초임계 이산화탄소 조건에서 다중벽 탄소 나노튜브(MWCNT)에 공유결합으로 조합된 폴리(2-에티닐피리디 늄 염) 복합체를 제조하였다. 초기 반응 단계에서 MWCNT 표면에서 형성된 4차염화 2-에티닐피리디늄 염의 활성 화된 아세틸렌 삼중 결합이 MWCNT 표면에서 연속적으로 중합되어 폴리(2-에티닐피리디늄 염)이 공유결합으로 조 합된 MWCNT가 용이하게 제조되었다. MWCNT/폴리(2-에티닐피리디늄 염)의 전기 광학 및 전기화학적 특성을 측 정하고 분석하였다. 해당 복합체의 광발광 피크는 2.04 eV의 광자 에너지에 해당하는 610 nm에서 관찰되었다. SnO2:F/TiO2/N719 염료/고체 전해질/Pt 장치가 있는 준고체 DSSC를 MWCNT/P2EP로 제조하였는데, 이의 최대 에 너지 변환효율은 5.33%였다.

노면결빙에 따른 전도사고 및 블랙아이스에 의한 사고 등이 증가하고 있으며 이를 해결하기 위한 발열 시멘트 복합체에 대한 관심이 증가하고 있다. 본 연구에서는 리튬이차전지 산업에서 발생되는 폐 CNT 폐 음극재 등 탄소계 산업부산물을 활용하여 고상탄소 캡슐을 제조 하고 이를 혼입하여 레미탈 및 모르타르 실험체를 제조하여 전기 인압에 따른 중심부 표면 온도 측정 및 열화상 카메라를 통하여 발열 성능을 평가하였다. 고상탄소캡슐 혼입량이 증가할수록 발열 성능이 우수하게 나타났으며 레미탈 실험체의 경우 DC 24 V에서 모든 실험체가 35분 내 표면온도 60℃ 이상 나타내었다. 모르타르 실험체의 경우 전기 인압 DC 24 V에서 고상탄소캡슐을 19% 이상 혼입 시 소요시간 30분 내 30℃ 이상의 발열 상승 목표를 만족하는 것으로 나타났다.

국내 수박(Citrullus lanatus) 품종의 발아율에 대한 Solid Matrix Priming(SMP)의 영향을 평가하였다. Micro cel-E가 SMP 처리에 가장 이상적인 matrix로 밝혀졌으며, 종자:matix:물의 비율은 10:5:10(w/w/w)로, 25°C 에서 3일 동안 처리했을 때 유근의 돌출없이 발아속도가 촉진되었다. SMP 처리 과정 동안 초기 4시간 동안의 수분 흡수율은 급격하게 증가했으며, 이후 72시간 동안은 더 느린 속도로 흡수되었고, 처리 마지막 시간까지 수분 흡수 율은 41%이었다. 발아 온도와 상관없이, SMP 처리된 종자는 발아 시간이 단축되면서 발아율이 향상되었다. 특히, 최적 발아 온도보다 낮은 온도에서 발아율이 높았다. 품종별 차이는 있었으나, 특히 ‘해찬꿀’과 ‘리코스위트’ 품종 에서 발아율이 유의미하게 증가하였다. 또한 일부 품종에서 SMP 처리 종자의 유묘출현율과 초장, 생체중이 무처 리에 비하여 증가한 값을 보였으며, SMP 처리로 종자의 발아속도 및 유묘활력을 증진시켜 우량 묘 확보가 가능한 것으로 판단되었다.

This study evaluated the suitability of using Wickerhamomyces anomalus A1-5 isolated from solid grain fermentation broth for winemaking by comparing the quality and functionality of Campbell Early wine produced with single and mixed inoculations. The pH ranged from 3.43 to 3.68, with the highest value in treatment B. Soluble solids ranged from 5.0 to 7.7 °Brix. Total acidity was measured at 0.42% to 0.47%. Color analysis indicated a significant decrease in lightness with an increase in redness across all treatment groups compared to the control. Among aroma compounds, 8 alcohols, 6 esters, 3 acids, and 11 other compounds were identified, with the control having the highest alcohol content and treatment D having the highest ester content. Tannin and total polyphenol contents ranged from 46.46 mg% to 95.92 mg% and from 87.66 mg% to 147.21 mg%, respectively. Antioxidant activities measured by DPPH and ABTS assays ranged from 33.84% to 69.02% and from 42.43% to 89.18%, respectively, with treatment B exhibiting the highest activities. These results suggest that W. anomalus A1-5 may positively influence the quality and functionality of Campbell Early wine, presenting potential as a novel yeast strain for winemaking.

고체전해질은 높은 에너지 밀도와 안전성을 갖춘 차세대 리튬이온전지에 꼭 필요한 핵심 요소다. 이러한 고체전 해질의 제작을 위해서 기존 고체전해질의 낮은 이온전도도와 높은 계면저항 문제를 해결해야 한다. 본 연구에서는 강화된 이 온 전도성과 계면 안정성을 지닌 PVDF-HFP 고분자에 분산된 Li7La3Zr2O12 (LLZO) 나노와이어 복합체를 기반으로 하는 새 로운 전해질(PVDF-HFP/LLZO/SN, PHLS membrane)을 제안한다. PHLS에 용매 열압착(Sovlent heat press, SHP)을 통해 계 면 저항과 내부 공극이 감소된 PHLS-(SHP)는 30°C에서 2.06 × 10-4 S/cm의 높은 이온 전도도, 4.5 V (vs. Li/Li+)의 넓은 전 기화학적 전위 창, 리튬 금속과 전해질 사이의 안정된 계면 안정성을 나타냈다. 0.2 mA/cm2에서 수행된 Li 대칭 셀을 사용한 전기화학적 테스트에서 150 시간 이상 안정성을 유지하는 것으로 확인되었으며, 이는 당사의 복합 기반 고체 전해질을 활용 하여 전기화학적 성능이 향상되었음을 시사한다.

This study aimed to manufacture emulsified asphalt for free-heated asphalt mixtures with high solid contents using the high internal phase ratio (HIPR) technique and utilize it as basic research data by evaluating the basic properties. The optimal emulsifier was selected by considering the physical and chemical properties of the emulsifier used in the emulsified asphalt, and the solid content in the emulsified asphalt was increased using the HIPR technique. Emulsified asphalt was produced with solid contents of 90%, 80%, 70%, and 62% (current standard) in emulsified asphalt, and the basic properties of the emulsified asphalt were evaluated for each content. In addition, a free-heated asphalt mixture for the surface layer was produced by applying the emulsified asphalt produced for each content, and the performance was evaluated based on the quality standard items presented in the current guidelines of the Ministry of Land, Infrastructure and Transport. When utilizing the HIPR technique, we could manufacture up to 90% of the asphalt solid content in the emulsified asphalt; however, applying it to unheated asphalt mixtures because of the increase in viscosity was impossible. We determined that it could be applied up to a maximum solid content of 80%. In addition, in the free-heated asphalt mixture test, the ratio of the air void increased as the solids content increased, but the strength decreased. An examination of the fracture surface after the strength test revealed that it was brown, which is a characteristic color of emulsified asphalt. This was because the curing time became insufficient as the solid content increased, resulting in insufficient time for strength development. To ensure the performance of the free-heated asphalt mixture, we observed that the viscosity of emulsified asphalt with a high solid content should be reduced; securing the curing time accordingly was an important factor, and it was determined that additional research is necessary.

In this study, ester co-solvents and fluoroethylene carbonate (FEC) were used as low-temperature electrolyte additives to improve the formation of the solid electrolyte interface (SEI) on graphite anodes in lithium-ion batteries (LIBs). Four ester co-solvents, namely methyl acetate (MA), ethyl acetate, methyl propionate, and ethyl propionate, were mixed with 1.0 M LiPF6 ethylene carbonate:diethyl carbonate:dimethyl carbonate (1:1:1 by vol%) as the base electrolyte (BE). Different concentrations were used to compare the electrochemical performance of the LiCoO2/ graphite full cells. Among various ester co-solvents, the cell employing BE mixed with 30 vol% MA (BE/MA30) achieved the highest discharge capacity at − 20 °C. In contrast, mixing esters with low-molecular-weight degraded the cell performance owing to the unstable SEI formation on the graphite anodes. Therefore, FEC was added to BE/MA30 (BE/MA30-FEC5) to form a stable SEI layer on the graphite anode surface. The LiCoO2/ graphite cell using BE/MA30-FEC5 exhibited an excellent capacity of 127.3 mAh g− 1 at − 20 °C with a capacity retention of 80.6% after 100 cycles owing to the synergistic effect of MA and formation of a stable and uniform inorganic SEI layer by FEC decomposition reaction. The low-temperature electrolyte designed in this study may provide new guidelines for resolving low-temperature issues related to LIBs, graphite anodes, and SEI layers.

This study investigates the thermal expansion characteristics of hydroxyl-terminated polybutadiene(HTPB) based solid propellants, focusing on batch-to-batch variability and accelerated aging effects. Coefficient of thermal expansion(CTE) measurements were conducted using thermomechanical analyzer(TMA) on samples from different manufacturing batches and specimens aged at various temperatures for different durations. Results indicate variations in CTE values between batches, highlighting the significance of manufacturing process control. Accelerated aging experiments reveal minimal systematic changes in CTE, suggesting stability of thermal expansion properties under short-term thermal stress. The overall distribution of CTE values shows concentration within a specific range, indicating consistency in thermal expansion characteristics. These findings provide insights into the thermal behavior of HTPB-based solid propellants, contributing to improved missile design and lifecycle prediction models.

본 연구는 대기 중 장기간 노출로 인해 열화된 Ni-rich NCM811(LiNi₀.₈Co₀.₁Mn₀.₁O₂) 양극 소재의 계면 저항 증가 및 전기화학적 성능 저하 문제를 해결하기 위해, 물리적 열처리 방법을 제안하였다. NCM811 양극 소재는 대기 중 수분 및 이산화탄소와의 반응에 의해 표면에 불순물이 형성되기 쉬우며, 이는 고체전해질과의 계면 저항을 증가시켜 전고 체전지 시스템에서의 성능 저하를 초래한다. 이러한 문제를 해결하기 위해, 열화된 NCM811 양극 소재를 O₂ 분위기 에서 열처리하여 표면의 불순물을 효과적으로 제거하고 양극 표면의 전도성을 향상시킴으로써, 양극-고체전해질 간의 계면 저항을 현저히 감소시키는 결과를 얻었다. SEM, XRD, ICP 분석을 통해 열화된 NCM811 양극 소재의 표면 특성 변화를 분석하였으며, 열처리 후 NCM811 소재의 계면 특성이 개선됨에 따라 전기화학적 성능 또한 상용 NCM811 소재와 유사한 수준으로 회복되는 것을 확인하였다. 특히, O₂ 분위기의 물리적 열처리 방법은 Ni-rich NCM811 양극 소재의 열화를 효과적으로 억제하고 고체전해질과의 계면 접촉을 개선하여, 황화물계 전고체전지의 전기화학적 성능 을 획기적으로 향상시킬 수 있는 유망한 기술임을 입증하였다. 이러한 결과는 전고체전지 상용화를 위한 핵심 전략으 로 적용될 수 있을 것으로 기대된다.

온실가스 배출량을 최소화하기 위하여 가열 없이 생산이 가능한 상온 아스팔트 포장 공법도 2000년 초부터 개발되어 활용되고 있으 나, 기술적 한계로 인해 성능 확보가 어려워 대부분 기층용으로 활용중에 있다. 상온 아스팔트 혼합물은 유화아스팔트를 사용하는데 양생하는 동안 혼합물 내부에 있는 물이 증가됨에 따라 혼합물 내부의 높은 공극률이 발생하게 되어 포장의 성능을 확보하는데 한계 가 있다. 따라서 본 연구에서는 유화 아스팔트 내 아스팔트 고형분 함량을 증가시켜 물 함량을 최소화함으로서, 양생시간을 단축하고 낮은 공극률 확보를 통한 상온 아스팔트 혼합물의 성능의 변화를 평가하였다. 시험결과, 고형분 함량이 변화에 따라 공극률 및 간접인 장강도, 터프니스 물성이 변화가 나타났다. 하지만 고함량 고형분의 유화 아스팔트를 상온 아스팔트 혼합물에 적용하기 위해서는 최적 함수비 결정방식 및 양생방식 등에 대한 추가적인 연구가 필요한 것으로 나타났다.

Natural gas pyrolysis produces hydrogen and solid carbon at high temperatures in an oxygen-free environment. This study has evaluated the characteristics of solid carbon obtained from the pyrolysis of methane and natural gas by using molten tin (Sn) at 900–1000 °C. Material characterization outcomes revealed that solid carbon produced at 1000 °C has a spherical morphology. At this temperature, methane and natural gas pyrolysis have resulted in the arrangement of nanocrystalline carbon spheres with average sizes of 635 and 287 nm, respectively. Similarly, pyrolysis at 900 °C and 950 °C has yielded nanocrystalline carbon featuring diverse morphologies such as spheres, fibrous, and irregularly shaped particles. Thermogravimetric analysis revealed that solid carbon products obtained from methane and natural gas pyrolysis at 1000 °C have higher thermal stability compared to commercial carbon black N991. Surface area analysis has indicated that solid carbon from natural gas pyrolysis at 1000 °C has 4.3- and 5.3-times higher surface area compared to the commercial carbon black N991 sample and graphite flakes, respectively. These findings offered insights into optimizing pyrolysis reactor design and operation to generate valuable solid carbon by-products while maximizing hydrogen production.

All-solid-state lithium batteries (ASSLBs) are receiving attention as a prospective next-generation secondary battery technology that can reduce the risk of commercial lithium-ion batteries by replacing flammable organic liquid electrolytes with non-flammable solid electrolytes. The practical application of ASSLBs requires developing robust solid electrolytes that possess ionic conductivity at room temperature on a par with that of organic liquids. These solid electrolytes must also be thermally and chemically stable, as well as compatible with electrode materials. Inorganic solid electrolytes, including oxide and sulfide-based compounds, are being studied as promising future candidates for ASSLBs due to their higher ionic conductivity and thermal stability than polymer electrolytes. Here, we present the challenges currently facing the development of oxide and sulfide-based solid electrolytes, as well as the research efforts underway aiming to resolve these challenges.

고형가유두상종양은 수술 후 95% 이상의 환자에서 완전 절제가 이루어지며 대부분 완치되는 것으로 알려져 있다. 하지만, 절제 후 재발하는 경우가 7% 정도로 보고되고 있어 수술 후에도 지속적인 추적 관찰이 필요하다. 또한, 췌장 내에서 다발성으로 종괴가 발생할 수 있으므로, 췌장 종괴에 대한 수술적 절제를 시행할 경우 수술 전에 반드시 영상 검사와 내시경 초음파 등을 통한 충분한 평가가 선행되어야 한다. 본 증례 보고에서는 건강 검진으로 발견된 췌장 종괴에 대해 추 적 관 찰 을 시 행 하 다 가 크 기 가 증 가 해 서 수 술 적 절제(췌장미부절제술)를 시행하였다. 수술 후 병리 결과 고형가유두상종양과 신경내분비종양이 동시에 진단되었다. 수술 12개월 후 남아 있는 췌장 두부에 종괴가 재발한 소견을 보여 추가적인 수술적 절제(전췌장절제술)을 시행 받았고, 수술 후 병리 결과 악성 고형가유두상종양으로 진단되었다. 현재까지 고형가유두상종양과 신경내분비종양이 동시에 발생하는 증례에 대한 보고가 많지 않고 국내에서는 아직 보고가 없다. 이에 수술 후 고형가유두상종양과 비기능성 신경내분비종양이 진단된 증례를 보고하는 바이다.

The dissolved air at the bottom layer of the deep aeration tank transforms into fine gas bubbles within the MLSS (Mixed Liquor Suspended Solid) floc when exposed to the atmosphere. MLSS floc flotation occurs when MLSS from the deep aeration tank enters the secondary clarifier for solid-liquid separation, as dissolved air becomes fine air within the MLSS floc. The floated MLSS floc causes a high SS (Suspended Solid) concentration in the secondary effluent. The fine air bubbles within the MLSS floc must be removed to achieve stable sedimentation in the secondary clarifier. Fine bubbles within the MLSS floc can be removed by air sparging. The settleability of MLSS was measured by sludge volume indexes (SVIs) after air sparging MLSS taken at the end of the deep aeration tank. MLSS settling tests were performed at MLSS heights of 200, 300, 400, and 500 mm, and compressed air was fed at the bottom of the settling column with air flow rates of 100, 300, and 500 ml/min at each MLSS height, respectively. Also, at each height and air flow rate, air was sparged for 3, 5, and 7 minutes, respectively. SVI was determined for each height, air flow rate, and sparging time, respectively. Experimental results showed that a 300 mm MLSS height, 300 ml/min air flow rate, and 3 minutes of sparging time were the least conditions to achieve less than 120 ml/g of SVI, which was the criterion for good MLSS settling in the secondary clarifier.

The structure and magnetic properties of composite powders prepared by ball milling a mixture of Fe2O3 ‧ (0.4-1.0)Fe were investigated. Hysteresis loops and differential scanning calorimetry (DSC) curves are used to characterize the materials and to examine the effect of the solid state reaction induced by ball milling. The results showed that a solid state reaction in Fe2O3 ‧ (0.4-1.0)Fe clearly proceeds after only 1 h of ball milling. The system is characterized by a positive reaction heat of +2.23 kcal/mole. The diffraction lines related to Fe2O3 and Fe disappeared after 1 h of ball milling and, instead, diffraction lines of the intermediate phase of Fe3O4 plus FeO formed. The magnetization and coercivity of the Fe2O3 ‧ 0.8Fe powders were changed by the solid state reaction process of Fe2O3 by Fe during ball milling. The coercivity of the Fe2O3 ‧ 0.8Fe powders increased with increasing milling time and reached a maximum value of 340 Oe after 5 h of ball milling. This indicates the grain size of Fe3O4 was clearly reduced during ball milling. The magnetic properties of the annealed powders depend on the amount of magnetic Fe and Fe3O4 phases.

This study focused on improving the solubility of silodosin, a drug poorly soluble in water, by utilizing solid dispersions. Three types of dispersions were examined and compared against the drug powder: surface-attached (SA), solvent-wetted (SW), and solvent-evaporated (SE). Polyvinyl alcohol (PVA) was identified as the most effective polymer in enhancing solubility. These dispersions were prepared using spray-drying techniques with silodosin and PVA as the polymer, employing solvents such as water, ethanol, and a water-acetone mix. The physicochemical properties and solubility of the dispersions were evaluated. The surface-attached dispersions featured the polymer on a crystalline drug surface, the solvent-wetted dispersions had the amorphous drug on the polymer, and the solvent-evaporated dispersions produced nearly round particles with both components amorphous. Testing revealed that the order of improved solubility was: solvent-evaporated, solvent-wetted, and surface-attached. The results demonstrated that the preparation method of the solid dispersions significantly impacted their physicochemical properties and solubility enhancement.

This review explores the potential of pillared bentonite materials as solid acid catalysts for synthesizing diethyl ether, a promising renewable energy source. Diethyl ether offers numerous environmental benefits over fossil fuels, such as lower emissions of nitrogen oxides (NOx) and carbon oxides (COx) gases and enhanced fuel properties, like high volatility and low flash point. Generally, the synthesis of diethyl ether employs homogeneous acid catalysts, which pose environmental impacts and operational challenges. This review discusses bentonite, a naturally occurring alumina silicate, as a heterogeneous acid catalyst due to its significant cation exchange capacity, porosity, and ability to undergo modifications such as pillarization. Pillarization involves intercalating polyhydroxy cations into the bentonite structure, enhancing surface area, acidity, and thermal stability. Despite the potential advantages, challenges remain in optimizing the yield and selectivity of diethyl ether production using pillared bentonite. The review highlights the need for further research using various metal oxides in the pillarization process to enhance surface properties and acidity characteristics, thereby improving the catalytic performance of bentonite for the synthesis of diethyl ether. This development could lead to more efficient, environmentally friendly synthesis processes, aligning with sustainable energy goals.