• 한국세라믹학회지
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• 제40권5호
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• pp.441-446
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• 2003

ZnO 미세 분말을 sol-gel법으로 제조하였다. Gel분말의 형상은 하소 열 처리 온도에 따라 판상, 침상,그리고 구형으로 변화하였고, $700^{\circ}C$ 이하 하소 온도에서는 온도에 따른 입자 성장 속도가 낮았지만, $700^{\circ}C$ 이상의 온도부터 급격한 입자 성장 속도를 나타내었다. 입자 사이즈가 커질수록 결정화 정도는 더 커졌고, gel분말의 유기 화합물들은 30$0^{\circ}C$ 이하 온도에서 휘발되었다. 열 처리 온도에 따른 ZnO 분말은 S자형(sigmoidal shape)의 전기전도성 거동을 보였고, gel분말의 열처리 온도가 감소할수록 일정한 전도성이 일정한 온도 구간이 좁게(narrow) 나타났다. 최적의 CO 기체 센싱 특성은 50$0^{\circ}C$의 하소 열처리한 시편에서 나타났고, 열처리 온도가 올라갈수록 센싱 특성은 감소하였다.

• 한국수소및신에너지학회논문집
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• 제27권1호
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• pp.95-105
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• 2016

Spray-dried NiO-based oxygen carriers developed for chemical looping combustion required high calcination temperatures above $1300^{\circ}C$ to obtain high mechanical strength applicable to circulating fluidized-bed process. In this study, the effect of CBB ($CaO{\cdot}BaO{\cdot}B_2O_3$) addition, as a binder, on the physical properties and oxygen transfer reactivity of spray-dried NiO-based oxygen carriers was investigated. CBB addition resulted in several positive effects such as reduction of calcination temperature and increase in oxygen transfer capacity and porosity. However, oxygen transfer rate was considerably decreased. This was more apparent when a higher amount of CBB was added and MgO was added together. From the experimental results, it is concluded that CBB added NiO-based oxygen carriers are not suitable for chemical looping combustion and a new method to reduce calcination temperature while maintaining high oxygen transfer rate of NiO-based oxygen carriers should be found out.

• 센서학회지
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• 제30권6호
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• pp.369-375
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• 2021

In this study, heterogeneous ZnO/CNTF composites were developed to improve the NO₂-sensing response, facilitated by the self-heating property. Highly conductive and mechanically stable CNTFs were prepared by a wet-spinning process assisted by the liquid crystal (LC) behavior of CNTs. Metal-organic frameworks (MOFs) of ZIF-8 were precipitated on the surface of the CNTF (ZIF-8/CNTF) via one-pot synthesis in solution. The subsequent calcination process resulted in the formation of the ZnO/CNTF composites. The calcination temperatures were controlled at 400, 500, and 600 ℃ in an N₂ atmosphere to confirm the evolution of the microstructures and NO₂-sensing properties. Gas sensor characterization was performed at 100 ℃ by applying a DC voltage to induce Joule heating through the CNTF. The results revealed that the ZnO/CNTF composite after calcination at 500 ℃ (ZnO/CNTF-500) exhibited an improved response (R_air/R_gas = 1.086) toward 20 ppm NO₂ as compared to the pristine CNTF (R_air/R_gas = 1.063). Selective NO₂-sensing properties were demonstrated with negligible responses toward interfering gas species such as H₂S, NH₃, CO, and toluene. Our approach for the synthesis of MOF-driven ZnO/CNTF composites can provide a new strategy for the fabrication of wearable gas sensors integrated with textile materials.

• 한국세라믹학회지
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• 제55권6호
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• pp.618-624
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• 2018

We developed a mass production method that simultaneously controls the phase transformation and crystal size of $TiO_2$ coatings on multiwalled carbon nanotubes (MWCNTs). Initially, MWCNTs were successfully coated with amorphous 15-20-nm-thick $TiO_2$ by an in-situ sol-gel method. As the calcination temperature increased in both air and argon atmospheres, the amorphous $TiO_2$ was gradually transformed into the fully anatase phase at approximately $600^{\circ}C$, a mixture of the anatase and rutile phases at approximately $700^{\circ}C$, and the fully rutile phase above approximately $800^{\circ}C$. The crystal size increased with increasing calcination temperature. Moreover, above $600^{\circ}C$, the size of crystals formed in air was approximately twice that of crystals formed in argon. The reason is thought to be that MWCNTs, which continuously supported the stresses associated with the reconstructive phase transformation, disappeared owing to complete oxidation in air at these high temperatures.

• Journal of Ceramic Processing Research
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• 제20권1호
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• pp.80-83
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• 2019

The Mn4+-activated Li2ZnSn2O6 (LZSO:Mn4+) red phosphors were synthesized by the solid-state reaction at temperatures of 1100-1400 ℃ in air. The synthesized LZSO:Mn4+ phosphors were confirmed to have a single hexagonal LZSO phase without the presence of any secondary phase formed by the Mn4+ addition. With near UV and blue excitation, the LZSO:Mn4+ phosphors exhibited a double band deep-red emission peaked at ~658 nm and ~673 nm due to the 2E → 4A2 transition of Mn4+ ion. PL emission intensity showed a strong dependence on the Mn4+ doping concentration and the 0.3 mol% Mn4+-doped LZSO phosphor produced the strongest PL emission intensity. Photoluminescence emission intensity was also found to be dependent on the calcination temperature and the optimal calcination temperature for the LZSO:Mn4+ phosphors was determined to be 1200 ℃. Dynamic light scattering (DLS) and field-effect scanning electron microscopy (FE-SEM) analysis revealed that the 0.3 mol% Mn4+-doped LZSO phosphor particles have an irregularly round shape and an average particle size of ~1.46 ㎛.

• 한국세라믹학회지
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• 제32권3호
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• pp.295-304
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• 1995

Stabilization of the perovskite phase and sequence of reactions occuring during calcination were studied with solid solutions formed between Pb(Zn1/3Nb2/3)O3 and Pb(Fe1/2Nb1/2)O3. In the PZN-PFN composition of equal molar ratio, rhombohedral type pyrochlore phase (Pb2Nb2O7) and PbO-rich distorted cubic type pyrochlore phase (Pb3Nb2O8) were coexisted as intermediate phases at temperatures below 85$0^{\circ}C$, and these phases transformed to a stable cubic type pyrochlore phase, Pb3Nb4O13 solid solution and a perovskite solid solution at temperatures above 85$0^{\circ}C$. The major stable phase as increasing sintering temperatures was a perovskite phase in this binary system and prominent suppression of the pyrochlore phase was achieved by substituting Zn2+ with Fe3+ or by increasing sintering temperature. The composition containing 20mol% PZN possessed the best dielectric properties, and the dissipation factor was lower than 5% in all compositions.

• 한국세라믹학회지
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• 제49권6호
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• pp.601-607
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• 2012

The alkali-activation reaction of two types of typical kaolin calcined at various lower temperatures was investigated at room temperature and at elevated temperatures. For the assessment of the reactivity, the temperature increase and the setting time of pastes prepared with calcined kaolin and sodium/potassium hydroxide solution were measured. Unlike raw kaolin, calcined kaolin samples prepared at various temperature showed an alkali-activation reaction according to the different aspects of the changes in the mineral phases. The reactivity with alkaline solutions was exceedingly activated in the samples calcined at $600-650^{\circ}C$, but the reactivity gradually decreased as the temperature increased in a higher temperature range, most likely due to the changes in the crystal structure of the dehydrated kaolin. The activation effect of the calcination treatment was achieved at reaction temperatures that exceeded $60^{\circ}C$ and was enhanced as the temperature increased. The reactivity of the calcined kaolin with an alkaline solution was more enhanced with the solution of a higher concentration and with a solution prepared from sodium hydroxide rather than potassium hydroxide.

• Korean Chemical Engineering Research
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• 제43권1호
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• pp.140-145
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• 2005

본 연구에서는 주 반응물질로 CuO를 사용하고, $Fe_2O_3$의 함량을 7.5 wt%, 15 wt%, 22.5 wt%로 변화시키고, 지지체 $SiO_2$의 함량을 25 wt%로 고정하여 흡수제를 제조하였다. 특히 소성온도의 변화에 따른 흡수제의 탈황성능의 변화를 조사하기 위하여, 흡수제의 소성 온도를 700, 900 그리고 $1,100^{\circ}C$로 달리하여 흡수제를 제조하였다. 제저된 흡수제는 GC/소형반응기를 이용하여 사이클 실험을 하였으며, 이때 흡수제의 황화온도는 $500^{\circ}C$, 재생온도는 $700^{\circ}C$로 하였다. 반응 전후의 XRD 분석을 통하여 화합물의 형태를 확인하였으며, BET 분석을 통하여 소성온도의 변화에 따른 흡수제의 표면적 변화를 조사하였다. 또한, 장기사이클에서 $700^{\circ}C$에서 소성된 CFS3 흡수제(CuO : $Fe_2O_3$ : $SiO_2$=52.5 wt% : 22.5 wt% : 25 wt%)의 $H_2O$의 유/무에 따른 탈황성능의 변화를 확인하였다. 그 결과 소성온도에 따른 비표면적의 변화는 크게 나타나지 않았다. 또한, 장기사이클에서 $H_2O$에 의한 탈황성능의 저하를 확인할 수 있었다. 특히 $1,100^{\circ}C$에서 소성된 CFS1 흡수제(CuO : $Fe_2O_3$ : $SiO_2$=67.5 wt% : 7.5 wt% : 25 wt%)의 경우에는 $H_2O$가 존재함에도 불구하고, 100 사이클이 지난 후에도 흡수제 100 g당 10 g의 황을 제거할 수 있는 탈황성능을 보였다.

• 청정기술
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• 제26권4호
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• pp.286-292
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• 2020

본 연구는 Cu/CeO2-X 촉매의 저온 CO 산화 활성에 미치는 영향을 촉매의 구조적 특성, 반응 특성을 통해 확인하였다. 사용된 촉매는 습윤 함침법으로 제조되었으며, 각기 다른 소성온도(300~600 ℃)에서 형성된 CeO2 (지지체)를 이용하여 Cu (활성금속)를 담지함으로써 Cu/CeO2-X 촉매를 제조하였다. 제조된 Cu/CeO2-X 촉매는 저온 CO 산화 활성을 평가하였다. 125 ℃에서 Cu/CeO2_300 촉매는 90% 이상의 활성을 나타냈으며, CeO2의 소성온도가 증가됨에 따라 활성이 점차 감소하여, Cu/CeO2_600 촉매는 65%를 나타냈다. 다음으로 촉매의 물리/화학적 특성을 Raman, BET, XRD, H2-TPR, XPS 분석으로 확인하였다. XPS 분석 결과, CeO2-X의 소성온도가 낮을 수록 불안정한 Ce3+ 종(비 화학양론 종) 비율이 증가하였다. 증가된 Ce3+종은 Cu와 결합함으로 써 치환결합을 형성하였으며 Raman 분석의 CeO2 peak 변화와 H2-TPR 분석의 치환결합 구조의 환원 peak를 통해 확인하였다. 결과적으로 Cu와 CeO2의 치환 결합 형성은 촉매의 redox 특성 및 저온 CO 산화 활성을 증진시켰다고 판단된다.

• 한국결정성장학회지
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• 제22권4호
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• pp.194-199
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• 2012

스피넬 구조로 이루어진 $LiMn_2O_4$에서 Mn의 일부분을 Ni로 치환한 $LiMn_{1.5}Ni_{0.5}O_4$은 4.7 V 전압 영역에서 높은 방전 용량 및 우수한 충 방전 사이클 특성을 가진다. 본 연구에서는 착체중합법을 이용하여 $LiMn_{1.5}Ni_{0.5}O_4$를 합성하였다. Citric acid : metal의 몰비(5 : 1, 10 : 1, 15 : 1, 30 : 1) 및 하소 온도($500{\sim}900^{\circ}C$) 변화에 따라 합성된 $LiMn_{1.5}Ni_{0.5}O_4$ 분말의 특성을 조사하였다. 합성된 분말의 XRD 분석을 통해 저온($500^{\circ}C$) 및 고온($900^{\circ}C$) 영역에서 모두 단일상인 $LiMn_{1.5}Ni_{0.5}O_4$ 결정상을 관찰할 수 있었고, 하소 온도가 증가함에 따라 결정화 및 결정자 크기도 함께 증가하였다. 합성된 $LiMn_{1.5}Ni_{0.5}O_4$ 분말의 형상 및 비표면적 분석 결과, 저온영역에서는 CA 몰비가 증가할수록 입자사이즈는 감소하고 비표면적은 증가하는 것을 확인할 수 있었다. 반면에 고온영역에서는 온도 증가에 따른 입자 성장에너지가 CA 몰비 증가에 따른 입자 사이즈 감소 및 비표면적 증가 효과를 감소시키는 것을 관찰하였다.