scholarly journals Adsorptive Removal of Antibiotic Ciprofloxacin from Aqueous Solution Using Protein-Modified Nanosilica

Polymers ◽  
2020 ◽  
Vol 12 (1) ◽  
pp. 57 ◽  
Author(s):  
Tien Duc Pham ◽  
Thi Ngan Vu ◽  
Hai Long Nguyen ◽  
Pham Hai Phong Le ◽  
Thi Sim Hoang
Keyword(s):  
Ionic Strength ◽  
Adsorption Isotherms ◽  
High Performance ◽  
Maximum Adsorption Capacity ◽  
Adsorption Mechanisms ◽  
Adsorptive Removal ◽  
Step Model ◽  
Anionic Species ◽  
Pseudo Second Order ◽  
Ft Ir

The present study aims to investigate adsorptive removal of molecular ciprofloxacin using protein-modified nanosilica (ProMNS). Protein was successfully extracted from Moringa seeds while nanosilica was synthesized from rice husk. Fourier-transform infrared (FTIR), ultraviolet visible (UV-Vis) and high-performance liquid chromatography (HPLC) were used to evaluate the characterization of protein. Adsorption of protein onto nanosilica at different pH and ionic strength was thoroughly studied to modify nanosilica surface. The removal efficiency of antibiotic ciprofloxacin (CFX) increased from 56.84% to 89.86% after surface modification with protein. Effective conditions for CFX removal using ProMNS were systematically optimized and found to be pH 7.0, adsorption time 90 min, adsorbent dosage 10 mg/mL, and ionic strength 1 mM KCl. A two-step model was successfully used to fit the adsorption isotherms of CFX onto ProMNS at different ionic strength while a pseudo-second-order model could fit adsorption kinetic of CFX onto ProMNS very well. Maximum adsorption capacity was very high that reached to 85 mg/g. Adsorption of CFX onto ProMNS decreased with increasing KCl concentration, suggesting that adsorption of CFX onto ProMNS is mainly controlled by electrostatic attraction between positively charged ProMNS surface and anionic species of CFX. Adsorption mechanisms of CFX onto ProMNS were discussed in detail based on adsorption isotherms, the change in surface charge by zeta potentail and the change in functional groups by FT-IR. The removal of CFX after three regenerations was greater than 73% while CFX removal from an actual hospital wastewater using ProMNS reached to 70%. Our results suggest that ProMNS is a new and eco-friendly adsorbent to remove antibiotics from aqueous solutions.

Efficient adsorption of chlorpyrifos onto modified activated carbon by gamma irradiation; a plausible adsorption mechanism

2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Mohamed S. Yahia ◽  
Ahmed S. Elzaref ◽  
Magdy B. Awad ◽  
Ahmed M. Tony ◽  
Ahmed S. Elfeky
Keyword(s):  
Gamma Irradiation ◽  
Area Measurement ◽  
Maximum Adsorption Capacity ◽  
X Ray Diffraction ◽  
X Ray ◽  
First Order ◽  
Pseudo Second Order ◽  
Ft Ir ◽  
Pseudo First Order ◽  
Kinetics Of

Abstract Commercial Granulated Active Carbon (GAC) has been modified using 10 Gy dose Gamma irradiation (GAC10 Gy) for increasing its ability of air purification. Both, the raw and treated samples were applied for removing Chlorpyrifos pesticide (CPF) from ambient midair. Physicochemical properties of the two materials were characterized by Fourier Transform Infrared (FT-IR) and Raman spectroscopy. The phase formation and microstructure were monitored using X-ray Diffraction (XRD), Scanning Electron Microscopy (SEM), supported with Energy-Dispersive X-ray (EDX). The Surface area measurement was detected using BET particle size prosometry. Obtained outcomes showed that, the maximum adsorption capacity, given by Langmuir equations, was greatly increased from 172.712 to 272.480 mg/g for GAC and GAC10 Gy, respectively, with high selectivity. The overall removal efficiency of GAC10 Gy was notably comparable to that of the original GAC-sorbent. The present study indicated that, gamma irradiation could be a promising technique for treating GAC and turned it more active in eliminating the pesticides pollutants from surrounding air. The data of equilibrium has been analyzed by Langmuir and Freundlich models, that were considerably better suited for the investigated materials than other models. The process kinetics of CPF adsorbed onto both tested carbon versions were found to obey the pseudo first order at all concentrations with an exception at 70 mg/l using GAC, where, the spontaneous exothermic adsorption of Chlorpyrifos is a strong function for the pseudo-first order (PFO) and pseudo second order (PSO) kinetics.

scholarly journals Sustainable Chromium (VI) Removal from Contaminated Groundwater Using Nano-Magnetite-Modified Biochar via Rapid Microwave Synthesis

Molecules ◽  
2020 ◽  
Vol 26 (1) ◽  
pp. 103
Author(s):  
Xiaoming Song ◽  
Yuewen Zhang ◽  
Nan Cao ◽  
Dong Sun ◽  
Zhipeng Zhang ◽  
...  
Keyword(s):  
Synthesis Method ◽  
Microwave Treatment ◽  
Contaminated Groundwater ◽  
Maximum Adsorption Capacity ◽  
Intraparticle Diffusion Model ◽  
Adsorption Mechanisms ◽  
Chromium Vi ◽  
Modified Biochar ◽  
Pseudo Second Order ◽  
Nano Fe3o4

This study developed a nano-magnetite-modified biochar material (m-biochar) using a simple and rapid in situ synthesis method via microwave treatment, and systematically investigated the removal capability and mechanism of chromium (VI) by this m-biochar from contaminated groundwater. The m-biochar was fabricated from reed residues and magnetically modified by nano-Fe3O4. The results from scanning electron microscopy (SEM) and X-ray diffraction (XRD) characterisations confirmed the successful doping of nano-Fe3O4 on the biochar with an improved porous structure. The synthesised m-biochar exhibited significantly higher maximum adsorption capacity of 9.92 mg/g compared with that (8.03 mg/g) of the pristine biochar. The adsorption kinetics followed the pseudo-second-order model and the intraparticle diffusion model, which indicated that the overall adsorption rate of Cr(VI) was governed by the processes of chemical adsorption, liquid film diffusion and intramolecular diffusion. The increasing of the pH from 3 to 11 significantly affected the Cr(VI) adsorption, where the capabilities decreased from 9.92 mg/g to 0.435 mg/g and 8.03 mg/g to 0.095 mg/g for the m-biochar and pristine biochar, respectively. Moreover, the adsorption mechanisms of Cr(VI) by m-biochar were evaluated and confirmed to include the pathways of electrostatic adsorption, reduction and complexation. This study highlighted an effective synthesis method to prepare a superior Cr(VI) adsorbent, which could contribute to the effective remediation of heavy metal contaminations in the groundwater.

Selective Removal of Hg2+ Ions from Water Using New Functionalized Silica Resin: Equilibrium, Thermodynamics and Kinetic Modeling Studies

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
Keyword(s):  
Adsorption Capacity ◽  
Adsorption Mechanism ◽  
Solid Phase ◽  
Maximum Adsorption Capacity ◽  
Adsorption Phenomenon ◽  
Column Adsorption ◽  
Pseudo Second Order ◽  
Ft Ir ◽  
Wastewater Samples ◽  
Ft Ir Spectroscopy

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.

scholarly journals Adsorption of Tea Polyphenols using Microporous Starch: A Study of Kinetics, Equilibrium and Thermodynamics

Molecules ◽  
2019 ◽  
Vol 24 (8) ◽  
pp. 1449 ◽  
Author(s):  
Xianchun Hu ◽  
Xianfeng Du
Keyword(s):  
Physical Adsorption ◽  
Tea Polyphenols ◽  
Adsorptive Capacity ◽  
Partial Hydrolysis ◽  
Maximum Adsorption Capacity ◽  
Solution Ph ◽  
Long Term Storage ◽  
Langmuir Isotherm Model ◽  
Pseudo Second Order ◽  
Ft Ir

Microporous starch (MPS) granules were formed by the partial hydrolysis of starch using α–amylase and glucoamylase. Due to its biodegradability and safety, MPS was employed to adsorb tea polyphenols (TPS) based on their microporous characteristics. The influences of solution pH, time, initial concentration and temperature on the adsorptive capacity were investigated. The adsorption kinetics data conformed to the pseudo second–order kinetics model, and the equilibrium adsorption data were well described by the Langmuir isotherm model. According to the fitting of the adsorption isotherm formula, the maximum adsorption capacity of TPS onto MPS at pH 6.7 and T = 293 K was approximately 63.1 mg/g. The thermodynamic parameters suggested that the adsorption of TPS onto MPS was spontaneous and exothermic. Fourier transform infrared (FT–IR) analysis and the thermodynamics data were consistent with a physical adsorption mechanism. In addition, MPS-loaded TPS had better stability during long-term storage at ambient temperature.

scholarly journals Valorization of Uncharred Dry Leaves of Ficus benjamina towards Cr (VI) removal from Water: Efficacy Influencing Factors and mechanism

2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Preeti S. Kulkarni ◽  
Varuna S. Watwe ◽  
Abubakar J. Hipparge ◽  
Sana I. Sayyad ◽  
Rutika A. Sonawane ◽  
...  
Keyword(s):  
Influencing Factors ◽  
Maximum Adsorption Capacity ◽  
Equilibration Time ◽  
Aqueous Samples ◽  
Sorption Data ◽  
Maximum Sorption ◽  
Pseudo Second Order ◽  
Ft Ir ◽  
Better Than ◽  
Work Treatment

AbstractThe potential of uncharred biomaterial derived from dry leaves of Ficusbenjamina (Family: Moraceae,local name: Weeping Fig) plant to remove Cr(VI) from aqueous samples was investigated. In the present work, treatment of dilute acids was used for activating the adsorption centres on the biomass instead of cumbersome charring process. The plant material was characterized using FT-IR, FE-SEM and EDX. Various influencing factors such as pH of equilibrating solution, contact time, Cr (VI) concentrations, adsorbent dose and temperature were optimized to obtain maximum sorption efficacy. The interactions among the biomaterial and Cr (VI) in water were studied by fitting the sorption data in four different adsorption isotherms. The data fitting and experimental evidences indicated formation of monolayer of Cr(VI) over the biomass surface. The process followed pseudo-second order kinetics and was thermodynamically spontaneous under laboratory conditions and reached equilibrium in 24 hours. Maximum adsorption capacity of 56.82 mg/g was obtained at the pH 2 when the concentration before adsorption was 200 mg L−1 of Cr(VI) with 24 hours of equilibration time and 2.50 g L−1 of dose of biomaterial at room temperature. The sorption efficiency was found to be better than many charred bio-based materials.

Alkaline deoxygenated graphene oxide as adsorbent for cadmium ions removal from aqueous solutions

2015 ◽  
Vol 71 (11) ◽  
pp. 1611-1619 ◽  
Author(s):  
Jun Liu ◽  
Hongyan Du ◽  
Shaowei Yuan ◽  
Wanxia He ◽  
Pengju Yan ◽  
...  
Keyword(s):  
Graphene Oxide ◽  
Aqueous Solutions ◽  
Batch Adsorption ◽  
Maximum Adsorption Capacity ◽  
Order Kinetic ◽  
Transmission Electron ◽  
Equilibrium Data ◽  
Order Kinetic Model ◽  
Pseudo Second Order ◽  
Ft Ir

Alkaline deoxygenated graphene oxide (aGO) was prepared through alkaline hydrothermal treatment and used as adsorbent to remove Cd(II) ions from aqueous solutions for the first time. The characterization results of transmission electron microscopy, X-ray diffraction, Raman spectroscopy, and Fourier transform infrared (FT-IR) spectra indicate that aGO was successfully synthesized. The batch adsorption experiments showed that the adsorption kinetics could be described by the pseudo-second-order kinetic model, and the isotherms equilibrium data were well fitted with the Langmuir model. The maximum adsorption capacity of Cd(II) on aGO was 156 mg/g at pH 5 and T = 293 K. The adsorption thermodynamic parameters indicated that the adsorption process was a spontaneous and endothermic reaction. The mainly adsorption mechanism speculated from FT-IR results may be attributed to the electrostatic attraction between Cd2+ and negatively charged groups (–CO−) of aGO and cation-π interaction between Cd2+ and the graphene planes. The findings of this study demonstrate the potential utility of the nanomaterial aGO as an effective adsorbent for Cd(II) removal from aqueous solutions.

Characterization of natural- and organobentonite by XRD, SEM, FT-IR and thermal analysis techniques and its adsorption behaviour in aqueous solutions

Clay Minerals ◽  
2012 ◽  
Vol 47 (1) ◽  
pp. 31-44 ◽  
Author(s):  
G. A. Ikhtiyarova ◽  
A. S. Özcan ◽  
Ö. Gök ◽  
A. Özcan
Keyword(s):  
Surface Area ◽  
Bet Surface Area ◽  
Maximum Adsorption Capacity ◽  
Textile Dye ◽  
Order Kinetic ◽  
Order Kinetic Model ◽  
Pseudo Second Order ◽  
Ft Ir ◽  
Thermal Analysis Techniques

AbstractIn this study, natural bentonite was modified with hexadecyltrimethylammonium (HDTMA) bromide to obtain organobentonite (HDTMA-bentonite). Bentonite and HDTMA-bentonite were then characterized using XRD, XRF, SEM, FT-IR, thermogravimetric (TG) analysis, elemental analysis and Brunauer-Emmett-Teller (BET) surface area techniques. The HDTMA+ cation was found to be located on the surface and enters the interlayer spaces of smectite according to the XRD and SEM results. FT-IR spectra indicated the existence of HDTMA functional groups on the bentonite surface. The BET surface area significantly decreased after the modification due to the coverage of the pores of natural bentonite. After the characterization, the adsorption of a textile dye, Reactive Blue 19 (RB19), onto bentonite and HDTMA-bentonite was investigated. The maximum adsorption capacity of HDTMA-bentonite for RB19 was 502 mg g-1 at 20°C. The adsorption process followed a pseudo-second-order kinetic model and it was exothermic and physical in nature.

scholarly journals Adsorption of Copper(II) and Mercury(II) Ions onto Chemically-Modified Chitosan Membranes: Equilibrium and Kinetic Properties

2012 ◽  
Vol 30 (1) ◽  
pp. 1-21 ◽  
Author(s):  
R.B. Rabelo ◽  
R.S. Vieira ◽  
F.M.T. Luna ◽  
E. Guibal ◽  
M.M. Beppu
Keyword(s):  
Adsorption Capacity ◽  
Metal Ion ◽  
Batch Process ◽  
Second Order ◽  
Infrared Spectrometry ◽  
Maximum Adsorption Capacity ◽  
Kinetic Properties ◽  
Pseudo Second Order ◽  
Ft Ir ◽  
Chitosan Membranes

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.

Removal of Mn(II) from Aqueous Solution Using Saponified Garlic Peel

2014 ◽  
Vol 694 ◽  
pp. 382-386 ◽  
Author(s):  
Bo Liang ◽  
Wan He Zhao ◽  
Kai Huang ◽  
Hong Min Zhu
Keyword(s):  
Metal Ion ◽  
Chemical Properties ◽  
Correlation Coefficients ◽  
Ion Concentration ◽  
Batch Adsorption ◽  
Maximum Adsorption Capacity ◽  
Pseudo Second Order ◽  
Ft Ir ◽  
Physical And Chemical ◽  
Garlic Peel

The removal of Mn (II) ion by saponified garlic peel (S-GP) was investigated using batch adsorption. SEM and FT-IR were employed to investigate the physical and chemical properties of S-GP. The adsorption was evaluated as a function of initial metal ion concentration, contact time and temperature. The maximum adsorption capacity for Mn (II) was 0.51 mol/kg, and the adsorption process followed the Langmuir model. Pseudo-second-order models fitted the experimental data well and kinetic parameters, rate constants, equilibrium sorption capacity and related correlation coefficients at various temperatures were calculated and discussed. A possible adsorption mechanism based on a cation exchange was proposed for the adsorption of Mn (II).

scholarly journals Enhanced cadmium removal from water by hydroxyapatite subjected to different thermal treatments

2020 ◽  
Vol 69 (7) ◽  
pp. 678-693
Author(s):  
R. Aouay ◽  
S. Jebri ◽  
A. Rebelo ◽  
J. M. F. Ferreira ◽  
I. Khattech
Keyword(s):  
Electron Microscopy ◽  
Sorption Process ◽  
Maximum Adsorption Capacity ◽  
Order Kinetic ◽  
Cadmium Removal ◽  
Sorption Behaviour ◽  
Adsorption Mechanisms ◽  
Transmission Electron ◽  
Order Kinetic Model ◽  
Pseudo Second Order

Abstract Hydroxyapatite powders were synthesized according to a wet precipitation route and then subjected to heat treatments within the temperature range of 200–800 °C. The prepared samples were tested as sorbents for cadmium in an aqueous medium. The best performances were obtained with the material treated at 200 °C (HAp200), as the relevant sorbent textural features (SBET – specific surface area and Vp – total volume of pores) were least affected at this low calcination temperature. The maximum adsorption capacity at standard ambient temperature and pressure was 216.6 mg g−1, which increased to 240.7 mg g−1 by increasing the temperature from 25 to 40 °C, suggesting an endothermic nature of the adsorption process. Moreover, these data indicated that a thermal treatment at 200 °C enhanced the ability of the material in Cd2+ uptake by more than 100% compared to other similar studies. The adsorption kinetic process was better described by the pseudo-second-order kinetic model. Langmuir, Freundlich, and Dubinin–Kaganer–Radushkevich isotherms were applied to describe the sorption behaviour of Cd2+ ions onto the best adsorbent. Furthermore, a thermodynamic study was also performed to determine ΔH°, ΔS°, and ΔG° of the sorption process of this adsorbent. The adsorption mechanisms were investigated by Fourier transform infrared spectroscopy (FTIR) and scanning electron microscopy-transmission electron microscopy (SEM-TEM) observations.

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