scholarly journals Photocatalytic Degradation of Cefixime Trihydrate by Bismuth Ferrite Nanoparticles

Materials ◽  
2021 ◽  
Vol 15 (1) ◽  
pp. 213
Author(s):  
Ammara Nazir ◽  
Shoomaila Latif ◽  
Syed Farooq Adil ◽  
Mufsir Kuniyil ◽  
Muhammad Imran ◽  
...  
Keyword(s):  
Combustion Synthesis ◽  
Degradation Kinetics ◽  
Bismuth Ferrite ◽  
Synthesis Method ◽  
Ferrite Nanoparticles ◽  
Solar Irradiation ◽  
X Ray Diffraction ◽  
Vis Spectroscopy ◽  
Different Types ◽  
Photoluminescence Studies

The present work was carried out to synthesize bismuth ferrite (BFO) nanoparticles by combustion synthesis, and to evaluate the photocatalytic activity of synthesized bismuth ferrite nanoparticles against cefixime trihydrate. BFO nanoparticles were successfully synthesized using bismuth (III) nitrate and iron (III) nitrate by a combustion synthesis method employing different types of fuels such as maltose, succinic acid, cinnamic acid, and lactose. The effects of the different types of fuels on the morphology and size of the bismuth ferrite nanoparticles were investigated. Characterization of the as-obtained bismuth ferrite nanoparticles was carried out by different techniques such as X-ray diffraction (XRD), scanning electron microscopy (SEM), Energy-Dispersive Spectroscopy (EDS), N2-sorption analysis, Fourier-transform infrared spectroscopy (FT-IR), and ultraviolet-visible (UV–vis) spectroscopy. Photoluminescence studies were also carried out for the various bismuth ferrite nanoparticles obtained. Degradation of cefixime trihydrate was investigated under sunlight to evaluate the photocatalytic properties of the bismuth ferrite nanoparticles, and it was found that the bismuth ferrite nanoparticles followed first-order degradation kinetics in solar irradiation in the degradation of antibiotic, cefixime trihydrate.

Flameless Solution Combustion Synthesis of Al3+ Doped LiMn2O4

2011 ◽  
Vol 186 ◽  
pp. 7-10 ◽  
Author(s):  
Gui Yang Liu ◽  
Jun Ming Guo ◽  
Bao Sen Wang ◽  
Ying He
Keyword(s):  
Combustion Synthesis ◽  
Synthesis Method ◽  
Solution Combustion Synthesis ◽  
Xrd Analysis ◽  
Cycling Performance ◽  
X Ray Diffraction ◽  
Solution Combustion ◽  
Electrochemical Test ◽  
Micro Morphology ◽  
Better Than

Single phase Al3+ doped LiMn2O4 has been prepared by flameless solution combustion synthesis method at 600oC for 1h. X-ray diffraction (XRD) and scanning electric microscope (SEM) were used to determine the phase composition and micro morphology of the products. XRD analysis indicates that the purities increase and the lattice parameters of the products decrease with increasing Al3+ content. Electrochemical test indicates that the cycling performance of the products with Al3+ doping are better than that of the product without Al3+ doping. The product LiAl0.10Mn1.90O4 gets the best electrochemical performance. At the current density of 30mA/g, the initial discharge capacity of LiAl0.10Mn1.90O4 is 124.8mAh/g, and after 20 cycles, the capacity retention is more than 89%. SEM investigation indicates that the particles of LiAl0.10Mn1.90O4 are sub-micron in size and well dispersed.

scholarly journals Green bio-inspired synthesis, characterization and activity of silver nanoparticle forms of Centaurea virgata Lam. and the isolated flavonoid eupatorin

2018 ◽  
Vol 7 (4) ◽  
pp. 372-379 ◽  
Author(s):  
Burcu Sümer Tüzün ◽  
Judit Hohmann ◽  
Bijen Kivcak
Keyword(s):  
Electron Microscopy ◽  
Zeta Potential ◽  
Synthesis Method ◽  
Gravimetric Analysis ◽  
X Ray Diffraction ◽  
Characteristic Absorption Band ◽  
X Ray ◽  
Vis Spectroscopy ◽  
Diffraction Patterns ◽  
Isolated Compound

AbstractA green synthesis method of silver nanoparticles (AgNPs) usingCentaurea virgataLam. extract and the isolated compound eupatorin was investigated in this study. Ultraviolet-visible (UV-Vis) spectroscopy, Fourier transform infrared (FTIR) spectroscopy, transmission electron microscopy (TEM), scanning electron microscopy (SEM)/energy-dispersive X-ray (EDX) spectroscopy, thermal gravimetric analysis, X-ray diffraction analysis and zeta potential were used for characterization of AgNPs. The UV-Vis spectrum exhibited a characteristic absorption band at 420 nm for monodisperse nanoparticles. FTIR measurements also proved the formation. X-ray diffraction patterns showed peaks at (110) and (112), which are characteristic for hexagonal crystals and also showed peaks at (111), (200) and (240), which are characteristic for orthorhombic crystals. The TEM images of AgNPs show that the morphology of AgNPs was predominantly spherical. Obtained AgNPs were highly stable according to the zeta potential values. The nitric oxide scavenging activity, which is also related to anticancer activity, of AgNPs was evaluated. It can be concluded thatC. virgataLam. extract and eupatorin can be used as a reducing agent for potential antioxidant AgNP formation.

scholarly journals Improved Aging Stability of Ethylene-Norbornene Composites Filled with Lawsone-Based Hybrid Pigment

Polymers ◽  
2019 ◽  
Vol 11 (4) ◽  
pp. 723 ◽  
Author(s):  
Anna Marzec ◽  
Bolesław Szadkowski
Keyword(s):  
Nmr Spectroscopy ◽  
Secondary Ion Mass Spectrometry ◽  
Solar Spectrum ◽  
Mechanical Analysis ◽  
Solar Irradiation ◽  
Mechanical And Thermal Properties ◽  
X Ray Diffraction ◽  
Lawsonia Inermis ◽  
Tof Sims ◽  
Vis Spectroscopy

In this study, we produced a new organic-inorganic hybrid pigment based on a natural chromophore. Lawsone was selected as the active organic compound and incorporated into aluminum-magnesium hydroxycarbonate (LH). The hydroxynaphthoquinone derivative lawsone (Lawsonia inermis L.) is a naturally occurring dye, which is commonly used as a colorant because of its nontoxicity and biological functions. The structure and stability of the hybrid colorant were investigated using 27-Al solid-state nuclear magnetic resonance (NMR) spectroscopy, X-ray diffraction (XRD), secondary ion mass spectrometry (TOF-SIMS), thermogravimetric analysis (TGA), scanning electron microscopy (SEM) and UV-Vis spectroscopy. TOF-SIMS and 27Al NMR spectroscopy revealed interactions between the dye molecules and metal ions present in the LH host, confirming successful formation of an LH-based hybrid (LH/lawsone). In the next part of the study, we examined the effect of the hybrid pigment on the mechanical and thermal properties of ethylene-norbornene (EN) materials, as well as the aging resistance of the colored composites to irradiation across the full solar spectrum. Dynamic mechanical analysis (DMA) and the results of tensile break tests revealed that the EN+LH/lawsone composite had significantly better resistance to solar irradiation in comparison to EN and EN with an unmodified carrier.

Effects of Synthesis Conditions on the Crystalline Phases and Photocatalytic Activities of Silver Vanadates via Hydrothermal Method

2009 ◽  
Vol 1171 ◽  
Author(s):  
Chao-Ming Huang ◽  
Guan T. Pan ◽  
Lung C. Chen ◽  
C.K. Thomas Yang ◽  
Wen S. Chang
Keyword(s):  
Photocatalytic Activity ◽  
Visible Light ◽  
Surface Area ◽  
Synthesis Method ◽  
Stoichiometric Ratio ◽  
X Ray Diffraction ◽  
Hydrothermal Conditions ◽  
Synthesis Conditions ◽  
Vis Spectroscopy ◽  
Visible Light Driven

AbstractVisible-light-driven Ag3VO4 photocatalysts were successfully synthesized using low-temperature hydrothermal synthesis method. Under various hydrothermal conditions, the structures of silver vanadates were tuned by manipulating the hydrothermal time and the ratio of silver to vanadium. X-ray diffraction (XRD) results reveal that the powders prepared in a stoichiometric ratio consisted of pure α-Ag3VO4 or mixed phases of Ag4V2O7 and α-Ag3VO4. With increasing the Ag-to-V mole ratio to 6:1, the resulting samples were identified as pure monoclinic structure α-Ag3VO4. UV-vis spectroscopy indicated that silver vanadate particles had strong visible light absorption with associated band gaps in the range of 2.2-2.5 eV. The sample synthesized in the excess silver exhibited higher photocatalytic activity than that synthesized in a stoichiometric ratio. The powder synthesized at silver-rich at 140℃ for 4 h (SHT4) exhibited the highest photocatalytic activity among all samples. The reactivity of SHT4 (surface area, 3.52 m2 g-1) on the decomposition of gaseous benzene was about 16 times higher than that of P25 (surface area, 49.04 m2 g-1) under visible light irradiation. A well developed crystallinity of Ag3VO4 of SHT 4 was considered to enhance the photocatalytic efficiency.

Temperature Dependence of LiMn2O4 Prepared by a Solution Combustion Synthesis in the System of Acetate Salts and Acetic Acid

2012 ◽  
Vol 485 ◽  
pp. 465-468
Author(s):  
Li Li Zhang ◽  
Gui Yang Liu ◽  
Jun Ming Guo ◽  
Bao Sen Wang ◽  
Ying He
Keyword(s):  
Acetic Acid ◽  
Combustion Synthesis ◽  
Raw Materials ◽  
Synthesis Method ◽  
Solution Combustion Synthesis ◽  
Electrochemical Performances ◽  
Metal Foil ◽  
X Ray Diffraction ◽  
Solution Combustion ◽  
Acid Ratio

Spinel LiMn2O4 have been prepared by the solution combustion synthesis method using acetate salts as raw materials and acetic acid as fuel. The phase compositions of the as-prepared products were determined by X-ray diffraction (XRD). The electrochemical performance of the products was tested by using a coin-type half battery versus lithium metal foil as anode material. XRD results suggested that the purities of the products prepared at 500oC are higher than these of the products prepared at 600oC. For the products prepared at 500oC, the purities of the products increase with increasing acetic acid ratios. But for the products prepared at 600oC, the purities of the products decrease with increasing acetic acid ratios. The performance tests indicated that the electrochemical performances of the products prepared at 500oC are better than these of the products prepared at 600oC. The product prepared at 500oC with the acetic acid ratio of 1.0 gets the best performance. The initial capacity of it reaches to 124.8mAh/g at the current density of 75mA/g, and after 50 cycles, the capacity retention is 93.7%.

LIGHT-INDUCED AGGREGATION OF NANOPARTICLES FUNCTIONALIZED WITH 7-AMINO-4-METHYLCOUMARIN

Nano LIFE ◽  
2012 ◽  
Vol 02 (03) ◽  
pp. 1241007 ◽  
Author(s):  
JOSHUA E. ROSEN ◽  
LYNDON JONES ◽  
FRANK X. GU
Keyword(s):  
Reductive Amination ◽  
Uv Light ◽  
Synthesis Method ◽  
The Body ◽  
Transmission Electron ◽  
Vis Spectroscopy ◽  
Different Types ◽  
Potential Applications ◽  
Nanoparticle Formulation ◽  
Induced Aggregation

Herein, we report on the modification of silica nanoparticles with the molecule 7-amino-4-methylcoumarin (AMC) via a hydrophilic dextran linker using reductive amination chemistry. The AMC-functionalized nanoparticles were shown to aggregate in response to irradiation by 350 nm UV light. The aggregation of the particles was studied using dynamic light scattering, UV-VIS spectroscopy, and transmission electron microscopy. The synthesis method described herein utilizes a classic reductive amination reaction, which can potentially be transferred to a variety of different types of nanoparticles. Particles displaying this behavior have many potential applications in the field of nanomedicine, as they can potentially allow one to modulate the particle size of a nanoparticle formulation after administration to the body. The AMC-functionalized particles studied in this report serve as a convincing proof-of-concept for synthesizing light-responsive nanoparticles.

LiAl0.1Mn1.9O4 Prepared by a Solution Combustion Synthesis Using Acetate as Raw Materials and Acetic Acid as Fuel: Effect of Further Calcination Time

2012 ◽  
Vol 485 ◽  
pp. 473-477
Author(s):  
Gui Yang Liu ◽  
Jun Ming Guo ◽  
Li Li Zhang ◽  
Jing Wang ◽  
Bao Sen Wang ◽  
...  
Keyword(s):  
Combustion Synthesis ◽  
Raw Materials ◽  
Synthesis Method ◽  
Solution Combustion Synthesis ◽  
Metal Foil ◽  
X Ray Diffraction ◽  
Calcination Time ◽  
Solution Combustion ◽  
X Ray ◽  
Discharge Capacities

LiAl0.1Mn1.9O4 materials were prepared by a solution combustion synthesis method. In order to improve the purity of the products, the effect of further calcination time was investigated. The phase compositions of the as-prepared products were determined by X-ray diffraction (XRD). The electrochemical performance of the products was tested by using a coin-type half battery versus lithium metal foil as anode material. XRD results suggested that the main phase of the products was LiAl0.1Mn1.9O4, and there was a trace amount Mn2O3 impurity in some of the products. The purity, crystallinity and grain size of the LiAl0.1Mn1.9O4 were increased with increasing further calcination time. Electrochemical experiments demonstrate that the initial discharge capacities of the products with further calcination time of 0, 6, 12 and 24h were 93.7, 105.7, 114.0 and 120.6mAh/g, and about 89.8, 89.5, 89.2 and 88.3% of the initial capacities were retained after 25 cycles, respectively. Further calcination time can enhance the initial capacity, but is not favorable for the cycle ability of the products.

Ni Doped LiMn2O4 Prepared by a Flameless Combustion Synthesis

2012 ◽  
Vol 625 ◽  
pp. 251-254 ◽  
Author(s):  
Gui Yang Liu ◽  
Bao Sen Wang ◽  
Ying He ◽  
Jun Ming Guo
Keyword(s):  
Combustion Synthesis ◽  
Raw Materials ◽  
Synthesis Method ◽  
Solution Combustion Synthesis ◽  
Electrochemical Performances ◽  
X Ray Diffraction ◽  
Galvanostatic Charge ◽  
Solution Combustion ◽  
Limn2o4 Spinel ◽  
X Ray

In this paper, LiNixMn2−xO4 materials were prepared by solution combustion synthesis method using acetic salts as raw materials and acetic acid as fuel. The phase structures are characterized by X-ray diffraction (XRD). Electrochemical performances of the materials are investigated by galvanostatic charge/discharge methods. XRD results revealed that the main phase of the products with increasing Ni3+ content is LiMn2O4, and there is a trace amount of Mn3O4 found in the product with Ni3+ content of 0.05. Electrochemical experiments showed that the capacity and the cyclability of the LiNixMn2−xO4 materials decrease with increasing Ni3+ content. Ni3+ doping has no significantly improvement for the capacity and the cyclability of the LiMn2O4 spinel.

Oxidation Behavior of NiAl Produced by Gel Combustion Synthesis

2016 ◽  
Vol 701 ◽  
pp. 122-126
Author(s):  
Tammy Anne Gonsalvez ◽  
Abreeza Manap ◽  
Nurfanizan Afandi ◽  
Halina Misran
Keyword(s):  
Combustion Synthesis ◽  
Oxidation Behavior ◽  
Mixed Oxides ◽  
Synthesis Method ◽  
Mass Gain ◽  
Isothermal Oxidation ◽  
X Ray Diffraction ◽  
Gel Combustion ◽  
Before And After ◽  
Different Temperatures

This paper presents the results of a study of the oxidation behavior of NiAl produced by gel combustion synthesis calcined at two different temperatures. The objective is to compare the oxide growth rates, oxide scale composition, morphology and elemental composition of the sample powder subjected to isothermal oxidation and calcined at 1050 °C and 1300 °C for 1, 2, 4 and 10 hours by means of mass gain measurements, X-ray diffraction (XRD), field emission scanning electron microsocopy (FESEM) and energy-dispersive spectrometry (EDX) in order to investigate the reliability of the gel combustion synthesis method and evaluate the effect of calcination temperature on the oxidation behaviour of the powder. It was found that for the sample calcined at 1300°C the sample was made up mainly of metastable and stable alumina before oxidation and stable alpha alumina after oxidation whereas for the powder calcined at 1050°C the sample was mainly composed of detrimental mixed oxides before and after oxidation. Overall findings indicate that the oxidation behavior of the powder calcined at 1300°C is more protective compared to the powder calcined at 1050°C.

scholarly journals Effect of Precursors on the Growth and Physiochemical Properties of Bio-mimetic ZnFe2O4 Nanocomposites for Photoelectrochemical Application

2020 ◽  
Vol 49 (12) ◽  
pp. 3219-3228
Author(s):  
Mohd Faizal Md Nasir ◽  
Wan Ramli Wan Daud ◽  
Mohamad Azuwa Mohamed ◽  
Mohamad Hafiz Mamat ◽  
Saifollah Abdullah ◽  
...  
Keyword(s):  
Zinc Ferrite ◽  
Synthesis Method ◽  
Photocurrent Density ◽  
Superior Performance ◽  
X Ray Diffraction ◽  
Physiochemical Properties ◽  
Fibril Structure ◽  
Vis Spectroscopy ◽  
Synthesized Materials ◽  
Transfer Properties

Zinc ferrite (ZnFe2O4) photocatalysts have been prepared with different types of zinc precursors using the bio-mimetic synthesis method. The kapok fibre (Ceiba pentandra (L.) Gaertn) used as a sacrificial template. The physiochemical of prepared bio-mimetic materials were carried out thoroughly in this work. The FESEM analysis in mimetic zinc ferrite catalysts shows a distinctly different structural transition under different precursors conditions. The acetate precursor formed a hollow tubular structure while other precursors formed a hierarchal fibril structure. X-ray diffraction analysis showed a distinctly different phase transition while UV-Vis spectroscopy recorded variable optical properties beneath different precursor conditions. The EDX and ATR-FTIR spectroscopy confirmed the formation of the pure composite after the annealing process. Different type of precursors that used have leads to tuneable of the magnetic properties of the prepared materials. Electrophoretic deposition (EPD) method has been used to fabricate the synthesized materials as photo-electrodes on the FTO substrate then evaluated for photoelectrochemical (PEC) application. Changing the precursors in the preparation method show a significant effect on physicochemical and PEC performance. The morphology and surface structure of the prepared catalysts are correlated with the alteration of the precursors, then attributed to the charge transfer properties of the photocurrent density in PEC system. The bio-templated zinc ferrite catalysts are promising photoanode in the photocatalytic activities. It is interesting to note that the various forms of multi-structure such as hollow fibril core-shell offers an enormous impact in designing active photocatalyst with superior performance.

Sign in / Sign up

Export Citation Format

Share Document