• 제목/요약/키워드: $Co_3O_4$ nanoparticles

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화염 분무 열분해법으로 합성된 Cr-Co3O4 나노입자 자일렌 가스센서 (Xylene Sensor Using Cr-doped Cr-Co3O4 Nanoparticles Prepared by Flame Spray Pyrolysis)

  • 정성용;조영무;강윤찬;이종흔
    • 센서학회지
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    • 제29권2호
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    • pp.112-117
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    • 2020
  • Xylene is a hazardous volatile organic compound that should be precisely measured to monitor indoor air quality. However, the selective and sensitive detection of ppm-level xylene using oxide-semiconductor gas sensors remains a challenge. In this study, pure and Cr-doped Co3O4 nanoparticles (NPs) were prepared using flame spray pyrolysis, and their gas-sensing characteristics to 5-ppm xylene at 250 ℃ were investigated. The 4 at% Cr-doped Co3O4 NPs exhibited a high gas response to 5-ppm xylene (resistance ratio to gas and air = 39.1) and negligible cross-responses to other representative and ubiquitous indoor pollutants such as ethanol, benzene, formaldehyde, carbon monoxide, and ammonia. In this paper, the enhancement of the gas response and selectivity of Co3O4 NPs to xylene by Cr doping was discussed in relation to the catalytic promotion of the gas-sensing reaction. This sensor can be used to monitor indoor xylene.

나노분말 CoGa0.1Fe1.9O4의 Mössbauer 분광학적 연구 (Mössbauer Studies of CoGa0.1Fe1.9O4 Nanoparticles)

  • 이승화
    • 한국자기학회지
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    • 제16권2호
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    • pp.144-148
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    • 2006
  • 초상자성 나노입자의 제작이 가능한 sol-gel법을 이용하여 초상자성 나노입자 $CoGa_{0.1}Fe_{1.9}O_4$를 제조하여 입자의 크기 및 자기적 성질을 x-선 회절법(XRD), 주사전자현미경(SEM) 측정과 $M\ddot{o}ssbauer$ 분광법, 진동시료 자화율 측정기(VSM)를 이용하여 연구하였다. SEM및 x-선 회절실험으로부터 250"C 이상에서 열처리한 입자가 순순한 cubic spinel구조를 가지며, $250^{\circ}C$에서 열처리한 $CoGa_{0.1}Fe_{1.9}O_4$의 평균입자 크기는 10 nm로 나타났으며 균일한 구형상 임을 알 수 있었다. VSM 측정 결과로부터 $250^{\circ}C$에서 열처리한 $CoGa_{0.1}Fe_{1.9}O_4$의 경우 상온에서 초상자성의 특성을 나타냈다. $M\ddot{o}ssbauer$ 분광실험으로 $250^{\circ}C$에서 열처리한 입자가 상온에서 초상자성의 특성을 가지고 있음을 확인할 수 있었으며 초상자성의 특성을 잃어버리는 차단온도 $T_B$는 250 K로 결정하였으며, 또한 자기이방성상수 $K=3.0X10^5\;ergs/cm^3$의 값을 얻었다 $250^{\circ}C$에서 열처리한$CoGa_{0.1}Fe_{1.9}O_4$의 경우 4.2K에서의 초미세 자기장은 $H_{hf}(B)=518,\;H_{hf}(A)=486\;kOe$이며, 이성질체 이동값은 $\delta_B=0.34$, $\delta_A=0.30$ 이 값은 A, B자리 모두 $Fe^{3+}$에 해당된다.

이중 전기방사법을 이용하여 SnO2-Sn-Ag3Sn 나노 입자가 균일하게 내재된 탄소 나노섬유의 합성 (Synthesis of Well-Distributed SnO2-Sn-Ag3Sn Nanoparticles in Carbon Nanofibers Using Co-Electrospinning)

  • 안건형;안효진
    • 한국재료학회지
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    • 제23권2호
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    • pp.143-148
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    • 2013
  • Well-distributed $SnO_2$-Sn-$Ag_3Sn$ nanoparticles embedded in carbon nanofibers were fabricated using a co-electrospinning method, which is set up with two coaxial capillaries. Their formation mechanisms were successfully demonstrated. The structural, morphological, and chemical compositional properties were investigated by field-emission scanning electron spectroscopy (FESEM), bright-field transmission electron microscopy (TEM), X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS). In particular, to obtain well-distributed $SnO_2$ and Sn and $Ag_3Sn$ nanoparticles in carbon nanofibers, the relative molar ratios of the Ag precursor to the Sn precursor including 7 wt% polyacrylonitrile (PAN) were controlled at 0.1, 0.2, and 0.3. The FESEM, bright-field TEM, XRD, and XPS results show that the nanoparticles consisting of $SnO_2$-Sn-$Ag_3Sn$ phases were in the range of ~4 nm-6 nm for sample A, ~5 nm-15 nm for sample B, ~9 nm-22 nm for sample C. In particular, for sample A, the nanoparticles were uniformly grown in the carbon nanofibers. Furthermore, when the amount of the Ag precursor and the Sn precursor was increased, the inorganic nanofibers consisting of the $SnO_2$-Sn-$Ag_3Sn$ nanoparticles were formed due to the decreased amount of the carbon nanofibers. Thus, well-distributed nanoparticles embedded in the carbon nanofibers were successfully synthesized at the optimum molar ratio (0.1) of the Ag precursor to the Sn precursor after calcination of $800^{\circ}C$.

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.

이산화탄소 분리를 위한 이온성 액체 1-butyl-3-methylimidazolium tetrafluoroborate/Al2O3 복합체 분리막 (1-Butyl-3-methylimidazolium tetrafluoroborate/Al2O3 Composite Membrane for CO2 Separation)

  • 윤기완;강상욱
    • 멤브레인
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    • 제27권3호
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    • pp.226-231
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    • 2017
  • 이산화탄소 분리를 위해 이온성 액체/금속 산화물 복합막이 제조되었으며, 이온성 액체로서 1-butyl-3-methylimidazolium tetrafluoroborate ($BMIM^+BF_4{^-}$)와 금속산화물로서 $Al_2O_3$가 사용되었다. 13 nm의 $Al_2O_3$가 이온성 액체 $BMIM^+BF_4{^-}$에 도입되었을 때, 복합체 분리막의 성능은 $CO_2/N_2$ 선택도 30.5과 $CO_2$ 투과도 45.7 GPU로 관찰되었다. neat $BMIM^+BF_4{^-}$ 분리막의 성능($CO_2/N_2$ 선택도 5와 $CO_2$ 투과도 17 GPU)에 비해서 성능이 증가한 이유는 $Al_2O_3$의 옥사이드 층과 이온성 액체 내 자유로운 이온농도의 상승으로 인해 $CO_2$ 용해도가 상승한 것으로 확인되었다. 특히 $Al_2O_3$ 나노입자는 질소 기체에 대해서 장애물로서 작용함으로써 질소기체의 투과도가 감소하여 결과적으로 이산화탄소 분리 성능은 급격히 증가하였다.

씨앗발아 및 발아지수에 근거한 나노입자 독성평가 (Toxicity Assessment of Nanopariticles Based on Seed Germination and Germination Index)

  • 구본우;공인철
    • 대한환경공학회지
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    • 제36권6호
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    • pp.396-401
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    • 2014
  • 나노물질은 다양한 분야에 널리 사용되고 있다. 본 연구에서는 Lactuca(상추)와 Raphanus(알타리무) 씨앗의 발아와 발아지수에 금속산화물 나노입자(CuO, NiO, $Fe_2O_3$, $Co_3O_4$, $TiO_2$, ZnO)가 미치는 영향을 조사하였다. 용액상 노출에서 CuO가 가장 큰 영향을 나타내었으며, 발아와 발아지수의 $EC_{50}$는 각 0.46 mg/L와 0.37%로 조사되었다. 씨앗 이용 식물독성 측정에서 상추가 알타리무보다 나노입자 노출에 대해 더욱 민감한 반응을 나타내었다. 일반적으로 나노입자의 씨앗발아와 발아지수에 근거한 영향은 다음의 순서로 조사되었다: CuO > ZnO >NiO > $TiO_2$, $Fe_2O_3$, $Co_3O_4$. 특히 $TiO_2$, $Fe_2O_3$$Co_3O_4$는 최대 노출 농도 1,000 mg/L 농도에서도 뚜렷한 영향을 나타내지 않았다.

수계 내 ZnO 나노입자의 제거 및 생태독성 저감 (Removal of ZnO Nanoparticles in Aqueous Phase and Its Ecotoxicity Reduction)

  • 김현상;김영훈;김영희;이상구
    • 청정기술
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    • 제22권2호
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    • pp.89-95
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    • 2016
  • 화장품이나 타이어에 주로 사용되는 ZnO 나노입자에 대한 나노위해성 문제가 대두되고 있다. 이에 본 연구에서는 수계상에 존재하는 ZnO 나노입자에 대한 제거 및 생물학적 독성평가를 실시하였다. 송사리(O. Latipes) 수정란을 이용한 단기 노출평가에서는 5 mg L−1에서는 일부 개체에서 기형이 관찰되었고, 10 mg L−1에서 성장지연에 의한 부화율저감이 관찰되었다. 이러한 결과를 바탕으로 ZnO 나노입자가 수생생물종에게 독성을 보인다는 것을 확인하고, 이를 제거하기 위한 방법인 침전법을 제안하였다. Na2S와 Na2HPO4를 이용하여 ZnO를 ZnS와 Zn3(PO4)2로 전환시켜 침전시켰으며, 이들의 침전에 의한 제거율은 거의 100%에 이르렀다. 또한 해당 침전물 대한 물벼룩(D. magna) 급성독성 평가에서 어떠한 독성 영향도 찾지 못하였다. 이는 ZnO의 황 및 인처리를 통한 변환이 독성 감소에 효과적이었음을 나타낸다.

Ultra-Drawing of Gel Films of Ultra High Molecular Weight Polyethylene/Low Molecular Weight Polymer Blends Containing $BaTiO_3$ Nanoparticles

  • Park Ho-Sik;Lee Jong-Hoon;Seo Soo-Jung;Lee Young-Kwan;Oh Yong-Soo;Jung Hyun-Chul;Nam Jae-Do
    • Macromolecular Research
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    • 제14권4호
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    • pp.430-437
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    • 2006
  • The ultra-drawing process of an ultra high molecular weight polyethylene (UHMWPE) gel film was examined by incorporating linear low-density polyethylene (LLDPE) and $BaTiO_3$ nanoparticles. The effects of LLDPE and the draw ratios on the morphological development and mechanical properties of the nanocomposite membrane systems were investigated. By incorporating $BaTiO_3$ nanoparticles in the UHMWPE/LLDPE blend systems, the ultra-drawing process provided a highly extended, fibril structure of UHMWPE chains to form highly porous, composite membranes with well-dispersed nanoparticles. The ultra-drawing process of UHMWPE/LLDPE dry-gel films desirably dispersed the highly loaded $BaTiO_3$ nanoparticles in the porous membrane, which could be used to form multi-layered structures for electronic applications in various embedded, printed circuit board (PCB) systems.

Facile Synthesis of Co3O4/Mildly Oxidized Multiwalled Carbon Nanotubes/Reduced Mildly Oxidized Graphene Oxide Ternary Composite as the Material for Supercapacitors

  • Lv, Mei-Yu;Liu, Kai-Yu;Li, Yan;Wei, Lai;Zhong, Jian-Jian;Su, Geng
    • Bulletin of the Korean Chemical Society
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    • 제35권5호
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    • pp.1349-1355
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    • 2014
  • A three-dimensional (3D) $Co_3O_4$/mildly oxidized multiwalled carbon nanotubes (moCNTs)/reduced mildly oxidized graphene oxide (rmGO) ternary composite was prepared via a simple and green hydrolysishydrothermal approach by mixing $Co(Ac)_2{\cdot}4H_2O$ with moCNTs and mGO suspension in mixed ethanol/$H_2O$. As characterized by scanning electron microscopy and transmission electron microscopy, $Co_3O_4$ nanoparticles with size of 20-100 nm and moCNTs are effectively anchored in mGO. Cyclic voltammetry and galvanostatic charge-discharge measurements were adopted to investigate the electrochemical properties of $Co_3O_4$/moCNTs/rmGO ternary composite in 6 M KOH solution. In a potential window of 0-0.6 V vs. Hg/HgO, the composite delivers an initial specific capacitance of 492 $Fg^{-1}$ at 0.5 $Ag^{-1}$ and the capacitance remains 592 $Fg^{-1}$ after 2000 cycles, while the pure $Co_3O_4$ shows obviously capacitance fading, indicating that rmGO and moCNTs greatly enhance the electrochemical performance of $Co_3O_4$.

Graphene/BaCrO4 Nanocomposites Catalyzed Photodegradation and Kinetics Study of Organic Dyes

  • Kim, Keun Hyung;Ko, Weon Bae
    • Elastomers and Composites
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    • 제50권1호
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    • pp.7-12
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    • 2015
  • The $BaCrO_4$ nanoparticles were synthesized from a 0.1 M $K_2CrO_4$ and 0.1 M $BaCO_3$ solution with stirring for 10 h. The product was washed several times with acetone and heated to $700^{\circ}C$ for 6 h. At that time, the color of mixture was a greenish yellow. The graphene/$BaCrO_4$ nanocomposites were prepared with graphene and $BaCrO_4$ nanoparticles by stirring in tetrahydrofuran and heated in an electric furnace at $700^{\circ}C$ for 2 h. The $BaCrO_4$ nanoparticles, graphene/$BaCrO_4$ and heated graphene/$BaCrO_4$ nanocomposites were characterized by X-ray diffraction, scanning electron microscopy and transmission electron microscopy. The graphene/$BaCrO_4$ nanocomposites and heated graphene/$BaCrO_4$ nanocomposites were evaluated as a photocatalyst and discussed about kinetics study for the degradation of organic dyes, such as methylene blue and rhodamine B under ultraviolet light irradiation at 254 nm.