scholarly journals Barium/Cobalt@Polyethylene Glycol Nanocomposites for Dye Removal from Aqueous Solutions

Polymers ◽  
2021 ◽  
Vol 13 (7) ◽  
pp. 1161
Author(s):  
Somayeh Rahdar ◽  
Abbas Rahdar ◽  
Mostafa Sattari ◽  
Laleh Divband Hafshejani ◽  
Athanasia K. Tolkou ◽  
...  
Keyword(s):  
Polyethylene Glycol ◽  
Aqueous Solutions ◽  
Removal Efficiency ◽  
Contact Time ◽  
Skin Diseases ◽  
Freundlich Isotherm ◽  
Order Kinetic ◽  
Initial Concentration ◽  
Adsorbent Dosage ◽  
Order Kinetic Model

Dyes are known as one of the most dangerous industrial pollutants which can cause skin diseases, allergy, and provoke cancer and mutation in humans. Therefore, one of the important environmental issues is the effective removal of dyes from industrial wastewater. In the current work, BaFe12O19/CoFe2O4@polyethylene glycol (abbreviated as BFO/CFO@PEG) nanocomposite was synthesized and evaluated regarding its capacity for adsorptive removal of a model dye Acid Blue 92 (denoted as AB92) from aqueous solutions. The characteristics of the prepared nanocomposite was determined by tests such as X-ray diffraction (XRD), scanning electron microscope (SEM), vibration sample magnetization (VSM), and Fourier transform infrared spectroscopy (FTIR). The effects of conditional parameters including pH (2–12), initial concentration of dye (20–100 mg/L), adsorbent dosage (0.02–0.1 g/L) and contact time (0-180 min) on the adsorption of dye were investigated and then optimized. The results indicated that with the increase of the adsorbent dosage from 0.02 to 0.1 g/L, the removal efficiency increased from 74.1% to 78.6%, and the adsorbed amount decreased from 148.25 to 31.44 mg/g. The maximum removal efficiency (77.54%) and adsorption capacity (31.02 mg/g) were observed at pH 2. Therefore, the general optimization conditions revealed that the maximum adsorption efficiency of dye was obtained in condition of initial concentration of 20 mg/L, contact time of 1 h and pH of solution equal 2. The adsorption isotherm and kinetic data were evaluated using a series of models. The pseudo-second order kinetic model and Freundlich isotherm model show the best fitting with experimental data with R2∼0.999.

scholarly journals Adsorption of Nickel and Chromium From Aqueous Solutions Using Copper Oxide Nanoparticles: Adsorption Isotherms, Kinetic Modeling, and Thermodynamic Studies

2019 ◽  
Vol 6 (2) ◽  
pp. 66-74 ◽  
Author(s):  
Raziyeh Hosseini ◽  
Mohammad Hossein Sayadi ◽  
Hossein Shekari
Keyword(s):  
Aqueous Solutions ◽  
Copper Oxide ◽  
Removal Efficiency ◽  
Contact Time ◽  
Removal Rate ◽  
Copper Oxide Nanoparticles ◽  
Isotherm Models ◽  
Oxide Nanoparticles ◽  
Initial Concentration ◽  
Adsorbent Dosage

The research was conducted with an aim to assess the efficiency of copper oxide nanoparticles as an adsorbent to remove Ni and Cr. The effect of pH, adsorbent dosage, contact time, initial concentration of metals (Ni and Cr) on the adsorption rate was evaluated and removal of these elements from aqueous solutions was measured using Atomic Absorption Spectrum System (Conter AA700). Moreover, the kinetic and isotherm besides thermodynamic adsorption models were assessed. The highest Ni and Cr removal rate occurred at an optimal pH of 7, and an initial concentration of 30 mg/L, a time period of 30 minutes, and 1 g/L of copper oxide nanoparticles. In fact, with the increase of adsorbent dosage and contact time, the removal efficiency increased and with initial concentration increase of Ni and Cr ions, the removal efficiency reduced. The correlation coefficient of isotherm models viz. Langmuir, Freundlich, Temkin, Redlich-Peterson, and Koble-Corrigan showed that Ni and Cr adsorption via copper oxide nanoparticles better follows the Langmuir model in relation to other models. The results showed that kinetic adsorption of Ni and Cr via copper oxide nanoparticles follows the second order pseudo model with correlation coefficients above 0.99. In addition, the achieved thermodynamic constants revealed that the adsorption process of metals (i.e., Ni and Cr) via copper oxide nanoparticles was endothermic and spontaneous and the reaction enthalpy values for these metals were 17.727 and 11.862 kJ/mol, respectively. In conclusion, copper oxide nanoparticles can be used as effective and environmentally compatible adsorbents to remove Ni and Cr ions from the aqueous solutions

scholarly journals Evaluation of insoluble xanthate and crosslinked starch-graft-polyacrylamide-co-sodium xanthate for the adsorption of Cu(II) in aqueous solutions

2015 ◽  
Vol 21 (4) ◽  
pp. 465-476
Author(s):  
Jun Tan ◽  
Xiaoyan Wei ◽  
Yuxia Ouyang ◽  
Rui Liu ◽  
Ping Sun ◽  
...  
Keyword(s):  
Aqueous Solutions ◽  
Removal Efficiency ◽  
Copper Ions ◽  
Physical Adsorption ◽  
Freundlich Isotherm ◽  
Absorption Capacity ◽  
Synthetic Wastewater ◽  
Ionic Exchange ◽  
Order Kinetic ◽  
Order Kinetic Model

The effectiveness of insoluble xanthate (ISX) and crosslinked starch-graft-polyacrylamide-co-sodium xanthate (CSAX) for Cu(II) removal from wastewater was evaluated. The two types of xanthates were characterized by SEM, XRD, FTIR, and elemental analysis. Also, the factors influencing adsorption behaviors of copper ions from aqueous solutions were investigated. The results indicated CSAX had higher absorption capacity for Cu(II) than ISX because it contained more N and S. While as far as the removal efficiency was concerned, ISX was better than CSAX for its strong ligand-CSS- groups. The removal efficiency of Cu(II) onto CSAX and ISX increased with the increase in pH. The mechanism for Cu(II) adsorption was ionic exchange for ISX whereas both ion exchange and physical adsorption contributed to adsorption by CSAX. The adsorption kinetics of ISX and CSAX for Cu(II) were favorably described by the pseudo-second-order kinetic model, and the adsorption isotherms were described well with the Freundlich isotherm model. The study with synthetic wastewater showed CSAX was a worthwhile alternative to the traditional ISX only when the wastewater contained both Cu(II) and turbidity.

scholarly journals Removal of metoprolol from aqueous solutions by the activated carbon prepared from pine cones

2019 ◽  
Vol 6 (2) ◽  
pp. 81-88 ◽  
Author(s):  
Dariush Naghipour ◽  
Abdoliman Amouei ◽  
Kamran Taher Ghasemi ◽  
Kamran Taghavi
Keyword(s):  
Activated Carbon ◽  
Aqueous Solutions ◽  
Adsorption Capacity ◽  
Removal Efficiency ◽  
Contact Time ◽  
Wastewater Treatment Plants ◽  
Order Kinetic ◽  
Initial Concentration ◽  
Pine Cones ◽  
Adsorbent Dose

Background: Metoprolol (MTP) with its low biodegradability is one of the most dominant micropollutant in the effluent of wastewater treatment plants. The aim of this study was to investigate the removal of metoprolol from aqueous solutions by the activated carbon prepared from pine cones. Methods: The pine cones were activated using thermal activation method. Characteristics of the adsorbent were determined using Brunauer-Emmett-Teller (BET) and scanning electron microscopy (SEM). In this study, the influent of different parameters such as pH, contact time, initial concentrations of metoprolol, adsorbent dose, temperature, adsorption isotherms, and kinetics were investigated. Results: The maximum removal efficiency of MTP (89.2%) was obtained at pH=8.5, adsorbent dose=1.5 g, contact time=60 min, and initial concentration=50 mg/L. By increasing the adsorbent dose, the removal efficiency also increased, but the adsorption capacity decreased, however, by increasing the initial concentration, the removal efficiency decreased, but the adsorption capacity increased. The isotherm experimental data for metoprolol was best fitted using the Langmuir model, and kinetic data were better described by pseudo-second-order kinetic model. The thermodynamic study indicated that the adsorption of MTP by the adsorbent was feasible, spontaneous, and endothermic. Conclusion: MTP removal by the activated carbon prepared from pine cones showed that this natural adsorbent is appropriate for removal of metoprolol from aqueous solutions regarding cost, efficiency, and production method.

scholarly journals The Removal of Uranium and Thorium from Their Aqueous Solutions by 8-Hydroxyquinoline Immobilized Bentonite

Minerals ◽  
2019 ◽  
Vol 9 (10) ◽  
pp. 626 ◽  
Author(s):  
Salah ◽  
Gaber ◽  
Kandil
Keyword(s):  
Aqueous Solutions ◽  
Metal Ions ◽  
Langmuir Isotherm ◽  
Freundlich Isotherm ◽  
Order Kinetic ◽  
X Ray Diffraction ◽  
Solution Ph ◽  
X Ray ◽  
Order Kinetic Model ◽  
Pseudo Second Order

The sorption of uranium and thorium from their aqueous solutions by using 8-hydroxyquinoline modified Na-bentonite (HQ-bentonite) was investigated by the batch technique. Na-bentonite and HQ-bentonite were characterized by X-ray fluorescence (XRF), X-ray diffraction (XRD), scanning electron microscopy (SEM), and Fourier Transform Infrared (FTIR) spectroscopy. Factors that influence the sorption of uranium and thorium onto HQ-bentonite such as solution pH, contact time, initial metal ions concentration, HQ-bentonite mass, and temperature were tested. Sorption experiments were expressed by Freundlich and Langmuir isotherms and the sorption results demonstrated that the sorption of uranium and thorium onto HQ-bentonite correlated better with the Langmuir isotherm than the Freundlich isotherm. Kinetics studies showed that the sorption followed the pseudo-second-order kinetic model. Thermodynamic parameters such as ΔH°, ΔS°, and ΔG° indicated that the sorption of uranium and thorium onto HQ-bentonite was endothermic, feasible, spontaneous, and physical in nature. The maximum adsorption capacities of HQ-bentonite were calculated from the Langmuir isotherm at 303 K and were found to be 63.90 and 65.44 for U(VI) and Th(IV) metal ions, respectively.

Preparation and Application of Electrospinning Membranes of Thermoplastic Carboxymethyl Cellulose/PLA for Removal of Cu2+ from Aqueous Solutions

2012 ◽  
Vol 724 ◽  
pp. 61-64
Author(s):  
Ying Li ◽  
Xiao Yan Lin ◽  
Zhe Chen ◽  
Xue Guang Luo ◽  
Wei Li Zuo
Keyword(s):  
Tensile Strength ◽  
Aqueous Solutions ◽  
Removal Efficiency ◽  
Composite Membrane ◽  
Carboxymethyl Cellulose ◽  
Contact Time ◽  
Electrospinning Process ◽  
Cross Linking ◽  
Initial Concentration ◽  
The Cross

A composite membrane of thermoplastic carboxymethyl cellulose (TCMC) /PLA was prepared by electrospinning process, and crossliked by epichlorohydrin solution at different temperature. The cross-linking temperature was optimized by characterizing the morphology and tensile strength of the film. The optimal cross-linking temperature was 50°C. A composite membrane was used to remove Cu2+ from aqueous solutions, and the effects of initial concentration of Cu2+ and contact time on the removal efficiency of Cu2+ were investigated. The removal efficiency of Cu2+ was 13.78%, at the initial concentration of 40 mg·L-1 and contact time of 30s.

Extraction of Heavy Metals from Aqueous Medium by Husk Biomass: Adsorption Isotherm, Kinetic and Thermodynamic study

2019 ◽  
Vol 233 (2) ◽  
pp. 201-223 ◽  
Author(s):  
Khalida Naseem ◽  
Rahila Huma ◽  
Aiman Shahbaz ◽  
Jawaria Jamal ◽  
Muhammad Zia Ur Rehman ◽  
...  
Keyword(s):  
Metal Ions ◽  
Aqueous Medium ◽  
Contact Time ◽  
Metal Ion ◽  
Adsorption Process ◽  
Maximum Adsorption Capacity ◽  
Order Kinetic ◽  
Adsorbent Dosage ◽  
Adsorption Sites ◽  
Order Kinetic Model

Abstract This study describes the adsorption of Cu (II), Co (II) and Ni (II) ions from wastewater on Vigna radiata husk biomass. The ability of adsorbent to capture the metal ions has been found to be in the order of Ni (II)>Co (II) and Cu (II) depending upon the size and nature of metal ions to be adsorbed. It has been observed that percentage removal of Cu (II), Co (II) and Ni (II) ions increases with increase of adsorbent dosage, contact time and pH of the medium but up to a certain extent. Maximum adsorption capacity (qmax) for Cu (II), Co (II) and Ni (II) ions has been found to be 11.05, 15.04 and 19.88 mg/g, respectively, under optimum conditions of adsorbent dosage, contact time and pH of the medium. Langmuir model best fits the adsorption process with R2 value approaches to unity for all metal ions as compared to other models because adsorption sites are seemed to be equivalent and only monolayer adsorption may occur as a result of binding of metal ion with a functional moiety of adsorbent. Pseudo second order kinetic model best interprets the adsorption process of Cu (II), Co (II) and Ni (II) ions. Thermodynamic parameters such as negative value of Gibbs energy (∆G°) gives information about feasibility and spontaneity of the process. Adsorption process was found to be endothermic for Cu (II) ions while exothermic for Co (II) and Ni (II) ions as signified by the value of enthalpy change (∆H°). Husk biomass was recycled three times for removal of Ni (II) from aqueous medium to investigate its recoverability and reusability. Moreover V. radiata husk biomass has a potential to extract Cu (II) and Ni (II) from electroplating wastewater to overcome the industrial waste water pollution.

Adsorption of Pb(II) from Aqueous Solutions on Dithizone-Immobilized Coal Fly Ash

2020 ◽  
Vol 840 ◽  
pp. 57-63
Author(s):  
Dina Fitriana ◽  
Mudasir Mudasir ◽  
Dwi Siswanta
Keyword(s):  
Fly Ash ◽  
Adsorption Isotherm ◽  
Contact Time ◽  
Coal Fly Ash ◽  
Order Kinetic ◽  
Adsorbent Dosage ◽  
Activated Coal ◽  
Concentration Of Ions ◽  
Order Kinetic Model ◽  
Pseudo Second Order

Adsorption of Pb(II) ions onto selective adsorbent of dithizone-immobilized coal fly ash (DCFA) from Holcim, Cilacap, Indonesia has been investigated in batch experiments. Prepared coal fly ash (CFA) modified by immobilization of dithizone previously were characterized by FT-IR and XRD. Several parameters influencing the adsorption of Pb(II) ions such as effect of pH, adsorbent dosage, contact time and initial concentration of ions on the efficiency of the adsorption were studied. The optimum condition of Pb(II) adsorption was found at pH 5, adsorbent dosage 0.1 g, contact time 60 min and initial Pb(II) ions concentration of 60 mg L–1. The adsorption kinetics of Pb(II) ions on DCFA was found to follow a pseudo-second-order kinetic model. The adsorption isotherm data were fitted to the Langmuir model. Kinetics and adsorption isotherm studies suggest that the capacity and affinity of the DCFA in adsorbing Pb(II) ions is significantly improved compared to those of non-immobilized activated coal fly ash (ACFA).

scholarly journals Nano-TiO2, ultrasound and sequential nano-TiO2/ultrasonic degradation of N-acetyl-para-aminophenol from aqueous solution

2017 ◽  
Vol 15 (6) ◽  
pp. 1015-1027 ◽  
Author(s):  
Olushola S. Ayanda ◽  
Simphiwe M. Nelana ◽  
Leslie F. Petrik ◽  
Eliazer B. Naidoo
Keyword(s):  
Electron Microscopy ◽  
Aqueous Solution ◽  
Removal Efficiency ◽  
Treatment Process ◽  
Freundlich Isotherm ◽  
Attenuated Total Reflection ◽  
Order Kinetic ◽  
Nano Tio2 ◽  
Transmission Electron ◽  
Order Kinetic Model

Abstract The application of nano-TiO2 as adsorbent combined with ultrasound for the degradation of N-acetyl-para-aminophenol (AAP) from aqueous solution was investigated. The nano-TiO2 was characterized by means of powder X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy dispersive spectroscopy (EDS), and attenuated total reflection–Fourier transform infrared spectroscopy (ATR-FTIR). Experimental results revealed that the adsorption of AAP by nano-TiO2 fitted the pseudo-second-order kinetic model, the equilibrium could be explained by the Freundlich isotherm and the treatment process is exothermic. The optimum removal efficiency of AAP (128.89 mg/g (77.33%)) was achieved at pH 4 when 0.03 g of nano-TiO2 was mixed with 50 mL of 100 mg/L AAP aqueous solution at ambient temperature, 60 min contact time, and a stirring speed of 120 rpm. Ultrasound at 20 kHz and pH 3 was favorable and it resulted in 52.61% and 57.43% removal efficiency with and without the addition of nano-TiO2, respectively. The degradation of AAP by ultrasound followed by nano-TiO2 treatment resulted in approximately 99.50% removal efficiency. This study showed that a sequential ultrasound and nano-TiO2 treatment process could be employed for the removal of AAP or other emerging water and wastewater contaminants.

scholarly journals UV Activation of Persulfate for Removal of Penicillin G Antibiotics in Aqueous Solution

2017 ◽  
Vol 2017 ◽  
pp. 1-6 ◽  
Author(s):  
Samira Norzaee ◽  
Edris Bazrafshan ◽  
Babak Djahed ◽  
Ferdos Kord Mostafapour ◽  
Razieh Khaksefidi
Keyword(s):  
Reaction Time ◽  
Removal Efficiency ◽  
Penicillin G ◽  
Aquatic Environments ◽  
Order Kinetic ◽  
Initial Concentration ◽  
First Order ◽  
The World ◽  
Order Kinetic Model ◽  
Activated Persulfate

Penicillin G (PG) is one of the most widely consumed antibiotics around the world. Release of PG in environment may lead to contamination of water resources. The aim of the present work is to assess feasibility of applying UV-activated persulfate process in removal of PG from aquatic environments. The study examined the effect of pH (3–11), persulfate initial concentration (0.5–3 mM), reaction time (15–90 minutes), and initial concentration of PG (0.02–0.14 mM) on PG decomposition. Also, the pseudo-first-order kinetic model was used for kinetic analysis of PG removal. The results indicated that UV-activated persulfate process can effectively eliminate PG from water. The highest PG removal efficiency was obtained as 94.28% at pH 5, and the decomposition percentage was raised by increasing persulfate dose from 0.5 to 3 mM and the reaction time from 15 to 90 minutes. Besides, the removal efficiency decreased through increasing the initial concentration of PG. UV-activated persulfate process effectively decomposes PG and eliminates it from water.

scholarly journals Benzene Removal by Iron Oxide Nanoparticles Decorated Carbon Nanotubes

2016 ◽  
Vol 2016 ◽  
pp. 1-10 ◽  
Author(s):  
Aamir Abbas ◽  
Basim Ahmed Abussaud ◽  
Ihsanullah ◽  
Nadhir A. H. Al-Baghli ◽  
Marwan Khraisheh ◽  
...  
Keyword(s):  
Carbon Nanotubes ◽  
Iron Oxide ◽  
Iron Oxide Nanoparticles ◽  
Contact Time ◽  
Batch Adsorption ◽  
Oxide Nanoparticles ◽  
Order Kinetic ◽  
Initial Concentration ◽  
Adsorbent Dosage ◽  
Benzene Removal

In this paper, carbon nanotubes (CNTs) impregnated with iron oxide nanoparticles were employed for the removal of benzene from water. The adsorbents were characterized using scanning electron microscope, X-ray diffraction, BET surface area, and thermogravimetric analysis. Batch adsorption experiments were carried out to study the adsorptive removal of benzene and the effect of parameters such as pH, contact time, and adsorbent dosage. The maximum removal of benzene was 61% with iron oxide impregnated CNTs at an adsorbent dosage 100 mg, shaking speed 200 rpm, contact time 2 hours, initial concentration 1 ppm, and pH 6. However, raw CNTs showed only 53% removal under same experimental conditions. Pseudo-first-order kinetic model was found well to describe the obtained data on benzene removal from water. Initial concentration was varied from 1 to 200 mg/L for isotherms study. Langmuir isotherm model was observed to best describe the adsorption data. The maximum adsorption capacities were 987.58 mg/g and 517.27 mg/g for iron oxide impregnated CNTs and raw CNTs, respectively. Experimental results revealed that impregnation with iron oxide nanoparticles significantly increased the removal efficiency of CNTs.

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