• Proceedings of the Membrane Society of Korea Conference
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• 1993.10a
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• pp.13-20
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• 1993

The sorption equilibria and permeation rates for carbon dioxide in such glassy polymer membranes with high glass-transition temperature as polyimide, polyetherimide, polysulfone and polyethersulfone membranes, were measured. The sorption isotherms for these systems can be described well by the dual-mode sorption model, whereas the pressure dependences of the mean permeability coefficients are simulated better by a modified dual-mode mobility model than the conventional dual-mode mobility model in which the Henry's law and Langmuir populations execute four kinds of diffusive movement.

• Membrane Journal
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• v.2 no.2
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• pp.129-134
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• 1992

The solubility of methane in poly(n-butyl methacrylate)(PnBMA) was determined at pressures up to 35 atm. These measurements were made by volumetric technique in the temperature range from -10 to 30$^{\circ}$C. The solubility was found to be a nonlinear function of the applied pressure and could be satisfactorily described by dual-mode sorption model at temperatures below the glass txansition temperature($T_g$) of the polymer. The Langmuir capacity constant decreased with increasing temperature and vanished near the glass transition temperature of PnBMA. The solubility isotherm became linear at temperatures above the glass transition temperature of PnBMA. The temperature dependence of the dual-mode sorption parameters was also discussed.

• KOREAN JOURNAL OF PACKAGING SCIENCE & TECHNOLOGY
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• v.4 no.1
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• pp.11-16
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• 1997

Sorption studies involving the sorption of n-propanol by an Amorphous Nylon(Nylon 6I/6T) were carried out as a function of sorbate vapor activity at $23^{\circ}C$. Vapor activity levels from 0.035 to 0.91 were investigated to evaluate the concentration dependency of sorption mechanism. Sorption behavior of propanol by Nylon 6I/6T showed distinctive two mode sorption phenomena as a function of Vapor activity. At Vapor activity levels below a=0.11, equilibrium sorption was achieved within a short period of time(less than 20hrs), which can be interpreted as following a Fickian diffusion model. A Langmuir-Flory-Muggins Dual Mode Sorption model can also be applied at these concentration levels. However, for Vapor activities above a=0.11, the sorption process appeared to be non-Fickian and resulted in a lack of equilibrium being attained.

• Proceedings of the Polymer Society of Korea Conference
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• 2006.10a
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• pp.339-339
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• 2006

In this study, the microvoids in glassy polymers were investigated by Xe sorption and $^{129}Xe$ NMR measurements. Xe sorption isotherms of glassy polymers have been successfully interpreted by the dual-mode sorption model. $^{129}Xe$ NMR chemical shift of the $^{129}Xe$ in the samples show nonlinear low-field shift with increasing sorption amount of Xe because of a fast exchange of Xe atoms between Henry and Langmuir sites, whereas it has showed linear shift against sorption amount of Xe into the Langmuir site. From this Xe-density dependence of the $^{129}Xe$ NMR chemical shift, it has been able to estimate mean size of the microvoids in glassy polymer. It is confirmed that there is correlation between ${C_H}'$ and volume or number of microvoids. From these findings, it is demonstrated that $^{129}Xe$ NMR spectroscopy is a powerful technique to determine the mean size and number of microvoids in glassy polymers.

• Membrane Journal
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• v.3 no.2
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• pp.79-82
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• 1993

The sorption equilibria and permeabilities for $CO_2$ in a homogeneous membrane of polystyrene with the glass transition temperature of $95^{\circ}C$ were measured at a temperature of $60^{\circ}C$ and gas pressures up to 1.6 MPa and 2.5 MPa, respectively. The sorption isotherm had the form af dual-mode sorption model at low gas pressures, but became linear at pressures above 1.3 MPa. The linear portion of the isotherm extrapolated to the origin. The pressure dependence of the rnean permeability coefficient deviated upward from the dualsrhode mobility model prediction. It was found that the glass transition was brought out by the plasticization action of sotbed $CO_2$ at a gas pressure of 1.3 MPa from the sorption isotherm. And this result was consistent with an increase in the mean permeability coefficient with applied gas pressure.

• Membrane Journal
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• v.9 no.1
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• pp.25-35
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• 1999

The sorption and permeation experiments with $O_2$ and $N_2$ were performed with poly sulfone hollow-fiber membrane to obtain oxygen-enriched air. Sorption of $O_2$ on poly sulfone membrane was 1.5'||'&'||'not;2.0 times higher than that of N2. Sorption of oxygen and nitrogen in poly sulfone membrane was described satisfactorily with "dual-mode sorption model". In the low pressure range below 3kgr!cm', about 85% of total sorption was Langmuir-type sorption and only 15% was Henry-type sorption. In the higher pressure above 3kgf/${cm}^2$, Langmuir sorption sites became almost saturated and reached asymptote, and the increase in total sorption with pressurizing might be due to the Henry~type sorption. The ideal separation factor ( P $O_2$/ P $N_2$) was in the range of 2~4, while the actual separation factor for the mixture was reduced to the value of 1.7~2.2.2.2.

• Proceedings of the Membrane Society of Korea Conference
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• 1991.10a
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• pp.37-38
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• 1991

몇가지 dianhydride와 diamine을 사용하여 합성한 PAA막을 가열온도와 가열시간을 달리하여 이미드화를 달리하는 막을 제조하고 이압법에 의하여 투과계수와 확산계수를 측정하였다. 이로부터 얻은 흡수계수는 Dual-Mode Sorption Model에 의하여 상관시켰다. 이로부터 polyimide막에 있어서 이미드화에 따른 기체루과 특성과 화학구조에 의한 기체투과 특성의 일부를 규명하였다.

• Food Science and Preservation
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• v.5 no.3
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• pp.239-246
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• 1998

Polyimide membrane system was designed for manufacturing nitrogen-enriched gas, and basic technical data was suggested for appling this system to controlled atmosphere storage. The permeability characteristics of pure oxygen and nitrogen could be explained by dual-mode sorption model. There was substantial decrease in the permeation rates of oxygen, which is the more permeable gas, through the polyimide membrane due to the presence of nitrogen in comparison with pure oxygen. However, the permeation rates of nitrogen was increased by the presence of oxygen. The ideal separation factor was in the range of 5 to 6 in the range of temperature and pressure difference studied, and the separation factor of air was lower than the ideal separation factor. The increase of ideal separation factor with increasing temperature is due to the fact that the activation energy for oxygen is larger than that for nitrogen. Nitrogen concentration decreased rapidly with increasing product recovery, and it was found that this is a major operating factor to obtain nitrogen concentration required for controlled atmosphere storage. A relation equation, by which nitrogen concentration in storehouse can be predicted, was suggested under the establishment of a hypothetical model for controlled atmosphere storage process using polyimide membrane system.

• Journal of Korean Society of Environmental Engineers
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• v.35 no.12
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• pp.897-905
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• 2013

In this study, sorption coefficients (${\log}K_{OC}$, n) for the binding of phenanthrene (PHE) to soil humins, insoluble fraction of soil humc substances (HS), were determined and relationship between the sorption coefficients and structural characteristics of the soil humins were investigated. The soil humins used in the present study were isolated from 7 different soils including 5 domestic soils, an IHSS standard and a peat soil, and characterized by elemental analysis and CPMAS $^{13}C$ NMR method. $^{13}C$ NMR spectral features indicate that the soil humins are mainly made up of aliphatic carbons (57.1~72.3% in total carbon) with high alkyl-C moiety, and the alkyl-C contents ($C_{Al-H,C}$, %) was in order of granite soil Hu (26~42%) > volcanic ash soil, HL Hu (23.9%) > Peat Hu (14.0%). The results of correlation study show that a positive relationship ($r^2$ = 0.77, p < 0.05) between organic carbon normalized-sorption coefficients ($K_{OC}$, mL/g) and alkyl-C contents($C_{Al-H,C}$, %), while negative relationship ($r^2$ = (-)0.74, p < 0.05) between Freundlich sorption parameter (n) and H,C-substituted aromatic carbon contents ($C_{Ar-H,C}$, %). The magnitude of $K_{OC}$ values are also negatively well correlated with polarity index (e.g., PI, N + O)/C) ($r^2$ = (-)0.74, p < 0.1). These results suggest that the binding capacity (e.g., $K_{OC}$) for PHE is increased in soil humin molecules having high contents of alkyl-C or lower polarity, and nonlinear sorption for PHE increased as the H,C-substituted aromatic carbon contents ($C_{Ar-H,C}$, %) in the soil humins increased. The PHE sorption characteristics on soil humins are discussed based on the dual reactive mode of sorption model.