• 제목/요약/키워드: Co catalyst metal

검색결과 267건 처리시간 0.027초

LNT용 PGM-free DeNOx 촉매 개발을 위한 기초연구 (Basic Research to Develop PGM-free DeNOx Catalyst for LNT)

  • 장길남;한광선;홍지숙;유영우;황택성
    • 청정기술
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    • 제21권2호
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    • pp.117-123
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    • 2015
  • 본 연구는 LNT (lean NOx trap)용 DeNOx 촉매를 개발하기 위해 시도하였다. 이를 위해서 예비실험을 통해 Pt등 귀금속류등의 PGM (platinum group metal)을 사용하지 않는 4개의 촉매, Al/Co/Mn, Al/Co/Ni/Mn, Al/Co/Mn/Ca, Al/Co/Ni 혼합 금속 산화물을 선정하였다. 또한, 이들의 물리화학적인 성질을 평가하기 위해 XRD, EDS, SEM, BET 및 TPD test를 실시하였다. 이러한 평가를 실시한 결과, 4종의 촉매들은 스피넬(spinel)구조를 가지는 결정으로 이루어졌으며 NOx 기체들의 산화-환원 반응이 이루어지기에는 충분한 기공부피와 기공크기를 갖고 있음을 알 수 있었다. 또한, TPD test를 통해서는 산화-환원이 일어날 수 있는 산점을 4종의 촉매가 모두 가지고 있음을 확인하였다. 더욱이 ramp test를 통해서는 상용(commercial) 촉매와 비슷한 NO 산화 능력을 가지고 있는 것도 확인할 수 있었다. 이상의 결과들을 바탕으로, 본 연구에서 선정된 촉매들을 기본으로 하여 조성성분의 변화 및 활성 성분 첨가 등을 한다면, 보다 개선된 LNT용 DeNOx 촉매를 얻을 수 있을 것이라 기대할 수 있었다.

금속담지 활성알루미나 촉매의 암모니아 저온연소반응 (Catalytic Oxidation of Ammonia over Metal Supported on Alumina at Low Temperature)

  • 임윤희;이주열;박병현
    • 한국응용과학기술학회지
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    • 제30권3호
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    • pp.371-379
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    • 2013
  • In order to improve the selective oxidation reaction of gaseous ammonia at a low temperature, various types of metal-impregnated activated alumina were prepared, and also physical and chemical properties of the conversion of ammonia were determined. Both types of metal (Cu, Ag) impregnated activated alumina show high conversion rate of ammonia at high temperature (over $300^{\circ}C$). However, at lower temperature ($200^{\circ}C$), Ag-impregnated catalyst shows the highest conversion rate (93%). In addition, the effects of lattice oxygen of the developed catalyst was studied. Ce-impregnated catalyst showed higher conversion rate than commercial alumina, but also showed lower conversion rate than Ag-impregnated sample. Moreover, 5 vol.% of Ag activation under hydrogen shows the highest conversion rate result. Finally, through high conversion at low temperature, it was considered that the production of NO and $NO_2$, toxic by-products, were effectively inhibited.

상이동촉매에 의한 GROUP 6 금속카르보닐의 CO 치환에 관한 연구(2) : 반응시간과 촉매량에 의한 영향 (A Study on CO Substitution of Group 6 Metal Carbonyls by Using Phase Transfer Catalyst(2))

  • 양현수;박하선
    • 공업화학
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    • 제3권3호
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    • pp.407-411
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    • 1992
  • 본 연구는 상이동 촉매를 이용하여 group 6 금속 카르보닐 착물($M(CO)_6$ [M=Cr, Mo, W])의 CO 리간드를 두자리 전자쌍 주게 리간드(L)인 2, 2'-bipyridine와 2, 2'-biquinoline에 의해서 치환된 $M(CO)_4(L)_2$를 생성할 때 반응 시간, 촉매의 첨가량, 리간드의 종류가 생성물의 수율에 미치는 영향을 관찰하였다.

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Sulfuric Acid Leaching of Valuable Metals from Spent Petrochemical Catalyst using Hydrogen Peroxide as a Reducing Agent

  • Park, Kyung-Ho;Sohn, Jeong-Soo;Kim, Jong-Seok
    • 대한전자공학회:학술대회논문집
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    • 대한전자공학회 2001년도 The 6th International Symposium of East Asian Resources Recycling Technology
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    • pp.478-481
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    • 2001
  • The spent petrochemical catalyst used in the manufacturing process of terephthalic-acid contains valuable metals such as cobalt and manganese. To recover these metals, sulfuric acid leaching was performed with hydrogen peroxide as a reducing agent. Low extractions of Mn, Co and Fe were obtained by sulfuric acid leaching without reducing agent. With adding hydrogen peroxide as a reducing agent, the high extraction of these metals could be obtained. Different from general leaching experiment, the extraction rates of metal components were decreased with increasing reaction temperature in this case. Under the optimum condition, the extraction rates of Mn, Co and Fe were 93.0%, 87.0% and 100% respectively.

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Effect of Support of Two-Dimensional Pt Nanoparticles/Titania on Catalytic Activity of CO Oxidation

  • Qadir, Kamran;Kim, Sang-Hoon;Kim, S.M.;Reddy, A.S.;Jin, S.;Ha, H.;Park, Jeong-Y.
    • 한국진공학회:학술대회논문집
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    • 한국진공학회 2012년도 제42회 동계 정기 학술대회 초록집
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    • pp.246-246
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    • 2012
  • Smart catalyst design though novel catalyst preparation methods can improve catalytic activity of transition metals on reducible oxide supports such as titania by enhancement of metal oxide interface effects. In this work, we investigated Pt nanoparticles/titania catalysts under CO oxidation reaction by using novel preparation methods in order to enhance its catalytic activity by optimizing metal oxide interface. Arc plasma deposition (APD) and metal impregnation techniques are employed to achieve Pt metal deposition on titania supports which are prepared by multi-target sputtering and Sol-gel techniques. In order to tailor metal-support interface for catalytic CO oxidation reaction, Pt nanoparticles and thin films are deposited in varying surface coverages on sputtered titania films using APD. To assess the role of oxide support at the interface, APD-Pt is deposited on sputtered and Sol-gel prepared titania films. Lastly, characteristics of APD-Pt process are compared with Pt impregnation technique. Our results show that activity of Pt nanoparticles is improved when supported over Sol-Gel prepared titania than sputtered titania film. It is suggested that this enhanced activity can be partly ascribed to a very rough titania surface with the higher free metal surface area and higher number of sites at the interface between the metal and the support. Also, APD-Pt shows superior catalytic activity under CO oxidation as compared to Pt impregnation on sputtered titania support. XPS results show that bulk oxide is formed on Pt when deposited through impregnation and has higher proportion of oxidized Pt in the form of $Pt^{2+/4+}$ oxidation states than Pt metal. APD-Pt shows, however, mild oxidation with large proportion of active Pt metal. APD-Pt also shows trend of increasing CO oxidation activity with number of shots. The activity continues to increase with surface coverage beyond 100%, thus suggesting a very rough and porous Pt films with higher active surface metal sites due to an increased surface area available for the reactant CO and $O_2$ molecules. The results suggest a novel approach for systematic investigation into metal oxide interface by rational catalysts design which can be extended to other metal-support systems in the future.

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12wt% Co 담지 FT 촉매 제조시 유기용매가 촉매활성에 미치는 영향연구 (The Effect of Organic Solvents on the Activity for the Synthesis of 12wt% Co-based FT Catalyst)

  • 이지윤;한자령;정종태;백영순
    • 한국수소및신에너지학회논문집
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    • 제26권4호
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    • pp.339-346
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    • 2015
  • The synthesis of Fischer-Tropsch (FT) oil is the catalytic hydrogenation of CO to give a range of products, which can be used for the production of high-quality diesel fuel, gasoline and linear chemicals. This studied catalyst was prepared Cobalt-supported alumina and silica by the incipient wet impregnation of the nitrates of cobalt, promoter and organic solvent with supports. Cobalt catalysts were calcined at $350^{\circ}C$ before being loaded into the FT reactors. After the reduction of catalyst has been carried out under $450^{\circ}C$ for 24h, FT reaction of the catalyst has been carried out at GHSV of 4,000/hr under $200^{\circ}C$ and 20atm. From these experimental results, we have obtained the results as following; In case of $SiO_2$ catalysts, the activity of 12wt% $Cobalt-SiO_2$ synthesized by organic solvent was about 2 or 3 times higher than the activity of 12wt% $Cobalt-SiO_2$ catalyst synthesized without organic solvent. In particular, the activity of the $Cobalt-SiO_2$ catalyst prepared in the presence of an organic solvent P was two to three times higher than that of the $Cobalt-SiO_2$ catalyst prepared without the organic solvent. Effect of Cr and Cu metal as a promoter was found little. 200 h long-term activity test was performed with a $Co/SiO_2$ catalyst prepared in the presence of an organic solvent of Glyoxal solution.

일산화탄소 저온 산화에서 금속산화물에 담지된 금촉매의 활성에 미치는 수분첨가의 영향 (Effect of Water Addition on Activity of Gold Catalysts Supported on Metal Oxide at Low Temperature CO Oxidation)

  • 안호근;김기중;정민철
    • Korean Chemical Engineering Research
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    • 제49권6호
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    • pp.720-725
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    • 2011
  • 금속질산염과 염화금산을 전구체로 사용하여 다양한 금속산화물($$Al_{2}O_{3}$, ZnO, $Fe_{2}O_{3}$, $Cr_{2}O_{3}$, $MnO_{2}$, CuO, NiO, $Co_{3}O_{4}$)에 담지된 금촉매를 공침법을 이용하여 제조한 후, 일산화탄소 산화반응에서 수분첨가의 영향을 검토하였다. 이들 중 $Co_{3}O_{4}$와 ZnO에 담지된 금촉매가 일산화탄소에 대하여 높은 활성을 보여주었다. 반응가스 중에 수분이 첨가될 때 Au/$Co_{3}O_{4}$ 촉매는 활성이 약간 감소하였으나, Au/ZnO 촉매에서는 활성이 크게 증가하여 수분에 의한 일산화탄소 산화 활성은 담체의 종류에 크게 의존함을 알 수 있었다. 반응가스 중에 포함된 수분에 관계없이 반응 전과 후의 Au(5 wt%)/ZnO 촉매의 금입자 크기는 거의 변하지 않아 활성이 감소되는 이유는 금입자들의 소결에 의한 영향보다는 카보네이트와 같은 화학종에 의해 불활성화가 일어남을 알 수 있었으며, 이 화학종은 수분의 첨가에 의해 이산화탄소로 분해되어 활성이 증가한 것으로 생각된다.

Ultrathin Titania Coating for High-temperature Stable $SiO_2$/Pt Nanocatalysts

  • Reddy, A. Satyanarayana;Kim, S.;Jeong, H.Y.;Jin, S.;Qadir, K.;Jung, K.;Jung, C.H.;Yun, J.Y.;Cheon, J.Y.;Joo, S.H.;Terasaki, O.;Park, Jeong-Young
    • 한국진공학회:학술대회논문집
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    • 한국진공학회 2011년도 제41회 하계 정기 학술대회 초록집
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    • pp.217-217
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    • 2011
  • Recently, demand for thermally stable metal nanoparticles suitable for chemical reactions at high temperatures has increased to the point to require a solution to nanoparticle coalescence. Thermal stability of metal nanoparticles can be achieved by adopting core-shell models and encapsulating supported metal nanoparticles with mesoporous oxides [1,2]. However, to understand the role of metal-support interactions on catalytic activity and for surface analysis of complex structures, we developed a novel catalyst design by coating an ultra-thin layer of titania on Pt supported silica ($SiO_2/Pt@TiO_2$). This structure provides higher metal dispersion (~52% Pt/silica), high thermal stability (~600$^{\circ}C$) and maximization of the interaction between Pt and titania. The high thermal stability of $SiO_2/Pt@TiO_2$ enabled the investigation of CO oxidation studies at high temperatures, including ignition behavior, which is otherwise not possible on bare Pt nanoparticles due to sintering [3]. It was found that this hybrid catalyst exhibited a lower activation energy for CO oxidation because of the metal-support interaction. The concept of an ultra-thin active metal oxide coating on supported nanoparticles opens-up new avenues for synthesis of various hybrid nanocatalysts with combinations of different metals and oxides to investigate important model reactions at high-temperatures and in industrial reactions.

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Sol-Gel법을 이용한 CuxCo3-xO4 산소 발생 촉매의 합성 및 전기화학 특성 분석 (Electrochemical Analysis of CuxCo3-xO4 Catalyst for Oxygen Evolution Reaction Prepared by Sol-Gel Method)

  • 박유세;정창욱;김치호;구태우;석창규;권일영;김양도
    • 한국재료학회지
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    • 제29권2호
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    • pp.92-96
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    • 2019
  • Transition metal oxide is widely used as a water electrolysis catalyst to substitute for a noble metal catalyst such as $IrO_2$ and $RuO_2$. In this study, the sol-gel method is used to synthesize the $Cu_xCo_{3-x}O_4$ catalyst for the oxygen evolution reaction (OER),. The CuxCo3-xO4 is synthesized at various calcination temperatures from $250^{\circ}C$ to $400^{\circ}C$ for 4 h. The $Cu_xCo_{3-x}O_4$ synthesized at $300^{\circ}C$ has a perfect spinel structure without residues of the precursor and secondary phases, such as CuO. The particle size of $Cu_xCo_{3-x}O_4$ increases with an increase in calcination temperature. Amongst all the samples studied, $Cu_xCo_{3-x}O_4$, which is synthesized at 300?, has the highest activity for the OER. Its onset potential for the OER is 370 mV and the overpotential at $10mA/cm^2$ is 438 mV. The tafel slope of $Cu_xCo_{3-x}O_4$ synthesized at $300^{\circ}C$ has a low value of 58 mV/dec. These results are mainly explained by the increase in the available active surface area of the $Cu_xCo_{3-x}O_4$ catalyst.

Co-P-B/FeCrAlloy 촉매를 이용한 NaBH4 가수분해 반응 (NaBH4 Hydrolysis Reaction Using Co-P-B Catalyst Supported on FeCrAlloy)

  • 황병찬;조아라;신석재;최대기;남석우;박권필
    • Korean Chemical Engineering Research
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    • 제51권1호
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    • pp.35-41
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    • 2013
  • Co-P-B/FeCrAlloy 촉매의 $NaBH_4$ 가수분해 특성과 내구성에 대해 연구하였다. 5 wt% $NaBH_4$ 농도에서 활성화 에너지가 25.2 kJ/mol로 귀금속 촉매와 비슷했고, $NaBH_4$ 농도가 증가할수록 활성화 에너지가 증가하였다. 20 wt% 이상의 $NaBH_4$ 농도에서 겔 형성이 수소발생과 촉매 내구성에 많은 영향을 줬다. $NaBH_4$ 농도가 높을 때 반응온도가 높을수록 겔 형성이 안 되므로 촉매 손실률이 낮았다. 수소발생과 촉매 내구성을 모두 고려했을 때 담지체를 $1,000^{\circ}C$에서 열처리하고, 초음파 진동없이 촉매를 담지하고, 촉매 담지 후 소성한 촉매가 우수하였다. 25 wt% $NaBH_4$에서는 촉매를 3회 이상 재사용하기 위해서는 $60^{\circ}C$ 이상의 온도에서 반응시켜야 함을 보였다.