The adsorption of Sb(III) in aqueous solution by Fe2O3-modified carbon nanotubes

2013 ◽  
Vol 68 (3) ◽  
pp. 658-664 ◽  
Author(s):  
Tingchao Yu ◽  
Chao Zeng ◽  
Miaomiao Ye ◽  
Yu Shao
Keyword(s):  
Electron Microscopy ◽  
Carbon Nanotubes ◽  
Aqueous Solution ◽  
Ph Value ◽  
Removal Rate ◽  
Nitrogen Adsorption ◽  
Solution Ph ◽  
Freundlich Adsorption Isotherm ◽  
Modified Carbon Nanotubes ◽  
Adsorption Desorption

A novel kind of iron oxide supported on carbon nanotubes (CNTs) was prepared for adsorption of antimony (Sb)(III) in aqueous solution. The iron (III) oxide (Fe2O3)-modified CNTs were characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, nitrogen adsorption–desorption and Fourier transform infrared spectrometer. Parameters affecting the adsorption efficiencies, including solution pH value, initial Sb(III) concentration, adsorbent dosage, adsorption time and temperature, were investigated. The results indicate that the removal rate of Sb(III) by Fe2O3-modified CNTs is 99.97% under the initial Sb(III) concentration of 1.5 mg/L, adsorbents dosage of 0.5 g/L, temperature of 25 oC and pH value of 7.00, which is 29.81% higher than that of the raw CNTs. The adsorption capacity increased correspondingly from 3.01 to 6.23 mg/g. The equilibrium adsorption data can be fitted to the Freundlich adsorption isotherm. In addition, it has been found that the solution pH values and adsorption temperatures have no significant influence on Sb(III) removal.

scholarly journals Adsorption of Arsenate from Aqueous Solution onto Modified Vietnamese Bentonite

2019 ◽  
Vol 2019 ◽  
pp. 1-13 ◽  
Author(s):  
Nguyen Le My Linh ◽  
Duc Hoang Van ◽  
Tran Duong ◽  
Mai Xuan Tinh ◽  
Dinh Quang Khieu
Keyword(s):  
Aqueous Solution ◽  
Nitrogen Adsorption ◽  
X Ray Diffraction ◽  
Solution Ph ◽  
X Ray ◽  
Surface Areas ◽  
Layered Clays ◽  
Monolayer Adsorption ◽  
Langmuir Isotherm Model ◽  
Adsorption Desorption

In this study, pillared layered clays were prepared by modifying Vietnamese bentonite with polymeric Al and Fe. The obtained materials were characteristic of X-ray diffraction analysis, thermal analysis, and nitrogen adsorption/desorption isotherms. The results indicated that hydroxy-aluminum ([Al13O4(OH)24(H2O)12]7+) and poly-hydroxyl-Fe or polyoxo-Fe cations were intercalated into layers of clay, resulting in an increase of d001 values and of the specific surface areas compared with those of initial bentonite. Modified bentonites were employed to adsorb As(V) from aqueous solution. The adsorption of As(V) was strongly dependent on solution pH, and the maximum adsorption of modified bentonites was obtained in the pH 3.0 for Fe-bentonite and the pH 4.0 for Al-bentonite. The equilibrium adsorption study showed that the data were well fit by the Langmuir isotherm model. The maximum monolayer adsorption capacity of As(V) at 30°C derived from the Langmuir equation was 35.71 mg/g for Al-bentonite and 18.98 mg/g for Fe-bentonite. Adsorption kinetics, thermodynamics, and reusability of modified bentonites have been addressed.

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.

Adsorption Behavior of Phenol in Aqueous Solution on MCM-41 Grafted by Different Functional Groups

2014 ◽  
Vol 955-959 ◽  
pp. 74-79
Author(s):  
Xiao Jun Sun ◽  
Xiao Chun Yan ◽  
Yu Jie Feng ◽  
Xian Bin Liu
Keyword(s):  
Aqueous Solution ◽  
Adsorption Capacity ◽  
Functional Groups ◽  
Ph Value ◽  
Nitrogen Adsorption ◽  
Adsorption Behaviors ◽  
Prepared Material ◽  
Adsorption Amount ◽  
Adsorption Desorption ◽  
Mcm 41

Four types of organo-functionalized mesoporous silicas were synthesized by post-grafting method, and characterized by powder X-ray diffraction, nitrogen adsorption/desorption and fourier transform infrared spectroscopy. In addition, adsorption behaviors of the prepared material modified with different functional groups were studied by adsorption of phenol in aqueous solution. When the concentration of phenol was 800 mg/L, the equilibrium adsorption capacity of N-aminoethyl-γ-aminopropyl-MCM-41, aminopropyl-MCM-41, mercaptopropyl-MCM-41 and propyl-MCM-41 was respectively as 2.5 times, 2.2 times, 1.9 times, and 1.7 times as that of MCM-41. It was due to the introduction of organo-functional groups, changing the polarity of the channel surface, and increasing the hydrophobic properties. N-aminoethyl-γ-aminopropyl and aminopropyl groups could generate acid-base interactions with phenol, therefore, their adsorption capacity increased much more. Besides, the pH value of the solution could significantly affect the adsorption amount of phenol on samples. The result showed that with the increase of pH, the adsorption amount of phenol increased at first, and then decreased. The maximum adsorption amount of all the prepared materials occurred at about pH value of 6.

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>.

Heterogeneous Fenton Catalytic Removal of Organic Pollutant in Aqueous Solution by using Coal Gangue as a Catalyst

2019 ◽  
Vol 12 (4) ◽  
pp. 312-325
Author(s):  
Jiwei Zhang ◽  
Jingjing Xu ◽  
Shuaixia Liu ◽  
Baoxiang Gu ◽  
Feng Chen ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Hydrogen Peroxide ◽  
Hydroxyl Radical ◽  
Removal Rate ◽  
Organic Pollutant ◽  
Coal Gangue ◽  
Ion Leakage ◽  
Heterogeneous Fenton ◽  
Solution Ph ◽  
X Ray

Background: Coal gangue was used as a catalyst in heterogeneous Fenton process for the degradation of azo dye and phenol. The influencing factors, such as solution pH gangue concentration and hydrogen peroxide dosage were investigated, and the reaction mechanism between coal gangue and hydrogen peroxide was also discussed. Methods: Experimental results showed that coal gangue has the ability to activate hydrogen peroxide to degrade environmental pollutants in aqueous solution. Under optimal conditions, after 60 minutes of treatment, more than 90.57% of reactive red dye was removed, and the removal efficiency of Chemical Oxygen Demand (COD) up to 72.83%. Results: Both hydroxyl radical and superoxide radical anion participated in the degradation of organic pollutant but hydroxyl radical predominated. Stability tests for coal gangue were also carried out via the continuous degradation experiment and ion leakage analysis. After five times continuous degradation, dye removal rate decreased slightly and the leached Fe was still at very low level (2.24-3.02 mg L-1). The results of Scanning Electron Microscope (SEM), energy dispersive X-Ray Spectrometer (EDS) and X-Ray Powder Diffraction (XRD) indicated that coal gangue catalyst is stable after five times continuous reuse. Conclusion: The progress in this research suggested that coal gangue is a potential nature catalyst for the efficient degradation of organic pollutant in water and wastewater via the Fenton reaction.

Comparison of Coal Ash and Activated Carbon for Removal of Humic Acid from Aqueous Solution

2013 ◽  
Vol 864-867 ◽  
pp. 1509-1512
Author(s):  
Xue Mei Zhang ◽  
Yan Zhang ◽  
Di Fan
Keyword(s):  
Aqueous Solution ◽  
Humic Acid ◽  
Activated Carbons ◽  
Removal Rate ◽  
Coal Ash ◽  
Cost Effective ◽  
Solution Ph ◽  
Adsorption Behaviors ◽  
Calcium Loading ◽  
Working Solution

This paper presents the adsorption behaviors of humic acid (HA) on coal ashes and powdered activated carbons (PACs). A bituminous coal, with or without calcium-loading, was used as a feedstock for coal ash preparation. The working solution of HA with a concentration of 20 mg/L was used in all adsorption tests. The results showed that calcium-enriched coal ash (CECA) gave rise to the removal rate of HA as high as 84.05%, much higher than those of raw coal ash (RCA) and PACs. The impacts of solution pH and adsorbent dosage on HA adsorption capacity were also investigated. It was found that lower pH facilitated to the removal of HA from aqueous solution by means of CECA, and the optimal CECA dosage was about 1.0g/L at pH 7.00. The data obtained in this study suggested that calcium-enriched coal ash could be useful and cost-effective in the treatment of wastewaters containing HA-like organic macro-molecules.

scholarly journals Adsorption of aquatic Cd2+ using a combination of bacteria and modified carbon fiber

2017 ◽  
Vol 36 (3-4) ◽  
pp. 857-871 ◽  
Author(s):  
Chao Xue ◽  
Peishi Qi ◽  
Yunzhi Liu
Keyword(s):  
Aqueous Solution ◽  
Composite Material ◽  
Carbon Fiber ◽  
Active Sites ◽  
Ph Value ◽  
Removal Rate ◽  
Sorption Process ◽  
Acid Sites ◽  
Heterogeneous Distribution ◽  
Carbon Fiber Material

Batch experiments were conducted to investigate the capacity and mechanisms for adsorbing Cd2+ from aqueous solutions by the composite material. The composite material was manufactured with Plesiomonas shigelloides strain H5 and modified polyacrylonitrile-based carbon fiber. Experimental results showed that the surface areas of modified polyacrylonitrile-based carbon fiber increased by 58.54% and pore width increased by 40.19% compared with unmodified polyacrylonitrile-based carbon fiber. Boehm’s titration results show the surface acid sites of composite material were increased by 712% compared with unmodified polyacrylonitrile-based carbon fiber. The field emission scanning electron microscope results show P. shigelloides H5 can be grown on the surface of modified polyacrylonitrile-based carbon fiber closely. The equilibrium removal rate and sorption quantity of composite material were 71.56% and 7.126 mg g−1, respectively. With the pH value of aqueous solution increased, the removal rate of Cd2+ ions was also increased, but the change of temperature and ionic strength had no significant effect on the removal rate. Furthermore, the results showed the whole sorption process was a good fit to Lagergren pseudo-second-order model and Freundlich isotherms model. Therefore, the results infer that there was a heterogeneous distribution of active sites, and then the sorption process was chemical adsorption and multilayer adsorption. In a word, microbial composite carbon fiber material can adsorb Cd2+ ions from aqueous solution effectively, which might be helpful in wastewater treatment in the future.

scholarly journals Electrochemical oxidation of sulfamethoxazole using Ti/SnO2-Sb/Co-PbO2 electrode through ANN-PSO

2019 ◽  
Vol 84 (7) ◽  
pp. 713-727 ◽  
Author(s):  
Jiteng Wan ◽  
Chunji Jin ◽  
Banghai Liu ◽  
Zonglian She ◽  
Mengchun Gao ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Electrochemical Oxidation ◽  
Removal Efficiency ◽  
Current Density ◽  
Ph Value ◽  
Ann Model ◽  
Solution Ph ◽  
Pbo2 Electrode ◽  
Artificial Neural Network Ann ◽  
Major Factors

Even in a trace amounts, the presence of antibiotics in aqueous solution is getting more and more attention. Accordingly, appropriate technologies are needed to efficiently remove these compounds from aqueous environments. In this study, we have examined the electrochemical oxidation (EO) of sulfamethoxazole (SMX) on a Co modified PbO2 electrode. The process of EO of SMX in aqueous solution followed the pseudo-first-order kinetics, and the removal efficiency of SMX reached the maximum value of 95.1 % within 60 min. The effects of major factors on SMX oxidation kinetics were studied in detail by single-factor experiments, namely current density (1?20 mA cm-2), solution pH value (2?10), initial concentration of SMX (10?500 mg L-1) and concentration of electrolytes (0.05?0.4 mol L-1). An artificial neural network (ANN) model was used to simulate this EO process. Based on the obtained model, particle swarm optimization (PSO) was used to optimize the operating parameters. The maximum removal efficiency of SMX was obtained at the optimized conditions (e.g., current density of 12.37 mA cm-2, initial pH value of 4.78, initial SMX concentration of 74.45 mg L-1, electrolyte concentration of 0.24 mol L-1 and electrolysis time of 51.49 min). The validation results indicated that this method can ideally be used to optimize the related parameters and predict the anticipated results with acceptable accuracy.

Preparation of PS@SiO2, PS@TiO2，PS@TiO2/SiO2 Core-Shell Composites by a Spray Drying Process and Their Hollow Spheres after Removing PS Cores by Calcinations

2011 ◽  
Vol 194-196 ◽  
pp. 389-392
Author(s):  
Ling Li ◽  
Hong Liang Li ◽  
Ying Chun Zhu ◽  
Ai Ping Fu ◽  
Yong Wan ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Spray Drying ◽  
Hollow Spheres ◽  
Nitrogen Adsorption ◽  
Core Shell ◽  
Drying Process ◽  
The Core ◽  
Adsorption Desorption ◽  
Drying Chamber ◽  
Scanning Electron

Polystyrene (PS) spheres encapsulated core-shell composites of SiO2or TiO2nanoparticles were prepared by the spray drying technique and hollow spheres of SiO2or TiO2nanoparticles were then derived by removing the PS cores with calcinations. The PS spheres were dispersed into the SiO2or TiO2colloids, forming a suspension and then the suspensions were sprayed to form micrometer-sized droplets, as the droplets rush through the drying chamber, the PS spheres were encapsulated into the core of SiO2or TiO2particles due to the high temperatures and the instant evaporation, obtaining PS@SiO2, PS@TiO2or PS@SiO2/TiO2core-shell composites. After removing the PS core by calcination at 550°C, SiO2or TiO2hollow spheres were then derived. The influence of drying temperature, the concentration of the SiO2or TiO2particles and the ratio of PS sphere to the particles on the structures and specific surface area of the hollow spheres were studied with scanning electron microscopy (SEM) and nitrogen adsorption-desorption measurements.

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