• 자원환경지질
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• 제31권4호
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• pp.277-290
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• 1998

The purpose of this research is to investigate the dispersion pattern of gold during skarnization and genesis of gold mineralization in the Sangdong skarn deposits. The Sangdong scheelite orebodies are embedded in the Cambrian Pungchon Limestone and limestone interbedded in the Myobong Slate of the Cambrian age. The tungsten deposits are classified as the Hangingwall Orebody, the Main Orebody and the Footwall Orebody as their stratigraphic locations. Recently, the Sangdong granite of the Cretaceous age (85 Ma) were found by underground exploratory drillings below the orebodies. In geochemisty, the W, Mo, Bi and F concentrations in the granite are significantly higher than those in the Cretaceous granitoids in southern Korea. Highest gold contents are associated with quartz-hornblende skarn in the Main Orebody and pyroxene-hornblende skarn in the Hangingwall Orebody. Also Au contents are closely related to Bi contents. This could be inferred that Au skarns formed from solutions under reduced environment at a temperature of $270^{\circ}C$. According to the multiple regression analysis, the variation of Au contents in the Main Orebody can be explained (87.5%) by Ag, As, Bi, Sb, Pb, Cu. Judging from the mineralogical, chemical and isotope studies, the genetic model of the deposits can be suggested as follows. The primitive Sangdong magma was enriched in W, Mo, Au, Bi and volatiles (metal-carriers such as $H_2O$, $CO_2$ and F). During the upward movement of hydrothermal ore solution, the temperature was decreased, and W deposits were formed at limestone (in the Myobong Slate and Pungchon Limestone). In addition, meteoric water influx gave rise to the retrogressive alterations and maximum solubility of gold, and consequently higher grade of Au mineralization was deposited.

• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 2001년도 하계학술대회 논문집
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• pp.624-627
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• 2001

Two kinds of Nd$_{1+x}$Ba$_{2-x}$Cu$_3$O$_{7-{\delta}}$, the sintering samples and zone melting samples, were heat treated under pure Ar at 95$0^{\circ}C$. The substitution of Nd ion for Ba ion in the Nd$_{1+x}$Ba$_{2-x}$Cu$_3$O$_{7-{\delta}}$ before and after the heat treatment were investigated by XRD. In order to know the effects of the heat treatment, the T$_{c}$ and J$_{c}$ of samples with the heat treatment and those without the heat treatment by Ar were comparatively studied. The results show that the substitution of Nd for Ba decreased, T$_{c}$, and J$_{c}$ increased after the treatment under Ar at 95$0^{\circ}C$. The Nd$_{1+x}$Ba$_{2-x}$Cu$_3$O$_{7-{\delta}}$ samples were oxygenated under pure oxygen at 30$0^{\circ}C$. From the XRD pattern it was found that the sample with x< 0.4 could transfer from tetragonal phase to orthorhombic phase after the oxygenation, but the sample with x>0.4 could not make the phase transition even after a long time oxygenation.ion even after a long time oxygenation.ation.n.ation.ation.

• Bulletin of the Korean Chemical Society
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• 제34권12호
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• pp.3755-3761
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• 2013

This study aims to assess the ecological risk of the hazardous air pollutants (HAPs) emitted in the semiconductor manufacturing processes in Korea by using Quantitative Structure Activity Relationship (QSAR, EPA, US, EPI $Suite^{TM}$ 4.1). Owing to the absence of environmental standards of hazardous air pollutants in the semiconductor manufacturing processes in Korea, 18 HAPs in the semiconductor field included in both the US EPA NESHAPs and the hazardous air pollutant list of Ministry of Environment in Korea were selected. As a results 8 chemicals (44.4%) of the selected 18 HAPs were VOCs. Cyanides (cyanides) and ethylene oxides (epoxy resins), and tetrachloro-ethylene (aliphatic compounds, halides) showed long half-lives. Cyanide HAPs especially had the highest half-life with the estimated value of 356.533 days. Nickel compounds (heavy metal compounds) possessed the highest water solubility followed by acetaldehyde (aldehyde compounds), ethylene oxides, and 1,4-dioxanes. The halides, including tetrachloro-ethylenes, carbon tetra-chlorides, benzene (aromatic compounds), and lead (heavy metals), are estimated to take the longest time for biodegradation. Tetrachloroethylene, with the acute toxicity end point of 3.685-7.033 mg/L, was assessed to be the most highly toxic substance among the 18 HAPs. However, considering the absence of the HAPs in the common category of log $K_{ow}{\geq}4$and $BCF{\geq}500$, which indicates the standard of bioconcentration potentials, potentials of the bioconcentration are considered to be low.

• 한국물환경학회지
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• 제20권6호
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• pp.670-675
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• 2004

Humic acids are macromolecules originated from natural water, soil, and sediment. The characteristics of humic acid enable it to change the distribution of metals as well as many kinds of organic contaminants and to determine the sorption of them from soil solution. To see the effect of humic acid on the removal rate of organic contaminants and heavy metals, batch-scale experiments were performed. As a natural geosorbent, black shale was used as a sorbent media, which showed hight sorption capacity of trichloroethylene (TCE), lead, cadmium and chromium. The effect of sorption-desorption, pH, ionic strength and the concentration of humic acid was taken into consideration. TCE sorption capacity by black shale was compared to natural bentonite and hexadecyltrimethylammonium (HDTMA) modified bentonite. The removal rate was good and humic acid also sorbed onto black shale very well. The organic part of humic acid could effectively enhance the partition of TCE and it act as an electron donor to reduce Cr(VI) to Cr(III). Cationic metal of Pb(II) and Cd(II) also removed from the water by black shale. With 3 mg/L of humic acid, both Pb(II) and Cd(II) were removed more than without humic acid. That could be explained by sorption and complexation with humic acid and that was possible when humic acid could change the hydrophobicity and solubility of heavy metals. Humic acid exhibited desorption-resistivity with black shale, which implied that black shale could be an alternative sorbent or material for remediation of organic contaminants and heavy metals.

• Applied Biological Chemistry
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• 제39권4호
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• pp.282-286
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• 1996

어류껍질 젤라틴의 수식에 의한 유화성 및 유화안정성과 같은 기능성을 개선하여 적색육어류 연제품의 품질개선제로 이용할 목적으로 붕장어껍질 젤라틴의 succinylation을 시도하였다. Succinylation의 정도는 젤라틴에 대하여 첨가하는 succinic anhydride의 비율 0.3까지는 첨가량에 따라 증가하였으나, 그 이상의 농도에서는 거의 변화가 없었다. 유지흡수성, 유화성 및 유화안정성은 무수식 젤라틴이 각각 1.8ml/g, 55% 및 49%이었고, 수식에 의해 개선되어 succinylation 정도가 89.9%일 때 이들의 값이 각각 5.8ml/g, 84% 및 78%이었고, 그 이상의 농도에서는 거의 변화가 없거나 서서히 감소하였다. 또한 용해도의 경우 40%, 보수력의 경우 50%, 거품성 및 거품안정성의 경우 0.4 및 0.3정도 개선되었다. 수식 젤라틴은 무수식 젤라틴에 비하여 아미노산조성의 경우 거의 차이가 없었고, 중금속함량은 오히려 낮았다.

• 한국표면공학회:학술대회논문집
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• 한국표면공학회 2018년도 춘계학술대회 논문집
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• pp.101-101
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• 2018

Quantitative measurement of chloride ion concentration has an important role in various fields of electrochemistry, medical science, biology, metallurgy, architecture, etc. Among them, its importance of architecture is ever-growing due to unexpected degradations of building structure. These situations are caused by corrosion of reinforced concrete (RC) structure of buildings. And chloride ions are the most powerful factors of RC structure corrosion. Therefore, precise inspection of chloride ion concentration must be required to increase the accuracy of durability monitoring. Multi-walled Carbon nanotubes (MWCNTs) have high chemical resistivity, large surface area and superior electrical property. Thus, it is suitable for the channels of electrical signals made by the sensor. Silver nanoparticles were added to giving the sensing property. CuBTC, one of the metal organic frameworks (MOFs), was employed as a material to improve the sensing property because of its hydrophilicity and high surface area to volume ratio. In this study, sensing element was synthesized by various chemical reaction procedures. At first, MWCNTs were functionalized with a mixture of sulfuric acid and nitric acid because of enhancement of solubility in solution and surface activation. And functionalized MWCNTs, silver nanoparticles, and CuBTC were synthesized on PTFE membrane, one by one. Electroless deposition process was performed to deposit the silver nanoparticles. CuBTC was produced by room temperature synthesis. Surface morphology and composition analysis were characterized by scanning electron microscope (SEM), energy dispersive X-ray spectroscopy (EDS), respectively. X-ray photoelectron spectroscopy (XPS) was also performed to confirm the existence of sensing materials. The electrical properties of sensor were measured by semiconductor analyzer. The chloride ion sensing characteristics were confirmed with the variation of the resistance at 1 V.

• 폴리머
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• 제32권1호
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• pp.43-48
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• 2008

본 연구는 벌크 중합을 이용하여 하이퍼브랜치 poly(styrene-co-divinylbenzene) (이하 PSD로 칭함)을 합성하고, 이를 설폰화하여 이온교환 용량이 큰 양이온 교환체를 합성하였다. 또한 FT-IR, $^1H-NMR$, 및 GPC 분석을 통하여 하이퍼브랜치 PSD 이온교환체의 분자량 및 구조 확인을 하였다. 하이퍼브랜치 PSD의 분자량과 점도는 DVB의 양이 증가함에 따라 모두 증가하였으며, 각각 최대값이 9410 g/mol과 338 cP로 나타났다. 또한, 가교제의 양이 증가함에 따라 반응속도가 증가하였으며, PSD의 용해도는 감소하였고, DVB 농도가 0.1 mlol%에서 용매 100 mL에 22g이 용해되었다. 또한, 하이퍼브랜치 PSD 이온교환체의 함수율과 이온교환 용량은 설폰 산기의 함량이 증가함에 따라 증가하였으며, 각각 최대 18.2%, 4.6 meq/g이었다. 구리 및 니켈에 대한 흡착이 40분 이내에 거의 100% 이루어졌다.

• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 1999년도 추계학술대회 논문집
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• pp.111-114
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• 1999

Electroluminescence(EL) devices based on organic thin films have been attracted lots of interests in large-area light-emitting display. In this stuffy, an emissive layer was fabricated using Langmuir-Blodgett(LB) technique in organic light-emitting (OLEDs). This emissive organic material was synthesized and named PECCP[poly(3.6-N-2-ethylhexyl carbazolyl cyanoterephthalidene)] which has a strong electron donor group and an electron acceptor group in main chain repeated unit. This material has good solubility in common organic solvents such as chloroform. THF, etc, and has a good stability in air. The Langmuir-Blodgett(LB) technique has the advantage of precise control of the thickness down to the molecular scale, In particular, by varying the film thickness it is possible to investigate the metal/polymer interface. Optimum conditions for the LB film deposition are usually determined by investigating a relationship between a surface pressure $\pi$ and an effective are A occupied by one molecule on the subphase. The LB films were deposited on an indium-tin-oxide(ITO) glass at a surface pressure of 10 mN/m and dipping speed of 12 mm/min after spreading PECCP solution on distilled water surphase at room temperature, Cell structure was ITO/PECCP LB film/Alq$_3$/Al. We considered PECCP as a hole -transport layer inserted between the emissive layer and ITO. We also used Alq$_3$ as an emissive layer and an electron transport layer. We measured current-voltage(I-V) characteristics, UV/visible absorption, PL spectrum and EL spectrum of the OLEDs.

• 한국지반환경공학회 논문집
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• 제14권10호
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• pp.59-64
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• 2013

화강풍화토의 풍화강도에 따른 중금속 흡착특성을 규명하기 위해 납과 구리를 이용하여 회분식 흡착실험을 수행하였다. 화강풍화토의 풍화가 진행됨에 따라 용해성이 높은 $SiO_2$, $K_2O$, $Na_2O$의 함량은 감소하며, 산화물인 $Fe_2O_3$의 함량은 증가하는 것으로 나타났으며, 강열감량과 비표면적은 증가하고 투수계수는 감소하는 것으로 나타났다. 화강풍화토의 풍화강도가 증가할수록 비표면적과 점토질 성분이 증가하므로 납과 구리의 흡착량이 증가하는 것으로 나타났다. 화강풍화토에 의한 납과 구리의 흡착속도는 1차 반응속도모델보다 2차 반응속도모델에 의해 적절하게 설명될 수 있는 것으로 나타났다.

• 자원환경지질
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• 제36권6호
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• pp.469-480
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• 2003

용출실험 연구는 서보 및 청양광산의 광미와 오염토양이 산성비(pH 5.0∼3.0)또는 강한 산성용액(pH 2.5∼l.0)과 반응하였을 때 용출될 수 있는 중금속의 함량을 예측하기 위하여 실시되었다. pH 5.0∼3.0인 용액에서, pH가 낮아질수록 광미 내 비소, 납, 아연의 용해도는 많이 증가하였다. 반면에 토양에서의 중금속의 용해도는 매우 제한적이었다. 이와 같은 결과로부터 산성비에 의하여 광미 내 납, 비소, 아연은 용출되나, 토양 내 이들 원소들은 고정되어 있음을 알 수 있다. pH 2.5∼l.0인 강한 산성과 반응시에는 pH가 낮아질수록 오염된 토양 내 아연, 카드뮴, 구리의 농도가 급격히 증가하는 반면, 광미 내에서는 납, 비소, 코발트의 용해도가 매우 증가한다 한편, CY4(청양광산)를 제외한 광미 내 아연, 카드뮴 및 구리의 용해도는 매우 낮은 pH(약 pH 1)에서 조차 낮은 용해도를 보여준다. 이것은 불완전 용해 또는 불용성의 광물상의 존재에 기인한다. 따라서 중금속의 용해도는 반응 용액의 pH뿐만 아니라 광미 및 오염토양 내 존재하는 금속의 존재형태에 영향을 받음을 알 수 있다. 반응용액의 pH가 5.0∼3.0인 경우, 광미에 함유된 원소들 간의 상대적인 이동도는 Pb>Zn>Cd)Co=Cu＞As이었다. 반응용액의 pH가 2.5∼l.0사이인 경우, 금속원소들의 상대적인 이동도는 오염 토양의 경우 Zn＞Cd>Cu≫Co>Pb=As이고, 광미로부터는 Pb≫Zn>Cd>As>Co>Cu이었다. 이러한 연구결과들은 이 지역에서 광산 폐기물의 환경적 영향에 대한 평가를 가능하게 하고, 복원 계획에 대한 유용한 자료로 사용될 수 있다.