• 생태와환경
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• 제49권4호
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• pp.289-295
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• 2016

The purpose of this study is to find out the effect of particle size of sediment on adsorption of fluoride. Particle size is classified as sand, silt and clay. Adsorption equilibrium time, adsorption isotherms and the effect of pH were investigated through batch tests. The $pH_{pzc}$ of sand, silt, clay was respectively 6, 8, 4.5 and AEC (anion exchange capacity) was highest in silt, respectively 0.0095, 0.0224, $0.014meq\;g^{-1}$. Adsorption of fluoride on the sediment was in equilibrium within 300 minutes from all particle size. The experimental data of isotherms at various pH were well explained by Freundlich equation. As the experimental results of the effect of pH, the adsorption efficiency of sand and silt were reduced after the $pH_{pzc}$. However, the adsorption efficiency of clay was maintained after the $pH_{pzc}$, and decreased rapidly higher than pH 12.

• EDISON SW 활용 경진대회 논문집
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• 제3회(2014년)
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• pp.464-466
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• 2014

We investigate the effect of hydrogen on adsorption of hydrocarbon molecules on graphene with density functional theory (DFT) calculations. In this study, we calculate the binding energies of hydrogen molecule, carbon atom and other hydrocarbon fragments such as CHx (x=1, 2, 3, 4) on graphene to find the most stable adsorption site. Then, to study the effect of hydrogen, we investigate the adsorption of hydrocarbon fragments in the presence of hydrogen atoms on graphene.

• 한국환경과학회지
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• 제16권2호
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• pp.143-149
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• 2007

The effect of precoating of silica with polyamine surfactants on the adsorption of five model compounds containing asphalt-like functionalities was studied. Hexadecyltrimethylammonium chloride (HDTMA) and 1-hexadecylamine were used for silica precoating. The model compounds representing five asphalt functionalities were benzoic acid, phenol, benzylbenzoate, benzophenone, and quinoline. All the adsorption isotherms conformed well to the Langmuir adsorption model. All the model compounds showed decreased adsorption with the HDTMA precoating. However, two acidic compounds, benzoic acid and phenol, showed enhanced adsorption on the silica precoated with 1-hexadecylamine. In aqueous solutions, the adsorption of the acidic compounds were in the following order: silica precoated with 1-hexadecylamine > silica precoated with HDTMA > uncoated silica.

• 한국재료학회지
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• 제14권3호
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• pp.229-234
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• 2004

All the applications of natural zeolites make use of one or more of their physical and chemical properties: adsorption, ion-exchange and related molecular sieve properties, dehydration and rehydration, and siliceous composition. Accordingly, the applications of zeolite have been carried out in the various aspects because of its large cation exchange capacity and adsorption properties. In this paper, the adsorption effect of heavy metal ions in wastewater on zeolite mineral by batch adsorption process is studied. The amounts of adsorbed ions were variable by original pH and ionic concentration, especially original pH of solution had an important effect on the adsorption. In case of low pH solution, e.g. below 3.0, clinoptilolite adsorbed $Pb^{2+}$ ,$ Cd ^{2+ }$ , $Cu^{2+}$ and $Zn^{ 2+}$ , but mordenite almost did not adsorb except $Pb^{2+}$ . Under the same conditions, these ions were more adsorbed on clinoptilolite than on mordenite mineral. The velocity of adsorption was relatively fast and it was confirmed by shaking test that the equilibrium of adsorption could be attained in about one hour. The species of exchangeable cation of zeolite had an effect on its removing ability and zeolite of the sodium-exchanged type was the best.

• Bulletin of the Korean Chemical Society
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• 제33권3호
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• pp.901-905
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• 2012

In this study, we investigated the pure geometrical effect of porous materials in gas adsorption using the grand canonical Monte Carlo simulations of primitive gas-pore models with various pore geometries such as planar, cylindrical, and random pore geometries. Although the model does not possess atomistic level details of porous materials, our simulation results provided many insightful information in the effect of pore geometry on the adsorption behavior of gas molecules. First, the surface curvature of porous materials plays a significant role in the amount of adsorbed gas molecules: the concave surface such as in cylindrical pores induces more attraction between gas molecules and pore, which results in the enhanced gas adsorption. On the contrary, the convex surface of random pores gives the opposite effect. Second, this geometrical effect shows a nonmonotonic dependence on the gas-pore interaction strength and length. Third, as the external gas pressure is increased, the change in the gas adsorption due to pore geometry is reduced. Finally, the pore geometry also affects the collision dynamics of gas molecules. Since our model is based on primitive description of fluid molecules, our conclusion can be applied to any fluidic systems including reactant-electrode systems.

• 한국환경농학회지
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• 제26권4호
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• pp.286-296
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• 2007

To increase phosphate (P) availability in soils, the efficiency of silicate (Si) in reducing P adsorption was investigated by competitive adsorption tests under changing conditions of pH, ion concentrations, and order of anion addition along with single adsorption properties of each ion at $20^{\circ}C$. In the single ion adsorption study, P and Si ions showed the opposite reaction patterns: phosphate adsorption decreased with increasing pH and attained adsorption maximum however, silicate adsorption increased with increasing pH without attaining adsorption maximum. Phosphorus and Si adsorption were influenced by pH in the range of 5.0 - 9.0 and the type and amount of P and Si concentration. Silicate added to soil before P or in a mixture with P significantly reduced P adsorption above pH 7.0; however, there was no significant Si-induced decreased in P adsorption at pH 5.0 when anions were added as mixture. The efficiency of Si in reducing P adsorption increased with increasing Si concentration and pH. The effect of P on Si adsorption was relatively small at pH 5.0 and no effect of P on silicate adsorption was observed at pH 9.0. The presence of Si strongly depressed P adsorption when Si was added before P compared to P and Si added as a mixture. These results suggest that application of Si may decrease P adsorption and increase the availability of P in soils. Furthermore, a Si source would be better to add before P application to enhance the availability of P in soils.

• 한국지반공학회논문집
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• 제16권4호
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• pp.157-170
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• 2000

본 연구에서는 자연점토에 대한 구리 흡착 및 구리와 아연의 경쟁 흡착 시 온도변화에 따른 흙의 각 구성성분별 흡착거동을 살펴보기 위해 혼합 흡착-연속추출법(combined adsorption-sequential extraction analysis, CASA)을 사용하였다. 실험결과 중금속 아연의 경우 농도에 따른 차이는 있지만 온도증가에 따라 주로 이온교환 형태로 흡착되는 것을 알 수 있고, 구리와 경쟁흡착의 경우 이러한 경향은 더욱 커져서 약 80~90%정도가 이온교환형태로 흡착되어진다. 반면 구리의 경우 실험을 수행한 거의 모든 농도 범위에서 약 50%이상이 탄산염 형태로 흡착되어진다. 탄산염형태로의 흡착 양상은 단일 흡착의 경우 온도증가에 따라 약 5% 증가하는 경향을 보이고, 경쟁흡착의 경우에는 약 10%정도 증가하는 경향을 나타내었다. 그리고 자연점토에서의 아연과 구리의 각 구성성분 별 흡착거동은 이온 교환 형태로 분배되는 경우를 제외하고는 온도증가에 따라 흡착량이 증가하는 흡열반응$(\DeltaH0>0)$인 것으로 나타났다.

• 한국지반환경공학회 논문집
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• 제2권3호
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• pp.17-35
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• 2001

본 연구에서는 자연점토에 납, 구리, 아연, 카드뮴의 단일 흡착 시 온도변화에 따른 흙의 구성성분별 흡착거동을 살펴보기 위해 혼합 흡착-연속추출법(combined adsorption-sequential extraction analysis, CASA)을 사용하였다. 실험결과 납과 구리의 경우 약 50%이상의 분배가 탄산염 형태로 나타났고, 카드뮴의 경우 약 80%이상의 분배가 이온교환 형태로 나타났다. 아연의 경우 $25^{\circ}C$이하의 온도에서는 이온교환 형태로의 분배가 약 60%로 나타났고, $40^{\circ}C$이상의 온도에서는 탄산염 형태로의 분배가 50%이상으로 나타났다. 흙의 각 구성성분에 대한 흡착용량의 온도에 따른 영향은 철.망간 산화물과 유기물 형태에서 주로 발생하는 것으로 나타났다. 또한 이온교환 형태를 제외한 모든 형태에 대한 중금속들의 흡착 반응은 온도의 증가에 따라 흡착량이 증가하는 흡열반응(${\Delta}H^0$ >0)인 것으로 나타났다.

• 한국환경과학회지
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• 제25권3호
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• pp.395-403
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• 2016

This study examined the adsorption effect of aromatic pesticides by hollow fiber NF membrane on rejection and removal properties. Batch type adsorption test and hollow fiber NF membrane filtration were conducted with 5 different kinds of aromatic pesticides. 3 to 15 days were required to reach the equilibrium concentration and $0.3181{\sim}0.8094{\mu}g/cm^2$ were adsorbed to hollow fiber NF membrane. Since 5 hours of separation test were too short to keep steady state for permeate due to the repetition of sorption and desorption, longer times were required to evaluate the rejection performance of NF membrane. Sorption and desorption were confirmed by the separation test equipped with membrane and without membrane. Adsorption contribution of aromatic pesticides to hollow fiber membranes were shown to be ranged from 16.1% to 36.3% and indicated the difference considering sorption effect.

• Bulletin of the Korean Chemical Society
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• 제2권2호
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• pp.56-59
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• 1981

In this paper a further generalization of the theory of multilayer physical adsorption previously developed by the authors is attempted so that the effect of vertical interactions between adsorbent and adsorbate can be explicitly taken into account. In this attempt we have to discard the previously adopted assumption that the molecules in the second layer or above are all in the same physical state. In order to estimate the effect of vertical interactions on the adsorption isotherm the interaction energy between an adsorbed molecule and the adsorbent surface is assumd to vary as $r^{-3}$ where r is the distance that the molecule under consideration is separated from the adsorbent surface. Resulting adsorption isotherm is applied to interpret the adsorption data of tetramethylsilane vapor on iron film and good agreements between observed and calculated values are obtained over wide range of pressure.