• Title/Summary/Keyword: Adsorption Isotherm

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Fabrication of Chitosan Nanoparticles with Lactococcus lactis for the Removal of Phthalate Endocrine Hormone (Phthalate계 환경호르몬 제거를 위한 Lactococcus lactis를 함유한 Chitosan Nanoparticles의 제조)

  • Yoon, Hee-Soo;Kang, Ik-Joong
    • Korean Chemical Engineering Research
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    • v.59 no.1
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    • pp.21-34
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    • 2021
  • Chitosan nanoparticles (CNPs) and Lactococcus lactis (L. lac.) were used as adsorbents to evaluate the adsorption performance of endocrine hormones, which are phthalates, in the healthy food packages. CNPs were produced through the cross bond with tripolyphosphate (TPP), and L. lac.-CNPs were prepared through the introduction of L. lac. during the preparation. The various functional groups of all adsorbents were identified using Fourier transform infrared spectroscopy (FTIR). Adsorption isotherm and adsorption kinetic confirmed the adsorption behavior and mechanism of CNPs, L. lac. and L. lac.-CNPs. The adsorption behavior of DBP and DEP for all particles was more suitable for the Freundlich adsorption isotherm model than for the Langmuir adsorption isotherm model, which means that the surface of the particles is heterogeneous. The adsorption mechanism was more suitable for the Pseudo-2nd-order model than for the Pseudo-1st-order model. This means that due to the presence of various functional groups on the particle surface, the adsorption of DBP and DEP is dominated by chemical adsorption such as electrostatic attraction and hydrogen bonding rather than physical adsorption. Finally, it was confirmed that the preparation of CNPs and L. lac.-CNPs can be performed easily and quickly, and it could be used as a cheaper adsorbent that can effectively remove phthalates.

Experiment on Chloride Adsorption by Calcium Aluminate Phases in Cement (시멘트내 칼슘 알루미네이트 상에 의한 염소이온의 흡착반응 연구)

  • Yoon, In-Seok
    • 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.

Comparative adsorption of crude oil using mango (Mangnifera indica) shell and mango shell activated carbon

  • Olufemi, Babatope Abimbola;Otolorin, Funmilayo
    • Environmental Engineering Research
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    • v.22 no.4
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    • pp.384-392
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    • 2017
  • Mango shell (MS) and mango shell activated carbon (MSAC) was used to adsorb crude oil from water at various experimental conditions. The MSAC was prepared by carbonization at $450^{\circ}C$ and chemical activation using strong $H_3PO_4$ acid. The adsorbents were characterized with Fourier Transform Infrared spectroscopy. Investigations carried out included the effects of parametric variations of different adsorbate dose, adsorbent dose, time, temperature, pH and mixing speed on the adsorption of crude oil. The equilibrium isotherm for the adsorption process was determined using Langmuir, Freundlich, Temkin and Dubinin Radushkevich isotherm models. Temkin isotherm was found to fit the equilibrium data reasonably well than others. The result demonstrated that MSAC was more effective for crude oil adsorption than raw mango shell. Optimum conditions were also presented. The enhanced effect from activation was justified statistically using Analysis of Variance and Bonferroni-Holm Posthoc significance test. The pseudo first order kinetics gave a better fit for crude oil adsorption with both MS and MSAC.

Study on Adsorption Characteristics of Tharonil from Aqueous Solution by Activated Carbon Adsorption (활성탄에 의한 Tharonil의 흡착특성에 관한 연구)

  • 이종집;유용호
    • 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.

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Synthesis and Phosphorus Adsorption Characteristics of Zirconium Magnetic Adsorbent Having Magnetic Separation Capability (자기분리가 가능한 지르코늄 자성 흡착제의 합성과 인 흡착 특성)

  • Lim, Dae-Seok;Kim, Yeon-Hyung;Kim, Dong-Rak;Lee, Tae-Gu;Lim, Hak-Sang
    • Journal of Korean Society of Water and Wastewater
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    • v.26 no.3
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    • pp.431-442
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    • 2012
  • The purpose of this study, is to separate magnetic separation devices using permanent magnets by using magnetization characteristics remaining in treated water after adsorption and synthesizing phosphorus adsorbent capable of magnetic separation for efficient removal of phosphorus. The synthesis of the adsorbent which set Zirconium(Zr) having high friendly features for phosphorus as an element, and by synthesizing Iron Oxide($Fe_3O_4$, another name of $Fe_3O_4$ is magnetite) being able to grant magnetism to Zirconium Sulfate($Zr(SO_4)_2$), zirconium magnetic adsorbent(ZM) were manufactured. In order to consider the phosphorus adsorption characteristics of adsorbent ZM, batch adsorption experiment was performed, and based on the results, pH effect, adsorption isotherm, adsorption kinetics, and magnetic separation have been explore. As the experiment result, adsorbent ZM showed a tendency that the adsorption number was decreased rapidly at pH 13; however, it was showed a high amount of phosphorus removal in other range and it showed the highest amount of phosphorus removal in pH 6 of neutral range. In addtion, the Langmuir adsorption isotherm model is matched well, and D-R adsorption isotherm model is ranged 14.43kJ/mol indicating ion exchange mechanism. The result shown adsorption kinetics match well to the Pseudo-second-order kinetic model. The adsorbent ZM's capablility of regenerating NaOH and $H_2SO_4$, was high selectivity on the phosphorus without impacts on the other anions. The results of applying the treated water after adsorption of phosphorus to the magnetic separation device by using permanent magnets, shows that capture of the adsorbent by the magnetization filter was perfect. And they show the possibility of utilization on the phosphorus removal in water.

A Study on Control of Trichloroethyene by Soil bed (토양상에 의한 Trichloroethyene처리에 관한 연구)

  • 이혜령;고경숙;임경택
    • Journal of Environmental Health Sciences
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    • v.24 no.3
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    • pp.41-47
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    • 1998
  • The purpose of this research is evaluation of adsorption capacity of the cast for TCE comparing with the yellow clay. Furthermore, the experimental data was fitted with the Langmuir and Freundlich isotherm and was found to be apllicable to the adsorption isotherm equation. The soil bed reactor used in this study was made of glass(10 cm in diameter, 100 cm in depth). The cast and yellow clay used as adsorbents were screened with 8-20 mesh mecanically. Results from Equilibrium test with adsorbents showed that the equibrium time of the cast and yellow clay was 9min independent of the amount of the adsorbents. The adsorption efficiencys of the cast and yellow clay for TCE was 66.3% and 56.2%, respectively. In the application of Freundlich isotherm, 1/n of the cast and yellow clay were 0.786 and 0.704, respectively. These results showed that the cast was more available than the yellow clay as TCE adsorbent. The best adsorption capacity was showed at 0% moisture content, 70 ppm inlet concentration and 25$^{\circ}$C temperature.

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On strong interaction dependence of the surface phase transition : Consideration through the partition function (표면상변이의 강인력 의존성 : 분배함수로 부터의 고찰)

  • Cheol Ho Kim;Bo Seung Hwang
    • Journal of the Korean Crystal Growth and Crystal Technology
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    • v.11 no.6
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    • pp.264-268
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    • 2001
  • We manipulate properly the partition function of the surface system to evaluate an adsorption isotherm. We explain the dependence of strong interaction on the surface phase transition via analysis of the derived adsorption isotherm. Our theoritical results for adsorption well reflect to the experiments.

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Adsorption Characteristic of Hydrogen and Methane on Activated Carbon (활성탄에 대한 수소화 메탄의 흡착특성)

  • Jin, Yinzhe;Choi, Dae-Ki;Row, Kyung-Ho
    • Transactions of the Korean hydrogen and new energy society
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    • v.16 no.4
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    • pp.307-314
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    • 2005
  • In this work, a static volumetric method was experimentally implemented to measure the adsorption isotherm of hydrogen and methane by the activated carbon. The equilibrium data of stationary phase and mobile phase were correlated into the Langmuir, Freundlich, Langmuir-Freundlich, and Toth isotherms, respectively. In addition, the comparison between prediction and experimental data was made. By a nonlinear regression analysis, the experimental parameters in the equilibrium isotherms were estimated and compared. Then, the linear and quadratic equations for pressure and temperature to adsorption amounts were expressed. The adsorption amounts were increased with the pressure increase and the temperature decrease.

Adsorption Isotherm Patterns According to the Interactions Between Adsorbed Particles (흡착입자간 상호작용에 따른 흡착등온선 패턴)

  • Kim, Cheol Ho
    • Korean Journal of Materials Research
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    • v.23 no.8
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    • pp.462-468
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    • 2013
  • We study and describe-from the point of view of the interactions of the adsorbed particles-three types of the adsorption isotherms, namely, Langmuir type adsorption isotherms, phase transition type adsorption isotherms, and adsorption limited type adsorption isotherms, which are observed by experiments. By introducing and using a one dimensional statistical occupancy model, we derived analytical adsorption isotherms for the no force, the attractive force, and the repulsive force exerted on the other adsorbed particles. Our derived adsorption isotherms qualitatively pretty well agree with the experimental results of the adsorption isotherms. To specify each adsorption type, Langmuir type adsorption is a phenomenon that occurs with no forces between the adsorbed particles, phase transition type adsorption is a phenomenon that occurs with the strong attractive forces between the adsorbed particles, and adsorption limited type adsorption is a phenomenon that occurs with the repulsive forces between the adsorbed particles. The theoretical analysis-only using fundamental thermodynamics and occupancy statistics though-qualitatively quite well explains the experimental results.

Determination of the Langmuir and Temkin Adsorption Isotherms of H for the Cathodic H2 Evolution Reaction at a Pt/KOH Solution Interface Using the Phase-Shift Method

  • Chun Jang-H.;Jeon Sang-K.;Chun Jin-Y.
    • Journal of the Korean Electrochemical Society
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    • v.9 no.1
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    • pp.19-28
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    • 2006
  • The phase-shift method for determining the Langmuir, Frumkin, and Temkin adsorption isotherms ($\theta_H\;vs.\;E$) of H for the cathodic $H_2$ evolution reaction (HER) at a Pt/0.1 M KOH solution interface has been proposed and verified using cyclic voltammetric, differential pulse voltammetric, and electrochemical impedance techniques. At the Pt/0.1 M KOH solution interface, the Langmuir and Temkin adsorption isotherms ($\theta_H\;vs.\;E$), the equilibrium constants ($K_H=2.9X10^{-4}mol^{-1}$ for the Langmuir and $K_H=2.9X10^{-3}\exp(-4.6\theta_H)mol^{-1}$ for the Temkin adsorption isotherm), the interaction parameters (g=0 far the Langmuir and g=4.6 for the Temkin adsorption isotherm), the rate of change of the standard free energy of $\theta_H\;with\;\theta_H$ (r=11.4 kJ $mol^{-1}$ for g=4.6), and the standard free energies (${\Delta}G_{ads}^{\circ}=20.2kJ\;mol^{-1}$ for $k_H=2.9\times10^{-4}mol^{-1}$, i.e., the Langmuir adsorption isotherm, and $16.7<{\Delta}G_\theta^{\circ}<23.6kJ\;mol^{-1}$ for $K_H=2.9\times10^{-3}\exp(-4.6\theta_H)mol^{-1}$ and $0.2<\theta_H<0.8$, i.e., the Temkin adsorption isotherm) of H for the cathodic HER are determined using the phase-shift method. At intermediate values of $\theta_H$, i.e., $0.2<\theta_H<0.8$, the Temkin adsorption isotherm ($\theta_H\;vs.\;E$) corresponding to the Langmuir adsorption isotherm ($\theta_H\;vs.\;E$), and vice versa, is readily determined using the constant conversion factors. The phase-shift method and constant conversion factors are useful and effective for determining the Langmuir, Frumkin, and Temkin adsorption isotherms of intermediates for sequential reactions and related electrode kinetic and thermodynamic data at electrode catalyst interfaces.