• Title/Summary/Keyword: Chemical diffusivity

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Diffusion-Selectivity Analysis of Permanent Gases through Carbon Molecular Sieve Membranes

  • Kang, Jong-Seok;Park, Ho-Bum;Lee, Young-Moo
    • Korean Membrane Journal
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    • v.5 no.1
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    • pp.43-53
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    • 2003
  • The selectivity of a gas in the carbon molecular sieve membrane (CMSM) can be expressed as the ratio of the product of the diffusivity and the solubility of two different gases. The diffusivity is also expressed as the product of the entropy and the total energy (kinetic and potential energy) in the nano-sized pore of the membrane. The present study calculates the entropic-energy and selectivity of penetrant gases such as H$_2$, O$_2$, N$_2$, and CO$_2$ from the gas-in-a box theory to physically analyze the diffusivity of penetrant gas in slit-shaped pore of CMSM focusing on the restriction of gas motion based on the size difference between penetrant gas pairs. The contribution of each energy term is converted to entropic term separately. By the conjugated calculation for each entropic-energy, the entropic effects on diffusivity-selectivity for gas pairs such as H$_2$/N$_2$, CO$_2$/N$_2$, and O$_2$/N$_2$ were analyzed within active pore of CMSM. In the activated diffusion domain, the calculated value of entropic-selectivity lies between 9.25 and 111.6 for H$_2$/N$_2$, between 3.36 and 6.0 for CO$_2$/N$_2$, and between 1.25 and 16.94 for O$_2$/N$_2$, respectively. The size decrement of active pore in CMSM had the direct effect on the reduction of translational entropic-energy and the contribution of vibrational entropic-energy for N$_2$, O$_2$, and H$_2$ was almost negligible. However, the vibrational entropic term of CO$_2$ might extravagantly affect on the entropic-selectivity.

Measured data of thermophysical properties of concrete for a temperature range of $20^{\circ}C$ to $1100^{\circ}C$ (상온에서 $1100^{\circ}C$까지 온도변화에 따른 콘크리트의 열물성 측정치)

  • Shin, Ki-Yeol;Chung, Mo;Kim, Sang-Baik;Kim, Jong-Chul
    • Transactions of the Korean Society of Mechanical Engineers B
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    • v.22 no.5
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    • pp.596-606
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    • 1998
  • Thermophysical properties and the compressive strength of concrete used in nuclear power plants in Korea were measured. The chemical composition of the concrete was also analyzed. The measured thermophysical properties include the density, the thermal conductivity, the thermal diffusivity and the specific heat for a wide temperature range of 20.deg. C to 1100.deg. C. The chemical composition of Korean concrete is similar to that of US basaltic concrete and the thermophysical properties are strongly temperature dependent. The density, the conductivity and the diffusivity decrease with an increase in temperature, and particularly the conductivity and the diffusivity are a 50-perdent decrease at 900.deg. C as compared with these values at room temperature. The specific heat increases until 500.deg. C, decreases from 700.deg. C to 900 .deg. C, and then increases again when temperature is above 900.deg. C. The measurement beyond 1100.deg. C is not acceptably accurate because the concrete decomposes to a liquid phase from a solid phase at that temperature. The results of this study can be applied, for example, to an analysis of the molten core-concrete interaction (MCCI) phenomenon of concrete structures at high temperature will also require those property data, especially for high temperature ranges.

A Study on the Eddy Diffusion in a Pulsed Turbulent System (脈動渦流裝置에 있어서의 渦流擴散)

  • Woong Ki Kang;Yung Wook Kim
    • Journal of the Korean Chemical Society
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    • v.7 no.3
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    • pp.203-206
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    • 1963
  • The eddy diffusion in the pulsed wetted wall column, where the spherical balls are consecutively arrayed along the axis of the column and turbulence is caused around the balls by pulsation, has been studied both theoretically and experimentally. A diffusion equation is solved for a longitudinal column where a concentration impulse is given at the top of the column, and the experimental results, which are the impulse response measurements at the half of the total height of the column, have shown a good agreement with the developed theory. A method of measuring the eddy diffusivity, which is based on the slope of concentration vs. time in the particular interval of concentration, is proposed and the measured diffusivity is used as a criterion of comparing the theory and the experiment. The eddy diffusion is remarkably increased as the amplitude and the frequency of the pulsation increase but the increasing rate is decreased as the pulsation increases.

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Analysis of Cyclic Adenosine Monophosphate (cAMP) Separation via RP-HPLC (reversed-phase high-performance liquid chromatography) by the Moment Method and the van Deemter Equation (역상 크로마토그래피에서 모멘트 방법과 van Deemter 식을 이용한 고리형 아데노신 일인산의 분리특성 연구)

  • Lee, Il Song;Ko, Kwan Young;Kim, In Ho
    • Korean Chemical Engineering Research
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    • v.53 no.6
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    • pp.723-729
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    • 2015
  • The moment analysis of cyclic adenosine monophosphate (cAMP) was performed using chromatograms that were obtained with the pulse input method from an octadecyl silica (ODS) high-performance liquid chromatography (HPLC) column. The general rate (GR) model was employed to calculate the first absolute moment and the second central moment. Three important coefficients for moment analysis, which are molecular diffusivity ($D_m$), external mass transfer coefficient ($k_f$), and intra-particle diffusivity ($D_e$), were estimated by the Wilke-Chang equation, Wilson-Geankoplis equation, and comparing van Deemter equation to theoretical plate number equation, respectively. Experiments were conducted by various conditions of flow rates, methanol volume ratio of the mobile phase, and solute concentration. After the moment analysis, results were organized by van Deemter plots. Also van Deemter coefficients were compared each other to effect $H_{ax}$, $H_f$, and $H_d$ on height equivalent to a theoretical plate (HETP, $H_{total}$). The value of intraparticle diffusion ($H_d$) was the primary factor which makes for HETP whereas external mass transfer ($H_f$) was disregardable factor.

Diffusion of Ethoprophos in Apple and Pear (사과와 배에서 Ethoprophos의 확산)

  • Park, Hyeon-Ju;Lee, Ki-Won;Chung, Kyong-Hwan;Park, Byung-Jun;Seo, Gon
    • Korean Journal of Environmental Agriculture
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    • v.26 no.2
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    • pp.171-178
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    • 2007
  • Diffusion and accumulation of ethoprophos in fruit such as apple and two types of pears were examined by dipping them into the solution of ethoprophos. The effective diffusivities of ethoprophos at the skin and flesh of apple and pear were determined by simulation their experimental accumulation curves with calculated ones from the model assuming consecutive diffusion of ethoprophos from skin to flesh. Its effective diffusivity at the flesh with higher content of water were higher, $\sim10^{-10}\;m^2/s$, regardless of the types of fruits, while that at the skin was small, $\sim10^{-12}\;m^2/s$ and increased with the order of 'Niitaka' pear < 'Whangkeumbae' pear < 'Fuji' apple. The variation in the concentration of ethoprophos in its solution did not induce any change in affecting its effective diffusivity at the flesh of 'Whangkeumbae' pear, but the increase in the concentration caused the increase in its effective diffusivity at the skin. The penetration rate of ethoprophos at the skin was an important factor in determining its accumulation rate in fruit.

Removal of Chlorinated Organic Compounds Using Crosslinked PDMS Pervaporation Membrane (가교된 PDMS 투과증발 막을 이용한 유기 염소계 화합물의 제거)

  • Kim, Yong Woon;Hong, Yeon Ki;Hong, Won Hi
    • Clean Technology
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    • v.7 no.3
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    • pp.195-202
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    • 2001
  • In this study the trace of chlorinated organic compound in aqueous solution was separated by pervaporation process using crosslinked PDMS (polydimethylsiloxane) membrane. The flux of trichloroethylene(TCE) increased linearly with feed composition but the flux of water was slightly increased. The partial flux of TCE was greater than that of tetrachloroethylene(PCE). The partial flux of TCE was not changed with operating temperature, but increased rapidly with feed flow rates. High crosslinking density causes the reduction of solubility and diffusivity for target component. The reduction of flux and selectivity for TCE is due to the chain immobilization and reduction of diffusivity with crosslinking density.

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Electrochemical Properties of Langmuir-Blodgett(LB) Film of Alkyl Bromides (브롬화 알킬화합물 LB막의 전기화학적 특성)

  • Park, Keun-Ho;Son, Tae-Chul;Min, Chang-Hun
    • Journal of the Korean Applied Science and Technology
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    • v.26 no.4
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    • pp.451-456
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    • 2009
  • We carried out this experiment to observe an electrochemical properties for LB films of alkyl compounds by the cyclic voltammetry. Alkyl bromides was deposited by using the Langmuir- Blodgett method on the ITO glass. We measured to an electrochemical measurement by using cyclic voltammetry with a three-electrode system(an Ag/AgCl reference electrode, a platinum wire counter electrode and LB film-coated ITO working electrode) in 0.5, 1.0, 1.5 and 2.0 N $NaClO_4$ solution. A measuring range was reduced from initial potential to -1350 mV, continuously oxidized to 1650 mV. The scan rate were 100 mV/s. As a result, an electrochemical properties of the LB films of alkyl bromides appeared irreversible process caused by only the oxidation current from the cyclic voltammogram. The diffusivity(D) effect of LB films decreased with increasing of alkyl compounds amount.

Experimental Verification of a Kinetic Model of Zr-Oxidation

  • Yoo, Han-Ill;Park, Sang-Hyun
    • Journal of the Korean Ceramic Society
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    • v.43 no.11 s.294
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    • pp.724-727
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    • 2006
  • It has long been known that the oxidation kinetics of Zr-based alloys undergoes a crossover from parabolic to cubic in the pretransition period (before breakaway of the oxide scale). This kinetic crossover, however, is not fully understood yet. We have earlier proposed a model for the Zr-oxidation kinetics, in a closed form for the first time, by taking into account a compressive strain energy gradient as a diffusional driving force in addition to a chemical potential gradient of component oxygen across the ZrO$_2$ scale upon Zr [J. Nucl. Mater., 299 (2001) 235]. In this paper, we experimentally reconfirm the validity of the proposed model by using the thermogravimetric data on mass gain of Zr in a plate and wire form, respectively, in air atmosphere at different temperatures in the range of 500$^{\circ}$ to 800$^{\circ}C$, and subsequently report on the numerical values for oxygen chemical diffusivity and strain energy gradient across the oxide scale.