• 한국환경과학회지
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• 제24권5호
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• pp.671-678
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• 2015

The adsorption characteristics of Sr and Cs ions were investigated by using PS-zeolite beads prepared by immobilizing zeolite with polysulfone (PS). The adsorption kinetics of Sr and Cs ions by PS-zeolite beads was described well by the pseudo-second-order model. The maximum adsorption capacities of Sr and Cs ions calculated from Langmuir isotherm model were 65.0 mg/g and 76.4 mg/g, respectively. In the binary system of Sr ion and Cs ion, the adsorption capacities of each ion decreased with increasing mole ratio of mixed counterpart ion, and Cs ion showed the higher hinderance than Sr ion. We found that thermodynamic properties of Sr and Cs ions on absorption reaction were spontaneous and endothermic at 293 to 323 K.

• 한국환경과학회지
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• 제32권5호
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• pp.343-353
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• 2023

A zeolite material (ZCH) was synthesized from coal fly ash in an HD thermal power plant using a fusion/hydrothermal method. ZCH with high crystallinity could be synthesized at the NaOH/CFA ratio of 0.9. Ion-exchanged ZCH adsorbents for ammonia removal were prepared by ion-exchanging various cation (Cu²⁺, Co²⁺, Fe³⁺, and Mn²⁺) on the ZCH. They were used to evaluate the ammonia adsorption breakthrough curves and adsorption capacities. The ammonia adsorption capacities of the ZCH and ion-exchanged ZCHs were high in the order of Mn-ZCH > Cu-ZCH ≅ Co-ZCH > Fe-ZCH > ZCH according to NH₃-TPD measurements. Mn-ZCH ion-exchanged with Mn has more Brønsted acid sites than other adsorbents. The ion-exchanged Cu²⁺, Co²⁺, Fe³⁺, or Mn²⁺ ions uniformly distributed on the surface or in the pores of the ZCH, and the number of acidic sites increased on the alumina sites to form the crystal structure of zeolite material. Therefore, when the ion-exchanged ZCH was used, the adsorption capacity for ammonia gas increased.

• Bulletin of the Korean Chemical Society
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• 제35권4호
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• pp.1139-1143
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• 2014

The adsorption behavior of the sulphate ($SO{_4}^{2-}$) on the external surface of (5,0), (8,0), and (10,0) zigzag AlNNTs was studied by using density functional calculations. Adsorption energies in the nanotubes are about -8.59, -8.04, -8.60 eV with a charge transfer of 0.59, 0.48, 0.56|e| from the sulphate ion to the nanotubes, respectively. The adsorption energies indicated that sulphate ion can be absorbed strongly on the nanotubes. Therefore, these nanotubes can be used for adsorption of sulphate ion from the environmental systems. It was found that diameter of the AlNNTs has slight role in the adsorption of sulphate ion. The electronic properties of the nanotubes showed notable changes upon the adsorption process.

• Journal of Industrial and Engineering Chemistry
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• 제67권
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• pp.312-315
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• 2018

Although the reversibility of 10,12-pentacosadiynoic amino meta-acid(PCDA-mBzA) against temperature and pH was reported, the modulation of reversibility by ion adsorption at terminal functional group has not been investigated. In this work, we developed a simple method for modulating the reversibility of PCDA-mBzA films upon a thermal stimulus by cadmium ion adsorption inducing the breakage of the outer hydrogen bonding of two hydrogen bonds, which are responsible for the reversible properties of PCDA-mBzA. External reflection-Fourier transform infrared (ER-FTIR) analyses revealed that the hydrogen bonding between the carboxylic acid groups was broken through ion adsorption and only a single hydrogen bond between the amide groups remained in the PCDA-mBzA polymer. In addition, PCDA-mBzA films could recover their original property through cadmium ion desorption. These results present that the transition between reversibility and irreversibility can be modulated artificially simply through the adsorption and desorption of metal ions.

• 폴리머
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• 제26권1호
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• pp.121-127
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• 2002

Acrylonitrile을 그라프트시킨 아미드옥심화 polypropylene 섬유이온교환체(AOPP-g-AN)의 충전 bed 높이를 변화시켜 간수 중 우라늄 이온 흡착 특성 및 흡착 공정 특성을 관찰하였다. 아미드옥심형 섬유이온교환체의 팽윤율은 그라프트율 100%, 물과 과산화수소 용매에 대하여 각각 8.54, 8.87 g/g을 나타내었다. 이온교환용량은 그라프트율이 증가함에 따라 증가하였으며, 그라프트율 100%에서 3.99 meq/g으로 최대를 나타내었다. 회분식 흡착에서 우라늄 흡착은 10분 이내에 초기 흡착 평형에 도달하며, 흡착 속도는 9.50 mg/min으로 나타났다. 최종 흡착 용량은 3.95 meq/g이었으며, pH에 따른 흡착 특성 변화는 관찰되지 않았다. 충전비에 따른 연속식 흡착시 흡착 용량은 L/D=1에서 3.92 meq/g으로 최대를 나타내었으며, L/D<2에서 편류 및 불균일 흡착에 의한 2단계 과정으로 파과가 나타남을 확인하였다. 실제 간수에 대한 우라늄 흡착 실험 결과, 흡착 용량 및 파과시간은 각각 3.63 meq/g, 26 min으로 모의용액과 비교 시 주목할만한 흡착능 저하는 관찰되지 않았다.

• 한국환경과학회지
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• 제26권3호
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• pp.363-371
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• 2017

This study evaluates the adsorption properties of Sr ions in an aqueous solution of the synthetic zeolite (Z-Y1) prepared using coal fly ash generated from a thermal power plant. In order to investigate the adsorption characteristics, the effects of various parameters such as the initial concentrations of Sr ion, contact time, and solution pH were investigated in a batch mode. The Langmuir and Redlich-Peterson model fitted the adsorption isotherm data better than the Freundlich model. The maximum adsorption capacity of Sr ions, as determined the Langmuir model, was 181.68 mg/g. It was found that by varying the Sr ion concentration, pH, and temperature, the pseudo-second-order kinetic model describes the adsorption kinetics of the Sr ion better than the pseudo-first-order kinetic model. The calculated thermodynamic parameters of ${\Delta}H^0$ and ${\Delta}G^0$ showed that the adsorption of Sr ions on Z-Y1 was occurred through a spontaneous and an endothermic reaction. We found that the adsorption of Sr ions by Z-Y1 was more affected by pH than by temperature and Sr ion concentration.

• 대한환경공학회지
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• 제37권8호
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• pp.450-457
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• 2015

본 연구에서는 제올라이트를 PVA에 고정화시켜 새로운 흡착제인 PVA-Zeolite 비드를 제조하고, XRD 및 SEM 분석을 통해 제조한 PVA-Zeolite 비드는 내부에 제올라이트가 잘 고정화된 다공성 구조를 가지고 있는 것을 확인할 수 있었다. 제조한 흡착제에 의한 Cs 이온과 Sr 이온에 대한 흡착특성을 살펴보기 위하여 pH의 영향, 흡착속도, 흡착등온을 검토하였다. Sr 및 Cs 이온에 대한 평형흡착시간은 약 540 min으로 나타났으며, 흡착속도는 유사 1차 속도식 보다는 유사 2차 속도식에 더 잘 부합하였다. 흡착평형 실험결과는 Langmuir 등온식에 잘 적용되었으며, Langmuir 등온식으로부터 구한 Sr 이온과 Cs 이온의 최대 흡착량은 각각 52.08 mg/g와 58.14 mg/g이었다. PVA-Zeolite 비드에 의한 Sr 이온과 Cs 이온의 흡착공정은 외부물질전달단계는 매우 빠르게 이루어지며, 내부입자확산에 의한 흡착반응은 느리게 진행되어 내부입자확산 단계가 흡착속도 결정단계인 것으로 판단된다.

• 통합자연과학논문집
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• 제10권4호
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• pp.225-231
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• 2017

Cryptand resins were synthesized by mixing 1-aza-18-crown-6 macrocyclic ligand with styrene divinylbenzene copolymer having 1%, 2%, 5%, and 10% crosslink by a substitution reaction. These synthetic resins were confirmed by chlorine content, elementary analysis, SEM, surface area, and IR-spectrum. As the results of the effects of pH, crosslink of synthetic resin, and dielectric constant of a solvent on uranium ion adsorption for resin adsorbent, the uranium ion showed high adsorption at pH 3 or over. Adsorption selectivity for the resin in methanol solvent was the order of uranium ($UO_2{^{2+}}$) > calcium ($Ca^{2+}$) > neodymium ($Nd^{3+}$) ion, adsorbability of the uranium ion was the crosslink in order of 1%, 2%, 5%, and 10% and it was increased with the lower dielectric constant.

• 통합자연과학논문집
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• 제6권2호
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• pp.104-110
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• 2013

1-Aza-12-crown-4 macrocyclic ligand was combined with styrene (2th petroleum in 4th class hazardous materials) divinylbenzene copolymer having 1%, 2%, 3%, and 6% crosslinks by a substitution reaction, in order to synthesize resin. These synthetic resins were confirmed by chlorine content, elementary analysis and IR-spectrum. As the results of the effects of pH, equilibrium arrival time, crosslink of synthetic resin, and dielectric constant of a solvent on uranium ion adsorption for resin adsorbent, the uranium ion showed high adsorption at pH 3 or over and adsorption equilibrium of uranium ion was about 2 hours. In addition, adsorption selectivity for the resin in methanol solvent was the order of uranium ($UO_2{^{2+}}$) > iron ($Fe^{3+}$) > lutetium ($Lu^{3+}$) ions, adsorbability of the uranium ion was in the crosslinks order of 1%, 2%, 3%, and 6% was increased with the lower dielectric constant.

• 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.