전기투석(ED)은 이온교환막을 통한 이온의 분리에서 중요한 과정이다. 해수담수화로 발생하는 염수 처리는 환경 적으로 큰 문제이며 막분리 기술을 통한 재활용 효율이 높다. 마찬가지로 알칼리는 가죽, 전기도금, 염색, 제련 등과 같은 여 러 화학 산업에서 생산된다. 폐기물의 고농도 알칼리는 부식성이 높고 화학적 산소 요구량(COD) 값이 높기 때문에 환경에 방출하기 전에 처리해야 합니다. 칼슘과 마그네슘의 농도는 염수의 거의 두 배이며 주요 환경 오염 물질인 이산화탄소의 흡 착에 완벽한 후보입니다. 수산화나트륨은 양극성 막 전기투석 공정으로 쉽게 생산되는 금속 탄산화 공정에 필수적입니다. 역 삼투압(RO), 나노여과(NF), 초여과(UF), ED 등 다양한 공정을 통해 회수가 가능하다. 본 검토에서는 알칼리 회수를 위한 이 온교환막에 의한 ED 공정에 대해 논의한다.

Vitrification is one of the best ways to immobilize high-level radioactive waste (HLW) worldwide over the past 50 years. Since the glass matrix has a medium (3.0-5.5 A) and short (1.5-3.0 A) periodicity, it can accommodate most elements from the periodic table. Borosilicate glass is the most suitable glass matrix for vitrification due to its high chemical durability, high waste-loading capacity, and good radiation resistance. Mo is a fission product contained in liquid waste generated in the process of reprocessing spent nuclear fuel and exists in the form of MoO4 2- in the glass. MoO4 2- forms a depolymerization region without directly connecting with the glass network former. When the concentration of Mo increases in the depolymerization region, it combines with nearby alkali or alkaline earth cations to form a crystalline molybdate phase. Phase separation and crystallization in the glass can degrade the performance of the material because it changes the physical and chemical properties of the glass. In particular, since alkali molybdate has high water solubility when it forms crystals containing radioactive elements such as Cs, there is a risk of leakage of radionuclides by groundwater during deep underground disposal. Therefore, in this study, the most stable glass-ceramic composition was developed using various alkali elements, and the difference in phase separation and crystallization behavior in glass and the stability of the solidified body were analyzed by structural analysis of the glass network and alkali molybdate. The cause of the difference in crystallization of alkali molybdate according to the type of alkali cation is structurally analyzed, and using this, research is conducted to increase the Mo content in the glass without crystallization.

As temporary storage facilities for spent nuclear fuel (SNF) are becoming saturated, there is a growing interest in finding solutions for treating SNF, which is recognized as an urgent task. Although direct disposal is a common method for handling SNF, it results in the entire fuel assembly being classified as high-level waste, which increases the burden of disposal. Therefore, it is necessary to develop SNF treatment technologies that can minimize the disposal burden while improving long-term storage safety, and this requires continuous efforts from a national policy perspective. In this context, this study focused on reducing the volume of high-level waste from light water reactor fuel by separating uranium, which represents the majority of SNF. We confirmed the chlorination characteristics of uranium (U), rare earth (RE), and strontium (Sr) oxides with ammonium chloride (NH4Cl) in previous study. Therefore, we prepared U-RE-SrOx simulated fuel by pelletizing each elements which was sintered at high temperature. The sintered fuel was again powdered by heating under air environment. The powdered fuel was reacted with NH4Cl to selectively chlorinate the RE and Sr elements for the separation. We will share and discuss the detailed results of our study.

Combination of liquid-phase exfoliation and hydrothermal method has progressed in recent years mainly on production of 2D materials. In this study, graphene was successfully synthesized via combinatorial of liquid-phase exfoliation and hydrothermal method with the aid of various conductive surfactants perylene-3, 4, 9, 10-tetracarboxylate (PTCA), lithium perylene-3, 4, 9, 10-tetracarboxylate (LiPTCA) and sodium perylene-3, 4, 9, 10-tetracarboxylate (NaPTCA). The effect of the lithium ( Li+) and sodium ( Na+) cations toward the efficiency of the graphene exfoliation process and its electrical properties was thoroughly investigated. Based on the characterization techniques, it is revealed that NaPTCA is the ideal conductive surfactant to exfoliate graphene sheets. X-ray diffraction spectra verified that the Na+ cation certainly can enhance the exfoliation process by expanding the interlayer spacing. The lateral size of the graphene sheets with Na-PTCA surfactant was the smallest (4.17 μm) as observed from SEM micrograph. The maximum concentration of the graphene yield was achieved up to 0.151 mgmL− 1 in NaPTCA surfactant alongside with excellent electrical conductivity of 746.27 Sm− 1 and relevant specific capacitance of 129 Fg− 1.

PURPOSES : In this study, the alkali aggregate reactivity and expansion characteristics of mortar mixed with waste glass (a recycled aggregate) were confirmed to verify the alkali-silica reaction (ASR) stability and review the appropriateness of the alkali aggregate reactivity test method following the replacement of recycled aggregate. METHODS : The alkali-aggregate reactivity of waste glass aggregates was measured using the chemical and physical methods described in KS F 2545 and ASTM C 1260, respectively. The reactivity was classified by comparing the results. Cement with a high-alkali content was used to simulate an environment that can induce ASR. Non-reactive fine aggregates, waste glass fine aggregates, reactive general aggregates, and Ferronickel slag aggregates were used as control groups. RESULTS : Waste glass fine aggregates were classified as reactive when applying the chemical method. In the physical method, they were classified as reactive at 100% and latent reactive at 1%, based on the mixing ratio. Additionally, we discovered that the reliability of the chemical method was low since the ASR of the aggregates was classified differently based on the evaluation method, while the results of the chemical and physical test methods were inconsistent. CONCLUSIONS : To determine the alkali reactivity of recycled aggregates, the complex use of chemical and physical methods and analysis based on the mixing ratio of the reactive aggregates are required. Small amounts of waste glass aggregate replacements affected the ASR. Because ASR reaction products can affect the long-term thermal expansion of the structure, further research is needed to use ASR aggregates in structures.

The Alkali-Metal Thermal to Electric Converter (AMTEC) can be used as a next-generation power generation technology related with a large thermal energy storage. In particular, this technology is expected for the higher efficiency by a cascade power generation with the thermoelectric generator(TEG), and the temperature distribution becomes a very important design parameter in this case. In this study, the temperature distribution of the AMTEC unit was analyzed through CFD analysis, and design points were discussed based on the results.

Tungsten carbide is widely used in carbide tools. However, its production process generates a significant number of end-of-life products and by-products. Therefore, it is necessary to develop efficient recycling methods and investigate the remanufacturing of tungsten carbide using recycled materials. Herein, we have recovered 99.9% of the tungsten in cemented carbide hard scrap as tungsten oxide via an alkali leaching process. Subsequently, using the recovered tungsten oxide as a starting material, tungsten carbide has been produced by employing a self-propagating high-temperature synthesis (SHS) method. SHS is advantageous as it reduces the reaction time and is energy-efficient. Tungsten carbide with a carbon content of 6.18 wt % and a particle size of 116 nm has been successfully synthesized by optimizing the SHS process parameters, pulverization, and mixing. In this study, a series of processes for the highefficiency recycling and quality improvement of tungsten-based materials have been developed.

Biomass porous carbons derived from Laminaria japonica were prepared by KOH and H3PO4 activation methods, respectively. The results indicated that the chemical activation had an apparent effect on the molecular framework and space of materials. To enhance the selective adsorption for organic acids, biomass carbons were modified by dopamine combined with N-(2-aminoethyl)-3-aminopropyltrimethoxysilane. The SEM and BET results illustrated the effect of the chemical activation approach on the morphology and porous texture. The biomass porous carbon using KOH activation method had the highest surface area (up to 1558 m2/ g). Compared with unmodified materials, the modified materials showed higher adsorption capacity for organic acids (27.90 μg/mL for chlorogenic acid and 25.47 μg/mL for caffeic acid). It was suggested that modification of porous carbons might be a viable pathway to increase the specific adsorption affinity and efficiency for organic acids in dried jujube samples.

알칼리 금속 이온과 염소 이온이 포함된 용액으로부터 이온교환수지를 이용한 이온 제거에 대한 연구를 진행하였다. 양이온인 금속이온(Na+와 K+)의 제거에는 양이온교환수지를, 음이온인 염소 이온(Cl-)의 제거에는 음이온교환수지를 사용하였다. 용액 A (Na+를 36,633 ppm, Cl-를 57,921 ppm 함유)의 경우, Na+ 이온과 Cl- 이온은 20분 이내에 99% 이상 제거되었다. 용액 B (K+를 1,638 ppm 함유)의 경우, K+ 이온은 3분 이내에 99% 이상 제거되었다.

Zirconia nanoparticles were widely used as filler in order to get high refractive index layer. However, dispersion of nanoparticles is difficult due to their agglomeration in solvent. In this study, the dispersibility of the zirconia suspension is promoted by controlling the steric hindrance and electrostatic interactions through the adsorption of PEI according to alkali treatment time. Also, to induce improved dispersibility on suspension, we changed the dispersion conditions variously and fabricated an ink formulation method for the coating layer. Zirconia suspension was characterized by dynamic light scattering (DLS), Zeta potential measurement, Transmission Electron Microscope (TEM) and FT-IR. We were able to confirm that good dispersion of zirconia suspension by alkali treatment and PEI led to high refractive index.

Salined water electrolysis is one of representative commercial processes to produce valued chemicals such as chlorine, hydrogen. The most important issue in the electrolysis is to reduce energy consumption. A plausible solution is to accelerate Na+ion transport through cation exchange membranes and to reduce interfacial resistance with electrodes. The conventional membrane materials are based on PFSAs such as Nafion®. In spite of their robust chemical resistance, there are several critical demerits including expensive production cost and difficult tuning capability. For this, a SPAES random copolymer-silica nanocomposite is used as a membrane matrix with a high ionic conductivity and radiation-grafted with a highly sulfonated poly(strylene) to provide a branched polymer architecture for improved interfacial characteristics.

The Chlor-alkali (CA) membrane cell is a major electrolysis system to produce valued chemicals such as chlorine gas and sodium hydroxide. The CA membrane process has been attracted in the industries, since it has relatively low energy consumption when compared with other CA processes. The key component in CA process is perfluorinated sulfonic acid ionomer membranes, which provide ion-selectivity and barrier properties to produced gases. Unfortunately, there is limited information to determine which factors should be satisfied for CA applications. In this study, the influences of PFSA membranes on CA performances are disclosed. They include ion transport behaviors, gas evolution capability, and chemical/electrochemical resistances under CA operation conditions.

Phosphorus is an essential and irreplaceable element for all living organisms and its resource is limited. Significant amount of used phosphorus is collected in sewage treatment plant as sludge. Sludge ash after incineration contains about 10% of phosphorus in dry mass basis, which is comparable to phosphate rocks, and it is an important source of phosphorus recovery. Acid and alkali were used to leach phosphorus from sludge ash and compared for their leaching kinetics and performance. Phosphorus leaching by NaOH was fast and 0.2 N and 2 N NaOH leached 49% and 56% of the total phosphorus in the sludge ash at the L/S ratio of 100. Phosphorus leaching by sulphuric acid and hydrochloric were very fast and most of the phosphorus was leached in 5 minutes. In case of sulphuric acid 95% of the total phosphorus in the sludge ash was leached by 0.2 N at the L/S ratio of 100 and 93% was leached by 1 N at the L/S ratio of 10. 1 N hydrochloric acid leached 99% of the total phosphorus at the L/S ratio of 10. The results showed acids were more effective than alkali for phosphorus leaching from sludge ash and hydrochloric acid leached more phosphorus than sulphuric acid.

Magnetite particles were synthesized by co-precipitation of water-soluble 밀 스케일-derived precursor by various concentrations of (0.5, 0.67, 1, 2 N) NaOH and (0.6, 0.8, 1.2, 2.4 N) NH4OH. It is theoretically known that as the concentration of the alkaline additive used in iron oxide synthesis increases, the particle size distribution of that iron oxide decreases. This trend was observed in both kind of alkaline additive used, NaOH and NH4OH. In addition, the magnetite synthesized in NaOH showed a relatively smaller particle size distribution than magnetite synthesized in NH4OH. Crystalline phase of the synthesized magnetite were determined by X-ray diffraction spectroscopy(XRD). The particles were then used as an adsorbent for phosphate(P) removal. Phosphorus adsorption was found to be more efficient in NaOH-based synthesized magnetite than the NH4OH-based magnetite.

PURPOSES : The objective of this study is to evaluate the effect of the residual mortar of recycled concrete aggregate on the expansion behavior during alkali silica reaction (ASR). METHODS: In order to evaluate the net effect of residual mortar on ASR expansion behavior, two aggregate samples with the same original virgin aggregate source but different residual mortar volumes were used. ASTM C1260 test was used to evaluate the ASR expansion behavior of these two aggregates and the original virgin aggregate. RESULTS: The greater the amount of residual mortar in recycled concrete aggregates, the less is the induced ASR expansion. Depending on the amount of residual mortar in recycled concrete aggregate, the ASR expansion of recycled concrete aggregate may be less than half of that of the original virgin aggregate. CONCLUSIONS: The residual mortar of recycled concrete aggregate may lead to the under estimation of the ASR expansion behavior of the original virgin aggregate.