• 제목/요약/키워드: Low temperature calcination

검색결과 134건 처리시간 0.021초

백금 담지 촉매상에서 에탄올의 저온연소 (Low-Temperature Combustion of Ethanol over Supported Platinum Catalysts)

  • 김문현
    • 한국환경과학회지
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    • 제26권1호
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    • pp.67-78
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    • 2017
  • Combustion of ethanol (EtOH) at low temperatures has been studied using titania- and silica-supported platinum nanocrystallites with different sizes in a wide range of 1~25 nm, to see if EtOH can be used as a clean, alternative fuel, i.e., one that does not emit sulfur oxides, fine particulates and nitrogen oxides, and if the combustion flue gas can be used for directly heating the interior of greenhouses. The results of $H_2-N_2O$ titration on the supported Pt catalysts with no calcination indicate a metal dispersion of $0.97{\pm}0.1$, corresponding to ca. 1.2 nm, while the calcination of 0.65% $Pt/SiO_2$ at 600 and $900^{\circ}C$ gives the respective sizes of 13.7 and 24.6 nm when using X-ray diffraction technique, as expected. A comparison of EtOH combustion using $Pt/TiO_2$ and $Pt/SiO_2$ catalysts with the same metal content, dispersion and nanoparticle size discloses that the former is better at all temperatures up to $200^{\circ}C$, suggesting that some acid sites can play a role for the combustion. There is a noticeable difference in the combustion characteristics of EtOH at $80{\sim}200^{\circ}C$ between samples of 0.65% $Pt/SiO_2$ consisting of different metal particle sizes; the catalyst with larger platinum nanoparticles shows higher intrinsic activity. Besides the formation of $CO_2$, low-temperature combustion of EtOH can lead to many other pathways that generate undesired byproducts, such as formaldehyde, acetaldehyde, acetic acid, diethyl ether, and ethylene, depending strongly on the catalyst and reaction conditions. A 0.65% $Pt/SiO_2$ catalyst with a Pt crystallite size of 24.6 nm shows stable performances in EtOH combustion at $120^{\circ}C$ even for 12 h, regardless of the space velocity allowed.

전기방사법에 의해 합성된 무방향성 산화아연 나노섬유의 일산화질소 가스 감지 특성 (Electrospun Non-Directional Zinc Oxide Nanofibers as Nitrogen Monoxide Gas Sensor)

  • 김옥길;김효진;김도진
    • 한국재료학회지
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    • 제22권11호
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    • pp.609-614
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    • 2012
  • We report on the NO gas sensing properties of non-directional ZnO nanofibers synthesized using a typical electrospinning technique. These non-directional ZnO nanofibers were electrospun on an $SiO_2$/Si substrate from a solution containing poly vinyl alcohol (PVA) and zinc nitrate hexahydrate dissolved in distilled water. Calcination processing of the ZnO/PVA composite nanofibers resulted in a random network of polycrystalline ZnO nanofibers of 50 nm to 100 nm in diameter. The diameter of the nanofibers was found to depend primarily on the solution viscosity; a proper viscosity was maintained by adding PVA to fabricate uniform ZnO nanofibers. Microstructural measurements using scanning electron microscopy revealed that our synthesized ZnO nanofibers after calcination had coarser surface morphology than those before calcination, indicating that the calcination processing was sufficient to remove organic contents. From the gas sensing response measurements for various NO gas concentrations in dry air at several working temperatures, it was found that gas sensors based on electrospun ZnO nanofibers showed quite good responses, exhibiting a maximum sensitivity to NO gas in dry air at an operating temperature of $200^{\circ}C$. In particular, the non-directional electrospun ZnO nanofiber gas sensors were found to have a good NO gas detection limit of sub-ppm levels in dry air. These results illustrate that non-directional electrospun ZnO nanofibers are promising for use in low-cost, high-performance practical NO gas sensors.

$ZnWO_4$ 세라믹의 마이크로파 유전특성 (Microwave Dielectric Properties of $ZnWO_4$ Ceramics)

  • 윤상옥;윤종훈;김대민;심상흥;강기성
    • 한국전기전자재료학회:학술대회논문집
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    • 한국전기전자재료학회 2002년도 하계학술대회 논문집 Vol.3 No.2
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    • pp.642-645
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    • 2002
  • Microwave dielectric properties of $ZnWO_4$ ceramic were investigated with calcination and sintering temperatures. The dielectric properties required for such application are high dielectric constant$(\varepsilon_r)$, high $Q{\times}f_o$ value and low temperature coefficient of resonant frequency$(\tau_f)$. These requirement correspond to necessities for size reduction, excellent frequency selectivity, good temperature stability of devices. $ZnWO_4$ ceramics could be sintered at low $1075^{\circ}C$, which was comparatively low temperature for microwave dielectrics. As a result, $ZnWO_4$ showed the dielectric constant of 13, quality factor($Q{\times}f_o$ value) of 22000 and 'temperature coefficient of resonant frequency$(\tau_f)$ of $-65{\pm}5ppm/^{\circ}C$.

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CoOx/TiO2 촉매상에 ConTiOn+2 화합물의 생성과 저온 CO 산화반응에 대한 촉매활성 (The Formation of ConTiOn+2 Compounds in CoOx/TiO2 Catalysts and Their Activity for Low-Temperature CO Oxidation)

  • 김문현;함성원
    • 한국환경과학회지
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    • 제17권8호
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    • pp.933-941
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    • 2008
  • The formation of $Co_nTiO_{n+2}$ compounds, i.e., $CoTiO_3$ and $CO_2TiO_4$, in a 5wt% $CoO_x/TiO_2$ catalyst after calcination at different temperatures has been characterized via scanning electron microscopy (SEM), Raman and X-ray photoelectron spectroscopy (XPS) measurements to verify our earlier model associated with $CO_3O_4$ nanoparticles present in the catalyst, and laboratory-synthesized $Co_nTiO_{n+2}$ chemicals have been employed to directly measure their activity profiles for CO oxidation at $100^{\circ}C$. SEM measurements with the synthetic $CoTiO_3$ and $CO_2TiO_4$ gave the respective tetragonal and rhombohedral morphology structures, in good agreement with the earlier XRD results. Weak Raman peaks at 239, 267 and 336 $cm^{-1}$ appeared on 5wt% $CoO_x/TiO_2$ after calcination at $570^{\circ}C$ but not on the catalyst calcined at $450^{\circ}C$, and these peaks were observed for the $Co_nTiO_{n+2}$ compounds, particularly $CoTiO_3$. All samples of the two cobalt titanate possessed O ls XPS spectra comprised of strong peaks at $530.0{\pm}0.1$ eV with a shoulder at a 532.2-eV binding energy. The O ls structure at binding energies near 530.0 eV was shown for a sample of 5 wt% $CoO_x/TiO_2$, irrespective to calcination temperature. The noticeable difference between the catalyst calcined at 450 and $570^{\circ}C$ is the 532.2 eV shoulder which was indicative of the formation of the $Co_nTiO_{n+2}$ compounds in the catalyst. No long-life activity maintenance of the synthetic $Co_nTiO_{n+2}$ compounds for CO oxidation at $100^{\circ}C$ was a good vehicle to strongly sup port the reason why the supported $CoO_x$ catalyst after calcination at $570^{\circ}C$ had been practically inactive for the oxidation reaction in our previous study; consequently, the earlier proposed model for the $CO_3O_4$ nanoparticles existing with the catalyst following calcination at different temperatures is very consistent with the characterization results and activity measurements with the cobalt titanates.

NaBH4 가수분해용 Co-P-B/Cu 촉매의 내구성 (Durability of Co-P-B/Cu Catalyst for NaBH4 Hydrolysis Reaction)

  • 황병찬;조아라;신석재;최대기;남석우;박권필
    • Korean Chemical Engineering Research
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    • 제50권4호
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    • pp.627-631
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    • 2012
  • 휴대용 고분자전해질 연료전지의 수소발생용으로써 $NaBH_4$는 많은 장점을 갖고 있다. 본 연구에서는 $NaBH_4$ 가수분해 반응용 Co-P-B/Cu 촉매의 내구성에 대해 연구하였다. Co-P-B/Cu 촉매의 내구성 미치는 반응 온도, $NaBH_4$ 농도, NaOH 농도, 촉매 소성온도 등의 영향에 대해 실험하였다. 촉매의 내구성은 가수분해 반응 중에 발생하는 gel 형성에 영향을 받았다. 즉 gel 형성에 의해 촉매 손실률이 증가하였다. $NaBH_4$ 농도가 고농도일 때는 $60^{\circ}C$ 이상에서는 gel 형성이 안 되어 촉매 손실률이 낮았다. 그러나 $40^{\circ}C$ 이하에서는 gel이 형성되어 촉매 손실률이 증가했다. $NaBH_4$ 20 wt%, $40^{\circ}C$에서 NaOH 농도증가에 따라 겔이 형성되어 촉매 손실률이 증가함을 보였다. Co-P-B/Cu 촉매의 높은 온도에서 소성은 내구성을 향상시켰지만 촉매 활성을 감소시켰다.

팔라듐 촉매의 메탄 부분산화에 관한 연구 - 반응온도에 따른 효과 - (A Study of Partial Oxidation of Methane by Pd Catalyst - Effects of Reaction Temperature -)

  • 이택홍;문영환
    • 한국수소및신에너지학회논문집
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    • 제15권3호
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    • pp.244-249
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    • 2004
  • Pd catalyst have been used in hydrogenation, oxidation, and low temperature combustion reaction. Recently, it has been candidated as a possible reagents in the partial oxidation of methanol reformers of the fuel cell. Pd catalysts, even though it is very precious and expensive, catalytic functioning is good, but it still need to be improved in the matter of durability and low catalytic activity after calcination. In this study, we synthesize the improved Pd catalyst and study their chemical functioning.

Immobilization of Metal lons Using Low-Temperature Calcination Techniques of Spinel-ferrites

  • Yen, Fu-Su;Kao, Hsiao-Chiun;Chen, Wei-Chien
    • 대한전자공학회:학술대회논문집
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    • 대한전자공학회 2001년도 The 6th International Symposium of East Asian Resources Recycling Technology
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    • pp.106-110
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    • 2001
  • Formation of stoichiometric lithium-, nickel-, and zinc- ferrites by calcining organo-metallic precursors a temperature below 40$0^{\circ}C$ is examined using DTA/TG, and XRD techniques. It attempts to simulate th immobilization of metal ions in industrial liquid influents (waste) through the synthesis of stoichiometric spinel ferrites (SSF). Two steps of the SSF formation during thermal treatments are noted. The transformation of magnetite to ${\gamma}$ - Fe$_2$O$_3$and subsequent first formation of SSF were observed at temperatures ranging from 200 to 45$0^{\circ}C$. Th formation of cation-containing ${\gamma}$-Fe$_2$O$_3$and subsequent second formation of the ferrite occurred at temperature ranges of < 45$0^{\circ}C$ and 500 to $650^{\circ}C$, depending on the heating rate used. Then the temperature range of 200t 45$0^{\circ}C$ is critical to the performance of the technique, because a calcination at the range would lead to a complete formation of SSF, avoiding the occurrences of ${\gamma}$-Fe$_2$O$_3$and ion-containing ${\gamma}$-Fe$_2$O$_3$. If not, so $\alpha$-Fe$_2$O$_3$would occur. And annealing at temperature above $650^{\circ}C$ must be employed by which solid-state reactio of $\alpha$-Fe$_2$O$_3$with metal ions (possibly metal oxides) to form SSF can be conducted.

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저온 상압에서 합성된 Na, TPA-ZSM-5의 결정화에 관한 분광학적 고찰 (Spectroscopic Studies on Crystallization of Na, TPA-ZSM-5 synthesized at Low Temperature and Atomospheric pressure)

  • 윤영자;하재목
    • 분석과학
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    • 제10권1호
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    • pp.18-30
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    • 1997
  • Si / Al비가 130 정도인 Na, TPA-ZSM-5를 저온 상압법으로 합성하였으며, 이들의 결정화 과정을 XRD, XRF, FT-IR, NMR 및 SEM을 이용하여 고찰하였다. 결정의 형성과정은 autoclave법과는 다소 다르게 나타났으나 최종 생성물의 분광학적 특성은 전형적인 ZSM-5 영역에서 나타났다. 또한 반응 도중 생성된 국부결함은 소성에 의해 제거됨을 알 수 있었으며, 저온상압하에서도 반응시간을 48시간 이내로 단축할 수 있음을 알 수 있었다.

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산업부산물을 활용한 제철·제강용 합성 칼슘 페라이트 특성 - (1) (The Properties of Synthetic Calcium Ferrite for Ironmaking and Steelmaking using Industrial By-products - (1))

  • 박수현;추용식;서성관;박재완
    • 자원리싸이클링
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    • 제23권5호
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    • pp.3-11
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    • 2014
  • 칼슘 페라이트는 기존 소결광용 결합제 및 제강용 융제보다 용융온도가 낮아 결합제 및 융제로서의 효과가 우수하다. 본 연구에서는 제조비용절감과 생산성 증대를 위해 기존 용융법이 아닌 시멘트 제조공정에서의 소성법으로 칼슘 페라이트를 제조하였다. 칼슘페라이트의 석회질 원료로 소성슬러지 및 석회석을 사용하였고, 철질 원료로 제강슬러지, 고로분진 및 철광석을 사용하였다. 이때 소성온도는 $950{\sim}1170^{\circ}C$이며, 저융점 특성을 가진 '소결광용 결합제' 또는 '전로 및 전기로용 융제'로의 사용 가능성을 검토하고자 원료를 분석하고 소결 특성을 평가하였다.

Low Temperature Catalytic Activity of Cobalt Oxide for the Emergency Escape Mask Cartridge

  • Park, Jae-Man;Kim, Deog-Ki;Shin, Chang-Sub
    • International Journal of Safety
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    • 제1권1호
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    • pp.58-61
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    • 2002
  • A preparation method of cobalt supported alumina catalyst for a emergency escape mask cartridge has been studied. Catalysts were prepared by incipient wetness impregnation method using pre-shaped $\gamma$=alumina powders of 70-100 mesh. The catalyst was tested in a continuous-flow reactor system and characterized by elemental analysis, BET and TGA-DTA techniques. Cobalt shows higher activity than platinum or nickel for carbon monoxide oxidation at room temperature. Optimum loading amount of cobalt was 10 wt.% for CO oxidation and the reaction activity increases gradually with the increase of calcination temperature up to $450^{\circ}C.