As frontier materials, graphene oxide (GO) and graphene have penetrated almost all research areas and advanced numerous technologies in sensing, electronics, energy storage, catalysis, water treatment, advanced composites, biomedical, and more. However, the affordable large-scale synthesis of high-quality GO and graphene remains a significant challenge that negatively affects its commercialisation. In this article, firstly, a simple, scalable approach was demonstrated to synthesise high-quality, high yield GO by modifying the improved Hummers method. The advantages of the optimised process are reduced oxidation time, straightforward washing steps without using coagulation step, reduction in cost as eliminating the use of phosphoric acid, use of minimum chemical reagents, and increased production of GO per batch (~ 62 g). Subsequently, the produced GO was reduced to reduced graphene oxide (rGO) using three different approaches: green reduction using ascorbic acid, hydrothermal and thermal reduction techniques. The GO and rGO samples were characterised using various microscopy and spectroscopy techniques such as XRD, Raman, SEM, TEM, XPS and TGA. The rGO prepared using different methods were compared thoroughly, and it was noticed that rGO produced by ascorbic acid reduction has high quality and high yield. Furthermore, surface (surface wettability, zeta potential and surface area) and electrical properties of GO and different rGO were evaluated. The presented synthesis processes might be potentially scaled up for large-scale production of GO and rGO.

Nitrophenol sensors have garnered interest in pharmaceuticals, agriculture, environment safety and explosives. Various methods have been proposed to detect 4-nitrophenol, but nitrophenol isomers such as 2,4-dinitrophenol (DNP) and 2,4,6-trinitrophenol have been comparatively less studied. For the first time, the present work explores graphitic nanocarbon, i.e., carbon black (CB) interface for sensing of DNP. Two reduction potentials were noted at − 0.48 and − 0.64 V for o-NO2 and p-NO2 moieties, respectively, at CB/GCE. At the same time, bare GCE (glassy carbon electrode) shows a single reduction potential at − 0.7 V. The electrocatalytic effect and adsorption ability of the interface was studied from the DNP concentration effect. Scan rate and pH studies suggest that the CB acquires four electrons for NO2 reduction by the diffusion phenomenon. A broad detection range of 10–250 μM DNP with a very low detection limit of 0.13 (o-form) and 0.15 μM (p-form) was achieved using the CB interface. The real-time applicability of the fabricated sensor was evaluated using commercially available beverages with excellent recovery values. The stability, repeatability and reproducibility of the CB interface were successfully confirmed. Comparison of the sensing parameters of the developed sensor with those reported in literature reveals excellent detection limit and response time for the CB-interfaced DNP sensor, indicating its potential for environmental and commercial applications.

본 연구에서는 액체감쇠역전회복(FLAIR) 시퀀스를 대체하였던 방법 중에 비교적 간단하면서 높은 재현성을 나타내었던 고신호 강도제거 원리를 MAGiC에 적용하여 MAGiC-FLAIR와 기존의 고속스핀에코-FLAIR 영상과 비교하여 고신호 강 도제거영상의 유용성과 임상적으로 유의미한 기준을 제시하고자 하였다. 연구방법은 MAGiC 적용 후 MAGiC-FLAIR와 MAGiC-고신호 강도제거 영상을 재구성하여, 기존의 고속스핀에코-FLAIR 영상과 각각 정성적, 정량적 평가를 비교하였 다. 정성평가결과 MAGiC-고신호 강도제거는 MAGiC-FLAIR 보다는 월등히 우수하며, 고속스핀에코-FLAIR와 유사한 결과를 보였고, 정량평가결과 MAGiC-고신호강도제거는 MAGiC-FLAIR보다 백질과 회백질 대조도는 더 우수할 뿐만 아 니라, 뇌척수액의 신호 억제도 우수한 결과를 나타냈다. Synthetic 영상을 통하여 획득한 다양한 대조도 영상 중 FLAIR의 부정확도를 고신호 강도제거기법을 적용한다면 진단적 가치를 개선하여 제공할 수 있을 것이다.

선박의 건조공정 중 강재의 절단과 곡 가공, 용접에 있어 화염의 사용은 필수적이다. 현재 조선소의 강재 절단과 가공 과정에서 는 아세틸렌이 화염 연료로 가장 많이 사용되고 있지만, 폭발 사고의 위험성과 상대적으로 적은 발열량의 한계로 최근에는 프로판 연료의 활용이 증가하고 있다. 하지만 프로판 연료는 상대적으로 가공 속도가 느리고, 가공 시 슬래그의 발생빈도가 높아 품질이 저하된다. 대체 연료로써 프로필렌이 주목받으며 가공 속도와 품질향상에 대한 기대가 증가하고 있다. 프로필렌은 발열량이 우수한 연료로 강재 가공 간 생산성과 가공 품질의 우수성을 갖추고 있다. 이에 본 논문에서는 프로판, 프로필렌 화염을 이용한 철판 가공 시 각 연료의 연소 특성을 분 석 및 비교하였다. 프로필렌 화염을 이용한 철판 가공 시 배출되는 온실가스와 유해가스를 프로판 연료의 배출량과 비교하여 저감효과를 실험적으로 확인하였다. 또한, 가공 연료에 따른 입열량이 선박용 강재의 기계적 강도 변화에 미치는 영향을 알아보기 위해 열 분포실험과 인장시험을 수행하였다. 실험 결과로, 대체 연료인 프로필렌을 사용할 때 프로판 연료에 비해 온도분포가 고르게 나타났다. 기계적 강도 실 험 결과로 인장강도의 저하는 관찰되지 않았으나, 변형률은 감소하는 경향을 보였다. 본 연구의 결과를 바탕으로 향후 실제 조선소의 강재 가공 및 절단과정에 적용하였을 때, 발생하는 문제점에 대한 분석 및 보완연구를 수행할 예정이다.

부분구조화 기법은 자유도가 많고 복잡한 구조물의 유한요소 해석 모델 단순화에 효율적으로 적용될 수 있는 기법이다. 대표적으 로 선형 문제에 대해서는 Craig-Bampton method 등이 있다. Craig-Bampton method는 경계 요소를 제외한 나머지 요소의 불필요한 자 유도를 제거함으로써 선형 구조물의 축소를 수행한다. 최근에는 부분구조화 기법과 더불어 구조물의 최적설계를 위해 멀티레벨 최적 화 기법이 많이 활용되고 있다. 시스템의 목표를 달성하기 위해 각 부구조에 새로운 목표를 할당하는 기법이다. 본 연구에서는 유전자 알고리즘을 이용하여 시스템 목표 달성을 위한 각 부구조별 내부 자유도 개수를 새로운 목표로 할당하고 최적화를 수행하였다. 최적 화 절차로부터 도출된 부구조별 내부 자유도 개수를 이용하여 시스템의 축소를 수행하였다. 다양한 수치예제들을 통해 축소 모델에 대한 결과를 확인하였으며, 90% 이상의 정확도를 가지는 것을 확인하였다.

In this study, a two-stage electrostatic precipitator (ESP) was developed using a novel automatic dry cleaning device to reduce the ultrafine particles in subway stations. Collection efficiency was evaluated with a pilot scale ESP (1.2m× 1.2m) and the scale of the test duct was half of the subway air handling unit. The maximum collection efficiency for 0.3 μm particles was 96.9%. In addition, we studied a method of automatic dry cleaning for maintenance of the ESP. The cleaning efficiency was analyzed according to the cleaning flow rate for each particle loading amount to achieve a recovery rate over 90%. In addition, we derived the equation to estimate the reduction in collection efficiency according to the particle loading amount. It was confirmed that the performance of the contaminated ESP was restored to the initial state by the automatic dry cleaning in this study and that the electrical energy consumption was 5 times lower compared to utilizing conventional water cleaning.

The rate of industrial accident reduction is slowing down as the attention of the Ministry of Employment and Labor and related agencies on risk assessment systems decreased. this paper focuses on weakness of legal system for the risk assessment in recent years. A survey was conducted to identify the status and condition of the risk assessment system applying on small and medium-sized manufacturing companies. A set of questionnaires is designed to reflect various perspectives of the companies regarding the problems and solutions of the system. The results refer that differentiated instructions and support systems in response to the actual conditions of the companies are mandatory to reinforce the efficiency of risk assessment system.

PURPOSES : The objective of this study is to evaluate the effectiveness of spraying dust suppressants in relation to the condition of road pavement in South Korea and to develop an optimal management method by continuously measuring re-suspended dust concentrations using a vehicle-based measurement. METHODS : Indoor experiments were conducted to select suppressants suitable for local conditions to reduce reducing road dust, which were identified through literature review. Data collection followed the evaluation method by selecting a section sprayed with dust suppressants and a non-sprayed section within the service road. RESULTS : The BPT experiment is designed to ensure the skid resistance of the road when dust suppressants are sprayed on the road. The Environmental toxic tests for PM10, HCHO, and TVOC all met the daily indoor air quality standards recommended in Korea for determining stability. Comparison of PM10 contents before and after spraying of the test road with dust suppressants and the non-sprayed section, it was confirmed that the dust suspended by the external environment may be reduced, but the amount of dust remaining on the road may increase. After 4 hours, when the water had evaporated, the dust suppressants remained effective and lasted for two-days. CONCLUSIONS : The concentration of fine dust in South Korea varies with the average duration of highly concentrated fine dust being 26.5 h nationwide, 20.5 h in the Seoul metropolitan area, and 25.1 h in Gyeonggi-province, suggesting a duration of one to two days. Thus, the fine dust problem can be solved by using dust suppressants.

A porous photocatalyst concrete filter was successfully produced to remove NOx, by mixing TiO2 photocatalyst with lightweight aerated concrete. Ultra Fine Bubbles were used to form continuous pores inside the porous photocatalytic concrete filter, which was mixed via a bubble generation experiment. The optimal mixing condition was determined to be with 4% of the bubble generation agent B. NO removal specimens were prepared for various photocatalytic loading conditions, and the specimen containing 3% P-25 removed NO at a concentration of 1.03 μmol in 1 h. The NO removal rate of the porous photocatalytic concrete filter prepared in this study was 10.99%. This photocatalytic filter performance was more than 9 times the amount of NO removed by a general photocatalytic filter. The porous photocatalyst concrete filter for removing NOx developed in this study can be applied to various construction sites and the air quality can be solved by reducing NOx contributing to the formation of fine particles.

The reduced graphene oxide (rGO) has attracted more and more attention in recent years. How to choose a suitable reduction method to prepare rGO is a critical problem in the preparation of graphene composites. In this work, the differences of rGO reduced by thermal, microwave, Ultraviolet (UV) and reducing agent were studied. The reduction degree and functional groups of rGO were compared by SEM, XPS, Raman, FTIR and TGA. Thermal can remove most of the oxygen-containing groups of graphene oxide (GO) and the thermal reduction is the most effective reduction method. UV light can directly act on the unstable oxygen-containing groups, and its reduction efficiency is second only to thermal reduction. The efficiency of chemical reduction is not as good as that of UV reduction, because the reducing agent only act on the surface of GO. Microwave reduction is a mild thermal reduction with the lowest efficiency, but the residual oxygen-containing groups increase the hydrophilicity of rGO. To sum up, this work studies that rGO prepared by different reduction methods has different characteristics, which provides a reference for selecting appropriate reduction methods to prepare graphene composites with better properties.

One-step hydrothermal reduction method was used to prepare three-dimensional carbon fiber brush-based graphene–platinum (CFB/Pt–G) composites to improve the electrocatalytic oxygen reduction activity of cathode materials for seawater oxygen-dissolved battery. Characterization results show that the reduced graphene oxide of as-prepared graphene–platinum composite displays the few-layer folded structure. In addition, Pt nanoparticles with the polycrystalline structure dispplay a preferential growth along the crystal plane of (111) and are mainly distributed around the defect cavities of folded graphene. Electrochemical results show that the diffusion-limited current density of CFB/Pt–G composite tested with 1600 rpm/min in 3.5% NaCl solution reaches 5 mA/cm2, while that of CFB/G is only 2.64 mA/cm2. Battery discharge results show that the maximum volume power density of CFB/Pt–G–Mg battery with a stable open voltage of 1.73 V is 81 times as much as the commercial seawater battery SWB1200.

2015년 ‘파리협정’ 및 2021년 ‘기후위기 대응을 위한 탄소중립·녹색성장 기본법’ 제정에 따라 2030년 국가 온 실가스 감축목표(NDC, 2018년 대비 40% 감축) 달성을 위해서는 지자체별 적절한 온실가스 감축 목표 설정과 이행 노 력이 필수적이다. 이에 이 연구에서는 충청북도 지역을 중심으로 1990-2018년 까지 온실가스 배출 현황을 시계열로 분석하였고, 2030년 국가 온실가스 감축목표와 시나리오를 바탕으로 충청북도의 2030년 온실가스 감축 목표를 제안하였 다. 또한 감축 목표 달성을 위해 BAU 대비 장래 배출량을 고려한 2030년까지의 감축 잠재량을 추정하였다. 그 결과, 첫째, 우리나라와 충북의 온실가스 배출량은 1990년 이래 인구 및 경제 성장에 따라 증가해온 것으로 나타났으며, 2018년 국가 대비 충북의 온실가스 배출량은 3.9%로 매우 낮은 편이였고, 시멘트 및 석회 생산, 제조업 및 건설업, 수 송업 등 연료연소에 의한 배출이 주를 이루는 것으로 나타났다. 둘째, 2030년 NDC 및 2050 탄소중립 시나리오를 반 영한 2030년 충청북도 온실가스 감축 목표는 2018년 대비 40.2%로 설정하였다. 이에 장래 배출량을 고려할 경우 목표 달성을 위한 감축 잠재량은 2018년 대비 46.8%인 것으로 추정되었다. 상기 결과는 국가 및 지자체의 온실가스 감축 목표 달성을 위해서는 분야별 온실가스 감축 수단을 통한 감축 잠재량을 충족하는 것이 중요하다는 것을 의미한다. 또 한 2030년 NDC 및 2050 탄소중립 시나리오 달성을 위해 충북을 포함한 국가 및 각 지자체는 온실가스 장래 배출량 을 연도별로 추정하여 매년 감축 목표와 감축 잠재량을 구하고 이를 삭감할 수 있는 구체적인 감축 수단을 마련할 필 요가 있음을 말해준다.

This study is to investigate the effect of material for GPF on the PM reduction characteristics before the improvement of filter efficiency in GPF. The material of GPF was changed to ceramic and metal. The ceramic material was applied to SiC, and the metal materials were employed to STS 310s, STS 316s, and STS 410s. The number of honeycomb and wall thickness were set to 200CPSI, 0.3987mm, respectively. The inlet mass flow was fixed at 0.00695kg/s. The inlet air temperature was changed from 500K(0s∼350s) to 1000K(400s∼900s). It was found that the differences in loading amount according to the GPF materials were difficult to observe because the pore density and porosity were set to be the same to affect only the mechanical properties. STS 310s with the highest temperature value had the fastest regeneration time. However, as time goes on, SiC had the highest regeneration rate characteristics. The reason is that the high-temperature region in the GPF by the high-temperature exhaust gas was rapidly transferred toward the outlet due to the high thermal conductivity of SiC.

Metal–organic frameworks (MOFs) are widely used as supports for single-atom catalysts (SACs) owing to their high specific surface area, porosity, and ordered metal–ligand structure. Their activity can be increased by increasing the number of electrochemically accessible active sites via the formation of atomically dispersed metal catalysts (M–Nx) that coordinate with nitrogen atoms on the MOF. Herein, we introduce the relationship between the size of the MOF as a starting material and the catalytic activity for the oxygen reduction reaction in alkaline media. The morphology and features of the MOFs are critically dependent on their size. Remarkably, cage-like MOFs below 33 nm are converted into collapsed structures and are connected between each MOF, even carbon fiber- or tube-like features, after carbonization. SACs derived from medium-sized MOFs exhibit excellent activity and are comparable to commercial Pt/C catalysts owing to their porous structure. Therefore, we believed that controlling the size of MOFs containing active atoms is an effective method of modulating the morphological properties of the support and even the number of active sites that are closely related to the activity.

Lately, Raman spectroscopy has become powerful tool for quality assessment of graphene analogues with identification of intensity ratio of Raman active D-band and G-band ( ID/IG ratio) as a vital parameter for quantification of defects. However, during chemical reduction of graphitic oxide (GrO) to reduced GrO (RGrO), the increased ID/ IG ratio is often wrongly recognized as defect augmentation, with “formation of more numerous yet smaller size sp2 domains” as its explanation. Herein, by giving due attention to normalized peak height, full-width half-maxima and integrated peak area of Raman D- and G-bands, and compliment the findings by XRD data, we have shown that in-plane size of sp2 domains actually increases upon chemical reduction. Particularly, contrary to increased ID/ IG ratio, the calculated decrease in integrated peak area ratio ( AD/AG ratio) in conjunction with narrowing of D-band and broadening of G-band, evinced the decrease in in-plane defects. Finally, as duly supported by reduction induced broadening of interlayer-spacing characteristic XRD peak and narrowing of ~ 43° centered XRD hump, we have also shown that the sp2 domains actually expands in size and the observed increase in ID/ IG ratio is indeed due to increase in across-plane defects, formed via along-the-layer slicing of graphitic domains.

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.