• Journal of Electrochemical Science and Technology
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• v.2 no.1
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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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• 2011.11a
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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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• v.2 no.1
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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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• v.17 no.9
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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.

• Journal of Korea Soil Environment Society
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• v.4 no.3
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• pp.77-84
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• 1999

Sequential extraction was applied to characterize the soil-metal binding mechanism in three kinds of soils contaminated with lead and copper The results showed that soil-metal binding was dependent on soil characteristics and metal species. In Munwha dong soil, lead was mainly carbonate form (37.7%), in agriculture soil was associated with amorphous Fe oxide form (23.9%) and in industry area was associated with exchangeable form (22.9%) Meanwhile for copper. organically bound form represented main fraction in most soil and also carbonate and amorphous Fe oxide form showed high fraction. Crystallized Fe oxide and residuals form of copper showed higher fraction than those of lead. Thus, it can be concluded that copper is bound with soil stronger and more difficult wash out Consequently, this mechanism analysis through sequential extraction can provide useful informations for better soil remediation.

• Nuclear Engineering and Technology
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• v.42 no.5
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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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• v.24 no.4
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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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• v.9 no.4
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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.

• 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.

• Animal Systematics, Evolution and Diversity
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• v.37 no.4
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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.