The major concern in the deep geological disposal of spent nuclear fuels include sulfide-induced corrosion and stress corrosion cracking of copper canisters. Sulfur diffusion into copper canisters may induce copper embrittlement by causing Cu2S particle formation along grain boundaries; these sulfide particles can act as crack initiation sites and eventually cause embrittlement. To prevent the formation of Cu2S along grain boundaries and sulfur-induced copper embrittlement, copper alloys are designed in this study. Alloying elements that can act as chemical anchors to suppress sulfur diffusion and the formation of Cu2S along grain boundaries are investigated based on the understanding of the microscopic mechanism of sulfur diffusion and Cu2S precipitation along grain boundaries. Copper alloy ingots are experimentally manufactured to validate the alloying elements. Microstructural analysis using scanning electron microscopy with energy dispersive spectroscopy demonstrates that Cu2S particles are not formed at grain boundaries but randomly distributed within grains in all the vacuum arc-melted Cu alloys (Cu-Si, Cu-Ag, and Cu-Zr). Further studies will be conducted to evaluate the mechanical and corrosion properties of the developed Cu alloys.

Carbon nanotube fiber is a promising material in electrical and electronic applications, such as, wires, cables, batteries, and supercapacitors. But the problem of joining carbon nanotube fiber is a main obstacle for its practical development. Since the traditional joining methods are unsuitable because of low efficiency or damage to the fiber structure, new methods are urgently required. In this study, the joining between carbon nanotube fiber was realized by deposited nickel–copper doublelayer metal via a meniscus-confined localized electrochemical deposition process. The microstructures of the double-layer metal joints under different deposition voltages were observed and studied. It turned out that a complete and defect-free joint could be fabricated under a suitable voltage of 5.25 V. The images of the joint cross section and interface between deposited metal and fiber indicated that the fiber structure remained unaffected by the deposited metal, and the introduction of nickel improved interface bonding of double-layer metal joint with fiber than copper joint. The electrical and mechanical properties of the joined fibers under different deposition voltages were studied. The results show that the introduction of nickel significantly improved the electrical and mechanical properties of the joined fiber. Under a suitable deposition voltage, the resistance of the joined fiber was 37.7% of the original fiber, and the bearing capacity of the joined fiber was no less than the original fiber. Under optimized condition, the fracture mode of the joined fibers was plastic fiber fracture.

This research studied the electrical characteristics, IR transmission characteristics, stealth functions, and thermal characteristics of infrared thermal-imaging cameras of copper-sputtered samples. Nylon samples were prepared for each density as a base material for copper-sputtering treatment. Copper-sputtered NFi, NM1, NM2, NM3, NM4, and NM5, showed electrical resistance of 0.8, 445.7, 80.7, 29.7, 0.3, and 2.2 Ω, respectively, all of which are very low values; for the mesh sample, the lower the density, the lower the electrical resistance. Measuring the IR transmittance showed that the infrared transmittance of the copper-sputtered samples was significantly reduced compared to the untreated sample. Compared to the untreated samples, the transmittance went from 92.0–64.1%. When copper sputtered surface was directed to the IR irradiator, the IR transmittance went from 73.5 to 43.8%. As the density of the sample increased, the transmittance tended to decreased. After the infrared thermal imaging, the absolute values of △R, △G, and △B of the copper phase increased from 2 to 167, 98 to 192, and 7 to 118, respectively, and the closer the density of the sample (NM5→NFi), the larger the absolute value. This proves that the dense copper phase-up sample has a stealth effect on the infrared thermal imaging camera. It is believed that the copper-sputtered nylon samples produced in this study have applications in multifunctional uniforms, bio-signal detection sensors, stage costumes, etc.

Due to its excellent processability, thermal conductivity and high corrosion resistance, copper tubes applied to heat exchangers are being joined through brazing to increase heat exchange efficiency. In order to improve performance, the issue of joint quality of copper tubes, a major member of heat exchangers, is emerging, so research is needed to obtain excellent joint quality of brazing joints that may be damaged. In this study, the quality change of joints according to process variables was studied through induction heating brazing experiments using high frequency. The depth of penetration, which indicates the quality of the junction, was measured, and the center position of the high-frequency electrode and the height of the electrode, which change the location of the heat source applied to the junction, were selected as process variables. Lastly, the thermal image data obtained between the brazing experiments were obtained and the joint quality according to the temperature gradient of the joint was analyzed.

Despite concerns about the significant toxicity of copper pyrithione (CuPT) at environmental concentrations, effects of CuPT on benthic organisms have received little attention. Here, we analyzed the detrimental effects of CuPT at sublethal concentrations (1/50, 1/20, and 1/10 of the 96 h-LC50 value) for 14 days in the marine polychaete Perinereis aibuhitensis. Reduced burrowing activity and significantly decreased the acetylcholinesterase activity in response to relatively high concentrations of CuPT were identified as CuPT-triggered cholinergic inhibition. The lipid peroxidation marker, malondialdehyde levels were dosedependently increased, whereas intracellular glutathione was depleted by relatively high concentrations. In the CuPT-treated polychaete, significant fluctuations in the enzymatic activities of the antioxidant defense system (catalase, superoxide dismutase, glutathione reductase, and glutathione peroxidase) were observed with significantly modulated glutathione S-transferase activity. These results indicate that even sublethal levels of CuPT would have detrimental effects on the health status of the marine polychaete.

본 연구는 전기투석과 용매추출을 융합한 희유금속 회수 공정에서 분리막과 음이온교환막의 개질을 통해 유기상 과 수상에 대한 분리막의 낮은 젖음성 및 AEM을 통한 수소이온 투과로 인한 금속이온의 회수 효율 감소를 개선하였다. 구체 적으로, 분리막 표면 중 한면은 polydopamine (PDA) 통한 친수성 개질, 다른 면은 SiO2 또는 graphene oxide를 통한 친유성 개질을 함으로써 분리막의 젖음성을 개선하였다. 또한, 음이온교환막의 표면을 polyethyleneimine, PDA, poly(vinylidene fluoride) 등을 이용, 개질해 수분 흡수(Water uptake) 감소 및 기공구조 변화를 통해 수소이온 수송을 억제해 수소이온 투과를 억 제할 수 있다. 개질된 막 표면 형상과 화학적 특성 및 조성은 주사전자현미경과 푸리에변환 적외선 분광법을 통해 확인되었 고, 이를 구리 이온 회수 시스템에 적용해 향상된 추출 및 탈거 효율과 수소이온 수송 억제능을 확인하였다.

The biocarbon (SKPH) was obtained from Sargassum spp., and it was evaluated electrochemically as support for the CO2 reduction. The biocarbon was synthesized and activated with KOH, obtaining a high surface area (1600 m2 g− 1) due to the activation process. Graphitic carbon formation after pyrolysis was confirmed by Raman spectroscopy. The XRD results show that SKPH has an amorphous structure with peaks corresponding to typical amorphous carbonaceous materials. FTIR was used to determine the chemical structure of SKPH. The bands at 3426, 2981, 2851, and 1604 cm− 1 correspond to O–H, C-H, and C-O stretching vibrations, respectively. Then, it compares SKPH films with different carbon films using two electrolytic systems with and without charge transfer. The SKPH film showed a capacitive behavior in the KOH, H2SO4, and, KCl systems; in the acid medium, the presence of a redox couple associated with carbon functional groups was shown. Likewise, in the [Fe(CN)6]−3 and Cu(II) systems, the charge transfer process coupled with a capacitive behavior was described, and this effect is more noticeable in the [Fe(CN)6]−3 system. Electrodeposition of copper on SKPH film showed two stages Cu(NH 3)2+ 4 /Cu(NH 3)+ 2 and Cu(NH 3)+ 2 ∕Cu in ammonia media. Hydrogen formation and the activity of CO2 are observed on SKPH film and are favored by the carbon’s surface chemistry. Cu/SKPH electrocatalyst has a catalytic effect on electrochemical reduction of CO2 and inhibition of hydrogen formation. This study showed that the SKPH film electrode responds as a capacitive material that can be used as an electrode for energy storage or as metal support.

The low-temperature sinterability of TiO2-CuO systems was investigated using a solid solution of SnO2. Sample powders were prepared through conventional ball milling of mixed raw powders. With the SnO2 content, the compositions of the samples were Ti1-xSnxO2-CuO(2 wt.%) in the range of x  0.08. Compared with the samples without SnO2 addition, the densification was enhanced when the samples were sintered at 900oC. The dominant mass transport mechanism seemed to be grain-boundary diffusion during heat treatment at 900oC, where active grain-boundary diffusion was responsible for the improved densification. The rapid grain growth featured by activated sintering was also obstructed with the addition of SnO2. This suggested that both CuO as an activator and SnO2 dopant synergistically reduced the sintering temperature of TiO2.

Copper is used for deep geological disposal canisters of spent nuclear fuels, because of excellent corrosion resistance in an oxygen-free environment. However, sulfide formation during the long-term exposure under deep geological disposal condition can be harmful for the integrity of copper canisters. Sulfur around the canisters can diffuse along grain boundaries of copper, causing grain boundary embrittlement by the formation of copper sulfides at the grain boundaries. The development of copper alloys preventing the formation of copper sulfides along grain boundaries is essential for the longterm safety of copper canisters. In this research, the mechanisms of copper sulfide formation at the grain boundary are identified, and possible alloying elements to prevent the copper sulfide formation are searched through the first principle calculations of solute atom-vacancy binding energy and the molecular dynamics calculation of grain boundary segregation energy. The comparison with the experimental literature results on the mitigation of copper embrittlement confirmed that the theoretically identified mechanisms of copper sulfide formation and the selected alloy elements are valid. Thereafter, binary copper alloys were prepared by using a vacuum arc melting furnace. Sulfur was added during casting of the copper alloys to induce the sulfide formation. The cast alloys were cold-rolled into a plate after homogenization heat treatment. The microstructure and mechanical property of each alloy were investigated after recrystallization in a vacuum tube heat treatment furnace. The copper alloys developed in this study are expected to contribute in increasing the long-term safety of deep geological disposal copper canisters by reducing the embrittlement caused by the sulfide formation.

Monitoring and assessing aquatic ecosystems using the behavior of organisms is essential for sustainable ecosystem management. Oligochaetes, which inhabit various freshwater ecosystems, are frequently used to evaluate the environmental conditions of freshwater ecosystems. Tubifex tubifex (Müller, 1774) (Oligochaeta, Tubificidae) is tolerant to organic pollution and has been used to evaluate the toxicity of toxicants, including heavy metals. We studied the behavioral responses of T. tubifex to three different copper concentrations (0.1, 0.5, and 1.0 mg L-1). The specimens were exposed to copper in an observation cage containing 150 mL of dechlorinated water. Movement behavior (diameter, speed, acceleration, meander, and turning rate) was continuously observed for two hours before and after the copper treatments. After the treatments, the diameter shrank and showed rapid twisting movement under all the copper conditions. The turning rate had a positive correlation with meander and acceleration both before and after treatment at all three concentrations, whereas speed and meander had a negative correlation. Length and turning rate also showed a negative correlation. The correlation coefficient between speed and acceleration in the highest copper concentration changed from positive before treatment (r=0.64) to negative (r= - 0.52) after treatment. Our results present the possibility of using behavioral parameters to detect copper contamination in freshwater ecosystems.

본 연구는 구리화합물계 목재방부제로 가압방부처리된 난주입수종이 국내 지상부 목재사용환경에서 방부성능을 유지할 수 있는 조건을 파악하기 위하여 수행되었다. 장기간(12년)의 지상부 야외노출시험을 통하여 방부성능이 입증된 방부처리 목재를 대상으로 목재 내부에 존재하는 주요 방부성 분인 구리의 분포 상태를 조사하였다. 구리 정색반응 결과를 살펴보면 변재는 대부분 균일하게 처리되었지만, 심재에서 구리의 침투는 목재 표면에 국한되어 있는 것으로 나타났다. 심재에서 구리의 침투는 국내 방부목 표준규격에서 요구하는 심재의 최소 침윤깊이(8 mm)를 만족하지 못하였다. 그러나 기준을 만족하지 못한 방부처리 시편들도 우수한 방부효능을 가지고 있다는 것을 알 수 있는데 이러한 결과는 난주입수종의 적절한 활용을 위해 국내 규격의 보완이 필요하다는 것을 의미한다.

Large-area graphene of the order of centimeters was deposited on copper substrates by low-pressure chemical vapor deposition (LPCVD) using hexane as the carbon source. The effect of temperature and the carrier gas flowrates on the quality and uniformity of the as-deposited graphene was investigated using the Raman analysis. The film deposited at 870 °C with a total carrier gas flowrate of 50 sccm is predominantly single-layer with very low defects according to the Raman spectra. The 2D/G peak intensity ratios obtained from the Raman spectra of samples from three different locations of graphene deposited on a whole copper catalyst was used to calculate the large-area uniformity. Based on the results, a very high uniformity of 89.6% was calculated for the graphene deposited at 870 °C. The uniformity was observed to decrease with increasing temperature. Similar to the thickness uniformity, the electrical conductivity values obtained as a result of I–V measurements and water contact angle measurements were found to be close to each other for the graphene deposited under the same deposition conditions.

Efficient capture and storage of radioactive iodine (consisting of two isotopes: 129I and 131I), produced or released from nuclear activities, are of paramount importance for sustainable development of nuclear energy due to their volatility and long half-life. Therefore, it is very important to develop new adsorbents for efficient utilization of radioactive iodine from nuclear waste. Various methods and materials are used for I2 capturing and removing, including MOFs due to their high porosity and fast adsorption kinetics, which are rightfully considered effective sorbents for removing I2. Metal–organic frameworks (MOFs) are porous crystalline materials which have diverse pore geometry and unique physicochemical properties, have attracted enormous attention for use in gas storage, separation and catalysis. The ability of MOFs to adsorb volatile products at room temperature can significantly improve the cost-effectiveness of the utilization process. This work describes the synthesis and characterization of three new metal-organic frameworks based on pyrazine (pyz), 44’bipyridine (bpy), 1,2 -bis(4 - pyridyl) – ethane (bpe) and copper (II) hexafluorozironate, as potential adsorbents for I2 capture. All of these three MOFs exhibit a two - dimensional (2D) crystal structure consisting from infinity non-crossing linear chains. The crystal structure of [Cu(pyz)2(ZrF6)2(H2O)2], [Cu(bpy)4(H2O)2ZrF6] and [Cu(bpe)4(H2O)2ZrF6] were characterized using powder X-ray diffraction (PXRD), single crystal X-ray diffraction (SC-XRD). Comparative characteristics of synthesized MOFs, including Fourier-transform infrared spectroscopy (FTIR) and thermogravimetric analysis (TGA) were also performed. The I2 sorption experiments were examined by UV-vis spectroscopy.

A method to effectively scavenge highly mobile radioiodide into a solid material was developed. Under an anaerobic condition, as copper(II) was strongly associated with bicarbonate (HCO3 −) in solution, malachite quickly formed, and then it was gradually transformed to a compact crystal of CuI (marshite) attracting iodide. The formation of CuI crystal was principally led by the spontaneous Cu-I redox reaction centering around the copper phase over the presence of sulfate (SO4 2−). The transformed CuI crystal was poorly soluble in water. Interestingly, this redox-induced iodide crystallization was rather promoted over the existence of anionic competitors (e.g., HCO3 − and SO4 2−). Unlike the conventional methods, these competing anions positively behaved in our system by supporting that the initial malachite was more apt to be reactive to largely attract highly mobile I−. Under practical environments, such a selective I− uptake and fixation into a crystalline form will be a promising way to effectively remove I− in a great capacity.

Corrosion cells that simulates engineering barrier system have been stored in an aerobic KURT environment for 10 years, which were recovered and dismantled in 2021. The test specimens were compressed copper (Com. Cu), Cold spray copper (CSC Cu), Ti Gr.2, STS 304, and Cast nodular iron. The specimens were buffered by compact Ca-type Gyeongju bentonite (KJ-I) and compact Na-type Wyoming bentonite. And the corrosion cells were exposed to KURT groundwater at 30°C for about 10 years (3,675 days). As a result of the long-term experiment in aerobic environment, it was confirmed that Na-bentonite is more advantageous for inhibiting corrosion than Ca-bentonite. The corrosion thickness of the most specimens in Ca bentonite was slightly lower than in Na bentonite until the initial 500 days, but after 10 years, the corrosion thickness of copper and cast iron specimens in Na bentonite was clearly lower. The corrosion thickness of the copper specimen in Na bentonite was very low about 0.5 um in both Com. Cu and CSC Cu. Moreover, the corrosion thickness in Ca bentonite was very high about 4 um for Com. Cu and 6 um for CSC Cu. In the case of cast iron, the corrosion thickness in Na bentonite was about 13 um, and 15 um in Ca bentonite. The common feature of copper and cast iron specimens in Ca bentonite, which showed a high corrosion thickness, is the forming of a white mineral deposition layer on the specimen surface, which was presumed to be some kind of feldspar. On the other hand, it was found that the STS304 and Ti specimens were hardly corroded even after 10 years. In conclusion, when a white mineral deposition layer was formed on the specimen surface, the corrosion thickness always increased sharply than before, and thus it was estimated that the generation of the mineral deposition layer cause the increase of bentonite permeability, and rather the weakening of existing passive corrosion film.

The use of heat exchangers in various applications such as chemical, air conditioning systems, fuel processing, and power industries is increasing. In order to improve the performance of the heat exchanger, the problem of bonding quality of the copper tube, which is a major member, is emerging. However, since the copper tube is in the form of a pipe, it is difficult to identify internal defects with external factors. In this study, a thermal imaging camera was used to develop and verify an algorithm for detecting defects in the brazing part, and in the process, the brazing performance characteristics were analyzed according to the electrode position, and finally, a learning model was developed and performance evaluation was performed. It was confirmed that the method of supplying heat to the base material and melting the filler metal through the heat transfer effect is more effective than supplying heat input to the filler metal in the bonding process of copper tubes through high-frequency induction heating brazing. Thermal image data was used to develop a defect discrimination model, and 80% of training data and 20% of test data were selected, and a neural network-based single-layer copper tube brazing defect discrimination model was developed through k-Flod cross-validation., the prediction accuracy of 95.2% was confirmed as a result of the error matrix analysis.

Copper nanoparticles (CuNPs) are considered of great importance due to their high catalytic and antimicrobial activities. This study focuses on the preparation and characterization of CuNPs, and on their antibacterial/antifungal activities. A copper salt (copper sulfate pentahydrate) as precursor, starch as stabilizing agent, and ascorbic acid as reducing agent were used to fabricate CuNPs. The resulting product was characterized via different techniques such as X-ray diffractrometry (XRD), Fourier Transform Infrared (FTIR) spectroscopy, and Scanning electron microscopy (SEM) to confirm its characteristic properties. Employing the Scherrer formula, the mean crystallite sizes of copper (Cu) and cuprous oxide (Cu2O) nanocrystals were found to be 29.21 and 25.33 nm, respectively, as measured from the main X-ray diffraction peaks. The functional groups present in the resulting CuNPs were confirmed by FTIR. In addition, the engineered CuNPs showed antibacterial and antifungal activity against tested pathogenic bacterial and fungal strains.

The adsorption process using GAC is one of the most secured methods to remove of phosphate from solution. This study was conducted by impregnating Cu(II) to GAC(GAC-Cu) to enhance phosphate adsorption for GAC. In the preparation of GAC-Cu, increasing the concentration of Cu(II) increased the phosphate uptake, confirming the effect of Cu(II) on phosphate uptake. A pH experiment was conducted at pH 4-8 to investigate the effect of the solution pH. Decrease of phosphate removal efficiency was found with increase of pH for both adsorbents, but the reduction rate of GAC-Cu slowed, indicating electrostatic interaction and coordinating bonding were simultaneously involved in phosphate removal. The adsorption was analyzed by Langmuir and Freundlich isotherm to determine the maximum phosphate uptake(qm) and adsorption mechanism. According to correlation of determination(R2), Freundlich isotherm model showed a better fit than Langmuir isotherm model. Based on the negative values of qm, Langmuir adsorption constant(b), and the value of 1/n, phosphate adsorption was shown to be unfavorable and favorable for GAC and GAC-Cu, respectively. The attempt of the linearization of each isotherm obtained very poor R2. Batch kinetic tests verified that ~30% and ~90 phosphate adsorptions were completed within 1 h and 24 h, respectively. Pseudo second order(PSO) model showed more suitable than pseudo first order(PFO) because of higher R2. Regardless of type of kinetic model, GAC-Cu obtained higher constant of reaction(K) than GAC.