• Journal of Korean Society on Water Environment
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• v.20 no.5
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• pp.520-524
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• 2004

As a feasibility study for the application of carbon nanotubes to the treatment of environmental pollutants, the adsorption characteristics of humic acid on carbon nanotubes has been investigated. The dispersion features of carbon nanotubes in aquatic environment were investigated by measuring the variation of their electrokinetic potentials with pH, and the effects of some dispersants on their dispersion features were also examined. Under the experimental conditions, humic acid was observed to mostly adsorb on nanotubes within a few minutes and reach the equilibrium state within about one hour. The adsorption features of humic acid on nanotubes were found to follow the Freundlich model better than the Langmuir Model. Humic acid adsorbed on carbon nanotubes endothermically and the change of enthalpy in adsorption reaction was estimated to be ca. 18.37kJ/mol at standard state. The entropic change in adsorption reaction for humic acid was ca. 0.0503kJ/mol at standard state and the activation energy for adsorption was also estimated based on the change of rate constants with temperature. FT-IR investigations showed that the functional groups such as alcohol, ester, and aromatics existing in the chemical structure of humic acid might work as the bridge in its adsorption on nanotubes.

• Journal of Korean Society on Water Environment
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• v.20 no.5
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• pp.466-472
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• 2004

Red mud is formed as a waste during bauxite refining known as Bayer's process. Its main constituents are iron, aluminium, sodium and silica. The disposal of large quantities of wasted red mud causes a serious ecological problem. In this study, the red mud wasted from the bauxite refinery was studied for phosphate removal from aqueous solution according to activation methods. The influence of heat treatment, and neutralization with sea water and acid treatment level for the optimum conditions for phosphate removal have been determined. Heat treatment combined with acid treatment is most suitable for the removal of phosphate from aqueous solution. The optimal condition was activated with 1 N HCl solution after heating in $600^{\circ}C$ during 4 hours. Acid and heat treatment causes sodalite compounds which hinder the phosphate adsorption to leach out. The adsorption data obtained followed a first-order rate expression and fitted well with the Freundlich Isotherm well.

• Journal of Korean Society of Water and Wastewater
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• v.30 no.1
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• pp.105-111
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• 2016

This paper presents the applicability of natural zeolite (Clinoptilolite) for recovery of ammonium nitrogen from high-strength wastewater stream. Isotherm experiments showed the ammonium exchange Clinoptilolite followed Freundlich isotherm and its maximum exchange capacity was $18.13mg\;NH_4{^+}-N/g$ zeolite. The X-ray photoelectron spectroscopy (XPS) analysis indicated that a significant amount of nitrogen was adsorbed to the Clinoptilolite. Optimal flowrate for recovery of high concentration ammonium nitrogen was determined at 16 BV/d (=19.2 L/min) throughout the lab-scale column studies operated under various flowrate conditions. This study also provided a method to determine the recovery rate of final product of nitrogen fertilizer based on the model application to the lab-scale continuous data.

• Applied Chemistry for Engineering
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• v.31 no.5
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• pp.495-501
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• 2020

In this study, zirconium fumarate of metal-organic framework (MOF-801) was solvothermally synthesized at 130 ℃ and characterized through powder X-ray diffraction (PXRD) analyses and porosity measurements from N₂ sorption isotherms at 77 K. The ability of MOF-801 to act as an adsorbent for the phosphate removal from aqueous solutions at 25 ℃ was investigated. The phosphate removal efficiency (PRE) obtained by 0.05 g/L adsorbent dose at an initial phosphate concentration of 60 ppm after 3 h was 72.47%, whereas at 5 and 20 ppm, the PRE was determined to be 100% and 89.88%, respectively, after 30 min for the same adsorbent dose. Brunauer-Emmett-Teller (BET) surface area and pore volume of the bare MOF-801 sample were 478.25 ㎡/g and 0.52 ㎤/g, respectively, whereas after phosphate adsorption (at an initial concentration of 60 ppm, 3 h), the BET surface area and pore volume were reduced to 331.66 ㎡/g and 0.39 ㎤/g, respectively. The experimental data of kinetic (measured at initial concentrations of 5, 20 and 60 ppm) and isotherm measurements followed the pseudo-second-order kinetic equation and the Freundlich isotherm model, respectively. This study demonstrates that MOF-801 is a promising material for the removal of phosphate from aqueous solutions.

• Korean Journal of Fisheries and Aquatic Sciences
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• v.38 no.3
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• pp.153-157
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• 2005

The biosorption of Pb and Cr by Sargassum thunbergii was investigated in a batch conditions. The Pb and Cr uptake capacity of Sargassum thunbergii was 232.5 mg Pb/g biomass and 91.6 mg Cr/g biomass, respectively. An adsorption equilibria was reached within about 0.5 hr for both the Pb and the Cr. The adsorption parameters for both the Pb and the Cr were determined according to the Langmuir and Freundlich model. With increasing pH values, more negative sites are becoming available for the adsorption of Pb and Cr. The selectivity of mixture solution showed an uptake order of Pb>Cu>Cr>Cd. Pb and Cr adsorbed by S. thunbergii could be recovered ken 0.1 M HCl, 0.1 M $HNO_3$ and 0.1M EDTA by a desorption process, and the efficiency of Pb desorption was above $95.8\%$, whereas the efficiency of the Cr desorption was below $50.7\%$.

• Journal of the Korean Chemical Society
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• v.17 no.5
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• pp.319-323
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• 1973

The state of carrier-free silver-111 has been studied by applying filtration method. The studies involved that the effects of pH and concentration of silver-111 in aqueous solution have been determined with membrane filters. The present studies revealed that the retainment of silver-111 on membrane filters followed Freundlish adsorption isotherm, and the adsorbed state of silver-111 was present in the form of AgOH. Also it was supposed that the formation of the non-adsorbed hydroxide of$Ag(OH)_{2}-$ may prohibit the existance of AgOH at higher pH, and it seems to be valid that the carrier-free silver-111 in aqueous solution exists in$Ag^+$state.

• Polymer(Korea)
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• v.38 no.5
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• pp.557-565
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• 2014

Sodium alginate and chitosan are added to a $CaCl_2$ solution to prepare calcium-alginate-chitosan and calciumalginate gels. After dehydration through stoving, two types of adsorbent particles are obtained. The adsorption process of the particles obtained for low concentrations of $Sr^{2+}$ satisfies a second-order kinetic equation and the Freundlich adsorption model. The thermodynamic behaviors of the particles indicate that adsorption occurs via a spontaneous physical process. XPS pattern analysis is used to demonstrate the adsorption of $Sr^{2+}$ by calcium alginate and chitosan. By building an interaction model of the molecules of chitosan and alginate with $Ca^{2+}$ and $Sr^{2+}$ to calculate energy parameters, Fukui index, Mulliken charge, and Mulliken population, adsorption of $Sr^{2+}$ on the molecular chains of chitosan as well as the boundary of calcium-alginate-chitosan is observed to show weak stability; by contrast, adsorption between molecular chains is high.

• Journal of Korean Society of Water and Wastewater
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• v.18 no.2
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• pp.137-144
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• 2004

In this study, several series of experiments were conducted to investigate the phosphorus (P) removal process in slag-containing solution using furnace and converter slags. High amount of $OH^-$, $Ca^{2+}$ and alkalinity were discharged from the slags and hydroxyapatites [$Ca_5(PO_4)_3(OH)$] were kept accumulated on the surface of slag. P removal capacity of the slag decreased with the increase of slag dosage. The maximum capacity was found to be 11.25 mg/g at the converter slag. Converter slag adsorbed P more than furnace slag(about four times in average). An experimental study on the effect of pH shows that the percentage removal of P increased upto 30% at the pH range of 56 than that of above pH 8. Langmuir isotherm constants gave a better correlation than Freundlich ones. P removal amount in the presence of $NH^+_4$ was less compared to the one in the absence of $NH^+_4$. Maximum percentage reduction was 23%.

• Journal of Korean Society of Water and Wastewater
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• v.21 no.1
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• pp.27-36
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• 2007

Milled Korean pine (Pinus densiflora) wood was used to evaluate its adsorption capacity of Cu(II) ions from aqueous solution by running a series of batch experiments. Prior to the tests, the milled woods were pretreated with 1N NaOH, 1N $NHO_3$, and distilled water, respectively, to examine the effect of pretreatment. Within the tested pH range in this study between 3 and 6, copper adsorption efficiency of NaOH-treated wood(96~99%) was superior than $NHO_3$-treated wood(19~31%) and distilled water-treated wood(18~35%). Adsorption behavior of copper onto both raw and $NHO_3$-treated woods was mainly attributed to interaction with carboxylic acid group. For NaOH-treated wood, carboxylate ion produced by hydrolysis was a major functional group responsible for Cu sorption. NaOH treatment of wood changed the ester and carboxylic acid groups into carboxylate group, whereas $NHO_3$ treatment did not affect the production of functional groups which could bind copper. A pseudo second-order kinetic model fitted well for the sorption of copper ion onto NaOH-treated wood. A batch isotherm test using NaOH-treated wood showed that equilibrium sorption data were better represented by the Langmuir model than the Freundlich model.

• Journal of Pharmaceutical Investigation
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• v.25 no.4
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• pp.331-338
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• 1995

In order to screen appropriate preservatives for the suspension containing sucralfate, neusilin and hydrotalcite, the patterns and mechanism of the adsorption and desorption of several preservatives on these antacids were studied. The employed preservatives were parabens(methyl, propyl, butyl), chlorhexidine diacetate and sorbic acid. While none of parabens were adsorbed on three antacids, chlorhexidine diacetate was strongly adsorbed on all the antacids employed, especially on hydrotalcite. Sorbic acid was not adsorbed on neusilin and hydrotalcite, however, 65% of sorbic acid was adsorbed on sucralfate. The adsorption of chlorhexidine diacetate on neusilin and hydrotalcite was partly physical and partly chemical, while its adsorption on sucralfate was almost chemical. Sorbic acid was completely deserted from sucralfate. In all cases, the adsorption isotherms were fitted well to both Freundlich equation and Langmuir equation. Based on these results, parabens and sorbic acid were the preservatives of choice for the suspension containing sucralfate, neusilin and hydrotalcite.