• Title/Summary/Keyword: ${\gamma}-Al_2O_3$

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Microstructural Observation of Scales formed on HVOF-sprayed NiCoCrAlY Coatings (HVOF 용사된 NiCoCrAlY 코팅의 산호막 관찰)

  • Ko J. H;Lee D. B
    • Korean Journal of Materials Research
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    • v.14 no.2
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    • pp.110-114
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    • 2004
  • High velocity oxy-fuel sprayed NiCoCrAlY coatings were oxidized between 1000 and $1200^{\circ}C$ in air, and the oxide scales were examined by XRD, SEM/EDS, and EPMA. The unoxidized coatings consisted mainly of ${\gamma}$'$-Ni_3$Al, with some ${\gamma}$-Ni. The major oxide formed on the coatings was $\alpha$ $-Al_2$$O_3$. Additionally, (CoCr$_2$$O_4$, $CoAl_2$$O_4$) spinels and $Al_{5}$ $Y_3$$O_{12}$ coexisted. NiO was not found, despite of high amount of Ni in the coating. Below the oxide layer, internally formed $Al_2$$O_3$ existed.

Catalytic Decomposition of NF3 by Thermal Decomposition and Hydrolysis of γ-Al2O3 (γ-Al2O3 촉매상에서 열분해와 가수분해에 의한 NF3 촉매분해 특성)

  • Kim, Yong Sul;Park, No-Kuk;Lee, Tae Jin
    • Applied Chemistry for Engineering
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    • v.26 no.2
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    • pp.154-158
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    • 2015
  • In this study, the catalytic activity of ${\gamma}-Al_2O_3$ was investigated for the decomposition of $NF_3$. Reactions for $NF_3$ decomposition were carried out in the range of reaction temperature of $330{\sim}730^{\circ}C$ and GHSV of $3,000{\sim}15,000mL/g-cat{\cdot}h$ in a fixed-bed catalytic reactor system. Thermal decomposition of $NF_3$ was also performed in order to compare with the catalytic decomposition of $NF_3$. The conversion of $NF_3$ by the catalytic decomposition at $400^{\circ}C$ was four times higher than that of the thermal decomposition. It was confirmed that the reaction behavior of $NF_3$ over ${\gamma}-Al_2O_3$ exhibited two reaction pathways in the presence of steam. Fluorine in $NF_3$ over ${\gamma}-Al_2O_3$ was chemically absorbed to $AlF_3$ by the gas-solid reaction in the absence of steam. The catalytic decomposition of $NF_3$ occurred by hydrolysis with steam. It was also confirmed by FT-IR analysis that $NF_3$ was completely decomposed to NOx and HF above $500^{\circ}C$.

Sintering and Microstructure of $Ce-TZP/Al_2O_3$ Ceramic Composite ($Ce-TZP/Al_2O_3$ 세라믹 복합재료의 소결과 미세구조)

  • 박홍채;홍상희;이윤복;오기동
    • Journal of the Korean Ceramic Society
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    • v.31 no.7
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    • pp.703-714
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    • 1994
  • Sintering and microstructure of Ce-TZP/Al2O3 composite with $\alpha$-Al2O3 matrix containing dispersed 5~50 vol% ZrO2 were discussed. Sintered density was increased with elevating forming pressure in range of 6~300 MPa and about >99.2% of theoretical density was obtained at 1$600^{\circ}C$ for 2h in case of 300 MPa of 6~300 MPa uniaxially cold-pressed compacts containing 20 vol% ZrO2. All kinds of different batch composition exhibited nearly the same shrinkage behaviour with end-point shrinkage between 20 and 24%, and had the maximum shrinkage rate (0.41~0.54%/min) around 140$0^{\circ}C$. Grain growth was occurred faster in $\alpha$-Al2O3 than in {{{{ gamma }}-Al2O3 starting matrix during sintering at 1$600^{\circ}C$. Bimodal pore size distribution of interaglomerate pores with size of 0.03~0.2 ${\mu}{\textrm}{m}$ and of interaglomerate pores with size of around 60 ${\mu}{\textrm}{m}$ was obtained in Ce-TZP/$\alpha$-Al2O3 composite sintered at 130$0^{\circ}C$. But unimodal pore size distribution with around 0.1 ${\mu}{\textrm}{m}$ was observed in Ce-TZP/{{{{ gamma }}-Al2O3 composite sintered at the same temperature. Microcracks were occurred due to the tlongrightarrowm transformation of ZrO2 on cooling process.

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1,1-Difluoroethane Synthesis from Acetylene over Fluorinated γ-Al2O3 (불화된 γ-Al2O3상에서 아세틸렌으로부터 1,1-difluoroethane의 합성)

  • Lee, Youn-Woo;Lee, Kyong-Hwan;Lim, Jong Sung;Kim, Jae-Duck;Lee, Youn Yong
    • Applied Chemistry for Engineering
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    • v.9 no.5
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    • pp.629-633
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    • 1998
  • The synthesis of 1,1-difluoroethane from acetylene as a function of HF/acetylene ratio, contact time and reaction temperature was studied on a fluorinated ${\gamma}-Al_2O_3$. The fluorination of ${\gamma}-Al_2O_3$ was treated with pure HF gas at high temperature. The crystallinity, the porosity, and the acid properties of the prepared samples were examined using XRD, the nitrogen adsorption, pyridine-IR and ammonia-TPD respectively. The activity was enhanced by further fluorination of alumina. The fraction of 1,1-difluoroethane was obtained above 90% at reaction temperature of about $200^{\circ}C$. The ratio of 1,1-difluoroethane to vinylfluoride over fluorinated ${\gamma}-Al_2O_3$ catalyst was increased with the mole ratio of HF/acetylene and contact time, and was found to be the highest ratio at reaction temperature of $200^{\circ}C$.

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Preferential CO Oxidation over Ce-Promoted Pt/γ-Al2O3 Catalyst (Ce가 첨가된 Pt/γ-Al2O3 촉매의 선택적 CO 산화반응 특성)

  • Kim, Kihyeok;Koo, Keeyoung;Jung, Unho;Yoon, Wanglai
    • Transactions of the Korean hydrogen and new energy society
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    • v.23 no.6
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    • pp.640-646
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    • 2012
  • The effect of Ce promotion over 1wt% $Pt/{\gamma}-Al_2O_3$ catalysts on the CO conversion and $CO_2$ selectivity was investigated in preferential CO oxidation (PrOx) to reduce the CO concentration less than 10 ppm in excess $H_2$ stream for polymer electrolyte membrane fuel cell (PEMFC). Ce-promoted 1wt% $Pt/{\gamma}-Al_2O_3$ catalysts were prepared by incipient wetness impregnation method and the loading amount of Pt was fixed at 1wt%. The content of Ce promoter which has excellent oxygen storage and transfer capability due to the redox property was adjusted from 0 to 1.5wt%. Ce-promoted 1wt% $Pt/{\gamma}-Al_2O_3$ catalysts exhibit high CO conversion and $CO_2$ selectivity at low temperatures below $150^{\circ}C$ due to the improvement of reducibility of surface PtOx species compared with the 1wt% $Pt/{\gamma}-Al_2O_3$ catalyst without Ce addition. When Ce content was more than 1wt%, the catalytic activity was decreased at over $160^{\circ}C$ in PrOx because of competitive $H_2$ oxidation. As a result, 0.5wt% Ce is optimal content not only to achieve high catalytic activity and good stability at low temperatures below $150^{\circ}C$ in the presence of $CO_2$ and $H_2O$ but also to minimize the $H_2$ oxidation at high temperatures.

A Study on Reaction Characteristics of $CO_2$ Conversion Methanation over Pt Catalysts for Reduction of GHG (온실가스 저감을 위한 Pt계 촉매상 $CO_2$ Methanation 전환반응 특성에 관한 연구)

  • Hong, Sung Chang
    • Applied Chemistry for Engineering
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    • v.23 no.6
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    • pp.572-576
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    • 2012
  • This study presents the $CO_2$ methanation reaction on Pt catalysts for reducing the amount of $CO_2$, one of greenhouse gases. The AlO(OH) of $Al_2O_3$precusor was used as a support via a thermal treatment and the Pt was used as an active metal. In XRD results, it was confirmed that the Pt was well dispersed and the support existed as the gamma $Al_2O_3$phase. The $Pt/Al_2O_3$ catalyst calcined at $600^{\circ}C$ showed the highest conversion efficiency and selectivity.

Decomposition of 1,2-dichlorobenzene over Al-MCM-41 (Al-MCM-41을 이용한 1,2-dichlorobenzene의 분해 반응)

  • Yim, Jin-Heong;Park, Young-Kwon;Jeon, Jong-Ki;Ko, Young Soo;Yoo, Kyung-Seun
    • Korean Chemical Engineering Research
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    • v.45 no.3
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    • pp.215-218
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    • 2007
  • The aim of this study is to test the feasibility of Pt/Al-MCM-41 for the dioxin decomposition reaction. For model reaction, 1,2-dichlorobenzene was decomposed instead of dioxin. $Pt/{\gamma}-Al_2O_3$ was compared with Pt/Al-MCM-41. Al-MCM-41 catlaysts were prepared by post grafting method and the Pt/Al-MCM-41 catalysts with Si/Al = 15, 30 showed higher catalytic activity than $Pt/{\gamma}-Al_2O_3$. Their higher catalytic activities were related with acid amounts. Especially Al-MCM-41 with ion exchanged with $H^+$ enhanced catalytic activity.

Effect of Al, Al2O3 Dispersants and Heat Treatment on Deposits from Watt′s Ni Plating Bamth (와트 Ni 도금욕에서 도금 피막에 미치는 Al, Al2O3 분산제 및 열처리의 영향)

  • Lee, Sang-Baek;Park, Hyeong-Ho;Bae, In-Seong;Yun, Jae-Sik;Kim, Byeong-Il
    • Korean Journal of Materials Research
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    • v.12 no.2
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    • pp.153-159
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    • 2002
  • The co-deposited behavior was investigated under varied bath compositions and current densities from Watt Ni plating bath containing Al and A1$_2$O$_3$powders. For single-particle bath, Al and A1$_2$O$_3$particles were agglomerated. The area percentage of A1$_2$O$_3$on plating surface decreased with increasing the current density, while that of Al on plating surface increased. On the other hand, in case of double-particle bath with 1.25g/$\ell$ of Al and 5.0g/$\ell$ of A1$_2$O$_3$5g, the area percentage of Ni-Al-A1$_2$O$_3$increased with increasing current density and the surface morphology was fine without agglomeration. Intermetallic compounds such as $\gamma$'and $\gamma$+$\gamma$' phases appeared when the co-deposited film was annealed.

The Effect of Carrier in CO2 Reforming of CH4 to Syngas over Ni-based catalysts

  • Seo, Ho Joon;Kang, Ung Il;Yu, Eui Yeon
    • Clean Technology
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    • v.5 no.2
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    • pp.63-68
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    • 1999
  • The activities of Ni(20wt%)/$La_2O_3$, Ni(20wt%)/${\gamma}-Al_2O_3$, and Ni(20wt%)/$SiO_2$ catalyst for $CO_2$ reforming of $CH_4$ were investigated in a fixed bed flow reactor under atmospheric condition. Catalyst characterization using XRD, TEM, SEM, BET analysis were also conducted. The catalytic activity of Ni(20wt%)/$La_2O_3$ catalyst has relatively superior to that of Ni(20wt%)/${\gamma}-Al_2O_3$ and Ni(20wt%)/$SiO_2$ catalyst. The good activity of Ni(20wt%)/$La_2O_3$ catalyst seems to depend on reduced $Ni^{\circ}$ phases of NiO($\rightarrow$ Ni + O), $LaNiO_3$($\rightarrow$ $Ni+La_2O_3$), Ni crystalline phases, and decoration of Ni phases by lanthanum species is also an important factor. Ni(20wt%)/${\gamma}-Al_2O_3$ and Ni(20wt%)/$SiO_2$ catalyst due to surface acidity resulted in the deposition of wisker type and encapsulate carbon on the surface of catalyst, but Ni(20wt%)/$La_2O_3$ catalyst did not show carbon on the surface of catalyst up to 8.5hr reaction.

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