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황화광물로부터 유용금속 침출을 위한 Acid Bake-water Leaching System 내 황산염 용매제의 적용성 (Application of Sulfate Solvent in Acid Bake-water Leaching System for Valuable Metal Leaching from Sulfide Mineral)

  • 고진석;톡토흐마;박천영
    • 한국광물학회지
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    • 제31권2호
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    • pp.67-73
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    • 2018
  • 본 연구는 acid bake-water leaching system (AWS)를 이용하여 Au 정광으로부터 경제적이고 친환경적인 유용금속 용출을 위하여 황산염 용매제의 적용성을 파악하는 것이다. AWS 실험은 전기로를 이용하여 다양한 baking 온도($100^{\circ}C{\sim}500^{\circ}C$)와 황산염 용매제($H_2SO_4$, $K_2SO_4$, $(NH_4)_2SO_4$, $MgSO_4$, $CaSO_4$) 조건에서 수행하였다. Baking 온도가 $400^{\circ}C$까지 증가할수록 유용금속의 용출률은 증가하였다. 용출시간에 따른 AWS 실험결과, 최대 용출률 조건은 $(NH_4)_2SO_4$ 용매제이었다. 본 연구를 통하여 $(NH_4)_2SO_4$ 용매제가 AWS를 이용한 유용금속 용출에 있어 효과적인 용매제로 사용가능함을 입증하였다.

비피리미딘계 배위자를 골격으로 하는 Pt(II)착체의 합성 및 특성 (A Synthesis and Characterization of Pt(II) Complexes with Bipyrimidin-based Back-bone System)

  • 손석환;안호근;정민철
    • Korean Chemical Engineering Research
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    • 제54권4호
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    • pp.555-559
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    • 2016
  • 본 연구에서는 2,2'-bispyrimidine (bpim), 2,2'-bipyridine (bpy), 5,5'-dimethyl-2,2'-bipyridine (5,5-mebpy), 5'-bromo-2,2'-bipyridine (5-brbpy), 5,5'-dibromo-2,2'-bipyridine (5,5-brbpy), 4,4'-dimethyl-2,2'-bipyridine (4,4-mebpy), 4,4'-dihexyl-2,2'-Bipyridine (4,4-hebpy), 1,10'-Phenanthroline (phen), 3,4,7,8'-tetramethyl-1,10'-Phenanthroline (3,4,7,8-phen)을 사용하여 단핵 Platinum착체를 합성하였다. 합성되어진 Platinum착체의 화학적 구조를 결정하기 위해서 $^1H(^{13}C)$-NMR, FT-IR을 사용하였으며, 광 물리학적 특성에 대한 측정은 UV-vis, PL을 통하여 측정하였다. 합성한 Platinum착체는 356 nm~421 nm영역에서 발광파장이 확인되었으며, DMSO용액에서 내부양자효율이 0.05~0.46으로 나타났다.

크롬(VI)-4,4'-Bipyridine 착물에 의한 치환 벤질 알코올류의 산화반응 속도론과 메카니즘 (Kinetics and Mechanism of the Oxidation of Substituted Benzyl Alcohols by Cr(VI)-4,4'-Bipyridine Complex)

  • 김영식;박영조
    • 한국산학기술학회논문지
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    • 제13권1호
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    • pp.462-469
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    • 2012
  • 크롬(VI)-4,4'-bipyridine 착물(4,4'-bipyridinium dichromate)를 합성하여, 적외선분광광도법(IR), 유도결합 플라즈마(ICP) 등으로 구조를 확인하였다. 여러 가지 용매하에서 4,4'-bipyridinium dichromate를 이용하여 벤질 알코올의 산화반응을 측정한 결과 유전상수(${\varepsilon}$) 값이 큰 용매 순서인 시클로헥센<클로로포름<아세톤$CH_3$, H, m-Br, m-$NO_2$)를 효과적으로 산화시켰다. 그리고 전자받개 그룹들은 반응속도가 감소한 반면에 전자주개 치환체들은 반응속도를 증가시켰다. 또한 Hammett 반응상수(${\rho}$) 값은 -0.63(303K) 이었다. 그러므로 본 실험에서 알코올의 산화반응 과정은 먼저 크토메이트 에스테르 형성과정을 거친 후, 속도결정단계에서 양성자 전이가 일어나는 메카니즘임을 알 수 있었다.

1,4-Thiazine Carboxanilide의 합성: Pummerer 반응에서의 인접기 참여효과 (A Synthesis of 1,4-Thiazine Carboxanilide: Neighboring Group Participation in Pummerer Reaction)

  • 한호규;남기달;마혜덕
    • 대한화학회지
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    • 제46권4호
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    • pp.330-336
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    • 2002
  • 새로운 ${\alpha},{\beta}$-불포화Carboxanilide계열의 살균제를 개발을 목적으로 4-acetyl-3-methyl-N-phenyl-1,4-thiazine-2-Carboxamide(6)의 합성에 대하여 기술하였다. Dihydro-1,4-thiazine methyl ester 11을 산화하여 생성된 sulfoxide 7을 Pummerer 반응하여 $\alpha$-acetoxy dihydro-1,4-thiazine 10a를 얻었다. 반며에 Dihydro-1,4-thiazine Carboxanilide sulfoxide14는 동일한 반응조건 하에서 중간체 sulfonium ion의 carboxanilide기가 관여한 vinylogous Pummerer 반응의 전위에 의하여 중간체를 15를 통하여 acetoxymethyl dihydro-1,4-thiazine 18이 생성되었다. 1,4-Thiazine carboxanilide 6은 $\alpha$-acetoxy dihydro-1,4-thiazine 10a를 산촉매로 처리한 다음 생성된 21a를 가수분해하고 아닐린과 결합하여 합성하였다

20세기초 4칸${\times}$4칸 교회의 평면구성 및 구조형식에 관한 연구 (A Study on the Plan and Structural System of 4 kan(間) by 4 kan(間) Church in the Early 20th Century)

  • 김기주
    • 건축역사연구
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    • 제17권5호
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    • pp.39-53
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    • 2008
  • This study aims to investigate and analyze the plan and structural system of 4 kan(間) by 4 kan(間) square church built in early 20th century. At that time, three kinds of traditional wooden structure church had been built under the circumstances of transitional era : Basilica style such as Ganghwa Anglican Church, 'ㄱ' shaped style such as Keumsan Church and $4{\times}4$ Square style such as Bukok Church and Jacheon Church that are concerned in this study. Traditional plans and structural system were mixed with new religious function and transformed into korean peculiar style. $4{\times}4$ Square style is a residual product in that process. Despite of it, little concerns on it till now. The results of this study are described as follows. 1. The plan of these $4{\times}4$ square churches is divided into three areas : cathedra($1{\times}1$), attendance($4{\times}2$), and intermediation($4{\times}2$). The location of cathedra is commonly the opposition part of main gate and projected out of the building. Attendance area was also divided into two, man and woman, because of keeping a distance with each other. 2. The structural system of these $4{\times}4$ square churches are somewhat different because of their size and roof style. In the case of Bukok church, $4{\times}4$ square fall off $3{\times}3$ and $2{\times}2$ gradually and turn into paljak(八作) roof, which enable us to get in traditional entering methods. On the contrary, Jacheon church use hipped roof but almost alike pyramidal roof, which could make us not to recognize entering in the aspect of gable part.

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A Novel Method for Preparing of Oxoruthenates Complexes: trans-[RuO3(OH)2]2-, [RuO4]-, (n-Pr4N)+[RuO4]- and [RuO4 and Their Use as Catalytic Oxidants

  • Shoair, Abdel-Ghany F.
    • Bulletin of the Korean Chemical Society
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    • 제26권10호
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    • pp.1525-1528
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    • 2005
  • The synthesis and characterization of ${K_3[Ru(C_2O_4)3]{\cdot}4H_2O\;(C_2O_4}^{2-}$ = oxalato anoin) complex are described, and its redox properties (in buffer solution of pH = 12) have been investigated. This complex is used for in situ generation of oxoruthenates complexes which have been characterized by electronic spectroscopy. Reaction of ${K_3[Ru(C_2O_4)3]{\cdot}4H_2O$ with excess ${S_2O_8}^{2-}$ in molar KOH generates trans-${[RuO_3(OH)_2]^{2-}/S_2O_8}^{2-}$ reagent while with excess ${BrO_3}^-$ in molar $Na_2CO_3$ generates ${[RuO_4]^-/BrO_3}^-$ reagent. Avoiding the direct use of [$RuO_4$] the organic-soluble $(n-Pr_4N)^+[RuO_4]^-$, (TPAP) has been isolated by reaction of $K_3[Ru(C_2O_4)3]{\cdot}4H_2O$ with excess ${BrO_3}^-$ in molar carbonate and n-$Pr_4$NOH. In a mixture of $H_2O/CCl_4$ ruthenium tetraoxide can be generated by reaction of $K_3[Ru(C_2O_4)3]{\cdot}4H_2O$ with excess ${IO_4}^-$. The catalytic activities of oxoruthenates that have been made from $K_3[Ru(C_2O_4)3]{\cdot}4H_2O$ towards the oxidation of benzyl alcohol, piperonyl alcohol, benzaldehyde and benzyl amine at room temperature have been studied.

Li4SiO4 slurry conditions and sintering temperature for fabricating Li4SiO4 pebbles as tritium breeders for nuclear-fusion reactors

  • Young Ah Park;Ji Won Yoo;Yi-Hyun Park;Young Soo Yoon
    • Nuclear Engineering and Technology
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    • 제55권8호
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    • pp.2966-2976
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    • 2023
  • A tritium breeder is a lithium-based material capable of producing tritium. Many researchers designing nuclear-fusion energy are studying tritium production using pebbles, which are solid-type breeders. The sphericity and size of the pebbles are critical in obtaining pebbles with good tritium-breeding efficiency. Furthermore, tritium-release efficiency can be increased by using pebbles with appropriate porosities. Promising raw materials for tritium-breeding materials include Li4SiO4 and Li2TiO3. Li4SiO4 has a higher lithium density than Li2TiO3 and exhibits excellent tritium-breeding efficiency. However, it has the disadvantage of being easily decomposed during the Li4SiO4-green-pebble sintering process because of its low structural stability at high temperatures and high lithium density. In this study, we attempted to determine the optimal conditions for manufacturing Li4SiO4 pebbles using the droplet-freeze-drying method. The optimal Li4SiO4 slurry conditions and sintering temperatures were determined. The optimal Li4SiO4 slurry-fabrication conditions were 3 wt% polyvinyl alcohol and 75 wt% Li4SiO4 based on the deionized-water weight content. The sintering temperature at which Li4SiO4 did not decompose and exhibited the optimum porosity of 10.8% was 900 ℃.

Dechlorination of 4-Chlorobenzoate by Pseudomonas sp. DJ-12

  • Chae, Jong-Chan;Kim, Chi-Kyung
    • Journal of Microbiology
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    • 제35권4호
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    • pp.290-294
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    • 1997
  • 4-Chlorobiphenyl-degrading Pseudomonas sp. DJ-12 was able to degrade 4-chlorobenzoate(4CBA), 4-iodobenzoate, and 4-bromobenzoate completely under aerobic conditions. During. the degradation of 4CBA by Pseudomonas sp. DJ-12, chloride ions were released by dechlorination and 4-hydroxybenzoate was produced as an intermediate metabolite. The NotI-KNA fragments of pKC157 containing dechlorination genes hybridized with the gene encoding 4CBA:CoA dehalogenase of Pseudomonas sp. CBS3 which is responsible for the hydrolytic dechlorination of 4CBA. These results imply that Pseudomonas sp. DJ-12 degrades 4CBA to 40hydroxybenzoate via dechlorination as the initial step of its degradativ pathway. The genes responsible for dechlorination of 4CBA were found to be blcated on the chromosomal DNA of Pseudomonas sp. DJ-12.

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$3CaO.SiO_2$ 생성 반응과 미세조직에 미치는 $K_2SO_4$$Na_2SO_4$의 영향 (Effects of $K_2SO_4$ and $Na_2SO_4$ on $3CaO.SiO_2$ Formation and its Microstructure)

  • 정해문;한기성;최상흘
    • 한국세라믹학회지
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    • 제30권10호
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    • pp.871-879
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    • 1993
  • Effects of K2SO4 and Na2SO4 on C3S formation and its microstructure were investigated. C3S formation was not influenced by addition up to 6.0wt% of K2SO4 as SO3 base, however it was prevented by only 1.0wt% of Na2SO4 addition. C3S prevention by added Na2SO4 was the reason why C2S stabilized by Na+ and SO42- could not react to C3S. Added K2SO4 appeared as K2SO4, however added Na2SO4 appeared as the form of Na2xCa3-xAl2O6, (Na0.8Ca0.1)SO4 and Na2SO4 in interstitial phase.

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Regioselective Nitration of Inactive 4,4-Dibromobiphenyl with Nitrogen Dioxide and Molecular Oxygen over Zeolites: An Efficient Preparation of 4,4'-Dibromo-2-nitrobiphenyl

  • Wang, Wei;Peng, Xinhua;Chen, Nan
    • 대한화학회지
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    • 제58권1호
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    • pp.72-75
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    • 2014
  • In the presence of zeolites, 4,4'-dibromobiphenyl could be region-selectively nitrated by the action of nitrogen dioxide and molecular oxygen. The ratio of 4,4'-dibromo-2-nitrobiphenyl to 4,4'-dibromo-3-nitrobiphenyl could reach 14 in a high yield of 90%. Zeolites could be easily regenerated by heating and reused four times to give the results similar to those obtained with fresh catalyst. Compared with the classic nitration method, no nitric acid and sulfuric acid were used, which suggested that the method was an environmentally economic process.