• Title/Summary/Keyword: equilibrium temperatures and pressures

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Equilibria and Dynamics of Toluene and Trichloroethylene onto Activated Carbon Fiber

  • Park, Jee-Won;Lee, Young-Whan;Choi, Dae-Ki;Lee, Sang-Soon
    • Clean Technology
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    • v.8 no.2
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    • pp.93-99
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    • 2002
  • Adsorption dynamics for toluene and trichloroethylene with an isothermal fixed bed of activated carbon fiber were investigated. Equilibrium isotherms were measured by a static method for toluene and trichloroethylene onto activated carbon fiber at temperatures of 298, 323, and 348 K and pressure up to 3 kPa for toluene and 6 kPa for trichloroethylene, respectively. These results were correlated by the Toth equation. And dynamic experiments in an isothermal condition of 298 K were examined. Breakthrough curves reflected the effects of the experimental variables such as partial pressures for adsorbate and interstitial bulk velocities of gas flow. To present the column dynamics, a dynamic model based on the linear driving force (LDF) mass transfer model was applied.

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Measurements and Correlations of Isobaric Vapor-Liquid Equilibrium for Glycerol-Water Systems (Glycerol-물 계에 대한 등압 기액평형의 측정과 상관관계)

  • Rho, Seon-Gyun;Kang, Choon-Hyoung
    • Applied Chemistry for Engineering
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    • v.8 no.6
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    • pp.893-900
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    • 1997
  • In this study, vapor-liquid equilibria of a binary system, which consists of glycerol and water, are measured using a vaporrecirculating modified Othmer still at various subatmospheric pressures. The constituent components of the binary system considered in this study exhibit a large difference in the boiling temperatures. Since it is generally observed that the properties of a mixture greatly differ from those of the pure components, the phase equilibrium characteristics of a mixture can not be predicted from the properties of the pure components. Furthermore, an abrupt increase in the boiling temperature occurs as the concentration of the higher boiling component exceeds a certain value. Therefore, it is essential to acquire realistic phase equilibrium data of the mixture for industrial applications. Using the UNIQUAC model, the experimental vapor-liquid equilibrium data are correlated with good accuracy. The thermodynamic consistency test is also performed to ensure soundness of the data.

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A Experimental Study of the Kinetic Characteristics of Methane Hydrate (메탄 하이드레이트 동적특성에 대한 실험적 연구)

  • Kim, Nam-Jin;Chun, Won-Gee
    • Journal of the Korean Solar Energy Society
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    • v.26 no.2
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    • pp.19-25
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    • 2006
  • Methane hydrate, non-polluting new energy resource, satisfies requirement and considered as a precious resource that can prevent the global warming. Fortunately, there are abundant resources of methane hydrate distribute in the earth widely. Therefore, developing the techniques that can utilize these gases effectively is highly desired. The work in this paper here is to develop a skill which can transport and store methane hydrate. As a first step, the equilibrium experiment was carried out by increasing temperatures in the cell at fixed pressures. The influence of gas consumption rates under variable degree of subcooling, stirring and water injection has been investigated formation to clarify kinetic characteristics of the hydrate. The results of present investigation showed that the enhancements of the hydrate formation in terms of the gas/water ratio are closely related to operational pressure, temperature, degrees of subcooling, and water injection.

Bubble-Point Measurement of Binary Mixture for the CO2 + Caprolactone Acrylate System in High Pressure

  • Jeong, Jong-Dae;Byun, Hun-Soo
    • Korean Chemical Engineering Research
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    • v.57 no.6
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    • pp.826-831
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    • 2019
  • Experimental data of phase equilibrium is reported for caprolactone acrylate in supercritical carbon dioxide. Bubble-point data was measured by synthetic method at temperatures ranging from (313.2 to 393.2) K and pressures up to 55.93 MPa. In this research, the solubility of carbon dioxide for the (carbon dioxide + caprolactone acrylate) system decreases as temperature increases at a constant pressure. The (carbon dioxide + caprolactone acrylate) system exhibits type-I phase behavior. The experimental result for the (carbon dioxide + caprolactone acrylate) system was correlated with Peng-Robinson equation of state using mixing rule. The critical property of caprolactone acrylate was predicted with the Joback and Lyderson method.

A geothermal gradient of the upper mantle beneath Jeju-do, Korea: evidence from mantle xenoliths

  • Choi, Seong-Hee;Jwa, Yong-Joo;Lee, Han-Yeang
    • Proceedings of the Mineralogical Society of Korea Conference
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    • 2000.05a
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    • pp.19-19
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    • 2000
  • ;Ultramafic xenoliths found in alkali basalts from Jeju-do, Korea are mostly spinel Iherzolites composed of olivine, orthopyroxene, clinopyroxene and spinel. A subordinate amount of spinel harzburgites and pyroxenites are also found. Temperatures for these xenoliths were estimated from the compositions of coexisting pyroxenes (Wood '||'&'||' Banno 1973; Wells 1977; Bertrand '||'&'||' Mercier 1985; Brey '||'&'||' Kohler 1990), the AI-solubility in orthopyroxene coexisting with olivine and spinel (Sachtleben '||'&'||' Seck 1981; Webb '||'&'||' Wood 1986), and from Fe/Mg partitioning between olivine and spinel (Ballhaus et al. 1991). Temperature estimates from the thermometers by Wells (1977) and Brey and Kohler (1990) are compatible. Average equilibrium temperatures by these two methods for spinel peridotites range from 890 to 1030$^{\circ}$C. Pressures for spinel peridotites were estimated from the geobarometer by Kohler and Brey (1991) derived from the equilibrium Ca content of olivine coexisting with clinopyroxene, and fall within the range of 12.9 to 26.3 kbar. The combination of the thermometer by Brey and Kohler (1990) and the geobarometer by Kohler and Brey (1991) yields P- T estimates for Jeju-do spinel peridotites that fall in experimentally determined spinel lherzolite field in CFMASCr system (O'Neill 1981). These P-T data sets have been used to construct the Quaternary Jeju-do geotherm, which is significantly different from the conventional conductive geotherm. The xenolith-derived geotherm has a higher T gradient at low P (13 kbar) than at high P, which may be due to perturbation of the conductive heat flow by magma underplating or overplating at the crust-mantle boundary. Temperature estimates and statistics on the xenoliths indicate that the crust/mantle boundary in Jeju-do lies at about 11 kbar (~39 km). Spinellherzolite is inferred as a main constituent rock of the uppermost lithospheric mantle beneath Jeju-do. Pyroxenites were intercalated in peridotites in similar depth and temperature as re-equilibrated veins or lens.

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Measurement and Modeling of Bubble Points for Binary Mixtures of Carbon Dioxide and N,N-Dimethylformamide (이산화탄소와 디메틸포름아마이드 혼합물의 기포점 측정 및 모델링)

  • Jung, Joon-Young;Lee, Byung-Chul
    • Clean Technology
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    • v.17 no.1
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    • pp.19-24
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    • 2011
  • The bubble point pressures of binary mixtures of carbon dioxide ($CO_2$) and N,N-dimethylformamide (DMF) were measured by using a high-pressure experimental apparatus equipped with a variable-volume view cell, at various $CO_2$ compositions in the range of temperatures above the critical temperature of $CO_2$ and below the critical temperature of DMF. The experimental bubble point pressure data were correlated with the Peng-Robinson equation of state (PR-EOS) to estimate the corresponding dew point compositions at equilibrium with the bubble point compositions. The experimentally measured bubble point pressures gave good agreement with those calculated by the PR-EOS. The variable-volume view cell equipment was verified to be an easy and quick way to measure the bubble point pressures of high-pressure compressible fluid mixtures.

Measurement of Bubble Points of Dimethyl Carbonate and Carbon Dioxide Mixtures (디메틸카보네이트와 이산화탄소 혼합물의 기포점 측정)

  • Ahn, Joon-Yong;Lee, Byung-Chul
    • Applied Chemistry for Engineering
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    • v.20 no.1
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    • pp.94-98
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    • 2009
  • The bubble point pressures of dimethyl carbonate and carbon dioxide mixtures were measured by using a high-pressure experimental apparatus equipped with a variable-volume view cell, at various $CO_2$ compositions in the range of temperatures above the critical temperature of $CO_2$ and below the critical temperature of dimethyl carbonate. The experimental bubble point pressure data were correlated with the Peng-Robinson equation of state (PR-EOS) to estimate the corresponding dew point compositions at equilibrium with the bubble point compositions. The experimentally measured bubble point pressures gave good agreement with those calculated by the PR-EOS. The variable-volume view cell equipment was verified to be an easy and quick way to measure the bubble point pressures of high-pressure compressible fluid mixtures.

Phase Equilibrium Conditions of Gas Hydrates for Natural Gas Solid Transportation and Storage (천연가스 고체수송 및 저장을 위한 가스 하이드레이트 상평형 조건에 대한 연구)

  • Jeon, Yong-Han;Kim, Jong-Yoon;Kim, Chong-Bo;Kim, Nam-Jin
    • Korean Journal of Air-Conditioning and Refrigeration Engineering
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    • v.20 no.4
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    • pp.266-273
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    • 2008
  • Natural gas hydrates are ice-like solid substances, which are composed of water and natural gas, mainly methane. They have three kinds of crystal structures of five polyhedra formed by hydrogen-bonded water molecules, and are stable at high pressures and low temperatures. They contain large amounts of organic carbon and widely occur in deep oceans and permafrost regions. Therefore, they are expected as a potential energy resource in the future. Especially, $1m^3$ natural gas hydrate contains up to $172Nm^3$ of methane gas, de pending on the pressure and temperature of production. Such large volumes make natural gas hydrates can be used to store and transport natural gas. In this study, three-phase equilibrium conditions for forming natural gas hydrate were numerically obtained in pure water and single electrolyte solution containing 3 wt% NaCl. The results show that the predictions match the previous experimental values very well, and it was found that NaCl acts as an inhibitor. Also, help gases such that ethane, propane, i-butane, and n-butane reduce the hydrate formation pressure at the same temperature.

High-Pressure Solubility of Carbon Dioxide in 1-Butyl-3-methylpiperidinium Bis(trifluoromethylsulfonyl)imide Ionic Liquid (1-Butyl-3-methylpiperidinium Bis(trifluoromethylsulfonyl)imide 이온성 액체에 대한 이산화탄소의 고압 용해도)

  • Nam, Sang-Kyu;Lee, Byung-Chul
    • Analytical Science and Technology
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    • v.27 no.2
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    • pp.79-91
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    • 2014
  • Solubility data of carbon dioxide ($CO_2$) in 1-butyl-3-methylpiperidinium bis(trifluoromethylsulfonyl)imide ($[bmpip][Tf_2N]$) ionic liquid are presented at pressures up to about 30 MPa and at temperatures between 303 K and 343 K. As far as we know, the data on the $CO_2$ solubility in the $[bmpip][Tf_2N]$ ionic liquid have never been reported in the literature by other investigators. The solubilities of $CO_2$ were determined by measuring the bubble point or cloud point pressures of the $CO_2+[bmpip][Tf_2N]$ mixtures with various compositions using a high-pressure equilibrium apparatus equipped with a variable-volume view cell. To observe the effect of the cation composing the ionic liquid on the $CO_2$ solubility, the $CO_2$ solubilities in $[bmpip][Tf_2N]$ used in this study were compared with those in 1-butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)-imide ($[bmim]Tf_2N]$). As the equilibrium pressure increased, the $CO_2$ solubility in $[bmpip][Tf_2N]$ increased sharply. On the other hand, the $CO_2$ solubility decreased with increasing temperature. The mole fraction-based $CO_2$ solubilities were almost the same for both $[bmpip][Tf_2N]$ and $[bmim][Tf_2N]$, regardless of temperature and pressure. The phase equilibrium data for the $CO_2+[bmpip][Tf_2N]$ systems have been correlated using the Peng-Robinson equation of state.

Temperature Effect on the Swelling Pressure of a Domestic Compacted Bentonite Buffer (국산 압축벤토나이트 완충재의 온도에 따른 팽윤압 특성 연구)

  • Lee, Ji-Hyeon;Lee, Min-Soo;Choi, Heui-Joo;Choi, Jong-Won
    • Journal of Nuclear Fuel Cycle and Waste Technology(JNFCWT)
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    • v.8 no.3
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    • pp.207-213
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    • 2010
  • The effect of temperature on swelling pressure was observed with a Korean domestic Ca-bentonite which has been considered as a potential buffer material in the engineering barrier of a high level radioactive waste (HLW) disposal system. The Ca-bentonite was compacted to a dry density of 1.6 g/$cm^3$, and then de-ionized water was supplied into it with a constant pressure of 0.69 MPa. The equilibrium swelling pressures were measured with different temperatures of $25^{\circ}C$, $30^{\circ}C$, $40^{\circ}C$, $50^{\circ}C$, $60^{\circ}C$, $70^{\circ}C$, respectively. The Ca-bentonite showed a sufficiently high swelling pressure of 5.3 MPa at room temperatures. Then it was clearly showed that the equilibrium swelling pressure was decreased with an increase of temperature. Interestingly, there were some differences in temperature effect on the equilibrium swelling pressure when the environmental temperature is increasing or decreasing. For further clarifying the swelling behaviour of a Korea domestic Ca-bentonite, the change of a compaction level, and the composition variation of a supplied water would be needed to use in conceptual design of HLW disposal system.