• 제목/요약/키워드: Silica Alumina

검색결과 263건 처리시간 0.022초

Sol-gel 및 CVD법을 이용한 고온 수소 분리용 silica/alumina 복합막의 합성 (Synthesis of Silica/Alumina Composite Membrane Using Sol-Gel and CVD Method for Hydrogen Purification at High Temperature)

  • 서봉국;이동욱;이규호
    • 멤브레인
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    • 제11권3호
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    • pp.124-132
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    • 2001
  • 고온에서 수소 분리 회수를 목적으로 silica/alumina 복합 막을 합성하였다. 막의 선택 투과 성능을 향상시키기 위해, sol-gel법에 의한 silica 및 alumina층을 중간층으로 도입하고, 그 위에 강제유동 CVD법에 의한 silica를 합성하였다. Sol-gel법에 의해 ${\alpha}$-alumina tube에 합성한 ${\gamma}$-alumina 및 silica 막은 Knudsen 확산 영역의 많은 mesopore를 포함하고 있어서 수소 선택 분리 막으로는 적합하지 못했다. 하지만, sol-gel법에 의해 합성한 silica/${\gamma}$-alumina층에 강제유동 CVD법으로 silica를 합성한 결과, 질소 투과 영역의 세공이 완전히 제거되어, 높은 수소 선택성을 가지는 복합 막이 형성되었다. 그 막은 온도에 따라 수소 투과 속도가 증가하여 $450^{\circ}C$에서 $5.57{\times}10^{-8}molm^2s^LPa^1$의 수소 투과 속도와, 9.52 kJ/mol의 활성화 에너지를 나타냈다. 분자체 효과에 의해 질소 투과가 완전히 배제되고, 수소만 선택적으로 투과되는 silica/alumina 복합막이 성공적으로 합성된다.

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전력기기용, 에폭시/마이크로 실리카 및 알루미나 복합제의 전기적·기계적 파괴 강도 특성 (Electrical and Mechanical Strength Properties of Epoxy/Micro Silica and Alumina Composites for Power Equipment)

  • 박주언;박재준
    • 한국전기전자재료학회논문지
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    • 제31권7호
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    • pp.496-501
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    • 2018
  • In this study, we prepared 40, 45, 50, 55, 60, 65, and 70 wt% content composites filled in epoxy matrix for two micro silica and three micro alumina types for use as a GIS heavy electric machine. As a filler type of epoxy composite, micro silica composites showed excellent AC breakdown strength properties compared to micro alumina composites in the case of electrical properties of micro silica and alumina. The electrical breakdown properties of micro silica composites increased with increasing filler content, whereas those of micro alumina decreased with increasing filler content. In the case of mechanical properties, the micro silica composite showed improved tensile strength and flexural strength compared with the micro alumina composite. In addition, mechanical properties such as tensile strength and flexural strength of micro silica and alumina composites decreased with increasing filler content. This is probably because O-H groups are present on the surface of silica in the case of micro silica but are not present on the surface of alumina in the case of micro alumina.

Fourier Transform Raman Studies of Methyl Red Adsorbed on γ-Alumina and Silica-Alumina

  • Park, Sun-Kyung;Lee, Choong-Keun;Min, Kyung-Chul;Lee, Nam-Soo
    • Bulletin of the Korean Chemical Society
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    • 제25권12호
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    • pp.1817-1821
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    • 2004
  • Fourier transform Raman spectra of methyl red adsorbed on untreated and pretreated ${\gamma}$-alumina and silicaalumina calcined at 900 $^{\circ}C$ under 1 atm steam flowing were recorded. Spectral analysis shows that the active species adsorbed on ${\gamma}$-alumina was to be deprotonated methyl red, and on silica-alumina to be di-protonated. This indicates that ${\gamma}$-alumina adapted in this work holds Bronsted basicity, and silica-alumina Bronsted acidity. Raman intensities of methyl red on pretreated ${\gamma}$-alumina are about three times stronger than on untreated ${\gamma}$-alumina, while spectral features are unchanged. For silica-alumina, spectral features show modified vibrational characteristics upon surface hydroxylations generated from pretreatment. Consequently, the acidity loss for silica-alumina and the basicity gain for ${\gamma}$-alumina were observed by increasing the surface hydroxyl groups on the catalysts through pretreatment of the steam calcination.

실리카 슬러리에 첨가된 알루미나가 Langasite의 기계.화학적 연마에 미치는 영향 (Effect of Alumina Addition tn the Silica Slurry on the Chemical Mechanical Polishing of Laugasite)

  • 장영일;윤인호;임대순
    • 한국윤활학회:학술대회논문집
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    • 한국윤활학회 1999년도 제30회 추계학술대회
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    • pp.263-268
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    • 1999
  • Langasite, a new piezoelectric material was polished by CMP(chemical mechanical polishing). To enhance the polishing rate, alumina abrasives were added to commercial ILD1300 slurry which contains silica abrasive. The effect of added alumina 0 the silica slurry on the polishing rate and damage of langasite was investigated, Experimental results show that the polishing rate and roughness increases with increasing added alumina particle size, Crystallinity of the langasite is also lowered by alumina addition.

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EVA 수지 이용 연료유 생성을 위한 열분해 반응에서 실리카-알루미나 계열 무기물의 영향 (The Effects of Silica-Alumina Type Inorganic Compounds on the Pyrolysis Reaction of EVA to Produce Fuel-Oil)

  • 박영철;최주홍;오세희
    • 한국수소및신에너지학회논문집
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    • 제22권5호
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    • pp.706-713
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    • 2011
  • The effects of silica-alumina type catalysts addition on the thermal decomposition of ethylene vinyl acetate (EVA) resin have been studied in a thermal analyzer (TGA, DSC) and a small batch reactor. The silica-alumina type compounds tested were kaolinite, bentonite, perlite, activated clay and clay. As the results of TGA experiments, pyrolysis starting temperature for EVA resin had the 1st pyrolysis temperature range of 300~$400^{\circ}C$ and the 2nd pyrolysis temperature range of 425~$525^{\circ}C$. The silica-alumina type catalysts did not affect the pyrolysis rate in EVA pyrolysis reaction. In the DSC experiments, addition of kaolinite and bentonite catalysts reduced the heat of fusion and heat of 2nd pyrolysis reaction. In the batch system experiments, the mixing of silica-alumina type catalysts enhanced the yield of fuel oil, and affected to the distribution of carbon numbers. In the silica-alumina type inorganic material used in this experiments, bentonite was the most effective from the pyrolysis heat, yields, and the characteristics of fuel oil.

기상 화학증착법에 의해 $\alpha$-Alumina 지지관 상에 제조한 Silica막의 수소투과 특성 (Hydrogen Permeance of Silica Membrane Prepared by Chemical Vapor Deposition Method on an $\alpha$-Alumina Support Tube)

  • 김성수;이재홍;서동수;박상욱;서봉국
    • 한국환경과학회지
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    • 제7권5호
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    • pp.669-677
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    • 1998
  • A porous $\alpha$-alumina tube of 2.5 mm O.D. and 1.9 mm I.D. was used as the support of an inorganic membrane. Macropores of the tube, about 150 nm in size, were plugged with silica formed by thermal decomposition of tetraethylorthosilicate at $600^{\circ}C$. The forced cross-flow CVD method that reactant was evacuated through the porous wall of the support was very effective in plugging macropores. The H$_2$ permeance of the prepared membrane was of the order of $10^{-8}/ molㆍs^{-1}/ㆍm^{-2}/. Pa{-1}$/, while the $N_2$ permeance was below $10^{-11}/ molㆍs^{-1}/ㆍm^{-2}/ㆍPa^{-1}$/ at $600^{\circ}C$. This was comparable to that of silica-modified Vycor glass whose size was 4 nm.

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De-soda Process Using Silica for Fabrication of Low Soda Alumina Powder

  • Park, Sang-Chun;Kim, Dae-Woong;Heo, In-Woong;Lee, Sang-Jin
    • 한국세라믹학회지
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    • 제52권3호
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    • pp.192-196
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    • 2015
  • Low soda alumina powder was fabricated using silica (${\alpha}$-quartz) as an agent for removing soda components in the alumina. Quartz powder 2 mm in size was added to aluminum hydroxide obtained through the Bayer process, and then the mixture was heated at various temperatures. Finally, the heat-treated powders were sieved for classification. In this study, the effects of the quartz amount and heating temperature on the mechanism of removing soda were examined. A minimum soda content of 0.005 wt% was observed at the conditions of 15 wt% quartz (based on $Al(OH)_3$ amount) heat-treated at $1600^{\circ}C$ for 8 h. The soda components, such as $Na_2O$, NaOH, and $Na_2CO_3$, in alumina were ionized and activated at high temperature, and this facilitated the reaction with quartz silica and alumina producing nepheline. The advantages of using quartz include low iron content and low cost in comparison with the conventional de-soda process using chamotte, another silicate mineral.

Adsorption of Colloidal Silica Particles on a Glass Substrate

  • Sim, Soo-Man
    • 한국세라믹학회지
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    • 제39권11호
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    • pp.1011-1016
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    • 2002
  • Colloidal particles of silica (100 nm in size) were electrostatically dispersed and adsorbed on a glass substrate coated with silica sol or alumina sol. Stability of the suspensions and microstructure of the adsorbed particle layers were discussed in terms of total potential energies between the particles and the substrate. Well-dispersed suspension resulted in a layer with densely packed and regularly arranged particles, whereas less stable suspension resulted in a porous layer with loosely packed and irregularly arranged particles. Despite repulsive interactions between the particles and the substrate coated with silica sol, the observed adsorption can be attributed to chemical bonds formed at the interface between the particle and silica sol. In contrast, the adsorption of the particles on the substrate coated with alumina sol formed a layer with strongly adhered and densely packed particles, due to large attractive interactions between the particles and alumina sol.

Mullite 합성에 있어서 조성에 따른 Mullite-seed 첨가효과 (Influence of mullite-seed on the mullite synthesis from various compositions)

  • 김인섭;강상원;박주석;이명웅;이병하;이경희
    • 한국결정성장학회지
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    • 제10권1호
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    • pp.48-54
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    • 2000
  • kaolin과 수산화알루미늄을 이용하여 mullite를 합성하는데 있어서 출발원료의 조성을 silica rich, stoichiometric, alumina rich 조성으로 준비하여 각각의 원료로부터 mullite를 합성할 때 mullite-seed가 미치는 영향을 연구하였다. 그 결과 silica rich 조성과 stoichiometric 조성에서는 mullite-seed의 첨가량이 증가할수록 꺾임강도값이 증가하며, alumina rich 조성에서는 mullite-seed의 첨가량이 증가할수록 꺾임강도값은 감소하는 경향을 보였다. 같은 양의 mullite-seed를 첨가했을 때 미세구조는 alumina 첨가 함량이 증가할수록 치밀도가 감소하고, aspect ratio는 증가하는 경향을 나타내었다. 순도면에서는 mullite정량결과 모든 조성에서 mullite-seed의 첨가량이 많을수록 합성된 mullite 결정상의 함량이 증가하는 경향을 보였다.

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(+)-Dihydromyricetin 분별침전에 미치는 제타전위의 영향 (Influence of Zeta Potential on Fractional Precipitation of (+)-Dihydromyricetin)

  • 하건수;김진현
    • Korean Chemical Engineering Research
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    • 제53권6호
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    • pp.831-835
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    • 2015
  • 본 연구에서는 바이오매스 유래 생리활성물질인 (+)-dihydromyricetin을 정제하기 위한 분별침전공정에서 분별침전용액의 제타전위가 분별침전 양상(순도, 수율, 침전물 형태와 크기)에 미치는 영향을 조사하였다. 제타전위 조절을 위한 실리카-알루미나의 첨가량(반응액 부피당 표면적) $100mm^{-1}$에서 가장 높은 수율을 얻을 수 있었다. 실리카-알루미나의 제타전위가 양(+)의 값으로 증가할수록 (+)-dihydromyricetin 수율과 침전물의 크기는 증가하였다. 가장 큰 제타전위 값(+4.99 mV)을 가진 실리카를 이용한 분별침전의 경우에는 가장 작은 제타전위 값(-19.00 mV)을 가진 알루미나를 이용한 분별침전의 경우보다 2배 이상 높은 수율을 얻을 수 있었다. 또한 분별침전 과정에서 제타전위 절대값이 증가할수록 (+)-dihydromyricetin 수율과 침전물의 크기는 감소하여 제타전위 절대값에 반비례함을 알 수 있었다. 반면 표면적증가물질 실리카-알루미나의 제타전위 변화에도 (+)-dihydromyricetin 순도는 거의 변화가 없었다.