• Journal of Korea Soil Environment Society
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• v.4 no.2
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• pp.77-86
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• 1999

Partitioning of two hydrophobic organic compounds (HOCs), phenanthrene and naphthalene, to kaolinite and sorbed surfactants was studied to evaluate the feasibility of surfactant-enhanced remediation (SER) of contaminated subsurface systems. Sorbed surfactant partition coefficients. $K_ss$, showed a strong dependence on the surfactant sorption isotherms at low sorbed surfactant levels $K_ss$ values were at their highest and then decreased with increasing surfactant sorption densities. $K_ss$ values for SDS were always larger than corresponding $K_mic$values. For Tween 80, however. $K_ss$ values $K_mic$ were higher than $K_mic$ values only at the lower sorbed surfactant densities. HOC distribution between immobile and mobile phases varied with surfactant dose distribution coefficients increased initially with increasing surfactant concentrations and then decreased at higher doses. This observation shows directly the competition between sorbed and micellar surfactants for HOC partitioning. Overall results of this study demonstrate that surfactant sorption to the solid phase can lead to increases in HOC retardation in some SER applications. Therefore, before an SER process is selected, appropriate consideration of surfactant sorption and HOC partitioning to immobile versus mobile phases pertinent to a specific subsurface system must be contemplated.

• Journal of Environmental Science International
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• v.19 no.5
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• pp.549-563
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• 2010

The environmental behaviors of polycyclic aromatic hydrocarbons (PAHs) are mainly governed by their solubility and partitioning properties on soil media in a subsurface system. In surfactant-enhanced remediation (SER) systems, surfactant plays a critical role in remediation. In this study, sorptive behaviors and partitioning of naphthalene in soils in the presence of surfactants were investigated. Silica and kaolin with low organic carbon contents and a natural soil with relatively higher organic carbon content were used as model sorbents. A nonionic surfactant, Triton X-100, was used to enhance dissolution of naphthalene. Sorption kinetics of naphthalene onto silica, kaolin and natural soil were investigated and analyzed using several kinetic models. The two compartment first-order kinetic model (TCFOKM) was fitted better than the other models. From the results of TCFOKM, the fast sorption coefficient of naphthalene ($k_1$) was in the order of silica > kaolin > natural soil, whereas the slow sorbing fraction ($k_2$) was in the reverse order. Sorption isotherms of naphthalene were linear with organic carbon content ($f_{oc}$) in soils, while those of Triton X-100 were nonlinear and correlated with CEC and BET surface area. Sorption of Triton X-100 was higher than that of naphthalene in all soils. The effectiveness of a SER system depends on the distribution coefficient ($K_D$) of naphthalene between mobile and immobile phases. In surfactant-sorbed soils, naphthalene was adsorbed onto the soil surface and also partitioned onto the sorbed surfactant. The partition coefficient ($K_D$) of naphthalene increased with surfactant concentration. However, the $K_D$ decreased as the surfactant concentration increased above CMC in all soils. This indicates that naphthalene was partitioned competitively onto both sorbed surfactants (immobile phase) and micelles (mobile phase). For the mineral soils such as silica and kaolin, naphthalene removal by mobile phase would be better than that by immobile phase because the distribution of naphthalene onto the micelles ($K_{mic}$) increased with the nonionic surfactant concentration (Triton X-100). For the natural soil with relatively higher organic carbon content, however, the naphthalene removal by immobile phase would be better than that by mobile phase, because a high amount of Triton X-100 could be sorbed onto the natural soil and the sorbed surfactant also could sorb the relatively higher amount of naphthalene.

• Journal of Korean Society of Water and Wastewater
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• v.20 no.3
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• pp.389-395
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• 2006

The use of pine bark, a natural adsorbent prepared from Korean Red Pine (Pinus densifloral), was studied for its adsorption behavior of lead ion from aqueous solution. Adsorption experiments were carried out on lead ion concentrations of 10mg/L. Adsorption of lead ion could be described by both Langmuir and Freundlich adsorption isotherms. Treatment of the bark with nitric acid greatly increased initial adsorption rate, and equilibrium sorption capacity increased by approximately 48%. A pseudo second-order kinetic model fitted well for the kinetic behavior of lead ion adsorption onto the bark. Acid-treated bark demonstrated its adsorption capacity quite close to that of granular activated carbon. Results of this study indicated that ion exchange and chelation were involved in the adsorption process.

• Proceedings of the Korean Society of Soil and Groundwater Environment Conference
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• 2001.09a
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• pp.115-119
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• 2001

Contaminant retardation factor is derived from the colloidal and contaminant transport equations for a four-phase porous medium: an aqueous phase, two mobile colloidal phases, and a solid matrix. It is assumed that the contaminant sorption to solid matrix and colloidal particles and the colloidal deposition on solid matrix follow the linear isotherms. The behavior of the contaminant retardation factor in response to the change of model parameters is examined employing the experimental data of Magee et al. (1991) and Jenkins and Lion (1993). In the four-phase system, the contaminant retardation factor is determined by both the contaminant association with solid matrix and colloidal particles and the colloidal deposition on solid matrix. The contaminant mobility is enhanced when the affinity of contaminants to mobile colloids increases. In addition, as the affinity of colloids to solid matrix decreases, the contaminant mobility increases.

• Journal of Korean Society on Water Environment
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• v.25 no.3
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• pp.370-374
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• 2009

Adsorption characteristics of glass fibers, obtained from the spent lithium primary batteries recycling process, were investigated for the removal of Acid Red 27 dye from aqueous solution. The batch data clearly showed that increasing the initial sorptive concentration apparently enhanced the amount adsorbed and the uptake process followed the pseudo-second order rate model. The equilibrium adsorption data at different initial sorptive concentrations were fitted well to Freundlich and Langmuir adsorption isotherms. Moreover, the increase in temperature, favored the uptake of dye on this solid, indicated the process was endothermic in nature. Further, using the temperature dependence sorption data obtained at different temperatures was used to estimate various thermodynamic parameters.

• Proceedings of the Korean Society of Soil and Groundwater Environment Conference
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• 2000.11a
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• pp.196-201
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• 2000

The influence of adsorption on cadmium toxicity to soil microorganisms in smectite-rich soils and sediments was quantified as a function of solution and sorbent characteristics. Adsorption and surface complexation experiments were conducted to infer Cd sorption mechanisms to a reference smectite and three fractions of a Veritsol soil, and to elucidate the effects of the surface complexation on Cd bioavailability and toxicity in soils and sediments. Cadmium adsorption isotherms conformed to the Langmuir adsorption model, with adsorptive capacities of the different samples dependent on their characteristics. Equilibrium geochemical modeling (MINTEQA2) was used to predict the speciation of Cd in the soil suspensions using Langmuir and Triple Layer surface complexation models. The influence of adsorption and surface complexation on cadmium toxicity to soil microorganisms was assessed indirectly through the relative change in microbial hydrolysis of fluorescein diacetate (FDA) as a function of total Cd concentration and sorbent characteristics. Adsorption decreased the toxicity of Cd to soil microorganisms. Inner-sphere complexation is more effective than outer-sphere complexation in reducing the bioavailability and toxicity of heavy metals in soils and sediments.

• Proceedings of the KSR Conference
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• 2009.05a
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• pp.1530-1535
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• 2009

Moisture evaporates, when concrete is exposed to fire, not only at concrete surface but also at inside the concrete to adjust the equilibrium and transfer properties of moisture. The equilibrium properties of moisture are described by means of water vapor sorption isotherms, which illustrate the hysteretical behavior of materials. In this paper, the prediction method of the moisture distribution inside the high strength concrete members under the high temperature is presented. Finite element method is employed to facilitate the moisture diffusion analysis for any position of member. And the moisture diffusivity model of high strength concrete by high temperature is proposed. To demonstrate the validity of this numerical procedure, the prediction by the proposed algorithm is compared with the test result of other researcher. The proposed algorithm shows a good agreement with the experimental results including the vaporization effect inside the concrete.

• Bulletin of the Korean Chemical Society
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• v.33 no.11
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• pp.3711-3718
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• 2012

Here, we report a chain-length dependent morphology and pore structure tailing of mesoporous silica templated from organogels, which is formed by primary alkylamine and ethylene glycol at room temperature. As the chain length of alkylamine changes from 12 to 18, the resulted materials exhibit a morphology change from layers to spheres and platelets, respectively. SEM and TEM observation revealed that these shapes appear to be inherited from their parent organogels. Further pore structure characterization by nitrogen sorption analysis demonstrates that all the resulted silicas exhibit typical IV isotherms indicative of uniform mesopores, and their pore sizes are dependent on the chain length of alkylamine used.

• Korean Journal of Agricultural Science
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• v.27 no.2
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• pp.135-140
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• 2000

The mobility of sulfate in soils defends on several factors including redox potential, soil mineralogy, pH, and the presence of other anions that compete for sorption sites with sulfate. The proposed model of adsorption mechanism for sulfate postulated that reaction is between anions in solution and charged surfaces of soil particles. With appropriate choice of parameters obtained from the adsorption-desorption experiments, the equation of transport model adapt an empirical approach, capable of handling most general equilibrium adsorption isotherms, suitable for multispecies systems.

• Proceedings of the KSEEG Conference
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• 2003.04a
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• pp.61-65
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• 2003

Zinc occurs in the nature as sulfide, carbonate, silicate, and oxide. In natural water, zinc is generally in the form of the divalent cation $Zn^{2+}$ as well as in the form of fairly weakly bound complexes. Human activities introduce zinc ion to the hydrosphere in many ways. The zinc complexes in the aqueous environment are accumulated not only in aquatic organisms but also in human body ultimately through physico-chemical and/or biological processes. (omitted)