• 제목/요약/키워드: 화학 반응

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Manganese Dioxide-Based Chlorination of Alcohols Using Silicon Tetrachloride (이산화망간 존재하에서 사염화규소를 이용한 알코올의 염소화반응)

  • Ha, Dong Soo;Yoon, Myeong Jong
    • Journal of the Korean Chemical Society
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    • 제41권10호
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    • pp.541-546
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    • 1997
  • Manganese dioxide may react with silicon tetrachloride to form manganese(Ⅳ) oxodichloride which reacts subsequently with another molecule of silicon tetrachloride leading to manganese tetrachloride eventually in chlorinated solvents. This in situ generated manganese(Ⅳ) oxodichloride or manganese tetrachloride were found to be very effective for the chlorination of a wide variety of alcohols to the corresponding chlorides. Primary, secondary and benzylic alcohols were converted into corresponding chlorides when treated with silicon tetrachloride in the presence of manganese dioxide at room temperature.

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Numerical Characteristics of Hypersonic Air Chemistry and Application of Partially Implicit Time Integration Method (극초음속 공기반응의 수치해석적 특성과 부분 내재적 적분법 적용)

  • Kim, Seong-Lyong;Ok, Ho-Nam;Ra, Seung-Ho;Kim, In-Sun
    • Journal of the Korean Society for Aeronautical & Space Sciences
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    • 제31권7호
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    • pp.1-8
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    • 2003
  • Numerical characteristics of air chemistry associated with hypersonic flows are described and are compared with those of hydrogen oxygen combustion, applying the partially implicit time integration method to air chemistry. This paper reveals that the time integration of air chemistry needs a chemical Jacobian for stable calculations. However the positive real eigenvalues in air chemistry are relatively smaller than those of hydrogen combustion, and the numerical integration is less sensitive than that with combustion. lt is also found that the application of the partia1ly irnplicit method reduces the computing time without numerical instabilities.

Study on Interfacial Reactions between Graphite Electrode and PC-base Electrolyte by In-situ AFM and In-situ Raman (In-situ 전기화학 AFM 및 Raman 분석방법을 이용한 흑연음극과 PC계 전해질 계면반응의 해석)

  • Song, Hee-Youb;Jeong, Soon-Ki;Kim, Yang-Su
    • Proceedings of the KAIS Fall Conference
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    • 한국산학기술학회 2011년도 춘계학술논문집 1부
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    • pp.155-157
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    • 2011
  • 본 논문에서는 In-situ 전기화학 AFM과 In-situ 전기화학 Raman을 주된 분석방법으로 리튬 이차전지의 흑연 음극과 PC계 전해질 계면에서의 반응을 이해하고자 하였다. In-situ 전기화학 AFM 분석방법을 통하여 PC계 전해질에서 용매화된 리튬의 삽입/탈리반응이 진행되는 것을 확인할 수 있었으며 In-situ 전기화학 Raman 분석방법을 이용하여 PC계 전해질에서는 삼원계 Li-GIC가 생성되는 것을 확인할 수 있었다.

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Development of high efficiency DSE for sterilization reaction (고효율 전기화학적 살균 반응용 DSE 개발)

  • Son, Seong-Ho;Kim, Hyeong-Mi;Park, Seong-Cheol;Kim, Jin-Hwa;Lee, Min-Hyeong;Yang, Se-Hun
    • Proceedings of the Korean Institute of Surface Engineering Conference
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    • 한국표면공학회 2014년도 추계학술대회 논문집
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    • pp.120-121
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    • 2014
  • 전기도금, 난분해성 오폐수 처리, 해수정화, 연료전지의 촉매전극 등 다양한 전기화학반응을 이용한 산업에 전기화학법 표면처리용 DSE(Dimensionally Stable Electrode)가 많이 사용되고 있다. 고효율 전기화학적 살균 반응용 DSE를 개발하기 위해 전기화학적 특성이 좋은 이리듐(Ir), 루테늄(Ru)등의 조성비, 전처리 및 열처리등의 실험을 통해 최적의 공정 조건을 확보하였다.

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Electrochemical Reduction of Triphenylphosphine Phenylimide (Triphenylphosphine Phenylimide의 전기화학적인 환원)

  • Pak Chong Min;Wilson M. Gulick, Jr.
    • Journal of the Korean Chemical Society
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    • 제18권5호
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    • pp.341-353
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    • 1974
  • The electrochemical reduction of triphenylphosphine penylimide in nonaqueous media has been examined by polarography, cyclic voltammetry, controlled-potential coulometry and electron spin resonance spectroscopy. The reduction of triphenylphosphine phenylimide proceeds by a one-electron transfer to form anion radical which undergoes both protonation and a second one-electron reduction followed by cleavage of the phosphorus-nitrogen double bond. Aniline is a major product. The cleavage of a phosphorus-phenyl bond was also observed after reduction of triphenylphosphine oxide which is one of the major products of the chemical reaction which follow the primary process.

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Characterization and Formation of Chemical Bonds of Silica-Coupling Agent-Rubber (실리카-커플링제-고무의 화학 결합 형성과 특성 분석)

  • Ko, Eunah;Choi, Sung-Seen
    • Elastomers and Composites
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    • 제49권3호
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    • pp.239-244
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    • 2014
  • Reaction between silica and silane coupling agent without solvent was investigated using transmission mode Fourier transform infrared spectroscopy (FTIR) and thermogravimetric analysis (TGA). Bis[3-(triethoxysilylpropyl) tetrasulfide] (TESPT) was used as a silane coupling agent. After removing the unreacted TESPT, formation of chemical bonds was analyzed using FTIR and content of reacted TESPT was determined using TGA. Content of the coupling agent bonded to silica increased with increase in the coupling agent content, but the oligomers were formed by condensation reaction between coupling agents when the coupling agent was used to excess. In order to identify bonds formed among silica, coupling agent, and rubber, a silica-coupling agent-BR model composite was prepared by reaction of the modified silica with liquid BR of low molecular weight and chemical bond formation of silica-coupling agent-BR was investigated. Unreacted rubber was removed with solvent and analysis was performed using FTIR and TGA. BR was reacted with the coupling agent of the modified silica to form chemical bonds. Polarity of silica surface was strikingly reduced and particle size of silica was increased by chemical bond formation of silica-coupling agent-BR.

Diversification of 4,5-disubstituted Pyrrolo[3,2-d]-pyrimidines by Microwave Assisted Metal Catalyzed Reaction (마이크로파와 금속 촉매를 이용한 Pyrrolo[3,2-d]-pyrimidine 유도체의 다양화)

  • Jeong Seob, Byeon;Eul Kgun, Yum;Yeong-Joon, Kim
    • Journal of the Korean Chemical Society
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    • 제66권6호
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    • pp.442-450
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    • 2022
  • Diverse pyrrolo[3,2-d]pyrimidines that are expected to exhibit bioactivity were synthesized through O-arylation and Suzuki coupling reactions. Microwave-assisted O-arylation was successfully performed using a Cu metal catalyst, so that 4 position of pyrrolo[3,2-d]pyrimidine could be substituted with phenol group. In addition, 4-aryl substituted pyrrolo[3,2-d]pyrimidines were synthesized with good to excellent yields by microwave-assisted Suzuki coupling reaction using a Pd metal catalyst. By using microwaves as reaction conditions for diversification of derivatives, it was possible to dramatically overcome the disadvantages of traditional heat reactions of long reaction times and heat transfer efficiency problems. The result of this study can be used to be diversify pyrrolo[3,2-d]pyrimidine derivatives, which are expected to play an important role in the drug discovery research.

1H NMR Kinetic Studies for Degradation of Nitramine Explosives Using PdO Nanoparticle (PdO 나노입자를 이용한 니트라민 폭발물 분해반응에 대한 1H NMR 반응속도연구)

  • Kye, Young-Sik;Kumbier, Mathew;Kim, Dongwook;Harbison, Gerard S.;Langell, Marjorie A.
    • Applied Chemistry for Engineering
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    • 제33권3호
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    • pp.302-308
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    • 2022
  • The PdO nanoparticle with large surface area was selected to solve the environmental pollution problem at fire range caused by high energy explosives research department explosive (RDX) and high melting explosive (HMX). By simulating water pollution, RDX and HMX nitramine explosives were dissolved in water, followed by the degradation reaction at 313 K by adding PdO. In order to measure the degradation reaction rate of explosives, 1H NMR was used, which can monitor the reaction rate without losing sample during reaction, and observe the progress of the reaction through the spectrum. The results showed that the degradation of RDX and HMX by PdO nanoparticles are pseudo-first order reaction. The degradation of explosives compounds were observed via the chemical shift and peak intensity analysis of NMR peaks. The measured rate constants for these reactions of RDX and HMX were 2.10 × 10-2 and 6.35 × 10-4 h-1, respectively. This study showed that the application of PdO nanoparticles for explosives degradation is a feasible option.

금속 프탈로시아닌 유도체의 제조 및 그의 소취 특성(1)

  • 김애경;최창남;조동련
    • Proceedings of the Korean Fiber Society Conference
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    • 한국섬유공학회 1998년도 봄 학술발표회 논문집
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    • pp.338-341
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    • 1998
  • 악취의 주원인은 염기성 취기의 대표인 암모니아, 산성 취기의 대표인 황화수소, 그리고 트리메틸아민이며, 이들은 법정 악취물질로써 지정되어 있다$^1$. 이와 같은 악취를 없애는 소취기구는 활성탄 및 제오라이트 등과 같은 물질에 대한 물리적 흡착에 의한 것, 산화제 및 환원제에 의한 화학반응에 의한 것, 미생물 및 효소에 의한 생물학적 반응에 의한 것으로 대별되지만, 물리 흡착은 재방출의 문제가 있고 화학 및 생물학적 반응에는 소취성분 자체의 유해성 및 반응후 물질의 유해성이 문제가 되는 경우가 있다.(중략)

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Chemical Fixation of Carbon Dioxide with Methane (메탄에 의한 이산화탄소의 화학적 고정화)

  • 조영복;김상채;서성규;유의연
    • Proceedings of the Korea Air Pollution Research Association Conference
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    • 한국대기환경학회 2000년도 추계학술대회 논문집
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    • pp.389-390
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    • 2000
  • 최근 지구 온난화의 55% 이상을 차지하고 있는 이산화탄소를 유용한 화합물로 전환하고자 메탄을 환원제로 사용한 이산화탄소 개질반응으로부터 합성가스 생성에 관한 연구가 활발히 진행되고 있다. 메탄의 이산화탄소 개질반응은 수증기 개질반응보다 낮은 합성 가스비의 생성, 온실효과를 유발하는 이산화탄소의 저감, 반응의 높은 흡열도를 이용한 화학에너지 전송 시스템의 응용 면에서 그 의의가 있다. (중략)

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