최근 지구온난화로 인해 발생하는 폭우 및 강설과 같은 비정상적인 기상 패턴으로 인해 도로 표면 결빙(블랙 아이스)으로 인 한 사고와 인명 피해가 증가하고 있으며, 이는 주요 문제로 대두되고 있습니다. 이러한 문제를 완화하기 위해 본 연구에서는 열저장 능력을 갖춘 상변화 물질(PCM)을 시멘트 복합재료에 포함시켰습니다. PCM은 상변화 과정에서 열에너지를 흡수, 저장 및 방출할 수 있어 온도 변동으로 인한 결빙을 최소화할 수 있습니다. PCM은 먼저 미세 캡슐화된 후 시멘트 복합재료에 강화되어 기계적 및 열적 성능 검증 연구가 수행되었습니다. 또한, 열전달 효율과 기계적 특성을 향상시키기 위해 다중벽 탄소나노튜브(CNT)와 실리카 퓸이 추 가되었습니다. 미세 캡슐화된 PCM의 열 성능은 열 거동을 측정하기 위한 재료 실험을 통해 검증되었습니다. 이후, 제조된 시멘트 복 합재의 기계적 및 열적 성능 테스트가 그 효과를 평가하기 위해 수행되었습니다. 이러한 테스트 동안 일정 온도와 습도 챔버를 사용한 열 주기 테스트가 열 성능을 검증하기 위해 수행되었습니다. 기계적 성능 실험에서는 CNT와 실리카 퓸의 포함이 미세 캡슐화된 PCM 의 포함으로 인한 강도 저하를 완화하는 것을 확인하였습니다. 더욱이, 열 주기 테스트를 통해 고효율 열저장 시멘트 복합재가 결빙 조건에서도 영하의 온도를 유지할 수 있음을 보여주었으며, 이는 효율적인 열저장 성능을 입증하였습니다.

In this investigation, we synthesized a novel quaternary nanocomposite, denoted as RGO-Ba(OH)2/CeO2/TiO2, through a straightforward and cost-effective solid-state synthesis approach. The as-prepared composites underwent a series of comprehensive characterizations, including XRD, FTIR, TGA-DTA, XPS, SEM, EDAX, and TEM analyses, affirming the successful synthesis of a quaternary nanocomposite with well-interconnected nanoparticles, nanorods, and sheet-like structures. Further, our electrochemical performance evaluations demonstrated that the electrochemical capacitance of the RGO-Ba(OH)2/CeO2/ TiO2 nanocomposite achieved an impressive value of 445 F g− 1 at a current density of 1.0 A g− 1, particularly when the mass ratio of CeO2 and TiO2 was maintained at 90:10. Furthermore, the specific capacitance retained a remarkable 65% even after 2000 cycles at a current density of 6 A g− 1 in a 3 mol KOH electrolyte. Comparatively, this outstanding electrochemical performance of the RGO-Ba(OH)2/CeO2/TiO2 (90:10) nanocomposite can be attributed to several factors. These include the favorable electrical conductivity and large specific surface area provided by graphene, TiO2, and Ba(OH)2, the enhanced energy density and extended cycle life resulting from the presence of CeO2, and the synergistic contributions among all four components. Therefore, the RGO-Ba(OH)2/CeO2/TiO2 nanocomposite emerges as a highly promising electrode material for supercapacitors.

Lead-free perovskite ceramics, which have excellent energy storage capabilities, are attracting attention owing to their high power density and rapid charge-discharge speed. Given that the energy-storage properties of perovskite ceramic capacitors are significantly improved by doping with various elements, modifying their chemical compositions is a fundamental strategy. This study investigated the effect of Zn doping on the microstructure and energy storage performance of potassium sodium niobate (KNN)-based ceramics. Two types of powders and their corresponding ceramics with compositions of (1-x)(K,Na)NbO3-xBi(Ni2/3Ta1/3)O3 (KNN-BNT) and (1-x)(K,Na)NbO3-xBi(Ni1/3Zn1/3Ta1/3) O3 (KNN-BNZT) were prepared via solid-state reactions. The results indicate that Zn doping retards grain growth, resulting in smaller grain sizes in Zn-doped KNN-BNZT than in KNN-BNT ceramics. Moreover, the Zn-doped KNNBNZT ceramics exhibited superior energy storage density and efficiency across all x values. Notably, 0.9KNN-0.1BNZT ceramics demonstrate an energy storage density and efficiency of 0.24 J/cm3 and 96%, respectively. These ceramics also exhibited excellent temperature and frequency stability. This study provides valuable insights into the design of KNNbased ceramic capacitors with enhanced energy storage capabilities through doping strategies.

Thermoelectric (TE) energy harvesting, which converts available thermal resources into electrical energy, is attracting significant attention, as it facilitates wireless and self-powered electronics. Recently, as demand for portable/wearable electronic devices and sensors increases, organic-inorganic TE films with polymeric matrix are being studied to realize flexible thermoelectric energy harvesters (f-TEHs). Here, we developed flexible organic-inorganic TE films with p-type Bi0.5Sb1.5Te3 powder and polymeric matrices such as poly(3,4-eethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) and poly (vinylidene fluoride) (PVDF). The fabricated TE films with a PEDOT:PSS matrix and 1 wt% of multi-walled carbon nanotube (MWCNT) exhibited a power factor value of 3.96 μW ‧ m-1 ‧ K-2 which is about 2.8 times higher than that of PVDF-based TE film. We also fabricated f-TEHs using both types of TE films and investigated the TE output performance. The f-TEH made of PEDOT:PSS-based TE films harvested the maximum load voltage of 3.4 mV, with a load current of 17.4 μA, and output power of 15.7 nW at a temperature difference of 25 K, whereas the f-TEH with PVDF-based TE films generated values of 0.6 mV, 3.3 μA, and 0.54 nW. This study will broaden the fields of the research on methods to improve TE efficiency and the development of flexible organic-inorganic TE films and f-TEH.

방충설비는 선박의 접안 및 양하역 과정에서 선박의 충격력을 흡수하여 선박과 접안시설을 모두 보호하는 매우 중 요한 역할을 수행한다. 하지만 이에 대한 최근 연구 및 설계 최적화의 노력이 매우 부족해 보인다. 이에 본 논문은 국내 항만 설계기준에서 제시하고 있는 방충재 설계에 사용되는 선박 접안에너지 산정식을 개선, 보완하기 위하여 연구를 수행하였다. 접 안에너지 산정과정에서 선박 및 접안시설의 조건을 고려하기 위하여 적용되는 영향계수의 변화에 따른 영향을 분석하였으며, 이 과정에서 국내외 설계코드에서 제시하고 있는 산정방법과 최신 선박제원, 국내 설계결과가 활용되었다. 분석에는 최신 선박 의 표준제원과 국내에서 실시된 실제 설계결과가 적용되었다. 그 결과, 국내 항만 설계기준에서 제시하고 있는 영향계수 결정방 법은 선박과 접안시설의 조건을 최적으로 반영하기에는 부족하며, 접안에너지가 20%이상 크게 산정되어 방충재 선정과정에서 과다 설계가 야기될 수 있는 것으로 판단되었다. 이에, 국내 항만 설계기준에서 제시하고 있는 영향계수를 선박 및 접안여건을 고려하여 설계할 수 있도록 최적화된 방법을 제시하였다.

Test of the operating characteristics and energy saving performance of a container cooling system that reduces the operating energy of a refrigeration system using a loop thermosyphon heat exchanger that removes heat by temperature difference between outdoor and indoor was performed. As a result of the experiments, when the loop thermosyphon and the refrigeration system were operated simultaneously, the refrigeration system operated intermittently by reducing the heat load. As the temperature difference between indoor and outdoor increased, the operating time of the refrigeration system decreased and the energy efficiency rate increased. Energy efficiency rate showed a tendency to increase with increasing temperature difference, and the predicted correlation of energy efficiency rate using the performance of the loop thermosyphon heat exchanger and the refrigeration system was relatively consistent with the experimental value.

The Calorifier is a device that supplies hot water to the crew for showering and cooking. In particular, problems such as hot water not coming out when a trainee and a crew member take a shower at the same time may occur due to a malfunction of the temperature control valve that controls the temperature. In particular, when the hot water usage time is almost constant, such as a training ship, a high calorific value is required. When there is no dissatisfaction with the use of hot water, satisfaction with the educational environment is improved. Therefore, in this study, a solenoid temperature control valve is applied to increase satisfaction with hot water use, and a mechanical time switch is applied to the hot water circulating water pump to save energy.

Recently, due to high theoretical capacitance and excellent ion diffusion rate caused by the 2D layered crystal structure, transition metal hydroxides (TMHs) have generated considerable attention as active materials in supercapacitors (or electrochemical capacitors). However, TMHs should be designed using morphological or structural modification if they are to be used as active materials in supercapacitors, because they have insulation properties that induce low charge transfer rate. This study aims to modify the morphological structure for high cycling stability and fast charge storage kinetics of TMHs through the use of nickel cobalt hydroxide [NiCo(OH)2] decorated on nickel foam. Among the samples used, needle-like NiCo(OH)2 decorated on nickel foam offers a high specific capacitance (1110.9 F/g at current density of 0.5 A/g) with good rate capability (1110.9 - 746.7 F/g at current densities of 0.5 - 10.0 A/g). Moreover, at a high current density (10.0 A/g), a remarkable capacitance (713.8 F/g) and capacitance retention of 95.6% after 5000 cycles are noted. These results are attributed to high charge storage sites of needle-like NiCo(OH)2 and uniformly grown NiCo(OH)2 on nickel foam surface.

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.

Recently, interest in technology for eco-friendly energy harvesting has been increasing. Polyvinylidene fluoride (PVDF) is one of the most fascinating materials that has been used in energy harvesting technology as well as micro-filters by utilizing an electrostatic effect. To enhance the performance of the electrostatic effect-based nanogenerator, most studies have focused on enlarging the contact surface area of the pair of materials with different triboelectric series. For this reason, one-dimensional nanofibers have been widely used recently. In order to realize practical energy-harvesting applications, PVDF nanofibers are modified by enlarging their contact surface area, modulating the microstructure of the surface, and maximizing the fraction of the β-phase by incorporating additives or forming composites with inorganic nanoparticles. Among them, nanocomposite structures incorporating various nanoparticles have been widely investigated to increase the β-phase through strong hydrogen bonding or ion-dipole interactions with -CF2/CH2- of PVDF as well as to enhance the mechanical strength. In this study, we report the recent advances in the nanocomposite structure of PVDF nanofibers and inorganic nanopowders.

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

기후변화로 인해 가속화되고 있는 충남 지역 가뭄현상에 대응하고 대산 임해산업단지의 증가하는 용수 수요를 만족하기 위해서, K-water에서는 100,000 m3/일 규모 역삼투 해수담수플랜트 건설 사업을 추진하고 있다. 이에 본 연구에서는 해수담수플랜트 운영비용의 70% 이상을 담당하는 역삼투 공정 성능에 영향을 미치는 주요 인자에 대한 성능 분석을 수행하였다. 대산 지역 해수 염분농도 및 수온 변화 조건에서 RO 공정의 전력소모는 2.39 ± 0.13 kWh/m3로 나타났으며, 막여과유속과 회수율이 낮을수록 전력소모가 절감되어 연간 운영비용이 감소하였다. 주요 막 제조사별 고유량 막의 성능 비교 결과, 전량 2단 여과공정(full two pass) 기준 생산수 TDS는 평균 3.84 mg/L로 양호하였고, 전력소모는 2.22 ± 0.13 kWh/m3 수준으로 확인되었다. 역삼투 공정 구성을 전량 2단 여과방식에서 partial 또는 split partial 방식으로 변경함에 따라 전력소모는 최대 0.29 kWh/m3, 막모듈 설치비용은 최대 15.6% 절감 가능할 것으로 기대된다.

Zn-ion supercapacitors (ZICs) show high energy densities with long cycling life for use in electronic devices. Porous Zn electrodes as anodes for ZICs are fabricated by chemical etching process using optimized conditions. The structures, morphologies, chemical bonding states, porous structure, and electrochemical behavior are examined. The optimized porous Zn electrode shows a root mean square of roughness of 173 nm and high surface area of 153 μm2. As a result, ZIC using the optimized porous Zn electrode presents excellent electrochemical performance with high specific capacitance of 399 F g−1 at current density of 0.5 A g−1, high-rate performance (79 F g−1 at a current density of 10.0 A g−1), and outstanding cycling stability (99 % after 1,500 cycles). The development of energy storage performance using synergistic effects of high roughness and high surface area is due to increased electroactive sites by surface functionalization of Zn electrode. Thus, our strategy will lead to a rational design and contribute to next-generation supercapacitors in the near future.

For electrodes in electrochemical double-layer capacitors, carbon nanofibers (CNFs) were prepared by thermal treatment of precursor polymer nanofibers, fabricated by electrospinning. Poly(acrylonitrile-co-vinylimidazole) (PAV) was employed as a precursor polymer of carbon nanofibers due to the effective cyclization of PAV polymer chains during thermal treatment compared to a typical precursor, polyacrylonitrile (PAN). PAV solutions with different comonomer compositions were prepared and electrospun to produce precursor nanofibers. Surface images obtained from scanning electron microscopy showed that their nanofibrous structure was well preserved after carbonization. It was also confirmed that electrospun PAV nanofibers were successfully converted to carbon nanofibers after the carbonization step by Raman spectroscopy. Carbon nanofiber electrodes derived from PAV showed higher specific capacitances and energy/power densities than those from PAN, which was tested by coin-type cells. It was also shown that PAV with an acrylonitrile/vinylimidazole composition of 83:17 is most promising for the carbon nanofiber precursor exhibiting a specific capacitance of 114 F/g. Their energy and power density are 70.1 Wh/kg at 1 A/g and 9.5 W/kg at 6 A/g, respectively. In addition, pouch cells were assembled to load the higher amount of electrode materials in the cells, and a box-like cyclic voltammetry was obtained with high capacitances.

Chlor-alkali (CA) membranes as key materials to generate chlorine gas and sodium hydroxide are composed of sulfonic acid layer (S-layer) and carboxylic acid layer (C-layer) to provide fast sodium ion transport and slow hydroxide ion diffusion, respectively. Aciplex F, a representative CA membrane is made in a double layer form via thermal adhesion of both layers after each single layer film is independently fabricated. Unfortunately, the membrane fabrication induces delamination particularly in their interface as a result of hydroxide ion diffusion occurring during CA operation, leading to rapid increase in electrochemical overpotential. In this study, selective chemical conversion technique was developed to solve the delamination issue. Their effectiveness was proved by applying the same concept to a wide range of PFSA membrane.

본 연구는 한우 암소비육에 있어서 고 에너지의 육성용 TMR(TDN 72.7%DM, CP 13.65%DM)을 육성기(8~12개월령) 및 비육기(13~24개월령)까지는 제한급여하고, 이후 비육 마무리기(25~32개월령)까지 자유 채식시켰을 때, 증체수준, 도체특성 및 경제성에 미치는 영향을 구명하고자 수행되었다. 공시축은 한우 암소 35두(8개월령)를 이용하여 Control구(5두), T1(10두), T2(10두) 및 T3(10두)구로 나누어 난괴법으로 배치하였다. 공시사료는 전기간 동일한 육성용 TMR을 Control구에서는 자유채식 시켰고, T1, T2, T3구에서는 각각 체중의 1.8%, 1.6% 및 1.5%로 제한하여 24개월령까지 급여하였다. 한우 암소의 체중은 비육마무리기간에서 Control구에 비해 T1, T2 및 T3 처리구가 각각 4.9%, 3.6% 및 2.5% 높은 것으로 나타났다 (p<0.05). 일일증체량은 육성기에는 Control구와 T1구가 다른 처리구에 비해 높았으며(p<0.05), 비육마무리기의 T1 처리구가 다른 처리구에 비해 높았다(p<0.05). 건물섭취량과 TDN 섭취량은 비육마무리기간에서 T1구가 가장 높았다(p<0.05). 고 에너지의 육성우용 TMR을 전 기간동안 급여함으로써 도체중과 배최장근 단면적이 일반적인 한우 암소비육 결과에 비해 현저히 증가되었다. 처리구별 도체중은 Control구에 비해 T1구가 약 11.6% 많았으며(p<0.05), 지방색과 성숙도는 Control구에서 높았다(p<0.05). 근내지방도, 육색 및 조직감은 처리구간 유의적 차이는 없었으나, 육량등급 출현율에 있어서는 Control구에서 A등급이 60%로서 다른 처리구에 비해 높았다. 육질등급에서 1++ 등급 출현율은 Control, T1, T2 및 T3구에서 각각 0%, 20%, 20% 및 0%로 나타났다. 순수익은 Control구에 비해 T1과 T2구가 각각 15% 및 13% 증가되었으나 T3구는 2% 감소한 것으로 나타났다. 결론적으로, 한우 미경산우 비육 시, 고에너지의 육성용 사료를 육성기부터 비육기(13~24개월령)까지 체중의 1.8% 수준으로 제한 급여하는 것이 전 기간 동안 자유채식시키는 것보다 도체중이나 육질등급 증가로 경제성이 향상되어 한우암소 고급육생산 프로그램 개발에 활용할 수 있을 것으로 판단된다.

We fabricated dual-phase free-standing polymeric membrane for high performance CO2/N2 separation, introducing amphiphilic, CO2-philic copolymer via one-step free radical polymerization, or (2-[3-(2H-benzotriazol-2-yl)-4-hydroxyphenyl]ethyl methacrylate)-graft-poly(oxyethylene methacrylate) (PBE). PBE filler partially interacts with Pebax polymer matrix to generate the interconnected CO2 philic network, exhibiting a microphase-separated, or dual-phase behavior in Pebax matrix. The performance of CO2/N2 separation was increased according to the PBE content, with the maximum selectivity at 5 wt%. The enhancement of Pebax/PBE CO2-philic membrane was attributed to the formation of CO2-philic channel consisting of ether oxygens and triazole groups. The best performance was CO2 permeability of 175.3 Barrer and CO2/N2 selectivity of 48.2.