• 분석과학
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• 제28권3호
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• pp.196-203
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• 2015

셀레늄 강화 사료를 먹인 모돈에 대하여 혈청에서의 셀레늄 화학종들 즉, 무기셀레늄, 셀레노아미노산 및 셀레노단백질들을 음이온 교환과 친화 크로마토 그라피를 ICP/MS에 연결사용하여 분석하였다. 무기 셀레늄(Se⁴⁺와 Se⁶⁺)과 셀레노 아미노산들은 PRP X-100 음이온 교환 컬럼을 사용하였고 셀레노 단백질들의 경우에는 HEP 컬럼을 사용하여 SelP을 GPx+SeAlb로 부터 분리하였다. 정량분석은 후 컬럼 동위원소 희석법을 사용하여 이 들의 농도를 결정하였다. 모돈 실험군을 3 그룹으로 나누고 셀레늄이 강화된 사료(유기셀레늄 0.3 mg/kg, 0.6 mg/kg 및 무기셀레늄 0.6 mg/kg)를 4주 동안 먹였을 때 셀레늄 화학종들의 변화 및 사료와의 상관관계를 알아보았다. 셀레노 아미노산의 경우, 실험군들은 무기셀레늄 강화사료를 제외하고 대조군에 비하여 높은 농도를 보여주었다. 유기셀레늄 강화사료에서는 큰 차이를 보이지 않았다. 셀레노 단백질의 경우는 실험군 모두가 대조군에 비하여 증가를 보여주었는데 특히 SelP가 다른 단백질에 비하여 1.5 배 정도 더 크게 증가한 것으로 나타났다.

• 한국물환경학회지
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• 제26권1호
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• pp.89-95
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• 2010

The electrokinetic potential of $CaCO_3$, which takes an important part in aquatic system, has been measured and the variation of total energy between $CaCO_3$ particles with the distance of particles was estimated based on DLVO theory. The electrokinetic potential of particles was observed to increase to positive direction as the charge valence of cations which was added to suspension was increased. Also, the total interaction energy between particles was estimated to be more negative as the charge valence of cation was higher and its concentrations was raised. When a mixture of cations with different charge valences was added, the influence of cation with a higher charge valence was more significant on the total interaction energy between particles. When anion was added to the suspension of $CaCO_3$, the total energy estimated by DLVO theory was examined to move to positive direction and the electrokinetic potential of particles became more negative. Likewise cations, the effect of anions on the electrokinetic potential of particles and total interaction energy between them was observed to be proportional to their charge valence and the influence of the mixture of anions with different charge valence became more remarkable as the mixing ratio of the anion with a higher charge valence was increased.

• Bulletin of the Korean Chemical Society
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• 제27권10호
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• pp.1587-1592
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• 2006

We report the preparation, structure and magnetic properties of a new pillared complex, copper(II) hydroxy-1,4-butanedisulfonate, $Cu_2(OH)_3(O_3SC_4H_8SO_3)_{1/2}$. The titled compound was obtained by anion exchange, using copper hydroxyl nitrate $(Cu_2(OH)_3NO_3)$ as the starting material. According to the XRD data, this compound exhibits a pillared layered structure with organic layers tilted between the copper hydroxide layers with a tilt angle of $21.8^{\circ}$. FTIR spectroscopy confirms total exchange of nitrate by the sulfonate and indicates that the sulfonate functions are linked to the copper(II) ions with each aliphatic chain bridging the adjacent hydroxide layers. According to the dc and ac magnetic measurements, the title compound is a metamagnet consisting of spin-canted antiferromagnetic layers, with a Neel temperature of 11.8 K.

• The Korean Journal of Physiology
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• 제30권2호
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• pp.279-288
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• 1996

Chronic exposure to cadmium impairs various renal tubular functions, including organic acid (anion) secretion. To investigate the mechanism of cadmium-induced alterations in the organic anion transport system, kinetics of p-aminohippurate (PAH) uptake was studied in renal cortical basolateral membrane vesicles (BLMV) isolated from cadmium-intoxicated rats (adult male Sprague-Dawley). Cadmium intoxication was induced by subcutaneous injections of $CdCl_{2}$ (2 mg Cd/kg per day) for 3 weeks. The renal plasma membrane vesicles were prepared by Percoll gradient centrifugation. The vesicular uptake of $^{14}C$-PAH was determined by rapid filtration technique using Millipore filter. Cadmium intoxication resulted in a marked attenuation of $Na^{+}$-dependent, ${\alpha}$-ketoglutarate (${\alpha}$KG)-driven PAH uptake with no changes in $Na^{+}$ and ${\alpha}$KG-independent transport component. Kinetic analysis indicated that Vmax, but not Km, of the $Na^{+}$-dependent, ${\alpha}$KG-driven component was reduced. A similar reduction of $Na^{+}$-dependent, ${\alpha}$KG-driven PAH uptake was observed in normal membrane vesicles directly exposed to inorganic cadmium in vitro, and this was accompanied by an inhibition of both $Na^{+}$-dependent ${\alpha}$KG uptake and ${\alpha}$KG-PAH exchange activity. These results indicate that during chronic exposure to cadmium, free cadmium ions liberated in the proximal tubular cytoplasm directly interact with the basolateral membrane and impair the active transport capacity for organic anions, most likely due to an inhibition of both $Na^{+}$-dicarboxylate cotransporter and dicarboxylate-organic anion antiporter activities.

• Journal of Electrochemical Science and Technology
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• 제8권3호
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• pp.183-196
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• 2017

The research efforts directed at advancing water electrolysis technology continue to intensify together with the increasing interest in hydrogen as an alternative source of energy to fossil fuels. Among the various water electrolysis systems reported to date, systems employing a solid polymer electrolyte membrane are known to display both improved safety and efficiency as a result of enhanced separation of products: hydrogen and oxygen. Conducting water electrolysis in an alkaline medium lowers the system cost by allowing non-platinum group metals to be used as catalysts for the complex multi-electron transfer reactions involved in water electrolysis, namely the hydrogen and oxygen evolution reactions (HER and OER, respectively). We briefly review the anion exchange membranes (AEMs) and electrocatalysts developed and applied thus far in alkaline AEM water electrolysis (AEMWE) devices. Testing the developed components in AEMWE cells is a key step in maximizing the device performance since cell performance depends strongly on the structure of the electrodes containing the HER and OER catalysts and the polymer membrane under specific cell operating conditions. In this review, we discuss the properties of reported AEMs that have been used to fabricate membrane-electrode assemblies for AEMWE cells, including membranes based on polysulfone, poly(2,6-dimethyl-p-phylene) oxide, polybenzimidazole, and inorganic composite materials. The activities and stabilities of tertiary metal oxides, metal carbon composites, and ultra-low Pt-loading electrodes toward OER and HER in AEMWE cells are also described.

• 대한화학회지
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• 제29권4호
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• pp.365-371
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• 1985

이온쌍크로마토그래피에 의한 유기 및 무기음이온을 분리하는데 반대이온으로서 양이온 염료인 메틸렌 부루$(MTB^+)$를 사용하여 흡수가 되지 않는 음이온 시료를 간접적으로 분광광도 검출기로서 가시영역인 665nm에서 검출할 수 있었으며 혼합시료의 분리를 시도한 결과 좋은 분리도와 높은 감도를 보여주었다. 또한 여러 실험조건에서 분리인자를 측정하여 머무름 기구를 조사하였다. 본 연구에서 머무름 기구는 $MTB^+$가 고정상에 일차층(primary layer)을 형성하고 반면 음이온 시료 또는 이동상에 존재하는 다른 음이온들이 경쟁적으로 이차층(secondary layer)을 형성하는 ion-interaction model임을 확인하였다.

• 한국군사과학기술학회지
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• 제16권5호
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• pp.690-702
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• 2013

Ionic liquids(ILs) have been the most investigated chemicals among green solvents including water, glycerol, supercritical carbon dioxdie($scCO_2$). ILs are attracting organic as well as inorganic chemicals because most ionic liquids' vapor pressures are very low so that ILs are liquids phase at ambient conditions. ILs are composed of various anions and cations, thus chemists can design functionalized solvents and/or catalysts that can be used in specific synthetic reactions by means of combinations of different ions. Many scientists believe ILs being green materials because of its low vapor pressure as well as the flexibility in controlling the chemical and physical properties. In this review the author describes recent development of ILs focused on imidazolium and pyridinium ILs which are being most investigated presently. In order to apply this materials in industrial level, the toxicity matter must be resolved first. In this regard, the author describes recent research trend regarding environmental effects by ILs as well as some meaningful results as well.

• 상하수도학회지
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• 제27권1호
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• pp.121-128
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• 2013

The concern for dissolved phosphate in water/wastewater has been increasing because of the risk for eutrophication. A variety of conventional and advanced technologies were applied to meet the enforced new regulation of phosphate around the world. However, there still remained a lot of challenge because most introduced/developed method, for example, biological and physic-chemical treatment is not easy to satisfy the new regulation of phosphate in water. In order to meet the new regulation, the application of ion exchanger has been tried which showed that the removal efficiency for phosphate was strongly determined by in the presence of the competing ion, especially sulfate. As results, a new class of ion exchanger governed by ligand exchange was developed and investigated to increase the selectivity for phosphate. The current study using organic/inorganic anion exchanger developed with Lewis acid-base interaction confirms the selectivity for phosphate over sulfate. According to isotherm test and column test, the value of the maximum phosphate uptake (Q) showed 64 mg/g as $po{_4}^{3-}$ and the breakthrough for phosphate occurs after 1000 min and completely finishes at 2500 min, respectively.

• 대한화학회지
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• 제17권6호
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• pp.411-415
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• 1973

Cyanide ion과 triphenylmethane dye와의 반응은 cetyltrimethyl ammonium bromide(CTABr)의 cationic micelle에 의하여 현저히 반응속도가 빨라지며 sodium lauryl sulfate(NaLS)의 anionic micelle에 의하여 반응속도가 늦어진다. 또한 CTABr존재하의 반응은 inorganic anion에 의하여 inhibition, 되며 NaLS존재하의 반응은 inorganic cation중의 몇가지, 특히 $Zn^{++},\;Cd^{++}$등에 의하여 현저하게 반응이 빨라지는 salt effect를 나타낸다. 물과 잘 혼합되는 몇가지 유기용매의 micelle catalysis에 대한 영향은 대체로 수용액 일때보다 작게 나타나서 반응속도가 늦어지거나 malachite green과의 반응에서 methanol은 수용액일때보다 반응속도가 빨라지는 특이한 solvent effect를 나타내었다.

• 한국대기환경학회지
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• 제14권5호
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• pp.479-490
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• 1998

The concentrations of ten inorganic (sodium, chloride, sulfate, ammonia, etc.) and three organic (acetate, formate, and MSA) ions associated with airborne particulate matter were measured from Cheju Island, Korea during the three field intensive campaigns conducted in (1) Sept./oct. 1997 (fall), (2) Dec. 1997 (winter), and (3) April 1998 (spring). The results of our measurements indicated that the concentration levels of most ionic species were decreasing significantly across the three experimental periods. The patterns of concentration reduction were clear as the sum of all cation and anion species changed dramatically across those periods such as 294> 144 > 65 and 193 >96>74 nequiv/m3, respectively. The changes were best explained in terms of the wind rose patterns of the study site. Since our sampling spot is located on the western-end point of Cheju Island, it is likely to reflect the effects of diverse sources such as natural, marine processes during NW and local non-maritime ones during SE winds. .Hence, the periodical changes in ionic concentrations may be accounted for by the comparable changes in wind direction. To further investigate environmental characteristics of these ionic components, correlation analysis was conducted not only between meteorological and ion data but between different ion-pairs. The results of these analyses confirm that the concentration levels of ionic species are strongly affected by wind speed and temperature and that there are certain patterns between ion species to which such effects apply. In light of the significance of the wind rose patterns in the area, we further extended these analyses into four data groups that were divided on the basis of wind direction. The results of these analyses showed that the strength of correlations between important pairs (e.g.:. between windspeed and most of major inorganic species including sodium and chloride) can be ranked on the distribution of major ions are very diverse, depending on data grouping scheme for such analysis. The results of this study thus suggest that environmental behavior of chemical components be analyzed in various respects, rather than simple standard, especially if measurements are made in complex environmental condition under which both natural and anthropogenic effects are competing each other.