• 제목/요약/키워드: Metal dissolution

검색결과 245건 처리시간 0.023초

고품위 형석의 신속 용량법 (Rapid Volumetric Assay of Fluorspar Concentrate)

  • 최규원;오준석;이광우
    • 대한화학회지
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    • 제8권3호
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    • pp.109-112
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    • 1964
  • A volumetric method of the determination of calcium carbonate and calcium fluoride in fluorspar concentrate is described. The carbonate is converted into solution by treatment of the sample in HNO$_3$-acetone (l% by volume) mixture, and the fluoride by treating the residue with H$_3BO_3$-HCl mixture. The calcium in the solution is determined volumetrically using EDTA standard solution. The selective dissolution of calcium carbonate by HNO$_3$-acetone mixture is superior to Bidtel's acetic method and little correction for the dissolution of calcium fluoride is needed. Triethanolamine is found to be superior to KCN in masking heavy metal ions.

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일방향응고 Ni기 초내열합금 천이액상화산접합부의 미세조직에 미치는 모재와 삽입금속 분말 혼합비의 영향 (The Mixing Ratio Effect of Insert Metal Powder and Insert Brazing Powder on Microstructure of the Region Brazed on DS Ni Base Super Alloy)

  • 예창호;이봉근;송우영;오인석;강정윤
    • Journal of Welding and Joining
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    • 제23권6호
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    • pp.99-105
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    • 2005
  • The mixing ratio effect of the GTD-111(base metal) powder and the GNI-3 (Ni-l4Cr-9.5Co-3.5Al-2.5B) powder on TLP(Transient Liquid Phase) bonding phenomena and mechanism was investigated. At the mixing ratio of the base metal powder under $50wt\%$, the base metal powders fully melted at the initial time and a large amount of the base metal near the bonded interlayer was dissolved by liquid inter metal. Liquid insert metal was eliminated by isothermal solidification which was controlled by the diffusion of B into the base metal. The solid phases in the bonded interlayer grew epitaxially from the base metal near the bonded interlayer inward the insert metal during the isothermal solidification. The number of grain boundaries farmed at the bonded interlayer corresponded with those of base metal. At the mixing ratio above $60wt\%$, the base metal powder melted only at the surface of the powder and the amount of the base metal dissolution was also less at the initial time. Nuclear of solids firmed not only from the base metal near the bonded interlayer but also from the remained base metal powder in the bonded interlayer. Finally, the polycrystal in the bonded interlayer was formed when the isothermal solidification finished. When the isothermal solidification was finished, the contents of the elements in the boned interlayer were approximately equal to those of the base metal. Cr-W borides and Cr-W-Ta-Ti borides formed in the base metal near the bonded interlayer. And these borides decreased with the increasing of holding time.

A New Chemical for the Separation of the CRT Panel Glass from its Funnel

  • Lee, Ki-Won;Byun, Ji-Young;Kim, Kyong-Tae;Oh, Jong-Kee
    • 대한전자공학회:학술대회논문집
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    • 대한전자공학회 2001년도 The 6th International Symposium of East Asian Resources Recycling Technology
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    • pp.71-75
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    • 2001
  • The first step for recycling the CRT bulb is to remove frist seals between the panel and funnel. For this purpose, various kinds of methods have been used. One of those is to use the nitric acid, which is a proven technology and widely used in CRT-making industries. The process. however. has a problem of NOx generation. Such a drawback can be overcome by using a new chemical. This new chemical can remove the frit without NOx generation. This paper describes the dissolution ability of the chemical for lead and zinc oxides and the application to the separation of the CRT panel from its funnel.

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중금속이온이 시멘트의 수화 및 미세구조에 미치는 영향 (The Effects of the Heavy Metal Ions on the Hydration and Microstructure of the Cement Paste)

  • 김창은;이승규
    • 한국세라믹학회지
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    • 제30권11호
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    • pp.967-973
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    • 1993
  • The effect on the hydration of cement was that Cu and Pb reacted with alkali to form soluble hydrates at theinitial stage and then there followed a slow reaction forming insoluble metal hydroxides. These hydroxides were deposited on the surface of cement particles providing a barrier against further hydration. But as a slow reaction continued, the insoluble layers were eventually destroyed and the hydration reaction resumed. Thereafter, another retardation occured by restricting the polymerization of silicates, shown by FT-IR spectroscopy analysis. In the case of Cr, as its reaction with cement caused H2O, the coordinator of Cr complex, to replace or polymerize with OH-, the formation of Cr complex promoted the leakage of OH- and increased the heat of dissolution. So the total heat evolution during hydration was larger than that in the case of Pb or Cu. The retarding effect of heavy metal ions was in the order Pb>Cu>Cr.

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각종 폐수로부터 중금속 이온을 제거하기 위한 Epichlorohydrine-가교키토산의 제조 및 가교도의 효과 (Preparations of the Cross-linked Chitosan Based on a Marine Natural Product with Epichlorohydrine for the Exclusion of Heavy Metal Ions from the Various Wastewater and Its Effect of Crosslinking Ratio)

  • 박영미;전동원
    • 한국의류산업학회지
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    • 제8권5호
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    • pp.577-584
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    • 2006
  • The binding of heavy metal ions onto cross-linked chitosan in dilute aqueous solution has been investigated as a function of pH (4.0 and 7.0), agitation period (10-180min) and concentration of various metal cations (5, 10, 50 and 100ppm). In order to obtain adsorbents that are insoluble and stable, and prevent the dissolution loss of chitosan into an acidic aqueous solution, chitosan flakes were cross-linked with epichlorohydrine (ECH) and its adsorption behavior was compared with that of the non cross-linked chitosan. An advantage of ECH is that it does not eliminate the cationic amine functional group of chitosan. In terms of adsorption ratio, the chitosan cross-linked at an ECH was inferior to original chitosan and was found that chitosan has a selectivity much remarkable than the cross-linked chitosan in low concentrated metal solutions. However, no significant decreases in the adsorption ratios were observed between the cross-linked ECH-chitosan and the non cross-linked chitosan concerning the adsorption of $Ni^{2+}$, $Co^{2+}$, $Pb^{2+}$ and $Zn^{2+}$ acidic solution.

Chemical-looping combustion을 위한 단일금속산화물인 산소운반체에 관한 연구 (Study of Oxygen Carriers with Single Metal Oxides for Chemical-Looping Combustion)

  • 이진배;박주식;최상일;송영욱;양현수;김영호
    • 한국수소및신에너지학회논문집
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    • 제14권3호
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    • pp.258-267
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    • 2003
  • A new kind of oxygen carrier material is tested for chemical-looping combustion. NiO, CoO, $Fe_2O_3$ is chosen as metal oxide and YSZ as a binder. Hydrogen fuel is reacted with metal oxide (reduction of metal oxide) and then the reduced metal is successively oxidized by air. Dissolution method is examined to prepare the oxygen carriers. The effects of reaction temperature are measured by a TGA, mechanical strength and regenerability after 10 cycle are examined. $Fe_2O_3/YSZ$ oxygen carrier is bested in mechanical strength and we consider that NiO/YSZ after 3rd cycle are good oxygen carrier in according to reactor design.

BIOGEOCHEMICAL ACTIVITIES OF MICROORGANISMS IN MINERAL TRANSFORMATIONS: CONSEQUENCES FOR METAL AND NUTRIENT MOBILITY

  • Gadd, Geoffrey M.
    • 한국미생물생명공학회:학술대회논문집
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    • 한국미생물생명공학회 2002년도 학술발표대회
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    • pp.39-61
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    • 2002
  • Bacteria and fungi are fundamental biotic components of natural biogeochemical cycles for metals and metalloids and play important roles in dissolution, precipitation, oxidation and reduction processes. Some processes catalyzed by microorganisms also have important applications in environmental biotechnology in the areas of ore leaching and bioremediation.

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모재 분말 혼합 삽입재를 이용한 니켈기 초내열합금의 천이액상확산접합에 있어서 가열속도가 접합부에 미치는 영향 (Effects of heating rate on the bonded interlayer in base metal powder mixture used transient liquid phase diffusion bonded Ni-base superalloy)

  • 김성욱;장중철;김재철;이창희
    • 대한용접접합학회:학술대회논문집
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    • 대한용접접합학회 2004년도 춘계 학술발표대회 개요집
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    • pp.48-50
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    • 2004
  • TLP 접합 공정에서 모재와 삽입금속 사이에서의 확산을 통하여 액상 삽입금속은 고온에서 등온으로 유지 시 등온 응고된다. D.S.Duvall은 느린 가열시 매우 빠른 속도로 가열 시 보다 낮은 온도에서 dissolution이 완료되고 응고가 발생할 것으로 예상하였다. (중략)

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Electrodeposition of Some Selective Metals Belonging to Light, Refractory and Noble Metals from Ionic Liquid Electrolytes

  • Dilasari, Bonita;Kwon, Kyung-Jung;Lee, Churl-Kyoung;Kim, Han-Su
    • 전기화학회지
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    • 제15권3호
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    • pp.135-148
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    • 2012
  • Ionic liquids are steadily attracting interests throughout a recent decade and their application is expanding into various fields including electrochemistry due to their unique properties such as non-volatility, inflammability, low toxicity, good ionic conductivity, wide electrochemical potential window and so on. These features make ionic liquids become an alternative solution for electrodeposition of metals that cannot be electroplated in aqueous electrolytes. In this review, we classify investigated metals into three categories, which are light (Li, Mg), refractory (Ti, Ta) and noble (Pd, Pt, Au) metals, rather than covering the exhaustive list of metals and try to update the recent development in this area. In electrodeposition of light metals, granular fine Li particles were successfully obtained while the passivation of electrodeposited Mg layers is an obstacle to reversible deposition-dissolution process of Mg. In the case of refractory metals, the quality of Ta and Ti deposit particles was effectively improved with addition of LiF and pyrrole, respectively. In noble metal category, EMIM TFSA ionic liquid as an electrolyte for Au electrodeposition was proven to be effective and BMP TFSA ionic liquid developed a smooth Pd deposit. Pt nanoparticle production from ionic liquid droplet in aqueous solution can be cost-effective and display an excellent electrocatalytic activity.