• 제목/요약/키워드: Calcination temperature

검색결과 548건 처리시간 0.023초

페롭스카이트 촉매의 제조와 메탄 산화에 응용 (Preparation of Perovskite Catalysts and Its Application to Methane Combustion)

  • 함현식;김규성;안성환;신기석;김송형;박홍수
    • 한국응용과학기술학회지
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    • 제24권1호
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    • pp.67-73
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    • 2007
  • Methane combustion over perovskite catalysts was investigated. For the preparation of catalysts, Co, Mn, Fe, and Ni were used as B-site components of the perovskite catalysts $(ABO_3)$ and La was used as A-site component. The effect of calcination temperature on methane combustion and perovskite structure was also investigated. The structure of perovskites, surface area, and adsorbed oxygen species were tested with XRD, BET apparatus, and $O_2-TPD$, respectively. The formation of perovskite structure was affected by the calcination temperature. The catalyst desorbing oxygen at a lower temperature showed better activity for the methane combustion, therefore, the oxygen species desorbing at lower temperatures is responsible for the methane combustion.

하소공정과 $ZrO_2$ 첨가량이 $BaTiO_3$의 전기적 특성에 미치는 영향 (Effects of Calcination Process and $ZrO_2$ Addition on the Electrical Properties of $BaTiO_3$ Ceramics)

  • 차진이;박재관;오태성;김윤호
    • 한국세라믹학회지
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    • 제28권11호
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    • pp.935-941
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    • 1991
  • Effects of calcination process and ZrO2 addition on the electrical properties of [(Ba0.82Sr0.08Ca0.1)O]m(Ti1-$\chi$Zr$\chi$)O2 ceramics have been investigated. With the variation of A/B-site ratio m of the dielectric formulations, sintering behavior and the resistivity after sintering in a reducing atmosphere have been affected by the calcination process. When the dielectric formulations of m=1.01 were sintered in a reducing atmosphere, the room-temperature resitivity of 109 {{{{ OMEGA }}.cm was obtained for samples processed with two-step calcination, which was much lower than 1012 {{{{ OMEGA }}.cm of samples calcined once. It was confirmed that high resistivity of Ca-doped BaTiO3 ceramics, after sintering in a reducing atmosphere, is maintained by acceptor-like behavior of CaTi" which is formed by Ca substitution to Ti-site. It was also found out that the critical amount of B-site Ca substitution for reduction inhibition of BaTiO3 is around 0.005 mol. With the increasing amount of ZrO2 addition to dielectric formulations, Curie peak was depressed and Curie temperature was lowered due to the enhanced diffuse phase transition.tion.

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비산회를 이용한 도금폐수의 응집처리 (Coagulation of the Metal-Plating Wastewater using Coal Fly Ash)

  • 연익준;김광렬
    • 환경위생공학
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    • 제17권3호
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    • pp.37-45
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    • 2002
  • The Purpose of this study is to reduce environmental problems caused by landfill of bituminous coal fly ash emitted from the power plant and to reuse it. First of all, we experimented that Al and Si elements were extracted from fly ash and investigated that extracted Al and Si elements night use a coagulant. The extraction was carried out under various conditions ; concentration of the extraction solution, calcination temperature and calcination time. As the results, it was found that the optimum conditions of the extraction of Al and Si elements from fly ash were as follows, concentration of NaOH was 5N for both of them, calcination temperature was $700^{\circ}C$ and $600^{\circ}C$ and calcination time was 1hr and 1.5hr, respectively The extracted solution was used as a coagulant to treat the diluted metal-plating solutions which contained Pb and Cu, respectively. As the result of treatment on the diluted Pb-plating solution with 315NTU, the removal efficiency of turbidity was more than 90%, and the removal efficiency of Pb was about 80%. As for treatment of the non-turbid diluted Cu-plating solution, the removal efficiency of Cu was about 98%.

달걀 껍질을 재활용한 탈황제의 제조에 관한 연구 (Study on Manufacturing Desulfurization Sorbent using Eggshell)

  • 이병호;이봉헌;박흥재;김우성
    • 한국환경과학회지
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    • 제7권5호
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    • pp.693-696
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    • 1998
  • We tried to develope a desulfurization sorbent using eggshell for recycling, practicability, and economic development. The calcination character of the eggshell was examined by thermal gravimetric analysis and qualitative-quantitative character by X-ray diffractometer(XRD) and scanning electron microscope(SEM). The calcination was occurred easily in the case of eggshell and its form was changed from calcite($CaCO_3$) to lime(CaO). The grain and pore sizes of the calcined sample after base-treatment were larger and more crystallic. The adsorption ability of the eggshell was two- to six-times in the calcination temperature more than in the grain size. Therefore, the eggshell was thought to be usable as the desulfurization sorbent.

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순산소연소 조건에서 석회석의 소성특성 및 로내탈황에 관한 연구 (Study on Calcination Characteristics of Limestones for In-Furnace Desulfurization in Oxy-Fuel Combustion)

  • 안영모;조항대;최원길;박영성;길상인;이형근
    • 대한환경공학회지
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    • 제31권5호
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    • pp.371-377
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    • 2009
  • 순산소연소 배가스 중 $CO_2$ 농도는 가스의 재순환으로 인해 95%까지 농축 가능하며, $CO_2$ 농도가 높은 조건에서 석회석의 소성특성은 기존의 공기 연소와 다르게 나타난다. 본 연구에서는 흡수제로 특성이 다른 세 종류의 국내산 석회석을 이용하여, 소성온도에 따른 석회석의 소성특성에 대해 알아보았다. 또한 흡수제 종류, 반응온도 등의 운전변수가 $SO_2$ 제거효율에 미치는 영향에 대하여 알아보고, 반응생성물을 포집하여 황 함량을 측정하였다. 소성온도가 증가함에 따라 석회석의 소성율 및 비표면적은 증가하는 경향을 보였으며, 반응온도가 증가함에 따라 $SO_2$ 제거효율은 증가하였으며 석회석의 종류에 따라 $SO_2$ 제거효율이 뚜렷한 차이를 보였다. 최고효율 나타낸 석회석 시료에 대한 반응생성물 분석결과 시료 내 황 함량은 약 10% 정도인 것으로 나타났다.

공침법으로 합성한 바륨 페라이트(BaM) 분말의 결정구조와 자기적 성질 (Magnetic Properties and Structure of Co-precipitated Barium Ferrite (BaM) Powders)

  • 백인승;남인탁
    • 한국자기학회지
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    • 제20권4호
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    • pp.134-142
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    • 2010
  • 바륨 페라이트($BaFe_{12}O_{19}$) 분말을 공침법을 이용하여 합성하였다. 출발물질의 조성은 $Fe^{3+}:Ba^{2+}$ 몰 비를 8로 고정하고 $Fe^{3+}$$Ba^{2+}$의 상대적인 양을 조절하였다. pH(= 8, 9, 10), 열처리 온도와 시간에 따른 자기적 성질과 결정구조 입자형상의 변화를 XRD, FESEM, VSM을 이용하여 조사하였다. pH, $Fe^{3+}$$Ba^{2+}$의 상대적인 양 그리고 열처리 온도와 시간에 따라 보자력과 자화 값이 다양하게 나타났다. pH가 9인 경우에는 $Fe^{3+}$$Ba^{2+}$의 비가 14.4 : 1.8인 경우를 제외한 모든 분말에서 바륨 페라이트의 단일 상을 얻을 수 있었다. $Fe^{3+}$$Ba^{2+}$의 비가 12.8 : 1.6이며 공기중에서 $900^{\circ}C$로 열처리한 분말이 가장 큰 자화 값(65.7 emu/g)을 얻을 수 있었으며 산소분위기에서 $900^{\circ}C$로 열처리한 분말이 가장 큰 보자력 값(5280 Oe)을 얻을 수 있었다.

열처리 온도가 전기방사방법을 이용하여 제조한 PEMFC용 TiO2 담체의 물리적 특성에 미치는 영향 (Effects of Calcination Temperature on Characteristics of Electrospun TiO2 Catalyst Supports for PEMFCs)

  • 권초롱;유성종;장종현;김형준;김지현;조은애
    • 한국수소및신에너지학회논문집
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    • 제24권3호
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    • pp.223-229
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    • 2013
  • Polymer Electrolyte Membrane Fuel Cell (PEMFC) is a power generation system to convert chemical energy of fuels and oxidants to electricity directly by electrochemical reactions. As a catalyst support for PEMFCs, carbon black has been generally used due to its large surface area and high electrical conductivity. However, under certain circumstances (start up/shut down, fuel starvation, ice formation etc.), carbon supports are subjected to serve corrosion in the presence of water. Therefore, it would be desirable to switch carbon supports to corrosion-resistive support materials such as metal oxide. $TiO_2$ has been attractive as a support with its stability in fuel cell operation atmosphere, low cost, commercial availability, and the ease to control size and structure. However, low electrical conductivity of $TiO_2$ still inhibits its application to catalyst support for PEMFCs. In this paper, to explore feasibility of $TiO_2$ as a catalyst support for PEMFCs, $TiO_2$ nanofibers were synthesized by electrospinning and calcinated at 600, 700, 800 and $900^{\circ}C$. Effects of calcination temperature on crystal structure and electrical conductivity of electrospun $TiO_2$ nanofibers were examined. Electrical conductivity of $TiO_2$ nanofibers increased significantly with increasing calcination temperature from $600^{\circ}C$ to $700^{\circ}C$ and then increased gradually with increasing the calcination temperature from $700^{\circ}C$ to $900^{\circ}C$. It was revealed that the remarkable increase in electrical conductivity could be attributed to phase transition of $TiO_2$ nanofibers from anatase to rutile at the temperature range from $600^{\circ}C$ to $700^{\circ}C$.

페로브스카이트 촉매에서 A-Site 치환에 따른 촉매활성 변화 (Catalytic Activity Change of Perovskite Catalysts with A-Site Substitution)

  • 함현식;김규성;안성환;신기석;김송형;박홍수
    • 한국응용과학기술학회지
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    • 제24권3호
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    • pp.272-277
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    • 2007
  • Catalytic activity changes of perovskite catalysts were examined with their A-site substitution. For the preparation of catalysts, Mn was used for B-site component and La, Ce, Sr, Ba, Ca, Ag were used for A-site component of the perovskite $catalysts(ABO_3)$ The effect of calcination temperature on methane combustion and perovskite structure was also investigated. The surface area and adsorbed oxygen species were tested with BET apparatus and $O_2-TPD$, respectively. Perovskite catalysts whose A-site was partially substituted needed higher calcination temperature than un-substituted one to form the perovskite structure. From $O_2-TPD$ experiment, it was found that methane combustion activity was directly related to the oxygen desorbing ability of the catalysts. The prepared catalyst(LM-7) was stable at $600^{\circ}C$ for 72 hours of reaction.

열처리 온도에 따른 8YSZ 후막의 미세구조 (Heat Treatment Effect on the Microstructure of 8YSZ Thick Film)

  • 한상훈;노효섭;나동명;김광호;이운영;박진성
    • 한국세라믹학회지
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    • 제48권1호
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    • pp.106-109
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    • 2011
  • In order to fabricate 8YSZ thick film by silk screen printing, YSZ(yttria-stabilized zirconia) commercial powder was used as starting materials. Paste for screen printing was made by mixing 8YSZ powder and organic vehicles. 8YSZ thick film was formed on $Al_2O_3$ substrate. The crystal structure, and microstructure were investigated. Grain size of 8YSZ was increased with increasing calcination temperature and rapid grain growth was shown after calcination at $1300^{\circ}C$. Microstructure showed the mixture of large and small grain size after $1400^{\circ}C$ sintering. Shrinkage rate of 8YSZ thick film sintered at $1400^{\circ}C$ was more than 40%.

Facile Preparation of ZnO Nanocatalysts for Ozonation of Phenol and Effects of Calcination Temperatures

  • Dong, Yuming;Zhao, Hui;Wang, Zhiliang;Wang, Guangli;He, Aizhen;Jiang, Pingping
    • Bulletin of the Korean Chemical Society
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    • 제33권1호
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    • pp.215-220
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    • 2012
  • ZnO nanoparticles were synthesized through a facile route and were used as ozonation catalysts. With the increase of calcination temperature ($150-300^{\circ}C$), surface hydroxyl groups and catalytic efficiency of asobtained ZnO decreased remarkably, and the ZnO obtained at $150^{\circ}C$ showed the best catalytic activity. Compared with ozonation alone, the degradation efficiency of phenol increased above 50% due to the catalysis of ZnO-150. In the reaction temperatures range from $5^{\circ}C$ to $35^{\circ}C$, ZnO nanocatalyst revealed remarkable catalytic properties, and the catalytic effect of ZnO was better at lower temperature. Through the effect of tertbutanol on degradation of phenol and the catalytic properties of ZnO on degradation of nitrobenzene, it was proposed that the degradation of phenol was ascribed to the direct oxidation by ozone molecules based on solidliquid interface reaction.