• Title/Summary/Keyword: 속도중합

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Polymerization of Methyl Methacrylate Initiated by Cobalt (II) Nitrate (질산코발트 (II)에 의한 Methyl Methacrylate의 중합)

  • Jang-oo Lee;Dong-ho Lee;Tae-oan Ahn
    • Journal of the Korean Chemical Society
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    • v.19 no.6
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    • pp.463-467
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    • 1975
  • The polymerization of methyl methacrylate(MMA) initiated by cobalt (II) nitrate in tetrahydrofuran (THF) has been studied. From the results of kinetic studies, the overall polymerization rate (Rp) could be expressed as following; $R_p=k\;[cobalt(Ⅱ)\;nitrate]^{0.5}\;[MMA]^{1.5}$ By considering the effects of chelating agent on the polymerization rate, it could be assumed that the monomer, MMA might form a coordination complex with cobalt(II) nitrate. In the presence of radical inhibitor hydroquinone, the inhibition time was observed. And the apparent overall activation energy was calculated to be 14.0 kcal/mole.

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Photopolymerization Kinetics of Urethane-acrylate Oligomer (우레탄-아크릴레이트 올리고머의 광경화 거동)

  • Kim, In-Beom;Song, Bong Jin;Lee, Myung Cheon
    • Applied Chemistry for Engineering
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    • v.17 no.1
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    • pp.33-36
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    • 2006
  • The kinetics of photopolymerization of urethane-acrylate oligomer which has many applications in photopolymerizable adhesives was analysed to investigate the influence of polymerization temperature and functionality of oligomer using the autocatalytic model. It was revealed that the maximum polymerization rate decreased as the polymerization temperature increased. The reaction rate constant, k, showed little change with the increase in polymerization temperature, while exponents m and n exhibited an increase. These results could be related to the diffusion and mobility restriction of reactive species during the cross-linking reaction. The decrease in photopolymerization rate with increase of temperature was mainly controlled by the reaction order n.

The Kinetic Study of Propylene Sulfide Polymerization Initiated by o-Sulfobenzoic Anhydride (Propylene Sulfide를 o-Sulfobenzoic Anhydride 개시제로 중합시킬 때 반응속도의 연구)

  • Man Jung Han
    • Journal of the Korean Chemical Society
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    • v.22 no.4
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    • pp.268-274
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    • 1978
  • The kinetics of the bulk polymerization of propylene sulfide initiated by o-sulfobenzoic anhydride were investigated, which proceeded by a zwitterionic mechanism.The instantaneous concentrations of monomer and initiator were determined by means of ir-and nmr-spectroscopy. The rate constant of propagation was found to be about three order of magnitude higher than that of initiation and this should be caused by a zwitterion mechanism.

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Zero-Offset VSP Data Processing for Gas Hydrate-Bearing Sediments in East Sea (동해 가스하이드레이트 부존지역 제로오프셋 VSP 탐사 자료의 자료처리)

  • Kim, Myung-Sun;Byun, Joong-Moo;Yoo, Dong-Geun
    • Geophysics and Geophysical Exploration
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    • v.12 no.3
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    • pp.255-262
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    • 2009
  • Conventionally, vertical-seismic-profiling (VSP) survey that provides high-resolution information has mainly performed to obtain the exact depth of the gas hydrate-bearing sediment, which is one of the key factors in the development of the gas hydrate. In this study, we extracted interval velocities and created corridor stacks from the first domestic zero-offset VSP data, which were acquired with three component receivers at UBGH09 borehole in Ulleung Basin where gas hydrate exists. Then we compared the corridor stacks with a CMP stacked section from surface seismic data. First of all, we converted the signals recorded with three component receivers to true vertical and horizontal components by phase rotation, and divided the data into direct waves and reflected waves by wavefield separation processing. The trend of the interval velocity extracted from the zero-offset VSP was similar to that of the sonic log obtained at the same borehole. Because the interval velocity of the gas hydrate-bearing sediment above the BSR was high, and it decreased suddenly through the BSR, we could infer that free gas is accumulated below the BSR. The results of comparing the corridor stacks to the CMP stacked section of the surface seismic data showed that most reflection events agreed well with those in the surface CMP stacked section and that the phase-rotated VSP data corresponded better with the surface seismic data than the VSP data without phase rotation. In addition, by comparing a corridor stack produced from the transverse component with the CMP stacked section of the surface seismic data, we could identify PS mode-converted reflections in the CMP stacked section.

Synthesis of High Molecular Weight Poly(Hexafluoropropylene Oxide) by Anionic Polymerization (음이온 중합에 의한 고분자량 헥사플루오르프로필렌 옥사이드 중합제의 합성)

  • Lee, Sang-Goo;Ha, Jong-Wook;Park, In-Jun;Lee, Soo-Bok;Lee, Jong-Dae
    • Polymer(Korea)
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    • v.32 no.4
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    • pp.385-389
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    • 2008
  • Chain propagation and chain transfer in anionic polymerization of hexafluoropropylene oxide were investigated under various reaction conditions such as the stabilization of reaction temperature, the amount of hexafluoropropylene solvent, and the feeding rate of hexafluoropropylene oxide monomer. Anionic initiator for the polymerization was synthesized from cesium fluoride and hexafluoropropylene oxide in tetraethyleneglycol dimethylether. It was possible to obtain a high molecular weight poly(HFPO) ($M_w$ 14800) using the anionic initiator in conditions of stabilized reaction temperature, and optimized addition of solvent and monomer feeding (HFP/initiator mole ratio=31.5 and HFPO feeding rate=11.67 g/hr). Otherwise, chain transfer reaction in anionic polymerization was increased. From the results of molecular weight in various reaction conditions, it was found that chain propagation and chain transfer in anionic polymerization of HFPO were very sensitive to reaction conditions.

Weighted Kirchhoff Prestack Depth Migration using Smooth Background Model (Smooth Background Model(SBM)을 이용한 가중 키리히호프 중합전 심도구조보정)

  • Ko, Seung-Won;Yang, Seung-Jin;Shin, Chang-Su
    • Geophysics and Geophysical Exploration
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    • v.4 no.3
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    • pp.84-88
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    • 2001
  • For the elastic migation, the velocity errors between the initial velocity model and true velocity model seriously affect the migrated images. The assumption of an initial velocity model, thus, is one of the critical factor for the successful migration. In case of applying the layered earth model as an initial velocity model, the layer boundary having large velocity contrast can not be defined well with conventional traveltime calculation algolithms and we have the difficulties for expressing the characteristics of the real subsurface. Smooth Background Model (SBM) we have applied as an initial velocity model in our study is characterized to be linearly varying the velocity with the depth, which can express the velocity variation in the subsurface properly. Thus it can properly be applied to traveltime calculation algolithms such as Vidale's method. In this study, Kirchhoff operator for prestack migration was used and the absolute amplitude obtained by modeling was applied as a weighted value to consider the true amplitude for initial model. Initial velocity model for migration was determined by using stacking velocity and we applied this model to real data.

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Electrochemical Properties of Pyrrole/Thiophene Polymer Composite (피롤/티오펜 고분자 복합체의 전기화학적 성질)

  • Cha, Seong Keuck;Choi, Kyu Seong;Ahn, Byuong Kee;Kang, Sang Jin
    • Journal of the Korean Chemical Society
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    • v.40 no.7
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    • pp.467-473
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    • 1996
  • Although a polypyrrole shows better electrical conductivity, 100∼400 ${\Omega}^{-1}cm^{-1}$, than other organic conducting polymers, its electrical conductivity will be worsen in the presence of the oxygen due to its easy oxidation. On the other hand, polythiophene shows better stability in the air while its electrcal conductivity is poor compared to the polypyrrole. We succeed to develope the mixed polymer electrode that is stable in the air and shows a good redox characteristics. The mixed polymer electrode has been prepared by the electrical polymerization of polypyrrole on the Pt electrode as 1.70 C$cm^{-2}$ and then coating with polythiophene as 0.34 C$cm^{-2}$. The polymerization rate of polythiophene was $3.89{\times}10^{-8}$ at the bare Pt electrode and $6.07{\times}10^{-8}cms^{-1}$ at the mixed polymer electrode. And the standard rate constants of each electrode were $5.16{\times}10^{-6}\;and\;3.94{\times}10^{-4} cms^{-1}$ respectively. Also, the electrocatalytic rate of the polypyrrole polymer electrode was $3.45{\times}10^{-3}cm^3mol^{-1}s^{-1}.$ We found the immobilized layer at the modified electrode acted as an electrocatalyst. Finally, this polymerization process at the Pt electrode was the electron transfer controlled, but that the mixed polymer electrode was the diffusion and charge transfer controlled.

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Iterative Least-Squares Method for Velocity Stack Inversion - Part B: CGG Method (속도중합역산을 위한 반복적 최소자승법 - Part B: CGG 방법)

  • Ji Jun
    • Geophysics and Geophysical Exploration
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    • v.8 no.2
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    • pp.170-176
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    • 2005
  • Recently the velocity stack inversion is having many attentions as an useful way to perform various seismic data processing. In order to be used in various seismic data processing, the inversion method used should have properties such as robustness to noise and parsimony of the velocity stack result. The IRLS (Iteratively Reweighted Least-Squares) method that minimizes ${L_1}-norm$ is the one used mostly. This paper introduce another method, CGG (Conjugate Guided Gradient) method, which can be used to achieve the same goal as the IRLS method does. The CGG method is a modified CG (Conjugate Gradient) method that minimizes ${L_1}-norm$. This paper explains the CGG method and compares the result of it with the one of IRSL methods. Testing on synthetic and real data demonstrates that CGG method can be used as an inversion method f3r minimizing various residual/model norms like IRLS methods.

Part 1 : Soap-Free Emulsion Copolymerization of Styrene with COPS-I (Part 1 : Styrene과 COPS-I의 무유화공중합)

  • Lee, KiChang;Choo, HunSeung;Ha, JeongMi
    • Journal of Adhesion and Interface
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    • v.15 no.3
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    • pp.93-99
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    • 2014
  • Monodisperse poly[styrene-co-(COPS-I)] latices in the size range of 165~550nm were successfully prepared by soap-free emulsion polymerization with various polymerization conditions (Styrene, COPS-I, KPS, DVB concentrations and polymerization temperature). In general, the COPS-I and KPS, DVB concentrations and polymerization temperature were closely related to the polymerization rate and the number of particles, molecular weight, and zeta potential. The polymerization rate and zeta potential increased, but molecular weight decreased, with increasing in the number of particles.

Basic Studies on Propellant Casting (II). Effects of Solid Additives on Urethane Polymerization (추진제 성형에 관한 기초연구 (제2보). 우레탄 중합에 미치는 첨가제 효과)

  • Young Gu Cheun;Ik Choon Lee;Shi Choon Kim
    • Journal of the Korean Chemical Society
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    • v.25 no.4
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    • pp.214-218
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    • 1981
  • Kinetic studies were carried out on urethane polymerization reaction of hydroxyl-terminated polybutadiene with isophorone diisocyanate under presence of Hexogen as solid additive. The rate was found to increase with the amount of Hexogen added. However the rate acceleration was not a catalytic effect but solely due to an increase of activation entropy. The reaction was a good 2nd order process with nearly constant activation energy of 8.4 kcal/mole.

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