• Title/Summary/Keyword: Sorption equilibrium

검색결과 200건 처리시간 0.026초

Batch and Flow-Through Column Studies for Cr(VI) Sorption to Activated Carbon Fiber

  • Lee, In;Park, Jeong-Ann;Kang, Jin-Kyu;Kim, Jae-Hyun;Son, Jeong-Woo;Yi, In-Geol;Kim, Song-Bae
    • Environmental Engineering Research
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    • 제19권2호
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    • pp.157-163
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    • 2014
  • The adsorption of Cr(VI) from aqueous solutions to activated carbon fiber (ACF) was investigated using both batch and flow-through column experiments. The batch experiments (adsorbent dose, 10 g/L; initial Cr(VI) concentration, 5-500 mg/L) showed that the maximum adsorption capacity of Cr(VI) to ACF was determined to 20.54 mg/g. The adsorption of Cr(VI) to ACF was sensitive to solution pH, decreasing from 9.09 to 0.66 mg/g with increasing pH from 2.6 to 9.9; the adsorption capacity was the highest at the highly acidic solution pHs. Kinetic model analysis showed that the Elovich model was the most suitable for describing the kinetic data among three (pseudo-first-order, pseudo-second-order, and Elovich) models. From the nonlinear regression analysis, the Elovich model parameter values were determined to be ${\alpha}$ = 162.65 mg/g/h and ${\beta}$ = 2.10 g/mg. Equilibrium isotherm model analysis demonstrated that among three (Langmuir, Freundlich, Redlich-Peterson) models, both Freundlich and Redlich-Peterson models were suitable for describing the equilibrium data. In the model analysis, the Redlich-Peterson model fit was superimposed on the Freundlich fit. The Freundlich model parameter values were determined to be $K_F$ = 0.52 L/g and 1/n = 0.56. The flow-through column experiments showed that the adsorption capacities of ACF in the given experimental conditions (column length, 10 cm; inner diameter, 1.5 cm; flow rate, 0.5 and 1.0 mL/min; influent Cr(VI) concentration, 10 mg/L) were in the range of 2.35-4.20 mg/g. This study demonstrated that activated carbon fiber was effective for the removal of Cr(VI) from aqueous solutions.

건조방법에 따른 복분자 분말의 갈변 및 흡습 특성 (Browning and Moisture Sorption Characteristics of Rubus coreanus Prepared by Different Drying Methods)

  • 정헌식;성종환;이영근;김한수;이주백;윤광섭
    • 한국식품저장유통학회지
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    • 제16권6호
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    • pp.797-803
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    • 2009
  • 건조방법이 복분자 분말의 갈변 및 흡습 특성에 미치는 영향을 조사하기 위하여, 신선 복분자를 천일, 적외선 및 동결 건조한 다음 분쇄하고 이 분말의 색도와 수분활성도 ($a_w$) 0.11-0.90 범위에서 평형수분함량(EMC)을 각각 측정하였다. 갈변지표인 $L^*$값과 $a^*$값은 동결 건조한 복분자 분말이 다른 방법으로 건조한 분말보다 높고 낮은 값을 나타내었고, 황색도인 $b^*$값은 동결 건조 분말에서 가장 높은 수준을 보였다. EMC는 $a_w$의 증가와 함께 증가하는 경향을 보였으며 특히, 0.75 $a_w$ 이상에서 급격하게 증가하였다. 동일한 $a_w$에서 분말의 EMC는 동결건조품이 천일과 적외선 건조품 보다 유의적으로 높게 나타났다. 복분자 분말의 흡습곡선은 전형적인 sigmoid 형태를 보였고, 천일건조 분말은 Halsey model, 적외선 건조 분말은 Kuhn model, 그리고 동결 건조 분말은 Oswin model이 적합도가 가장 높았다. 단분자층 수분함량은 GAB 방정식으로 설명 할 수 있었으며, 적외선 건조 분말에서 0.005 g $H_2O/g$ dry solid, 천일 및 동결 건조 분말에서 0.019 g $H_2O/g$ dry solid를 각각 나타내었다. 이로써 건조방법은 복분자 분말의 갈변과 흡습 특성에 영향을 미치는 것으로 확인되었다.

녹차잎과 인삼잎의 중금속 흡착능 평가 연구 (Adsorption of Heavy Metals by Natural Adsorbents of Green Tea and Ginseng Leaves)

  • 김소현;송진영;윤광석;강은미;송호철
    • 한국지하수토양환경학회지:지하수토양환경
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    • 제22권5호
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    • pp.128-134
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    • 2017
  • This work presents the adsorption capability of green tea and ginseng leaves to adsorb heavy metals such as Cd(II), Cu(II), and Pb(II) in aqueous solution. FT-IR analysis indicates the presence of oxygen containing functional groups (carboxyl groups) in two kinds of leaves. High pH condition was favorable to the adsorption of heavy metal ions due to the enhanced electrostatic attraction and the precipitation reaction of metal ions. The adsorption of Cd(II), Cu(II), and Pb(II) reached equilibrium within 10 min, achieving high removal efficiencies of 80.3-97.5%. The adsorption kinetics data of heavy metal ions were fitted well with the pseudo-second-order kinetic model. The maximum adsorption amounts of Cd(II), Cu(II), and Pb(II) ions were 8, 3.5, and 15 mg/g, respectively, in the initial concentration range from 0.15 to 0.75 mM. Based on the fitting data obtained from isotherm models, heavy metal adsorption by green tea and ginseng leaves could occur via multi-layer sorption.

Remediation of cesium-contaminated fine soil using electrokinetic method

  • Kim, Ilgook;Kim, June-Hyun;Kim, Sung-Man;Park, Chan Woo;Yang, Hee-Man;Yoon, In-Ho
    • Membrane and Water Treatment
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    • 제11권3호
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    • pp.189-193
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    • 2020
  • In this study, electrokinetic remediation equipment was used to remove cesium (Cs) from clay soil and waste solution was treated with sorption process. The influence of electrokinetic process on the removal of Cs was evaluated under the condition of applied electric voltage of 15.0-20.0 V. In addition to monitoring the Cs removal, electrical current and temperature of the electrolyte during experiment were investigated. The removal efficiency of Cs from soil by electrokinetic method was more than 90%. After electrokinetic remediation, Cs was selectively separated from soil waste solution using sorbents. Various adsorption agents such as potassium nickel hexacyanoferrate (KNiHCF), Prussian blue, sodium tetraphenylborate (NaTPB), and zeolite were compared and KNiHCF showed the highest Cs removal efficiency. The Cs adsorption on KNiHCF reached equilibrium in 30 min. The maximum adsorption capacity was 120.4 mg/g at 0.1 g/L of adsorbent dosage. These results demonstrated that our proposed process combined electrokinetic remediation of soil and waste solution treatment with metal ferrocyanide can be a promising technique to decontaminate Cs-contaminated fine soil.

Saccharomyces cerevisiae에 의한 Pb 생체흡착 (Pb Biosorption by Saccharomyces cerevisiae)

  • 안갑환;서근학
    • KSBB Journal
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    • 제11권2호
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    • pp.173-180
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    • 1996
  • S. CereVlSWe를 이용하여 Pb 이온의 흡착 능력을 조사하였다. 살아있는 S. CereVlSWe 및 멸균된 S. cereVlswe 보다 건조분쇄 된 S. cerevisiae가 Pb 흡착 능력이 가장 좋았다. 통일의 중금속 농도에서 중금 속 단위 흡착량은 미생물 농도가 높아짐에 감소하였다. 살아있는 S. cereVlsiae의 흡착 능력 순서는 Pb > >Cu> Cd = Co>Cr > Zn = Ni순이었다. 중금속 흡 착에서 0.1 M NaOH로 24시간 전처리하여 흡착량을 1.5배 증가시킬 수 있었다. 0.1 M HCl 및 0.1 M $H_2S_O4$ 로 Pb이온을 효과적으로 탈착시킬 수 있었다. Pb 이온의 흡착평형은 Freundlich 흡착등온식과 Langmuir 흡착등온식으로 설명할 수 있었다.

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Removal of Cd(II) and Cu(II) from Aqueous Solution by Agro Biomass: Equilibrium, Kinetic and Thermodynamic Studies

  • Reddy, Desireddy Harikishore Kumar;Lee, Seung-Mok;Seshaiah, Kalluru
    • Environmental Engineering Research
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    • 제17권3호
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    • pp.125-132
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    • 2012
  • The removal of Cd(II) and Cu(II) from aqueous solution by an agricultural solid waste biomass prepared from Moringa oleifera bark (MOB) was investigated. The biosorbent was characterized by Fourier transform infrared spectroscopy and elemental analysis. Furthermore, the effect of initial pH, contact time, biosorbent dosage, initial metal ion concentration and temperature on the biosorption of Cd(II) and Cu(II) were studied using the batch sorption technique. Kinetic studies indicated that the biosorption process of the metal ions followed the pseudo-second order model. The biosorption data was analyzed by the Langmuir, Freundlich, Dubinin-Radushkevich, and Temkin isotherm models. Based on the Langmuir isotherm, the maximum biosorption capacities for Cd(II) and Cu(II) onto MOB were 39.41 and 36.59 mg/g at 323 K, respectively. The thermodynamic parameters, Gibbs free energy (${\Delta}G^o$), enthalpy (${\Delta}H^o$), and entropy (${\Delta}S^o$) changes, were also calculated, and the values indicated that the biosorption process was endothermic, spontaneous and feasible in the temperature range of 303-323 K. It was concluded that MOB powder can be used as an effective, low cost, and environmentally friendly biosorbent for the removal of Cd(II) and Cu(II) ions from aqueous solution.

해양 퇴적물에서 인 용출 차단을 위한 반응성 피복 소재로서 제강슬래그의 적용성 검토 (Applicability Assessment of Steel Slag as Reactive Capping Material for Blocking Phosphorus Release from Marine Sediment)

  • 조성욱;박성직
    • 한국농공학회논문집
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    • 제56권3호
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    • pp.11-17
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    • 2014
  • We investigated the applicability of steel slag as a capping material in order to minimize phosphorus(P) release into seawater. Steel slag is a byproduct from the iron and steel industries and the use of steel slag has some advantages in respect of both cost and environmental concern. P removal by steel slag were studied in a batch system with respect to changes in contact time and initial concentration. Kinetic adsorption data were described well by pseudo 2nd order model, indicating rate limiting step for P adsorption to steel slag is chemical sorption. Equilibrium adsorption data fitted well to Langmuir isotherm model which describes for single layer adsorption. The maximum P adsorption capacity of steel slag was 7.134 mg-P/L. Increasing the depth of steel slag produced a positive effect on interruption of P release. More than 3 cm of steel slag was effective for blocking P release and 5 cm of steel slag was recommended as the depth for capping of P contaminated marine sediments. Increasing P concentration and flow rate had a negative effect on P removal ratio. It was concluded that the steel slag has a potential capping material for blocking P release from marine sediments.

Effects of Iron on Arsenic Speciation and Redox Chemistry in Acid Mine Water

  • Bednar A.J.;Garbarino J.R.;Ranville J.F.;Wildeman T.R.
    • 대한자원환경지질학회:학술대회논문집
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    • 대한자원환경지질학회 2004년도 International Symposium
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    • pp.9-28
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    • 2004
  • Concern about arsenic is increasing throughout the world, including areas of the United States. Elevated levels of arsenic above current drinking-water regulations in ground and surface water can be the result of purely natural phenomena, but often are due to anthropogenic activities, such as mining and agriculture. The current study correlates arsenic speciation in acid mine drainage and mining influenced water with the important water-chemistry properties Eh, pH, and iron(III) concentration. The results show that arsenic speciation is generally in equilibrium with iron chemistry in low pH AMD, which is often not the case in other natural-water matrices. High pH mine waters and groundwater do not 짐ways hold to the redox predictions as well as low pH AMD samples. The oxidation and precipitation of oxyhydroxides depletes iron from some systems, and this also affects arsenite and arsenate concentrations differently through sorption processes.

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Kinetics of water vapor adsorption by vacuum-dried jujube powder

  • Lee, Jun Ho;Zuo, Li
    • 한국식품저장유통학회지
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    • 제24권4호
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    • pp.505-509
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    • 2017
  • Water vapor adsorption kinetics of vacuum-dried jujube powder were investigated in temperature and relative humidity ranges of 10 to $40^{\circ}C$ and 32 to 75%, respectively. Water vapor was initially adsorbed rapidly and then reached equilibrium condition slowly. Reaction rate constant for water vapor adsorption of vacuum-dried jujube powder increased with an increase in temperature. The temperature dependency of water activity followed the Clausius-Clapeyron equation. The net isosteric heat of sorption increased with an increase in water activity. Good straight lines were obtained with plotting of $1/(m-m_0)$ vs. 1/t. It was found that water vapor adsorption kinetics of vacuum-dried jujube powder was accurately described by a simple empirical model, and temperature dependency of the reaction rate constant followed the Arrhenius-type equation. The activation energy ranged from 50.90 to 56.00 kJ/mol depending on relative humidity. Arrhenius kinetic parameters ($E_a$ and $k_0$) for water vapor adsorption by vacuum-dried jujube powder showed an effect between the parameters with the isokinetic temperature of 302.51 K. The information on water vapor adsorption kinetics of vacuum-dried jujube powder can be used to establish the optimum condition for storage and processing of jujube.

Moisture Sorption Isotherm Characteristics of Chaga Mushroom Powder as Influenced by Particle Size

  • Lee, Min-Ji;Lee, Jun-Ho
    • Food Science and Biotechnology
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    • 제16권1호
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    • pp.154-158
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    • 2007
  • Adsorption isotherms for chaga mushroom powder as influenced by particle size were investigated using a gravimetric technique. Samples were equilibrated in desiccators containing sulfuric acid solutions of known water activity (0.11-0.93), then placed in temperature-controlled chambers for approximately ten days. Equilibrium moisture content (EMC) of chaga mushroom powder increased with water activity in all samples. EMC was slightly greater in the samples comprised of smaller particle size, however there was no marked difference in appearance between the three samples. The chaga mushroom powder exhibited Type II behavior. When the BET model was used to determine mean monolayer values, 0.077, 0.077, and 0.070 $H_2O/dry$ solid was observed for <250, 250-425, and $425-850\;{\mu}m$ sized samples, respectively, however mean monolayer values were 0.121, 0.111, and 0.101 $H_2O/dry$ solid, respectively, when the GAB model was used. The experimental EMC values were related to the computed values from Henderson's model. The coefficient of determination and standard error for the linear regression were 0.997 and 0.003, respectively.