본 연구에서는 “이온젤” 이라고 불리는 고분자 기반의 PVA(polyvinyl alcohol) 기반의 고체 전 해질에 이온성 액체 BMIMBF4 (1-buthyl-3-methylimidazolium tetrafluoroborate)를 첨가하여 제조한 전 고체 전해질과 활성탄소와 금속유기골격체 복합재료 기반의 전극 재료를 이용하여 슈퍼커패시터를 제작 하였으며, 유기골격체의 유 무에 따른 전기화학적 특성을 분석하여 보았다. 슈퍼커패시터의 전기화학적 특 성은 순환전압전류법(CV), 전기화학적 임피던스 분광법(EIS) 및 전정류 충·방전법(GCD)을 통하여 비교 및 분석하여 보았다. 그 결과로, 금속유기골격체가 함유되지 않은 슈퍼커패시터의 전기용량값은 380 F/g 으로 확인 할 수 있었고, 이 값은 금속유기골격체를 첨가하였을 때 340 F/g로 감소하는 현상을 확인할 수 있었 다. 이러한 결과로 1 wt%의 금속유기골격체의 함유량은 전기화학적 특성 감소에 영향을 주는 것으로 사료 되며 이러한 결과를 바탕으로 금속유기골격체의 첨가량을 최적화 할 필요가 있다고 판단된다

ZnO thin films are of considerable interest because they can be customized by various coating technologies to have high electrical conductivity and high visible light transmittance. Therefore, ZnO thin films can be applied to various optoelectronic device applications such as transparent conducting thin films, solar cells and displays. In this study, ZnO rod and thin films are fabricated using aqueous chemical bath deposition (CBD), which is a low-cost method at low temperatures, and environmentally friendly. To investigate the structural, electrical and optical properties of ZnO for the presence of citrate ion, which can significantly affect crystal form of ZnO, various amounts of the citrate ion are added to the aqueous CBD ZnO reaction bath. As a result, ZnO crystals show a nanorod form without citrate, but a continuous thin film when citrate is above a certain concentration. In addition, as the citrate concentration increases, the electrical conductivity of the ZnO thin films increases, and is almost unchanged above a certain citrate concentration. Cu(In,Ga)Se2 (CIGS) solar cell substrates are used to evaluate whether aqueous CBD ZnO thin films can be applicable to real devices. The performance of aqueous CBD ZnO thin films shows performance similar to that of a sputter-deposited ZnO:Al thin film as top transparent electrodes of CIGS solar cells.

본 연구는 (주)퓨어엔비텍에서 제조한 multi-bore 형태의 중공사 막을 이용하여 오염된 원수의 투과 후 오염된 막의 재사용을 위해 화학적 세정효율에 대해 파악하고자 하였으며 이를 위해 제조된 중공사 막의 재료는 내화학성이 좋은 PSf (polysulfone) 소재를 사용하였다. 실험은 소혈청 알부민(BSA)을 이용한 내오염성 평가 및 염기성 용액인 차아염소산나트륨 (NaOCl), 산성 용액인 구연산(citric acid)을 이용해 장기 함침하여 내화학성 평가를 진행하였다. 시간에 따른 수투과도와 인장강도를 측정하여 분리막의 기계적 강도와 성능의 감소에 대한 결과를 관찰하였다. 이후 소혈청 알부민으로 오염된 막의 화학적 용액에 따른 역세척 후 회복효율을 파악하였다. PSf 중공사 막은 뛰어난 내화학성을 가졌으며 화학적세척결과 차아염소 산나트륨의 효율이 높음을 확인하였다.

A facile one-pot wet chemical process to prepare pure anatase TiO2 hollow structures using ammonium hexafluorotitanate as a precursor is developed. By defining the formic acid ratio, we fabricate TiO2 hollow structures containing fluorine on the surface. The TiO2 hollow sphere is composed of an anatase phase containing fluorine by various analytical techniques. A possible formation mechanism for the obtained hollow samples by self-transformation and Ostwald ripening is proposed. The TiO2 hollow structures containing fluorine exhibits 1.2 - 2.7 times higher performance than their counterparts in photocatalytic activity. The enhanced photocatalytic activity of the TiO2 hollow structures is attributed to the combined effects of high crystallinity, specific surface area (62 m2g-1), and the advantage of surface fluorine ions (at 8%) having strong electron-withdrawing ability of the surface ≡ Ti-F groups reduces the recombination of photogenerated electrons and holes.

PURPOSES : The purpose of this research was to select sites that are appropriate for the storage of individual protective gear that can be used by traffic-controlling police when chemical terrorism occurs. METHODS : A storage facility, which is classified as Class A in the Act on Safety Action at Facilities Vulnerable to Terrorism, is defined for use in the event of soft-target chemical terrorism. Considering the number of controlled intersections and the police stations/substations within a radius of 750 m, the jurisdiction of traffic police and grade of protective gear were identified using ammonia, which has the widest protection boundary among known chemical terrorism substances. RESULTS : The results indicate that mobilization should only occur after the police have put on protective gear at the nearby station, regardless of the police district. Additionally, Class B protective gear should be furnished if there is a police station/substation within the jurisdiction, whereas Class C protective gear should be furnished if there is police station/substation outside of the jurisdiction. CONCLUSIONS : Because it is inefficient to keep protective gear at all police stations/substations, appropriate sites should be selected in accordance with chemical terrorism action strategy.

PURPOSES : Asphalt pavements are damaged by various causes, such as cracks, potholes due to climate, and traffic environment. Asphalt aging has a significant effect on cracks, which may also form potholes. The purposes of this study are to estimate the change in asphalt binder and mixture performance and to correlate the physicochemical changes of the asphalt binder and mixture performance with aging. METHODS : The aging process of the asphalt was determined in the laboratory, based on the methods used in previous studies. In terms of consistency (stiffness), crack-resistance performance, moisture susceptibility, SK investigated the binder part, and Shoreki investigated the mixture part depending on the aging time. RESULTS : The consistency (stiffness) and brittleness of both the asphalt binder and mixture tended to increase with aging. In particular, the crack-resistance performance of the asphalt binder (G*sinδ, ductility, and ΔTc) and mixture (flexural fatigue test and Cantabro test) deteriorated because of asphalt aging. Furthermore, the aging mechanisms (oxidation and polymerization) were identified based on the chemical structure analysis. CONCLUSIONS : It is confirmed that the aging affected the chemical composition change and the physical properties of the asphalt. Asphalt pavements are significantly affected by the aging characteristics of the binder. It is concluded that the crack-resistance performance of the mixture decreases with aging due to these physical and chemical changes.

용존 6가 우라늄은 다양한 화학종으로 존재하며, 화학종의 분포는 수용액의 pH에 의존한다. 산성 및 중성 근처의 pH 환경 에서는 대표적으로 UO2 2+, UO2OH+, (UO2)2(OH)2 2+, (UO2)3(OH)5 + 화학종이 공존한다. 수용액 속에 비결정성 실리카가 콜로이드 성질의 부유입자 상태로 존재할 때 용존 화학종은 실리카 표면에 쉽게 흡착된다. 이 연구에서는 표면 흡착 화학종의 분 포가 용존 화학종의 분포를 따르는지 조사하였다. 시료의 pH 값이 3.5-7.5인 조건에서 3종의 용존 화학종(UO2 2+, UO2OH+, (UO2)3(OH)5 +)과 2종의 표면 흡착 화학종(≡SiO2UO2, ≡SiO2(UO2)OH‐ 또는 ≡SiO2(UO2)3(OH)5 ‐)의 시간 분해 발광(luminescence) 스펙트럼을 측정하였다. pH 변화에 따른 각 화학종의 스펙트럼 변화 양상을 비교한 결과로 표면 흡착 U(VI) 화학종의 분포는 용존 U(VI) 화학종의 분포와 다르다는 것을 확인하였다.

PURPOSES: This study aims to evaluate the resistance to chemical attack of combined organic and inorganic hybrid mortars as the repair materials (i.e., HRM mortar) used for concrete road facilities through a comparison with mortars made from cement repair materials (i.e., IRM mortar). METHODS: Inorganic materials used as a binder and two mineral fillers were adopted to produce HRM mortars. The ratio of the main resin versus the hardener was fixed at 2:1. For comparison, IRM mortars made of cement repair materials were also manufactured. The mortars were exposed to chemical solutions, such as NaCl, MgSO4, Na2SO4, and H2SO4, with the same concentration of 5% after 7 days of curing. The compressive strength, compressive strength loss, mass ratio, and relative bulk density of the mortar samples exposed to the chemical solutions were measured at predetermined periods. In addition, a scanning electron microscope observation was performed to evaluate the microstructures and the products formed by the chemical reaction of the mortar samples. RESULTS : As a result, the resistance to chemical attack of the HRM mortars was found to be much better than that of the IRM mortars, regardless of the types of attacking sources. This finding implies that HRM is a highly promising and versatile material because of its excellent resistance to chemical attack. CONCLUSIONS: The application of the combined organic and inorganic hybrid mortars is a possible option for repair of concrete road facilities exposed to aggressive environments.

BiFeO3 with perovskite structure is a well-known material that has both ferroelectric and antiferromagnetic properties called multiferroics. However, leaky electrical properties and difficulty of controlling stoichiometry due to Bi volatility and difficulty of obtaining high relative density due to high dependency on the ceramic process are issues for BiFeO3 applications. In this work we investigated the sintering behavior of samples with different stoichiometries and sintering conditions. To understand the optimum sintering conditions, nonstoichiometric Bi1±xFeO3±δ ceramics and Ti-doped Bi1.03Fe1-4x/3TixO3 ceramics were synthesized by a conventional solid-state route. Dense single phase BiFeO3 ceramics were successfully fabricated using a two-step sintering and quenching process. The effects of Bi volatility on microstructure were determined by Bi-excess and Ti doping. Bi-excess increased grain size, and Ti doping increased sintering temperature and decreased grain size. It should be noted that Ti-doping suppressed Bi volatility and stabilized the BiFeO3 phase.

리튬 덴드라이트의 효과적인 억제를 위해 유/무기 복합체를 리튬메탈 전극의 보호층으로 사용하였다. 유기물로는 PVDF-HFP가 사용되었으며 무기물로는 TiO2가 사용되었다. 유기물로 사용된 PVDF-HFP는 높은 유연성을 가지는 고분자로서 무기물의 matrix 역할을 하며, 무기물로 사용된 TiO2 나노입자는 보호막의 기계적 강도와 이온전도성을 향상시켜주는 역할을 하였다. 합성된 보호막은 SEM, AFM, XRD를 통하여 PVDF-HFP matrix에 TiO2가 잘 분산되어 있는 형태인 것을 확인할 수 있 었다. 또한 전기화학적 분석 결과, 향상된 기계적 물성과 이온전도성으로 인해 polymer-inorganic composite은 비교 샘플(untreated 와 PVDF-HFP 보호층) 대비 100번째 사이클까지 80%의 높은 쿨롱 효율 및 20 mV 미만의 낮은 과전압을 나타내었다.

화학물질 취급공정에서 발생하는 화학사고를 예방하기 위해 기본적으로 요구되는 위험성 분석 (Risk Analysis)시 공정의 특성을 잘 반영하는 것이 매우 중요하다. 본 연구에서는 CFD (computational fluid dynamics) 언어를 활용하여 화학공장의 고위험 공정을 대상으로 신뢰성 있는 사고 피해 결과를 분석하고 안전확보 방안을 제시하였다. 이를 위한 방법론적 사례로 화학공장의 RHDS (잔사유수첨탈황공정) 공정을 대상으로 실제공정의 운전조건, 설비 및 장치의 형태와 밀집도, 대기상태, 바람의 영향 등 여러 복합적 변수를 고려하여 FEA (Finite Element Analysis)와 CFD 시뮬레이션을 수행 하여 확산, 폭발 시뮬레이션을 수행하였으며, 3D Scanning 기술, 누출공 크기 산정, 누출량 산정을 위한 CFD 적용 가능성을 검토하였다.

The self-discharge behavior of zinc-air batteries is a critical issue induced by corrosion and hydrogen evolution reaction (HER) of zinc anode. The corrosion reaction and HER can be controlled by a gelling agent and concentration of potassium hydroxide (KOH) solution. Various concentrations of KOH solution and polyacrylic acid have been used for gel electrolyte. The electrolyte solution is prepared with different concentrations of KOH (6 M, 7 M, 8 M, 9 M). Among studied materials, the cell assembled with 6 M KOH gel electrolyte exhibits the highest specific discharge capacity and poor capacity retention. Whereas, 9 M KOH gel electrolyte shows high capacity retention. However, a large amount of hydrogen gas is evolved with 9 M KOH solution. In general, the increase in concentration is related to ionic conductivity. At concentrations above 7 M, the viscosity increases and the conductivity decreases. As a result, compared to other studied materials, 7 M KOH gel electrolyte is suitable for Zn-air batteries because of its higher capacity retention (92.00 %) and specific discharge capacity (351.80 mAh/g) after 6 hr storage.

The performance of Li-ion hybrid supercapacitors (asymmetric-type) depends on many factors such as the capacity ratio, material properties, cell designs and operating conditions. Among these, in consideration of balanced electrochemical reactions, the capacity ratio of the negative (anode) to positive (cathode) electrode is one of the most important factors to design the Li-ion hybrid supercapacitors for high energy storing performance. We assemble Li-ion hybrid supercapacitors using activated carbon (AC) as anode material, lithium manganese oxide as cathode material, and organic electrolyte (1 mol L−1 LiPF6 in acetonitrile). At this point, the thickness of the anode electrode is controlled at 160, 200, and 240 μm. Also, thickness of cathode electrode is fixed at 60 μm. Then, the effect of negative and positive electrode ratio on the electrochemical performance of AC/LiMn2O4 Li-ion hybrid supercapacitors is investigated, especially in the terms of capacity and cyclability at high current density. In this study, we demonstrate the relationship of capacity ratio between anode and cathode electrode, and the excellent electrochemical performance of AC/LiMn2O4 Li-ion hybrid supercapacitors. The remarkable capability of these materials proves that manipulation of the capacity ratio is a promising technology for high-performance Li-ion hybrid supercapacitors.

본 연구는 1M Li2SO4 및 1M Na2SO4 수용액에서 CoSe 나노 입자의 전기 화학적 성능을 조사 하였다. CoSe 나노 입자의 전기 화학적 효율은 1M Na2SO4 전해질에서 더 높은 비정전 용량을 보여주는 결 과를 얻었고 이것은 주로 1M Na2SO4 용액의 벌크 전해질에서 수화 된 이온의 빠른 이동과 활물질에 의해 제공되는 낮은 전기 화학적 임피던스가 원인이라 사료된다. 또한, 순환 전압 전류법 안정성 실험에서 25 mV s-1의 스캔 속도로 1000 회 연속 순환 전압 전류 측정주기 후에도 각각 1M Na2SO4 및 1M Li2SO4에서 약 92 % 및 89 %의 특정 정전 용량의 유지를 보여주었다. 이 연구는 새로운 하이브리드 슈퍼 커패시터를 개발하기 위한 기초 데이터를 제공하며 비대칭 슈퍼 커패시터의 양극으로 사용될 수 있음을 시사한다.

The basalt fiber is expected to become a trend for industrial fibers as they have better properties of heat-resistant, non-combustion, absorbent, soundproof, moistureproof, lightweight, corrosion resistant, and high strength properties. Also, the fiber is found to be non-toxic and harmless to the human body. Therefore, in this study, we analyzed the chemical and mineral compositions of powdered sludge of basalt produced at seven sites on Jeju Island for the development of fire resistance insulating material for a building. The results showed that the basalt stone sludge is made from only sodium calcium aluminum silicate and ferridioside components unlike the basalt rock.

In this study, using a wet chemical process, we evaluate the effectiveness of different solution concentrations in removing layers from a solar cell, which is necessary for recovery of high-purity silicon . A 4-step wet etching process is applied to a 6-inch back surface field(BSF) solar cell. The metal electrode is removed in the first and second steps of the process, and the anti-reflection coating(ARC) is removed in the third step. In the fourth step, high purity silicon is recovered by simultaneously removing the emitter and the BSF layer from the solar cell. It is confirmed by inductively coupled plasma mass spectroscopy(ICP-MS) and secondary ion mass spectroscopy(SIMS) analyses that the effectiveness of layer removal increases with increasing chemical concentrations. The purity of silicon recovered through the process, using the optimal concentration for each process, is analyzed using inductively coupled plasma atomic emission spectroscopy(ICP-AES). In addition, the silicon wafer is recovered through optimum etching conditions for silicon recovery, and the solar cell is remanufactured using this recovered silicon wafer. The efficiency of the remanufactured solar cell is very similar to that of a commercial wafer-based solar cell, and sufficient for use in the PV industry.

Geopolymer is an alumina silicate-based ceramic material that has good heat-resistance and fire-resistance; it can be cured at room temperature, and thus its manufacturing process is simple. Geopolymer can be used as a reinforcement or floor finish for high-speed curing applications. In this manuscript, we investigate a high-speed curing geopolymer achieved by adding calcium to augment the curing rate. Metakaolin is used as the main raw material, and aqueous solutions of KOH and K2SiO3 are used as the activators. As a result of optimizing the high bending strength as a target factor for geopolymers with SiO2 / Al2O3 ratio of 4.1 ~ 4.8, the optimum ranges of the active agent are found to be 0.1 ≤ K2O / SiO2 ≤ 0.4 and 10 ≤ H2O / K2O ≤ 32.5, and the optimum range of the curing accelerator is found to be 0.82 Ca (OH)2 / Al2O3 2.87. The maximum flexural strength is found to be 1.35 MPa at Ca (OH)2 / Al2O3 = 2.82, K2O / SiO2 = 0.3, and H2O / K2O = 11.3. The physical and thermal properties are analyzed to validate the applicability of these materials as industrial insulating parts or repairing·finishing materials in construction.