In this study, we explored the potential of the Maillard reaction-based time-temperature indicators (TTI) as a tool for predicting and visualizing moisture variations during high-temperature drying. Using activation energy analysis, we found that the Maillard reaction-based TTI could not only visualize but also predict changes in moisture contents during high-temperature drying of 60-80oC. The color changes of the Maillard reaction solutions were distinct enough to be discerned with the naked eye, transitioning from colorless to black via the shift of yellow, light brown, brown, and dark brown. The dynamic characteristics for the color change in the Maillard reaction solutions and the moisture changes in the drying of thin-layer apples could be expressed with high suitability using a logistic model. This suggests that the Maillard reaction-based TTI can potentially be a practical and reliable tool for predicting the moisture changes for the high-temperature drying of thin-layer apples, offering a promising avenue for future research and applications.

아산화질소(N2O, Nitrous Oxide)는 6대 온실가스 중 하나로 대기 중에서 적외선을 흡수하여 온실효과를 유발하는 것으로 알려져 있다. 특히 지구온난화지수(GWP)는 CO2에 비해 310배 높아 국내뿐만 아니라 전 세계적으로 이슈화되고 있으며, 그에 따른 강력한 환경 규 제 강화법들이 발의되고 있다. N2O 저감 기술에는 물리적인 방식에 따라 농축회수, 촉매분해, 그리고 열분해로 구분할 수 있는데, 본 연구 에서는 그 중 가장 효과적인 열분해 처리방식에 대해 논의하고자 일반적인 연소 조건 내 고온 열분해 방식을 이용하여 비용 저감과 함께 질소산화물을 저감시키는 온도 조건 및 반응 시간에 대한 정보를 제공하고자 한다. 열분해 조건으로 선정된 고온 영역은 1073 K부터 1373 K 까지 100 K 간격을 두고 계산을 수행하였다. 1073 K과 1173 K의 온도조건에 경우, N2O 저감율과 일산화질소 농도가 체류시간에 따라 비례관 계를 이루는 것이 관측되었으며, 1273 K에 경우, 체류시간이 증가함에 따라 발생되는 역반응으로 인해 N2O 저감율이 감소되는 것이 관측되 었다. 특히 1373 K에 경우, 모든 체류시간에 대해 정반응과 역반응이 화학 평형상태에 도달하여 N2O 저감에 대한 반응진행율이 오히려 감 소하는 것으로 확인되었다.

To solve the common problems of concrete preparation in low-temperature environments, calcium formate (C2H2O4Ca), anhydrous sodium sulfate (Na2SO4), triethanolamine (C6H15O3N), calcium bromide (CaBr2), and triisopropanolamine (C9H21NO3) are selected as early strength agents and mixed with C40 concrete in different dosages under low-temperature environments of 5 oC and 10 oC to develop a high-efficiency low-temperature compound early strength agent based on the effect of single-doped early strength agents. The effects of the compound early strength agent on the early strength of the concrete, the cement paste setting time, and cement fluidity at 5 oC and 10 oC are investigated, and the corresponding reaction mechanism is discussed from the perspective of micro-products. The best compound early strength agent ratio is found to be 2% of calcium formate + 0.08 % of TEA (C6H15O3N). The compound early strength agent effectively promotes the formation of hydration products, such as Ca(OH)2 and C-S-H gel. In comparison with the control group, the strength of the concrete cured for 18 h, 1 d, 3 d, and 7 d under simulated natural conditions at 5 oC increases by 700%, 540%, 11.4 % and 10 %, respectively, whereas at 10 oC, the corresponding values are 991%, 400%, 19.6 % and 11 %, respectively. The strength of the concrete at each age is close to the normal temperature standard of the curing strength. The addition of the compound early strength agent causes a reduction in cement fluidity and initial and final setting times, and also yields a good effect on the porosity of the early concrete.

SiC is a material with excellent strength, heat resistance, and corrosion resistance. It is generally used as a material for SiC invertors, semiconductor susceptors, edge rings, MOCVD susceptors, and mechanical bearings. Recently, SiC single crystals for LED are expected to be a new market application. In addition, SiC is also used as a heating element applied directly to electrical energy. Research in this study has focused on the manufacture of heating elements that can raise the temperature in a short time by irradiating SiC-I2 with microwaves with polarization difference, instead of applying electric energy directly to increase the convenience and efficiency. In this experiment, Polydimethylsilane (PDMS) with 1,2 wt% of iodine is synthesized under high temperature and pressure using an autoclave. The synthesized Polycarbosilane (PCS) is heat treated in an argon gas atmosphere after curing process. The experimental results obtain resonance peaks using FT-IR and UV-Visible, and the crystal structure is measured by XRD. Also, the heat-generating characteristics are determined in the frequency band of 2.45 GHz after heat treatment in an air atmosphere furnace.

HMDS를 리간드로 하는 PbS 콜로이드 양자점 물질을 만들었다. 양자점 물질의 전자광학적 밴드갭 의 크기는 UV/VIS과 IR 스펙트럼을 측정하여 알아낼 수 있었다. PbS 콜로이드 양자점 물질을 합성할 때 만 들어 지는 입자의 크기를 조절하기 위하여 반응온도를 100~160℃ 사이에서 변화시켰으며 이에 따라 흡수스펙 트럼의 피크위치에 변화가 있음을 관찰할 수 있었다. HOMO와 LUMO 사이에 해당하는 밴드갭은 800~1200nm 에서의 피크 위치변화를 보였으며 피크위치의 변화량은 반응물질을 섞었을 때 반응용기 온도에 선형적으로 변화하는 관계를 얻을 수 있었다.

The study analyzed performance assessment factors of odor sensors from 4 different manufacturers, including minimum detection limit, humidity stability and temperature stability. In the minimum detection limit assessment, only one electrochemical gas sensor was able to detect ammonia and hydrogen sulfide at the concentration of 5 ppb. The standard deviation ratio was over 10%, and it increased as humidity rose. The range of temperatures in which the electrochemical and photoionization gas sensors could function well was between 25oC and 40oC, and the sensor output values were unstable at low temperatures. Regarding the temperature stability of the metal oxide semiconductor sensor for measuring complex odors, the sensor output values dropped considerably to 0~10oC, and were similar to the concentrations of odor gases generated at 25oC. The results of the test of odor sensor outputs after temperature and humidity pre-treatment revealed that the respective stable output values at 50% humidity and 25oC were similar to the concentrations of manufactured odors. In terms of temperature and humidity stability of the NH3, H2S and Complex odor sensors, all target substances had stable output values at 25~40oC and 50~65% relative humidity, and unstable values at low temperatures and high humidity. Therefore, implementing pretreatment systems including temperature and humidity correction (25~40oC, 50~65% RH) is necessary for the stable use of odor sensors.

Compared with bulk material, quantum dots have received increasing attention due to their fascinating physical properties, including optical and electronic properties, which are due to the quantum confinement effect. Especially, Luminescent CdSe quantum dots have been highly investigated due to their tunable size-dependent photoluminescence across the visible spectrum. They are of great interest for technical applications such as light-emitting devices, lasers, and fluorescent labels. In particular, quantum dot-based light-emitting diodes emit high luminance. Quantum dots have very high luminescence properties because of their absorption coefficient and quantum efficiency, which are higher than those of typical dyes. CdSe quantum dots were synthesized as a function of the synthesis time and synthesis temperature. The photoluminescence properties were found strongly to depend on the reaction time and the temperature due to the core size changing. It was also observed that the photoluminescence intensity is decreased with the synthesis time due to the temperature dependence of the band gap. The wavelength of the synthesized quantum dots was about 550-700 nm and the intensity of the photoluminescence increased about 22~70%. After the CdSe quantum dots were synthesized, the particles were found to have grown until reaching a saturated concentration as time increased. Red shift occurred because of the particle growth. The microstructure and phase developments were measured by transmission electron microscopy (TEM) and X-ray diffractometry (XRD), respectively.

A formation of aluminum hydroxide by hydrolysis reaction in the water has been studied by using nano aluminum powder fabricated by pulsed wire evaporation(PWE) method. The hydroxide type and morphology depending on temperature and pH were examined by structural analysis. The Boehmite(. or AIO(OH)) was predominantly formed in high temperature region over 4, while the Bayerite(. or ) below of hydrolysis temperature. The Boehmite formation was preferred to the Bayerite in acidic solution in the same hydrolysis temperature. The slowly formed Bayerite phase showed facet crystalline structure, while the fast formed Boehmite was fine fiber with a large aspect ratio of several nm in diameter and several hundred nm in length, and with much larger specific surface area(SSA) than that of Bayerite. The highest SSA was about /g.

Pure tantalum powder has been produced by combining Na as a reducing agent, as feed material, KCl and KF as a diluent in a stainless steel(SUS) bomb, using the method of metallothermic reduction. The present study investigated the effect of the amount of the diluent and reaction temperature on the characteristics of tantalum powder in the production process. The temperature applied in this study and the amount of the additional reductant from +5% of the theoretical amount used for the reduction of the entire . The results showed that as the amount of the diluent increased, the reaction temperature became lower because the diluent prevented a temperature rise. Also, according to the mixture ratio of the feed materials and the diluent changed from 1 : 0.25 to 1 : 2, the particle size decreased from to and a particle size distribution which is below 325 mesh in fined powder increases from 71% to 83%. The average size of Tantalum powder, , was close to that of the commercial powders(). Also under this condition, impurities contained in the powder were within the range allowed for the commercial Ta powders.

니켈기 주조용 합금 738LC를 816˚C와 982˚C에서 크리프 파단 시험과 열간 노출시험을 통해 온도와 응력 변화에 따른 파단양상, 탄화물과 σ상의 석출 거동에 대해 조사하였다. 816˚C/440MPa에서는 크리프 파단양상이 전단변형에 의한 입내파괴를 나타내었으나, 982˚C/152MPa에서는 표면과 접하는 결정입계에서 입계산화에 의해 표면에너지의 감소로 균열이 나타나 진행되는 입계파괴가 나타났다. M(sub)23C(sub)6 탄화물이 816˚C에서는 주로 결정입계에서와 전단변형에 의한 입내균열을 따라 석출하였으나, 982˚C에서는 결정입계 뿐만 아니라 입내에서는 석출하였으며 석출양은 증가하였다. σ상은 Cr(sub)23C(sub)6 탄화물에서 핵생성 후 기지로 성장하며, 온도가 높고 응력이 주어지면 Cr(sub)23C(sub)6 탄화물의 양이 증가하여 σ상의 석출도 많아졌다.

This study was carried out to synthesis the zeolite using the bituminous coal fly ash emitted from power plant that occurs several environmental problems. In spite of fly ash has contained high content of SiO2 and Al2O3, it disposed mainly landfill. If the effective methods to recover the SiO2 and Al2O3 were developed, the fly ash could be utilized valuable raw materials. In this study, fly ash was used as raw material to synthesize the zeolite by pressurized hydrothermal reaction. Also, experimental parameters included temperature(70~110℃, and pressure(140~200 psi) of crystallization were investigated. The more crystallization pressure was increased, the more Zeolite 4A was synthesized at 70 and 90℃. Zeolite 4A of metastable phase tend to be transformed into sodalite of stable phase at 110℃.

본 연구는 티타늄과 활성탄소 원료분말을 반응밀링법에 의해 합성시, 밀링시간에 따른 Ti-TiC 복합재료의 미세조직과 기계적 성질에 미치는 TiC vol.% 및 열간압축성형온도의 영향에 관해 조사하였다. 티타늄과 활성 탄소 원료분말을 300시간 밀링 후 5μm이하의 미세한 구형의 Ti-TiC복합분말을 생성시킬 수 있었다. 반응밀링된 분말을 1000˚C이상에서 1시간동안 진공열간압축성형한 경우 이론밀도의 98%에 가까운 우수한 성형체를 얻었으며, TiC입자가 티타늄 기지 전반에 걸쳐 고르게 분산되어 Ti-TiC 복합재료의 기계적 특성을 향상시켰다. Ti-TiC복합재료의 고온안정성을 고찰하기 위해 600˚C등온열처리한 결과 80시간까지는 경도의 큰 변화없이 열적으로 안정하였다. Ti-20vol%TiC 복합재료를 700˚C에서 고온압축시험을 한 경우 330MPa의 높은 항복강도값을 나타내었다.

The structure of the scale formed on the surface of Fe - Cr - X alloys exposed to 1143K high sulfidation(Ps2 = 1.11×10-7 atm, Po2 = 3.11×10-20 atm) or sulfidation/oxidation((Ps2= 1.06×10-7 atm, (Po2 = 3.11×10-18 atm) environment has been observed and analysed using XRD, SEM/EDS. To investigate the possibility of protective film formed on the surface of the alloys, Aluminium, Nickel were selected as alloying elements. Thermodynamic phase stability diagram was used to predict the reaction path of scale formed on Fe - Cr - X alloys. Parabolic rate constant(Kp) value with 6wt% Al in Fe - 25Cr alloy decreased significantly compared with the Fe - 25Cr alloy without 6wt% Al. Since thin layer of defect free sulfide film, (Al, Cr)Sx, was formed at the alloy/scale interface. Fe - rich sulfide scale at outer layer and Cr - rich sulfide scale containing porosity at inner layer of Fe - 25Cr alloy have been observed. The reaction path for these scales could be predicted by the thermodynamic stability diagram.

상업적으로 HTS (High Temperature Shift reaction) 반응에서 사용되는 Fe2O3/Cr2O3 촉매는 사용 후 6가 크롬 (Cr6+)의 침출에 따른 환경적/인체적 문제를 일으킬 수 있는 잠재성을 가지고 있어 친환경 크롬-프리 촉매개발을 위한 연구가 활발히 진행되고 있다. 본 연구에서는 크롬을 사용하지 않고 우수한 성능을 나타낼 수 있는 Fe/Al, Fe/Al/Cu, 그리고, Fe/Al/Ni 촉매를 제조하고 성능을 비교 평가하였다. 단계함침법으로 금속산화물(Cu와 Ni)과 알루미늄이 함유된 Fe계 촉매를 제조하고 촉매반응장치를 이용하여 각 촉매의 활성을 분석하였다. 그 결과 Fe/Al/Cu 촉매는 가혹한 조건(COconc. = 38.2%; 천연가스 대비 약 5.7 배 높은 CO 농도)에서도 탁월한 성능(XCO = 84.3% at 400 ℃)을 나타내었다. 이 결과는 Fe/Al/Cu 촉매의 강한 환원력과 활성종인 Fe3O4의 높은 열적 안정성에 기인한 것으로 확인되었다. 또한 강한 소결 저항성을 가진 Fe/Al/Cu 촉매는 400°C에서 100시간 동안 뚜렷한 비활성화를 보이지 않아 높은 안정성을 지닌 것으로 확인되었다.