scholarly journals Influence of Magnetic Nanoparticles on Modified Polypyrrole/m-Phenylediamine for Adsorption of Cr(VI) from Aqueous Solution

Polymers ◽  
2020 ◽  
Vol 12 (3) ◽  
pp. 679 ◽  
Author(s):  
Thabiso Carol Maponya ◽  
Kabelo Edmond Ramohlola ◽  
Nazia Hassan Kera ◽  
Kwena Desmond Modibane ◽  
Arjun Maity ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Adsorption Capacity ◽  
Entropy Change ◽  
Significant Loss ◽  
Batch Adsorption ◽  
Maximum Adsorption Capacity ◽  
Transmission Electron ◽  
Magnetite Fe3o4 ◽  
Application Potential ◽  
Adsorption Desorption

A novel, modified polypyrrole/m-phenylediamine (PPy–mPD) composite, decorated with magnetite (Fe3O4) nanoparticles, and prepared via an in-situ oxidative polymerisation, was investigated. The PPy–mPD/Fe3O4 nanocomposite was employed for the removal of highly toxic oxyanion hexavalent chromium Cr(VI) from an aqueous solution. The structure and successful formation of the PPy–mPD/Fe3O4 nanocomposite was confirmed and investigated using various techniques. The presence of Fe3O4 was confirmed by high resolution transmission electron microscopy, with an appearance of Fe lattice fringes. The estimation of the saturation magnetisation of the nanocomposite, using a vibrating sample magnetometer, was observed to be 6.6 emu/g. In batch adsorption experiments, PPy–mPD/Fe3O4 nanocomposite (25 mg) was able to remove 99.6% of 100 mg/L of Cr(VI) at pH 2 and 25 °C. Adsorption isotherms were investigated at different Cr(VI) concentration (100–600 mg/L) and temperature (15–45 °C). It was deduced that adsorption follows the Langmuir model, with a maximum adsorption capacity of 555.6 mg/g for Cr(VI) removal. Furthermore, isotherm data were used to calculate thermodynamic values for Gibbs free energy, enthalpy change and entropy change, which indicated that Cr(VI) adsorption was spontaneous and endothermic in nature. Adsorption–desorption experiments revealed that the nanocomposite was usable for two consecutive cycles with no significant loss of adsorption capacity. This research demonstrates the application potential for the fascinating properties of PPy–mPD/Fe3O4 nanocomposite as a highly efficient adsorbent for the removal of heavy metal ions from industrial wastewater.

Removing Cd(II) from Aqueous Solution by Inverse Opal Hybrid SiO2

NANO ◽  
2020 ◽  
Vol 15 (04) ◽  
pp. 2050047
Author(s):  
Yanhong Wang ◽  
Xiuli Wang ◽  
Cuihong Wu ◽  
Xiaomei Wang ◽  
Xu Zhang
Keyword(s):  
Aqueous Solution ◽  
Adsorption Capacity ◽  
Ph Value ◽  
Pore Wall ◽  
Ionic Concentration ◽  
Batch Adsorption ◽  
Maximum Adsorption Capacity ◽  
Inverse Opal ◽  
Solution Ph ◽  
Adsorption Desorption

A hybrid adsorbent with inverse opal (IO) structure was prepared for removing Cd(II) from aqueous solution. The functional polymeric chains were grafted from the pore wall of IO silica to prepare the porous hybrid material by surface-initiated atom-transfer radical polymerization. Furthermore, the amidation reaction was carried out to obtain diethylenetriamine-modified hybrid adsorbent (IO SiO2-g-PAA-DETA). Batch adsorption of removing Cd(II) onto IO SiO2-g-PAA-DETA was studied as the effect of solution pH, adsorbent doses, contact time, ionic concentration, and temperature. When the grafted amount was 73%, the maximum adsorption capacity was obtained. The optimum adsorbent dose and pH value for adsorbing Cd(II) were found to be 5[Formula: see text]g/L and 0.5[Formula: see text]g/L, respectively. The adsorption capacity was almost unaffected by Na[Formula: see text] at low concentrations. The adsorption data was depicted by the corresponding models and the results displayed that adsorbing Cd(II) on IO SiO2-g-PAA-DETA followed the Freundlich and pseudo-first-order model. In addition, after six adsorption–desorption cycles, IO adsorbent could remain above 80% of the first adsorption ability while it was washed using 0.025[Formula: see text]M EDTA.

scholarly journals OXIDATION OF CARBON NANOTUBES USING FOR Cu(II) ADSORPTION FROM AQUEOUS SOLUTION

2019 ◽  
Vol 128 (1B) ◽  
pp. 5
Author(s):  
Nguyễn ĐỨC Vũ Quyên ◽  
Trần Ngọc Tuyền ◽  
Đinh Quang Khiếu ◽  
Đặng Xuân Tín ◽  
Bùi Thị Hoàng Diễm ◽  
...  
Keyword(s):  
Carbon Nanotubes ◽  
Aqueous Solution ◽  
Electron Microscope ◽  
Adsorption Capacity ◽  
Chemical Vapour ◽  
Nitrogen Adsorption ◽  
Maximum Adsorption Capacity ◽  
X Ray ◽  
Transmission Electron ◽  
Adsorption Desorption

Carbon nanotubes (CNTs) synthesized by chemical vapour deposition without using hydrogen were oxidized with 0.1 M potassium permanganate at 40<sup>o</sup>C for 2 hours and exhibited high Cu<sup>II</sup> adsorption capacity from aqueous solution. X-ray diffraction (XRD), energy-dispersive X-ray spectroscopy (EDS), scanning electron microscope (SEM), transmission electron microscope (TEM) and nitrogen adsorption/desorption isotherms were used to characterize the oxidized CNTs. After oxidizing, the obtained CNTs were used to remove Cu<sup>II</sup> from aqueous solution. With Cu<sup>II</sup> initial concentration of 20 mg.L<sup>-1</sup>, at pH of 4 and adsorbent dosage of 0.2 g.L<sup>-1</sup>, the oxidized CNTs exhibited high Cu<sup>II</sup> adsorption ability with maximum adsorption capacity of 174.4 mg.g<sup>-1</sup>.

scholarly journals Biochar of Spent Coffee Grounds as Per Se and Impregnated with TiO2: Promising Waste-Derived Adsorbents for Balofloxacin

Molecules ◽  
2021 ◽  
Vol 26 (8) ◽  
pp. 2295
Author(s):  
Marwa El-Azazy ◽  
Ahmed S. El-Shafie ◽  
Hagar Morsy
Keyword(s):  
Adsorption Capacity ◽  
Batch Adsorption ◽  
Maximum Adsorption Capacity ◽  
Spent Coffee Grounds ◽  
Thermal Stabilities ◽  
Coffee Grounds ◽  
Bet Analysis ◽  
Pseudo Second Order ◽  
Set Up ◽  
Adsorption Desorption

Biochars (BC) of spent coffee grounds, both pristine (SCBC) and impregnated with titanium oxide (TiO2@SCBC) were exploited as environmentally friendly and economical sorbents for the fluroquinolone antibiotic balofloxacin (BALX). Surface morphology, functional moieties, and thermal stabilities of both adsorbents were scrutinized using SEM, EDS, TEM, BET, FTIR, Raman, and TG/dT analyses. BET analysis indicated that the impregnation with TiO2 has increased the surface area (50.54 m2/g) and decreased the pore size and volume. Batch adsorption experiments were completed in lights of the experimental set-up of Plackett-Burman design (PBD). Two responses were maximized; the % removal (%R) and the adsorption capacity (qe, mg/g) as a function of four variables: pH, adsorbent dosage (AD), BALX concentration ([BALX]), and contact time (CT). %R of 68.34% and 91.78% were accomplished using the pristine and TiO2@SCBC, respectively. Equilibrium isotherms indicated that Freundlich model was of a perfect fit for adsorption of BALX onto both adsorbents. Maximum adsorption capacity (qmax) of 142.55 mg/g for SCBC and 196.73 mg/g for the TiO2@SCBC. Kinetics of the adsorption process were best demonstrated using the pseudo-second order (PSO) model. The adsorption-desorption studies showed that both adsorbents could be restored with the adsorption efficiency being conserved up to 66.32% after the fifth cycles.

Removal of Cd(II) from Water System Using Novel Biosorbent Derived from Persimmon Fallen Leaves

2015 ◽  
Vol 1130 ◽  
pp. 685-688
Author(s):  
Rui Yi Fan ◽  
Qing Ping Yi ◽  
Qing Lin Zhang ◽  
Zheng Rong Luo
Keyword(s):  
Aqueous Solution ◽  
Metal Ions ◽  
Adsorption Capacity ◽  
Water System ◽  
Raw Material ◽  
Batch Adsorption ◽  
Diospyros Kaki ◽  
Cadmium Metal ◽  
Fallen Leaves ◽  
Adsorption Desorption

A biosorbent was prepared by treating the persimmon (Diospyros kaki Thunb.) fallen leaves with sodium hydroxide (NaOH). The NaOH concentration and stirring period for the preparation of the biosorbent were adjusted to optimise the Cd(I) adsorption capacity of the biosorbents. Removal of highly toxic Cadmium metal ions from water system using the optimal biosorbent named ‘NPFL’ was investigated using a mimic industrial column. The result showed that NPFL could remove Cd(II) in large quantities from aqueous solution with coexisting metal ions. The raw material, NPFL and Cd(II) loaded NPFL were characterized by SEM-EDS. The reusability of NPFL was also studied by batch adsorption-desorption test.

scholarly journals Removal of Arsenite from Water by Ce-Al-Fe Trimetal Oxide Adsorbent: Kinetics, Isotherms, and Thermodynamics

2016 ◽  
Vol 2016 ◽  
pp. 1-8 ◽  
Author(s):  
Cuizhen Sun ◽  
Jinwei Qiu ◽  
Zhibin Zhang ◽  
Taha F. Marhaba ◽  
Yanhao Zhang
Keyword(s):  
Adsorption Capacity ◽  
Standard Free Energy ◽  
Entropy Change ◽  
Maximum Adsorption Capacity ◽  
Transmission Electron ◽  
Adsorbent Surface ◽  
Adsorption Mode ◽  
Freundlich Adsorption Isotherm ◽  
Pseudo Second Order ◽  
Isotherms And Thermodynamics

Ce-Al-Fe trimetal oxide adsorbent was prepared. The morphology characteristics of the new adsorbent were analysed by the transmission electron microscope (SEM) method. The SEM results implied its ability in the adsorption of As (III). To verify the analyses, bench-scale experiments were performed for the removal of As (III) from water. In the experiments of adsorption, As (III) adsorption capacity of the trimetal oxide adsorbent was presented significantly higher than activated aluminium oxide and activated carbon. As (III) adsorption kinetics resembled pseudo-second-order adsorption mode. When initial As (III) concentration was 3, 8, and 10 mg·L−1, the maximum adsorption capacity achieved was 1.48, 3.73, and 5.12 mg·g−1, respectively. In addition, the experimental adsorption data were described well by the Freundlich adsorption isotherm model at 20, 30, and 40°C. The enthalpy change(ΔS), the standard free energy(ΔG), and entropy change(ΔH)indicated that the nature of As (III) adsorption was exothermic and spontaneous with increasing randomness on the interface of solid and liquid. And the adsorption mechanism can be interpreted as chemisorption with As (III) multilayer coverage formation on the adsorbent surface.

Cd(II) removal on surface-modified activated carbon: equilibrium, kinetics and mechanism

2016 ◽  
Vol 74 (8) ◽  
pp. 1800-1808 ◽  
Author(s):  
Jianjun Liang ◽  
Meiling Liu ◽  
Yufei Zhang
Keyword(s):  
Aqueous Solution ◽  
Activated Carbon ◽  
Adsorption Capacity ◽  
Orthogonal Experiment ◽  
Xrd Analysis ◽  
Bet Surface Area ◽  
Batch Adsorption ◽  
Maximum Adsorption Capacity ◽  
Modified Activated Carbon ◽  
Surface Modified

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.

scholarly journals Selective and rapid removal of Mo(VI) from water using functionalized Fe3O4-based Mo(VI) ion-imprinted polymer

2020 ◽  
Author(s):  
Lang Wu ◽  
Zhengwei Luo ◽  
Hui Jiang ◽  
Zijian Zhao ◽  
Wenhua Geng
Keyword(s):  
Adsorption Capacity ◽  
Isotherm Model ◽  
Batch Adsorption ◽  
Maximum Adsorption Capacity ◽  
Ion Imprinted Polymer ◽  
Imprinted Polymer ◽  
Adsorption Selectivity ◽  
X Ray ◽  
Ion Imprinted ◽  
Adsorption Desorption

Abstract Fe3O4 nanoparticles-based magnetic Mo(VI) surface ion-imprinted polymer (Mo(VI)-MIIP) was elaborated employing 4-vinyl pyridine as a functional monomer. The adsorbent preparation was confirmed by Fourier-transform infrared spectroscopy, scanning electron microscopy, energy dispersive X-ray spectrometry, X-ray diffraction, vibrating sample magnetometer, thermogravimetric analysis, and surface area analysis. Batch adsorption experiments displayed that the maximum adsorption capacity of Mo(VI)-MIIP was 296.40 mg g−1 at pH 3, while that of the magnetic non-imprinted polymer (MNIP) was only 147.10 mg g−1. The adsorption isotherm model was well-fitted by the Langmuir isotherm model. The adsorption experiments revealed that Mo(VI)-MIIP reached adsorption equilibrium within 30 min, and the kinetics data fitting showed that the pseudo-second-order kinetics model suitably described the adsorption process. Mo(VI)-MIIP exhibited an excellent adsorption selectivity to Mo(VI) in binary mixtures of Mo(VI)/Cr(VI), Mo(VI)/Cu(II), Mo(VI)/H2PO44-, Mo(VI)/Zn(II), and Mo(VI)/I–, with relative selectivity coefficients toward MNIP of 13.71, 30.27, 20.01, 23.53, and 15.89, respectively. After six consecutive adsorption-desorption cycles, the adsorption capacity of Mo(VI)-MIIP decreased by 9.5% (from 228.4 mg g−1 to 206.7 mg g−1 at initial Mo(VI) concentration of 250 mg L−1), demonstrating its reusability.

scholarly journals Removal of Phosphorus from Wastewater by Different Morphological Alumina

Molecules ◽  
2020 ◽  
Vol 25 (13) ◽  
pp. 3092
Author(s):  
Jianchuan Sun ◽  
Awang Gao ◽  
Xuhui Wang ◽  
Xiangyu Xu ◽  
Jiaqing Song
Keyword(s):  
Adsorption Capacity ◽  
Maximum Adsorption Capacity ◽  
X Ray Diffraction ◽  
Phosphorus Adsorption ◽  
X Ray ◽  
Transmission Electron ◽  
Ft Ir ◽  
Series Of Experiments ◽  
Level 1 ◽  
Adsorption Desorption

In this work, an organic-free method was used to synthesize different morphological boehmite by controlling the crystallization temperature, and alumina adsorbents were obtained by baking the boehmites at 500 °C. The alumina adsorbents were characterized by X-ray diffraction (XRD), High resolution transmission electron microscope (HRTEM), Fourier transform infrared (FT-IR), N2 adsorption/desorption analysis, and their phosphorus adsorption properties were comparatively investigated by a series of experiments. The results showed that the self-prepared alumina adsorbents were lamellar and fibrous material, while the industrial adsorbent was a granular material. The lamellar alumina adsorbents had the largest specific surface area and showed better phosphorus adsorption capacity. The maximum adsorption capacity could reach up to 588.2 mg·g−1; and only 0.8 g·L−1 of lamellar alumina adsorbent is needed to treat 100 mg·L−1 phosphorus solution under the Chinese level 1 discharge standard (0.5 mg·L−1). Further investigation suggests that the lamellar alumina adsorbent kept high adsorption capacity in various solution environments.

scholarly journals Synthesis and Characterization of CuFe2O4 Nanoparticles Modified with Polythiophene: Applications to Mercuric Ions Removal

Nanomaterials ◽  
2020 ◽  
Vol 10 (3) ◽  
pp. 586 ◽  
Author(s):  
Ayman H. Kamel ◽  
Amr A. Hassan ◽  
Abd El-Galil E. Amr ◽  
Hadeel H. El-Shalakany ◽  
Mohamed A. Al-Omar
Keyword(s):  
Electron Microscopy ◽  
Aqueous Solution ◽  
Maximum Adsorption Capacity ◽  
X Ray Diffraction ◽  
Solution Ph ◽  
X Ray ◽  
Transmission Electron ◽  
Enhanced Adsorption ◽  
Co Precipitation ◽  
Adsorption Desorption

In this research, CuFe2O4 nanoparticles were synthesized by co-precipitation methods and modified by coating with thiophene for removal of Hg(II) ions from aqueous solution. CuFe2O4 nanoparticles, with and without thiophene, were characterized by x-ray diffraction (XRD), Field emission scanning electron microscopy (FESEM), energy dispersive x-ray (EDX), high-resolution transmission electron microscopy (HRTEM) and Brunauer–Emmett–Teller (BET). Contact time, adsorbent dose, solution pH, adsorption kinetics, adsorption isotherm and recyclability were studied. The maximum adsorption capacity towards Hg2+ ions was 7.53 and 208.77 mg/g for CuFe2O4 and CuFe2O4@Polythiophene composite, respectively. Modification of CuFe2O4 nanoparticles with thiophene revealed an enhanced adsorption towards Hg2+ removal more than CuFe2O4 nanoparticles. The promising adsorption performance of Hg2+ ions by CuFe2O4@Polythiophene composite generates from soft acid–soft base strong interaction between sulfur group of thiophene and Hg(II) ions. Furthermore, CuFe2O4@Polythiophene composite has both high stability and reusability due to its removal efficiency, has no significant decrease after five adsorption–desorption cycles and can be easily removed from aqueous solution by external magnetic field after adsorption experiments took place. Therefore, CuFe2O4@Polythiophene composite is applicable for removal Hg(II) ions from aqueous solution and may be suitable for removal other heavy metals.

scholarly journals Preparation of ureido-functionalized PVA/silica mesoporous fibre membranes via electrospinning for adsorption of Pb2+ and Cu2+ in wastewater

2017 ◽  
Vol 76 (9) ◽  
pp. 2526-2534 ◽  
Author(s):  
Meimei Zhou ◽  
Weizhen Tang ◽  
Pingping Luo ◽  
Jiqiang Lyu ◽  
Aixia Chen ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Adsorption Capacity ◽  
Freundlich Isotherm ◽  
Isotherm Model ◽  
Maximum Adsorption Capacity ◽  
X Ray Diffraction ◽  
Transmission Electron ◽  
Langmuir Isotherm Model ◽  
Pseudo Second Order ◽  
Adsorption Desorption

Abstract Ureido-functionalized mesoporous polyvinyl alcohol/silica composite nanofibre membranes were prepared by electrospinning technology and their application for removal of Pb2+ and Cu2+ from wastewater was discussed. The characteristics of the membranes were investigated by scanning electron microscopy, transmission electron microscopy, X-ray diffraction, and N2 adsorption-desorption analysis. Results show that the membranes have long fibrous shapes and worm-like mesoporous micromorphologies. Fourier transform infrared spectroscopy confirmed the membranes were successfully functionalized with ureido groups. Pb2+ and Cu2+ adsorption behavior on the membranes followed a pseudo-second-order nonlinear kinetic model with approximately 30 minutes to equilibrium. Pb2+ adsorption was modelled using a Langmuir isotherm model with maximum adsorption capacity of 26.96 mg g−1. However, Cu2+ adsorption was well described by a Freundlich isotherm model with poor adsorption potential due to the tendency to form chelating complexes with several ureido groups. Notably, the membranes were easily regenerated through acid treatment, and maintained adsorption capacity of 91.87% after five regeneration cycles, showing potential for applications in controlling heavy metals-related pollution and metals reuse.

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