scholarly journals Synthesis of Manganese Ferrite/Graphene Oxide Magnetic Nanocomposite for Pollutants Removal from Water

Processes ◽  
2021 ◽  
Vol 9 (4) ◽  
pp. 589
Author(s):  
Khadijah Mohammedsaleh M Katubi ◽  
Norah Salem Alsaiari ◽  
Fatimah Mohammed Alzahrani ◽  
Saifeldin M. Siddeeg ◽  
Mohamed A. Tahoon
Keyword(s):  
Electron Microscopy ◽  
Adsorption Capacity ◽  
Photoelectron Spectroscopy ◽  
Neutral Red ◽  
Magnetic Nanocomposite ◽  
Lead Ion ◽  
X Ray ◽  
Adsorbent Surface ◽  
Pollutants Removal ◽  
Adsorbent Dose

These days, environmental pollution, notably water pollution, has increasingly caused severe human health problems. The major water pollutants are heavy metals. MnFe2O4/GO nanocomposite was prepared in the current work via in situ method and tested to remove lead ion Pb2+ and neutral red (NR) dye from water. The prepared nanocomposite was characterized using different techniques, including X-ray diffraction, transmission electron microscopy, Fourier transform infrared spectroscopy, scanning electron microscopy, X-ray photoelectron spectroscopy, Raman spectra, and vibrating sample magnetometer. The prepared nanocomposite showed high adsorption capacity toward Pb2+ and NR dye removal according to Langmuir fitting indicating the monolayer homogeneous adsorption of pollutants over the adsorbent surface and can be separated easily with an external magnet. The effect of different factors, including contact time, pH, initial concentration, and adsorbent dose on the adsorption, were also studied. The increased concentration of pollutants led to increased adsorption capacity from 63 to 625 mg/g for Pb2+ ions and from 20 to 90 mg/g for NR dye. The increased adsorbent dose led to increased removal efficiency from 39% to 98.8% and from 63% to 94% for Pb2+ and NR dye, respectively. The optimum pH for the adsorption of both pollutants was found to be 6.0. The reusability of MnFe2O4/GO nanocomposite was studied for up to five cycles. The nanocomposite can keep its efficiency even after the studied cycles. So, the prepared magnetic nanocomposite is a promising material for water treatment.

scholarly journals Fabrication and Characterization of Porous Core–Shell Graphene/SiO2 Nanocomposites for the Removal of Cationic Neutral Red Dye

2020 ◽  
Vol 10 (23) ◽  
pp. 8529
Author(s):  
Junyi Wang ◽  
Tianlu Chen ◽  
Biao Xu ◽  
Yueqiu Chen
Keyword(s):  
Electron Microscopy ◽  
Water Vapor ◽  
Adsorption Capacity ◽  
Photoelectron Spectroscopy ◽  
Neutral Red ◽  
Water Vapor Adsorption ◽  
Core Shell ◽  
X Ray ◽  
Adsorption Sites ◽  
Sio2 Nanocomposites

Porous rGO/SiO2 nanocomposites with a “core-shell” structure were prepared as an efficient adsorbent for the liquid-phase adsorption of cationic neutral red (NR) dye. The samples were characterized with powder X-ray diffraction (XRD), field-emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), thermogravimetric analysis (TG), X-ray photoelectron spectroscopy (XPS), Raman spectroscopy, and N2 and water vapor adsorption/desorption methods. The NR removal ability and kinetics of the adsorption process of SiO2 and the rGO/SiO2 nanocomposites were investigated at 298 K. The rGO/SiO2 nanocomposite SG 0.30 showed a superior adsorption of NR dye. In regard to NR at pH 5, we measured a superior adsorption capacity of 66.635 mg/g at an initial NR concentration of 50 mg/L. The experimental adsorption capacity of SG 0.30 was 3.791 times higher than that of SiO2. Then, we compared the results with similar materials used for NR removal. Moreover, the water adsorption sites provided by the nitrogen- and oxygen-containing groups might be one of the reasons for the increased adsorption of water vapor. The broad range of properties of the rGO/SiO2 nanocomposite, including its simple synthesis, ability to be mass prepared, and strong adsorption properties, makes it a truly novel adsorbent that can be industrially produced, and shows potential application in the treatment of wastewater-containing dyes.

scholarly journals Superior Adsorption and Photocatalytic Degradation Capability of Mesoporous LaFeO3/g-C3N4 for Removal of Oxytetracycline

Catalysts ◽  
2020 ◽  
Vol 10 (3) ◽  
pp. 301 ◽  
Author(s):  
Ke Xu ◽  
Xiaosheng Yang ◽  
Luda Ruan ◽  
Shaolv Qi ◽  
Jianling Liu ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Degradation ◽  
Adsorption Capacity ◽  
Photoelectron Spectroscopy ◽  
Thermal Polymerization ◽  
X Ray ◽  
Practical Applications ◽  
Ultrathin Nanosheets ◽  
Lafeo3 Nanoparticles ◽  
Reheating Process

Mesoporous LaFeO3/g-C3N4 Z-scheme heterojunctions (LFC) were synthesized via the incorporation of LaFeO3 nanoparticles and porous g-C3N4 ultrathin nanosheets. The as prepared LFC were characterized by transmission electron microscopy, scanning electron microscopy, atomic force microscopy, X-ray photoelectron spectroscopy, powder X-ray diffraction, Raman spectra and N2 adsorption analysis. The structural analysis indicated that the reheating process and the addition of NH4Cl in the thermal polymerization were the key factors to get porous g-C3N4 ultrathin nanosheets and to obtain high specific surface areas of LFC. It remarkably enhanced the adsorption capacity and photocatalytic degradation of LFC for removal of oxytetracycline (OTC). The effect of the mass percentage of LaFeO3 in LFC, pH and temperature on the OTC adsorption was investigated. The LaFeO3/g-C3N4 heterojunction with 2 wt % LaFeO3 (2-LFC) exhibited highest saturated adsorption capacity (101.67 mg g−1) and largest photocatalytic degradation rate constant (1.35 L g−1 min−1), which was about 9 and 5 times higher than that of bulk g-C3N4 (CN), respectively. This work provided a facile method to prepare mesoporous LaFeO3/g-C3N4 heterojunctions with especially well adsorption and photocatalytic activities for OTC, which can facilitate its practical applications in pollution control.

A novel iron modified montmorillonite composite and its enhanced performance for tetracycline hydrochloride adsorption

2019 ◽  
Vol 12 (02) ◽  
pp. 1950014 ◽  
Author(s):  
Wei Yang ◽  
Sheng Guo ◽  
Jinyi Chen ◽  
Abdul Naeem ◽  
Hussain Fida ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Adsorption Capacity ◽  
Photoelectron Spectroscopy ◽  
Adsorption Process ◽  
Interlayer Spacing ◽  
Tetracycline Hydrochloride ◽  
Maximum Adsorption Capacity ◽  
X Ray ◽  
Modified Montmorillonite ◽  
Wide Ph Range

Iron-modified montmorillonite (Mt) composites with controlled interlayer spacing were successfully synthesized through Fenton-like process with the addition of different concentrations of Rhodamine B (RhB). The physicochemical properties of the resulting samples were characterized by X-ray powder diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS). It was worth noting that the adsorption efficiency of the composite for tetracycline hydrochloride (TC) increased with the increase of the RhB concentration during preparation. The maximum adsorption capacity of the as-prepared composite toward TC was 192.4[Formula: see text]mg/g, which was much higher than that of the Mt (144.9[Formula: see text]mg/g). Moreover, the as-prepared adsorbent showed high adsorption capacity of TC in a wide pH range of 3.0–9.0. The adsorption process followed the pseudo-second-order equation and the Langmuir isotherm model, suggesting the mono-layer chemisorption of the adsorption process. The present work may provide a new strategy for the design and fabrication of functional clay-based materials.

EFFECTS OF ACTIVATED TIME ON STRUCTURAL PROPERTIES OF PLATED PLANT FIBER NONWOVEN SHEETS

2019 ◽  
Vol 26 (01) ◽  
pp. 1850124 ◽  
Author(s):  
ZHIPING SUN ◽  
YAJUN ZHANG ◽  
JUNJUN HUANG
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Adsorption Capacity ◽  
Structural Properties ◽  
Photoelectron Spectroscopy ◽  
Saturation Point ◽  
Plant Fiber ◽  
X Ray ◽  
Activating Solution ◽  
Scanning Electron

In this work, the effects of activated time on the structural properties of plated plant fiber nonwoven sheet were investigated systematically using scanning electron microscopy (SEM) and X-ray photoelectron spectroscopy (XPS). Results showed that there existed a saturated adsorption state on the surface of sheet in the PdCl2 solution. The adsorbed rate and saturated adsorption capacity increased with the increase of PdCl2 concentration. As a result, the deposited quantity and crystallization characteristics of plated nonwoven sheets were firstly enhanced and then unchanged with increase of activated time. The Pd-adsorbed capacity reached saturation point when the activated time was 16[Formula: see text]min. The maximum plated quantity was 0.02 and 0.028[Formula: see text]g/cm2 when the concentration of activating solution was 0.015 and 0.15[Formula: see text]g/L on the surface of sheet.

scholarly journals Montmorillonite-anchored magnetite nanocomposite for recovery of ammonium from stormwater and its reuse in adsorption of Sc3+

2021 ◽  
Vol 6 (3) ◽  
Author(s):  
Jianzhi Song ◽  
Varsha Srivastava ◽  
Tomas Kohout ◽  
Mika Sillanpää ◽  
Tuomo Sainio
Keyword(s):  
Electron Microscopy ◽  
Adsorption Capacity ◽  
Photoelectron Spectroscopy ◽  
Selective Adsorption ◽  
Maximum Adsorption Capacity ◽  
Suitable Model ◽  
Transmission Electron ◽  
Adsorbent Surface ◽  
Langmuir Isotherm Model ◽  
Co Precipitation

AbstractThe treatment of stormwater to remove and recover nutrients has received increasing interest. The objective of this study was to develop a novel adsorbent that is easy to handle, has good adsorption capacity, and is economical to use. A novel nanocomposite of montmorillonite (MT)-anchored magnetite (Fe3O4) was synthesised by co-precipitation as an adsorbent for ammonium. The MT/Fe3O4 nanocomposite had pore sizes (3–13 nm) in the range of narrow mesopores. The dispersion of the anchored Fe3O4 was confirmed by transmission electron microscopy, scanning electron microscopy, and X-ray photoelectron spectroscopy (XPS). The nanocomposite exhibited higher affinity towards ammonium than the original MT. The Langmuir isotherm model was found to be the most suitable model to explain the ammonium adsorption behaviour of the nanocomposite. The maximum adsorption capacity for ammonium was 10.48 mg/g. The adsorption mechanism was a combination of ion exchange and electrostatic interaction. In an authentic stormwater sample, the synthesised adsorbent removed 64.2% of ammonium and reduced the amount of heavy metal contaminants including Mn, Ni, Cu and Zn. Furthermore, the ammonium loading on MT/Fe3O4 during adsorption functionalised the adsorbent surface. Additionally, the spent nanocomposite showed potential for rare earth elements (REEs) adsorption as a secondary application, especially for the selective adsorption of Sc3+. The versatile application of montmorillonite-anchored magnetite nanocomposite makes it a promising adsorbent for water treatment. Graphic abstract

scholarly journals Effective Interactions of Ag Nanoparticles on the Surface of SBA-15 in Performing Deep Desulfurization of Real Diesel Fuel

Catalysts ◽  
2020 ◽  
Vol 10 (5) ◽  
pp. 593 ◽  
Author(s):  
Clenildo de Longe ◽  
Rafael Viana Sales ◽  
Anne Beatriz Figueira Câmara ◽  
Heloise Oliveira Medeiros de Araújo Moura ◽  
Enrique Rodríguez-Castellón ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Diesel Fuel ◽  
Photoelectron Spectroscopy ◽  
Ag Nanoparticles ◽  
Dark Field ◽  
X Ray ◽  
Adsorbent Surface ◽  
Scanning Transmission ◽  
Annular Dark Field ◽  
Equilibrium Data

SBA-15 materials as-synthesized and impregnated with Ag nanoparticles were applied to perform adsorptive desulfurization of real diesel fuel. High-angle annular dark-field scanning transmission electron microscopy and field-emission scanning electron microscopy coupled with energy-dispersive X-ray spectroscopy (HAADF-STEM-EDX and FESEM-EDX) and X-ray photoelectron spectroscopy (XPS) results confirmed that there is uniform distribution of Ag nanodomains on the surface and in the channels of a 2AgSBA-15 (2% Ag) sample. The interaction between sulfur compounds and adsorbent mainly occurred via π-complexation mechanisms, as observed via XPS and equilibrium data. The kinetic results for 2AgSBA-15 were better fitted to the pseudo-second-order model (R2 > 0.9999), indicating that the determining step of the adsorptive process is chemisorption, whereas the equilibrium results were better fitted to the Langmuir model (R2 > 0.9994), thus indicating that the adsorption occurs on the adsorbent surface monolayer with significant adsorption capacity (qm = 20.30 mgS/g), approximately two times greater than that observed for pure SBA-15. The mean desulfurization reached by the adsorbents was up to 86.8% for six recycling steps.

scholarly journals Trimethoprim Antibiotic Adsorption from Aqueous Solution onto Eco-Friendly Zr-Metal Organic Framework Material

Materials ◽  
2021 ◽  
Vol 14 (24) ◽  
pp. 7545
Author(s):  
Marwa Elkady ◽  
Kamal E. Diab ◽  
Hassan Shokry
Keyword(s):  
Electron Microscopy ◽  
Aqueous Solution ◽  
Removal Efficiency ◽  
Photoelectron Spectroscopy ◽  
Metal Organic Framework ◽  
Physical Nature ◽  
Polluted Water ◽  
Solution Ph ◽  
X Ray ◽  
Adsorbent Dose

The synthesis of Bio-MOF using aspartic acid as an organic linker and water as a solvent was performed to create an environmentally friendly material. The chemical composition, structure, and morphology of the synthesized zirconium Bio-MOF (MIP-202) was evaluated using X-ray diffraction (XRD), energy dispersive X-ray (EDX) spectroscopy, transmission electron microscopy (TEM), scanning electron microscopy (SEM), and X-ray photoelectron spectroscopy (XPS). The synthesized Bio-MOF was used as an adsorbent for trimethoprim antibiotic as pollutants from an aqueous solution under various operating parameters. The increase in the initial trimethoprim concentration from 2.5 mg/L to 20 mg/L decreased the decontamination efficiency from 77.6% to 35.9% at a solution pH of 7 with 0.5 g/L adsorbent dose after 60 min reaction time. The rise of adsorbent dose from 0.1 g/L to 1.5 g/L increased the removal efficiency from 47.7% to 87.6%. The maximum trimethoprim removal efficiency of 95% was attained at a solution pH of 11. Langmuir and pseudo-second order models described the adsorption process of trimethoprim antibiotic onto zirconium Bio-MOF and the chemo-physical nature of trimethoprim adsorption onto the synthesized zirconium Bio-MOF. Accordingly, it was evident that the prepared zirconium Bio-MOF (MIP-202) is an ecofriendly and efficient adsorbent for antibiotic decontamination from polluted water.

Antibacterial silver-diatomite nanocomposite ceramic with low silver release

2019 ◽  
Vol 20 (2) ◽  
pp. 633-643
Author(s):  
Xiaopeng Qi ◽  
Junwei Chen ◽  
Qian Li ◽  
Hui Yang ◽  
Honghui Jiang ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Water Treatment ◽  
Photoelectron Spectroscopy ◽  
Bactericidal Effect ◽  
Ceramic Filter ◽  
Ceramic Filters ◽  
X Ray ◽  
E Coli ◽  
Point Of Use ◽  
Silver Release

Abstract There is an urgent need for an effective and long-lasting ceramic filter for point-of-use water treatment. In this study, silver-diatomite nanocomposite ceramic filters were developed by an easy and effective method. The ceramic filters have a three-dimensional interconnected pore structure and porosity of 50.85%. Characterizations of the silver-diatomite nanocomposite ceramic filters were performed using scanning electron microscopy, transmission electron microscopy, X-ray diffraction, and X-ray photoelectron spectroscopy. Silver nanoparticles were confirmed to be formed in situ in the ceramic filter. The highest silver concentration in water was 0.24 μg/L and 2.1 μg/L in short- and long-term experiments, indicating very low silver-release properties of silver-diatomite nanocomposite ceramic filter. The nanocomposite ceramics show strong bactericidal activity. When contact time with Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus) of 105 colony forming units (CFU)/mL exceeded 3 h, the bactericidal rates of the four different silver content ceramics against E. coli and S. aureus were all 100%. Strong bactericidal effect against E. coli with initial concentration of 109 CFU/mL were also observed in ceramic newly obtained and ceramic immersed in water for 270 days, demonstrating its high stability. The silver-diatomite nanocomposite ceramic filters could be a promising candidate for point-of-use water treatment.

scholarly journals Phytosynthetic Fabrication of Lanthanum Ion-Doped Nickel Oxide Nanoparticles Using Sesbania grandiflora Leaf Extract and Their Anti-Microbial Properties

Crystals ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 124
Author(s):  
Srihasam Saiganesh ◽  
Thyagarajan Krishnan ◽  
Golla Narasimha ◽  
Hesham S. Almoallim ◽  
Sulaiman Ali Alhari ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Optical Properties ◽  
Rare Earth ◽  
Nickel Oxide ◽  
Photoelectron Spectroscopy ◽  
Metal Oxide Nanoparticles ◽  
Oxide Nanoparticles ◽  
Nio Nanoparticles ◽  
X Ray ◽  
Sesbania Grandiflora

Over the past few years, the photogenic fabrication of metal oxide nanoparticles has attracted considerable attention, owing to the simple, eco-friendly, and non-toxic procedure. Herein, we fabricated NiO nanoparticles and altered their optical properties by doping with a rare earth element (lanthanum) using Sesbania grandiflora broth for antibacterial applications. The doping of lanthanum with NiO was systematically studied. The optical properties of the prepared nanomaterials were investigated through UV-Vis diffuse reflectance spectra (UV-DRS) analysis, and their structures were studied using X-ray diffraction analysis. The morphological features of the prepared nanomaterials were examined by scanning electron microscopy and transmission electron microscopy, their elemental structure was analyzed by energy-dispersive X-ray spectral analysis, and their oxidation states were analyzed by X-ray photoelectron spectroscopy. Furthermore, the antibacterial action of NiO and La-doped NiO nanoparticles was studied by the zone of inhibition method for Gram-negative and Gram-positive bacterial strains such as Escherichia coli and Bacillus sublitis. It was evident from the obtained results that the optimized compound NiOLa-04 performed better than the other prepared compounds. To the best of our knowledge, this is the first report on the phytosynthetic fabrication of rare-earth ion Lanthanum (La3+)-doped Nickel Oxide (NiO) nanoparticles and their anti-microbial studies.

scholarly journals Thermoelectric Generator Using Polyaniline-Coated Sb2Se3/β-Cu2Se Flexible Thermoelectric Films

Polymers ◽  
2021 ◽  
Vol 13 (9) ◽  
pp. 1518
Author(s):  
Minsu Kim ◽  
Dabin Park ◽  
Jooheon Kim
Keyword(s):  
Electron Microscopy ◽  
Electrical Conductivity ◽  
Field Emission ◽  
Photoelectron Spectroscopy ◽  
Thermoelectric Generator ◽  
Hydrothermal Reaction ◽  
Water Evaporation ◽  
Pani Film ◽  
Portable Devices ◽  
X Ray

Herein, Sb2Se3 and β-Cu2Se nanowires are synthesized via hydrothermal reaction and water evaporation-induced self-assembly methods, respectively. The successful syntheses and morphologies of the Sb2Se3 and β-Cu2Se nanowires are confirmed via X-ray powder diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Raman spectroscopy, field emission scanning electron microscopy (FE-SEM), and field emission transmission electron microscopy (FE-TEM). Sb2Se3 materials have low electrical conductivity which limits application to the thermoelectric generator. To improve the electrical conductivity of the Sb2Se3 and β-Cu2Se nanowires, polyaniline (PANI) is coated onto the surface and confirmed via Fourier-transform infrared spectroscopy (FT-IR), FE-TEM, and XPS analysis. After coating PANI, the electrical conductivities of Sb2Se3/β-Cu2Se/PANI composites were increased. The thermoelectric performance of the flexible Sb2Se3/β-Cu2Se/PANI films is then measured, and the 70%-Sb2Se3/30%-β-Cu2Se/PANI film is shown to provide the highest power factor of 181.61 μW/m·K2 at 473 K. In addition, a thermoelectric generator consisting of five legs of the 70%-Sb2Se3/30%-β-Cu2Se/PANI film is constructed and shown to provide an open-circuit voltage of 7.9 mV and an output power of 80.1 nW at ΔT = 30 K. This study demonstrates that the combination of inorganic thermoelectric materials and flexible polymers can generate power in wearable or portable devices.

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