scholarly journals In Situ Synthesis of MIL-100(Fe) at the Surface of Fe3O4@AC as Highly Efficient Dye Adsorbing Nanocomposite

2019 ◽  
Vol 20 (22) ◽  
pp. 5612 ◽  
Author(s):  
Asma Hamedi ◽  
Francesco Trotta ◽  
Mahmood Borhani Zarandi ◽  
Marco Zanetti ◽  
Fabrizio Caldera ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Surface Area ◽  
Activated Charcoal ◽  
Order Kinetic ◽  
X Ray Diffraction ◽  
Transmission Electron ◽  
Order Kinetic Model ◽  
Langmuir Isotherm Model ◽  
Pseudo Second Order ◽  
Kinetics And Isotherms

A new magnetic nanocomposite called MIL-100(Fe) @Fe3O4@AC was synthesized by the hydrothermal method as a stable adsorbent for the removal of Rhodamine B (RhB) dye from aqueous medium. In this work, in order to increase the carbon uptake capacity, magnetic carbon was first synthesized and then the Fe3O4 was used as the iron (III) supplier to synthesize MIL-100(Fe). The size of these nanocomposite is about 30–50 nm. Compared with activated charcoal (AC) and magnetic activated charcoal (Fe3O4@AC) nanoparticles, the surface area of MIL-100(Fe) @Fe3O4@AC were eminently increased while the magnetic property of this adsorbent was decreased. The surface area of AC, Fe3O4@AC, and MIL-100(Fe) @Fe3O4@AC was 121, 351, and 620 m2/g, respectively. The magnetic and thermal property, chemical structure, and morphology of the MIL-100(Fe) @Fe3O4@AC were considered by vibrating sample magnetometer (VSM), thermogravimetric analysis (TGA), zeta potential, X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), Brunner-Emmet-Teller (BET), and transmission electron microscopy (TEM) analyses. The relatively high adsorption capacity was obtained at about 769.23 mg/g compared to other adsorbents to eliminate RhB dye from the aqueous solution within 40 min. Studies of adsorption kinetics and isotherms showed that RhB adsorption conformed the Langmuir isotherm model and the pseudo second-order kinetic model. Thermodynamic amounts depicted that the RhB adsorption was spontaneous and exothermic process. In addition, the obtained nanocomposite exhibited good reusability after several cycles. All experimental results showed that MIL-100(Fe) @Fe3O4@AC could be a prospective sorbent for the treatment of dye wastewater.

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 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 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.

scholarly journals Organobentonite: Characterization and adsorptive properties towards phenol and its derivatives

2016 ◽  
Vol 48 (2) ◽  
pp. 167-176
Author(s):  
Sanja Marinovic ◽  
Marija Ajdukovic ◽  
Natasa Jovic-Jovicic ◽  
Predrag Bankovic ◽  
Zorica Mojovic ◽  
...  
Keyword(s):  
Point Of Zero Charge ◽  
Hexadecyltrimethylammonium Bromide ◽  
Order Kinetic ◽  
X Ray Diffraction ◽  
Phenol Derivatives ◽  
Order Kinetic Model ◽  
Langmuir Isotherm Model ◽  
Pseudo Second Order ◽  
Nitro Derivatives

Bentonite from Mecji Do locality in Serbia was modified with hexadecyltrimethylammonium bromide (HDTMA-Br), and the sample was denoted as HDTMA-MD. The characterization of the material included X-Ray diffraction, elemental analysis and point of zero charge determination. The adsorption of phenol and its nitro derivatives: 2-nitrophenol (2NP), 3-nitrophenol (3NP) and 4-nitrophenol (4NP) on HDTMA-MD was investigated. The adsorption capacity of HDTMA-MD toward phenol derivatives increased in the following order qe (phenol) < qe (3NP) < qe (2NP) < qe (4NP). The influence of adsorption time and initial concentration on the adsorption efficiency of HDTMA-MD was studied for 4NP. The data were best fitted with Langmuir isotherm model and the pseudo-second-order kinetic model.

scholarly journals Insights into Starch Coated Nanozero Valent Iron-Graphene Composite for Cr(VI) Removal from Aqueous Medium

2016 ◽  
Vol 2016 ◽  
pp. 1-10 ◽  
Author(s):  
Prasanna Kumarathilaka ◽  
Vimukthi Jayaweera ◽  
Hasintha Wijesekara ◽  
I. R. M. Kottegoda ◽  
S. R. D. Rosa ◽  
...  
Keyword(s):  
Point Of Zero Charge ◽  
Inert Material ◽  
Maximum Adsorption Capacity ◽  
Order Kinetic ◽  
X Ray Diffraction ◽  
Graphene Composite ◽  
Removal Capacity ◽  
Order Kinetic Model ◽  
Pseudo Second Order ◽  
First Time

Embedding nanoparticles into an inert material like graphene is a viable option since hybrid materials are more capable than those based on pure nanoparticulates for the removal of toxic pollutants. This study reports for the first time on Cr(VI) removal capacity of novel starch stabilized nanozero valent iron-graphene composite (NZVI-Gn) under different pHs, contact time, and initial concentrations. Starch coated NZVI-Gn composite was developed through borohydrate reduction method. The structure and surface of the composite were characterized by scanning electron microscopy (SEM), X-ray diffraction spectroscopy (XRD), Fourier transform infrared spectroscopy (FTIR), Brunauer-Emmett-Teller (BET), and point of zero charge (pHpzc). The surface area and pHpzc of NZVI-Gn composite were reported as 525 m2 g−1 and 8.5, respectively. Highest Cr(VI) removal was achieved at pH 3, whereas 67.3% was removed within first few minutes and reached its equilibrium within 20 min obeying pseudo-second-order kinetic model, suggesting chemisorption as the rate limiting process. The partitioning of Cr(VI) at equilibrium is perfectly matched with Langmuir isotherm and maximum adsorption capacity of the NZVI-Gn composite is 143.28 mg g−1. Overall, these findings indicated that NZVI-Gn composite could be utilized as an efficient and magnetically separable adsorbent for removal of Cr(VI).

scholarly journals The Removal of Uranium and Thorium from Their Aqueous Solutions by 8-Hydroxyquinoline Immobilized Bentonite

Minerals ◽  
2019 ◽  
Vol 9 (10) ◽  
pp. 626 ◽  
Author(s):  
Salah ◽  
Gaber ◽  
Kandil
Keyword(s):  
Aqueous Solutions ◽  
Metal Ions ◽  
Langmuir Isotherm ◽  
Freundlich Isotherm ◽  
Order Kinetic ◽  
X Ray Diffraction ◽  
Solution Ph ◽  
X Ray ◽  
Order Kinetic Model ◽  
Pseudo Second Order

The sorption of uranium and thorium from their aqueous solutions by using 8-hydroxyquinoline modified Na-bentonite (HQ-bentonite) was investigated by the batch technique. Na-bentonite and HQ-bentonite were characterized by X-ray fluorescence (XRF), X-ray diffraction (XRD), scanning electron microscopy (SEM), and Fourier Transform Infrared (FTIR) spectroscopy. Factors that influence the sorption of uranium and thorium onto HQ-bentonite such as solution pH, contact time, initial metal ions concentration, HQ-bentonite mass, and temperature were tested. Sorption experiments were expressed by Freundlich and Langmuir isotherms and the sorption results demonstrated that the sorption of uranium and thorium onto HQ-bentonite correlated better with the Langmuir isotherm than the Freundlich isotherm. Kinetics studies showed that the sorption followed the pseudo-second-order kinetic model. Thermodynamic parameters such as ΔH°, ΔS°, and ΔG° indicated that the sorption of uranium and thorium onto HQ-bentonite was endothermic, feasible, spontaneous, and physical in nature. The maximum adsorption capacities of HQ-bentonite were calculated from the Langmuir isotherm at 303 K and were found to be 63.90 and 65.44 for U(VI) and Th(IV) metal ions, respectively.

scholarly journals Visible-light-driven photocatalytic degradation of rhodamine B in water by BiOClxI1−x solid solutions

2020 ◽  
Vol 81 (5) ◽  
pp. 1080-1089
Author(s):  
Huan-Yan Xu ◽  
Dan Lu ◽  
Qu Tan ◽  
Xiu-Lan He ◽  
Shu-Yan Qi
Keyword(s):  
Electron Microscopy ◽  
Solid Solutions ◽  
Rhodamine B ◽  
Diffuse Reflectance Spectroscopy ◽  
Bet Surface Area ◽  
Order Kinetic ◽  
X Ray Diffraction ◽  
Sunlight Irradiation ◽  
Transmission Electron ◽  
Visible Light Driven

Abstract Bismuth oxyhalides (BiOXs, X = Cl, Br and I) are emerging photocatalytic materials with unique layered structure, flexible band structure and superior photocatalytic activity. The purpose of this study was to develop a facile alcoholysis route to prepare BiOClxI1−x nanosheet solid solutions at room temperature. X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), UV-vis diffuse reflectance spectroscopy (UV-vis DRS), photoluminescence emission spectroscopy (PL) and Brunauer–Emmett–Teller (BET) surface area analyzer were used to characterize the as-prepared photocatalysts. These results revealed that two-dimension BiOClxI1−x nanosheet solid solutions could be obtained with high percentage of {001} crystal facets exposed. Moreover, the formation of solid solution could regularly change the optical absorption thresholds and band gaps of BiOClxI1−x photocatalysts. The photocatalytic experiments indicated that BiOCl0.75I0.25 exhibited the highest photocatalytic performance for the degradation of Rhodamine B (RhB) under simulated sunlight irradiation and the photocatalytic process followed a pseudo-first-order kinetic equation. A possible mechanism of RhB photodegradation over BiOClxI1−x solid solutions was proposed based on the structural properties of BiOClxI1−x solid solutions and RhB photosensitization.

Fast Removal of Pb2+ from Aqueous Solution by Water Insoluble Konjac Glucomannan

2009 ◽  
Vol 610-613 ◽  
pp. 65-68 ◽  
Author(s):  
Xue Gang Luo ◽  
Feng Liu ◽  
Xiao Yan Lin
Keyword(s):  
Aqueous Solution ◽  
Correlation Coefficients ◽  
Konjac Glucomannan ◽  
Maximum Adsorption Capacity ◽  
Order Kinetic ◽  
Order Kinetic Model ◽  
Langmuir Isotherm Model ◽  
Pseudo Second Order ◽  
Equilibrium Process ◽  
Fast Removal

Konjac glucomannan (KGM) was converted into water insoluble konjac glucomannan (WIKGM) by treating with NaOH through completely deacetylated reaction. Adsorption study was carried out for the adsorption of Pb2+ from aqueous solution using water insoluble konjac glucomannan. The influences of pH, contact time, temperature and initial Pb2+ concentration on the absorbent were studied. Results of kinetic data showed that the Pb2+ adsorption rate was fast and good correlation coefficients were obtained for the pseudo second-order kinetic model. The equilibrium process was described well by the Langmuir isotherm model with maximum adsorption capacity of 9.18 mg/g on WIKGM at 25°C.

Efficient synthesis of carbon nanotubes with improved surface area by low-temperature solvothermal route from dichlorobenzene

2013 ◽  
Vol 67 (11) ◽  
Author(s):  
Gantigaiah Krishnamurthy ◽  
Sarika Agarwal
Keyword(s):  
Electron Microscopy ◽  
Carbon Nanotubes ◽  
Carbon Source ◽  
Surface Area ◽  
Heating Temperature ◽  
Outer Diameter ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Scanning Electron

AbstractThe synthesis of well-aggregated carbon nanotubes in the form of bundles was achieved by the catalytic reduction of 1,2-dichlorobenzene by a solvothermal approach. The use of 1,2-dichlorobenzene as a carbon source yielded a comparably good percentage of carbon nanotubes in the range of 60–70 %, at a low reaction temperature of 200°C. The products obtained were analysed by X-ray diffraction, Raman spectroscopy, scanning electron microscopy, and transmission electron microscopy techniques. The X-ray diffraction studies implied the presence of pure, crystalline, and well-ordered carbon nanotubes. The scanning electron and transmission electron microscopic images revealed the surface morphology, dimensions and the bundled form of the tubes. These micrographs showed the presence of multi-walled carbon nanotubes with an outer diameter of 30–55 nm, inner diameter of 15–30 nm, and lengths of several hundreds of nanometers. Brunauer-Emmett-Teller-based N2 gas adsorption studies were performed to determine the surface area and pore volume of the carbon nanotubes. These carbon nanotubes exhibit a better surface area of 385.30 m2 g−1. In addition, the effects of heating temperature, heating time, amount of catalyst and amount of carbon source on the product yield were investigated.

Sign in / Sign up

Export Citation Format

Share Document