• 한국지하수토양환경학회지:지하수토양환경
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• 제27권6호
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• pp.11-21
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• 2022

Sorption of phenanthrene (PHE) and pyrene (PYR) in several sorbents, i.e., natural soil, BionSoil^®, Pahokee peat, vermicompost and Devonian Ohio Shale and a surfactant (hexadecyltrimethyl ammonium chloride)-modified montmorillonite (HDTMA-M) were investigated. Pyrene exhibited higher sorption tendency than phenanthrene, as predicted by its higher octanol to water partition coefficient (K_ow). Several sorption models: linear, Freundlich, solubility-normalized Freundlich model, and Polanyi-Manes model (PMM) were used to analyze sorption isotherms. Linear isotherms were observed for natural soil, BionSoil^®, Pahokee peat, vermicompost, while nonlinear Freundlich isotherms fitted for Ohio shale and HDTMA-M. The relationship between sorption model parameters, organic carbon content (f_oc), and elemental C/N ratio was studied. In the binary competitive sorption of phenanthrene and pyrene in natural soil, competition between the solutes caused reduction in the sorption of each solute compared with that in the single-solute system. The ideal adsorbed solution theory (IAST) coupled with the single-solute Freundlich model was not successful in describing the binary competitive sorption equilibria. This was due to the inherent nature of linear sorption of phenanthrene and pyrene in natural soil. The result indicates that the applicability of IAST for the prediction of binary competitive sorption is limited when the sorption isotherms are inherently linear.

• 한국지하수토양환경학회:학술대회논문집
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• 한국지하수토양환경학회 2001년도 총회 및 춘계학술발표회
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• pp.15-18
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• 2001

Sorption/desorption studies were conducted to determine sorption/desorption characteristics of phenolic compounds (phenol and 4-chlorophenol) in organically modified natural bentonite. The cationic exchange capacity (CEC) of bentonite was exchanged with a cationic surfactant, hexadecyltrimethylammonium (HDTMA), to enhance the removal capacity of organic phenol contaminants dissolved in aqueous solution. This modification produces a change of the surface property of bentonite from hydrophilic to organophilic. The single-solute and bi-solute competitive adsorptions were performed In batch mode to investigate the removal of two toxic organic Phenols, chlorophenol and 4-chlorophenol on the HDTMA-bentonite. The adsorption affinity of the 4-chlorophenol was higher than phenol due to higher octanol:water partition coefficient (Kow). The single-solute and bi-solute competitive desorptions were also performed investigate the competitive desorption of the phenolic compounds from HDTMA-bentonite. Freundlich model was used to analyze the single-solute adsorption/desorption results, while the IAST model predicted the hi-solute adsorption/desorption equilibria. The IAST model well predicted hi-solute competitive adsorption/desorption behaviors.

• 상하수도학회지
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• 제28권1호
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• pp.83-89
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• 2014

The aim of this study is to investigate the sorption/ion exchange of radioactive nuclides such as $Cs^+$ and $Sr^{2+}$ by synthetic Na-micas. In order to prepare Na-micas, two natural micas (phlogopite and biotite) were used as precursor materials. XRD, SEM, and EDS analyses were used to examine material characterization of synthetic Na-micas. Analyses of materials revealed that Na-micas were successfully obtained from natrual micas by K removal treatment. On the other hand, single solute (Cs or Sr) and bi-solute (Cs/Sr) sorption experiments were carried out to determine sorption capacity of Na-micas for Cs and Sr under different pH and ionic strength conditions. Uptake of Cs and Sr by micas in bi-solute system was lower than in single-solute system. Additionally, Langmuir and Langmuir competitive models were applied to describe sorption isotherm of Na-micas. bi-solute system was well described by Langmuir competitive models. For the results obtained in this study, Na-micas could be promising sorbents to treat multi-radioactive species from water and groundwater.

• 한국지하수토양환경학회:학술대회논문집
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• 한국지하수토양환경학회 2002년도 추계학술발표회
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• pp.302-305
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• 2002

Scoria is a bomb-sized, generally vesicular pyroclast that is red or black in color and light in weight. In this study, scoria from Cheju was examined for the use as a sorbent. It is composed of plagioclase, olivine, hornblende, pyroxene, and glass, with an average composition of 49.84% SiO$_2$, 14.07% A1$_2$O$_3$, End 9.14% Fe$_2$O$_3$. Studies on kinetic isotherm sorption of Zn(II) onto scoria under various parameters such as initial zinc concentration, particle size, and adsorbent/adsorbate ratio were carried out using an agitated batch. The results suggest that the smaller scoria size and the larger adsorbent/adsorbate ratio produce the higher degree of Zn(II) removal. More effective removal also appears at lower initial Zn concentration. The sorption behavior of Zn(II) onto scoria seems to be mainly controlled by cation exchange. Studies on equilibrium isotherm sorption of other heavy metals (Pb, Cu, Cd) onto scoria were also conducted and compared with those onto powdered activated carbon (PAC) and non-organic matter scoria (NOS), The results suggest that the Cheju scoria has the slightly higher sorption capability than PAC and NOS, and the order of the effective sorption onto scoria and PAC is Pb > Cu > Zn > Cd. The monometal sorption onto scoria is more stronger than the competitive sorption.

• 한국지하수토양환경학회:학술대회논문집
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• 한국지하수토양환경학회 2001년도 추계학술발표회
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• pp.19-22
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• 2001

The effects of pH on the sequential sorption/desorption of chlorinated phenols (2-chlorophenol, 2.4-dichlorophenol and 2,4,5-trichlorophenol) in HDTMA-montmorillonite were investigated by maintaining pH 4.85 or 9.15 in the sequential batch sorption and desorption experiments. The chlorinated phenols are hydrophobic ionizable orginic compounds; they can exist as either neutral (pH << pKa) or anionic (pH >> pKa) forms. Among the tested chlorinated phenols, 2,4,5-trichlorophenol showed the highest sorption affinity at pH 4.85 as expected by the $K_{ow}$ . Neutral speciation at pH 4.85 exhibited higher sorption affinity than anionic speciation at pH 9.15. Our results indicates that desorption of chlorinated phenols is strongly dependent on pH of the aqueous phase. Freundlich model was used to analyze the single-solute sorption/desorption results. The ideal adsorbed solution theory(IAST) was employed to predict the hi-solute sorption/desorption equilibria.

• 한국환경보건학회지
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• 제21권3호
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• pp.77-86
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• 1995

Lead(II) removal efficiency by natural kaolinite was investigated through laboratory experiments. This study was conducted in two phases-sorption and desorption. In the adsorption study, the influence of sorption kinetics and sorption isotherm and various parameters such as pH, temperature, coexisting other heavy metal ions on the lead adsorption was investigated. And desorption study was carried out in order to find the re-usability of kaolinite as an adsorbent. The results of the study are as follows. 1. Sorption kinetics was investigated under the condition of 2.5 mg/l adsorbent concentration, pH 6.5$\pm$0.05, temperature $30\pm 0.5\circ$C, initial lead(II) concentration 25 mg/l. Adsorption rate was initially rapid and the extent of adsorption arrived at adsorption equilibrium with 73% adsorption efficiency in an hour. 2. The sorption isotherm experiment was made with different initial lead(II) concentration. A linearized Freundlich equation was used to fit the acquired experimental data. As a result, Freundlich constants, the sorption intensity (1/n) was 0.47 and the measure of sorption (k) was 2.44. So, it was concluded that sorption of lead(II) by kaolinite is effective. 3. The effect of pH on lead(II) sorption by kaolinite shows that at a pH of 3, only 6% of the total lead(II) was adsorbed and at a pH 9, 97% of the lead(II) was removed. And the effect of temperature on lead(II) sorption by kaolinite shows that as the temperature increased, the amount of lead(II) sorption per unit weight of kaolinite increased. But the effect was minor (p<0.05). 4. Sorption isotherm of lead coexisting cadmium (II) or zinc (II) was lower than that of lead itself. It was caused by the result of competitive sorption to adsorption site. And there was no difference between the sorption isotherm of cadmium and zinc. 5. In desorption studies, only 5.12% desorption took place in distilled water, while 52.08% in 0.1 N hydrochloric acid. Consequently used kaolinite could be regenerated by hydrochoric acid.

• 한국방사성폐기물학회:학술대회논문집
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• 한국방사성폐기물학회 2018년도 추계학술논문요약집
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• pp.253-254
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• 2018

• 농업과학연구
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• 제23권2호
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• pp.250-260
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• 1996

Observed results of the adsorption between two competing anions for the shared sorption sites represent that the adsorption phenomena may depends on the characteristics of anion and available sorption sites in a given conditions. In binary systems, adsorption of one species can significantly influence the fate of the other anion, resulting in control of the extent of solute-adsorbate distributions throughout soil profile. And the proton-donation mechanisms by organic anions having a carboxyl as a functional group can also influence the adsorption of inorganic anions onto the hydroxylated sites of Fe and Al oxides. However, study of competitive adsorption of specifically adsorbed anions illustrates some of difficulties which arise in interpretation of reactions at oxide/aqueous solution interfaces. At least two factors prevented a simple analysis of reactions. First, at any pH value the maximum amount of adsorbate taken up at the surface depends on the identity of the anion. Second, it was necessary to postulate the sorption sites where the anion can be adsorbed. Hence, anions having non-specific adsorption characteristics are less capable for sorption sites, compared to those of specific adsorption characteristics, even though competition complies both ordinary and electrostatic interactions for sorption sites. Therefore, competition among chemical species in soil matrix can be of major significance in determining the effective mobility of any reactive anions with sorption sites.

• 한국토양비료학회지
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• 제38권5호
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• pp.238-246
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• 2005

두 가지 이상의 중금속이온이 토양에 존재할 때 토양입자표면에 흡착되는 중금속 이온은 복합적인 경쟁이온치환과 특정결합기작에 따라 흡착량이 결정된다. 본 연구는 충남 논산과 대전시 유성에 소재하는 밭토양에서 채취한 사질식양토와 식토를 공시토양으로 하여 중금속의 다중경쟁흡착특성을 조사하였다. 경쟁흡착은 조사 대상 중금속인 Cr, Cd, 및 Pb를 토양용액에 처리 농도를 달리하여 단일, 이중, 삼중체계로 처리하였다. 등온흡착은 평형농도가 증가함에 따라 흡착이 증가하는 경향을 보여주었으며 이중과 삼중체계에서는 동일 평형농도에서 흡착량은 각각의 중금속이온의 농도와 중금속 전하에 의해 영향을 받는 것으로 조사되었다. 3가지 중금속이온의 이중경쟁 흡착특성은 전기음성도는 낮으나 이온포텐셜이 높은 Cr 이온이 경쟁이온 보다 선택적 흡착특성을 보여주고 있으며 Cd와 Pb가 Cr 흡착에 미치는 영향은 유사한 것으로 조사되었다. 따라서 본 연구 결과 3중 경쟁 흡착 시 중금속 이온의 흡착량이 단일과 이중 경쟁흡착보다 증가하는 특성을 구명하기 위해서는 다중 형태로 존재하는 중금속이온의 흡착기작과 다중 형태상의 중금속이온의 반응식, 그리고 반응식에 따른 가수분해상수를 구하여 흡착정도와 경쟁 상태에 대한 추가 연구가 필요하다. 결론적으로 다중 중금속이온이 존재하는 상태 하에서 흡착친화도는 토양 내 중금속이온의 이동성과 불용화 및 가용화 사이의 분배특성에 영향을 주는 것으로 판단되었다.

• Membrane and Water Treatment
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• 제15권2호
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• pp.67-78
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• 2024

In this study, a nickel hexacyanoferrate and manganese dioxide-polyacrylonitrile (NM-PAN) composite was synthesized and used for the sorptive removal of Co²⁺, Sr²⁺, and Cs⁺ Cs⁺ in radioactive laundry wastewater. Single- and multi-solute competitive sorptions onto NM-PAN were investigated. The Freundlich (Fr), Langmuir (Lang), Kargi-Ozmıhci (K-O), Koble-Corrigan (K-C), and Langmuir-Freundlich (Lang-Fr) models satisfactorily predicted all the single sorption data. The sorption isotherms were nonlinearly favorable (Freundlich coefficient, N_F = 0.385-0.426). Cs⁺ has the highest maximum sorption capacity (q_mL = 0.855 mmol g^-1) for NM-PAN compared to Co²⁺ and Sr²⁺, wherein the primary mechanism was the physical process (mainly ion-exchange). The competition between the metal ions in the binary and ternary systems reduced the respective sorption capacities. Binary and ternary sorption models, such as the ideal adsorbed solution theory (IAST) model coupled with single sorption models of IAST-Fr, IAST-K-O, IAST-K-C and IAST-Lang-Fr, were fitted to the experimental data; among these, the IAST-Freundlich model showed the most satisfactory prediction for the binary and ternary systems. The presence of cationic surfactants highly affected the sorption on NM-PAN due to the increase in distribution coefficients (K_d) of Co²⁺ and Cs⁺.