• 약학회지
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• 제47권6호
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• pp.356-360
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• 2003

Nitroso-2-naphthol-3,6-disulfonic acid, disodium salt (NRS) was used as an organic ligand to prepare basic drug-selective polymeric membrane electrode. The sensing membrane of the electrode consited of basic drug-meta1(II)-NRS as an ion-exchanger site in a poly(vinyl chloride) matrix plasticized with 2-nitrophenyl octyl ether (NPOE). The metal ions used were Fe$^{2+}$, Co$^{2+}$, Ni$^{2+}$ and Cu$^{2+}$. The electrodes exhibited fast and wide linear response in the basic drug concentration of 10$^{-5}$ ∼10$^{-3}$ mol/l with a response slope of 50∼60 mV/decade in a buffer solution of pH 4∼8. The electrodes exhibited good selectivity for many basic compounds.mpounds.

• 한국세라믹학회지
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• 제37권11호
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• pp.1065-1070
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• 2000

TiO$_2$의 첨가가 Mn-Zn ferrites의 전자기적 물성에 미치는 효과에 대해 연구하였다. TiO$_2$의 첨가량이 증가함에 따라 밀도와 전기비저항이 증가된 반면 초기투자율은 감소하였다. TiO$_2$의 첨가에 따라 Fe$^{2+}$ ion의 증가에 기인하여 전력손실의 최소 값을 나타내는 온도가 저온으로 이동하였다. TiO$_2$를 0.12wt% 첨가한 시편의 경우, 100 kHz, 200 mT, 8$0^{\circ}C$ 측정 조건에서는 소결온도가 증가함에 따라 전력손실이 감소하였으며 125$0^{\circ}C$ 소결한 시편이 340 mW/㎤으로 가장 낮은 값을 보였다. 500 kHz, 50 mT, 8$0^{\circ}C$의 측정 조건에서는 소결 온도가 감소함에 따라 전력손실이 감소하였으며 115$0^{\circ}C$ 소결한 시편이 105 mW/㎤으로 가장 낮은 전력손실 값이 관찰되었다.

• 분석과학
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• 제14권6호
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• pp.530-534
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• 2001

Effect of stripping solutions on the Duolite GT-73 chelating resin for ten elements, Ag(I), Al(III), Ca(II), Cd(II), Cu(II), Fe(II), Hg(II), Mn(II), Pb(II), and Zn(II), was investigated. Relation between affinities of the metal ions and solubility products of metal sulfides was studied. The smaller the solubility product of metal sulfideis, the larger the affinitie with the ionsis. The ions which have the solubility products larger than $10^{-23}$ could be effectively desorbed with nitric acid. Complexation with chloride ion enhanced the desorption efficiencies of the ions having moderately strong affinity with the resin. The ions which have very strong affinity by the chelating resin can be desorbed by complextion with thiourea and hydrochloric acid.

• 한국식품영양학회지
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• 제7권2호
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• pp.128-136
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• 1994

Mackerel muscle protein hydrolysates, which were prepared from defatted mackerel meal by proteases such as complex enzyme, alcalase, bromelain, pancrease, pepsin, w-chymotrypsin, trypsin and papain, were tested for the antioxidative action against linoleic acid. Among proteases tested, the hydrolysates obtained from the treatment of complex enzyme, bromelain and alcalase showed higher antioxidative effects. Also, the hydrolysates showed the synergistic effects with o-tocopherol and the inhibitory effects for peroxidation of metal ions(Fe3+, Cua+) From the profiles of fractionation of the hydrolysates with Bio-gel P-2 column, the most active fractions, part I(complex enzyme-derived) and part e(bromelain-derived), had below MW 1,400 and the antioxidative effects were closely related to the binding capacity with metal ion(Cua+). Amno acid composition of the part I was abundant in histidine, arginine, phenylalanine and lysine, and the part e was abundant in lysine, glutamic acid and leucine.

• Bulletin of the Korean Chemical Society
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• 제4권2호
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• pp.76-79
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• 1983

The elution behaviors of a series of metal complexes, such as $Co(gly)_{3}$, $[Ni(en)_{3}]^{2+}$, $[Ni(phen)_3]^{2+}$, $[Fe(phen)_3]^{2+}$, $[Co(phen)_3]^3+$, $[Co(tn)_3]^3+$, $[Co(en)_3]^3+$ and $[Co(NH_3)_6]^3+$ (where gly; glycine, phen; phenanthroline, tn; trimethylenediamine, en; ethylenediamine), were studied in aqueous solution by measuring the retention volumes (v values) on SP-Sephadex C-25, cation exchange resin. It was found that the elution behaviors of metal complexes were apparently affected by salt concentrations, kinds of cations in eluent and kinds of anions in eluent, and according to the degrees of their effects coulombic forces, ion exchange capacities, the 'solvent effect' of resin backbone, hydrophobicity and hydrophilicity were applied to explain the elution mechanism.

• Bulletin of the Korean Chemical Society
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• 제18권7호
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• pp.706-710
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• 1997

Isotope ratios of K, Ca, Cr and Fe are measured at cool plasma condition generated using high carrier flow rate and relatively low RF power of 900 W. Background molecular ions are suppressed to below 100 counts which give isobaric interference to the analytes. The background ions show different attenuation characteristics at increased carrier flow rate and hence for each element different carrier flow rate should be used to measure isotope ratios without isobaric interference. Isotope ratios are measured at both scan and peak-hopping modes and compared with certified or accepted ratios. The measured isotope ratios show some mass discrimination against low mass due to low ion energy induced from a copper shield to eliminate capacitive coupling of plasma with load coil.

• Journal of the Optical Society of Korea
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• 제17권1호
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• pp.10-15
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• 2013

Adsorption behavior of counterions under a Langmuir monolayer was investigated by sum-frequency generation (SFG) spectroscopy. By comparing SFG spectra of arachidic acid (AA) Langmuir monolayer/water interface with and without added salt, it was found that the simple trivalent cation $La^{3+}$ adsorbed on AA monolayer only when the carboxylic headgroups are charged (deprotonated), implying that counterion adsorption is induced by Coulomb interaction. On the other hand, metal hydroxide complex $Fe(OH)_3$ adsorbed even on a charge-neutral AA monolayer, indicating that the adsorption of iron hydroxide is due to chemical interaction such as covalent or hydrogen bonding to the headgroup of the molecules at the monolayer.

• Corrosion Science and Technology
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• 제18권2호
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• pp.49-54
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• 2019

The purpose of this paper is to present failure analysis, of the heat exchanger tube in a district heating system. SS304 stainless steel is used, as material for the heat exchanger tube. The heat exchanger operates in a soft water environment containing a small amount of chloride ions, and regularly repeats operation and standstill period. This causes concentration of chloride ions on the outer surface of the tube, as well as repeat of thermal expansion, and shrinkage of the tube. As a result of microscopic examination, cracks showed transgranular as well as branched propagation, and many pits were present, at the initiation point of each crack. Energy disperstive spectroscopy analysis showed Fe and O peak, as well as Cl peak, meaning that cracks were affected by Cl ion. Failure of the tube was caused by chloride-induced stress corrosion cracking by thermal stress, high temperature, and localized enrichment of chloride ions.

• 한국결정성장학회:학술대회논문집
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• 한국결정성장학회 1998년도 PROCEEDINGS OF THE 15TH KACG TECHNICAL MEETING-PACIFIC RIM 3 SATELLITE SYMPOSIUM SESSION 4, HOTEL HYUNDAI, KYONGJU, SEPTEMBER 20-23, 1998
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• pp.71-71
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• 1998

Transition metal ions, such as Sc, V, Cr and Fe, doped rutile crystals were grown by Floating Zone method. Growth conditions for high quality of crystals depending on the concentration of doped ions were investigated. Grown crystals were cut and polished to thin wafers, and then various types of defects such as homogeneities, low angle grain boundaries, scattering centers, and oxygen vacancies were analyzed. The effects of transition metal ions on defect formation are discussed. Results and discussions on absorption and fluorescence spectra and electrical properties of grown crystals were also reported.

• 자원환경지질
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• 제56권2호
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• pp.125-138
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• 2023

수계 내 세슘(cesium: Cs)을 제거하기 위하여 개발된 대부분의 기존 Cs 흡착제들은 원재료 값이 고가라는 단점과, 해수와 같이 높은 이온 강도와 낮은 Cs 농도를 가지는 대규모의 오염수를 실질적으로 정화하는데 한계를 가지고 있었다. 본 연구에서는 석탄광산배수를 처리하는 과정에서 생성되는 슬러지(CMDS)에 Na와 S를 첨가하여 친환경적이고 높은 Cs 제거 효율을 가지는 Cs 흡착제를 개발하였다. Fe 및 Ca 함량이 풍부한 CMDS를 1차 소재로 사용하였고, 열처리 과정으로 Na와 S를 첨가하여 새로운 Cs 흡착제를 제조하였다(이하 본 연구에서 개발한 흡착제는 Na-S-CMDS라 명명함). Na-S-CMDS의 Cs 흡착능 및 흡착 기작을 평가하기 위해 실험실 규모의 실험과 흡착 동역학 및 등온 모델링 연구를 수행하였으며, XRF, XRD, SEM/EDS, XPS 등의 분석을 통해 Na-S-CMDS의 물리화학적, 광물학적 특성을 조사함으로써 Cs 흡착 기작을 규명하였다. 흡착 배치 실험 결과, Cs은 빠르게 Na-S-CMDS에 흡착되어 1시간 내 평형에 도달하였으며, 낮은 Cs 농도(0.5 mg/L) 조건에서도 높은 Cs 제거 효율(> 90.0%)을 보였다. 흡착 등온 모델링 결과, 단일 흡착을 가정하는 Langmuir 흡착 등온 모델에 대응되는 경향을 보였으며, 흡착 동역학 모델링 결과 흡착 경향이 유사 2차 속도(pseudo second order kinetic) 모델과 일치하는 경향을 보였고, 이러한 결과는 단순한 물리적 흡착보다 이온 교환과 같은 화학적 흡착이 우세함을 의미한다. 고농도의 Cs 용액으로 반응시킨 Na-S-CMDS의 XRF/XRD 분석 결과, Na-S-CMDS 내 Na 함량은 감소하고 흡착 전 존재하던 erdite (NaFeS₂·2(H₂O))가 관찰되지 않는 것을 통해, Na⁺과 Cs⁺ 사이에서 활발한 이온 교환 반응이 진행되었음을 알 수 있었다. XPS 분석 결과, Na-S-CMDS에서 Cs와 S 사이의 강한 결합 작용이 관찰되었으며, 이러한 Cs와 S(또는 S-복합체)내 결합에너지 감소도 Na-S-CMDS의 Cs 흡착능을 증가시키는 요인으로 판단되었다. 본 연구를 통해 기존에 폐기물로 처리되었던 석탄광산배수슬러지를 개량하여 제조한 Na-S-CMDS는 기존의 Cs 흡착제보다 제조 비용이 저렴하고, 해수 및 지하수와 같이 이온 강도는 높지만 Cs 농도가 낮은 대규모 오염 수계에서도 Cs 흡착능이 높게 유지되어, 현장에서 효과적인 Cs 흡착제로 사용할 수 있을 것으로 기대한다.