scholarly journals Diverse Surface Chemistry of Cobalt Ferrite Nanoparticles to Optimize Copper(II) Removal from Aqueous Media

Materials ◽  
2020 ◽  
Vol 13 (7) ◽  
pp. 1537 ◽  
Author(s):  
Kosmas Vamvakidis ◽  
Theodora-Marianna Kostitsi ◽  
Antonis Makridis ◽  
Catherine Dendrinou-Samara

Water pollution by heavy metals is one of the most serious worldwide environmental issues. With a focus on copper(II) ions and copper complex removal, in the present study, ultra-small primary CoFe2O4 magnetic nanoparticles (MNPs) coated with octadecylamine (ODA) of adequate magnetization were solvothermally prepared. The surface modification of the initial MNPs was adapted via three different chemical approaches based on amine and/or carboxylate functional groups: (i) the deposition of polyethylimide (PEI), (ii) covalent binding with diethylenetriaminepentaacetic acid (DTPA), and (iii) conjugation with both PEI and DTPA, respectively. FT-IR, TGA, and DLS measurements confirmed that PEI or/and DTPA were successfully functionalized. The percentage of the free amine (−NH2) groups was also estimated. Increased magnetization values were found in case of PEI and DTPA-modified MNPs that stemmed from the adsorbed amine or oxygen ligands. Comparative UV–Vis studies for copper(II) ion removal from aqueous solutions were conducted, and the effect of time on the adsorption capacity was analyzed. The PEI-modified particles exhibited the highest adsorption capacity (164.2 mg/g) for copper(II) ions and followed the pseudo-second-order kinetics, while the polynuclear copper(II) complex Cux(DTPA)y was also able to be immobilized. The nanoadsorbents were quickly isolated from the solution by magnetic separation and regenerated easily by acidic treatment.

Author(s):  
Joshua O. Ighalo ◽  
Ibrahim O. Tijani ◽  
Oluwaseun J. Ajala ◽  
Fisayo O. Ayandele ◽  
Omodele A. Eletta ◽  
...  

Background: Modified bio-based adsorbents from plant sources can be used for pollution remediation by adsorption due to their low cost and availability in large quantities. Objective: In this study, the competitive biosorption of Pb(II) and Cu(II) by Micropogonias undulates functionalised fish scales (FFS) was conducted. The functionalisation was done by wet impregnation with Fe2+. Method: The biosorbent was characterised by Fourier Transform Infrared Spectroscopy (FT-IR), Scanning Electron Microscopy with Energy-Dispersive X-ray Spectroscopy (SEM-EDS) and Branueur–Emmett–Teller (BET) analyses. Results: The major constituents in the FFS were calcium and phosphorus from the collagen and apatite on the scales. Optimum removal efficiency for both metals was >99% at 10 g/l dosage. It was observed that the Langmuir isotherm model and the pseudo second order kinetics model were the best fit for the experimental data. The monolayer adsorption capacity of FFS for Pb(II) and Cu(II) was observed to be 96.15 mg/g and 100 mg/g respectively. Conclusion: The study revealed that the competitive biosorption of heavy metals can be achieved (at a good adsorption capacity) using functionalised Micropogonias undulates fish scales.


2021 ◽  
Vol 43 (4) ◽  
pp. 436-436
Author(s):  
Nida Shams Jalbani Nida Shams Jalbani ◽  
Amber R Solangi Amber R Solangi ◽  
Shahabuddin Memon Shahabuddin Memon ◽  
Ranjhan Junejo Ranjhan Junejo ◽  
Asif Ali Bhatti Asif Ali Bhatti

In current study, the diphenylaminomethylcalix[4]arene (3) was synthesized and immobilized onto silica surface to prepare a selective, regenerable and stable resin-4. The synthesized resin-4 has been characterized by FT-IR spectroscopy, scanning electron microscopy, energy-dispersive X-ray spectroscopy (EDX) and Brunauer-Emmett-Teller (BET) techniques. To check the adsorption capacity of resin-4, the batch and column adsorption methodology were applied and it has observed that the resin-4 was selectively removed Hg2+ ions under the optimized parameters. The maximum adsorption capacity was obtained at pH 9 using 25 mg/L of resin-4. Under the optimal conditions, different equilibrium, kinetic and thermodynamic models were applied to experimental data. The results show that adsorption mechanism is chemical in nature following Langmuir model with good correlation coefficient (R2=0.999) and having 712.098 (mmol/g) adsorption capacity. The energy of calculated from D-R model suggests the ion exchange nature of the adsorption phenomenon. Dynamic adsorption experiments were conducted using Thomas model. The maximum solid phase concentration (qo) was 7.5 and rate constant was found to be 0.176 with (R2=0.938) for Hg2+ ions. The kinetic study describes that the adsorption mechanism follows pseudo second order (R2=0.999). The thermodynamic parameters such as ∆H (0.032 KJ/mol) and ∆S (0.127 KJ/mol /K) and ∆G (-5.747,-6.306, -7.027 KJ/mol) shows that the adsorption of Hg2+ ion is endothermic and spontaneous. The reusability of resin-4 was also checked and it has observed that the after 15 cycle only 1.2 % adsorption reduces. Moreover, the resin-4 was applied on real wastewater samples obtained from local industrial zone of Karachi, Sindh-Pakistan.


2020 ◽  
Vol 10 (8) ◽  
pp. 2726 ◽  
Author(s):  
Roxana Nicola ◽  
Otilia Costişor ◽  
Mihaela Ciopec ◽  
Adina Negrea ◽  
Radu Lazău ◽  
...  

Magnetic iron oxide-silica shell nanocomposites with different iron oxide/silica ratio were synthesized and structurally characterized by Fourier transform infrared (FT-IR) spectroscopy, X-ray diffraction (XRD), small-angle neutron scattering, magnetic and N2-sorption studies. The composite that resulted with the best properties in terms of contact surface area and saturation of magnetization was selected for Pb2+ adsorption studies from aqueous media. The material presented good absorption capacity (maximum adsorption capacity 14.9 mg·g−1) comparable with similar materials presented in literature. Its chemico-physical stability and adsorption capacity recommend the nanocomposite as a cheap adsorbent material for lead.


Author(s):  
Qingqing Liu ◽  
Xiaoyan Li

The activated MgO was synthesized by microwave homo-precipitator method and characterized by SEM, EDS and FT-IR methods. It was used to adsorption of U(VI) from aqueous solution with batch system. The paper discussed the effect of pH, temperature, contact time, adsorbent dose and initial U(VI) concentration on the adsorption. The results showed that activated MgO has good adsorption capacity for U(VI), the removal rate and equilibrium adsorption capacity reached 83.5% and 84.04mg·g−1 at pH 5.0, 15mg dose and 313K,respectively. The adsorption kinetics of U(VI) onto activated MgO were better fitted with pseudo-second-order kinetic.The adsorption isotherm data were fitted well to Freundlich isotherm model.The thermodynamic parameters showed that the adsorption process is endothermic and spontaneous.


2016 ◽  
Vol 2016 ◽  
pp. 1-11 ◽  
Author(s):  
Shaojun Huang ◽  
Chengzhang Ma ◽  
Yaozu Liao ◽  
Chungang Min ◽  
Ping Du ◽  
...  

Poly(1-amino-5-chloroanthraquinone) (PACA) nanofibrils were applied as novel nanoadsorbents for highly toxic mercury removal from aqueous solutions. A series of batch adsorption experiments were conducted to study the effect of adsorbent dose, pH, contact time, and metal concentration on Hg(II) uptake by PACA nanofibrils. Kinetic data indicated that the adsorption process of PACA nanofibrils for Hg(II) achieved equilibrium within 2 h following a pseudo-second-order rate equation. The adsorption mechanism of PACA nanofibrils for Hg(II) was investigated by Fourier transform-infrared (FT-IR) spectra and X-ray photoelectron spectroscopy (XPS) analyses. The adsorption isotherm of Hg(II) fitted well the Langmuir model, exhibiting superb adsorption capacity of 3.846 mmol of metal per gram of adsorbent. Lastly, we found out that the as-synthesized PACA nanofibrils are efficient in Hg(II) removal from real wastewater. Furthermore, five consecutive adsorption-desorption cycles demonstrated that the PACA nanofibrils were suitable for repeated use without considerable changes in the adsorption capacity.


2012 ◽  
Vol 30 (1) ◽  
pp. 1-21 ◽  
Author(s):  
R.B. Rabelo ◽  
R.S. Vieira ◽  
F.M.T. Luna ◽  
E. Guibal ◽  
M.M. Beppu

Cross-linked chitosan was synthesized with glutaraldehyde (chitosan–GLA) and epichlorohydrin (chitosan–ECH). The structures of these matrices were characterized by elemental analysis, Fourier-transform infrared spectrometry (FT-IR), the degree of de-acetylation and the surface topography as determined via scanning electron microscopy (SEM). After promoting interaction with the metal ion, the adsorbent was also studied using FT-IR and energy dispersive X-ray spectroscopy (EDXS). Adsorption studies for Cu(II) and Hg(II) ions were carried out in a batch process. The adsorption kinetics were tested using three models, viz. pseudo-first-order, pseudo-second-order and intra-particle diffusion. The experimental kinetic data were best fitted by the pseudo-second-order model for Cu(II) ions (R2 ≥ 0.98) and for Hg(II) ions (R2 = 0.99). Higher rate constants (k2) were obtained for the adsorption of Cu(II) ions onto chitosan–GLA [1.40 g/(mmol h)] and for Hg(II) ions onto raw chitosan [5.65 g/(mmol h)]. The adsorption rate depended on the concentration of Cu(II) and Hg(II) ions on the adsorbent surface and on the quantity of ions adsorbed at equilibrium. At 293 K, the Langmuir–Freundlich model provided a better fit to the adsorption isotherms on both raw and cross-linked chitosan membranes. The maximum adsorption capacity for Cu(II) ions was obtained with the chitosan–GLA matrix (2.7 mmol/g). A maximum adsorption capacity of 3.1 mmol/g was attained for Hg(II) ions onto the chitosan–ECH matrix.


2020 ◽  
Vol 9 (3) ◽  
pp. 197-206
Author(s):  
Thaharah Ramadhani ◽  
Faisal Abdullah ◽  
Indra Indra ◽  
Abrar Muslim ◽  
Suhendrayatna Suhendrayatna ◽  
...  

The use of a low-cost biosorbent prepared from Ipomoea pes-caprae stem for the adsorption of Cd(II) ions from aqueous solution at different contact times, biosorbent sizes, pH values, and initial Cd(II) ions concentration solution was investigated. The biosorbent was analyzed using Fourier-transform infrared spectroscopy (FT-IR) to find important IR-active functional groups. A scanning electron microscope (SEM) was used to examine the biosorbent morphology. The experimental results showed the highest Cd(II) ions adsorption was 29.513 mg/g  under an optimal condition as initial Cd(II) ions concentration of 662.77 mg/L, 1 g dose, 80-min contact time, pH 5, 75 rpm of stirring speed, 1 atm, and 30 oC. Cd(II) ions' adsorption kinetics obeys the linearized pseudo-second-order kinetics (R2 = 0.996), and the adsorption capacity is based on the optimal condition, and the rate attained was 44.444 mg/g and 0.097 g/mg. Min, respectively. Besides, the adsorption isotherms were very well fitted by the linearized Langmuir isotherm model, and the monolayer adsorption capacity and pore volume determined was 30.121 mg/g and 0.129 L/mg, respectively. These results indicated the chemisorption nature


2021 ◽  
Vol 185 (1) ◽  
pp. 42-50
Author(s):  
Gabriela BUEMA ◽  
Nicoleta LUPU ◽  
Horia CHIRIAC ◽  
Dumitru Daniel HEREA ◽  
Lidia FAVIER ◽  
...  

The fly ash generated from a Romanian power plant was used as a starting material in this study. The aim of the study was to obtain a low cost material based on the treatment of fly ash with Fe3O4 for utilization as an adsorbent for cadmium ion removal. The adsorbent that was synthesized was characterized using different techniques. The adsorption process was investigated by the batch technique at room temperature. The quantity of cadmium ion adsorbed was measured spectrophotometrically. The experimental data showed that the material can remove cadmium ions at all three working concentrations. The adsorption capacity increased with an increase in concentration, respectively contact time. The results were analyzed through two kinetic models: pseudo first order and pseudo second order. The kinetics results of cadmium adsorption onto a magnetic material are in good agreement with a pseudo second order model, with a maximum adsorption capacity of 4.03 mg/g, 6.73 mg/g, and 9.65 mg/g. Additionally, the pseudo second order model was linearized into its four types. The results indicated that the material obtained show the ability to remove cadmium ions from an aqueous solution.


2021 ◽  
Author(s):  
Chengchen Liu ◽  
Jiaxin Lin ◽  
Haojia Chen ◽  
Wanjun Wang ◽  
Yan Yang

Abstract The potential application of biochar in water treatment is attracting interest due to its sustainability and low production cost. In the present study, H3PO4-modified biochar (H-PBC), ethylenediaminetetraacetic acid-modified biochar (E-PBC), and NaOH-modified biochar (O-PBC) were prepared for Ni(II) and Pb(II) adsorption in an aqueous solution. Scanning electron microscopy (SEM), X-ray diffraction analysis, Brunauer–Emmett–Teller analysis, and Fourier transform infrared (FT-IR) spectroscopy were employed to characterize the as-obtained samples, and their capacities for Ni(II) and Pb(II) adsorption were determined. SEM showed that H-PBC retained the hierarchical porous structure of pristine biochar, and projections were observed on its surface. FT-IR showed that H-PBC possessed abundant oxygen-containing and phosphorus-containing functional groups on the surface. H-PBC, E-PBC, and O-PBC all exhibited excellent performance at Ni(II) and Pb(II) adsorption with qmax values of 64.94 mg/g, 47.17 mg/g, and 60.24 mg/g, and 243.90 mg/g, 156.25 mg/g, and 192.31 mg/g, respectively, which were significantly higher than the adsorption capacity (19.80 mg/g and 38.31 mg/g) of pristine biochar. Pseudo-second order models suggested that the adsorption process was controlled by chemical adsorption. Regeneration analysis showed that H-PBC had superior reusability characteristics. H-PBC had a greater adsorption capacity than other adsorbents due to its large specific surface area, and abundant oxygen-containing and phosphorus-containing functional groups. The results obtained in this study suggest that H-PBC is a promising adsorbent for the removal of heavy metals from aqueous solutions.


2010 ◽  
Vol 178 ◽  
pp. 8-16
Author(s):  
Liang Dong Feng ◽  
Bo Qing Chen ◽  
Ying Ying Shi ◽  
Ying Wei Guo ◽  
Jing Huang ◽  
...  

1, 10-phenanthroline and triethylamine modified palygorskites were prepared by microwave irradiation, and characterized with FT-IR technique. The effects of contact time, adsorbent dosage, and pH value of the initial solution on the adsorption characters of Mn2+ were investigated. The adsorption of Mn2+ from aqueous solutions using 1, 10-phenanthroline or triethylamine modified palygorskites were investigated. Experiment results indicated that 1,10-phenanthroline and triethylamine molecules have been successfully grafted to palygorskite. The adsorption was rapid during the first 5 minuts and equilibrium were attained within 60 minutes in the initial concentration of Mn2+ of 50 and 100 mg•L-1, and fast adsorption in the first 10 minutes and slowly increased with the contact time due to the adsorption of palygorskite. The 1, 10-phenanthroline modified palygorskites had higher adsorption capacity than triethylamine modified palygorskites. Compared with natural palggorskites, the Mn2+ ions adsorption capacities of palggorskite modified by 1, 10-phenanthroline or triethylamine were significantly improved. There were less difference in the adsorption capacity between different dasages of 1, 10-phenanthroline modified palygorskites, but the adsorption capacity of Mn2+ adsorbed onto triethylamine modified palygorskites decreased with increasing the dosages. A Lagergren pseudo-second order model best described the kinetics of adsorption of Mn2+ onto the modified palygorskites.


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