• Journal of the Korean Geotechnical Society
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• v.27 no.4
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• pp.43-50
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• 2011

Steel-making slag was investigated as reactive material for removal of cadmium in coastal area. Batch experiments of the sorption isotherm experiment and kinetic sorption experiment were performed. Result of sorption isotherm was more adequately described by Langmuir model than Freundlich model and theoretical maximum capacity (${\beta}$) of cadmium onto steel-making slag was found. Results of kinetic sorption experiments were evaluated by pseudo second order model to investigate sorption characteristics of cadmium onto steel-making slag. Results showed that the equilibrium sorption amount of cadmium (q$q_e$) increased and the rate constant ($k_2$) and initial sorption rate (h) decreased as the initial cadmium concentration increased. The $q_e$ with simulated sea water was similar to that with deionized water and $k_2$ and h with simulated sea water was lower than those with deionized water. Results of kinetic experiments could be used to predict the result from sorption isotherm, since equilibrium sorption amounts calculated by pseudo second order model generally agreed with those measured from sorption isotherm. The reaction time for the target removal rate could be calculated by the pseudo second order model using kinetic sorption tests results.

• Analytical Science and Technology
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• v.17 no.6
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• pp.454-463
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• 2004

The sorption behavior of some metal ions on XAD-16-CTA chelating resin was investigated by batch method. The sorption of chelating resin was highly selective for Hf(IV), Zr(IV) and Th(IV) at pH 3.0 ~ 6.0 and the maximum sorption capacity of Zr(IV) ion was 0.81 mmol/g. It was successfully applied to the separation of several rare metal ions from mixed metal solutions by using CDTA, EDTA, NTA and $NH_4F$ as masking agent. The elution order of metal ions obtained from breakthrough capacity and the overall capacity at pH 4.0 was Zr(IV)>Th(IV)>Hf(IV)>U(VI)>Cu(II)>In(III)>Pb(II). Desorption characteristics for metal ions was investigated with desorption agents such as HCl, $HNO_3$, $HClO_4$. 2 M HCl showed high desorption efficiency. Th(IV) ion can be successfully separated from mixed metal ions by using XAD-16-CTA cheating resin.

• Korean Journal of Soil Science and Fertilizer
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• v.49 no.6
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• pp.789-794
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• 2016

Continuous excessive application of phosphorus (P) fertilizer and manure in plastic film house soils can lead to an accumulation of P in soils. The understanding of P sorption by soils is important for fertilizer management. In this study, 9 samples were collected for acidic and calcareous soils as non-cultivated soil and plastic film house soils as cultivated soil Phosphorus sorption data of acidic soils fit the Langmuir equations, Freundlich equations in calcareous and plastic film house soils. In calcareous and plastic film house soils, the slope of isotherm adsorption changed abruptly, which could be caused P precipitation with $CaCO_3$. The calculated Langmuir adsorption maximum ($S_{max}$) varied from 217 to 1,250, 139 to 1,429, and $714mg\;kg^{-1}$ for acidic soils, calcareous soils, and plastic film house soils with low available phosphate concentration, respectively. From this result, maximum P adsorption by the Langmuir equation could be regarded as threshold of P concentration to induce the phosphate precipitation in soil. Phosphate-sorption values estimated from one-point isotherm for acidic and calcareous soils as non-cultivated soils were comparable with the $S_{max}$ values calculated from the Langmuir isotherm.

• Journal of the Korean GEO-environmental Society
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• v.15 no.12
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• pp.5-13
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• 2014

In this study, exfoliated vermiculite (EV) coated with glycerol was tested for its abiility to remove phosphorus in aqueous solution. The glycerol modified vermiculite (GS) was prepared with EV/glycerol ratio of 1/4 where glycerol contained 4 mol% $H_2SO_4$ and heated until designated temperature. GS heated at $380^{\circ}C$ showed that the specific surface area was $53.1m^2/g$ and mass loss due to oxidation of carbon was maximum from TGA analysis. Removal of phosphorus using GS heated at $380^{\circ}C$ was well explained by Langmuir isotherm model and maximum sorption capacity of 714.3 mg/kg is comparable or greater than those of other clay orignated sorbents for phosphorus.

• Proceedings of the Korean Society of Soil and Groundwater Environment Conference
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• 2002.09a
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• pp.92-95
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• 2002

Bioavailability study was conducted to elucidate the relationship between sorption/desorption and biodegradation of sorbed phenanthrene in seven different soils. Mineralization kinetics was determined for phenanthrene-sorbed soil slurries inoculated with Pseudomonas putida (ATCC strain 17484). Two biodegradation models were used to fit mineralization kinetics; (i) a first-order degradation model and (ii) a coupled degradation-desorption model. The biodegradation rates were in order of vermicompost >Bion peat > 50% organoclay > Pahokee > blank (no soil, medium only) > montmorillonite > Ohio shale. The mineralization rate constants increased as desorption-resistance of phenanthrene increased. Among the tested sorbents, active biodegradation of phenanthrene was observed in vermicompost and Bion peat. Biodegradation in these two sorbents exhibited little lag time and a high maximum mineralized capacity. The role of sorption/desorption in bioavailability of phenanthrene sorbed in soils was discussed.

• Journal of Korean Society of Environmental Engineers
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• v.30 no.9
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• pp.907-912
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• 2008

In order to reduce the availability of dissolved inorganic phosphorus in surface water, lakes, and estuaries, black shale and zero valent iron can be used as reacitve materials. Sorption of phosphate to sampled sediment, black shale, and zero valent iron was quantitatively evaluated in this research. Effect of coexistence of calcium was also tested, since coexisting ions can enhance the precipitation of phosphate. An empirical kinetic model with fast sorption(k$_t$), slow sorption(k$_s$), and precipitation(k$_p$) was well fitted to experiment data from this research. Langmuir and Freundlich sorption isotherms were also used to evaluated phosphate maximum sorption capacity. Calcium ions at 0, 1 and 5 mM affected the precipitation kinetic coefficient in empirical kinetic model but did not have impact on the maximum sorbed concentration.

• Advances in Traditional Medicine
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• v.7 no.2
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• pp.171-181
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• 2007

Metal binding activity of the pectin samples with different physicochemical properties was studied. It was found that in vitro copper binding capacity of pectins is depending on the following factors: degree of esterification, content of non-methylated anhydrogalacturonic acid, and pH of solution. There was found that the maximum copper uptake capacity increases correspondingly to reduction of the degree of esterification of pectin, rise of the non-methylated anhydrogalacturnic acid content and the solution pH. It is proposed to use for standardization of pectin samples such parameters as the degree of esterification, content of anhydrogalacturonic acid, and intrinsic viscosity.

• Journal of Microbiology and Biotechnology
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• v.8 no.1
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• pp.53-60
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• 1998

This study examines the effect of pH, temperature, metal ion concentration and culture density on metal biosorption by the nuisance cyanobacterium Microcystis aeruginosa. Ni biosorption was higher at pH 9.2 than at neutral and acidic pH. In contrast the biosorption of Cu and Zn was maximum at pH 7.0. However, biosorption of Zn was difficult to measure at pH values 9.2 and 10.5, owing to the formation of insoluble complexes. All the test metals (Cu, Zn, and Ni) showed maximum biosorption rate at low culture densities of 40 mg dry wt $1^{-1}$. The biosorption of Cu, Zn, and Ni was maximum at $40^{\circ}C$. However, no worthwhile difference in Zn and Ni sorption was noticed at 4 and $29^{\circ}C$ as compared to $40^{\circ}C$. Of these three metals used Microcystis showed a greater binding capacity ($K_{f}$ value=0.84, Freundlich adsorbent capacity) and accelerated biosorption rate for Cu under various environmental conditions. Fitness of mathematical models on metal biosorption by Microcystis confirmed that the biological materials behave in the same way as physical materials. These results suggest that before using a biosorbent for metal recovery, the environmental requirements of the biosorbent must be ascertained.

• Journal of Korean Society of Environmental Engineers
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• v.29 no.8
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• pp.930-937
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• 2007

Korean pine(Pinus densiflora) bark was evaluated for its adsorption capacity of Cu(II) ions from aqueous solution by running a series of batch experiments. Prior to the tests, the milled barks were treated with 1 N NaOH or 1 N HCl to examine the effect of surface modification. For comparison, untreated bark was tested under same condition. Within the tested pH range between 3 and 6, NaOH treatment increased Cu(II) adsorption capacity by $139\sim184%$, while HCl treatment decreased it by $37\sim42%$. Maximum copper ion uptake by bark was observed at pH $5\sim6$, but pH of solution was not a potent influence. A pseudo second-order kinetic model fitted well for the sorption of copper ion onto bark. For NaOH-treated bark, the calculated sorption capacity$(q_e)$ increased from 6.58 to 12.77 mg/g, while the equilibrium rate constant$(k_2)$ decreased from 0.284 to 0.014 g/mg/min as initial Cu(II) concentration doubled from 100 mg/L. A batch isotherm test using NaOH-treated bark showed that equilibrium sorption data were represented by both the Langmuir model and the Freundlich model. It was confirmed that carboxylic acid of bark was involved in the Cu(II) adsorption. For NaOH-treated bark, in particular, carboxylate ion produced by hydrolysis or saponification appeared to be a major functional roup responsible for the enhanced Cu(II) sorption.

• Clean Technology
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• v.13 no.3
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• pp.215-221
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• 2007

Biosorption is considered to be a promising alternative to replace the present methods for the treatment of dye-containing wastewater. In this study, sewage sludge was used as a biosorbent which could be one of the cheapest and most abundant biomaterials. The objective of this work is to develop a surface-modified biosorbent with enhanced sorption capacity and binding affinity. The FT-IR and potentiometric titration studies revealed that carboxyl, phosphateand amine groups played a role in binding of dye molecules. The binding sites for reactive dye Reactive Red 4 (RR 4) were identified to be amino groups present in the biomass. In this work, based on the biosorption mechanism, the performance of biosorbentcould be enhanced by the removal of inhibitory carboxyl groups from the biomass for practical application of the biosorbents. As a result, the maximum capacity of biomass was increased up to 130% and 210% of the increment of sorption capacity at pH 2 and 4, respectively. Therefore, chemically modified sewage sludge can be used as an effective and low-cost biosorbent for the removal of dyes from industrial discharges.