• Journal of Electrochemical Science and Technology
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• 제2권1호
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• pp.8-13
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• 2011

Interfacial compatibility between the Si-Cu electrode and diluted ionic liquid electrolyte containing 50 vol.% of 1M lithium bis(trifluoromethanesulfonyl)imide (LiTFSI)/1-methyl-1-propylpyrrolidinium bis(trifluoromethylsulfonyl)imide (MPP-TFSI) and 50 vol.% dimethyl carbonate (DMC) in a lithium cell and dilution effect on surface chemistry are examined. ex-situ ATR FTIR analysis results reveal that the surface of the Si-Cu electrode cycled in the diluted ionic liquid electrolyte is effectively passivated with the SEI layer mainly composed of carboxylate salts-containing polymeric compounds produced by the decomposition of DMC. Surface species by the decomposition of TFSI anion and MPP cation are found to be relatively in a very low concentration level. Passivation of electrode surface with the SEI species contributes to protect from further interfacial reactions and to preserve the electrode structure over 200 cycles, delivering discharge capacity of > 1670 $mAhg^{-1}$ and capacity retention of 88% of maximum discharge capacity.

• 한국신재생에너지학회:학술대회논문집
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• 한국신재생에너지학회 2011년도 추계학술대회 초록집
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• pp.82.2-82.2
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• 2011

A channel design which is closely related with the mass transport overpotential is one of the most important procedures to optimize the whole fuel cell performance. In this study, three dimensional results of a numerical study for gas distribution in channels of a molten carbonate fuel cell (MCFC) unit cell for a 1kW class stack was presented. The relationship between the fuel and air distribution in the anode and cathode channels of the unit cell and the electric performance was observed. A charge balance model in the electrodes and the electrolyte coupled with a heat transfer model and a fluid flow model in the porous electrodes and the channels was solved for the mass, momentum, energy, species and charge conservation. The electronic and ionic charge balance in the anode and cathode current feeders, the electrolyte and GDEs were solved for using Ohm's law, while Butler-Volmer charge transfer kinetics described the charge transfer current density. The material transport was described by the diffusion and convection equations and Navier-Stokes equations govern the flow in the open channel. It was assumed that heat is produced by the electrochemical reactions and joule heating due to the electrical currents.

• Journal of Electrochemical Science and Technology
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• 제2권1호
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• pp.20-25
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• 2011

This work focuses on the behavior of the overpotential increase due to a utilization rise in a molten carbonate fuel cell. The behavior is generally explained by Nernst loss, which is a kind of voltage loss due to the thermodynamic potential gradients in a polarization state due to the concentration distribution of reactant species through the gas flow direction. The evaluation of Nernst loss is carried out with a traditional experimental method of constant gas utilization (CU). On the other hand, overpotential due to the gas-phase mass-transport resistance at the anode and cathode shows dependence on the utilization, which can be measured using the inert gas step addition (ISA) method. Since the Nernst loss is assumed to be due to the thermodynamic reasons, the voltage loss can be calculated by the Nernst equation, referred to as a simple calculation (SC) in this work. The three values of voltage loss due to CU, ISA, and SC are compared, showing that these values rise with increases in the utilization within acceptable deviations. When we consider that the anode and cathode reactions are significantly affected by the gas-phase mass transfer, the behavior strongly implies that the voltage loss is attributable not to thermodynamic reasons, namely Nernst loss, but to the kinetic reason of mass-transfer resistance in the gas phase.

• Bulletin of the Korean Chemical Society
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• 제17권9호
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• pp.814-819
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• 1996

In search of simple host molecules for uranyl ion which form 1: 1-type complexes with high formation constants that can be used either in extraction of uranium from seawater or in catalysis of biologically important organic reactions, the uranophile activities of dihydroxyazobenzene derivative 1 were studied. Uranyl ion and 1 form a 1: 1-type complex with a very large formation constant. The formation constant was measured at pH 7-11.6 by competition experiments with carbonate ion. From the resulting pH dependence, ionization constants of the two aquo ligands coordinated to the uranium of the uranyl complex of 1 were calculated. The ionization constants were also measured by potentiometric titration of the uranyl complex of 1. Based on these results, the pKa values of the two aquo ligands were estimated as 7.1 and 11.0, respectively. At pH 7.5-9.5, therefore, the complex exists mostly as monohydroxo species. Under the conditions of seawater, 1 possesses greater affinity toward uranyl ion compared with other uranophiles such as carbonate ion, calixarene derivatives, or a macrocyclic octacarboxylate. In addition, complexation of 1 with uranyl ion is much faster than that of the calixarene or octacarboxylate uranophiles.

• 한국토양환경학회지
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• 제4권3호
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• pp.77-84
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• 1999

본 논문에서는 고농도의 중금속 (납, 구리)으로 오염된 세 가지의 토양을 대상으로 sequential extraction 방법을 사용하여 토양과 중금속의 차이에 따른 결합 특성을 밝혀내고자 하였다. 고농도의 납과 구리로 오염된 토양을 형태별로 추출하였을 때 토양의 특성과 중금속의 종류에 따라 다른 결과를 보였다. 납은 문화동 토양에서는 Carbonate 형태가 37.7%로 가장 높았고 농토는 Amorphous Fe oxide 형태가 23.9%, 공단 토양에서는 Exchangeable 형태가 22.9%로 나타났다. 이에 비하여 구리는 세 가지 토양에서 공통적으로 Organically bound 형태가 농토에서 26.1%, 문화동 토양은 20.4%. 공단 토양에서는 24.1%로 높게 나타났고 Carbonate 형태와 Amorphous Fe oxide형태의 비율도 높게 나타났다. 또한 Crystallized Fe oxide 형태와 Residuals 형태도 납보다 높은 비율을 나타냄으로서 구리가 납보다는 토양과 강한 결합을 형성하는 것으로 생각된다. 이러한 토양과 중금속의 결합 특성은 오염 토양의 복원시 유용한 자료가 될 수 있다.

• Nuclear Engineering and Technology
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• 제42권5호
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• pp.552-561
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• 2010

This study investigates the solubility of neptunium (Np) in the deep natural groundwater of the Korea Atomic Energy Research Institute Underground Research Tunnel (KURT). According to a Pourbaix diagram (pH-$E_h$ diagram) that was calculated using the geochemical modeling program PHREEQC 2.0, the redox potential and the carbonate ion concentration both control the solubility of neptunium. The carbonate effect becomes pronounced when the total carbonate concentration is higher than $1.5\;{\times}\;10^{-2}$ M at $E_h$ = -200 mV and the pH value is 10. Given the assumption that the solubility-limiting stable solid phase is $Np(OH)_4(am)$ under the reducing condition relevant to KURT, the soluble neptunium concentrations were in the range of $1\;{\times}\;10^{-9}$ M to $3\;{\times}\;10^{-9}$ M under natural groundwater conditions. However, the solubility of neptunium, which was calculated with the formation constants of neptunium complexes selected in an OECD-NEA TDB review, strongly deviates from the value measured in natural groundwater. Thus, it is highly recommended that a prediction of neptunium solubility is based on the formation constants of ternary Np(IV) hydroxo-carbonato complexes, even though the presence of those complexes is deficient in terms of the characterization of neptunium species. Based on a comparison of the measurements and calculations of geochemical modeling, the formation constants for the "upper limit" of the Np(IV) hydroxo-carbonato complexes, namely $Np(OH)_y(CO_3)_z^{4-y-2z}$, were appraised as follows: log $K^{\circ}_{122}\;=\;-3.0{\pm}0.5$ for $Np(OH)_2(CO_3)_2^{2-}$, log $K^{\circ}_{131}\;=\;-5.0{\pm}0.5$ for $Np(OH)_3(CO_3)^-$, and log $K^{\circ}_{141}\;=\;-6.0{\pm}0.5$ for $Np(OH)_4(CO_3)^{2-}$.

• ALGAE
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• 제24권4호
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• pp.213-229
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• 2009

A monographic reassessment of Padina Adanson species from the Gulf of California was developed based on an exhaustive review of the character and characters states that have been used to delimit species in recent and historically valuable collections. Eight names (P. caulescens Thivy in Taylor, P. concrescens Thivy in Taylor, P. crispata Thivy in Taylor, P. durvillaei Bory Saint-Vincent, P. gymnospora [Kutzing] Sonder, P. mexicana Dawson, P. tetrastromatica Hauck and P. vickersiae Hoyt in Howe) were reported from the region. An analysis of 1,200 specimens led to the conclusion that only three species (P. durvillaei, P. concrescens and P. mexicana) can be recognized for the area based on four discriminating characters: presence of calcium carbonate in the cell wall; number of medullary cell layers in the basal area; number of medullary cell layers in the middle part and presence/absence of cortical cells. Comparative analysis of the species in the Gulf of California in relation to other recently evaluated species has shown a clear distinction among them suggesting Padina species were overestimated in our area.

• Journal of Species Research
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• 제9권4호
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• pp.427-442
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• 2020

We collected indigenous Korean ciliate species from diverse aquatic and terrestrial habitats in 2018 and 2019. The morphology of these ciliates was revealed based on the observations of living cells, and protargol-impregnated and/or silver carbonate-impregnated specimens. During this study, we found 16 previously unrecorded Korean ciliate species, which are as follows: 1) class Heterotrichea - Stentor introversus; 2) class Spirotrichea - Aspidisca orthopogon, Amphisiella sinica, Epiclintes auricularis rarisetus, Apokeronopsis wrighti, Pseudokeronopsis carnea, Trachelostyla pediculiformis, Strombidium apolatum, and Varistrombidium kielum; 3) class Phyllopharyngea - Chlamydodon obliquus, Dysteria aculeata, and Hartmannula angustipilosa; 4) class Litostomatea - Paraspathidium apofuscum; and 5) class Oligohymenophorea - Frontonia angusta solea, Metanophrys sinensis, and Uronemita binucleata. Here, we provide a diagnosis for each species with a brief remark. Among them, the infraciliature of the poorly known species, Stentor introversus and Dysteria aculeata, is described for the first time. Further, we revise the Korean population of Pseudokeronopsis pararubra, which was previously misidentified as Pseudokeronopsis carnea.

• 공업화학
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• 제10권5호
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• pp.754-760
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• 1999

직접 내부개질형 MCFC용 촉매의 반응 전과 후의 특성분석을 ICP, BET, CHN, EDS, $H_2$ 화학흡착 분석을 통하여 수행하였다. 반응을 거치는 동안 탄산염 전해질의 구성 성분인 K와 Li가 촉매에 전달되고, 그 누적량은 단위전지 내의 위치에 따라 입구, 출구, 중간 순으로 감소하였다. 알칼리 전달량 증가에 따라 BET 표면적과 Ni 분산도가 감소하고 촉매 표면에 증착된 알칼리 탄산염 물질이 존재하는 것으로부터, 촉매 표면상에 존재하는 알칼리성분의 물리적 피복이 촉매 활성을 감소시키는 중요한 원인임을 확인하였다. SEM 분석 결과, 입구, 중간, 출구 순으로 알칼리 성분의 표면 피복율이 감소하였으나, 실제 메탄에 대한 수증기 개질반응의 촉매활성은 출구부분 촉매가 입구나 중간 부분 촉매보다 낮은 활성을 보임으로써, 알칼리 탄산염의 물리적 피복에 의한 활성감소 이외의 다른 화학적 피독 요인이 존재함을 예측하였고, 이를 FT-IR 분석을 통해 확인하였다.

• Animal Systematics, Evolution and Diversity
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• 제37권4호
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• pp.280-286
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• 2021

During a field survey on Korean coastal marine waters, two ciliates belonging to the genera Pseudovorticella Foissner & Schiffmann, 1975 and Frontonia Ehrenberg, 1838 in the class Oligohymenophorea de Puytorac et al., 1974, were collected. Even though the two genera are very common in the aquatic ecosystems, they had been superficially studied in Korean habitats. Using the observation of living cells and specimens impregnated by protargol, silver carbonate, and silver nitrate, two newly recorded ciliate are identified as P. paramarina Sun, Ji, Warren & Song, 2009 and F. ocularis Bullington, 1939. A brief diagnosis, remark, and comprehensive micrographs are provided for each species.