• Title/Summary/Keyword: reaction mechanism

검색결과 2,672건 처리시간 0.037초

추가 이동 질량을 이용한 선형 모터용 반발력 보상 기구 (A Passive Reaction Force Compensation Mechanism for a Linear Motor Motion Stage using an Additional Movable Mass)

  • 응웬덕칸;안형준
    • 한국정밀공학회지
    • /
    • 제31권10호
    • /
    • pp.929-934
    • /
    • 2014
  • Reaction force compensation (RFC) mechanism can relieve the vibration of base system caused by acceleration and deceleration of mover. In this paper, we propose a new passive RFC mechanism with a movable additional mass to reduce vibration of the system base as well as displacement of the magnet track. First, equation of motion for the new passive RFC mechanism is derived and simulated to tune design parameters such as masses and spring coefficients. Simulation results show that the vibration of the system base of the stage with the new RFC mechanism.

Studies on the Regioselective and Diastereoselective Amination using Chlorosulfonyl Isocyanate (CSI)

  • Kim, In-Su;Jung, Young-Hoon
    • 대한약학회:학술대회논문집
    • /
    • 대한약학회 2003년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.1
    • /
    • pp.239.2-240
    • /
    • 2003
  • We have recently described the novel synthetic method for N-protected amines from various ethers using chlorosulfonyl isocyanate(CSI) and found that the mechanism of our CSI reaction is a competitive reaction of SN1 and SNi mechanism according to the stability of carbocation intermediate. Forthermore. we developed the regioselective and diastereoselective one-pot synthetic method for 1,2-amino alcohol, through the reaction of di-and tribenzyl thers with CSI, and invetigated its mechanism. (omitted)

  • PDF

APPLICATION OF HP-DISCONTINUOUS GALERKIN FINITE ELEMENT METHODS TO THE ROTATING DISK ELECTRODE PROBLEMS IN ELECTROCHEMISTRY

  • Okuonghae Daniel
    • Journal of applied mathematics & informatics
    • /
    • 제22권1_2호
    • /
    • pp.1-20
    • /
    • 2006
  • This paper presents the interior penalty discontinuous Galerkin finite element methods (DGFEM) for solving the rotating disk electrode problems in electrochemistry. We present results for the simple E reaction mechanism (convection-diffusion equations), the EC' reaction mechanism (reaction-convection-diffusion equation) and the ECE and $EC_2E$ reaction mechanisms (linear and nonlinear systems of reaction-convection-diffusion equations, respectively). All problems will be in one dimension.

하동 고령토로부터 Zeolite A 합성 반응기구 (Reaction Mechanism for Zeolite A Synthesis from Hadong Kaolin)

  • 권영수;김면섭
    • 한국세라믹학회지
    • /
    • 제20권3호
    • /
    • pp.255-259
    • /
    • 1983
  • Am(rphous aluminosilicate zeolite A and hydroxysodalite were obtained by reaction of Hadong kaolin(halloysite) with IN sodium hydroxide solntion in the temperature range of 60 to 10$0^{\circ}C$ For determination of the mechanism of the reaction Various possible mechanisms were compared with the experimental results. It was observed that the reaction mechamism of zeolite A synthesis from Hadong kaolin was first order consecu-tive reaction as follows : halloysitelongrightarrowamorphous aluminosilicatelongrightarrowzeolite Alongrightarrowhydroxysodalite

  • PDF

Mechanism Studies on the CSI Reaction with Allyl Ethers by Varying p-Substituent

  • Jung, Young-Hoon;Kim, Ji-Duck
    • Archives of Pharmacal Research
    • /
    • 제26권9호
    • /
    • pp.667-678
    • /
    • 2003
  • We examined the effect of p-substituents in p-substituted cinnamyl methyl ethers and 1-(p-substituted phenyl)allyl methyl ethers with CSI, and confirmed that the CSI reaction of allyl ethers (p-substituted ethers) is a competitive reaction of $S_Ni{\;}and{\;}S_N1$ mechanism according to the stability of the carbocation. And, the only terminal allylic amine was obtained through the migration reaction in thermodynamic reaction condition.

중성 및 알카리성수용액에서 Cupferron 의 전극환원메카니즘 (Mechanism of the Electrode Reduction of Cupferron in Neutral and Alkaline Media)

  • 황금소;황정의
    • 수산해양기술연구
    • /
    • 제11권1호
    • /
    • pp.32-55
    • /
    • 1975
  • The ammonium salt of N-Nitrosophenylhydroxiamine, namely Cupferron, is a well-known analytical reagent which precipitates a great number of metal ions in acid medium. Various structures of electrode reduction for N-Nitrosophenylhydroxiamine have been suggested in acid and alkaline media by many researchers, but not in neutral medium. So the mechanism of electrode reaction of Cupferron was investigated by both chronopotentiometric and polarographic methods. It was estimated that the reduction of Cupferron occurs in a three-step mechanism through which a chemical step is interposed between two charge transfer, the ECE (charge transfer-chemical reaction-charge transfer) mechanism, over a range of neutral and alkaline media. The chemical reaction of the process was assumed to be acid-base catalyzed from the fact that kapp (over all rate constant) of chemical reaction is pH dependent.

  • PDF

Catalytic mechanism and inhibition studies of purine nucleoside phosphorylase (PNP) in micrococcus luteus

  • Choi, Hye-Seon
    • Journal of Microbiology
    • /
    • 제35권1호
    • /
    • pp.15-20
    • /
    • 1997
  • Kinetic studies were done to elucidate the reaction mechanism of purine nucleoside phosphorylase (PNP) in Micrococcus Luteus. PNP catalyzes the reversible phosphorolysis of ribonucleosides to their respective base. The effect of alternative competing substrates suggested that a single enzyme was involved in binding to the active site for all purine nucleosides, inosine, deoxyiosine, guanosine, deoxyguanosine, adenosine and deoxyadenosine. Affinity studies showed that pentose moiety reduced the binding capacity and methylation of ring N-1 of inosine and guanosine had little effect on binding to bacterial enzyme, whereas these compounds did not bind to the mammalian enzymes. The initial velocity and product inhibition studies demonstrated that the predominant mechanism of reaction was an ordered bi, bi reaction. The nucleoside bound to the enzyme first, followed by phosphate. Ribose 1-phosphate was the first product to leave, followed by base.

  • PDF

용융 Si-C-SiC계에서 $\beta$-SiC 생성기구 ($\beta$-SiC Formation Mechanisms in Si Melt-C-SiC System)

  • 서기식;박상환;송휴섭
    • 한국세라믹학회지
    • /
    • 제36권6호
    • /
    • pp.655-661
    • /
    • 1999
  • ${\beta}$-SiC formation mechanism in Si melt-C-SiC system with varying in size of carbon source was investigated. A continuous reaction sintering process using Si melt infiltration method was adopted to control the reaction sintering time effectively. It was found that ${\beta}$-SiC formation mechanism in Si melt-C-SiC system was directly affected by the size of carbon source. In the Si melt-C-SiC system with large carbon source ${\beta}$-SiC formation mechanism could be divided into two stages depending on the reaction sintering time: in early stage of reaction sintering carbon dissolution in Si melt and precipitation of ${\beta}$-SiC was occurred preferentially and then SIC nucleation and growth was controlled by diffusion of carbon throughy the ${\beta}$-SiC layer formed on graphite particle. Furthmore a dissolution rate of graphite particles in Si melt could be accelerated by the infiltration of Si melt through basal plane of graphite crystalline.

  • PDF

Ethylacrylate에 대한 n-Butylmercaptan의 친핵성 첨가반응에 관한 연구 (The Kinetics and Mechanism of Nucleophilic Addition of n-Butylmercaptan to Ethylacrylate)

  • 권동숙;김태린
    • 대한화학회지
    • /
    • 제16권4호
    • /
    • pp.232-240
    • /
    • 1972
  • Ethylacrylate에 대한 n-butylmercaptan의 첨가반응속도상수를 iodometry로 측정하여 넓은 pH범위에서 잘 맞는 속도식을 구하였다. 이 식에 의하면 pH 4 이하에서는 n-butylmercaptan분자가 첨가하여 pH 7 이상에서는 n-butylmercaptide ion이 첨가함을 알 수 있고 pH 4∼7 사이에서 일어나는 복잡한 첨가반응 메카니즘도 이 식으로 잘 설명 될 수 있음을 알았다.

  • PDF