• 한국지하수토양환경학회:학술대회논문집
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• 한국지하수토양환경학회 2003년도 추계학술발표회
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• pp.132-135
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• 2003

Solution chemistry, sorbate chemistry, and sorbent chemistry were widely investigated to find important factors that affect PAH sorption on mineral surfaces and to elucidate its microscopic mechanism. The solution chemistry, pH and ionic strength caused measurable change of HOC sorption reaction to minerals. The detectable change of Ka occurred at a pH region crossing the PZC (Point of Zero Charge) of each mineral. The PAH hydrophobicity, one of sorbate chemistry, was observed to have a strong correlation with PAM sorption to mineral. Mineral surface area was not found to be a predominant factor controlling PAH sorption. The mineral type might be more likely to play a crucial role in controlling the PAH sorption behavior. The CEC (Cation Exchange Capacity) of mineral, representing surface charge density, has meaningful correlation with regression slope of sorption coefficients (log $K_{d}$) versus aqueous activity coefficients (log Υ$_{w}$).).).

• Environmental Engineering Research
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• 제14권3호
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• pp.186-194
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• 2009

Understanding the environmental fate of human and animal pharmaceuticals and their risk assessment are of great importance due to their growing environmental concerns. Although there are many potential pathways for them to reach the environment, effluents from sewage treatment plants (STPs) are recognized as major point sources. In this study, the removal efficiencies of the 43 selected priority pharmaceuticals in a conventional STP were evaluated using two simple models: an equilibrium partitioning model (EPM) and STPWIN$^{TM}$ program developed by US EPA. It was expected that many pharmaceuticals are not likely to be removed by conventional activated sludge processes because of their relatively low sorption potential to suspended sludge and low biodegradability. Only a few pharmaceuticals were predicted to be easily removed by sorption or biodegradation, and hence a conventional STP may not protect the environment from the release of unwanted pharmaceuticals. However, the prediction made in this study strongly relies on sorption coefficient to suspended sludge and biodegradation half-lives, which may vary significantly depending on models. Removal efficiencies predicted using the EPM were typically higher than those predicted by STPWIN for many hydrophilic pharmaceuticals due to the difference in prediction method for sorption coefficients. Comparison with experimental organic carbon-water partition coefficients ($K_{ocs}) revealed that log KOW-based estimation used in STPWIN is likely to underestimate sorption coefficients, thus resulting low removal efficiency by sorption. Predicted values by the EPM were consistent with limited experimental data although this model does not include biodegradation processes, implying that this simple model can be very useful with reliable Koc values. Because there are not many experimental data available for priority pharmaceuticals to evaluate the model performance, it should be important to obtain reliable experimental data including sorption coefficients and biodegradation rate constants for the prediction of the fate of the selected pharmaceuticals.

• Nuclear Engineering and Technology
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• 제33권3호
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• pp.261-269
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• 2001

In this study, sorption experiments of uranium onto silica colloids were carried out and the effects of important geochemical parameters such as pH, ionic strength, carbonate concentration, colloid concentration, and total concentration of uranium were investigated. The sorption coefficients of uranium for silica colloids named as pseudo-colloid formation constants were about 10$^4$~ 10$^{5}$ mL/g depending on the experimental conditions. The effects of the geochemical parameters were found to be important in the sorption of uranium onto silica colloids. A Langmuir type sorption isotherm of uranium between silica colloids and the solution phase was also presented. The sorption mechanisms were explained by analyzing the effects of the geochemical parameters.

• 한국환경과학회지
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• 제11권9호
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• pp.961-969
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• 2002

This study was performed : 1) to establish the experimental analysis conditions for the sorption and desorption of toxic organic contaminants to/from the activated sludge, sediment, and clay, and 2) to determine the sorption and desorption equilibrium coefficients of some representative halogenated aliphatic compounds. Through the preliminary sorption test using Azo dye, a setting of quantitative experimental conditions to determine the sorption and desorption characteristics was decided as follows; equilibration time of 180 minutes, centrifuge for 15 minutes at 5000$\times$g, and 500mg/$\ell$ of TOC concentration. The sorption and desorption characteristics of halogenated aliphatic compounds onto activated sludge, sediment and clay could be described very well using the Freundlich isotherm. The preference of the average sorption capacity of the overall compounds showed in the sequence sediment 0.26mg/g, clay 0.23mg/g, and activated sludge 0.11 mg/g. The desorption rate of the sorbed compounds onto activated sludge, sediment and clay was approximately 89.8%, 35.3%, and 66.4%, respectively.

• 한국지하수토양환경학회지:지하수토양환경
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• 제10권1호
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• pp.26-34
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• 2005

토양과 유기화합물의 접촉시간은 흡착과 탈착의 특성에 영향을 미치는 중요한 요소 중의 하나이다. 본 연구에서는 atrazine의 토양 흡착과 탈착에 미치는 접촉시간의 영향을 연구하였다. 등온 흡착실험을 수행하여 토양과 수용액 사이의 분배계수를 구하였고, 탈착에 대한 동력학 실험을 수행하고 three-site desorption모델을 이용, 회기분석 하여 탈착속도 계수들을 추산하였다. atrazine과 토양의 접촉시간은 2일에서부터 8개월까지 변화시켰다. 2일 흡착에 대한 atrazine의 흡착등온 곡선은 거의 선형이었고$(r^2>0.97)$, 흡착분배계수는 토양의 유기탄소 함량과 강한 양의 상관관계를 가졌으며 사용한 모든 토양에서 접촉시간이 길어질수록 증가하였다. 흡착곡선에서의 비선형성은 Houghton muck토양을 제외하고는 접촉시간에 따라 증가하지 않았다. 탈착실험 분석으로부터 접촉시간이 증가함에 따라 equilibrium site분율은 감소하고 non-desorbable site 분율은 증가함을 알 수 있었다. 사용한 모든 토양에서 토양유기탄소 함량으로 표준화한 경우 desorbable sites 에서의 atrazine농도는 접촉시간에 따라 비교적 일정한 것에 비해 non-desorbable site에서의 atrazine농도는 접촉시간이 증가함에 따라 증가하였다.

• 한국막학회:학술대회논문집
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• 한국막학회 1993년도 추계 총회 및 학술발표회
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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.

• Macromolecular Research
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• 제12권1호
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• pp.26-31
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• 2004

Using gravimetry, we have studied the diffusion of water into sulfonated polystyrene ionomers. Diffusion coefficients were calculated from Fick's equation. The water sorption was found to be dependent on the ion content (3.6-11 mol％) and the nature of the cation (H, Na, Li, or Zn). The sorption kinetics indicates a slight deviation from Fickian behavior. We used the analytical solution of Fick's equation to evaluate the concentration profiles, which are in good agreement with the experimental results.

• Nuclear Engineering and Technology
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• 제34권5호
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• pp.445-454
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• 2002

The sorption of U(Vl) on a domestic granite is studied as a function of experimental conditions such as contact time, solution-solid ratio, ionic strength, and pH using a batch procedure. The distribution coefficients, $K_{d}$＇s, of U(VI) are about 1-100mL/g depending on the experimental conditions. The sorption of U(VI) onto granite particles is greatly dependent upon the contact time, solution-solid ratio, and pH, but very little is dependent on the ionic strength. It is noticed that an U(VI)-carbonate ternary surface complex can be formed in the neutral range of pH. In the alkaline range of pH above 7, U(VI) sorption onto granite particles is greatly decreased due to the formation of anionic U(VI)-carbonate aqueous complexes.s.

• 한국지하수토양환경학회:학술대회논문집
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• 한국지하수토양환경학회 2005년도 총회 및 춘계학술발표회
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• pp.191-194
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• 2005

Characteristics of sorption and desorption in soils affect chemical fate, soil-remediation time, and selection of remediation technology. The sorption and desorption behavior of atrazine and naphthalene on soils was studied. Six soils collected at Gwangju area were used as sorbents and the organic matter contents ranged from 1.28 to 5.21%. Sorption and desorption experiments were conducted and sorption distribution coefficients(Kd) of atrazine and naphthalene were nearly linear$(R^2=0.93{\sim}0.97)$. Desorption parameters were evaluated using three site desorption model included equilibrium, nonequilibrium and nondesorption sites. Non-desorbable site fraction for atrazine was evaluated, but for naphthalene it was not enumerated during the experimental period. Through the series dilution desorption experiments, non-desorpbable sites were observed for both chemicals.

• Nuclear Engineering and Technology
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• 제53권3호
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• pp.894-900
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• 2021

This paper examines sorption of Pd(II) onto illite, MX-80 bentonite, and Queenston shale in Na-Ca-Cl solutions of varying ionic strength (IS) from 0.01 to 6.0 mol/L (M) and pH_c ranging from 3 to 9 under atmospheric conditions. A 2-site protolysis non-electrostatic surface complexation and cation exchange model was applied to the Pd sorption onto illite and MX-80 using PHREEQC, and the model results were compared to the experimental ones obtained in this work. Surface complexation and cation exchange constants were estimated for both illite and MX-80 through the optimization process to bring the predicted distribution coefficients from the model into alignment with the experimentally derived values. These optimized surface complexation constants were compared to existing linear free energy relationships (LFER).