Removal of Arsenate from Aqueous Solution Using Nanoscale Iron Particles

2006 ◽  
Vol 41 (2) ◽  
pp. 210-215 ◽  
Author(s):  
Ching Yuan ◽  
Hsing-Lung Lien

Abstract Removal of As(V) using nanoscale iron particles was examined in batch reactors. Nanoscale iron particles, utilizing zerovalent iron with a diameter less than 100 nm as reactive materials, have been demonstrated to effectively remediate a wide variety of common environmental contaminants. In this study, characterization of nanoscale iron particles and their corrosion products was conducted using SEM-EDX, XRD, BET surface area analyzer and Laser Zee Meter. SEM-EDX results indicated adsorption of arsenic onto the iron surface, and XRD analysis found the formation of iron corrosion products including lepidocrocite, magnetite and/or maghemite at a reaction period of 7 d. Measurements of zeta potential revealed that the nanoscale iron particles have a zero point of charge at pH 4.4. Increasing adsorption amounts of arsenic with decreasing pH can therefore be attributed to the positive surface charge of the particles at lower pH. The maximum adsorption capacity of nanoscale iron particles determined by the Langmuir equation was about 38.2 mg/g. Normalization of the adsorption capacity to specific surface areas provides insight into the importance of iron types and the contact time of reactions in influencing arsenic uptake.

2016 ◽  
Vol 74 (8) ◽  
pp. 1800-1808 ◽  
Author(s):  
Jianjun Liang ◽  
Meiling Liu ◽  
Yufei Zhang

Commercial pulverous activated carbon (AC-0) was modified through two steps: oxidize AC-0 acid firstly, impregnate it with iron using ferric chloride secondly. Orthogonal experiment was conducted then to prepare modified activated carbon with high Cd(II) adsorption capacity (ACNF). Batch adsorption experiments were undertaken to determine the adsorption characteristics of Cd(II) from aqueous solution onto AC-0 and ACNF and the effect of pH, contact time and initial Cd(II) concentration. The results indicate that: the adsorption behavior of Cd(II) on ACNF can be well fitted with Langmuir model, and the maximum adsorption capacity of ACNF was 2.3 times higher than that of AC-0, supporting a monolayer coverage of Cd(II) on the surface. The kinetics of the adsorption process can be described by pseudo-second-order rate equation very well, and the adsorption capacity increased from 0.810 mg/g to 0.960 mg/g after modification. Compared with AC-0, the kinetic parameters of ACNF showed a higher adsorption rate through the aqueous solution to the solid surface and a lower intraparticle diffusion rate. Surface modification resulted in a lower Brunauer–Emmett–Teller (BET) surface area and pore size because of the collapse and blockage of pores, according to the X-ray diffraction (XRD) analysis, while the total number of surface oxygen acid groups increased, and this was supposed to contribute to the enhanced adsorption capacity of modified activated carbon.


Materials ◽  
2020 ◽  
Vol 14 (1) ◽  
pp. 63
Author(s):  
Maria Harja ◽  
Gabriela Buema ◽  
Nicoleta Lupu ◽  
Horia Chiriac ◽  
Dumitru Daniel Herea ◽  
...  

Fly ash/magnetite material was used for the adsorption of copper ions from synthetic wastewater. The obtained material was characterized by scanning electron microscopy (SEM), energy dispersive X-ray analysis (EDAX), X-ray diffractometer (XRD), Fourier transform infrared spectroscopy (FTIR), Brunauer–Emmett–Teller (BET) surface area, and vibrating sample magnetometer (VSM). Batch adsorption experiments were employed in order to investigate the effects of adsorbent dose, initial Cu (II) concentration and contact time over adsorption efficiency. The experimental isotherms were modeled using Langmuir (four types of its linearization), Freundlich, Temkin, and Harkins–Jura isotherm models. The fits of the results are estimated according to the Langmuir isotherm, with a maximum adsorption capacity of 17.39 mg/g. The pseudo-second-order model was able to describe kinetic results. The data obtained throughout the study prove that this novel material represents a potential low-cost adsorbent for copper adsorption with improved adsorption capacity and magnetic separation capability compared with raw fly ash.


Author(s):  
Lorena Alcaraz ◽  
María Esther Escudero ◽  
Francisco J. Alguacil ◽  
Irene Llorente ◽  
Ana Urbieta ◽  
...  

This paper describes the physico-chemical study of the adsorption of dysprosium (Dy3+) in aqueous solution onto two types of activated carbons synthesized from spent coffee ground. KOH activated carbon is a microporous material with a specific BET surface area of 2330 m2·g-1 and pores with a diameter of 3.2 nm. Carbon activated with water vapor and N2 is a solid mesoporous, with pores of 5.7 nm in diameter and a specific surface of 982 m2·g-1. A significant dependence of the adsorption capacity on the solution pH was found, while it does not depend significantly neither on the dysprosium concentration nor on the temperature. A maximum adsorption capacity of 31.26 mg·g-1 and 33.52 mg·g-1 for the chemically and physically activated carbons, respectively, were found. In both cases, the results obtained from adsorption isotherms and kinetic study were better fit to a Langmuir model and a pseudo-second-order kinetics. In addition, thermodynamic results indicate that dysprosium adsorption onto both activated carbons is an exothermic, spontaneous and favorable process.


2020 ◽  
Vol 82 (5) ◽  
pp. 984-997
Author(s):  
Tatyana Kouznetsova ◽  
Andrei Ivanets ◽  
Vladimir Prozorovich ◽  
Ahmad Hosseini-Bandegharaei ◽  
Hai Nguyen Tran ◽  
...  

Abstract The research aimed to develop a novel mesoporous aluminosilicate/zeolite composite by the template co-precipitation method. The effect of aluminosilicate (AlSi) and zeolite (NaY) on the basic properties and adsorption capacity of the resultant composite was conducted at different mass ratios of AlSi/NaY (i.e., 5/90, 10/80, 15/85, 20/80, and 50/50). The adsorption characteristics of such composite and its feedstock materials (i.e., aluminosilicates and zeolite) towards radioactive Sr2+ ions and toxic metals (Cu2+ and Pb2+ ions) in aqueous solutions were investigated. Results indicated that BET surface area (SBET), total pore volume (VTotal), and mesopore volume (VMeso) of prepared materials followed the decreasing order: aluminosilicate (890 m2/g, 0.680 cm3/g, and 0.644 cm3/g) > zeolite (623 m2/g, 0.352 cm3/g, and 0.111 cm3/g) > AlSi/NaY (20/80) composite (370 m2/g, 0.254 cm3/g, and 0.154 cm3/g, respectively). The Langmuir maximum adsorption capacity (Qm) of metal ions (Sr2+, Cu2+, and Pb2+) in single-component solution was 260 mg/g, 220 mg/g, and 161 mg/g (for zeolite), 153 mg/g, 37.9 mg/g, and 66.5 mg/g (for aluminosilicate), and 186 mg/g, 140 mg/g, and 77.8 mg/g for (AlSi/NaY (20/80) composite), respectively. Ion exchange was regarded as a domain adsorption mechanism of metal ions in solution by zeolite; meanwhile, inner-surface complexation was domain one for aluminosilicate. Ion exchange and inner-surface complexation might be mainly responsible for adsorbing metal ions onto the AlSi/NaY composite. Pore-filling mechanism was a less important contributor during the adsorption process. The results of competitive adsorption under binary-components (Cu2+ and Sr2+) and ternary-components (Cu2+, Pb2+, and Sr2) demonstrated that the removal efficacy of target metals by the aluminosilicate, zeolite, and their composite remarkably decreased. The synthesized AlSi/NaY composite might serve as a promising adsorbent for real water treatment.


2020 ◽  
Vol 7 (12) ◽  
pp. 3773-3782
Author(s):  
Junmin Deng ◽  
Sungjun Bae ◽  
Sunho Yoon ◽  
Mathieu Pasturel ◽  
Rémi Marsac ◽  
...  

Surface bound Fe(ii) on NZVI secondary minerals would affect the fate and mobility of quinolone antibiotics in the environment.


Metals ◽  
2020 ◽  
Vol 10 (12) ◽  
pp. 1630
Author(s):  
Vesna Marjanovic ◽  
Aleksandra Peric-Grujic ◽  
Mirjana Ristic ◽  
Aleksandar Marinkovic ◽  
Radmila Markovic ◽  
...  

Hybrid adsorbent, based on the cross-linked copolymer impregnated with hydrous iron oxide, was applied for the first time for Se(VI) adsorption from water. The influence of the initial solution pH, selenate concentration and contact time to adsorption capacity was investigated. Adsorbent regeneration was explored using a full factorial experimental design in order to optimize the volume, initial pH value and concentration of the applied NaCl solution as a reagent. Equilibrium state was described using the Langmuir model, while kinetics fitted the pseudo-first order. The maximum adsorption capacity was found to be 28.8 mg/g. Desorption efficiency increased up to 70%, and became statistically significant with the reagent concentration and pH increase, while the applied solution volume was found to be insignificant in the investigated range. Based on the results obtained, pH influence to the adsorption capacity, desorption efficiency, Fourier transform infrared (FTIR) and X-ray diffraction (XRD) analysis of loaded adsorbent, it was concluded that the outer- and inner-sphere complexation are mechanisms responsible for Se(VI) separation from water. In addition to the experiments with synthetic solutions, the adsorbent performances in drinking water samples were explored, showing the purification efficiency up to 25%, depending on the initial Se(VI) concentration and water pH. Determined sorption capacity of the cross-linked copolymer impregnated with hydrous iron oxide and its ability for regeneration, candidate this material for further research, as a promising anionic species sorbent.


2019 ◽  
Vol 39 (2) ◽  
Author(s):  
Viviana Eloisa Gomez Rengifo ◽  
Adriana Herrera Barros ◽  
Jorge Hernan Sanchez Toro

The adsorption capacity of acetylsalicylic acid was evaluated using carbon xerogel (CX) and carbon xerogel modified with TiO2 nanoparticles (CXM). These materials were characterized by different techniques such as Scanning Electron Microscopy (SEM), X-Ray Diffraction (XRD), and Fourier Transform Infrared (FTIR) spectroscopy. BET surface area measurements found values of 762 m2/g and 214 m2/g for CX and CXM, respectively. Batch experiments show that the Langmuir-Freundlich model best represents the experimental adsorption isotherm, in addition to show a maximum adsorption capacity of 17,48 mg/g.  In continuous experiments, the effect of the inlet concentration and flow rate on the adsorption capacity of the micro-packed bed adsorber were evaluated. Breakthrough curves agree well with the axial dispersion model. In view of their adsorption capacity, carbon xerogels provide a potential material for the removal of emergent contaminants from the pharmaceutical industry. Besides, the incorporation of TiO2 nanoparticles allows the implementation of complementary techniques, e.g. photodegradation, as an alternative to achieve higher elimination of aqueous contaminants.


Nanomaterials ◽  
2019 ◽  
Vol 9 (10) ◽  
pp. 1372 ◽  
Author(s):  
Lorena Alcaraz ◽  
María Esther Escudero ◽  
Francisco José Alguacil ◽  
Irene Llorente ◽  
Ana Urbieta ◽  
...  

This paper describes the physicochemical study of the adsorption of dysprosium (Dy3+) in aqueous solution onto two types of activated carbons synthesized from spent coffee ground. Potassium hydroxide (KOH)-activated carbon is a microporous material with a specific Brunauer–Emmett–Teller (BET) surface area of 2330 m2·g−1 and pores with a diameter of 3.2 nm. Carbon activated with water vapor and N2 is a solid mesoporous, with pores of 5.7 nm in diameter and a specific surface of 982 m2·g−1. A significant dependence of the adsorption capacity on the solution pH was found, but it does not significantly depend on the dysprosium concentration nor on the temperature. A maximum adsorption capacity of 31.26 mg·g−1 and 33.52 mg·g−1 for the chemically and physically activated carbons, respectively, were found. In both cases, the results obtained from adsorption isotherms and kinetic study were better a fit to the Langmuir model and pseudo-second-order kinetics. In addition, thermodynamic results indicate that dysprosium adsorption onto both activated carbons is an exothermic, spontaneous, and favorable process.


2012 ◽  
Vol 479-481 ◽  
pp. 250-254
Author(s):  
Wen Jun Xiang

Iron oxides-coated kaolinite (Fe-Kaolinite) was prepared by co-precipitation and indentified using X-ray diffraction (XRD). Moreover, the surface properties and fluoride adsorption characteristics of Fe-Kaolinite were investigated and compared with those of kaolinite. Compared to kaolinite, the BET surface area and surface fractal dimension of Fe-Kaolinite increased significantly. The pH at zero point of charge (pHZPC) of kaolinite and Fe-Kaolinite was 3.16 and 6.24, respectively. In the suspensions of pH 6.0, the fitted maximum adsorption capacity (qmax) for fluoride of kaolinite and Fe-Kaolinite was 1.32 and 5.86 mg/g, respectively. The adsorption data for fluoride by Fe-Kaolinite could be fitted using Freundlich isotherm (R2 =0.987), and Langmuir isotherm was very suitable for describing the fluoride adsorption of kaolinite (R2 =0.991).


2020 ◽  
Vol 15 (2) ◽  
pp. 525-537 ◽  
Author(s):  
Neza Rahayu Palapa ◽  
Tarmizi Taher ◽  
Bakri Rio Rahayu ◽  
Risfidian Mohadi ◽  
Addy Rachmat ◽  
...  

The preparation of CuAl LDH and biochar (BC) composite derived from rice husk and its application as a low-cost adsorbent for enhanced adsorptive removal of malachite green has been studied. The composite was prepared by a one-step coprecipitation method and characterized by X-ray Diffraction (XRD), Fourier Transform Infra Red (FTIR), Brunauer-Emmett-Teller (BET), and Scanning Electron Microscopy - Energy Dispersive X-ray (SEM−EDX). The result indicated that CuAl LDH was successfully incorporated with the biochar that evidenced by the broadening of XRD peak at 2θ = 24° and the appearance of a new peak at 1095 cm−1 on the FTIR spectra. The BET surface area analysis revealed that CuAl/BC composite exhibited a larger surface area (200.9 m2/g) that the original CuAl LDH (46.2 m2/g). Surface morphological changes also confirmed by SEM image, which showed more aggregated particles. The result of the adsorption study indicated the composite material was efficient in removing malachite green with Langmuir maximum adsorption capacity of CuAl/BC reaching 470.96 mg/g, which is higher than the original CuAl LDH 59.523 mg/g. The thermodynamic analysis suggested that the adsorption of malachite green occurs spontaneously (ΔG < 0 at all tested temperature) and endothermic nature. Moreover, the CuAl/BC composite showed strong potential as a low-cost adsorbent for cationic dye removal since it showed not only a high adsorption capacity but also good reusability. Copyright © 2020 BCREC Group. All rights reserved


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