• Journal of the Korean Geosynthetics Society
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• v.10 no.1
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• pp.53-61
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• 2011

This study was conducted to confirm the adsorption capacity of CFW(Carbonized Foods Waste), which is produced by the process of recycling waste, in PRB method that Electrokinetic(E/K) method was applied. The batch test was carried out to analyze the adsorption characteristics of CFW for adsorbing the organic compounds. The organic compounds used in the batch test were Phenanthrene and Trichloroethylene(TCE), and the anionic surfactant(SDS) and the nonionic surfactant(Brij$^{(R)}$30) were used for the surfactants. The results of the batch test confirmed that the adsorption efficiency of Phenanthrene was 99% and TCE was 26%. The each compounds compared with the adsorption isotherms, which is calculated by the Langmuir and Freundlich models. The results indicated that Phenanthrene is fitted to the linear Langmuir model, whereas the distribution of TCE is unclear. The results of the batch test used in surfactants confirmed that the adsorption efficiency of CFW using Phenanthrene was reduced to 6~8%. However, the adsorption efficiency of CFW in TCE was increased up to 81% by surfactants. Especially, the nonionic surfactant was excellent in the adsorption of CFW using TCE. Nevertheless, the adsorption efficiency of CFW in Phenanthrene was still higher than TCE. Therefore, the adsorption efficiency of CFW in Phenanthrene was better than in TCE. In PRB method using E/K method, the adsorption of CFW used nonionic surfactant is better to use than the anion surfactants on the organic compounds.

• Journal of the Korean Geosynthetics Society
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• v.13 no.2
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• pp.59-67
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• 2014

The amount of the contaminants that can be adsorbed on the drain was evaluated for the effective remediation of the contaminated soil, and the contaminants adsorptivity of the drain was evaluated by comparing the isothermal adsorption model after carrying out the contaminants adsorption test of the reactants coated on the surface of the drain. The reactant used in the experiment is a natural zeolite, and the contaminants are copper, lead and cadmium. The results that Freundlich and Langmuir adsorption isotherm model are compared to the adsorption amount according to the change of the initial concentration by the contaminants. As a result of the component analysis, because Si, Al and O are contained approximately 28%, 11% and 48%, respectively, it is identified that the material coated on the surface of the drain is the component of the zeolite which is the reactant for the adsorption of the heavy-metal (Cu, Pb, Cd) contaminants. The heavy-metal adsorption kinetic of the zeolite which is the reactant was decreased in order of lead, copper and cadmium. The important factor of the performance evaluation of the adsorbent is the reaction rate, and if zeolite is used as the reactant in the relationship between the maximum amount of adsorption and reaction rate, it can be utilized as the design factor that determine the removal order of the complex heavy-metal. In other words, because the maximum adsorption quantity of lead is smaller compared to copper but the reaction rate is relatively fast, it can be primarily removed, and copper can be removed after removing the lead. It was analyzed that Cadmium can be finally removed after that other heavy-metal is removed.

• Journal of the Korean Chemical Society
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• v.55 no.2
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• pp.208-217
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• 2011

The effects of pH and temperature on the removal of two dyes (neutral red; NR and malachite green oxalates; MG) from aqueous effluents using Maghnia montmorillonite clay in a batch adsorption process were investigated. The results showed the stability of the optical properties of MG in aqueous solution and adsorbed onto clay under wide range of pH 3-9. However, the interaction of NR dye with clay is accompanied by a red shift of the main absorption bands of monomer cations under pH range of 3-5, whereas, those of neutral form remains nearly constant over the pH range of 8-12. The optimal pH for favorable adsorption of the dyes, i.e. ${\geq}$90% has been achieved in aqueous solutions at 6 and 7 for NR and VM respectively. The most suitable adsorption temperatures were 298 and 318 K with maximum adsorption capacities of 465.13mg/g for NR and 459.89 mg/g for MG. The adsorption equilibrium results for both dyes follow Langmuir, Freundlich isotherms. The numerical values of the mean free energy $E_a$ of 4.472-5.559 kj/mol and 2.000-2.886 kj/mol for NR and MG respectively indicated physical adsorption. Various thermodynamic parameters, such as ${\Delta}H^{\circ}$, ${\Delta}S^{\circ}$, ${\Delta}G^{\circ}$ and Ea have been calculated. The data showed that the adsorption process is spontaneous and endothermic. The sticking probability model was further used to assess the potential feasibility of the clay mineral as an alternative adsorbent for organic ion pollutants in aqueous solution.

• Clean Technology
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• v.21 no.1
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• pp.22-32
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• 2015

In this study, we studied the characteristics of ion exchange for treatment of HSS (heat stable salts) which cause performance reduction in CO₂ gas capture amine solution using anion exchange resins. The optimum HSS removal efficiency, 96.1% was obtained when using strong base anion exchange resin SAR10 at dosage 0.05 g/mL, 316 K, pH 12 and the best resin regeneration efficiency, 78.8% was obtained using NaOH solution of 3 M at 316 K. The adsorption data were described well by the Freundlich model and the sorption intensity(n) was 2.0951 lying within the range of favorable adsorption. The adsorption selectivity coefficients were increased by increasing valences and size of ion and desorption selectivity coefficients showed a contradictory tendency to adsorption selectivity coefficients. By continuous HSS removal experiments, 13.3 BV of HSS contaminated solution was effectively treated and the optimum NaOH solution consumption was 5.2 BV to regenerate resins.

• Journal of the Korean Chemical Society
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• v.64 no.5
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• pp.249-258
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• 2020

The potential use of egg shell and calcined egg shell as adsorbent was evaluated and compared to remove Cd²⁺ from aqueous solution. The samples were characterized using Thermogravimetry and Differential Thermal Analysis (TG/DTA), Scanning Electron Microscope (SEM), X-ray Diffractometer (XRD), Energy Dispersive X-ray Spectrometer (EDX) and BET Surface Analyzer. The batch-type adsorption experiment was conducted by varying diverse variables such as contact time, pH, initial Cd²⁺ concentrations and adsorbent dosage. The results showed that, under the initial Cd²⁺ concentrations ranged from 25 to 200 mg g^-1, the removal efficiencies of Cd²⁺ by egg shell powder (ESP) were decreased steadily from 96.72% to 22.89% with increase in the initial Cd²⁺ concentration at 2.5 g of dosage and 8 h of contact time. However, on the contrary to this, calcined egg shell powder (CESP) showed removal efficiencies above 99% regardless of initial Cd²⁺ concentration. The difference in the adsorption behavior of Cd²⁺ may be explained due to the different pH values of ESP and CESP in solution. Cd²⁺ seems to be efficiently removed from aqueous solution by using the CESP with a basicity nature of around pH 12. It was also observed that an optimum dosage of ESP and CESP for nearly complete removal of Cd²⁺ from aqueous solution is approximately 5.0 g and 1.0 g, respectively. Consequently, Cd²⁺ is more favorably adsorbed on CESP than ESP in the studied conditions. Adsorption data were applied by the pseudo-first-order and pseudo-second-order kinetics models and Freundlich and Langmuir isotherm models, respectively. With regard to adsorption kinetics tests, the pseudo-second-order kinetics was more suitable for ESP and CESP. The adsorption pattern of Cd²⁺ by ESP was better fitted to Langmuir isotherm model. However, by contrast with ESP, CESP was described by Freundlich isotherm model well.

• Journal of Life Science
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• v.23 no.12
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• pp.1471-1476
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• 2013

The present study deals with the immobilization of Kluyveromyces lactis ${\beta}$-galactosidase on a weak ionic exchange resin (Duolite A568) as polymer support. ${\beta}$-Galactosidase was immobilized using the adsorption method. A kinetic study of the immobilized enzyme was performed in a packed-bed reactor. The adsorption of the enzyme followed a typical Freundlich adsorption isotherm. The adsorption parameters of k and n were 14.6 and 1.74, respectively. The initial rates method was used to characterize the kinetic parameters of the free and immobilized enzymes. The Michaelis-Menten constant ($K_m$) for the immobilized enzyme (120 mM) was higher than it was for the free enzyme (79 mM). The effect of competitive inhibition kinetics was studied by changing the concentration of galactose in a recycling packed-bed reactor. The kinetic model with competitive inhibition by galactose was best fitted to the experimental results with $V_m$, $K_m$, and $K_I$ values of 46.3 $mmolmin^{-1}mg^{-1}$, 120 mM, and 24.4 mM, respectively. In a continuous packed-bed reactor, increasing the flow rate of the lactose solution decreased the conversion efficiency of lactose at different input lactose concentrations. Continuous operation of 11 days was conducted to investigate the stability of a long-term operation. The retained activity of the immobilized enzymes was 63% and the half-life of the immobilized enzyme was found to be 15 days.

• Korean Journal of Environmental Agriculture
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• v.6 no.2
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• pp.46-52
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• 1987

This study of adsorption and column percolation was conducted to examine the utilization of natural zeolite for the removal of heavy metals from waste water to compare with that of absorption activated carbon. The adsorption of heavy metals by natural zeolite was conformed to the Freundlich isotherm (1/n values: $0.12{\sim}0.45$, K values: $18.77{\sim}59.48$) and natural zeolite was turned out to be an effective adsorbent of heavy metals. At the same particle size and percolation velocity, zeolite adsorbed a greater amount of heavy metals was adsorbed on natural zeolite than activated carbon. The smaller the particle size, the more heavy metals that were adsorbed. It was postulated that the most effective size as an adsorbent of heavy metals from waste water ranged from 0.5 to 2.0mm. The slower the percolation velocity that of the heavy metal solution in column, the more heavy metals were adsorbed. Natural zeolite in a single solution adsorbed more heavy metals than that in mixed solution, and the order of the adsorption amount on natural zeolite was Cu>Zn>Cd.

• Journal of Korean Society of Environmental Engineers
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• v.22 no.6
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• pp.1045-1053
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• 2000

The adsorption and desorption of herbicides such as napropamide and pendimethalin was studied in three kinds of soil. sandy loam. silty clay and loam. The results of batch tests performed with various shaking time, pH, organic matter content and temperature in soil were summarized as follows. The shaking times reached to the equilibrium of the adsorption and desorption for napropamide and pendimethalin in soil were 12 and 6 hours. respectively. For each soil. the adsorption rates of napropamide were 23.35%. 31.57% and 25.95%, the desorption rates of them were 18.42%, 13.42% and 15.89%, respectively. And the adsorption rates of pendimethalin were 59.61%, 77.26% and 64.02%, and the desorption rates of them were 3.23%, 2.93% and 3.07%, respectively. The adsorption isotherms with the Freundlich equation showed better consistency than those with the Langmuir one. The adsorption was affected by the organic matter content when it exceed 2.0%. But if the organic matter content is below 2.0%, it was affected by the clay content. When the organic matter content is 0.95~7.45%, the adsorption coefficients ($K_{fa}$) of napropamide and pendimethalin were 1.17~2.50 and 4.74~16.08 and the desorption coefficients($K_{fd}$) of them were 5.33~34.06 and 24.25~134.00, respectively. Because of the physical adsorption between herbicide molecules and soil surface, little effect of pH variation of soils was appeared for the adsorption and desorption. Because of the solubility of herbicide is related to the temperature, the adsorption rate was decreased and the desorption rate was increased with the temperature increase, respectively.

• Journal of Korean Society of Environmental Engineers
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• v.32 no.10
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• pp.936-941
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• 2010

This study was conducted to investigate formaldehyde removals by silver nano-particles attached on the surface of granular activated carbon (Ag-AC) and to compare the results to those obtained with ordinary activated carbon (AC). The BET analysis showed that the overall surface area and the fraction of micropores (less than $20{\AA}$ diameter) of the Ag-AC were significantly decreased because the silver particles blocked the small pores on the surface of the Ag-AC. The formaldehyde removal capacity of the Ag-AC determined using the Freundlich isotherm was higher than that of AC. Despite the decreased BET surface area and micropore volume, the Ag-AC had the increased removal capacity for formaldehyde, presumably due to catalytic oxidation by silver nano-particles. In contrast, the adsorption intensity of the Ag-AC, estimated by 1/n in the Freundlich isotherm equation, was similar to that of the ordinary AC, indicating that the surface modification using silver nano-particles did not affect the adsorption characteristics of AC. In a column experiment, the Ag-AC also showed a longer breakthrough time than that of the AC. Simulation results using the homogeneous surface diffusion model (HSDM) were well fitted to the breakthrough curve of formaldehyde for the ordinary AC, but the predictions showed substantial deviations from the experimental data for the Ag-AC. The discrepancy was due to the catalytic oxidation of silver nano-particles that was not incorporated in the HSDM. Consequently, a new numerical model that takes the catalytic oxidation into accounts needs to be developed to predict the combined oxidation and adsorption process more accurately.

• Korean Journal of Environmental Agriculture
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• v.7 no.2
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• pp.96-101
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• 1988

It is important to assess the effects of ionic strength and type of anions when studying the adsorption of heavy metals on zeolite because the background salt may complex with heavy metals and compete for adsorption sites. This experiment was carried out to determine the effect of ionic strength and anion species($Cl^-$, $SO^{2-}\;_4$, and $ClO^-\;_4$) on heavy metal adsorption. Heavy metal adsorption by zeolite from solutions in the range of 10 to 50ppm was studied in the presence of NaCl, $Na_2SO_4$ and $NaClO_4$, with different concentrations. The ionic strength ranged from 0.01 to 1.00. Adsorption of heavy metal cations could be described by the Freundlich isotherm equation. Increasing the ionic strength of equilibrium solutions, the amounts of heavy metal adsorbed on the zeolite surfaces decreased in all three of the anion systems. This fact could be attributed to the competition of background salt cation and the decrease in initial activity of heavy metal cations. In the presence of Cl anion, less adsorption resulted than in the presence of $SO_4$ or $ClO_4$ anions of the same ionic strength, indicating the presence of uncharged and negatively charged complexes of heavy metal with Cl ligands.