• Title/Summary/Keyword: 해리

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Characteristic of formation and decomposition for the Methane-Ethane / Methane-Propane gas hydrate (($CH_4$-$C_2_H_6$ / $CH_4$-$C_3H_8$ 혼합가스 하이드레이트의 형성 및 분해에 관한 특성연구)

  • Lee, Jin-Woo;Park, Dae-Won;Kim, Young-Seok;Lee, Ju-Dong
    • 한국신재생에너지학회:학술대회논문집
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    • 2007.11a
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    • pp.569-572
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    • 2007
  • 천연가스의 주요 구성성분은 메탄, 에탄, 프로판으로 99%이상 차지하고 있으며 천연가스 하이드레이트(NGH)는 압축천연가스(CNG)에 비해 체적당 질량이 크고 액화천연가스(LNG) 보다 상대적으로 유리한 온도 및 압력조건으로 인해 천연가스의 경제적인 저장 및 수송 수단으로 주목 받고 있다. $CH_4$ - $C_2H_6$, $CH_4$ - $C_3H_8$ 혼합가스 하이드레이트의 제조시 반응시간에 따른 하이드레이트의 거동을 관찰하였으며 생성조건의 변화에 따른 하이드레이트의 생성속도를 비교하였다. 하이드레이트의 생성이 진행될 때 기상에서의 $C_2H_6$, $C_3H_8$의 몰 비는 감소함을 보여주었고 이러한 변화는 $CH_4$ - $C_3H_8$$CH_4$ - $C_2H_6$보다 더욱 빠르게 진행되었다. 또한 생성된 하이드레이트의 해리과정이 진행될 때 역시 서로 다른 해리속도에 의해 조성의 변화를 관찰 할 수 있었다.

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Kinetic Studies on the Reaction of Thiocyanate with Di-$\mu$-oxobis-(aquaoxalatooxomolybdate (V)) in Acid Media (산성수용매에서 이-$\mu$-옥소비스-(아쿠아옥살라토옥소몰리브덴 (V)) 산이온과 티오시안산이온의 반응)

  • Chang-Su Kim;Chang-Yong Kwon;Moon-Pyoung Yi;Chann-Woo Kim
    • Journal of the Korean Chemical Society
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    • v.29 no.6
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    • pp.623-628
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    • 1985
  • Rate constants for complexing with thiocyanate after ring opening of molybdenum-oxalate in acid media were obtained spectrophotometrically at 460nm. The acid-assisted dissociation of molybdenum-oxalate and the reaction of thiocyanate with oxalatooxomolybdenum (V) complex in acid media were investigated with thiocyanate and hydrogen ion concentration. The kinetic data indicate that molybdenum-oxalate is protonated to a limited extent in acid media and the protonated complex is responsible for an increase in rate for the reaction of thiocyanate with oxalatooxomolybdenum (V) complex. Replacement of an oxalate ligand in acid media has been interpreted in terms of dissociative mechanism involving bond-breaking of the oxygen trans to the yl oxygen.

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A Study on the Ionic Dissociation Rate of $\alpha$-Chlorobenzyl Ethyl Ether by Dynamic NMR Spectroscopy-Chlorobenzyl Ethyl Ether by Dynamic NMR Spectroscopy (動的 NMR에 依한 $\alpha$-Chlorobenzyl Ethyl Ether의 이온解離速度에 關한 硏究)

  • Chang-Yol Kim
    • Journal of the Korean Chemical Society
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    • v.24 no.1
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    • pp.44-52
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    • 1980
  • Ionic dissociation rates of $\alpha$-chlorobenzyl ethyl ether in each solvent of toluene-$d_8$ and carbon tetrachloride were measured by the method of dynamic NMR spectroscopy. The spin system of these 1H NMR spectra was $AB_3$. The theoretical spectrum was calculated by computer simulation of dynamic NMR spectra, which agreed very well with observed spectra. From this computer simulation, the ionic dissociation rate constant k was obtained, and by Eyring plot with it, slope and intercept length was gained, from which kinetic parameters were calculated.The easiness of ionic dissociation depended upon solvent polarity. Activation enthalpy was 4.7 kcal/mole in toluene-$d_8$, 10.7 kcal/mole in carbon tetrachloride, and activation entropy was -35. 8 e.u. in toluene-$d_8$, -14.4 e.u. in carbon tetrachloride. It was understood that though the ${\Delta}H^{neq}$ value was small, this ionic dissociation had an easier procession in nonpolar solvents with increasing temperatures. Considering that the ionic dissociation could be thought as the first step of $S_N1$ mechanism, attention might be paid to the results that the value of ${\Delta}S^{neq}$ had a large negative value in comparison with a small ${\Delta}H^{neq}$.

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Signal Coverages of DGPS Beacon Stations in Korea (우리나라 DGPS 보정국의 위치보정신호의 이용범위)

  • Ahn, Jang-Young;Choi, Chan-Moon
    • Journal of the Korean Society of Fisheries and Ocean Technology
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    • v.40 no.1
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    • pp.47-53
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    • 2004
  • For the purpose of comparison between the designed coverage and actual coverage of Korean DGPS (Differential Global Position System) beacon stations, we have received the ship‘s positions with states and IDs of their stations on the navigation route of Jeju-Tianjin by automatic selection mode of DGPS receiver and on them of Jeju-Inchun and Jeju-Vladibostok by manual mode. Also in case that some obstructions were on propagation routes from DGPS beacon stations to receiving positions, a restriction on available ranges of DGPS beacon signals was investigated. The results obtained are as follows : 1. The coverage of Korean DGPS beacon stations was designed 100NM (Nautical mails) at 40.0dB(over ${\mu}$V/m). But the actual coverages of them according to their stations and propagation routes were 0.3-3.6 times as wide as designed coverage. 2. In case that the propagation route of beacon signals from DGPS beacon stations was on the sea, the propagation distance of north direction from the stations was longer than south direction. 3. The coverages of Echongdo and Ulungdo stations were 366NM on the yellow sea and 342.3NM on the east sea of Korea respectively, and were widest than any other stations. 4. The coverage of Marado station on the south and yellow seas of Korea was very unstable because of the Halla mountain on the propagation route. Maximum receiving range to be measured by automatic selection mode of DGPS receiver was 145NM on the route of Jeju-Tianjin on June 22-July 1, 2002. Minimum receiving range to be not measured by manual selection mode was 28.7NM on the route of Jeju-Inchun on June 26-28, 2003

Pressure Effects on the Ionic Dissociation of $[Co(en)]_3Cl_3\;and\;[Co(NH_3)_6Cl_3$ in Aqueous Solutions (수용액에서 $[Co(en)_3]Cl_3$$[Co(NH_3)_6]Cl_3$착물의 이온 해리에 미치는 압력의 영향)

  • Jong Jae Chung;Rho Byung Gill
    • Journal of the Korean Chemical Society
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    • v.30 no.4
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    • pp.335-450
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    • 1986
  • The thermodynamic dissociation constants of $[Co(en)]_3Cl_3\;and\;[Co(NH_3)_6Cl_3$ in aqueous solutions at $25{\circ}$ and at the pressure from 1 bar to 2000 bars were measured by conductometric method. The dissociation constants were increased with pressure elevation because of volume decreasing by the formation of charged ions during dissociation reaction. That is, the $pK^T$ values of $[Co(en)]_3Cl_3$ were 2.16 for I bar, 2.08 for 500 bars, 2,08 for 1000 bars, 2.05 for 1500 bars and 2.03 for 2000 bars, respectively and those of $[Co(NH_3)_6Cl_3$ were 2.02 for 1 bar 1.96 for 500 bars, 1.90 for 1000 bars, 1. 88 for 1500 bars and 1. 87 for 2000 bars, respectively. Comparing and analyzing the values of Stokes' radii and $K^T$, the formation of ion pair compound was affected by not only the electrostatic interaction, but also the Interal Conjugate Base(ICB), which was increased by the elevation of the pressure.

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An Experimental Analysis of Hydrate Production using Multi-Well, Plate-Type Cell Apparatus (다중공 평판형 셀기기에서 하이드레이트 생산실험 분석연구)

  • Bae, Jaeyu;Sung, Wonmo;Kwon, Sunil
    • Korean Chemical Engineering Research
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    • v.45 no.3
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    • pp.304-309
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    • 2007
  • In this study, the "Multi Well Plate-type cell Apparatus" was designed and setup for performing the producing experiments of methane hydrate by depressurization, heat stimulating methods. In order to characterizing the producing mechanism of hydrate through porous materials, the experiments for various producing methods have been conducted with the aid of the apparatus which has high permeability. In the experimental result of depressurization method, the pressure is temporarily increased unlikely conventional gas reservoir due to the sourcing effect of hydrate dissociation in the pore. Meanwhile, the temperature is decreased because of the endothermic reaction while hydrate is dissociated. In the experimental results of heat stimulating method, the dissociation in depressurization method is more slowly processed than that in thermal method, and hence, its gas production is lower. In the case of production right after heating, hydrate is dissociated only near injecting point and the permeability becomes greater at that area only. It infers that the more gas is produced during relatively earlier producing period. Since then, the hydrate is more slowly dissociated than the case of production after heating and soaking. This time, the performances of pressure and production obtained by thermal method have been analyzed in order to investigate the effect of soaking time on gas recovery. As a result, the gas recoveries in the case of 2 min and 4 min soaking are higher than case in 6 min soaking. This is reason that hydrate is reformed due to the decrease of temperature. It is expected that the experimental results obtained in this work may be more clearly explained by utilizing the lower permeable porous system with the greater hydrate saturation.