The main objective of the research was to deposit thin films of silver on a graphite carbon paste in a phosphate buffer medium using an electrochemical method. To construct a nitrofurazone detection sensor that is highly sensitive. Different manufacturing parameters, such as electrodeposition potential, pH effect, potential scan rate effect, and number of scan cycles, were examined in this section. The parameters were optimized to improve the deposited silver layers various electrocatalytic characteristics. The Nitrofurazone reduction process is diffusion controlled, as seen by the linear variation of Epc with log(v). The constructed Ag-NPs@CPE electrod has excellent electrical characteristics a large active surface area and low background with extremely high electrical conductivity, according to structural and electrochemical characterizations such as Scanning electron microscopy, X-ray diffraction (XRD) and cyclic voltammetry. The constructed sensor has a very remarkable analytical performance for nitrofurazone molecule identification, with a very low detection limit of about 10– 8 M. The detection of nitrofurazone using our Ag-NPs@CPE sensors in real samples contaminated with the antibiotic nitrofurazone, such as tap water and urine. In the selected sample, the electroanalytical findings reveal a very satisfactory recovery rate of more than 94 percent.

Coal-based graphite has become the main material of emerging industries. The microstructure of coal-based graphite plays an important role in its applications in many fields. In this paper, the effect of carbon disulfide/N-methyl-2-pyrrolidone solvent mixture extraction on the microstructure of bituminous coal-based graphite was systematically studied through preliminary extraction coupled with high-temperature graphitization. The graphitization degree g (75.65%) of the coal residue-based graphite was significantly higher than that of the raw coal-based graphite. The crystallite size La of the coal residue-based graphite was reduced by 47.06% compared with the raw coal-based graphite. The ID/ IG value of the coal residue-based graphite is smaller than that of the raw coal-based graphite. The specific surface area (16.72 m2/ g) and total pore volume (0.0567 m3/ g) of the coal residue-based graphite are increased in varying degrees compared with the raw coal-based graphite. This study found a carbon source that can be used to prepare coal-based graphite with high graphitization degree. The results are expected to provide a theoretical basis for further clean and efficient utilization of the coal residue resources.

North Korea claimed to have tested a hydrogen bomb in its fourth nuclear test in 2016, and declared that the hydrogen bomb was completed after the sixth nuclear test in 2017. North Korea’s operation of Yongbyon Graphite-moderated reactor has been thought to be aimed at producing plutonium, but it has been strongly argued that the restart of the Graphite-moderated reactor is, indeed, aimed at supplying tritium recently. Tritium can be used not only to manufacture hydrogen bombs, but also to miniaturize nuclear weapons, making it as a key material for nuclear weapon capability. Since upgrading nuclear weapons and developing hydrogen bombs through the use of tritium by North Korea could pose a major threat to the security of the Korean Peninsula, it is important to accurately evaluate North Korea’s nuclear weapon capabilities through the analysis of nuclear material production scenarios based on its nuclear facilities. However, researches on North Korea’s nuclear materials such as HEU (Highly Enriched Uranium) and Pu production has been actively conducted, while no research has been shown on tritium production yet. Therefore, this study aims to evaluate the tritium productivity based on the analysis of hypothetical nuclear material production facilities and possible tritium production scenarios. Basic research was conducted about the existing theoretical methodology for tritium production, the analysis of the global tritium production history, and the analysis of nuclear facilities. Based on this basic investigation, feasible tritium production scenarios were constructed. Subsequently, based on design criteria of an hypothetical Graphite-moderated reactor, possible tritium production scenario was modeled by applying the TPBAR (Tritium Production Burnable Absorber Rod). In addition, the factors such as 6Li concentration, design parameters, material compositions, and the number of TPBARs, which may affect tritium throughput were analyzed in terms of sensitivity study such that the maximum and minimum throughput can be predicted.

This work describes the facile synthesis of silver nanoparticle-decorated zinc oxide nanocomposite through a simple glycol reduction method. The silver nanoparticle-decorated zinc oxide nanocomposite-based pencil graphite electrode has been validated as a perceptive electrochemical sensing podium towards nitrite. The morphology of the prepared nanocomposite has been characterized via specific spectroscopic and electrochemical techniques. The sensor exhibits a notable enhancement in the cyclic voltammetric response to nitrite oxidation at an ideal peak potential of 0.76 V in pH 6.0 acetate buffer. Under optimum conditions of nitrite directly expanded with their concentration in the range from 30 to 1400 μM with a detection limit of 14 μM.

Thermal reduction of graphite oxide (GO) is considered as a prospective method for the preparation of high-performance graphene-based materials. However, this method has certain limitations, and the major is that this exothermic process is difficult to control. In this research, we focused on the kinetic studies of the reduction of graphite oxide using non-isothermal differential calorimetry (DSC) method. Six GO nanocomposites with dyes were tested to study the shift in kinetic parameters. The apparent reaction order is determined to be ca 0.7 for the thermal decomposition of pure GO, while in the presence of dye molecules it increases sometimes reaching a value of 2.0 for higher dye concentrations. Decisively, the thermal decomposition of pure GO can be presented as an intermediate between a zero- and first-order reaction, while the introduction of dye molecules turns a certain part of the energy consumption via the bimolecular pathway. Our research revealed that the process of GO thermal decomposition can be operated and properties of the final product (reduced graphene oxide (rGO) and its derivatives) can be adjusted more precisely using additive molecules, which interact with GO sheets.

Graphite Isotope Ratio Method (GIRM) can be used to estimate plutonium production in a graphite-moderated reactor. This study presents verification results for the GIRM combined with a 3-D polynomial regression function to estimate cumulative plutonium production in a graphite-moderated reactor. Using the 3-D Monte-Carlo method, verification was done by comparing the cumulative plutonium production with the GIRM. The GIRM can estimate plutonium production for specific sampling points using a function that is based on an isotope ratio of impurity elements. In this study, the 10B/11B isotope ratio was chosen and calculated for sampling points. Then, 3-D polynomial regression was used to derive a function that represents a whole core cumulative plutonium production map. To verify the accuracy of the GIRM with polynomial regression, the reference value of plutonium production was calculated using a Monte-Carlo code, MCS, up to 4250 days of depletion. Moreover, the amount of plutonium produced in certain axial layers and fuel pins at 1250, 2250, and 3250 days of depletion was obtained and used for additional verification. As a result, the difference in the total cumulative plutonium production based on the MCS and GIRM results was found below 3.1% with regard to the root mean square (RMS) error.

Tin/graphite composites are prepared as anode materials for Li-ion batteries using a dry ball-milling process. The main experimental variables in this work are the ball milling time (0–8 h) and composition ratio (tin:graphite=5:95, 15:85, and 30:70 w/w) of graphite and tin powder. For comparison, a tin/graphite composite is prepared using wet ball milling. The morphology and structure of the different tin/graphite composites are investigated using X-ray diffraction, Raman spectroscopy, energy-dispersive X-ray spectroscopy, and scanning and transmission electron microscopy. The electrochemical properties of the samples are also examined. The optimal dry ball milling time for the uniform mixing of graphite and tin is 6 h in a graphite-30wt.%Sn sample. The electrode prepared from the composite that is dry-ballmilled for 6 h exhibits the best cycle performance (discharge capacity after 50th cycle: 308 mAh/g and capacity retention: 46%). The discharge capacity after the 50th cycle is approximately 112 mAh/g, higher than that when the electrode is composed of only graphite (196 mAh/g after 50th cycle). This result indicates that it is possible to manufacture a tin/graphite composite anode material that can effectively buffer the volume change that occurs during cycling, even using a simple dry ball-milling process.

본 논문은 에너지를 실시간으로 저장할 수 있는 저장장치 중 열에너지 저장 콘크리트를 대상으로 재료의 미세구조와 물성(열전도 도)의 상관관계를 분석하는 연구를 수행하였다. 에너지 저장 콘크리트의 열전도 성능을 증가시키기 위해 혼화재인 그라파이트 (graphite)를 사용하였다. 그라파이트가 시멘트 질량의 10%와 15%를 치환한 시편과 일반 콘크리트(OPC) 시편을 제작하여 그라파이 트의 혼입에 따른 미세구조 변화 및 열전도도의 영향을 마이크로 스케일에서 분석하였다. 마이크로-CT를 활용하여 OPC와 그라파이 트를 사용한 콘크리트의 공극률을 비교하였으며, 확률함수를 사용하여 미세구조 특성을 정량화하였다. 미세구조 특성 차이가 열전도 도에 미치는 영향을 확인하기 위해 3차원 가상 시편을 제작하여 열해석을 수행하였으며, 이를 열평판법을 사용하여 측정한 열전도도 실험 결과와 비교하였다. 열해석 수행 시 그라파이트 재료가 지닌 열전도도 성능을 반영하기 위하여 해석 결과와 실험 결과를 기반으 로 고체상의 열전도도를 역해석을 통해 계산하였으며, 그라파이트가 시편의 열전도도에 미치는 영향에 대해 분석하였다.

In the present study, pyrolyzed fuel oil (PFO)-based pitch without impurities was used to prepare coke under pressure, and the preparation yield and the powder resistance depending on the graphitization were investigated. The preparation yield of green coke by pressurized coking at 500 °C was about 26–27% higher than that at normal pressure. However, the coke yield after the thermal treatment of green coke at 900 °C was lower by 10.6–14.8% at the pressurization conditions than under normal pressure. This may be because the substances that are not vaporized under the pressurized conditions remain in the reactants and then are discharged later. The coke yield after the thermal treatment at 900 °C was higher by 14.9–28.3% under the pressurized conditions than under the normal pressure, indicating that the low-boiling point materials of the pitch participated more in coke polymerization under the pressurized conditions. The density of the coke prepared under the pressurized conditions was lower than that of the coke prepared under normal pressure, because the low-boiling point materials of the pitch participated in the reaction. However, after graphitization, the density values became similar (2.27–2.26 g/cm3). The volume resistivity of the graphitized samples was in a range of 0.499 × 10–2–0.384 × 10–2 Ω cm, indicating that the coke samples have similar electrical properties. The results of the present study show that, in comparison with the conventional normal-pressure process, the pressurized coking process can improve the yield through the participation of low-boiling point materials in the polymerization reaction, while maintaining the properties of the prepared coke and graphite, such as the conductivity and density.

The use of recycled materials, such as the fine recycled aggregate made from concrete waste and carbon fiber (CF) product of industrial waste, for the manufacture of conductive recycled mortars (CRM), transforms the mortar base cement normally made with cement:sand in a sustainable multifunctional material, conferring satisfactory mechanical and electrical properties for non-structural uses. This action provides ecological benefits, reducing the use of natural fine aggregates from rivers and the amount of concrete waste deposited in landfills resulting from construction waste. In this investigation the effect of the addition of CF on electrical properties in hardened, wet and dry state, electric percolation in dry state and fluidity of the wet mixture of a cement based CRM was evaluated: fine recycled aggregate: graphite powder, CRM specimens with dimensions of 4 × 4 × 16 cm. were manufactured for 3, 7 and 28 days of age and sand/cement ratios = 1.00, graphite/cement = 1.00, water/cement = 0.60 and CF = 0.1, 0.3, 0.5, 1.0, 1.5, 2.0, 2.5 and 3.0% compared to the weight of cement. The results demonstrated the effect of the addition of CF in CRM, reducing fluidity of the mixtures due to the opposition generated by its physical interaction of CF with recycled sand or recycled fine aggregate and graphite powder (GP), in its case, placing the electric percolation percolation at 0.30% and 0.45% of CF for CRM with and without GP, respectively. Increases in electrical conductivity (EC) without the presence of GP are defined by the contact between the CF and the conductive paths formed. In contrast, with the presence of GP, the EC is defined by the contact between the CF and the GP simultaneously, forming conductive routes with greater performance in its EC.

Owing to its low cost, easy fabrication process, and good ionic properties, aqueous supercapacitors are under strong consideration as next-generation energy storage devices. However, the limitation of the current collector is its poor electrochemical stability, leading to low energy storage performance. Therefore, a reasonable design of the current collector and the acidic electrolyte is a necessary, as well as interfacial engineering to enhance the electrochemical performance. In the present study, graphite foil, with excellent electrochemical stability and good electrical properties, is suggested as a current collector of aqueous supercapacitors. This strategy results in excellent electrochemical performance, including a high specific capacitance of 215 F g−1 at a current density of 0.1 A g−1, a superior high-rate performance (104 F g−1 at a current density of 20.0 A g−1), and a remarkable cycling stability of 98 % at a current density of 10.0 A g−1 after 9,000 cycles. The superior energy storage performance is mainly ascribed to the improved ionic diffusion ability during cycling.

Accurate and effective powder compaction analyses are performed for brittle materials such as graphite, utilized as a solid lubricant, by using the discrete element method (DEM). The reliability of the DEM analysis is confirmed by comparing the results of graphite powder compaction analyses using the DEM particle bonding contact model and particle non-bonding contact model with those from the powder compaction experiment under the same conditions. To improve the characteristics, the parameters influencing the compaction properties of the metal-graphite mixtures are explored. The compressibility increases as the size distribution of the graphite powder increases, where the shape of the graphite particles is uniform. The improved compaction characteristics of the metal-graphite (bonding model) mixtures are further verified by the stress transmission and compressive force distribution between the top and bottom punches. It is confirmed that the application of graphite (bonding model) powders resulted in improved stress transmission and compressive force distribution of 24% and 85%, respectively.

Bulk graphite is manufactured using graphite scrap as the filler and phenolic resin as the binder. Graphite scrap, which is the by-product of processing the final graphite product, is pulverized and sieved by particle size. The relationship between the density and porosity is analyzed by measuring the mechanical properties of bulk graphite. The filler materials are sieved into mean particle sizes of 10.62, 23.38, 54.09, 84.29, and 126.64 μm. The bulk graphite density using the filler powder with a particle size of 54.09 μm is 1.38 g/cm3, which is the highest value in this study. The compressive strength tends to increase as the bulk graphite density increases. The highest compressive strength of 43.14 MPa is achieved with the 54.09 μm powder. The highest flexural strength of 23.08 MPa is achieved using the 10.62 μm powder, having the smallest average particle size. The compressive strength is affected by the density of bulk graphite, and the flexural strength is affected by the filler particle size of bulk graphite.

In the manufacturing of bulk graphite, pores produced by vaporization and discharge of volatile materials in binders during carbonization reduce the density of bulk graphite, which adversely affects the electrical conductivity, strength and mechanical properties. Therefore, an impregnation process is introduced to fill the pores and increase the density of bulk graphite. In this study, bulk graphite is prepared by varying the viscosity of the impregnant. The microstructure of bulk graphite is observed. The flexural strength and electrical resistivity are measured. As the viscosity of the impregnants decreases and the number of impregnations increases, it is shown that the number of pores decreases. The density before impregnation is 1.62 g/cm3. The density increases to 1.67 g/cm3 and porosity decreases by 18.6 % after three impregnations using 5.1 cP impregnant, resulting in the best pore-filling effect. After three times of impregnation with a viscosity of 5.1 cP, the flexural strength increases by 55.2 % and the electrical resistivity decreases by 86.76 %. This shows that a slight increase in density due to the pore-filling effect improves the properties of bulk graphite.

Pores produced by carbonization in bulk graphite process degrade the mechanical and electrical properties of bulk graphite. Therefore, the pores of bulk graphite must be reduced and an impregnation process needs to be performed for this reason. In this study, bulk graphite is impregnated by varying the viscosity of the impregnant. The pore volume and pore size distribution, according to the viscosity of the impregnant, are analyzed using a porosimeter. The total pore volume of bulk graphite is analyzed from the cumulative amount of mercury penetrated. The volume for a specific pore size is interpreted as the amount of mercury penetrating into that pore size. This decreases the cumulative amount of mercury penetrating into the recarbonized bulk graphite after impregnation because the viscosity of the impregnant is lower. The cumulative amount of mercury penetrating into bulk graphite before impregnation and after three times of impregnation with 5.1cP are 0.144 mL/g and 0.125 mL/gm, respectively. Therefore, it is confirmed that the impregnant filled the pores of the bulk graphite well. In this study, the impregnant with 5.1 cP, which is the lowest viscosity, shows the best effect for reducing the total pore volume. In addition, it is confirmed by Raman analysis that the impregnant is filled inside the pores. It is confirmed that phenolic resin, the impregnant, exists inside the pores through micro-Raman analysis from the inside of the pore to the outside.

Zinc-ion Batteris (ZIBs) are recently being considered as energy storage devices due to their high specific capacity and high safety, and the abundance of zinc sources. Especially, ZIBs can overcome the drawbacks of conventional lithium ion batteris (LIBs), such as cost and safety issues. However, in spite of their advantages, the cathode materials under development are required to improve performance of ZIBs, because the capacity and cycling stability of ZIBs are mainly influenced by the cathode materials. To design optimized cathode materials for high performance ZIBs, a novel manganese oxide (MnO2) coated graphite sheet is suggested herein with improved zinc-ion diffusion capability thanks to the uniformly decorated MnO2 on the graphite sheet surface. Especially, to optimize MnO2 on the graphite sheet surface, amounts of percursors are regulated. The optimized MnO2 coated graphite sheet shows a superior zinc-ion diffusion ability and good electrochemical performance, including high specific capacity of 330.8 mAh g−1 at current density of 0.1 A g−1, high-rate performance with 109.4 mAh g−1 at a current density of 2.0 A g−1, and remarkable cycling stability (82.2 % after 200 cycles at a current density of 1.0 A g−1). The excellent electrochemical performance is due to the uniformly decorated MnO2 on the graphite sheet surface, which leads to excellent zinc-ion diffusion ability. Thus, our study can provide a promising strategy for high performance next-generation ZIBs in the near future.

신축성 전극을 다양한 소재와과 방식을 통해 제조되고 있으며 많은 기계적 특성 분석이 연구되고 있다. 은, 구리, 금, 나노와이어 등 다양한 금속이나 CNT, graphene, 플러렌 등을 기반으로 연구되고 있으며 대부분 높은 전도성과 신축특성을 요구하는 어플리케이션에 사용되지만 고가라는 단점이 있다. 본 연구에서는 저비용 소재와 공정으로 높은 신축특성과 반복 특성을 보유한 신축성 전극을 개발하였다. 값싼 전도성 탄소 와 흑연을 혼합하여 페이스트를 개발하였고 개발된 페이스트를 메탈마스크 인쇄 공정을 통해 TPU기판 위에 인쇄하였고 120℃에서 2시간 경화를 진행하였다. 이렇게 개발된 전극을 인장 시험과 인장 반복 시험을 통해 특성을 증명하였고 향후 어플리케이션 적용 가능여부를 확인하기 위해 무릎에 임시로 고정 후 간이 시험을 진행한 결과 20회 반복하는 동안 일정한 저항 변화를 보여줬다.