity. This was caused by the chemical interaction between the alkali species and the catalyst at the outlet where temperature was highest in the cell body, which was detected by FT-IR analyses.