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 Efficient Adsorption of Lead (II) from Aqueous Phase Solutions Using Polypyrrole-Based Activated Carbon

Materials ◽  
2019 ◽  
Vol 12 (12) ◽  
pp. 2020 ◽  
Author(s):  
Abdulaziz Ali Alghamdi ◽  
Abdel-Basit Al-Odayni ◽  
Waseem Sharaf Saeed ◽  
Abdullah Al-Kahtani ◽  
Fahad A. Alharthi ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Activated Carbon ◽  
Freundlich Isotherm ◽  
Ion Concentration ◽  
Morphological Properties ◽  
Order Kinetic ◽  
Isotherm Equation ◽  
Transmission Electron ◽  
Order Kinetic Model ◽  
Adsorbent Dose

In this study, polypyrrole-based activated carbon was prepared by the carbonization of polypyrrole at 650 °C for 2 h in the presence of four-times the mass of KOH as a chemical activator. The structural and morphological properties of the product (polypyrrole-based activated carbon (PPyAC4)), analyzed by scanning electron microscopy, transmission electron microscopy, X-ray diffraction, and thermogravimetric analysis, support its applicability as an adsorbent. The adsorption characteristics of PPyAC4 were examined through the adsorption of lead ions from aqueous solutions. The influence of various factors, including initial ion concentration, pH, contact time, and adsorbent dose, on the adsorption of Pb2+ was investigated to identify the optimum adsorption conditions. The experimental data fit well to the pseudo-second-order kinetic model (R2 = 0.9997) and the Freundlich isotherm equation (R2 = 0.9950), suggesting a chemisorption pathway. The adsorption capacity was found to increase with increases in time and initial concentration, while it decreased with an increase in adsorbent dose. Additionally, the highest adsorption was attained at pH 5.5. The calculated maximum capacity, qm, determined from the Langmuir model was 50 mg/g.

scholarly journals Adsorption of Ni2+ from aqueous solution by magnetic Fe@graphite nano-composite

2016 ◽  
Vol 18 (4) ◽  
pp. 96-103 ◽  
Author(s):  
Wojciech Konicki ◽  
Rafał Pelka ◽  
Walerian Arabczyk
Keyword(s):  
Aqueous Solution ◽  
Adsorption Capacity ◽  
Diffraction Method ◽  
Chemical Vapor ◽  
Bet Surface Area ◽  
Order Kinetic ◽  
Solution Ph ◽  
Transmission Electron ◽  
Order Kinetic Model ◽  
Nanocrystalline Iron

Abstract The removal of Ni2+ from aqueous solution by iron nanoparticles encapsulated by graphitic layers (Fe@G) was investigated. Nanoparticles Fe@G were prepared by chemical vapor deposition CVD process using methane as a carbon source and nanocrystalline iron. The properties of Fe@G were characterized by X-ray Diffraction method (XRD), High-Resolution Transmission Electron Microscopy (HRTEM), Fourier Transform-Infrared Spectroscopy (FTIR), BET surface area and zeta potential measurements. The effects of initial Ni2+ concentration (1–20 mg L−1), pH (4–11) and temperature (20–60°C) on adsorption capacity were studied. The adsorption capacity at equilibrium increased from 2.96 to 8.78 mg g−1, with the increase in the initial concentration of Ni2+ from 1 to 20 mg L−1 at pH 7.0 and 20oC. The experimental results indicated that the maximum Ni2+ removal could be attained at a solution pH of 8.2 and the adsorption capacity obtained was 9.33 mg g−1. The experimental data fitted well with the Langmuir model with a monolayer adsorption capacity of 9.20 mg g−1. The adsorption kinetics was found to follow pseudo-second-order kinetic model. Thermodynamics parameters, ΔHO, ΔGO and ΔSO, were calculated, indicating that the adsorption of Ni2+ onto Fe@G was spontaneous and endothermic in nature.

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.

scholarly journals SURFACE MODIFICATION OF CANARIUM OVATUMENGL.(PILI) SHELL AS ADSORBENT OF LEAD(Pb2+) FROM AQUEOUS SOLUTION

2021 ◽  
Author(s):  
Ernesto Jr. S. Cajucom ◽  
◽  
Lolibeth V. Figueroa ◽  
Keyword(s):  
Aqueous Solution ◽  
Adsorption Capacity ◽  
Freundlich Isotherm ◽  
Cost Effective ◽  
Maximum Adsorption Capacity ◽  
Order Kinetic ◽  
Carboxylic Groups ◽  
Equilibrium Data ◽  
Order Kinetic Model ◽  
Surface Modified

This study was carried out to investigate the efficiency of raw pili shell (RPS) and the surface modified pili shell using EDTA (EMPS) and oxalic acid (OMPS). A comparative study on the adsorption capacity of the adsorbents was performed against lead (Pb2+) from aqueous solution. The adsorbents were characterized by FTIR, which showed higher peak of adsorption bands of carboxylic groups on the acid modified pili shells. Scanning electron microscope orSEM was also used to describe the surface morphology of the adsorbents. The linear form of Langmuir and Freundlich models were applied to represent adsorption data. The calculated equilibrium data of Pb (II) best fitted to Langmuir compare to Freundlich isotherm model with maximum adsorption capacity (qmax) of 27.03 mg/g and 45.45 mg/g using EMPS and OMPS, respectively. Kinetic sorption models were used to determine the adsorption mechanism and the kinetic data of all the adsorbents correlated (R2=1) wellwith the pseudo second order kinetic model. Among the three adsorbents, OMPS shown higher percent removal of lead compared to RPS and EMPS. The large adsorption capacity rate indicated that chemically modified pili shell in present study has great potential to be used as a cost-effective adsorbent for the removal of lead ions from the water.

scholarly journals Phragmites karkaas a Biosorbent for the Removal of Mercury Metal Ions from Aqueous Solution: Effect of Modification

2015 ◽  
Vol 2015 ◽  
pp. 1-12 ◽  
Author(s):  
Muhammad Hamid Raza ◽  
Aqsa Sadiq ◽  
Umar Farooq ◽  
Makshoof Athar ◽  
Tajamal Hussain ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Metal Ion ◽  
Freundlich Isotherm ◽  
Agitation Speed ◽  
Second Order ◽  
Ion Concentration ◽  
Order Kinetic ◽  
Order Kinetic Model ◽  
Pseudo Second Order ◽  
Phragmites Karka

Batch scale studies for the adsorption potential of novel biosorbentPhragmites karka(Trin), in its natural and treated forms, were performed for removal of mercury ions from aqueous solution. The study was carried out at different parameters to obtain optimum conditions of pH, biosorbent dose, agitation speed, time of contact, temperature, and initial metal ion concentration. To analyze the suitability of the process and maximum amount of metal uptake, Dubinin-Radushkevich (D-R) model, Freundlich isotherm, and Langmuir isotherm were applied. The values ofqmaxfor natural and treated biosorbents were found at 1.79 and 2.27 mg/g, respectively. The optimum values of contact time and agitation speed were found at 50 min and 150 rpm for natural biosorbent whereas 40 min and 100 rpm for treated biosorbent, respectively. The optimum biosorption capacities were observed at pH 4 and temperature 313 K for both naturalP. karkaand treatedP. karka.RLvalues indicate that comparatively treatedP. karkawas more feasible for mercury adsorption compared to naturalP. karka. Both pseudo-first-order and pseudo-second-order kinetic models were applied and it was found that data fit best to the pseudo-second-order kinetic model. Thermodynamic studies indicate that adsorption process was spontaneous, feasible, and endothermic.

Adsorption of azo dyes from aqueous solution by the hybrid MOFs/GO

2016 ◽  
Vol 73 (7) ◽  
pp. 1728-1737 ◽  
Author(s):  
Ling Li ◽  
Zhennan Shi ◽  
Hongyang Zhu ◽  
Wei Hong ◽  
Fengwei Xie ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Azo Dyes ◽  
Metal Organic Framework ◽  
Freundlich Isotherm ◽  
Order Kinetic ◽  
Sunset Yellow ◽  
Order Kinetic Model ◽  
Metal Organic ◽  
Pseudo Second Order ◽  
The Stability

In this work, a hybrid of chromium(III) terephthalate metal organic framework (MIL-101) and graphene oxide (GO) was synthesized and its performance in the removal of azo dyes (Amaranth, Sunset Yellow, and Carmine) from water was evaluated. The adsorption for azo dyes on MIL-101/GO was compared with that of MIL-101, and it was found that the addition of GO enhanced the stability of MIL-101 in water and increased the adsorption capacity. The maximum adsorption capacities of MIL-101/GO were 111.01 mg g−1 for Amaranth, 81.28 mg g−1 for Sunset Yellow, and 77.61 mg g−1 for Carmine. The adsorption isotherms and kinetics were investigated, showing that the adsorption fits the Freundlich isotherm and the pseudo-second-order kinetic model. The recyclability of MIL-101/GO was shown by the regeneration by acetone. The high adsorption capability and excellent reusability make MIL-101/GO a competent adsorbent for the removal dyes from aqueous solution.

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 Gum Arabic-Magnetite Nanocomposite as an Eco-Friendly Adsorbent for Removal of Lead(II) Ions from Aqueous Solutions: Equilibrium, Kinetic and Thermodynamic Studies

Separations ◽  
2021 ◽  
Vol 8 (11) ◽  
pp. 224
Author(s):  
Ismat H. Ali ◽  
Mutasem Z. Bani-Fwaz ◽  
Adel A. El-Zahhar ◽  
Riadh Marzouki ◽  
Mosbah Jemmali ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Aqueous Solutions ◽  
Contact Time ◽  
Gum Arabic ◽  
Ion Concentration ◽  
Maximum Adsorption Capacity ◽  
Order Kinetic ◽  
Transmission Electron ◽  
Order Kinetic Model ◽  
Langmuir Isotherm Model

In this study, a gum Arabic-magnetite nanocomposite (GA/MNPs) was synthesized using the solution method. The prepared nanocomposite was characterized by Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), vibrating sample magnetometer (VSM), and thermogravimetric analysis (TGA). The prepared composite was evaluated for the adsorption of lead(II) ions from aqueous solutions. The controlling factors such as pH, contact time, adsorbent dose, initial ion concentration, and temperature were investigated. The optimum adsorption conditions were found to be 0.3 g/50 mL, pH = 6.00, and contact time of 30 min. The experimental data well fitted the pseudo-second-order kinetic model and the Langmuir isotherm model. The maximum adsorption capacity was determined as 50.5 mg/g. Thermodynamic parameters were calculated postulating an endothermic and spontaneous process and a physio-sorption pathway.

scholarly journals The Preparation of Pd/Foam-Ni Electrode and Its Electrocatalytic Hydrodechlorination for Monochlorophenol Isomers

Catalysts ◽  
2018 ◽  
Vol 8 (9) ◽  
pp. 378 ◽  
Author(s):  
Junjing Li ◽  
Huan Wang ◽  
Liang Wang ◽  
Chang Ma ◽  
Cong Luan ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
Catalytic Performance ◽  
Order Kinetic ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Order Kinetic Model ◽  
Good Catalytic Activity ◽  
Promising Application

Noble metal palladium modified foamed nickel electrode (Pd/foam-Ni) was prepared by electrodeposition method. The fabricated electrode showed better catalytic performance than the Pd/foam-Ni prepared by conventional electroless deposition. The catalysts were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and transmission electron microscopy (TEM). Electrocatalytic activity of the Pd/Ni was studied for the hydrodechlorination of monochlorophenol isomers. The Pd/Ni exhibited good catalytic activity for 3-chlorophenol (3-CP). Complete decomposition of chlorophenol isomers could be achieved within 2 h, and the hydrodechlorination process conformed to the pseudo-first-order kinetic model. It showed a supreme stability after recycling for 5 times. The Pd/Ni exhibited a promising application prospect with high effectiveness and low Pd loading.

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.

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