• Title/Summary/Keyword: $Co-Al_{2}O_{3}$

검색결과 1,035건 처리시간 0.024초

Production of uranium tetrafluoride from the effluent generated in the reconversion via ammonium uranyl carbonate

  • Neto, Joao Batista Silva;de Carvalho, Elita Fontenele Urano;Garcia, Rafael Henrique Lazzari;Saliba-Silva, Adonis Marcelo;Riella, Humberto Gracher;Durazzo, Michelangelo
    • Nuclear Engineering and Technology
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    • 제49권8호
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    • pp.1711-1716
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    • 2017
  • Uranium tetrafluoride ($UF_4$) is the most used nuclear material for producing metallic uranium by reduction with Ca or Mg. Metallic uranium is a raw material for the manufacture of uranium silicide, $U_3Si_2$, which is the most suitable uranium compound for use as nuclear fuel for research reactors. By contrast, ammonium uranyl carbonate is a traditional uranium compound used for manufacturing uranium dioxide $UO_2$ fuel for nuclear power reactors or $U_3O_8-Al$ dispersion fuel for nuclear research reactors. This work describes a procedure for recovering uranium and ammonium fluoride ($NH_4F$) from a liquid residue generated during the production routine of ammonium uranyl carbonate, ending with $UF_4$ as a final product. The residue, consisting of a solution containing high concentrations of ammonium ($NH_4^+$), fluoride ($F^-$), and carbonate ($CO_3^{2-}$), has significant concentrations of uranium as $UO_2^{2+}$. From this residue, the proposed procedure consists of precipitating ammonium peroxide fluorouranate (APOFU) and $NH_4F$, while recovering the major part of uranium. Further, the remaining solution is concentrated by heating, and ammonium bifluoride ($NH_4HF_2$) is precipitated. As a final step, $NH_4HF_2$ is added to $UO_2$, inducing fluoridation and decomposition, resulting in $UF_4$ with adequate properties for metallic uranium manufacture.

저온환경에서 알루미나시멘트를 사용한 모르타르의 단열양생에 따른 기초물성 평가 (Fundamental Properties of Alumina Cement Mortar by Insulation Curing Method under Low Temperature)

  • 박정훈;기경국
    • 한국건축시공학회지
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    • 제17권5호
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    • pp.419-427
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    • 2017
  • 동절기에 콘크리트를 시공할 경우 초기동해와 강도발현이 지연되는 문제가 있으며, 이를 방지하기 위해서는 콘크리트가 동결하기 이전에 시멘트의 수화반응이 일정수준 이하 진행되는 것이 중요하다. 이에 본 연구는 저온에서도 수화열이 높게 발생되는 $Al_2O_3$성분이 함량이 높은 CSA, 알루미나시멘트를 OPC에 치환하여 물성평가를 수행하였다. 그 결과 CSA, 알루미나시멘트를 사용하여 $-5^{\circ}C$의 저온환경에서 초기에 수화반응이 빠르게 진행되며, 급결현상 및 유동성저하현상이 발생되었고, 석고를 사용하여 응결시간을 지연하며 유동성을 확보하여 작업성을 개선하였다. 또한 단열양생공법을 적용하여 모르타르의 동결시간을 지연하였으며 수축보상효과를 증진시켰고 3일, 7일 강도가 증진되었다. 따라서 본 연구 결과 저온환경에서 CSA, 알루미나시멘트 및 석고를 사용하여 조기에 강도발현 증진효과가 우수하였으며, 석고 및 단열양생공법을 적용하여 작업성, 동결저항성, 조기강도 발현 성능이 개선되어 초기동해를 방지하는데 효과가 있을 것으로 판단된다.

EVALUATION OF NOx REDUCTION CATALYST BY MODEL GAS FOR LEAN-BURN NATURAL GAS ENGINE

  • LEE C. H.;CHO B. C.
    • International Journal of Automotive Technology
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    • 제6권6호
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    • pp.591-598
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    • 2005
  • A three-way catalyst system of a natural gas vehicle (NGV) has characteristics of higher fuel consumption and higher thermal load than a lean-bum catalyst system. To meet stringent emission standards in the future, NGV with the lean-bum engine may need a catalyst system to reduce the amounts of HC, CO and NOx emission, although natural gas system has low emission characteristics. We conducted experiments to evaluate the conversion efficiency of the NOx reduction catalyst for the lean-burn natural gas engine. The NOx reduction catalysts were prepared with the ${\gamma}-Al_{2}O_3$ washcoat including Ba based on Pt, Pd and Rh precious metal. In the experiments, effective parameters were space velocity, spike duration of the rich condition, and the temperature of flowing model gas. From the results of the experiments, we found that the temperature for maximum NOx reduction was around $450^{\circ}C$, and the space velocity for optimum NOx reduction was around $30,000\;h^{-1}$ And we developed an evaluation model of the NOx reduction catalyst to evaluate the conversion performance of each other catalysts.

세라믹 패키지를 이용한 표면 실장형 다이오드의 제작과 특성 평가 (Manufacture and Characteristic of Surface Mounted Device Type Fast Recovery Diode with Ceramic Package)

  • 전명표;조상혁;조정호;김영익;유인기
    • 한국전기전자재료학회:학술대회논문집
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    • 한국전기전자재료학회 2006년도 추계학술대회 논문집 Vol.19
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    • pp.221-221
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    • 2006
  • The SMD type P-N junction diode with ceramic package for diode case were fabricated. It was made this diode with simple process from $Al_2O_3$ ceramic chip, solder preform, diode chip, coating reagent and conductive paste for chip terrmination. Its merit is small size, easy manufacture. fast cooling with ceramic case. The electric characteristics of the diode such as reverse recovery time, breakdown voltage, forward voltage, and leakage current were 5 28ns, 1322V, 1.08V, $0.45{\mu}A$.

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알루미나-아연붕규산염 유리를 이용한 저온 소결 다공성 세라믹스의 제조 및 특성 (Properties of Low Temperature Sintered Porous Ceramics from Alumina-Zinc Borosilicate Glass)

  • 김관수;송기영;박상엽;김신;김성진;윤상옥
    • 한국세라믹학회지
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    • 제46권6호
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    • pp.609-614
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    • 2009
  • The low-temperature preparation of porous ceramics was carried out using mixtures of alumina-zinc borosilicate (ZBS) glass. The compositions of alumina-ZBS glass mixture with PMMA pore-former were unfortunately densified. Because PMMA was evaporated below the softening point of ZBS glass ($588{^{\circ}C}$), the densification through the pore-filling caused by the capillary force might occur. Howerver, those with carbon possessed pores where carbon was evaporated above the softening point. The porous ceramic having 35% porosity was successively fabricated by the low-temperature sintering process below $900{^{\circ}C}$ using 45 vol% of alumina, 45 vol% ZBS of glass, and 10 vol% of carbon as starting materials.

SiC 필러 함량이 탄소 함유 Polysiloxane으로부터 제조된 고기공률 탄화규소 세라믹스의 미세조직과 꺾임강도에 미치는 영향 (Effect of SiC Filler Content on Microstructure and Flexural Strength of Highly Porous SiC Ceramics Fabricated from Carbon-Filled Polysiloxane)

  • 엄정혜;김영욱;송인혁
    • 한국세라믹학회지
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    • 제49권6호
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    • pp.625-630
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    • 2012
  • Highly porous silicon carbide (SiC) ceramics were fabricated from polysiloxane, SiC and carbon black fillers, AlN-$Y_2O_3$ additives, and poly (ether-co-octene) (PEOc) and expandable microsphere templates. Powder mixtures with a fixed PEOc content (30 wt%) and varying SiC filler contents from 0-21 wt% were compression-molded. During the pyrolysis process, the polysiloxane was converted to SiOC, the PEOc generated a considerable degree of interconnected porosity, and the expandable microspheres generated fine cells. The polysiloxane-derived SiOC and carbon black reacted and synthesized nano-sized SiC with a carbothermal reduction during a heat-treatment. Subsequent sintering of the compacts in a nitrogen atmosphere produced highly porous SiC ceramics with porosities ranging from 78 % to 82 % and a flexura lstrength of up to ~7 MPa.

제강슬래그와 석회석을 이용한 비소오염 농경지 토양 안정화 연구 (Study for the Stabilization of Arsenic in the Farmland Soil by Using Steel Making Slag and Limestone)

  • 이민희;전지혜
    • 자원환경지질
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    • 제43권4호
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    • pp.305-314
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    • 2010
  • 제강슬래그와 석회석을 이용하여 비소로 오염된 농경지 토양으로부터 비소 용출을 안정화 시키는 배치 및 대형 칼럼 실험을 실시하여, 제강슬래그와 석회석이 토양 내 비소안정화에 효과적으로 사용될 수 있음을 입증하였다. 토양의 비소 농도가 토양오염우려기준 농도의 약 2배(12.3 mg/kg)인 전남 광양 주변 초남광산 주변에 위치한 밭토양을 대상으로 안정화 실험을 실시하였으며, 안정화제로 사용한 제강슬래그 이화학분석 결과 비소 공침 효과가 높은 Ca, Fe, Al, Mg 산화물 함량이 70% 이상을 차지하는 것으로 나타났다. 안정화제 종류별 비소 용출 저감 효과를 규명하고 최적 안정화제 주입 비율을 선정하기위한 배치실험을 실시하였다. 오염토양 대비 석회석(또는 제강슬래그)의 첨가 비율을 1, 2, 3% 로 설정하여 비소 용출 저감 효율을 규명하는 실험을 실시하였으며, 석회석과 제강슬래그를 다양한 비 율로 혼합한 혼합안정화제도 실험에 사용하였다. 배치실험 결과 오염토양으로부터 용출되는 비소 농도는 1% 와 3% 석회석 첨가에 의해 안정화제를 첨가하지 않은 오염 토양의 비소 용출 농도 대비 각각 51%, 62% 감소하였다. 1%와 3% 제강슬래그를 오염토양에 첨가한 경우 비소 용출 농도는 각각 46%, 52% 감소하였다. 석회석 1%+제강슬래그 1%, 석회석 1%+제강슬래그 2%, 석회석 2%+제강슬래그 1%를 첨가하여 실험한 경우, 비소 용출농도는 각각 63%, 62%, 72% 감소하였다. 비소 용출 농도 및 용출 누적량을 계산하여 안정화공법에 의한 비소 오염 토양의 장기적 안정화를 예측하고자 인공강우에 의한 연속 용출 실험을 실시하였다. 배수시스템 및 격자형의 하부 스크린이 설치된 직경 15 cm, 높이 100 cm 의 대형 아크릴 칼럼을 제작하였으며, 용출시험 결과로부터 비소 용출 저감 효과가 뛰어난 석회석 2%+제강슬래그 1%를 혼합하여 연속 칼럼 실험의 안정화제로 사용하였다. 안정화제를 첨가하지 않은 칼럼의 경우 인공강우에 의한 비소 용출 농도는 시간이 지남에 따라 약 $50-80\;{\mu}g/L$ 를 유지하였다. 2% 석회석과 1% 제강슬래그를 오염토양과 혼합한 칼럼의 경우 비소 용출 농도는 1년 이내에 80% 이상 감소하였으며, 지하수 생활용수기준치인 $50\;{\mu}g/L$ 보다 낮게 나타나 오염토양으로부터의 비소의 안정화 효과는 매우 높은 것으로 나타났다. 석회석과 제강슬래그의 비소 안정화 기작을 규명하기위해 석회석과 제강슬래그를 3가비소(arsenite) 용액과 혼합하여 반응시 켜 공침된 광물 결정에 대하여 SEM/EDS 분석을 실시한 결과 방해석($CaCO_3$) 이외에 포틀랜다이트(portlandite)와 칼슘-비소 산화물(Ca-As-O 계열)이 추가로 생성된 것으로 나타났으며, 이러한 추가 생성 광물에 의한 비소 포획이 주요 비소 고정 기작인 것으로 나타났다.

Methyl Methacrylate의 Emulsion Polymerization에 關한 硏究 (A Study on the Emulsion Polymerization of Methyl Methacrylate)

  • 이형규;민태익
    • 대한화학회지
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    • 제12권1호
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    • pp.4-11
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    • 1968
  • With the selected emulsifiers for the emulsion polymerization of methyl methacrylate, the HLB of the emulsifier in the reaction system has been studied on the effect of the ratio of tetra sodium-N-(1,2-dicarboxy ethyl)-N-octadecyl sulfosuccinamate(Aerosol 22) to polyethylene glycol nonyl phenyl ether (Noigen EA 160), and also sodium lauryl sulfate(Quolac EX-UB), Disodium-N-octadecyl sulfosuccinamate (Aerosol 18) and Aerosol 22 as emulsifiers having various hydrophilic groups in the molecules have been studied. Results are as follows; 1) The viscosity of the emulsions and the molecular weight of the polymers have maximum values at a constant HLB value of emulsifiers, but their stabilities show minimum point at the value with the titration with the three kinds of mono, bi, tri-valent electrolytes. These results are agreed on the theory of Greth & Wilson in which the properties of polymer emulsions depend upon the HLB system of emulsifiers. 2) The viscosity of the emulsions and the molecular weights of the produced polymers increase more in the case of blending of Aerosol 22 to Noigen EA-160 than of the separate using. 3) The coagulation effects of the divalent electrolytes($ex,\;Ca^{++},\;Zn^{++}$) are contrast to the effects of monovalent($ex,\;Na^+$) and trivalent($ex,\;Al^{+++}$) in the emulsions with Aerosol 18 or Aerosol 22 which have more than two hydrophilic groups. It seems that the stability of the O/W emulsions by electrolytes is directly related to the parameters of surface physical chemistry such as surface geometry of surface chemical constitution of polymer particles.

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유지요소의 크기와 형태가 간접복합레진과 금속간의 결합강도에 미치는 영향 (THE EFFECT OF SIZE AND SHAPE OF RETENTION ELEMENT ON COMPOSITE TO METAL BOND STRENGTH)

  • 이윤정;전영찬;정창모
    • 대한치과보철학회지
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    • 제45권5호
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    • pp.665-674
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    • 2007
  • Purpose: The purpose of this study was to investigate the effect of sire and shape of retention element on the bond strength of indirect composite resin and metal. Material and method: The metal disk specimens, each 6mm in diameter, were cast from CrCo alloy. They were divided into 8 groups by applied retention element. retention bead group $B2\;({\phi}\;0.2mm),\;B4\;({\phi}\;0.4mm),\;B6\;({\phi}\;0.6mm),\;B8\;({\phi}\;0.8mm)$, retention crystal group C2 (0.2mm), C5 (0.5mm), C8 (0.8mm) and sandblasting group SB ($110{\mu}m\;Al_2O_3$ blasting) as control. Eighty-eight metal specimens were veneered with $TESCERA^{(R)}$ Indirect resin system. One specimen of each group was sectioned and the resin-metal bonding pattern at the interface was observed under measuring microscope. Other specimens were then tested for tensile bond strength on an Instron universal testing machine at a crosshead speed of 2mm/min. Results: 1. Compared to sandblasting, beads or crystals increased the resin-metal bond strength (P<.05). 2. 0.2mm retention crystals were most effective in improving the resin-metal bond strength (P>.05). 3. 0.2mm beads showed the highest bond strength among retention bead groups, but there was no statistically significant difference (P>.05). 4. Retention crystals tend to be higher in bond strength than retention beads due to wider surface area. 5. The larger retention element, the larger the undercut for the mechanical retention, but the gap at resin-metal interface was also increased. Conclusion: Within the limitations of this study, 0.2mm retention crystals were most effective in improving the resin-metal bond strength.

용융침투법으로 제조한 유리-알루미나 복합체: II. Kinetic 연구 (Glass-alumina Composites Prepared by Melt-infiltration: II. Kinetic Studies)

  • 이득용;장주웅;이명현;이준강;김대준;박일석
    • 한국세라믹학회지
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    • 제39권2호
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    • pp.145-152
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    • 2002
  • 상용 알루미나 분말(0.5, 2.8, 12, 45 ${\mu}m$)을 die-press법을 이용하여 1120$^{\circ}C$에서 2시간 1차 소결하여 다공성 전성형체를 제조하고 1100$^{\circ}C$에서 0∼2시간까지 $La_2O_3-Al_2O_3-SiO_2$계 유리를 용융 침투시켜 유리 침투 깊이와 침투 시간간의 kinetic을 조사하였다. 침투시간이 증가할수록 유리 침투깊이는 Washburn 식의 포물선 관계를 가지면서 증가하였으며 침투 상수인 K는 알루미나 입도가 증가할수록 증가하였다. 유리-알루미나 복합체의 강도값은 2.8${\mu}m$ 알루미나가 분산된 복합체까지 충진률의 증가로 인하여 증가하다가 알루미나 입도가 증가할수록 감소하였다. 파괴인성은 알루미나 입도가 증가할수록 균열 휨 현상과 균열과 알루미나 입자간 결합에 의하여 증가하였다.