• KSCE Journal of Civil and Environmental Engineering Research
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• v.2 no.1
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• pp.63-68
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• 1982

This study was aimed ultimately to develop an adsorption process treating heavy metal industrial wastewater by utilizing domestically abundant natural zeolite and the study was conducted in a series of investigations. Presented if1 this paper are the results of the preliminary batch mode test. Factors affecting an adsorption process of heavy metals of aqueous waste stream by zeolite are numerous. Factors such as hydrogen ion concentration and temperature are taken into consideration in the investigation to evaluate adsorptive capacity. The mechanisms of adsorption may better be described by an evaluation of adsorption isotherm andi of adsorption kinetics. It is observed from the preliminary investigation that an optimum adsorption occurs at higher pH's than 4. It is further demonstrated that $Cd^{+2}$ adsorption by zeolite follows the BET model better than the Freundlich and the Langmuir model and that the reaction time of at least 10 minutes is required. It is interesting to note that higher adsorptive capacity was found at higher temperature, suggesting that the adsorption is not only due to simple physisorption but also due to chemisorption.

• Journal of Environmental Science International
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• v.28 no.6
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• pp.561-570
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• 2019

A zeolitic material (Z-Y2) was synthesized from Coal Fly Ash (CFA) using a fusion/hydrothermal method under low-alkali condition (NaOH/CFA = 0.6). The adsorption performance of the prepared zeolite was evaluated by monitoring its removal efficiencies for Sr and Cs ions, which are well-known as significant radionuclides in liquid radioactive waste. The XRD (X-ray diffraction) patterns of the synthesized Z-Y2 indicated that a Na-A type zeolite was formed from raw coal fly ash. The SEM (scanning electron microscope) images also showed that a cubic crystal structure of size $1{\sim}3{\mu}m$ was formed on its surface. In the adsorption kinetic analysis, the adsorption of Sr and Cs ions on Z-Y2 fitted the pseudo-second-order kinetic model well, instead of the pseudo-first-order kinetic model. The second-order kinetic rate constant ($k_2$) was determined to be $0.0614g/mmol{\cdot}min$ for Sr and $1.8172g/mmol{\cdot}min$ for Cs. The adsorption equilibria of Sr and Cs ions on Z-Y2 were fitted successfully by Langmuir model. The maximum adsorption capacity ($q_m$) of Sr and Cs was calculated as 1.6846 mmol/g and 1.2055 mmol/g, respectively. The maximum desorption capacity ($q_{dm}$) of the Na ions estimated via the Langmuir desorption model was 2.4196 mmol/g for Sr and 2.1870 mmol/g for Cs. The molar ratio of the desorption/adsorption capacity ($q_{dm}/q_m$) was determined to be 1.44 for Na/Sr and 1.81 for Na/Cs, indicating that the amounts of desorbed Na ions and adsorbed Sr and Cs ions did not yield an equimolar ratio when using Z-Y2.

• Journal of Korean Society on Water Environment
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• v.37 no.6
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• pp.483-492
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• 2021

This study evaluated the removal efficiencies of methylene blue (MB) and humic acids (HA) using a rice husk (RH) biochar and powdered activated carbon (PAC). The pseudo-second-order model better presented the adsorption of MB and HA onto a RH biochar than the pseudo-first-order model. Furthermore, better description of the adsorption behavior of MB and HA by the Langmuir isotherm model (R² of the RH biochar: MB = 0.986 and HA = 0.984; R² of PAC: MB = 0.997 and HA = 0.989) than the Freundlich isotherm model (R² of the RH biochar: MB = 0.955 and HA = 0.965; R² of PAC: MB = 0.982 and HA = 0.973) supports the assumption that monolayer adsorption played key roles in the removal of MB and HA using the RH biochar and PAC. Batch experiments were performed on the effects of dosage, temperature, and pH. For all experiments, PAC showed higher efficiencies than RH biochar and MB adsorption efficiencies were higher than those of HA. Adsorption efficiencies increased with increasing amounts of adsorbents and temperature. As the pH increased, adsorption efficiencies of MB were increased while adsorption efficiencies of HA were decreased.

• Membrane and Water Treatment
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• v.15 no.3
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• pp.107-115
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• 2024

This study proposes the recycling of MVS as a value-added product for the removal of phosphate from aqueous solutions. By comparing the phosphate adsorption capacity of each calcined adsorbent at each temperature of MVS, it was determined that the optimal heat treatment temperature of MVS to improve the phosphate adsorption capacity was 800 ℃. MVS-800 suggests an adsorption mechanism through calcium phosphate precipitation. Subsequent kinetic studies with MVS-800 showed that the PFO model was more appropriate than the PSO model. In the equilibrium adsorption experiment, through the analysis of Langmuir and Freundlich models, Langmuir can provide a more appropriate explanation for the phosphate adsorption of MVS-800. This means that the adsorption of phosphate by MVS-800 is uniform over all surfaces and the adsorption consists of a single layer. Thermodynamic analysis of thermally activated MVS-800 shows that phosphate adsorption is an endothermic and involuntary reaction. MVS-800 has the highest phosphate adsorption capacity under low pH conditions. The presence of anions in phosphate adsorption reduces the phosphate adsorption capacity of MVS-800 in the order of CO 3 2-, SO 4 2-, NO 3- and Cl-. Based on experimental data to date, MVS-800 is an environmentally friendly adsorbent for recycling waste resources and is considered to be an adsorbent with high adsorption capacity for removing phosphates from aqueous solutions. This paper combines the advantages of gray predictor and AI fuzzy. The gray predictor can be used to predict whether the bear point exceeds the allowable deviation range, and then perform appropriate control corrections to accelerate the bear point to return to the boundary layer and achieve.

• Journal of Environmental Science International
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• v.7 no.6
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• pp.773-782
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• 1998

The adsorption experiment of phenol(Ph) from aqueous solution on granular activated carbon was studied in order to design the fixed-bed adsorption column. The experimental data were analyzed by unsteady-state, one-dimensional heterogeneous model. Finite element method(FEM) was applied to analyze the sensitivity of parameter and to predict the fixed-bed adsorption column performance on operation variable changes. The prediction model showed similar effect to mass transfer and intraparticle diffusion coefficient changes suggesting that both parameter present mass transfer rate limits for GAC-phenol system. The Freundlich constants had a greater effect than kinetic parameters for the performance of fixed-bed adsorption column. FEM solution facilitated prediction of concentration history in solution and within adsorbent particle.

• Journal of Environmental Science International
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• v.24 no.11
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• pp.1331-1341
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• 2015

The removal of Sr ion and Cs ion was investigated to evaluate adsorption properties by using SAN-Zeolite beads immobilized with styrene acrylonitrile (SAN). The adsorption capacities increased with the decrease of SAN/zeolite ratio (SAR) from 2.5 to 0.83. The relationship of adsorption capacity ($q_e$) and SAR was described by experimental equation such as $q_e=20.88+137.81e^{-1.96SAR}$ ($r^2=0.9980$). The adsorption kinetics of Sr ion and Cs ion with SAN-Zeolite beads were fitted well by the pseudo-second-order model. The maximum adsorption capacities of Sr ion and Cs ion calculated from Langmuir isotherm model were 66.97 mg/g and 81.97 mg/g, respectively.

• Journal of Environmental Science International
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• v.20 no.11
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• pp.1437-1445
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• 2011

The adsorption performance of lead ion was studied using five zeolites (Na-P1, sodalite (SOD), analcime (ANA), nepheline hydrate (JBW), cancrinite (CAN)) synthesized from Jeju scoria. The adsorption performances of lead ion decreased in the order of Na-P1 > SOD > ANA > JBW > CAN. These results showed that the synthetic zeolite with a higher cationic exchange capacity showed a higher adsorption performance. The uptake of lead ion by synthetic zeolites were described by Freundlich model better than Langmuir model. The adsorption kinetics of lead ion by synthetic zeolites fitted the pseudo 2nd order kinetics better than pseudo 1st order kinetics. The effective diffusion coefficients of lead ion by synthetic zeolites were ten times higher than the zeolite A synthesized from coal fly ash.

• Korean Journal of Soil Science and Fertilizer
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• v.49 no.5
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• pp.489-494
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• 2016

Carbon-based sorbents such as biochar and activated carbon have been proven to be cost-effective in removing pollutants containing heavy metals from wastewater. The aim of this study was using batch experiment to evaluate the adsorption characteristics of heavy metals in single-metal conditions onto reed biochar for treating wastewater containing heavy metals. The removal rates of heavy metals were in the order of Pb > $Cu{\fallingdotseq}Cd{\fallingdotseq}Zn$, showing the adsorption efficiency of Pb was higher than the other heavy metals. Freundlich and Langmuir adsorption isotherms were used to model the equilibrium adsorption data obtained from adsorption of Pb on reed biochar. For reed biochar, the Langmuir model provided a slightly better fit than the Freundlich model. Lead was observed on the biochar surface after adsorption by scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDS). The main functional groups of reed biochar were aromatic carbons. Overall, the results suggested that reed biochar could be useful adsorbent for treating wastewater containing Pb.

• Journal of the Korean GEO-environmental Society
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• v.12 no.11
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• pp.31-37
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• 2011

This study investigated on the adsorption and photocatalysis of Reactive Black 5(RB5) by the hydroxyapatite(HAP)/Titanium dioxide($TiO_{2}$) media. The adsorption of RB5 on $TiO_{2}$, HAP and $TiO_{2}$/HAP was investigated during a series of batch adsorption experiments. The amounts adsorbed at equilibrium were measured. Langmuir and Freundlich isotherm models were tested for their applicability. The result of equilibrium studies of $TiO_{2}$, HAP and $TiO_{2}$/HAP adsorbent were found to follow Langmuir isotherm model. The adsorbed amounts(Qmax) were found to be 5.28mg/g on single $TiO_{2}$, 12.45mg/g on single HAP and 9.03mg/g on $TiO_{2}$/HAP, respectively. The experimental data were analysed using the pseudo-first-order adsorption and photocatalysis kinetic models. According to these models, RB5 degradation by $TiO_{2}$/HAP was affected by interaction effect of photocatalysis and adsorption.

• Environmental Engineering Research
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• v.19 no.2
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• pp.157-163
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• 2014

The adsorption of Cr(VI) from aqueous solutions to activated carbon fiber (ACF) was investigated using both batch and flow-through column experiments. The batch experiments (adsorbent dose, 10 g/L; initial Cr(VI) concentration, 5-500 mg/L) showed that the maximum adsorption capacity of Cr(VI) to ACF was determined to 20.54 mg/g. The adsorption of Cr(VI) to ACF was sensitive to solution pH, decreasing from 9.09 to 0.66 mg/g with increasing pH from 2.6 to 9.9; the adsorption capacity was the highest at the highly acidic solution pHs. Kinetic model analysis showed that the Elovich model was the most suitable for describing the kinetic data among three (pseudo-first-order, pseudo-second-order, and Elovich) models. From the nonlinear regression analysis, the Elovich model parameter values were determined to be ${\alpha}$ = 162.65 mg/g/h and ${\beta}$ = 2.10 g/mg. Equilibrium isotherm model analysis demonstrated that among three (Langmuir, Freundlich, Redlich-Peterson) models, both Freundlich and Redlich-Peterson models were suitable for describing the equilibrium data. In the model analysis, the Redlich-Peterson model fit was superimposed on the Freundlich fit. The Freundlich model parameter values were determined to be $K_F$ = 0.52 L/g and 1/n = 0.56. The flow-through column experiments showed that the adsorption capacities of ACF in the given experimental conditions (column length, 10 cm; inner diameter, 1.5 cm; flow rate, 0.5 and 1.0 mL/min; influent Cr(VI) concentration, 10 mg/L) were in the range of 2.35-4.20 mg/g. This study demonstrated that activated carbon fiber was effective for the removal of Cr(VI) from aqueous solutions.