• Journal of the Korean Society of Safety
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• v.15 no.4
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• pp.88-94
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• 2000

The adsorption characteristics of Tharonil on granular activated carbon were experimentally investigated in an adsorber and in a packed column. It was estabilished that the adsorption equilibrium of Tharonil on granular activated carbon was more successfully fitted by Freundlich isotherm equation than Langmuir isotherm equation in the concentration range from 1 to 1000 mg/1. Intraparticle diffusivities (pore and surface diffusivity) of Tharonil were estimated by the concentration-time curve and adsorption isotherm. The estimated values of pore diffusivity and surface diffusivity are $6.70{\times}10^{-6}$ and $2.0{\times}10^{-9}cm^2/s$, respectively. From comparison of intraparticle diffusivities, it was found that surface diffusion was the limiting step for adsorption rate. The break time and breakthrough curve predicted by constant pattern-linear driving force model were shown to agree with the experimental results.

• Journal of Environmental Science International
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• v.12 no.10
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• pp.1061-1069
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• 2003

The adsorption behaviors of strontium and cesium ions on fly ash, natural zeolites, and zeolites synthesized from fly ash were investigated. The zeolites synthesized from fly ash had greater adsorption capabilities for strontium and cesium ions than the original fly ash and natural zeolites. The maximum adsorption capacity of synthetic zeolite for strontium and cesium ions was 100 and 154 mg/g, respectively, It was found that the Freundlich isotherm model could fit the adsorption isotherm. The distribution coefficients (K$\_$d/) for strontium and cesium ions were also calculated from the adsorption isotherm data, The distribution coefficients decreased with increasing equilibrium concentration of strontium and cesium ions in solution. By studying the removal of cesium and strontium ions in the presence of calcium, magnesium, sodium, potassium, sulfate, nitrate, nitrite, and EDTA (in the range of 0.01 - 5 mM) it was found that these coexistence ions competed for the same adsorption sites with strontium and cesium ions.

• Journal of the Korea Concrete Institute
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• v.29 no.4
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• pp.389-397
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• 2017

Friedel's salt is an important product of chemical adsorption between cement hydrate and chloride ions because it contains chlorine in its structure. When cement reacts with water in the presence of chloride ions, the $C_3A$ phase, and $C_4AF$ phase react with chloride to produce Friedel's salt. If chloride ions penetrate into concrete from external environments, many calcium aluminate hydrates, including AFm, can bind chloride ions. It is very important, therefore, to investigate the chloride binding isotherm of $C_3A$ phase, $C_4AF$ phase, and AFm phase to gain a better understanding of chloride binding in cementitious materials. Meanwhile, the adsorption isotherm can provide us with the fundamental information for the understanding of adsorption process. The experimental results of the isotherm can supply not only the quantitative knowledge of the cement-Friedel's salt system, but also the mechanism of adsorption and the properties of their interactions. The purpose of this study is to explore the time dependant behaviors of chloride ions adsorption with $C_3A$, $C_4AF$ and AFm phases. The chloride adsorption isotherm was depicted with Langmuir isotherm and the adsorption capacity was low in terms of the stoichiometric point of view. However, the chloride adsorption of AFm phase was depicted with Freundlich isotherm and the value was very low. Since the amount of the adsorption was governed by temperature, the affecting parameters of isotherm were expressed as a function of temperature.

• Journal of Microbiology and Biotechnology
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• v.33 no.2
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• pp.251-259
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• 2023

Immobilizing microalgae cells in a hyphal matrix can simplify harvest while producing novel mycoalgae products with potential food, feed, biomaterial, and renewable energy applications; however, limited quantitative information to describe the process and its applicability under various conditions leads to difficulties in comparing across studies and scaling-up. Here, we demonstrate the immobilization of both active and heat-deactivated marine diatom Phaeodactylum tricornutum (UTEX 466) using different loadings of fungal pellets (Aspergillus sp.) and model the process through kinetics and equilibrium models. Active P. tricornutum cells were not required for the fungal-assisted immobilization process and the fungal isolate was able to immobilize more than its original mass of microalgae. The Freundlich isotherm model adequately described the equilibrium immobilization characteristics and indicated increased normalized algae immobilization (g algae removed/g fungi loaded) under low fungal pellet loadings. The kinetics of algae immobilization by the fungal pellets were found to be adequately modeled using both a pseudo-second order model and a model previously developed for fungal-assisted algae immobilization. These results provide new insights into the behavior and potential applications of fungal-assisted algae immobilization.

• Journal of Korean Society of Water and Wastewater
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• v.29 no.6
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• pp.609-615
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• 2015

This study was carried out for characterization of MIO synthesized in our laboratory by co-precipitation method and applied isotherm and kinetic models for adsorption properties. XRD analysis were conducted to find crystal structure of synthesized MIO. Further SEM and XPS analysis was performed before and after phosphate adsorption, and BET analysis for surface characterization. Phosphate stock solution was prepared by KH2PO4 for characterization of phosphate adsorption, and batch experiment was conducted using 50 ml conical tube. Langmuir and Freundlich models were applied based on adsorption equilibrium test of MIO by initial phosphate solution. Pseudo first order and pseudo second order models were applied for interpretation of kinetic model by temperature. Surface area and pore size of MIO were found $89.6m^2/g$ and 16 nm respectively. And, the determination coefficient ($R^2$) value of Langmuir model was 0.9779, which was comparatively higher than that of Freundlich isotherm model 0.9340.

• Journal of Korean Society on Water Environment
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• v.25 no.6
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• pp.943-950
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• 2009

Cadmium (Cd) adsorption onto the activated carbon containing hydroxyapatite (HAP) was investigated in batch experiments and response surface methodology (RSM) using the Box-Behnken methods were applied to the experimental results. Cd adsorption with different HAP mass ratio of from 10% to 30%. With more HAP, Cd was more adsorbed. These results suggest that the higher HAP mass causes an increase of the ion exchange potential of the HAP sorbent. Equilibrium experimental results from Cd adsorption was fitted to Langmuir and Freundlich isotherm models. Cd adsorption on HAP sorbent were found to follow the Freundlich isotherm model well in the initial adsorbate concentration range. Also, Cd adsorption was a function of the HAP mass ratio ($x_1$), initial Cd concentration ($x_2$), and initial pH ($x_3$) from the application of the RSM. Statistical results showed the order of significance of the independent variables to be initial Cd concentration > HAP mass ratio > initial pH.

• Advances in environmental research
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• v.4 no.2
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• pp.119-133
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• 2015

Water pollution means that the physical, chemical and biological properties of water are changing. In this study, adsorption was chosen as the treatment method because it is an eco-friendly and low cost approach. Magnetite is a magnetic material that can synthesize chemical precipitation. Magnetite was used for the removal of copper in artificial water samples. For this purpose, metal removal from water dependent on the pH, initial concentration of metal, amount of adsorbent and effect of sorption time were investigated. Magnetite was characterized using XRD, SEM and particle size distribution. The copper ions were determined by atomic absorption spectrometry. The adsorption of copper on the magnetite was studied in a batch process, with different aqueous solutions of Cu (II) at concentrations ranging from 10 to $50mg\;l^{-1}$. Optimum conditions for using magnetite were found to be concentration of $10mg\;L^{-1}$, pH: 4.5, contact time: 40 min. Optimum adsorbent was found to be 0.3 gr. Furthermore, adsorption isotherm data were analyzed using the Langmuir and Freundlich equations. The adsorption data fitted well with the Freundlich ($r^2=0.9701$) and Langmuir isotherm ($r^2=0.9711$) equations. Kinetic and equilibrium aspects of the adsorption process were studied. The time-dependent Cu (II) adsorption data were described well by a pseudo-second-order kinetic model.

• Journal of the Korean GEO-environmental Society
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• v.12 no.10
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• pp.23-28
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• 2011

This study was conducted to investigate the adsorption characteristics of various surfactants including biosurfactant, SWA 1503, Triton X-100 and sodium dodecyl sulfate(SDS) on soil. The Freundlich adsorption isotherm equation was found to be the best to describe experimental results. The amount of adsorbed surfactant on soil increased as the content of clay increased. The results showed that surfactant was adsorbed mainly on the surface and the pores of soil since the surface area of clay was larger than that of sand. The amount of adsorbed surfactants on soil was as follows: Biosurfactant > SWA 1503 > Triton X-100 > SDS.

• Journal of the Korean Society of Groundwater Environment
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• v.4 no.2
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• pp.78-84
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• 1997

Batch and column tests were performed to investigate the sorption capacity of bottom soils of Kimpo metropolitan waste landfill. Sorption capacity and sorption isotherm from the batch test for inorganic and heavy metal substances and retardation capacity of heavy metals from the column test are obtained. It was recognized from the tests that the samples match well with Freundlich isotherm and marine clay has good sorption capacity for potassium and heavy metals such as lead and cadmium. The soil samples with different geologic origins did not show significant differences in the sorption capacity of tested components.

• Journal of Life Science
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• v.8 no.2
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• pp.208-215
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• 1998

It was investigated the biosorption performances of copper by the immobilized biomass of nonliving marine brown alge h. fusiformis by each of the Ca-alginate method(Ca-ALG), Ba-alginate method(Ba-ALG), polyethylene glycol method(PEG), and carrageenan method (CARR). The copper removal performance increased but the copper uptake decreased as the biomass amount was increased. However, the copper uptake by the immobilized biomass increased with increasing initial copper concentration. The copper uptake by the immobilized biomass of the immobilization method decreased in the following sequence; Ca-ALG>Ba-ALG>PEG>CARR among the immoblization emthods. The copper uptake by the immobilized biomass followed the Langmuir isotherm better than the Freundlich isotherm.