• 한국지하수토양환경학회:학술대회논문집
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• 한국지하수토양환경학회 2001년도 총회 및 춘계학술발표회
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• pp.89-92
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• 2001

This study aims at investigating the relationship between dispersion coefficient ratio to molecular diffusion coefficient (D$_{l}$ /D$_{m}$) and Peclet number (Pe) for multi-solute system in non-Darcian flow regime. Existing understanding on solute dispersion is primarily derived from one-solute system in Darcian flow regime. We found that solute dispersion in rock fractures can be characterized by the mechanism of both macrodispersion and Taylor dispersion, even for non-Darcian f]ow domain. For the Darcian flow regime even different solutes lead to the same D$_{l}$ /D$_{m}$ at same Pe. However, as the flow becomes non-Darcian, solute with a higher molecular diffusion coefficient result in higher D$_{l}$ /D$_{m}$ at tile same Pe than that with a lower diffusion coefficient.cient.

• Fisheries and Aquatic Sciences
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• 제7권2호
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• pp.90-95
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• 2004

An analytical model for predicting the convection-diffusion of solute dumped in a homogeneous open sea of constant water depth has been developed in a time-integral form. The model incorporates spatially uniform, uni-directional, mean and oscillatory currents for horizontal convection, the settling velocity for the vertical convection, and the anisotropic turbulent diffusion. Two transformations were introduced to reduce the convection-diffusion equation to the Fickian type diffusion equation, and then the Galerkin method was then applied via the expansion of eigenfunctions over the water column derived from the Sturm-Liouville problem. A series of calculations has been performed to demonstrate the applicability of the model.

• Membrane and Water Treatment
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• 제8권5호
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• pp.411-421
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• 2017

Forward osmosis (FO) is an emerging technology which can possibly make the desalination process more cost and energy efficient. One of the major factors impeding its growth is the lack of an appropriate draw solute. The present study deals with the identification of potential draw solutes, and rank them. The comparison was carried out among ten draw solutes on the basis of four main parameters namely; water flux, reverse salt diffusion, flux recovery and cost. Each draw solute was given three 24 hour runs; corresponding to three different concentrations; and their flux and reverse salt diffusion values were calculated. A fresh membrane was used every time except for the fourth time which was the flux recovery experiment conducted for the lowest concentration and the change of flux and reverse salt diffusion values from the initial run was noted. The organic solutes inspected were urea and tartaric acid which showed appreciable values in other parameters viz. reverse salt diffusion, flux recovery and cost although they generated a lower flux. They ranked 5th and 8th respectively. All the experimented draw solutes were ranked based on their values corresponding to each of the four main parameters chosen for comparison and Ammonium sulfate was found to be the best draw solute.

• 대한기계학회논문집B
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• 제20권4호
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• pp.1437-1448
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• 1996

This paper presents a simplified model for approximate analysis of the solute redistribution in coarsening dendrite arms during solidification of binary metal alloys. By introducing a quadratic concentration profile with a time-dependent coefficient, the integral equation for diffusion in the solid phase is reduced to a simple differential relation between the coefficient and the solid-liquid interface position. The solid fraction corresponding to the system temperature is readily determined from the relation, phase equilibrium and the overall solute balance in which the liquid phase is assumed to be completely mixed. In order to validate the developed model, calculations are performed for the directional solidification of Al-4.9 mass Cu alloy. The predicted eutectic fractions for a wide range of the cooling rate reasonably agree with data from the well-known experiment as well as sophisticated numerical analyses. Also, the results for the back diffusion limits are consistent with available references. Additional calculations show that the characteristic parameters such as the coarsening, density variation and nonlinarity in the phase diagram significantly affect the microsegregation. Owing to the simplicity, efficiency and compatibility, the present model may be suitable for the micro-macroscopic solidification model as a microscopic component.

• 대한화학회지
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• 제34권4호
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• pp.377-383
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• 1990

용매 존재하에서 2-hydroxyethylmethacrylate와 acrylamide, N, N-dimethylamide 및 methylmethacrylate를 함량에 따라 3종류의 공중합체 수화겔막을 제조한 다음 이들 막에 알코올용질의 투과 및 분배계수를 측정하였으며, 이 측정값들을 이용하여 용질의 투과 메카니즘을 논의하였다. 수화겔막에서 유기용질의 투과계수는 그 분자의 크기에 주로 의존하였다. 그러나 수화겔막 내에 존재하는 물의 함량이 낮아지면 막에 대한 용질의 용해도가 점차 중요해짐을 또한 알 수 있었다. 분배계수의 측정 결과에 의하면 수화겔막에서의 용질의 분배는 주로 막과 용질사이에 존재하는 소수성 상호작용에 의해 조절되었다. 그리고 수화겔막에 유기용질의 확산은 전적으로 빈자리에 의존하며, 물분자와 용질 사이에 극성-편극성 및 수소결합도 부분적으로 영향을 미치나 그 정도가 아주 미약함을 확인하였다.

• Journal of Electrochemical Science and Technology
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• 제13권3호
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• pp.347-353
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• 2022

Agarose hydrogel, a solid electrolyte, was investigated voltammetrically in terms of transport properties and natural convection effects using a ferrocenyl compound as a redox probe. To confirm the diffusion properties of solute on the agarose interface, the diffusion coefficients (D) of ferrocenemethanol in agarose hydrogel were determined by cyclic voltammetry (CV) according to the concentration of agarose hydrogel. While the value of D on the agarose interface is smaller than that in the bulk solution, the square root of the scan rate-dependent peak current reveals that the mass transport behavior of the solute on the agarose surface shows negligible convection or migration effects. In order to confirm the reduced natural convection on the gel interface, scan rate-dependent CV was performed in the solution phase and on the agarose surface, respectively. Slow scan voltammetry at the gel interface can determine a conventional and reproducible diffusion-controlled current down to a scan rate of 0.3 mV/s without any complicated equipment.

• 한국지하수토양환경학회:학술대회논문집
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• 한국지하수토양환경학회 1999년도 정기총회 및 춘계 공동 학술발표회
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• pp.6-7
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• 1999

• Nuclear Engineering and Technology
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• 제44권1호
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• pp.79-88
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• 2012

Migration tests were performed with conservative tracers in a fractured zone that had a single fracture of about 2.5 m distance at the KURT. To interpret the migration of the tracers in the fractured rock, a solute transport model was developed. A two dimensional variable aperture channel model was adopted to describe the fractured path and hydrology, and a particle tracking method was used for solute transport. The simulation tried not only to develop a migration model of solutes for open flow environments but also to produce ideas for a better understanding of solute behaviours in indefinable fracture zones by comparing them to experimental results. The results of our simulations and experiments are described as elution and breakthrough curves, and are quantified by momentum analysis. The main retardation mechanism of nonsorbing tracers, including matrixdiffusion, was investigated.

• 한국항행학회논문지
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• 제16권4호
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• pp.657-664
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• 2012

용질분자를 용매를 통하여 전달시키는 기법중의 하나는 확산에 의한 것이다. 이러한 기전은 각개 용질분자의 열운동에 의한 것이다. 유체는 정지해 있는 상태로서 용질 전달의 핵심기전은 농도차에 의하여 결정된다. 인체 내에서 각종 하전 이온을 포함한 입자나 분자들은 체내의 농도차에 의해서 또는 외부 전계에 의해서 영향을 받아 고농도에서 저농도쪽으로 확산되어간다. 이러한 현상은 픽이 제안한 확산에 관한 제1법칙과 제2법칙에 의하여 정량적으로 전개할 수 있다. 본 논문에서는 체내의 물질이 확산되는 과정을 픽의 법칙을 이용하여 해석하고 그것을 실례를 통하여 구현하였다. 각 시간별 공간상의 확산현상에서 확산계수가 클 때는 시간이 경과함에 따라 발생지점의 농도는 현저히 낮아지고 그 농도가 주위로 급속히 확산되어감을 알 수 있었다. 그러나 어느 정도의 시간이 경과되면 그 농도의 감소는 매우 약해진다.

• Bulletin of the Korean Chemical Society
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• 제6권3호
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• pp.128-131
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• 1985

A series of copolymer membranes of 2-hydroxyethylmethacrylate (HEMA) with selected hydrophobic monomers were prepared without crosslinking agents. The equilibrium water content, the partition coefficient, and the permeability of the solutes such as urea, methylurea, 1,3-di-methylurea, and acetamide via these membranes were measured. The partition coefficient data show that as the hydrophobicity of solutes increased, the partition of solutes were dictated by hydrophobic interaction between solute and polymer matrix. Diffusion coefficients obtained in these experiments decrease as the water content of polymer membrane decreases. This decrease is blunt as the excess heat capacities, ${\phi}C^0_p$ (excess) in aqueous solution at infinite dilution of solute increases. To investigate the relationship between water content and diffusion coefficient, the results of the diffusion experiments were examined in light of a free-volume model of diffusive transport. The remarkable increase of urea mobility in the polymer network containing relatively larger bulk water can be considered as water structure breaking effect.