• 대한기계학회논문집B
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• 제22권4호
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• pp.499-509
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• 1998

In the absorption process of water vapor in a liquid film, the composition of the gas phase, in which a non-absorbable gas is combined with the absorbate influences the transport characteristics remarkably. In the present study, the absorption processes of water vapor into aqueous solution of lithium bromide in the presence of non-absorbable gases were investigated analytically. The continuity, momentum, energy and diffusion equations for the solution film and gas phase were formulated in integral forms and solved numerically. It was found that the mass transfer resistance in gas phase increased with the concentration of non-absorbable gas. However the primary resistance to mass transfer was in the liquid phase. As the concentration of non-absorbable gas in the absorbate increased, the liquid-vapor interfacial temperature and concentration of absorbate in solution decreased, which resulted in the reduction of absorption rate. The reduction of mass transfer rate was found to be significant for the addition of a small amount of non-absorbable gas to the pure vapor, especially at the outlet of an absorber where non-absorbable gases accumulated. At higher non-absorbable gas concentration, the decrease of absorption flux was almost linear to the volumetric concentration of non-absorbable gas.

• Journal of Electrochemical Science and Technology
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• 제2권1호
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• pp.20-25
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• 2011

This work focuses on the behavior of the overpotential increase due to a utilization rise in a molten carbonate fuel cell. The behavior is generally explained by Nernst loss, which is a kind of voltage loss due to the thermodynamic potential gradients in a polarization state due to the concentration distribution of reactant species through the gas flow direction. The evaluation of Nernst loss is carried out with a traditional experimental method of constant gas utilization (CU). On the other hand, overpotential due to the gas-phase mass-transport resistance at the anode and cathode shows dependence on the utilization, which can be measured using the inert gas step addition (ISA) method. Since the Nernst loss is assumed to be due to the thermodynamic reasons, the voltage loss can be calculated by the Nernst equation, referred to as a simple calculation (SC) in this work. The three values of voltage loss due to CU, ISA, and SC are compared, showing that these values rise with increases in the utilization within acceptable deviations. When we consider that the anode and cathode reactions are significantly affected by the gas-phase mass transfer, the behavior strongly implies that the voltage loss is attributable not to thermodynamic reasons, namely Nernst loss, but to the kinetic reason of mass-transfer resistance in the gas phase.

• 공업화학
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• 제10권2호
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• pp.310-318
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• 1999

공기분리 PSA 공정설계에 적용할 물질전달계수를 구하기 위하여 흡착탑을 통과하는 질소와 산소의 농도에 대한 동적파과곡선을 실험적으로 측정하였다. 그 결과를 전산모사에 의한 파과곡선과 비교하여 벌크흐름 중의 물질전달속도를 예측하였다. 전산모사에서 흡착은 coupled Langmuir isotherm을 따른다고 보았으며, 물질전달은 LDF 모델에 의해 표현된다고 가정하였다. 실험과 이론의 비교를 통해 얻은 물질전달계수는 유속에는 거의 영향을 받지 않았으나 압력 조건에 따라 민감한 변화를 보였다. 이를 통해 물질전달저항이 거대기공 확산영역에 있음을 예측할 수 있었으며, 물질전달계수를 압력변화에 대해 지수함수의 형태로 표현하였다. 질소나 산소 단일 성분에 대해서 얻은 물질전달계수는 질소와 산소 혼합 벌크기체의 파과곡선에 적용했을 경우에도 5% 이하의 오차로 잘 일치함을 보여주었다.

• 설비공학논문집
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• 제11권6호
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• pp.912-920
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• 1999

The forced convective boiling heat transfer coefficients of R-407C were measured inside a horizontal tube 6.0mm I.D. and 4.0m long. The heat transfer coefficients increased according to an increase in heat flux at constant mass flux. Because nucleation was completely suppressed in the two-phase flow region with high quality, heat transfer coefficients in forced convective evaporation were higher than those in nucleate boiling region. Average heat transfer coefficients of R-407C were about 30 percent lower than the pure refrigerant correlation, due to mass transfer resistance at the gas-liquid interface. However, the total experimental data shows an agreement with the predicted data for ternary refrigerant mixtures with a mean deviation of 30%.

• 대한기계학회논문집
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• 제18권12호
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• pp.3305-3314
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• 1994

In this study, the influence of a frost formed on the vertical plate for different operating conditions(the temperature of the air, the humidity of the air, the velocity of the air, and the temperature of the cooling plate) is investigated. The performance of the heat exchanger is examined by introducing a parameter such as the energy transfer resistance. Correlations which relate frost density, frost thickness and energy transfer resistance to Reynolds number, air temperature and humidity, and cooling plate temperature are developed. Static pressure drop and air flow rate are expressed as a function of free flow area of air.

• Membrane and Water Treatment
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• 제1권2호
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• pp.159-169
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• 2010

The effect of external recycle on the performance of dialysis in countercurrent-flow rectangular membrane modules was investigated both theoretically and experimentally. Theoretical analysis of mass transfer in parallel-flow device with and without recycle is analogous to heat transfer in parallel-flow heat exchangers. Experiments were carried out with the use of a microporous membrane to dialyze urea aqueous solution by pure water. In contrast to a device with recycle, improvement in mass transfer is achievable if parallel-flow dialysis is operated in a device of same size with recycle which provides the increase of fluid velocity, resulting in reduction of mass-transfer resistance, especially for rather low feed volume rate.

• 폴리머
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• 제28권2호
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• pp.121-127
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• 2004

폴리(에틸렌 나프탈레이트)의 축중합 반응은 가역반응이므로 부반응 물질인 에틸렌 글라이콜의 신속한 제거가 높은 분자량의 제품을 얻는데 매우 중요하다. 본 연구에서는 폴리(에틸렌 나프탈레이트)올리고머로 박막을 제조하여 실제 반응기와 동일한 조건 하에서 (28$0^{\circ}C$, <0.1mmHg) 반응시켜 이 때 일어나는 물질 전달 현상을 관찰하고자 하였다. 여러 가치 두께의 박막을 제조하여 반응 실험한 결과 두께가 0.025cm 이하의 영역에서는 박막에서의 물질 전달 저항이 크지 않아 총괄 반응 속도에 영향을 미치지 않음을 관찰하였다. 물질 전달 모델 및 확산 모델을 사용하여 반응 결과를 예측한 결과 두 모델 모두 실험 결과를 잘 예측하였으나 확산 모델의 경우 중합도가 낮은 영역에서 물질 전달 모델에 비해 반응이 더 빨리 진행되는 경향을 보였다. 두 모델을 이용하여 물질 전달 관련 계수를 예측한 결과 폴리(에틸렌 나프탈레이트)에서의 확산 계수는 4.7${\times}$$10^{-6}$$\textrm{cm}^2$/sec, 물질 전달 계수는 1.4${\times}$$10^{-4}$cm/sce로 폴리(에틸렌 테레프탈레이트) 경우보다 작은 값을 보였다.

• 한국수소및신에너지학회논문집
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• 제34권3호
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• pp.283-291
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• 2023

The physical properties were analyzed for four gas diffusion layers, and gas diffusion electrodes (GDEs) for the cathode of high-temperature polymer electrolyte membrane fuel cell were fabricated through bar coating with three binder to carbon (B/C) ratios. Among them, The GDE from JNT30-A6P showed a significant change in secondary pore volume at a B/C ratio of 0.31, which had the largest pore volume among all GDEs. In the polarization curve, JNT30-A6P GDE showed the best membrane electrode assembly (MEA) performance with a peak power density of 384 mW/cm² at a a B/C ratio of 0.31. From the distribution of relaxation time analysis, the peak 1 corresponding to mass transfer resistance of oxygen reduction reaction (ORR) was significantly reduced in the JNT30-A6P GDE. This is the result that when the binder content decreased, the volume of the secondary pore increased, and the mass transfer resistance of ORR decreased, which played an essential role in the MEA performance.

• 한국지하수토양환경학회:학술대회논문집
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• 한국지하수토양환경학회 2000년도 추계학술대회
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• pp.171-176
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• 2000

Bioremediation of hazardous hydrophobic organic compounds, such as polycyclic aromatic hydrocarbons (PAHs), is a major environmental concern due to their toxic and carcinogenic properties. Due to their hydrophobicity, the hydrophobic organic compounds are mainly associated with the soil organic matter or nonaqueous-phase liquids. A major question concerns the relationships between biodegradation and sorption. This work develops and utilizes a non- steady state model for evaluating the interactions between sorption and biodegradation of phenanthrene, a 3-ring PAH compound, in soil-slurry systems. The model includes sorption/desorption of a target compound, its utilization by microorganisms as a primary substrate existing in the dissolved phase and/or the sorbed phase in biomass and soil, oxygen transfer, and oxygen utilization as an electron acceptor. Biodegradation tests with phenanthrene were conducted in liquid and soil-slurry systems. The soil-slurry tests were performed with very different mass transfer rate: fast mass transfer in a flask test at 150 rpm, and slow mass transfer in a roller-bottle test at 2 rpm. In the slurry tests, phenanthrene was degraded more rapidly than in liquid tests, but with a similar rate in both slurry systems. Modeling analyses with several hypotheses indicate that a model without biodegradation of compound sorbed to the soil was not able to account for the rapid degradation of phenanthrene, particularly in the roller bottle slurry test. Reduced mass-transfer resistance to bacteria attached to the soil is the most likely phenomenon accounting for rapid sorbed-phase biodegradation.

• 한국막학회:학술대회논문집
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• 한국막학회 1994년도 춘계 총회 및 학술발표회
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• pp.51-52
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• 1994

High permeability, selectivity and stability are the basic properties also required for membrane gas separations. The $CO_2$ separation by liquid membranes has been developed as a new technique to improve the permeability and selectivity of polymeric membranes. Sirkar et al.(1) have atlempted the hollow-fiber contained liquid membrane technique under four different operational modes, and permeation models have been proposed for all modes. Compared to a conventional liquid membrane, the diffusional resistance decreased by the work of Teramoto et al.(2), who referred to a moving liquid membrane. Recently, Shelekhin and Beckman (3) considered the possibility of combining absorption and membrane separation processes in one integrated system called a membrane absorber. Their analysis could be predicted effectively the performance of flat sheet membrane, however, there are restrictions for considering a flow effect. The gas absorption rate is determined by both an interfacial area and a mass transfer coefficient. It can be easily understood that although the mass transfer coefficients in hollow fiber modules are smaller than in conventional contactors, the substantial increase of the interfacial area can result in a more efficient absorber (4). In order to predict a performance in the general system of hollow-fiber membrane absorber, a gas-liquid mass transfor should be investigated inevitably. The influence of liquid velocity on both a mass transfer and a performance will be described, and then compared with experimental results. A present study is attempted to provide the fundamentals for understanding aspects of promising a hollow-fiber membrane absorber.