• 한국신재생에너지학회:학술대회논문집
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• 2010.06a
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• pp.96.1-96.1
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• 2010

현재 태양광 시장에 진출한 대부분의 Si계열 태양전지는 복잡한 공정과 원재료 고갈, 높은 가격으로 인해 한계에 직면에 있는 상태이다. 최근 많은 연구소나 학교에서는 기존의 Si계열 태양전지를 대체할 대안으로 염료 감응형 태양전지에 대해서 높은 관심을 보이고 있으며, 그동안의 연구개발로 단위 셀 면적에서는 상용화에 근접한 효율을 확보한 상태이다. 염료 감응형 태양전지의 작동과정을 간단히 단계별로 살펴보면 나노 결정 산화물 반도체 표면에 흡착된 염료분자가 가시광선을 흡수하면 전자는 HOMO에서 LUMO로 천이하고 이 들뜬 상태의 전자는 다시 에너지 준위가 낮은 반도체 산화물의 전도띠로 주입된다. 주입된 전자는 나노 입자간 계면을 통하여 투명 전도성막으로 확산, 전달되고 산화된 염료분자는 전해질 I-에 의해 다시 환원되어 중성 분자가 된다. 그러나 표면상태 전자 중 일부는 산화된 염료와 다시 결합하거나, 전해질의 $I^{3-}$ 이온을 환원시키기도 한다. 이와 같은 과정은 암전류를 증가시키면서 반도체 전극 막의 성능을 저해하는 주원인이 된다. 전자의 재결합은 투명 전극을 통해서도 가능하기 때문에 투명 전극에 얇은 blocking layer를 도포한 후 나노 결정 산화물 반도체 전극을 제작하면 전지 특성을 향상시킬 수 있다. 본 실험에서 우리는 졸-젤 법으로 $TiO_2$ blocking layer 졸을 만들었고 간단하며 저가공정이 가능한 스크린 프린팅 방법으로 blocking layer를 형성하는 실험을 진행하였다. 전도띠 에너지가 높은 반도체 물질로 표면을 처리하면 $TiO_2$-전해질 간 계면에 에너지 장벽이 형성되어 재결합을 줄여 모든 광전특성이 향상 되었다.

• Proceedings of the Korean Society of Dyers and Finishers Conference
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• 2011.03a
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• pp.56-56
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• 2011

알코올 환원법(alcohol reducing process)은 화학적 환원제가 필요하지 않은 화학합성법으로 메탄올, 에탄올, 프로판올, 이소프로판올, 부탄올 등 C1-C4의 알코올류, 에틸렌 글라이콜, 디에틸렌 글라이콜, 프로필렌 글라이콜과 같은 글리콜류 등이 용매이자 환원제로써 사용된다. 전형적으로 금속 전구체를 상기의 알코올류나 글리콜류에 용해 또는 분산시킨 후 그 용액을 환류 조건하에서 가열하게 되면 금속 이온과 용매간의 산화, 환원반응에 의하여 금속이온이 금속원자로 환원되며, 환원된 금속 입자들은 핵 행성과 성장 과정을 거쳐서 입자를 형성하게 된다. 본 연구에서는 알코올환원법을 이용하여 나노크기의 은입자제조를 시도하였고, 이를 PET 칩과의 마스터배치 제조을 시도하였으며, 이의 항균성능을 연구 고찰하였다. 30 ~ 80 nm의 은파우더를 제조할 수 있었으며, 우수한 항균성능을 갖는 Ag/PET 마스터배치를 제조할 수 있었다. 이를 활용하여 나노은입자기반의 항균섬유을 제조하여 이를 활용한 기모경편성물 제조의 기초데이타로 활용이 가능하리라고 사료된다.

• Applied Chemistry for Engineering
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• v.31 no.3
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• pp.299-304
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• 2020

Nanoparticles play an important role as a catalyst in many chemical syntheses. Colloidal nanoparticles were usually synthesized with reducing, capping, and shape directing agents which induce surface poisoning of catalysts. A new green synthesis for silver nanoparticles was developed by utilizing less additives which could be a hazardous waste. A crystallization technique was employed to reduce the amount of reducing and capping agents during synthesis resulting in less surface poisoning of the nanoparticle. The synthesized Ag nanoparticles using monosaccharides and disaccharides as reducing agents could be used as a catalyst for the redox reaction of resazurin and the mechanism of the reaction using Ag nanoparticles was studied.

• Journal of the Korean Chemical Society
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• v.32 no.1
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• pp.22-29
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• 1988

The reaction of methanol-water mixture to $CO_2$ and $H_2$ on alkaline earth metal-copper-zinc oxide has been studied in the temperature range of 150 ${\sim}\;300^{\circ}C$. Generally the addition of the alkaline earth metal to Cu/ZnO resulted in an enhancement of selectivity for $CO_2$ formation and a reduction of catalytic activity. Measurable activities were found from 150$^{\circ}C$, 200$^{\circ}C$, and 250$^{\circ}C$ on Mg/Cu/ZnO, Ca/Cu/ZnO, and Ba/Cu/ZnO respectively. However, the highest selectivity for $CO_2$ formation was observed in Ba/Cu/ZnO catalyst at 250$^{\circ}C$. The effect of alkaline earth metal or ZnO on the reactivity was investigated using temperature programmed desorption of $CO_2$ or temperature programmed reduction with $H_2$ over catalysts respectively. It was found that $CO_2$ interacts more strongly in the sequence of MgO < CaO < BaO and ZnO decereases the reduction temperature of CuO. From the results, it was suggested that ZnO activates $H_2$ in the redox process of Cu component and alkaline earth metals adsorbs $CO_2$ in the catalytic process.

• Resources Recycling
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• v.30 no.2
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• pp.61-67
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• 2021

Scraps are a byproduct of the machining process used for transforming titanium ingots into useful mechanical parts. Scraps take two forms, namely, bulky scraps, which are produced by cutting, and chipped scraps, which are produced by milling. Bulky scraps are comparatively easier to recycle because of their small surface area and less oxygen content; as a result, they pose only a small risk of explosion. In contrast, chipped scraps pose a higher risk of explosion, because of which, their recycling is complicated, resulting in most such scraps being discarded. With the aim of avoiding this waste, we proposed a novel process for converting chipped scraps into stable carbide materials. Methods typically applied to reduce particle size and impair the formation of solid solution type phase in the carbide materials were used to improve the mechanical properties of carbides prepared from chipped scraps. Our novel recycling process reduced carbide production costs and improved carbide quality.

• Korean Chemical Engineering Research
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• v.51 no.6
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• pp.700-708
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• 2013

Pyroprocessing has been developed for the purpose of resolving the current spent nuclear fuel management issue and enhancing the recycle of valuable resources. Pyroprocessing has been developed with the dry technologies which are performed under high temperature conditions excluding any aqueous processes. Pyro-processes which are based on the electrochemical principles require pretreatment processes and a voloxidation process is considered as a pretreatment step for an electrolytic reduction process. Various kinds of gas conditions are applicable to the voloxidation process and the understanding of Cs behavior during the process is of importance for the analyses of waste characteristics and heat load on the overall pyroprocessing. In this study, the changes of chemical compounds with the gas conditions were calculated by analyzing gas-solid reaction behavior based on the chemical equilibria on a Cs-Te-O system. $Cs_2TeO_3$ and $Cs_2TeO_4$ were selected after a Tpp diagram analysis and it was confirmed that they are relatively stable under oxidizing atmospheres while it was shown that Cs and Te would be removed by volatilization under reducing atmosphere at a high temperature. This work provided basic data for predicting Cs behavior during the voloxidation process at which compounds are chemically distributed as the first stage in the pyroprocessing and it is expected that the results would be used for setting up material balances and related purposes.

• Journal of the Korean Chemical Society
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• v.63 no.6
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• pp.486-504
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• 2019

This study analyzed achievement standards in the 2015 Science Education Standards as well as activities and assessment items in the Integrated Science, Chemistry I, and Chemistry II textbooks using science core competencies and subcomponents. All five scientific core competencies, in order of scientific thinking capacity, scientific inquiry capacity, scientific communication capacity, scientific problem solving capacity, and scientific participation and lifelong learning capacity, were included in the achievement standards of Integrated Science. Scientific thinking capacity, scientific inquiry capacity, and scientific communication capacity were included in the achievement standards of Chemistry I. The achievement standards of Chemistry II only included scientific thinking capacity. All five scientific core competencies were involved in activities of Integrated Science, Chemistry I, and Chemistry II textbooks and the highest propotion was scientific thinking capacity and scientific inquiry capacity. All five scientific core competencies were involved in assessment items of Integrated Science, Chemistry I, and Chemistry II textbooks and the highest proportion was scientific thinking capacity.

• Journal of the Korean Chemical Society
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• v.31 no.3
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• pp.250-257
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• 1987

The electrical conductances for the thorium (IV) complexes with crown ethers have been measured in DMSO, and water solvents, and the oxidation-reduction reaction mechanisms, electron number and diffusion coefficients in the reversible reduction process have been examined by polarography and cyclic voltammography. The dissociation mole ratio of $Th^{4+}$ and nitrate ion are 1:1 and in aprotic solvent, and 1:4 in protic solvent like as water. The limiting molar conductances of all complexes in aprotic solvent have been found to be in the range of $92.2{\times}159$ $ohm^{-1}cm^2mol^{-1}$. In aprotic solvent, DMSO, the reduction of each complex is reversible by one electron reduction of one step, and the range of diffusion coefficients is obserbed to be $5.83\;10^{-6}{\sim}6.90{\times}10^{-6}$. The complexes which have reduction step were hydrolyzed above at 1.8volt with reference saturated calomel electrode, generating the hydrogen gas. The reaction mechanisms of thorium (IV)-crown ether complexes appear as follows. ${Th_m(IV)L_n(H_2O)_x(NO_3)_{4y}}_=^{DMSO} {\overline{{Th_m(IV)L_n(H_2O)_x(NO_3)_{4y-1}}}^+ + NO_3-$

• Clean Technology
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• v.27 no.3
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• pp.207-216
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• 2021

Major anthropogenic emissions of elemental mercury (Hg⁰) occur from coal-fired power plants, and the emissions can be controlled successfully using NH₃-SCR (selective catalytic reduction) systems with catalysts. Although the catalysts can easily convert the gaseous mercury into Hg²⁺ species, the reactions are greatly dependent on the flue gas constituents and SCR conditions. Numerous deNO_xing catalysts have been proposed for considerable reduction in power plant mercury emissions; however, there are few studies to date of elemental mercury oxidation using SCR processes with MW- and full-scale coal-fired boilers. In these flue gas streams, the chemistry of the mercury oxidation is very complicated. Coal types, deNO_xing catalytic systems, and operating conditions are critical in determining the extent of the oxidation. Of these parameters, halogen element levels in coals may become a key vehicle for obtaining better Hg⁰ oxidation efficiency. Such halogens are Cl, Br, and F and the former one is predominant in coals. The chlorine exists in the form of salts and is transformed to gaseous HCl with a trace amount of Cl₂ during the course of coal combustion. The HCl acts as a very powerful promoter for high catalytic Hg⁰ oxidation; however, this can be strongly dependent on the type of coal because of a wide variation in the chlorine contents of coal.

• Proceedings of the Korea Concrete Institute Conference
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• 2008.04a
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• pp.897-900
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• 2008

Some substances of cement could make underestimate concentration of hexavalent chromium(Cr(VI)) as they reduce Cr(VI) to Cr(III) in acidic condition during the determination of Cr(VI) content in cement. The reduction of Cr(VI) increased with elapsed time after acidification in this study. The reduction rate varied with various cements. From our result, we can conclude that simultaneous additions of acid and DPC were required for the accurate measurement of Cr(VI) in cement. The high recovery rate of 94.3 to 106.7% with the simultaneous acid-DPC addition method can also support our conclusion.