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.

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.

This paper reports an enhanced strategy for improving the mechanical flexibility and ionic kinetic properties of a double network hydrogel based on Co2+- coordination assistance. The modified double-network hydrogel was obtained by using acrylic acid and N, N-dimethylacrylamide as monomers, adding cross-linking agents and 3D nitrogen-doped graphenes. The tensile fracture rate of the modified hydrogel was 1925% and its tensile strength was 1696 kPa. In addition, the hydrogel exhibited excellent ionic dynamics, and its application to an all-solid-state supercapacitor was able to achieve a specific capacitance of up to 182.8 F g− 1. The supercapacitor exhibited an energy density of 34.2 Wh kg− 1, even when operating at a power density of 5 kW kg− 1, highlighting its significant potential for practical applications.

In this study, NASICON-type Li1+XGaXTi2-X(PO4)3 (x = 0.1, 0.3 and 0.4) solid-state electrolytes for all-solid-state batteries were synthesized through the sol-gel method. In addition, the influence on the ion conductivity of solid-state electrolytes when partially substituted for Ti4+ (0.61Å) site to Ga3+ (0.62Å) of trivalent cations was investigated. The obtained precursor was heat treated at 450 °C, and a single crystalline phase of Li1+XGaXTi2-X(PO4)3 systems was obtained at a calcination temperature above 650 °C. Additionally, the calcinated powders were pelletized and sintered at temperatures from 800 °C to 1,000 °C at 100 °C intervals. The synthesized powder and sintered bodies of Li1+XGaXTi2-X(PO4)3 were characterized using TGDTA, XRD, XPS and FE-SEM. The ionic conduction properties as solid-state electrolytes were investigated by AC impedance. As a result, Li1+XGaXTi2-X(PO4)3 was successfully produced in all cases. However, a GaPO4 impurity was formed due to the high sintering temperatures and high Ga content. The crystallinity of Li1+XGaXTi2-X(PO4)3 increased with the sintering temperature as evidenced by FE-SEM observations, which demonstrated that the edges of the larger cube-shaped grains become sharper with increases in the sintering temperature. In samples with high sintering temperatures at 1,000 °C and high Ga content above 0.3, coarsening of grains occurred. This resulted in the formation of many grain boundaries, leading to low sinterability. These two factors, the impurity and grain boundary, have an enormous impact on the properties of Li1+XGaXTi2-X(PO4)3. The Li1.3Ga0.3 Ti1.7(PO4)3 pellet sintered at 900 °C was denser than those sintered at other conditions, showing the highest total ion conductivity of 7.66 × 10-5 S/cm at room temperature. The total activation energy of Li-ion transport for the Li1.3Ga0.3Ti1.7(PO4)3 solidstate electrolyte was estimated to be as low as 0.36 eV. Although the Li1+XGaXTi2-X(PO4)3 sintered at 1,000 °C had a relatively high apparent density, it had less total ionic conductivity due to an increase in the grain-boundary resistance with coarse grains.

This study aimed to provide an accurate estimate of sodium intake from jangajji by examining the changes in sodium content according to the type of jangajji and the length of storage period, specifically differentiating between the solid ingredients and the seasoning liquid. It focused on six types of jangajji: chili pepper, perilla leaf, onion, radish, garlic scape, and cucumber. The sodium content in the solid ingredients and the seasoning was measured using a salinometer and ICP-AES. The results indicated that across all types of jangajji, the seasoning liquid consistently contained significantly higher levels of sodium than the solid ingredients. When comparing the sodium content measured by ICP-AES with that from a salinometer, the salinometer readings were significantly lower for both the solid ingredients and the seasoning liquid in all types of jangajji. Additionally, when comparing the sodium content of the solid ingredients with that listed in the nation’s representative nutritional databases, a substantial discrepancy was noted, with some cases potentially overstating the actual sodium intake from jangajji. Overall, this study suggests that an urgent review should be conducted to identify and resolve the causes of such discrepancies and accurately estimate the actual sodium intake from jangajji.

Paecilomyces tenuipes (P. tenuipes) is a fungus cultivated artificially by South Korean researchers, utilizing rice bran as its substrate. The increased demand for this fungus has not been met with successful cultivation methods for fruiting body production in natural environments. Therefore, we tested the effect on the growth of P. tenuipes using a Solid media based on pests. In this results, the Solid media based on M.alternatus was effective in increasing the growth of P. tenuipes and the content of cordycepin. Moreover, we confirmed the conditions for manufacturing a Solid media based on M.alternatus for P. tenuipes growth. We suggested that the growth-promoting compounds offers valuable insights for optimizing fungal cultivation conditions, thereby enhancing productivity and contributing to a broader understanding of fungal physiology in varying nutritional environments.

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.

Recently, separation membranes have been applied to fields such as water supply, sewage treatment, gray water reuse, and air pollution control. Chemical cleaning technology is attracting attention among the methods of reusing these expensive separation membranes. It was found that the separation membrane could be regenerated using chemical cleaning. Specifically, it was found that the use time of the separation membranes regenerated by chemical cleaning was sustainable for more than 1,700 hours. Additionally, it was found that the flux recovery ratio after chemical cleaning was maintained at least 60%. In addition, the flux recovery ratio of HYDREX 4710, an organic membrane cleaner, and 4703, an inorganic membrane cleaner, was 76% and 62%, respectively, showing the highest flux recovery ratio among the chemicals used. Considering that the target raw water of this study is biological secondary treatment water, it was suggested that chemical cleaning could be actively used to regenerate separation membranes in future water treatment.

본 실험에서는 외인성 효소 첨가제 및 혼합 세균 배양을 통한 고상발효(Solid-state fermentation, SSF)가 채종박(Rapeseed meal, RSM)의 체외건물소화율(In vitro dry matter digestibility, IVDMD) 및 단쇄지방산(Short chain fatty acid) 생성에 미치는 영향을 조사하기 위해 수행되었다. 외인성 효소 칵테일(첨가 및 미첨가) 및 RSM에 대한 SSF(발효 및 비발효)를 나타내는 2 x 2 요인 설계가 적용되었다. 3-step 돼지 소화율 모델을 적용하여 채종박의 건물 소화율을 분석하였으며, 72시간 대장발효 후 상층액을 수집하여 단쇄지방산 생성량을 분석한 후 칼로리 단위로 변환하여 가소화에너지 소화율을 분석하였다. 소장 (IVDMDh) 및 전장 (IVDMDt) 건물소화율에서는 고상발효된 채종박이 더 높게 나타났다 (각각 p < 0.01). 마찬가지로, 외인성 효소 첨가제 처리구에서 채종박의 소장 소화율(IVDMDh)이 증가하는 경향을 나타냈다(p = 0.06). Acetic acid 및 butyric acid의 생산은 대조구에 비해 고상발효 처리 시 유의하게 더 생산되었으며 (각각 p < 0.01), 이는 총 단쇄지방산의 생산 증가 경향을 나타냈다(p = 0.09). 에너지 소화율에서는 채종박의 고상발효 및 외인성 효소제 첨가가 유의적으로 높게 나타났다 ( p < 0.01). 그러므로 채종박의 고상발효 처리는 단백질 이용성을 비롯한 영양적 가치를 향상시키는데 효과적이라고 사료된다.

This study aimed to develop a solid self-nanoemulsifying drug delivery system (solid-SNEDDS) to enhance the formulation of ketoconazole (KTZ), a BCS Class II drug with poor solubility. Ketoconazole, which is insoluble above pH 3, requires solubilization for effective delivery. This SNEDDS comprises oil, surfactant, and co-surfactant, which spontaneously emulsify in the gastrointestinal tract environment to form nanoemulsions with droplet sizes less than 100 nm. The optimal SNE-vehicle composition of oleic acid, TPGS, and PEG 400 at a 10:80:10 weight ratio was determined based on the smallest droplet size achieved. This composition was used to prepare liquid SNEDDS containing ketoconazole. The droplet size and polydispersity index (PDI) of the resulting liquid SNEDDS were analyzed. Subsequently, solid-SNEDDS was fabricated using a spray-drying method with solidifying carriers such as silicon dioxide, crospovidone, and magnesium alumetasilicate. The physicochemical properties of the solid-SNEDDS were characterized by scanning electron microscopy and powder X-ray diffraction, and its solubility, droplet size, and PDI were evaluated. In particular, the solid-SNEDDS containing ketoconazole and crospovidone in a 2:1 weight ratio exhibited significantly enhanced solubility, highlighting its potential for improved medication adherence and dissolution rates.