• 제목/요약/키워드: freundlich model

검색결과 309건 처리시간 0.025초

입상활성탄에 의한 합성폐수의 용존유기물질의 새로운 흡착등온 모델 및 운동학적 흡착 연구 (Study of new adsorption isotherm model and kinetics of dissolved organic carbon in synthetic wastewater by granular activated carbon)

  • 김성현;신성훈;김진혁;우달식;이호선
    • 한국산학기술학회논문지
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    • 제15권4호
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    • pp.2029-2035
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    • 2014
  • 본 논문은 입상활성탄에 의해서 합성폐수에서의 용존유기탄소의 흡착평형과 회분식 실험을 통해 흡착성질을 파악하고자 하였다. 흡착평형의 새로운 모델식을 제안하였고 이 식을 바탕으로 회분식 실험데이터를 모사하였다. 합성폐수의 유기성분은 Beef extract, Peptone, Humic acid, Tannic acid, Sodium lignin sulfonate, Sodium lauryle sulfate, Arabic gum powder, Arabic acid (polysaccharide), $(NH_4)_2SO_4$, $K_2HPO_4$, $NH_4HCO_3$, $MgSO_4{\cdot}7H_2O$ 등으로 구성되었다. 농도가 낮은 영역 (0~2.5 mg/L)에서는 선형적인 흡착평형을 보여주었고, 농도가 높은 영역 (2.5~6mgl/L)에서는 우호적인 흡착평형을 보여주었다. 사용되어진 생물학적 처리방법에서 나오는 유출수의 합성폐수는 알려진 양으로 준비되어졌다. 흡착평형 모델링은 Freundlich, Langmuir, Sips 및 하이브리드 식을 이용하여 모사하였다. 특히, 선형과 Sips를 이용한 하이브리드 흡착평형식은 낮은 농도와 높은 농도 역에서 매우 좋은 흡착평형식이었다. 용수 및 폐수처리에 활성탄 흡착에 있어서, 선형식과 Sips식을 합친 새로운 하이브리드 식은 새로운 흡착평형식이 될 수 있었다. 하이브리드 흡착평형식 (선형+Sips)을 이용하여 LDFA 운동학적식을 통하여 다양한 흡착제 양에 따른 회분식 반응조에서의 실험데이터를 잘 모사할 수 있었다.

등온 및 동적 흡착 실험을 통한 제강 슬래그의 비소 흡착 특성 (Sorption Characteristics of Arsenic on Furnace Slag by Adsorption Isotherm and Kinetic Sorption Experiments)

  • 오참뜻;이성수;;권호진;이원택;박준범
    • 한국지반공학회논문집
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    • 제26권9호
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    • pp.37-45
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    • 2010
  • 본 연구에서는 지하수에 존재하는 비소를 산업 폐기물인 제강 슬래그를 이용하여 제거하고자, 제강 슬래그에 대한 비소의 흡착특성을 규명하였다. 이를 위해 등온흡착 실험과 동적흡착 실험을 수행하였고, 흡착반응 후 용액의 화학적 특성을 분석하였다. 실험 결과, 흡착 실험을 수행한 모든 용액은 염기 상태로 존재하였으며(pH 9이상), 칼슘의 농도가 가장 높았다(30~50mg/L). 등온흡착 실험결과는 Langmuir 모델보다Freundlich 모델에 적용하는 젓이 더 합리적이였으며, 제강 슬래그에 As(V)가 As(III)보다 약 87% 더 많이 흡착되는 것으로 확인됐다. 동적흡착 실험결과의 경우, 유사일차모델보다 유사이차모델을 통해 해석하는 것이 더 적합하였다. 비소의 초기농도가 높을수록 평형 흡착량($q_e$)과 완화시간($t_r$) 이 모두 증가하였으며, As(V)는 As(III)보다 평형 흡착량이 많고 완화시간은 짧은 것을 확인할 수 있었다. 또한, 유사이차모델을 통해 예측된 평형 흡착량이 등온흡착 실험에서 구한 평형 흡착량과 유사해 동적흡착 실험결과로 등온흡착 실험결과를 예측하는 것이 가능함을 확인하였다.

Studies on the Influence of Mercaptoacetic Acid (MAA) Modification of Cassava (Manihot sculenta Cranz) Waste Biomass on the Adsorption of Cu2+ and Cd2+ from Aqueous Solution

  • Horsfall, M. Jnr.;Spiff, A.I.;Abia, A.A.
    • Bulletin of the Korean Chemical Society
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    • 제25권7호
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    • pp.969-976
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    • 2004
  • Cassava peelings waste, which is both a waste and pollutant, was chemically modified using mercaptoacetic acid (MAA) and used to adsorb $Cu^{2+}\;and\;Cd^{2+}$ from aqueous solution over a wide range of reaction conditions at $30^{\circ}C$. Acid modification produced a larger surface area, which significantly enhanced the metal ion binding capacity of the biomass. An adsorption model based on the $Cu^{2+}/Cd^{2+}$ adsorption differences was developed to predict the competition of the two metal ions towards binding sites for a mixed metal ion system. The phytosorption process was examined in terms of Langmuir, Freundlich and Dubinin-Radushkevich models. The models indicate that the cassava waste biomass had a greater phytosorption capacity, higher affinity and greater sorption intensity for $Cu^{2+}\;than\;Cd^{2+}$. According to the evaluation using Langmuir equation, the monolayer binding capacity obtained was 127.3 mg/g $Cu^{2+}$ and 119.6 mg/g $Cd^{2+}$. The kinetic studies showed that the phytosorption rates could be described better by a pseudo-second order process and the rate coefficients was determined to be $2.04{\times}10^{-3}\;min^{-1}\;and\;1.98{\times}10^{-3}\;min^{-1}\;for\;Cu^{2+}\;and\;Cd^{2+}$ respectively. The results from these studies indicated that acid treated cassava waste biomass could be an efficient sorbent for the removal of toxic and valuable metals from industrial effluents.

흡착제의 흡착특성 규명을 위한 흡착모델의 적용성 평가(1)-흡착등온식을 이용한 평가 (Applicability of Theoretical Adsorption Models for Studies on Adsorption Properties of Adsorbents(1))

  • 나춘기;한무영;박현주
    • 대한환경공학회지
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    • 제33권8호
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    • pp.606-616
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    • 2011
  • 본 연구는 흡착제의 흡착특성을 이해하는데 이용되는 각종 흡착모델의 적용성을 평가하는데 목적이 있다. 이를 위해 상용의 음이온교환수지(PA-308)를 이용하여 $NO_3^-$에 대한 흡착특성을 회분식 실험을 통해 조사하였다. 흡착등온과 흡착속도 실험결과는 일반적으로 널리 이용되고 있는 다양한 흡착등온식과 반응속도식을 통해 모델화하였다. 흡착평형실험은 흡착등온식을 적용하는데 있어 실험조건이 미치는 영향을 확인하기 위해 흡착제의 투여량을 일정한 값으로 고정하고 흡착질의 농도변화에 따른 조건과 흡착질의 농도를 일정한 값으로 고정하고 흡착제의 투여량 변화에 따른 조건으로 나누어 수행하였다. 흡착질의 농도를 변화시키는 조건에서의 흡착평형은 Langmuir와 Freundlich 흡착등온식을 결합한 형태의 Sips 흡착등온식과 Redlich-Perterson 흡착등온식에 의해 수식화가 가능하였다. 한편, 흡착제의 무게를 변화시키는 조건에서의 흡착평형은 단층 흡착, 균일표면을 가정하는 Langmuir 흡착등온식과 잘 일치하는 경향을 보였다. 이상의 결과는 $NO_3^-$에 대한 음이온교환수지의 흡착 메커니즘이 흡착실험 조건에 의해 달라질 수 있음을 시사한다.

해수에서 6가 크롬 제거를 위한 흡착제로서의 산처리 적니 적용성 검토 (Applicability Assessment of Acid Treated Red Mud as Adsorbent Material for Removal of Six-valent Chromium from Seawater)

  • 강구;엄병환;김영기;박성직
    • 한국농공학회논문집
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    • 제55권5호
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    • pp.17-23
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    • 2013
  • Six-valent chromium ($Cr^{6+}$) is a highly toxic pollutant, supplied in a variety of industrial activities such as leather tanning, cooling tower blowdown, and plating. Herein, we investigated the removal of $Cr^{6+}$ from aqueous phase using low-cost adsorbents. Steel slag, montmorillonite, illite, kaolinite, red mud, and acid treated red mud with 0.5, 1.0, and 2.0 M HCl were used as adsorbent for the removal of $Cr^{6+}$ and the results showed that acid treated red mud with 2.0 M HCl (ATRM-2.0 M) had higher adsorption capacity of $Cr^{6+}$ than other adsorbents used. Accordingly, $Cr^{6+}$ removal by ATRM-2.0 M were studied in a batch system with respect to changes in initial concentration of $Cr^{6+}$, initial solution pH, adsorbent dose, adsorbent mixture, and seawater. Equilibrium sorption data were described well by Freundlich isotherm model. The influence of initial solution pH on $Cr^{6+}$ adsorption was insignificant. The use of the ATRM-2.0 M alone was more effective than mixing it with other adsorbents including red mud, zeolite, oyster shell, lime stone, and montmorillonite for the removal of $Cr^{6+}$. The $Cr^{6+}$ removal of the ATRM-2.0 M was slightly less in seawater than deionized water, resulting from the presence of anions in seawater competing for the favorable adsorption site on the surface of ATRM-2.0 M. It was concluded that the ATRM-2.0 M can be used as a potential adsorbent for the removal of $Cr^{6+}$ from the aqueous solutions.

Improving the permeability and adsorption of phenol by organophilic clay in clay liners

  • Heidarzadeh, Nima;Parhizi, Paria
    • Environmental Engineering Research
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    • 제25권1호
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    • pp.96-103
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    • 2020
  • The aim of this study is to investigate the effect of five different combinations including: sand 70%, bentonite 30% (S70B30)- sand 80%, bentonite 20% (S80B20)- sand 80%, organophilic 20% (S80M20)- sand 60%, bentonite 20%, organophilic 20% (S60B30M20) and sand 75% - bentonite 15% - organophilic 10% (S75B15M10) on landfill linear structure in order to decrease phenol leaching. Hydraulic conductivity and adsorption behavior of the samples were investigated. The results demonstrated that the lowest hydraulic conductivity coefficient ($1.16{\times}10^{-11}{\frac{m}{s}}$) was obtained for S70B30. Furthermore, adding more than 20% of bentonite had no significant effect on reducing permeability. Moreover, Freundlich isotherm was introduced as the best model explaining adsorption behaviour due to its highest determination coefficient (0.945). The best samples for adsorption capacity of phenol and for both permeability and adsorption are S80M20 and S60B30M20, respectively. Although the presence of bentonite was effective in reducing hydraulic conductivity, organic clay had no considerable impact on reducing permeability. Though, it's an exceptional role in adsorbing organic contaminants including phenol cannot be ignored. To meet all regulatory constraints, the optimal compound is made up of 10.2% of bentonite and 2.8% of organophilic clays with a minimized cost of 13.64 ($/ton).

Maghnia 산 Montmorillonite 수용액으로부터 양이온 염료의 제거 비교연구 (Comparison Study on the Removal of Cationic Dyes from Aqueous Suspension of Maghnia Montmorillonite)

  • Elaziouti, A.;Laouedj, N.
    • 대한화학회지
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    • 제54권3호
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    • pp.300-309
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    • 2010
  • 대상 수용액으로부터 상업용 염료인 메틸렌 블루(MB)와 말라카이트 그린 옥살레이트(MG)의 제거를 위한 소듐-교환된 점토 입자의 흡착능을 다양한 실험조건에서 조사하였다. 용액의 pH, 교반 시간, 흡착물 농도, 흡착제 투여량 등의 효과를 조사하였다. pH 7, 298 K 조건에서 0.03 그람 점토를 사용한 경우 수용액으로부터 최대 > 90%의 염료가 제거되었다. 흡착과정은 빨랐으며 5분 내에 평형에 도달하였다. 사용된 염료들의 흡착반응에 대해 반응속도론 실험에서 유사 2차반응이 관찰되었고 실험 데이터와 잘 일치하였다. 흡착평형은 높은 회귀계수 $R^2$ > 0.98로 Langmuir 와 Dubini-Radushkevich (D-R) 등온에 따랐다. 이 D-R 모델로부터 평균자유에너지 $E_a$ 는 MB와 MG 염료에 대해 각기 3.779와 2.564가 이었으며, 이것은 물리적 흡착과 정에 해당된다.

수용액 중 Orange II 흡착 제거를 위한 우모폐기물의 이용가능성 (Effectiveness of Feather Waste for Orange II Removal from Aqueous Solutions)

  • 박수연;유지연;손홍주
    • 한국환경과학회지
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    • 제27권9호
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    • pp.743-751
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    • 2018
  • The objective of this study was to investigate the adsorption potential of chicken feathers for the removal of OrangeII (AO7) from aqueous solutions. Batch experiments were performed as a function of different experimental parameters such as initial pH, reaction time, feather dose, initial OrangeII concentration and temperature. The highest OrangeII uptake was observed at pH 1.0. Most of the OrangeII was adsorbed at 2 h and an adsorption equilibrium was reached at 6 h. As the amount of chicken feather was increased, the removal efficiency of OrangeII increased up to 99%, but its uptake decreased. By increasing the initial concentration and temperature, OrangeII uptake was increased. The experimental adsorption isotherm exhibited a better fit with the Langmuir isotherm than with the Freundlich isotherm, and maximum adsorption capacity from the Langmuir constant was determined to be 0.179244 mmol/g at $30^{\circ}C$. The adsorption energy obtained from the Dubinin-Radushkevich model was 7.9 kJ/mol at $20^{\circ}C$ and $30^{\circ}C$ which indicates the predominance of physical adsorption. Thermodynamic parameters such as ${\Delta}G^0$, ${\Delta}H^0$, and ${\Delta}S^0$ were -12.28 kJ/mol, 20.64 kJ/mol and 112.32 J/mol K at $30^{\circ}C$, respectively. This indicates that the process of OrangeII adsorption by chicken feathers was spontaneous and endothermic. Our results suggest that as a low-cost biomaterials, chicken feather is an attractive candidate for OrangeII removal from aqueous solutions.

Equilibrium and kinetic studies of an electro-assisted lithium recovery system using lithium manganese oxide adsorbent material

  • Lee, Dong-Hee;Ryu, Taegong;Shin, Junho;Kim, Young Ho
    • Carbon letters
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    • 제28권
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    • pp.87-95
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    • 2018
  • This study examined the influence of operating parameters on the electrosorptive recovery system of lithium ions from aqueous solutions using a spinel-type lithium manganese oxide adsorbent electrode and investigated the electrosorption kinetics and isotherms. The results revealed that the electrosorption data of lithium ions from the lithium containing aqueous solution were well-fitted to the Langmuir isotherm at electrical potentials lower than -0.4 V and to the Freundlich isotherm at electrical potentials higher than -0.4 V. This result may due to the formation of a thicker electrical double layer on the surface of the electrode at higher electrical potentials. The results showed that the electrosorption reached equilibrium within 200 min under an electrical potential of -1.0 V, and the pseudo-second-order kinetic model was correlated with the experimental data. Moreover, the adsorption of lithium ions was dependent on pH and temperature, and the results indicate that higher pH values and lower temperatures are more suitable for the electrosorptive adsorption of lithium ions from aqueous solutions. Thermodynamic results showed that the calculated activation energy of $22.61kJ\;mol^{-1}$ during the electrosorption of lithium ions onto the adsorbent electrode was primarily controlled by a physical adsorption process. The recovery of adsorbed lithium ions from the adsorbent electrode reached the desorption equilibrium within 200 min under reverse electrical potential of 3.5 V.

Adsorption Behavior and Mechanism of Tripolyphosphate on Synthetic Goethite

  • Zhong, Yong;Sheng, Dandan;Xie, Fazhi;Li, Guolian;Li, Hui;Han, Xuan;Xie, Wenjie;Oh, Won-Chun
    • 한국세라믹학회지
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    • 제56권2호
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    • pp.146-152
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    • 2019
  • In order to study the transport behavior of tripolyphosphate (TPP) in aqueous solutions, the adsorption process of TPP on synthetic goethite, which exists stably in supergene environment, has been systematically studied. The adsorption properties under different conditions (pH, electrolyte presence, and temperature) were investigated. The adsorption of TPP in the presence of humic acid (HA)/fulvic acid (FA) has also been discussed in this paper. The results indicated that the adsorption capacity quickly increased within the first hour and equilibrium was reached within 24 h. The adsorption capacity decreased from 1.98 to 0.27 mg·g-1 upon increasing the pH from 8.5 to 11.0, whereas the adsorption of TPP on goethite hardly changed with increasing electrolyte concentration. The results of analysis of the kinetic and isothermal models showed that the adsorption was more in accord with the pseudo second-order equation and Freundlich model. The adsorption capacity decreased obviously regardless of the order of addition of TPP, HA, and goethite. Subsequent addition of FA led to a large increase in the adsorption capacity, which might be attributed to the adsorption ability of FA. According to the predictions of the kinetic and isothermal models and the spectroscopic evidence (X-ray diffraction (XRD), Fourier Transform infrared spectroscopy (FT-IR), and scanning electron microscope (SEM)), the adsorption mechanism may be mainly based on surface complexation and physical adsorption.