Preparation of Polyaniline–ZnO Photocatalyst and its Photocatalytic Property

2011 ◽  
Vol 356-360 ◽  
pp. 519-523
Author(s):  
Hong Chao Ma ◽  
Yang Zhang ◽  
Ying Huan Fu ◽  
Chun Ling Yu ◽  
Yu Song ◽  
...  
Keyword(s):  
Visible Light ◽  
Zno Nanoparticles ◽  
Oxidative Polymerization ◽  
Photocatalytic Property ◽  
X Ray Diffraction ◽  
Anthraquinone Dye ◽  
X Ray ◽  
Transmission Electron ◽  
Diffraction Patterns

ZnO nanoparticles were modified by polyaniline (PANI) using ‘in situ’ chemical oxidative polymerization method. The morphology, structure, and light absorption properties of PANI-ZnO composites were examined by powder X-ray diffraction (XRD), transmission electron microscopy (TEM) and UV–vis spectra. UV–vis spectra reveal that PANI-ZnO composites showed stronger absorption than neat ZnO under the whole range of visible light. New characteristic peaks were found in PANI-ZnO composites according to the X-ray diffraction patterns after hybridization of PANI and ZnO, which indicating that there was a strong interaction between PANI and ZnO nanoparticles. The resulting PANI-ZnO composites exhibit significantly higher photocatalytic activity than that of neat ZnO for degradation of anthraquinone dye (reactive brilliant blue KN-R) aqueous solution under visible light irradiation (λ > 420 nm).

Preparation of Polyaniline Supported TiO2 Photocatalyst and its Photocatalytic Property

2011 ◽  
Vol 356-360 ◽  
pp. 524-528 ◽  
Author(s):  
Chun Ling Yu ◽  
Rui Xue Wu ◽  
Ying Huan Fu ◽  
Xiao Li Dong ◽  
Hong Chao Ma
Keyword(s):  
Electron Microscopy ◽  
Hydrothermal Process ◽  
Photocatalytic Property ◽  
Visible Spectrum ◽  
X Ray Diffraction ◽  
Visible Spectroscopy ◽  
Anthraquinone Dye ◽  
X Ray ◽  
Transmission Electron ◽  
Uv Visible

A polyaniline supported titanium dioxide photocatalyst was prepared by an impregnation-hydrothermal process and characterized by powder X-ray diffraction, transmission electron microscopy and UV-visible spectroscopy. It was found that the TiO2 nanoparticles were well dispersed on the surface of the polyaniline and the photocatalyst has a stronger absorption compared with that of pure TiO2 over the whole of the visible spectrum. The photocatalyst exhibited higher photocatalytic activity than pure TiO2 for the photodegradation of solutions of the anthraquinone dye, reactive brilliant blue KN-R, under visible light irradiation.

Hydrothermal Synthesis and Photocatalytic Properties of TiO2/SnS2 Nanocomposite

2014 ◽  
Vol 898 ◽  
pp. 23-26
Author(s):  
Jing Li ◽  
Wei Sun ◽  
Wei Min Dai ◽  
Yong Cai Zhang
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Visible Light ◽  
Diffuse Reflectance ◽  
Photocatalytic Property ◽  
Deionized Water ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Chloride Pentahydrate

TiO2/SnS2 nanocomposite was synthesized via hydrothermal treatment of tin (IV) chloride pentahydrate, thioacetamide and TiO2 nanotubes in deionized water at 150 °C for 3 h. The structure, composition and optical property of the as-synthesized nanocomposite were characterized by X-ray diffraction, energy dispersive X-ray spectroscopy, transmission electron microscopy and UV-vis diffuse reflectance spectra, and its photocatalytic property was tested in the reduction of aqueous Cr6+ under visible-light (λ > 420 nm) irradiation. It was observed that TiO2 nanotubes exhibited no photocatalytic activity, whereas TiO2/SnS2 nanocomposite exhibited photocatalytic activity in the reduction of aqueous Cr6+ under visible-light (λ > 420 nm) irradiation.

scholarly journals Facile Solvothermal Synthesis of CuCo2S4 Yolk-Shells and Their Visible-Light-Driven Photocatalytic Properties

Materials ◽  
2018 ◽  
Vol 11 (11) ◽  
pp. 2303 ◽  
Author(s):  
Yinxia Chen ◽  
Xianbing Ji ◽  
Vadivel Sethumathavan ◽  
Bappi Paul
Keyword(s):  
Electron Microscopy ◽  
Visible Light ◽  
Photocatalytic Property ◽  
Shell Shape ◽  
X Ray Diffraction ◽  
Exchange Method ◽  
X Ray ◽  
Transmission Electron ◽  
Visible Light Driven ◽  
Photocatalytic Applications

In this present work, we synthesized a yolk-shell shaped CuCo2S4 by a simple anion exchange method. The morphological and structural properties of the as-synthesized sample were characterized using X-ray diffraction (XRD), UV-vis diffuse reflectance spectra (UV-vis DRS), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). The SEM and TEM results confirmed that the uniform yolk-shell structure was formed during the solvothermal process. The band gap was about 1.41 eV, which have been confirmed by UV–vis DRS analysis. The photocatalytic property was evaluated by the photocatalytic degradation of methylene blue (MB) dye as a target pollutant under the visible-light irradiation. The experimental results confirmed the potential application of yolk-shell shape CuCo2S4 in visible-light photocatalytic applications.

Synthesis and characterization of organic–inorganic poly(3,4-ethylenedioxythiophene)/MoS2 nanocomposite via in situ oxidative polymerization

2006 ◽  
Vol 21 (1) ◽  
pp. 112-118 ◽  
Author(s):  
A. Vadivel Murugan ◽  
Mathieu Quintin ◽  
Marie-Helene Delville ◽  
Guy Campet ◽  
Annamraju Kasi Viswanath ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Oxidative Polymerization ◽  
X Ray Diffraction ◽  
Rechargeable Lithium Batteries ◽  
X Ray ◽  
Transmission Electron ◽  
Basal Distance ◽  
New Type

Here we demonstrate the synthesis of a new type of layered poly(3,4-ethylenedioxy- thiophene) (PEDOT)/MoS2 nanocomposite via flocculation of delaminated MoS2 with subsequent in situ oxidative polymerization of 3,4-ethylenedioxythiophene. The resulting nanocomposite was characterized by Fourier transform infrared spectroscopy, powder x-ray diffraction, x-ray photoelectron spectroscopy, thermal analysis, transmission electron microscopy, and four-probe electrical conductivity measurements with respect to temperature. X-ray diffraction results indicated that the exfoliated MoS2 and PEDOT are restacked to produce a novel nanoscale composite material containing alternate nanoribbons of PEDOT in between MoS2 with a basal distance of ∼1.38 nm. The nanocomposite, which could be used as a cathode material for small power rechargeable lithium batteries, has also been demonstrated by the electrochemical insertion of lithium into the PEDOT/MoS2 nanocomposite, where a significant enhancement in the discharge capacity is observed, compared to that of respective pristine molybdenum disulfide.

scholarly journals Synthesis and Antibacterial Aspects of Graphitic C3N4@Polyaniline Composites

Coatings ◽  
2020 ◽  
Vol 10 (10) ◽  
pp. 950
Author(s):  
Mohammad Oves ◽  
Mohammad Omaish Ansari ◽  
Reem Darwesh ◽  
Afzal Hussian ◽  
Mohamed F. Alajmi ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Morphological Analysis ◽  
Oxidative Polymerization ◽  
X Ray Diffraction ◽  
X Ray ◽  
E Coli ◽  
Transmission Electron ◽  
Aging Conditions ◽  
Polyaniline Composites

In this work, Pani and Pani@g-C3N4 was synthesized by in situ oxidative polymerization methodology of aniline, in the presence of g-C3N4. The as prepared Pani@g-C3N4 was characterized by scanning electron microscopy, transmission electron microscopy and X-ray diffraction (XRD). The morphological analysis showed well dispersed Pani in g-C3N4, as well as the coating of Pani on g-C3N4. The XRD further revealed this, and peaks of Pani as well as g-C3N4 was observed, thereby suggesting successful synthesis of the composite. The DC electrical conductivity studies under isothermal and cyclic aging conditions showed high stability of composites over 100 °C. Further, the synthesized composite material proved to be an excellent antimicrobial agent against both type i.e., gram positive Streptococcus pneumoniae and negative bacteria Escherichia coli. In the zone inhibition assay 18 ± 0.5, 16 ± 0.75 and 20 ± 0.5, 22 ± 0.5 mm zone diameter were found against E. coli and S. pneumoniae in presence of pure g-C3N4 and Pani@g-C3N4 at 50 µg concentrations, respectively. Further antimicrobial activity in the presence of sunlight in aqueous medium showed that Pani@g-C3N4 is more potent than pure g-C3N4.

Synthesis of SnS2/SnO2 Nanocomposite for Visible Light-Driven Photocatalytic Reduction of Aqueous Cr(VI)

2013 ◽  
Vol 538 ◽  
pp. 46-49 ◽  
Author(s):  
Min Yang ◽  
Yong Cai Zhang ◽  
Wei Min Dai ◽  
Ke Hang ◽  
Yue Quan Pan
Keyword(s):  
Visible Light ◽  
Diffuse Reflectance ◽  
Reflectance Spectrum ◽  
Sno2 Nanoparticles ◽  
Diffuse Reflectance Spectrum ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Visible Light Driven

SnS2/SnO2 nanocomposite was synthesized by a simple in situ hydrothermal oxidation route, and characterized by X-ray diffraction, energy dispersive X-ray spectroscopy, transmission electron microscopy and UV-vis diffuse reflectance spectrum. The as-synthesized SnS2/SnO2 nanocomposite displayed much superior photocatalytic activity to SnS2 and SnO2 nanoparticles in the reduction of aqueous Cr(VI) under visible light (λ > 420 nm) irradiation.

Deposition Kinetics and Microstructural Evolution in Sputtered TA Films: a Real-Time/In-Situ Study

1999 ◽  
Vol 562 ◽  
Author(s):  
J. F. Whitacre ◽  
S. M. Yalisove ◽  
J. C. Bilello
Keyword(s):  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Film Layer ◽  
Pressure Increment ◽  
Diffraction Patterns ◽  
Set Up ◽  
Film Development ◽  
Porous Microstructures

ABSTRACTTa films were grown using sputter gas (Ar) pressures ranging from 1.7 to 20 mTorr. This produced growth environments where incoming adatom kinetic energies ranged from over 100 eV to less than 1 eV. Film development was monitored in-situ using a x-ray diffraction set-up that allowed complete diffraction patterns to be rapidly collected without interrupting the growth process. Traditional x-ray diffraction methods, transmission electron microscopy (TEM), and transmission electron diffraction (TED) were used to examine film microstructure after growth. It was found that lower Ar pressures, which allow higher adatom kinetic energies, produced films that displayed significant grain growth, texturing, and a smooth surface morphology. Those films grown at increasingly higher Ar pressures displayed smaller grain sizes, less texturing, and increasingly porous microstructures. To further explore this effect, the Ar pressure was varied during deposition for several films. The in-situ probe allowed the effects of each pressure increment to be analyzed and compared with previous x-ray and microscopy results. It was found that the microstructure of any particular film layer depended more on the deposition conditions during its formation rather than the structure or crystallography of previous layers.

Preparation and characterization of poly(2-hydroxyethyl methacrylate)/ Na-montmorillonite intercalated nanocomposites

2013 ◽  
Vol 33 (1) ◽  
pp. 27-32 ◽  
Author(s):  
Zafer Koç ◽  
Meltem Çelik ◽  
Müşerref Önal ◽  
Yüksel Sarıkaya ◽  
Yesim Mogulkoc
Keyword(s):  
Interlayer Spacing ◽  
Hydroxyethyl Methacrylate ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Monomer Content ◽  
Diffraction Patterns ◽  
Thermal Stability Of

Abstract A series of intercalated nanocomposites were prepared via in situ polymerization of 2-hydroxyethyl methacrylate (HEMA) between the interlayer spacing of hydrous Na-montmorillonite (Na-MMT) using benzoyl peroxide (Bz2O2) as a radical initiator. X-ray diffraction patterns showed the absence of any intercalation up to 61.7 mass% of HEMA, but anhydrous Na-MMT formed by the hydrophilic effect of HEMA. The interlayer spacing (d001) values of hydrous and anhydrous Na-MMT were calculated as 1.19 and 1.03 nm, respectively. At higher monomer contents, the increase in the value of d001 from 1.19 to 2.01 nm indicated intercalation of polymer in the interlayer spacing of Na-MMT. Besides, transmission electron microscopy results supported the formation of the intercalated nanocomposites. Thermogravimetric analysis showed that the thermal stability of the nanocomposites increased considerably by intercalation of pure poly-HEMA. Specific surface area and specific nanopore volume of the nanocomposites decreased with the increasing of the monomer content taken by the preparations. The decrease is due to the nonporous nature of the polymer matrix.

The Use of Advanced Analytical Techniques for Characterization of the Chemical, Physical, and Crystallographic Nature of a Surface

1973 ◽  
Vol 31 ◽  
pp. 132-133 ◽  
Author(s):  
R. E. Herfert
Keyword(s):  
Surface Characterization ◽  
Analytical Techniques ◽  
X Ray Diffraction ◽  
Depth Of Penetration ◽  
X Ray ◽  
The Past ◽  
Transmission Electron ◽  
Scanning Electron

Studies of the nature of a surface, either metallic or nonmetallic, in the past, have been limited to the instrumentation available for these measurements. In the past, optical microscopy, replica transmission electron microscopy, electron or X-ray diffraction and optical or X-ray spectroscopy have provided the means of surface characterization. Actually, some of these techniques are not purely surface; the depth of penetration may be a few thousands of an inch. Within the last five years, instrumentation has been made available which now makes it practical for use to study the outer few 100A of layers and characterize it completely from a chemical, physical, and crystallographic standpoint. The scanning electron microscope (SEM) provides a means of viewing the surface of a material in situ to magnifications as high as 250,000X.

scholarly journals Controlled Synthesis of CuS and Cu9S5 and Their Application in the Photocatalytic Mineralization of Tetracycline

Catalysts ◽  
2021 ◽  
Vol 11 (8) ◽  
pp. 899
Author(s):  
Murendeni P. Ravele ◽  
Opeyemi A. Oyewo ◽  
Damian C. Onwudiwe
Keyword(s):  
Electron Microscopy ◽  
Visible Light ◽  
Blue Shift ◽  
X Ray Diffraction ◽  
X Ray ◽  
Copper Sulfides ◽  
Transmission Electron ◽  
Single Source Precursor ◽  
Pure Phase ◽  
Pure Phases

Pure-phase Cu2−xS (x = 1, 0.2) nanoparticles have been synthesized by the thermal decomposition of copper(II) dithiocarbamate as a single-source precursor in oleylamine as a capping agent. The compositions of the Cu2−xS nanocrystals varied from CuS (covellite) through the mixture of phases (CuS and Cu7.2S4) to Cu9S5 (digenite) by simply varying the temperature of synthesis. The crystallinity and morphology of the copper sulfides were studied using X-ray diffraction (XRD), scanning electron microscopy (SEM), and transmission electron microscopy (TEM), which showed pure phases at low (120 °C) and high (220 °C) temperatures and a mixture of phases at intermediate temperatures (150 and 180 °C). Covellite was of a spherical morphology, while digenite was rod shaped. The optical properties of these nanocrystals were characterized by UV−vis–NIR and photoluminescence spectroscopies. Both samples had very similar absorption spectra but distinguishable fluorescence properties and exhibited a blue shift in their band gap energies compared to bulk Cu2−xS. The pure phases were used as catalysts for the photocatalytic degradation of tetracycline (TC) under visible-light irradiation. The results demonstrated that the photocatalytic activity of the digenite phase exhibited higher catalytic degradation of 98.5% compared to the covellite phase, which showed 88% degradation within the 120 min reaction time using 80 mg of the catalysts. The higher degradation efficiency achieved with the digenite phase was attributed to its higher absorption of the visible light compared to covellite.

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