scholarly journals CuAl LDH/Rice Husk Biochar Composite for Enhanced Adsorptive Removal of Cationic Dye from Aqueous Solution

2020 ◽  
Vol 15 (2) ◽  
pp. 525-537 ◽  
Author(s):  
Neza Rahayu Palapa ◽  
Tarmizi Taher ◽  
Bakri Rio Rahayu ◽  
Risfidian Mohadi ◽  
Addy Rachmat ◽  
...  
Keyword(s):  
Adsorption Capacity ◽  
Surface Area ◽  
Malachite Green ◽  
Rice Husk ◽  
Low Cost ◽  
Bet Surface Area ◽  
Maximum Adsorption Capacity ◽  
Cationic Dye ◽  
X Ray ◽  
Adsorptive Removal

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

scholarly journals Fly Ash Coated with Magnetic Materials: Improved Adsorbent for Cu (II) Removal from Wastewater

Materials ◽  
2020 ◽  
Vol 14 (1) ◽  
pp. 63
Author(s):  
Maria Harja ◽  
Gabriela Buema ◽  
Nicoleta Lupu ◽  
Horia Chiriac ◽  
Dumitru Daniel Herea ◽  
...  
Keyword(s):  
Fly Ash ◽  
Adsorption Capacity ◽  
Copper Ions ◽  
Synthetic Wastewater ◽  
Bet Surface Area ◽  
Isotherm Models ◽  
Batch Adsorption ◽  
Maximum Adsorption Capacity ◽  
Copper Adsorption ◽  
X Ray

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.

scholarly journals Magnetically Recyclable Wool Keratin Modified Magnetite Powders for Efficient Removal of Cu2+ Ions from Aqueous Solutions

Nanomaterials ◽  
2021 ◽  
Vol 11 (5) ◽  
pp. 1068
Author(s):  
Xinyue Zhang ◽  
Yani Guo ◽  
Wenjun Li ◽  
Jinyuan Zhang ◽  
Hailiang Wu ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Aqueous Solutions ◽  
Adsorption Capacity ◽  
Surface Area ◽  
Ion Concentration ◽  
Bet Surface Area ◽  
Chemical Compositions ◽  
Ion Adsorption ◽  
X Ray ◽  
Wool Keratin

The treatment of wastewater containing heavy metals and the utilization of wool waste are very important for the sustainable development of textile mills. In this study, the wool keratin modified magnetite (Fe3O4) powders were fabricated by using wool waste via a co-precipitation technique for removal of Cu2+ ions from aqueous solutions. The morphology, chemical compositions, crystal structure, microstructure, magnetism properties, organic content, and specific surface area of as-fabricated powders were systematically characterized by various techniques including field emission scanning electron microscopy (FESEM), energy dispersive spectroscopy (EDS), X-ray diffraction (XRD), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), vibrating sample magnetometer (VSM), thermogravimetric (TG) analysis, and Brunauer–Emmett–Teller (BET) surface area analyzer. The effects of experimental parameters such as the volume of wool keratin hydrolysate, the dosage of powder, the initial Cu2+ ion concentration, and the pH value of solution on the adsorption capacity of Cu2+ ions by the powders were examined. The experimental results indicated that the Cu2+ ion adsorption performance of the wool keratin modified Fe3O4 powders exhibited much better than that of the chitosan modified ones with a maximum Cu2+ adsorption capacity of 27.4 mg/g under favorable conditions (0.05 g powders; 50 mL of 40 mg/L CuSO4; pH 5; temperature 293 K). The high adsorption capacity towards Cu2+ ions on the wool keratin modified Fe3O4 powders was primarily because of the strong surface complexation of –COOH and –NH2 functional groups of wool keratins with Cu2+ ions. The Cu2+ ion adsorption process on the wool keratin modified Fe3O4 powders followed the Temkin adsorption isotherm model and the intraparticle diffusion and pseudo-second-order adsorption kinetic models. After Cu2+ ion removal, the wool keratin modified Fe3O4 powders were easily separated using a magnet from aqueous solution and efficiently regenerated using 0.5 M ethylene diamine tetraacetic acid (EDTA)-H2SO4 eluting. The wool keratin modified Fe3O4 powders possessed good regenerative performance after five cycles. This study provided a feasible way to utilize waste wool textiles for preparing magnetic biomass-based adsorbents for the removal of heavy metal ions from aqueous solutions.

scholarly journals Steel slag as low-cost adsorbent for the removal of phenanthrene and naphthalene

2018 ◽  
Vol 36 (3-4) ◽  
pp. 1160-1177 ◽  
Author(s):  
Liyun Yang ◽  
Xiaoming Qian ◽  
Zhi Wang ◽  
Yuan Li ◽  
Hao Bai ◽  
...  
Keyword(s):  
Adsorption Capacity ◽  
Low Cost ◽  
Steel Slag ◽  
Maximum Adsorption Capacity ◽  
Order Kinetic ◽  
Batch Experiments ◽  
Obvious Effect ◽  
X Ray ◽  
Order Kinetic Model ◽  
Langmuir Isotherm Model

This study investigates the removal effectiveness and characteristics of phenanthrene and naphthalene using low-cost steel slag with batch experiments. The adsorption characteristics of steel slag were measured and analysed using X-ray fluorescence, X-ray diffraction, and Fourier transform infrared spectroscopy. The batch experiments investigated the effect of the time gradient, pH, and steel slag dosage gradient on the adsorption of the steel slag. The results show that with time and dosage of steel slag increased, the adsorption capacity of phenanthrene and naphthalene increased and gradually became balanced, but pH had no obvious effect on the adsorption of phenanthrene and naphthalene. The Langmuir isotherm model best describes the phenanthrene and naphthalene removal by the steel slag, which shows the adsorption occurring in a monolayer. The maximum adsorption capacity of the steel slag to phenanthrene and naphthalene is 0.043 and 0.041 mg/g, respectively. A pseudo-first-order kinetic model can better represent the adsorption of phenanthrene and naphthalene by steel slag. The research demonstrates that the steel slag has a certain adsorption capacity for phenanthrene and naphthalene.

The Behaviors of Removing Silver Ions by Low-Cost Expanded Rice Husk, Nature Diatomite and Nature Bentonite as Sorbents

2012 ◽  
Vol 724 ◽  
pp. 472-475
Author(s):  
Xuan Liang ◽  
Xue Gang Luo ◽  
Xiao Yan Lin ◽  
Qiang Mei
Keyword(s):  
Adsorption Capacity ◽  
Rice Husk ◽  
Ph Value ◽  
Low Cost ◽  
Silver Ions ◽  
Maximum Adsorption Capacity ◽  
Removal Of Heavy Metals ◽  
Initial Ph ◽  
Influence Of Ph ◽  
By Products

Low cost industrial and agricultural by-products are promising materials for water pollution treatment such as removal of heavy metals. This work deals with removal of silver ions from solutions using expanded rice husk (ERH), nature diatomite (ND) and nature bentonite (NB). Firstly the influence of pH value of the solution on adsorption capacity for silver ions was studied, and then the effect of initial silver concentration on adsorbents adsorption capacity was investigated. The silver ions removal percentage increases with initial pH and achieves a maximum value of nearly 94% at pH= 5.0 ± 0.5 for ERH. The maximum adsorption capacity is 18.6 mg/g for ERH.

scholarly journals Adsorptive removal of azithromycin from aqueous solutions using raw and saponin-modified nano diatomite

2019 ◽  
Vol 80 (5) ◽  
pp. 939-949
Author(s):  
Siavash Davoodi ◽  
Behnaz Dahrazma ◽  
Nasser Goudarzi ◽  
Hajar Ghasemian Gorji
Keyword(s):  
Aqueous Solutions ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Low Cost ◽  
Maximum Adsorption Capacity ◽  
X Ray ◽  
Low Concentrations ◽  
Intra Particle Diffusion ◽  
High Concentrations

Abstract This study aims to investigate the performance and mechanism of raw (R-ND) and saponin-modified nano diatomite (M-ND) in the removal of azithromycin from aqueous solutions. Adsorbent characterization was performed using X-ray fluorescence, Brunauer–Emmett–Teller (BET), scanning electron spectroscopy, dynamic light scattering and energy-dispersive X-ray analyses. It was shown that the specific surface area of R-ND was 119.5 m2/g, 14-fold higher than that for raw diatomite, and for M-ND it was 90.1 m2/g. Various adsorption conditions, i.e. adsorbent dosage, pH, initial concentration and contact time were investigated. According to the results, despite reducing the specific surface area by 25%, modification of nano diatomite by saponin markedly enhanced its performance in the removal of azithromycin. The maximum adsorption capacity of R-ND and M-ND in the removal of azithromycin was 68 and 91.7 mg/g, respectively. Fourier transform infrared spectroscopy results revealed that azithromycin was adsorbed by O-H groups on the diatomite surface. Weber–Morris intra-particle diffusion (IPD) model suggested that while IPD is not the rate-controlling step in high concentrations of azithromycin, it is the only step that controls the rate of adsorption in low concentrations. In comparison to R-ND, M-ND showed a higher efficiency in the removal of azithromycin and, therefore, it can be used as a promising low-cost adsorbent to remove azithromycin from aqueous solutions.

scholarly journals The Role of the Aluminum Source on the Physicochemical Properties of γ-AlOOH Nanoparticles

2020 ◽  
Vol 39 (1) ◽  
pp. 89
Author(s):  
Rafael Romero Toledo ◽  
Luis M. Anaya Esparza ◽  
J. Merced Martínez Rosales
Keyword(s):  
Electron Microscopy ◽  
Physicochemical Properties ◽  
Surface Area ◽  
Low Cost ◽  
Nitrogen Adsorption ◽  
Bet Surface Area ◽  
Precipitation Method ◽  
X Ray ◽  
Aluminum Salts ◽  
Adsorption Desorption

The effect on the physicochemical properties of aluminum salts on the synthesis of γ-AlOOH nanostructures has been investigated in detail using a hydrolysis-precipitation method. X-ray fluorescence (XRF), Fourier transform infrared spectroscopy (FTIR), X-ray powder diffraction (XRD), field-emission scanning electron microscopy (FESEM) and transmission electron microscopy (TEM), were used to characterize the synthesized samples. The specific surface area, pore size distribution and pore diameter of the different γ-AlOOH structures were discussed by the N2 adsorption-desorption analysis. According to the results of the nanostructure, characterization revealed that for synthesized γ-AlOOH nanostructures from AlCl3 and Al(NO3)3, obvious XRD peaks corresponding to the bayerite phase are found indicating an impure γ-AlOOH phase. Furthermore, the nitrogen adsorption-desorption analysis indicated that the obtained γ-AlOOH nanoparticles from Al2(SO4)3 of technical grade (95.0 % of purity) and low cost, possess a high BET surface area of approximately 350 m2/g, compared to the obtained nanostructures from aluminum sources reactive grade, which was attributed to the presence of Mg (0.9 wt.%) in its nanostructure.

Methanol Dehydration to Dimethyl Ether over Silica Derived from Rice Husk as the Component-Based Catalysts

2014 ◽  
Vol 931-932 ◽  
pp. 17-21
Author(s):  
Nattaporn Chaba ◽  
Sutasinee Neramittagapong ◽  
Arthit Neramittagapong
Keyword(s):  
Surface Area ◽  
Dimethyl Ether ◽  
Rice Husk ◽  
Reaction Temperature ◽  
Methanol Conversion ◽  
Packed Bed Reactor ◽  
Bet Surface Area ◽  
Gravimetric Analysis ◽  
Methanol Dehydration ◽  
X Ray

Dimethyl Ether (DME) an alternative fuel was synthesized by methanol dehydration over the silica-based catalysts. Silica extracted from both rice husk (A) and rice-husk ash (B) was used as the precursors for preparing the catalysts. The SiO2/Al2O3 and the SAPO catalysts prepared from that silica were analyzed using X-ray diffraction (XRD), N2 adsorption (BET surface area), X-ray fluorescence (XRF), NH3 temperature-programmed desorption (NH3-TPD), and thermal gravimetric analysis (TGA). The effects of reaction temperature on the methanol selectivity and conversion to dimethyl ether were investigated. The methanol dehydration reactions were carried out in a packed-bed reactor at the reaction temperature of 250-350°C. DME was the major product and formed with selectivity of 57% over SAPO-B. An increasing of the reaction temperatures resulted in the enhancing of methanol conversion. The highest methanol conversion of 93% was achieved at 325°C. The method of silica extraction had an effect on the selectivity to DME due to the higher BET surface area.

scholarly journals Adsorptive Removal of Fe (II) By NaOH Treated Rice Husk: Adsorption Equilibrium And Kinetics

2021 ◽  
Vol 14 (14) ◽  
pp. 75-82
Author(s):  
Sunita Shrestha ◽  
Anita Kumari Dhami ◽  
Armila Rajbhandari Nyachhyon
Keyword(s):  
Surface Area ◽  
Rice Husk ◽  
Adsorption Process ◽  
Low Cost ◽  
Second Order ◽  
Maximum Efficiency ◽  
Maximum Adsorption Capacity ◽  
Adsorption Method ◽  
Equilibrium And Kinetics ◽  
Pseudo Second Order

The low cost adsorbents were prepared from raw rice husk (RRH) and NaOH treated rice husk (NRH). Then prepared materials were characterized by XRD, FTIR and surface area of rice husk adsorbent were determined by methylene blue adsorption method. XRD showed amorphous nature with low crystallinity of the material. The FTIR spectra showed the presence of oxygenated functional groups such as ester, phenol, carbonyl and silica on the material. The surface area of RRH and NRH were found to be 387 and 417 m2/g respectively. Thus, prepared adsorbents were used for the removal of Fe(II) ion from aqueous solution. The influence of various parameters like pH, adsorbent doge, and contact time were studied for the better adsorption of Fe(II) on rice husk adsorbents. Results revealed that the maximum efficiency was achieved at pH 3 for Fe(II). The adsorption process was found to be best fitted to Langmuir adsorption isotherm model controlled by pseudo-second–order kinetics with the rate constant value i.e. 0.0218 and 0.0235 g/(mg·min) for RRH and NRH respectively.  The χ2 values of pseudo second order was found to be lower which confirmed chemisorption, involving ion exchange and valence forces through sharing or exchange of electrons between adsorbent and adsorbate. The maximum adsorption capacity for Fe(II) on RRH and NRH was found to be 2.9 mg/g and 5.6 mg/g respectively. The positive ∆G value represents the randomness of the system during adsorption process. The slope of the linear plot of Qt vs t0.5 was linear but not passed through the origin, which indicates that, the intraparticle diffusion was not only rate controlling step. Temkin value showed the maximum binding energy (KT) for NRH was 16.4 L/g and for RRH it was 12.2 L/g. 

Tamanrasset’s Clay Characterization and Use as Low Cost, Ecofriendly and Sustainable Material for Water Treatment: Progress and Challenge in Copper Cu (II)

2021 ◽  
Vol 406 ◽  
pp. 457-472
Author(s):  
Aicha Kourim ◽  
Moulay Abderrahmane Malouki ◽  
Aicha Ziouche ◽  
Mouna Boulahbal ◽  
Madjda Mokhtari
Keyword(s):  
Adsorption Capacity ◽  
Metal Ion ◽  
Low Cost ◽  
Ion Concentration ◽  
Maximum Adsorption Capacity ◽  
X Ray Diffraction ◽  
X Ray ◽  
Pseudo Second Order ◽  
Equilibrium Process

In this study, the adsorption of copper Cu (II) from aqueous solution, on Tamanrasset’s clay which is low cost adsorbent, was studied using batch experiments. The adsorption study includes both equilibrium adsorption isotherms and kinetics. The characterization of the adsorbent necessitated several methods such as X-Ray Diffraction, Scanning Electron Microscopy coupled with Energy Dispersive X-ray, BET for specific surface area determination, Fourier transform infrared spectroscopy and thermogravimetric analysis. Indeed, various parameters were investigated such as contact time, initial metal ion concentration, mass of solid, pH of the solution and temperature. The adsorption process as batch study was investigated under the previews experimental parameters. The results revealed that the adsorption capacity of Cu2+ is maximized at naturel pH of metal 5.5. Removal of copper by the clay of Tamanrasset (kaolinite) achieved equilibrium within 50 minutes; the results obtained were found to be fitted by the pseudo-second order kinetics model. The equilibrium process was well described by the Langmuir model and the maximum adsorption capacity was found to be 26.59 mg/g.

scholarly journals COPPER HEXACYANOFERRATE (II): SYNTHESIS, CHARACTERIZATION, AND CESIUM, STRONTIUM ADSORBENT APPLICATION

2021 ◽  
Author(s):  
Dinh Trung Nguyen ◽  
Vu Tram Anh Le ◽  
Dong Phuong Truong ◽  
Thi Dan Thy Kieu ◽  
Tran Thuy Hong Nguyen ◽  
...  
Keyword(s):  
Low Cost ◽  
Bet Surface Area ◽  
Precipitation Method ◽  
Maximum Adsorption Capacity ◽  
X Ray Diffraction ◽  
Copper Hexacyanoferrate ◽  
X Ray ◽  
Transmission Electron ◽  
High Concentrations ◽  
Co Precipitation

Low-cost nanoscale copper hexacyanoferrate (CuHF), a good selective adsorbent for cesium (Cs+) removal, was prepared using the chemical co-precipitation method. Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), energy-dispersive X-ray spectroscopy (EDS), and high-resolution transmission electron microscopy (HR-TEM) were conducted to determine the CuHF morphology. Copper hexacyanoferrate, Cu13[Fe(CN)6]14.(2K).10H2O, has a cubic structure (space group F-43m) in the range of 10-30 nm and a Brunauer-Emmett-Teller (BET) surface area of 462.42 m2/g. The removal of Cs+ and Sr2+ is dependent on pH; the maximum adsorption capacity (qmax) of CuHF is achieved at a pH = 6. From the Langmuir model, qmax = 143.95 mg/g for Cs+ and 79.26 mg/g for Sr2+, respectively. At high concentrations, Na+, Ca2+, and K+ ions have very little effect on Cs+ removal, and Na+ and K+ ions have a higher affinity for removing Sr2+ than Ca2+ at all concentrations. CuHF has a high affinity for alkaline cations in the order: Cs+ > K+ > Na+ > Ca2+ > Sr2+, as proposed and discussed.

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