scholarly journals Voltammetric detection of sumatriptan in the presence of naproxen using Fe3O4@ZIF-8 nanoparticles modified screen printed graphite electrode

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Somayeh Tajik ◽  
Mahboobeh Shahsavari ◽  
Iran Sheikhshoaie ◽  
Fariba Garkani Nejad ◽  
Hadi Beitollahi
Keyword(s):  
Electron Microscopy ◽  
Detection Limit ◽  
Graphite Electrode ◽  
Diffraction Field ◽  
Gravimetric Analysis ◽  
X Ray ◽  
Sensing Applications ◽  
Voltammetric Detection ◽  
Sensing Performance ◽  
Screen Printed

AbstractA novel electrochemical sensing platform was designed and prepared for the simultaneous detection of sumatriptan and naproxen by exploiting the prowess of the Fe3O4@ZIF-8 nanoparticles (NPs); as-synthesized Fe3O4@ZIF-8 NPs were characterized by energy-dispersive X-ray spectroscopy, fourier transform infrared spectroscopy, X-ray diffraction, field emission scanning electron microscopy (FESEM), transmission electron microscopy and thermal gravimetric analysis. The immobilized Fe3O4@ZIF-8 NPs on a screen printed graphite electrode (SPGE) was evaluated electrochemically via cyclic voltammetry, linear sweep voltammetry, and differential pulse voltammetry as well as chronoamprometery means; Fe3O4@ZIF-8/SPGE exhibited good sensing performance for sumatriptan in a range of 0.035–475.0 µM with detection limit of 0.012 µM. Also, Fe3O4@ZIF-8/SPGE exhibited good sensing performance for naproxen in a range of 0.1–700.0 µM with detection limit of 0.03 µM. The modified electrode showed two separate oxidative peaks at 620 mV for sumatriptan and at 830 mV for naproxen with a peak potential separation of 210 mV which was large enough to detect the two drugs simultaneously besides being stable in the long-run with considerable reproducibility. Real sample analyses were carried out to identify the function of fabricated electrode in sensing applications wherein trace amounts of sumatriptan and naproxen could be identified in these samples.

scholarly journals Synthesis and Characterization of Nano-Tungsten Oxide Precipitated onto Natural Inorganic Clay for Humidity-Sensing Applications

Ceramics ◽  
2018 ◽  
Vol 1 (1) ◽  
pp. 120-127 ◽  
Author(s):  
Ahmed Afify ◽  
Ahmed Elsayed ◽  
Mohamed Hassan ◽  
Mohamed Ataalla ◽  
Amr Mohamed ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Tungsten Oxide ◽  
Diffraction Field ◽  
Oxide Nanoparticles ◽  
X Ray Diffraction ◽  
X Ray ◽  
Sensing Applications ◽  
Transmission Electron ◽  
Tungsten Oxide Nanoparticles ◽  
Inorganic Clay

A wet chemical method was used to obtain tungsten oxide nanoparticles from tungsten tetrachloride and natural microfibrous inorganic clay (sepiolite) as a starting material. Precipitation of tungsten oxide species onto sepiolite under basic conditions and subsequent thermal treatment was investigated, prompted by the abundance of sepiolite in nature and the useful environmental applications that could be attained. Laser granulometry, X-ray diffraction, field emission scanning electron microscopy (FE-SEM), energy dispersive X-ray spectroscopy (EDX), and high-resolution transmission electron microscopy (HR-TEM) techniques were used to study the particle-size distribution, the morphology, and the composition of the prepared sample. Our findings show the presence of tungsten oxide nanoparticles, which are less than 50 nm, on the needles of the modified sepiolite.

scholarly journals Rapid four-component synthesis of dihydropyrano[2,3-c]pyrazoles using nano-eggshell/Ti(IV) as a highly compatible natural based catalyst

BMC Chemistry ◽  
2021 ◽  
Vol 15 (1) ◽  
Author(s):  
Arefeh Dehghani Tafti ◽  
Bi Bi Fatemeh Mirjalili ◽  
Abdolhamid Bamoniri ◽  
Naeimeh Salehi
Keyword(s):  
Thermo Gravimetric Analysis ◽  
Reaction Times ◽  
Diffraction Field ◽  
Gravimetric Analysis ◽  
X Ray Diffraction ◽  
X Ray ◽  
Solvent Free Conditions ◽  
High Yields ◽  
Work Up

AbstractNano-eggshell/Ti(IV) as a novel naturally based catalyst was prepared, characterized and applied for the synthesis of dihydropyrano[2,3-c]pyrazole derivatives. The characterization of nano-eggshell/Ti(IV) was performed using Fourier Transform Infrared spectroscopy, X-ray Diffraction, Field Emission Scanning Electron Microscopy, Energy-Dispersive X-ray Spectroscopy, and Thermo Gravimetric Analysis. Dihydropyrano[2,3-c]pyrazoles were synthesized in the presence of nano-eggshell/Ti(IV) via a four component reaction of aldehydes, ethyl acetoacetate, malononitrile and hydrazine hydrate at room temperature under solvent free conditions. The principal affairs of this procedure are mild condition, short reaction times, easy work-up, high yields, reusability of the catalyst and the absence of toxic organic solvents.

scholarly journals Enhanced Photocatalytic Activity of Cu2O Cabbage/RGO Nanocomposites under Visible Light Irradiation

Polymers ◽  
2021 ◽  
Vol 13 (11) ◽  
pp. 1712
Author(s):  
Appusamy Muthukrishnaraj ◽  
Salma Ahmed Al-Zahrani ◽  
Ahmed Al Otaibi ◽  
Semmedu Selvaraj Kalaivani ◽  
Ayyar Manikandan ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Thermo Gravimetric Analysis ◽  
Visible Region ◽  
Catalytic Performance ◽  
Precipitation Method ◽  
Gravimetric Analysis ◽  
X Ray Diffraction ◽  
X Ray ◽  
Dye Pollutants ◽  
Transmission Electron

Towards the utilization of Cu2O nanomaterial for the degradation of industrial dye pollutants such as methylene blue and methyl orange, the graphene-incorporated Cu2O nanocomposites (GCC) were developed via a precipitation method. Using Hummers method, the grapheme oxide (GO) was initially synthesized. The varying weight percentages (1–4 wt %) of GO was incorporated along with the precipitation of Cu2O catalyst. Various characterization techniques such as Fourier-transform infra-red (FT-IR), X-ray diffraction (XRD), UV–visible diffused reflectance (UV-DRS), Raman spectroscopy, thermo gravimetric analysis (TGA), energy-dispersive X-ray analysis (EDX), and electro chemical impedance (EIS) were followed for characterization. The cabbage-like morphology of the developed Cu2O and its composites were ascertained from field-emission scanning electron microscopy (FESEM) and high-resolution transmission electron microscopy (HR-TEM). In addition, the growth mechanism was also proposed. The results infer that 2 wt % GO-incorporated Cu2O composites shows the highest value of degradation efficiency (97.9% and 96.1%) for MB and MO at 160 and 220 min, respectively. Further, its catalytic performance over visible region (red shift) was also enhanced to an appreciable extent, when compared with that of other samples.

scholarly journals Structural and optical properties of SnO2–Al2O3 nanocomposite synthesized via sol-gel route

2015 ◽  
Vol 33 (4) ◽  
pp. 714-718 ◽  
Author(s):  
Neeraj K. Mishra ◽  
Chaitnaya Kumar ◽  
Amit Kumar ◽  
Manish Kumar ◽  
Pratibha Chaudhary ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Optical Properties ◽  
Sol Gel ◽  
Physical Interaction ◽  
X Ray Diffraction ◽  
Structural And Optical Properties ◽  
X Ray ◽  
Sensing Applications ◽  
Scanning Electron

AbstractA nanocomposite of 0.5SnO2–0.5Al2O3 has been synthesized using a sol-gel route. Structural and optical properties of the nanocomposite have been discussed in detail. Powder X-ray diffraction and scanning electron microscopy with energy-dispersive X-ray diffraction spectroscopy confirm the phase purity and the particle size of the 0.5SnO2–0.5Al2O3 nanocomposite (13 to 15 nm). The scanning electron microscopy also confirms the porosity in the sample, useful in sensing applications. The FT-IR analysis confirms the presence of physical interaction between SnO2 and Al2O3 due to the slight shifting and broadening of characteristic bands. The UV-Vis analysis confirms the semiconducting nature because of direct transition of electrons into the 0.5SnO2–0.5Al2O3 nanocomposites.

Effect of Synthesis Temperature on Particles Size and Morphology of Zirconium Oxide Nanoparticle

2017 ◽  
Vol 50 ◽  
pp. 18-31 ◽  
Author(s):  
Rudzani Sigwadi ◽  
Simon Dhlamini ◽  
Touhami Mokrani ◽  
Patrick Nonjola
Keyword(s):  
Electron Microscopy ◽  
Particle Size ◽  
Zirconium Oxide ◽  
Thermo Gravimetric Analysis ◽  
Gravimetric Analysis ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Crystallite Sizes ◽  
Ft Ir

The paper presents the synthesis and investigation of zirconium oxide (ZrO2) nanoparticles that were synthesised by precipitation method with the effects of the temperatures of reaction on the particles size, morphology, crystallite sizes and stability at high temperature. The reaction temperature effect on the particle size, morphology, crystallite sizes and stabilized a higher temperature (tetragonal and cubic) phases was studied. Thermal decomposition, band structure and functional groups were analyzed by Brunauer-Emmett-Teller (BET), Scanning Electron Microscopy (SEM), Transmission electron microscopy (TEM), X-ray diffraction (XRD), Thermo-gravimetric analysis (TGA) and Fourier transform infrared (FT-IR). The crystal structure was determined using X-ray diffraction. The morphology and the particle size were studied using (SEM) and (TEM). The shaped particles were confirmed through the SEM analysis. The transmission electron microscopic analysis confirmed the formation of the nanoparticles with the particle size. The FT-IR spectra showed the strong presence of ZrO2 nanoparticles.

The Evaporative Decomposition of Solutions Method (Eds) for the Production of Ultrafine Y1Ba2Cu3O7 from Nitrate and Mixed Anion Precursor Solutions

1989 ◽  
Vol 169 ◽  
Author(s):  
Rollin E. Lakis ◽  
Sidney R. Butler
Keyword(s):  
Electron Microscopy ◽  
Particle Size ◽  
Barium Carbonate ◽  
Hollow Spheres ◽  
Particle Size Analysis ◽  
Size Analysis ◽  
Gravimetric Analysis ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron

AbstractY1Ba2Cu3O7 has been prepared by the evaporative decomposition of solutions method. Nitrate and mixed anion solutions were atomized and decomposed at temperatures ranging from 300°C to 950°C. The resulting materials have been characterized using x-ray powder diffraction, Thermal Gravimetric Analysis (TGA), particle size analysis, Scanning Electron Microscopy (SEM), and Transmission Electron Microscopy (TEM). The powder consists of 0.3 micron agglomerated hollow spheres with a primary particle size of 0.06 micron. TGA and x-ray diffraction indicate the presence of barium nitrate and barium carbonate due to incomplete decomposition and/or product contamination by the process environment.

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 Synthesis of SnO2 nanowires forCO, CH4 and CH3OH gases sensing

2018 ◽  
Vol 14 (8) ◽  
pp. 155014771879075 ◽  
Author(s):  
Khurram Shehzad ◽  
Nazar Abbas Shah ◽  
Muhammad Amin ◽  
Murrawat Abbas ◽  
Waqar Adil Syed
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Gas Sensing ◽  
Reduction Process ◽  
X Ray ◽  
Sensing Applications ◽  
Microscopy Investigation ◽  
Sno2 Nanowires ◽  
Visible Spectra ◽  
Scanning Electron

Synthesis of one-dimensional nanostructures, such as nanowires, is of vigorous significance for achieving the desired properties and fabricating functional devices. In this work, we report the synthesis of tin oxide (SnO2) nanowires on gold-catalyzed silicon substrate by carbothermal reduction process. SnO2 nanowires were synthesized with SnO2 and graphite powders as the source materials at atmospheric pressure and temperature of 900°C in the ambience of nitrogen (N2) gas. First, the effect of source material ratio SnO2:C on growth of SnO2 nanowires was studied. The structural, morphological and compositional properties of the samples were investigated by X-ray diffraction, scanning electron microscopy and energy dispersive X-ray spectroscopy. The scanning electron microscopy investigation reveals that uniform dense nanowires of SnO2 (diameter ~127 nm and length ~40 µm) were synthesized with vapour–liquid–solid mechanism. Ultraviolet–visible spectra estimate that the optical band gap of the synthesized SnO2 nanowires was 3.72 eV. Second, the gas sensing performance of synthesized SnO2 nanowires was investigated by testing with carbon monoxide (CO), Methane (CH4) and methanol (CH3OH) gases at different operating temperatures and concentrations. Results indicate that the synthesized SnO2 nanowires are highly promising for gas sensing applications.

Peroxidase Mimic Activities of Copper Selenide (CuSe) Nanoplates for Sensing H2O2 and L-Cysteine

2020 ◽  
Vol 20 (9) ◽  
pp. 5369-5375
Author(s):  
Bai Maojuan ◽  
Xu Chengcheng ◽  
Huang Xuanye ◽  
Liu Yanan ◽  
Wan Jun
Keyword(s):  
Electron Microscopy ◽  
Detection Limit ◽  
Energy Dispersive Spectrometer ◽  
Catalytic Efficiency ◽  
Relative Standard Error ◽  
Colorimetric Determination ◽  
Peroxidase Mimic ◽  
Biomedical Analysis ◽  
X Ray ◽  
Relative Standard

Compared with natural enzymes, artificial mimic enzymes have been widely studied for their high stability and cost effectiveness. In this study, CuSe nanoplates as a simulated enzyme which does not contain precious metals, has peroxidase activity. CuSe nanoplates were prepared and characterized by powder X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and X-ray energy dispersive spectrometer (EDS). Kinetic studies show that CuSe nanoplates exhibits a higher affinity for 3,3′,5,5′-teramethylbenzidine (TMB) than horseradish peroxidase (HRP). The rapid colorimetric determination of H2O2 and L-cysteine were developed based on the catalytic efficiency. The linear range of detection for H2O2 is 5.0×10−6~8.0×10−5 M, and the detection limit is 2.9×10−6 M, while the relative standard error is less than 5%. In addition, L-cysteine was detected with a detection limit of 0.2×10−6 M. The good selectivity of the determination to H2O2 and L-cysteine in aqueous solution was also achieved. CuSe nanoplates as a simulated enzyme for sensor applications would be used in environmental monitoring and biomedical analysis.

Synthesis of MoS2 Nanoparticles with Inorganic Fullerene-Like Structure from Molybdenum Trioxide and Sulfur

2012 ◽  
Vol 554-556 ◽  
pp. 601-604
Author(s):  
Bin Gao ◽  
Xiao Jun Zhang
Keyword(s):  
Electron Microscopy ◽  
Molybdenum Trioxide ◽  
Raw Materials ◽  
Heating Temperature ◽  
Chemical Vapor ◽  
Diffraction Field ◽  
Chemical Vapor Deposition Method ◽  
X Ray ◽  
Inorganic Fullerene ◽  
Transmission Electron

MoS2 nanoparticles with fullerene-like (IF-MoS2) structure were successfully obtained at heating temperature higher than 840 °C by chemical vapor deposition method in a three-tube furnace using MoO3 and S (sulfur) powders as raw materials. The synthesized samples were characterized by X-ray diffraction, field emission scanning electron microscopy, transmission electron microscopy, and energy dispersion X-ray spectrometerrespectively. IF-MoS2 nanoparticles can be obtained only in the narrow temperature range of 840 °C-870 °C, and the diameter of IF-MoS2 nanoparticles increases with temperature. A gradual formation mechanism of IF-MoS2 nanoparticles was discussed in detail.

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