• 제목/요약/키워드: Mg catalyst

검색결과 255건 처리시간 0.019초

Nitrate reduction by iron supported bimetallic catalyst in low and high nitrogen regimes

  • Hamid, Shanawar;Lee, Woojin
    • Advances in environmental research
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    • 제4권4호
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    • pp.263-271
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    • 2015
  • In this study, the effect of initial nitrate loading on nitrate removal and byproduct selectivity was evaluated in a continuous system. Nitrate removal decreased from 100% to 25% with the increase in nitrate loading from 10 to $300mg/L\;NO_3-N$. Ammonium selectivity decreased and nitrite selectivity increased, while nitrogen selectivity showed a peak shape in the same range of nitrate loading. The nitrate removal was enhanced at low catalyst to nitrate ratios and 100% nitrate removal was achieved at catalyst to nitrate ratio of ${\geq}33mg\;catalyst/mg\;NO_3-N$. Maximum nitrogen selectivity (47%) was observed at $66mg\;catalyst/mg\;NO_3-N$, showing that continuous Cu-Pd-NZVI system has a maximum removal capacity of 37 mg $NO_3{^-}-N/g_{catalyst}/h$. The results from this study emphasize that nitrate reduction in a bimetallic catalytic system could be sensitive to changes in optimized regimes.

Synthesis of thin-multiwalled carbon nanotubes by Fe-Mo/MgO catalyst using sol-gel method

  • Dubey, Prashant;Choi, Sang-Kyu;Kim, Bawl;Lee, Cheol-Jin
    • Carbon letters
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    • 제13권2호
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    • pp.99-108
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    • 2012
  • The sol-gel technique has been studied to fabricate a homogeneous Fe-Mo/MgO catalyst. Ambient effects (air, Ar, and $H_2$) on thermal decomposition of the citrate precursor have been systematically investigated to fabricate an Fe-Mo/MgO catalyst. Severe agglomeration of metal catalyst was observed under thermal decomposition of citrate precursor in air atmosphere. Ar/$H_2$ atmosphere effectively restricted agglomeration of bimetallic catalyst and formation of highly-dispersed Fe-Mo/MgO catalyst with high specific surface-area due to the formation of Fe-Mo nanoclusters within MgO support. High-quality thin-multiwalled carbon nanotubes (t-MWCNTs) with uniform diameters were achieved on a large scale by catalytic decomposition of methane over Fe-Mo/MgO catalyst prepared under Ar-atmosphere. The produced t-MWCNTs had outer diameters in the range of 4-8 nm (average diameter ~6.6 nm) and wall numbers in the range of 4-7 graphenes. The as-synthesized t-MWCNTs showed product yields over 450% relative to the utilized Fe-Mo/MgO catalyst, and indicated a purity of about 85%.

Chemical Poisoning of Ni/MgO Catalyst by Alkali Carbonate Vapor in the Steam Reforming Reaction of DIR-MCFC

  • 문형대;임태훈;이호인
    • Bulletin of the Korean Chemical Society
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    • 제20권12호
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    • pp.1413-1417
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    • 1999
  • Chemical poisoning of Ni/MgO catalyst was induced by hot alkali carbonate vapor in molten carbonate fuel cell (MCFC), and the poisoned (or contaminated) catalyst was characterized by TPR/TPO, FTIR, and XRD analysis. Carbonate electrolytes such as K and Li were transferred to the catalyst during DIR-MCFC operation at 650 ℃. The deposition of alkali species on the catalyst consequently led to physical blocking on catalytic active sites and structural deformation by chemical poisoning. TPR/TPO analysis indicated that K species enhanced the reducibility of NiO thin film over Ni as co-catalyst, and Li species lessened the reducibility of metallic Ni by chemical reaction with MgO. FTIR analysis of the poisoned catalyst did not exhibit the characteristic ${\vector}_1$$(D_{3h})$ peaks (1055 $cm^{-1},\;1085\;cm{-1})$ for pure crystalline carbonates, instead a new peak (1120 $cm^{-1})$ was observed proportionally with deformed alkali carbonates. From XRD analysis, the oxidation of metallic Ni into $Ni_xMg_{1-x}O$ was confirmed by the peak shift of MgO with shrinking of Ni particles. Conclusively, hot alkali species induced both chemical poisoning and physical deposition on Ni/MgO catalyst in DIR-MCFC at 650 ℃.

KF/MgO 촉매를 이용한 대두유의 전이에스테르화 반응 (Transesterification Reaction of Soybean Oil over KF/MgO Catalyst)

  • 조용범;전종기;박성훈;박영권
    • 공업화학
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    • 제23권3호
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    • pp.344-347
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    • 2012
  • 본 연구에서는 기존 MgO의 염기세기를 증가시켜 전이에스테르화 반응에 있어 보다 좋은 활성을 가지는 촉매를 만들고자 하였다. MgO를 실험실에서 제조한 후 지지체로 사용하였으며 염기세기를 증가시키기 위하여 KF를 함침법으로 담지하였다. BET, XRD, XRF, $CO_2$ TPO로 촉매의 특성분석을 하였고, 대두유과 메탄올을 사용하여 바이오디젤을 합성한 후 지방산메틸에스테르 함유량을 측정함으로써 촉매의 활성을 알아보았다. 결과적으로, KF를 30% 담지한 촉매가 활성이 가장 좋은 것으로 나타났다. 이는 전이에스테르화 반응에서 중간세기 염기도가 더 많이 관여하기 때문으로 보인다.

Eco-AZ91 MgH2의 반응열 제어에 미치는 촉매 분산 효과 (Effects of Catalyst Dispersion for Reaction Energy Control on Eco-AZ91 MgH2)

  • 이수선;석송;홍태환
    • 한국수소및신에너지학회논문집
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    • 제34권6호
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    • pp.631-640
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    • 2023
  • This study selected Eco-AZ91 MgH2, which shows high enthalpy as a material for this purpose, as the basic material, and analyzed the change in characteristics by synthesizing TiNi as a catalyst to control the thermodynamic behavior of MgH2. In addition, the catalyst dispersion technology using graphene oxide (GO) was studied to improve the high-temperature aggregation phenomenon of Ni catalyst and to secure a source technology that can properly disperse the catalyst. XRD, SEM, and BET analysis were conducted to analyze the metallurgical properties of the material, and TGA and DSC analysis were conducted to analyze the dehydrogenation temperature and calorific value, and the correlation between MgH2, TiNi catalyst, and GO reforming catalyst was analyzed. As a result, the MgH2-5 wt% TiNi at GO composite could lower the dehydrogenation temperature to 478-492 K due to the reduction of the catalyst aggregation phenomenon and the increase in the reaction specific surface area, and an experimental result for the catalyst dispersion technology by GO could be ensured.

Effects of Magnesium Catalyst on the Nitridation of Aluminum Melt in the Synthesis of Aluminum Nitride Powder

  • Kim, Hyo-Jin;Kim, Sung-Hun;Lim, Sung-Min;Seo, Jong-Hyun;Lee, Kon-Bae;Lee, Jae-Chul;Ahn, Jae-Pyoung
    • Applied Microscopy
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    • 제44권2호
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    • pp.79-82
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    • 2014
  • Aluminum nitride (AlN) powder was easily synthesized by the direct nitridation of Al melt containing ~20 wt.% Mg catalyst and the nitriding behavior was investigated by thermodynamic calculation and through observations of electron microscopy and X-ray diffraction. The addition of Mg catalyst decreased the nitriding temperature below $1,000^{\circ}C$, which is comparable to the high nitriding temperature of $1,400^{\circ}C$ required in carbothermal method. It was caused by a significant increase of the solubility of nitrogen gas due to the increase of Mg catalyst in Al melt. The dissolved nitrogen gas met Mg catalyst and was transformed into metastable $Mg_3N_2$. Finally the metastable phase reacted with Al to AlN.

저급탄화수소 수증기 개질에 의한 수소 제조용 니켈계 촉매개발 (Development of Ni-based Catalyst for Hydrogen Production with Steam Reforming of Light Hydrocarbon)

  • 김대현;이상득;이병권;김명준;홍석인;문동주
    • 신재생에너지
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    • 제4권4호
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    • pp.80-87
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    • 2008
  • Steam reforming of LPG was investigated over spc-Ni/MgAl catalyst in a temperature range of $600{\sim}850^{\circ}C$, feed molar ratio of $H_2O/C=1.0{\sim}3.0$, space velocity of $10,000{\sim}90,000h^{-1}$ and at atmospheric pressure. spc-Ni/MgAl catalyst was prepared by a co-precipitation method, whereas Ni/MgO and $Ni/Al_2O_3$ catalysts were prepared by an incipient wetness method. The characteristics of catalysts were analyzed by N2 Physisorption, CO chemisorption, XRD, TOF-SIMS, SEM and TEM techniques. The Ni/MgO and $Ni/Al_2O_3$ catalysts were deactivated by the formation of carbon. However, the spc-Ni/MgAl catalyst showed higher conversion and $H_2$ selectivity than the other catalysts, even though carbon was formed on the surface of the catalyst during the reaction under the tested reaction conditions.

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니켈계 유사 하이드로탈사이트 촉매상에서 n-헥사데칸의 수증기 개질에 의한 수소 생산 (Hydrogen Production from Steam Reforming of n-Hexadecane over Ni-Based Hydrotalcite-Like Catalyst)

  • 이승환;문동주
    • 한국수소및신에너지학회논문집
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    • 제21권5호
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    • pp.412-418
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    • 2010
  • Steam reforming of n-hexadecane, a major component of diesel over Ni-based hydrotalcite-like catalyst was carried out at $900^{\circ}C$ at atmospheric pressure with space velocity of $10,000h^{-1}$ and feed molar ratio of steam/carbon=3.0. Ni-based hydrotalcite catalyst was prepared by a solid phase crystallization (spc) method and characterized by $N_2$-physisorption, CO chemisorption, TPR., XRD, and TEM techniques. It was found that spc Ni/MgAl catalyst showed higher catalytic stability and inhibition of carbon formation than Ni/$\gamma-Al_2O_3$ catalyst under the tested conditions. The results suggest that the modified spc-Ni/MgAl catalyst after optimization may be applied for the SR reaction of diesel.

알칼리 및 알칼리 토금속에 의한 SCR 촉매 비활성 거동 (The deactivation behavior of SCR catalyst by alkali and alkali earth metal)

  • 한승윤;신민철;이희수
    • 한국결정성장학회지
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    • 제26권6호
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    • pp.238-242
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    • 2016
  • 알칼리(토)금속이 SCR(Selective Catalytic Reduction) 촉매 비활성화에 미치는영향을 미세구조, 촉매 비표면적, 기공 부피 변화, 탈질 성능 분석을 통해 규명하였다. 신촉매를 $350^{\circ}C$에서 6시간 동안 $H_3PO_4$, $K_2CO_3$, $Na_2CO_3$, $Ca(CH_3COO)_2{\cdot}H_2O$, $C_4H_6MgO_4{\cdot}4H_2O$ 수용액을 분사 시켜, 모사 피독된 SCR 촉매를 제조하였다. 피독 촉매 표면의 미세구조는 신촉매와 거의 유사한 형태를 보이지만, 비표면적과 기공 부피 변화를 신촉매와 비교하였을 때, Na < Mg < K < Ca < P 순으로 감소하는 것으로 나타났다. 특히 Na에 의해 피독된 촉매는 비표면적은 $10.20m^2/g$, 기공부피는 $0.061cm^2/g$ 정도 감소하였다. $150{\sim}450^{\circ}C$에서 신촉매 및 피독 촉매의 탈질성능을 평가한 결과, 알칼리 금속(K, Na)에 피독된 SCR 촉매가 가장 낮은 탈질효율을 보였으며, 알칼리 토금속(Ca, Mg)에 피독된 SCR 촉매는 알칼리 금속(K, Na)에 피독된 촉매에 비해 상대적으로 높은 탈질 효율을 보였으며, 인(P)에 의해 피독된 촉매는 SCR 신촉매와 거의 유사한 탈질 성능을 나타내는 것을 확인하였다. 이러한 결과는 SCR 촉매 비표면적이나 기공 부피 감소에 따른 물리적인 비활성화가 SCR 촉매 탈질 성능에 영향을 미치는 것으로 보인다.

NI/$MgAl_2O_4$코팅된 금속 모노리스 촉매의 수소 생산을 위한 천연가스 수증기 개질 반응특성에 관한 연구 (The Performance of NI/$MgAl_2O_4$ Coated Metal Monolith in Natural Gas Steam Reforming for Hydrogen Production)

  • 최은정;구기영;정운호;이영우;윤왕래
    • 한국수소및신에너지학회논문집
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    • 제21권6호
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    • pp.500-506
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    • 2010
  • The metal monolith catalyst coated with 15wt% Ni/$MgAl_2O_4$ is applied to the natural gas steam reforming for hydrogen production. To address the improvement of adherence between metal monolith and catalyst coating layer, the pre-calcination temperature as well as the coating conditions of $Al_2O_3$ sol are optimized. When the Fe-Cr alloy monolith is pre-calcined at $900^{\circ}C$ for 6 h, $Al_2O_3$ layer was formed uniformly on the entire surface of the metal substrate. It is seen that the formation of $Al_2O_3$ layer on the monolith surface is essential for the uniform coating of $Al_2O_3$ sol onto the monolith substrate. The monolith catalyst coated with 10wt% $Al_2O_3$ sol shows high $CH_4$ conversion and good thermal stability as compared with the monolith catalyst without $Al_2O_3$ sol coating under severe reaction conditions with high GHSV of 30,000 $h^{-1}$ at $700^{\circ}C$. In addition, the metal monolith catalyst shows higher catalytic activity and better thermal conductivity than 15wt% Ni/$MgAl_2O_4$ pellet catalyst.