• Title/Summary/Keyword: Freundlich 등온흡착식

Search Result 177, Processing Time 0.029 seconds

Kinetic and Thermodynamic Studies of Brilliant Green Adsorption onto Carbon/Iron Oxide Nanocomposite (탄소/산화철 나노복합재료의 Brilliant Green 흡착에 대한 반응속도론적, 열역학적 연구)

  • Ahmad, Rais;Kumar, Rajeev
    • Journal of the Korean Chemical Society
    • /
    • v.54 no.1
    • /
    • pp.125-130
    • /
    • 2010
  • In the present work, we have investigated the adsorption efficiency of carbon/iron oxide nanocomposite towards removal of hazardous brilliant green (BG) from aqueous solutions. Carbon/iron oxide nanocomposite was prepared by chemical precipitation and thermal treatment of carbon with ferric nitrate at $750^{\circ}C$. The resulting material was thoroughly characterized by TEM, XRD and TGA. The adsorption studies of BG onto nanocomposite were performed using kinetic and thermodynamic parameters. The adsorption kinetics shows that pseudo-second-order rate equation was fitted better than pseudo-first-order rate equation. The experimental data were analyzed by the Langmuir and Freundlich adsorption isotherms. Equilibrium data was fitted well to the Langmuir model with maximum monolayer adsorption capacity of 64.1 mg/g. The thermodynamic parameters were also deduced for the adsorption of BG onto nanocomposite and the adsorption was found to be spontaneous and endothermic.

Sorption of Radioactive Cobalt and Ruthenium on Soil Minerals (방사성 코발트 및 루테늄의 토양 흡착)

  • Lee, Byung-Hun;Hands, J.D.
    • Journal of Radiation Protection and Research
    • /
    • v.15 no.2
    • /
    • pp.7-16
    • /
    • 1990
  • The sorption of radioactive cobalt and ruthenium on alumina, silica gel, zeolite 3A, kaolin and Na-bentonite has been studied as a function of pH. nuclide concentration and ionic strength. Retardation factor for cobalt and ruthenium on soil minerals was determined through porosity measurement. Hydrolysed species, cobalt and ruthenium interact with solid surfaces by physical adsorption processes. Freundlich sorption isotherms for cobalt and ruthenium are effectively linear. The sorption decreases with increasing ionic strength for cobalt and ruthenium. The effect of increasing porosity on the retardation factor countered the effect of a significant increase in the distribution coefficient.

  • PDF

Evaluation of Removal Characteristics of Taste and Odor Causing Compounds using Meso-Porous Absorbent (메조공극 흡착제를 이용한 상수원수내 맛·냄새 유발물질 제거특성 평가)

  • Kim, Jong-Doo;Park, Chul-Hwi;Yun, Yeo-Bog;Lee, Dae-Sung;Kim, Hyo-Jeon;Kang, Seok-Tae
    • Journal of Korean Society of Environmental Engineers
    • /
    • v.39 no.1
    • /
    • pp.26-33
    • /
    • 2017
  • The objective of this study was to evaluate the characteristic of adsorption by using a meso-porous adsorbent (MPA), and investigate the removal efficiency of geosmin which taste and odor causing compounds in drinking water supplies through batch test. The results for the adsorption isotherm was analyzed by using the Langmuir equation and Freundlich equation, generally being applied. And the study showed that the both Langmuir and Freundlich equation explains the results better. Both of pseudo-first-order model and pseudo-second-order model were respectively applied for evaluation of kinetic sorption property of geosmin onto MPA. The adsorption experiment results using MPA showed that maximum adsorption capacity of MPA was lower 7 times than that of GAC, and adsorption rate of MPA was faster 11 times than that of GAC, on the basis of pseudo-first-order model. Therefore, it was determined that MPA was effectively able to remove geosmin in drinking water supplies in short EBCT condition, but regeneration cycle in MAP process was shorter than that in conventional process.

Leaching Test and Adsorption Characteristics of Porphyry for Removal of Heavy Metals (맥반석의 용출시험 및 중금속 흡착특성)

  • Kim, Jong-Boo;Shen, Ming-Guo;Sung, Nak-Whan;Choi, Moon-Jeong;Kim, Kyung-Joo;Rhee, Dong Seok
    • Journal of Industrial Technology
    • /
    • v.20 no.A
    • /
    • pp.57-62
    • /
    • 2000
  • This experiment was done to investigate the leaching and adsorption properties of heavy metals on porphyry. The comparison with respect to the leachability of heavy metals from porphyry between the Korea Standard Leaching Test (KSLT) and the Toxicity Characteristic Leaching Procedure (TCLP) was carried out. The fractional composition of leachate and the total concentration of heavy metal of porphyry were studied through Sequential Extraction Procedure (SEP) and EPA Method 3050. Adsorption experiment of porphyry has pointed out that the optimum dosage of porphyry for 50ppm Pb was over 10g/L, the effective particle size for absorption was below 200 mesh and the optimum pH was about 7. From the Freundlich' adsorption equation, 1/n was 1.0722, and k was 0.0041. After adsorption, the fractional composition of Pb was changed. The exchangeable, carbonate, reducible fractions were increased, and the organic fraction was not changed, and the residual fraction was decreased.

  • PDF

Effects of Change in Soil pH and Treatment of Gibbsite and Organic Matter on Sulfate Adsorption in Soils (Gibbsite와 유기물(有機物) 처리(處理) 및 pH변화(變化)가 토양(土壤)의 SO4= 흡착(吸着)에 미치는 영향(影響))

  • Yoon, Sun-Kang;Yoo, Sun-Ho
    • Korean Journal of Soil Science and Fertilizer
    • /
    • v.19 no.2
    • /
    • pp.107-113
    • /
    • 1986
  • Laboratory experiments were carried out to investigate the effects of pH, gibbsite, and organic matter on sulfate adsorption by soils. Samples of five soil series (Songjeong, Gopyung, Yeasan, Gyorae, and Namwon), different in physical and chemical properties, were used in this study. The results obtained from sulfate adsorption experiment with sulfate solutions of the concentrations ranging from 50 to 400 ppm were as follows: 1. The adsorption phenomena for five soils were well described by the Freundlich adsorption isotherm over a given range of sulfate concentration. 2. The amounts of sulfate adsorbed and K value of Freundlich adsorption isotherm increased as the initial pH of the suspension decreased. 3. Although the changes in pH of the suspension on the adsorption equilibrium were hardly observed in the soil treated with gibbsite, the sulfate adsorption rates were increased with amount of gibbsite treated. 4. The effects of pH of the suspension on the adsorption rates in the soils treated with gibbsite were remarkable at the level of 0.1% but were little at the level of 1.5%. 5. The adsorption rates of soils, treated with organic matter and incubated for three weeks, were in the order: starch > straw > compost. At the relatively high levels (5 and 10%) of treatments, compost treatment resulted in the sulfate desorption phenomena.

  • PDF

Effect of Immobilization Method in the Biosorption and Desorption of Lead by Algae, Chlorella pyrenoidosa (Chlorella pyrenoidosa에 의한 납 흡.탈착시 고정화 방법의 영향)

  • Shin, Taek-Soo;Lim, Byung-Seo;Lee, Sang-Woo;Rhu, Kwon-Gul;Jeong, Seon-Ki;Kim, Kwang-Yul
    • Journal of Korean Society of Environmental Engineers
    • /
    • v.31 no.8
    • /
    • pp.663-672
    • /
    • 2009
  • In this studies, the adsorption test using Chlorella pyrenoidosa was conducted to examine the effect of Pb adsorption according to various immobilized methods such as Ca-alginate, K-carrageenan, and Polyacrylamide. From the results, the duration to need to reach adsorption equilibrium was delayed according to the immobilization. And, the higher adsorption capacity of immobilized Chlorella pyrenoidosa was represented in the higher concentration of Pb, the smaller amount of immobilizing agent, and the higher pH of solution. The maximum adsorption capacity of Pb was shown in the adsorption test using Chlorella pyrenoidosa immobilized with Ca-alginate even though it was sensitive pH. The adsorption results properly represented with Freundlich isotherm equations. And, pseudo second-order chemisorption kinetic rate equation was applicable to all the biosorption data over the entire time range. The FT-IR analysis showed that the mechanism involved in biosorption of Pb by Chlorella pyrenoidosa was mainly attributed to Pb binding of carbo-acid and amide group. Adsorbed Pb on immobilized Chlorella prenoidosa was easily desorbed in the higher concentration of desorbents(NTA, HCl, EDTA, $H_2SO_4,\;Na_2CO_3$). Among the several desorbents, NTA showed the maximum desoption capacities of Pb from Chlorella pyrenoidosa immobilized with Ca-alginate and K-carrageenan and EDTA was the most effective in Chlorella pyrenoidosa immobilized with polyacrylamide. The desoprtion efficiency in the optimum condition was 90.0, 83.0, and 80.0%, respectively.

Adsorption characteristics of Pb by various particle sizes of microplastics in aqueous solution (수용액에서 입자크기에 따른 미세플라스틱의 Pb 흡착특성)

  • Taejung Ha;Minjune Yang
    • Proceedings of the Korea Water Resources Association Conference
    • /
    • 2023.05a
    • /
    • pp.149-149
    • /
    • 2023
  • 미세플라스틱은 입자크기가 5 mm 이하인 플라스틱으로 정의되며, 수계로 유입된 미세플라스틱은 내분비계 교란물질로 작용하여 생태계에 환경독성을 유발하고 오염물질을 흡착·운반할 수 있는 독성 물질의 매개체로서 미세플라스틱의 위해성에 대한 우려가 증가하고 있다. 본 연구는 수용액에서 다양한 미세플라스틱의 납(Pb) 흡착특성을 평가하고 미세플라스틱의 비표면적에 따른 흡착 효과를 비교하고자 하였다. 플라스틱 종류 중 HDPE (High-density Polyethylene)와 PVC (Polyvinyl Chloride)를 각각 세 가지 크기(Group 1: 2.5 mm - 1.0 mm, Group 2: 1.0 mm - 0.3 mm, Group 3: < 0.3 mm)로 제조하여 분류하였으며, 미세플라스틱 입자크기의 비표면적은 BET(Brunauer, Emmett, Teller)분석을 통하여 측정하였다. 담수환경 조성을 위해 pH 7로 조절한 Pb 용액의 농도(0, 0.5, 1, 5, 10, 30 mg/L)별 흡착실험을 수행하였으며 실험결과를 3가지 흡착등온식(Langmuir, Freundlich, Sips 모델)을 사용하여 미세플라스틱에서 Pb 흡착 거동을 나타내었다. BET 분석 측정결과, PVC의 경우 Group 3 > Group 2 > Group 1 순으로 PVC의 입자크기가 작을수록 비표면적이 크게 나타났으며, HDPE 비표면적 또한 비슷한 경향을 보였다. HDPE와 PVC에서 Pb의 흡착은 Langmuir 모델(R2 > 0.97)과 Freundlich 모델(R2 > 0.82)보다 Sips 모델(R2 > 0.98)이 흡착 거동을 설명하기에 가장 적합하였다. 최대흡착능(Qm) 상수는 입자크기가 작아질수록 흡착능이 높아지는 추세를 보였으며, 흡착세기(KF)와 흡착강도(n-1)는 각 플라스틱의 Group 3(HDPE KF = 0.028, PVC KF = 0.032; HDPE n-1 = 0.225, PVC n-1 = 0.547)에서 가장 높게 나타났다. 본 연구를 통해 HDPE와 PVC에서 Pb의 흡착특성은 Sips모델로 설명이 가능했으며, 이에 따라 Pb 흡착과정에 복수의 흡착메커니즘이 작용하고 있음을 유추해볼 수 있었다. 미세플라스틱의 입자크기와 비표면적이 Pb 흡착량에 영향을 미치는 것을 알 수 있었으며, 미세플라스틱이 중금속을 흡착하여 생물체 내로 전이시킬 수 있는 매개체 역할의 가능성을 확인하였다.

  • PDF

A Study of Ground Tire as a Sorption Media for the Passive Treatment Wall: Sorption of MTBE (Methyl tertiary Butyl Ether) (파쇄 폐타이어를 이용한 반응벽체에 관한 연구: 폐타이어 내의 MTBE(Methyl tertiary Butyl Ether)흡착 중심)

  • 박상현;이재영;최상일
    • Journal of Soil and Groundwater Environment
    • /
    • v.8 no.3
    • /
    • pp.37-44
    • /
    • 2003
  • Fuel oxygenates, such as Methyl tertiary Butyl Ether (MTBE) is additive in gasoline used to reduce air pollution. Gasoline components and fuel additives can leak: form underground storage tanks. MTBE is far more water soluble than gasoline hydrocarbons like BTEX then it travels at essentially the same velocity as groundwater. MTBE in drinking water causes taste and odor problems. Therefore, the purpose of the this study is to examine the ability of ground tire to sorb MTBE in water. The study consisted of running both batch and column tests to determine the sorption capacity, the required sorption equilibration time, and the flow through utilization efficiency of ground tire. The batch test result indicated that ground tire can attain equilibrium sorption capacities about 0.5 mg of MTBE. The result of column test indicate that ground tire has on the 36% utilization rate. Finally, it is clear that ground tire represented an attractive and relatively inexpensive sorption medium for a MTBE. Authors thought that to determine the economic costs of ground tire utilization, the cost to sorb a given mass of contaminant by ground tire will have to be compared to currently accepted sorption media. The cost comparison will also have to include regeneration and disposal cost.

Adsorption Equilibrium, Kinetics and Thermodynamics Studies of Malachite Green Using Granular Activated Carbon (입상 활성탄을 이용한 말라카이트 그린의 흡착평형, 동력학 및 열역학 연구)

  • Lee, Jong-Jib
    • Applied Chemistry for Engineering
    • /
    • v.24 no.2
    • /
    • pp.184-189
    • /
    • 2013
  • In the present study, batch experiments were carried out for the utilizatioin of activated carbon as a potential adsorbent to remove a hazardous malachite green from an aqueous solution. The effects of various parameters such as temperature, contact time, initial concentration on the adsorption system were investigated. On the basis of adsorption data Langmuir and Freundlich adsorption isotherm model were also confirmed. The equilibrium process was described well by Langmuir isotherm model. From determined separation factor, the activated carbon could be employed as an effective treatment for removal of malachite green. From kinetic experiments, the adsorption process followed the pseudo second order model, and the adsorption rate constant ($k_2$) decreased with increasing both the initial concentration of malachite green and the adsoprtion temperature. Thermodynamic parameters like that activation energy, change of free energy, enthalpy, and entropy were also calculated to predict the adsorption nature. The activation energy calculated from Arrhenius equation indicated that the adsortpion of malachite green on the zeolite was physical process. The negative Gibbs free energy change ($\Delta$G = -3.68~-7.76 kJ/mol) and the positive enthalpy change ($\Delta$H = +26.34 kJ/mol) indicated the spontaneous and endothermic nature of the adsorption in the temperature range of 298~318 K.

Sorption of copper ion on waste pig bone (돼지 폐(廢) 골분(骨粉)에 의한 구리이온 흡착(吸着))

  • Kim, Eun-Jung;Woo, Sung-Hoon;Park, Seung-Cho
    • Resources Recycling
    • /
    • v.15 no.2 s.70
    • /
    • pp.45-49
    • /
    • 2006
  • The removal of copper ion from aqueous solution by adsorption with bone char that made from spent pig bone has been studied. This paper was studied the effects of bone char dosage and pH. The optimal results show that bone char adsorbs about 96.5 percent of copper ion in aqueous solution containing 50 mg/L as initial concentration at pH 5.0 when the bone char of 5g/L is used for 30 hours. Increase in the initial pH of the copper solution resulted in an increase in the copper ion uptake per weight of the sorbent Freundlich isotherm model was found to be applicable for the experimental data of $Cu^{2+}$.