scholarly journals Synthesis, Characterization, and Photocatalytic Evaluation of Manganese (III) Phthalocyanine Sensitized ZnWO4 (ZnWO4MnPc) for Bisphenol A Degradation under UV Irradiation

Nanomaterials ◽  
2020 ◽  
Vol 10 (11) ◽  
pp. 2139 ◽  
Author(s):  
Chukwuka Bethel Anucha ◽  
Ilknur Altin ◽  
Zekeriya Biyiklioglu ◽  
Emin Bacaksiz ◽  
Ismail Polat ◽  
...  
Keyword(s):  
Bisphenol A ◽  
Uv Irradiation ◽  
Photoelectron Spectroscopy ◽  
Photocatalytic Performance ◽  
Diffuse Reflectance Spectroscopy ◽  
Degradation Process ◽  
X Ray Diffraction ◽  
X Ray ◽  
Uv Visible ◽  
Adsorption Desorption

ZnWO4MnPc was synthesized via a hydrothermal autoclave method with 1 wt.% manganese (iii) phthalocyanine content. The material was characterized for its structural and morphological features via X-ray diffraction (XRD) spectroscopy, Fourier transform infrared (FTIR) spectroscopy, transmission emission microscopy (TEM), scanning electron microscopy-Energy dispersive X-ray spectroscopy (SEM-EDX), N2 adsorption–desorption at 77K, X-ray photoelectron spectroscopy (XPS), and UV-visible/diffuse reflectance spectroscopy(UV-vis/DRS). ZnWO4MnPc photocatalytic performance was tested on the degradation of bisphenol A (BPA). The ZnWO4MnPc material removed 60% of BPA after 4 h of 365 nm UV irradiation. Degradation process improved significantly to about 80% removal in the presence of added 5 mM H2O2 after 4 h irradiation. Almost 100% removal was achieved after 30 min under 450 nm visible light irradiation in the presence of same concentration of H2O2. The effect of ions and humic acid (HA) towards BPA removal was also investigated.

ZnO-SiO2/Laponite Photocatalyst: Kinetic Study on Photocatalytic Decolorization of Methylene Blue

2014 ◽  
Vol 896 ◽  
pp. 541-544
Author(s):  
Is Fatimah ◽  
N. Nunani Yuyun
Keyword(s):  
Methylene Blue ◽  
Energy Dispersive Spectrometry ◽  
Photocatalytic Performance ◽  
Sol Gel ◽  
X Ray Diffraction ◽  
X Ray ◽  
Photocatalytic Decolorization ◽  
Uv Visible ◽  
Gel Preparation ◽  
Adsorption Desorption

ZnO-SiO2/Laponite was prepared by sol-gel preparation procedure consit of SiO2 pillarization to laponite followed by ZnO dispersion by using zinc acetate as precursor. The obtained material was characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive spectrometry (EDS), diffuse reflectance UV-Visible (DRUV-Vis) and N2 adsorption-desorption analysis. The photocatalytic performance of the amterial in methylene blue decolorization was also investigated. Compared with ZnO-SiO2 nanoparticles, it is concluded that ZnO-SiO2/Laponite possess higher photocatalytic activity which obey Temkin isotherm model.

Facile deposition of carbon-doped TiO2 films by two-electrode electrodeposition setup

2021 ◽  
pp. 2150175
Author(s):  
Necati Basman ◽  
Mehmet Gokcen
Keyword(s):  
Photoelectron Spectroscopy ◽  
Diffuse Reflectance Spectroscopy ◽  
Carbon Doping ◽  
Silicon Substrates ◽  
X Ray Diffraction ◽  
High Carbon ◽  
X Ray ◽  
Carbon Doped ◽  
Surface Areas ◽  
Uv Visible

This study presents a simple electrochemical deposition route to obtain carbon-doped TiO2 films. The deposition of the films is carried out on silicon substrates from a mixture of methanol (CH3OH) and Titanium (IV) isopropoxide (Ti[OCH(CH3)2]4) solution using a simple two-electrode electrodeposition setup. The obtained films are characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), UV-Visible diffuse reflectance spectroscopy (DRS) and conductivity measurements. Depending on the deposition conditions, both amorphous and crystalline TiO2 films could be obtained. It is found that carbon is doped both substitutionally and interstitially. High carbon doping (up to 18.96%) enables to obtain TiO2 film with narrowed bandgap and high conductivity to about 2.3 eV and [Formula: see text] S cm[Formula: see text], respectively. This study suggests that the proposed electrodeposition route offers an easy way of obtaining conductive and narrowed bandgap TiO2 films on large surface areas.

scholarly journals Au/TiO2Reusable Photocatalysts for Dye Degradation

2013 ◽  
Vol 2013 ◽  
pp. 1-10 ◽  
Author(s):  
Silija Padikkaparambil ◽  
Binitha Narayanan ◽  
Zahira Yaakob ◽  
Suraja Viswanathan ◽  
Siti Masrinda Tasirin
Keyword(s):  
Photoelectron Spectroscopy ◽  
Diffuse Reflectance ◽  
Diffuse Reflectance Spectroscopy ◽  
Dye Degradation ◽  
Analytical Techniques ◽  
X Ray Diffraction ◽  
X Ray ◽  
Dye Pollutants ◽  
Transmission Electron ◽  
Uv Visible

Nanogold doped TiO2catalysts are synthesized, and their application in the photodegradation of dye pollutants is studied. The materials are characterized using different analytical techniques such as X-ray diffraction, transmission electron microscopy, UV-visible diffuse reflectance spectroscopy, and X-ray photoelectron spectroscopy. The results revealed the strong interaction between the metallic gold nanoparticles and the anatase TiO2support. Au doped systems showed very good photoactivity in the degradation of dye pollutants under UV irradiation as well as in sunlight. A simple mechanism is proposed for explaining the excellent photoactivity of the systems. The reusability studies of the photocatalysts exhibited more than 98% degradation of the dye even after 10 repeated cycles.

Effect of Ag+ and PO43− ratios on the microstructure and photocatalytic activity of Ag3PO4

2016 ◽  
Vol 09 (05) ◽  
pp. 1650063 ◽  
Author(s):  
Jiaqian Qin ◽  
Xinyu Zhang ◽  
Chengwu Yang ◽  
Aijun Song ◽  
Bing Zhang ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Photocatalytic Activity ◽  
Diffuse Reflectance ◽  
Photocatalytic Performance ◽  
Diffuse Reflectance Spectroscopy ◽  
Precipitation Method ◽  
X Ray Diffraction ◽  
X Ray ◽  
Uv Visible ◽  
The Rich

In this work, the catalyst silver phosphate (Ag3PO[Formula: see text] with different initial ratios of Ag[Formula: see text] and PO[Formula: see text] in aqueous solution was synthesized by a simple precipitation method from AgNO3 and NH4H2PO4 which were used as the precursor. After that, the prepared samples were characterized by different techniques such as field emission scanning electron microscopy (FE-SEM), X-ray diffraction (XRD), UV-visible diffuse reflectance spectroscopy (UV-DRS) and decomposition evolution of rhodamine B (RhB) solution. The results indicate that the initial ratios of Ag[Formula: see text]/PO[Formula: see text] in aqueous solution can modify the morphology and also it can significantly affect the photocatalytic performance. During photocatalytic process, the rich Ag[Formula: see text] ion Ag3PO4 can form the surface plasmon resonance (SPR) of Ag nanoparticles, which inhibit the reduction of Ag3PO4 resulting in higher photocatalytic activity and stability.

scholarly journals Mechanochemical synthesis of zincite doped with cadmium in various amounts

2019 ◽  
Vol 26 (1) ◽  
pp. 482-490
Author(s):  
S. Kurajica ◽  
V. Mandić ◽  
G. Matijašić ◽  
I. K. Munda ◽  
K. Mužina
Keyword(s):  
Mechanochemical Synthesis ◽  
Diffuse Reflectance Spectroscopy ◽  
Degradation Process ◽  
X Ray Diffraction ◽  
Methylene Blue Degradation ◽  
X Ray ◽  
Cd Doping ◽  
Reflectance Ftir ◽  
Atr Spectroscopy ◽  
Adsorption Desorption

AbstractThis work investigates the limit of Cd doping in ZnO derived by means of mechanochemical synthesis using CdCl2, ZnCl2 and Na2CO3 as precursors and NaCl as diluent. The prepared samples were characterized using X-ray diffraction (XRD), Fourier transformed infrared attenuated total reflectance (FTIR ATR) spectroscopy, UV-Vis diffuse reflectance spectroscopy (DRS),N2 adsorption-desorption isotherms, scanning electron microscope (SEM) and energy-dispersive X-ray spectroscopy (EDS), while photocatalytic efficiency has been evaluated for methylene blue degradation process. Zn for Cd replacement limits in the crystal lattice of ZnO derived via mechanochemical synthesis were found to be only 2%. For Cd present in a larger portion, CdO and CdCO3 phases appear. Cd doping limits in ZnO were not affected by the milling interval. However, it was observed that Cd doping impairs the nanocrystallinity of ZnO. The morphology and the electronic structure of ZnO and thus photocatalytic activity was inappreciably affected by the Cd doping.

Dye-Sensitized-Assisted, Enhanced Photocatalytic Activity of TiO2/Bi4V2O11

NANO ◽  
2018 ◽  
Vol 13 (03) ◽  
pp. 1850028 ◽  
Author(s):  
Mengjun Liang ◽  
Zhiyuan Yang ◽  
Ying Mei ◽  
Haoran Zhou ◽  
Shuijin Yang
Keyword(s):  
Photocatalytic Activity ◽  
Photoelectron Spectroscopy ◽  
Diffuse Reflectance Spectroscopy ◽  
X Ray Diffraction ◽  
X Ray ◽  
Dye Sensitized ◽  
Transmission Electron ◽  
Efficient Charge ◽  
Degradation Activity ◽  
Adsorption Desorption

In this study, the TiO2/Bi4V2O[Formula: see text] nanocomposite photocatalysts were prepared by loading different amount of TiO2 nanoparticles onto the surface of Bi4V2O[Formula: see text] nanospheres via a facile hydrothermal method. Afterwards, the as-synthesized samples were characterized by high-resolution transmission electron microscopy (HRTEM), X-ray diffraction (XRD), N2 adsorption–desorption isotherms, X-ray photoelectron spectroscopy (XPS), UV-Vis diffuse reflectance spectroscopy (DRS) and photocurrent techniques. The optimal TiO2/Bi4V2O[Formula: see text] composite with 20[Formula: see text]wt.% TiO2 loading (TB2) exhibited the best photocatalytic activity, which could degrade almost RhB completely within 30[Formula: see text]min under visible light irradiation. The enhanced photocatalytic activity of TiO2/Bi4V2O[Formula: see text] composites for RhB degradation could be mainly ascribed to the efficient charge separation over dye-induced sensitized and the increased specific surface area. Also, the photocatalytic activities of TiO2/Bi4V2O[Formula: see text] for CIP degradation were tested. After five consecutive recycling experiments, the photocatalytic degradation activity of TB2 could still reach 99% which indicated that the catalysts had superior stability. Based on the experimental and bandgap calculations, a possible photocatalytic mechanism of TiO2/Bi4V2O[Formula: see text] for RhB degradation was proposed.

MgO-based nanosheets loaded with ZnxMg1−xO nanoparticles with UV light-driven photocatalytic performance

2017 ◽  
Vol 10 (06) ◽  
pp. 1750072 ◽  
Author(s):  
Junshu Wu ◽  
Linlin Wang ◽  
Jinshu Wang ◽  
Yucheng Du ◽  
Yongli Li
Keyword(s):  
Photoelectron Spectroscopy ◽  
Photocatalytic Performance ◽  
Uv Light ◽  
Controlled Synthesis ◽  
Dye Wastewater ◽  
X Ray Diffraction ◽  
X Ray ◽  
Uv Light Irradiation ◽  
Uv Visible ◽  
High Temperature Calcination

This paper reports the synthesis of MgO-based nanosheets loaded with UV-light absorbed, wurtzite ZnxMg[Formula: see text]O nanoparticles based on calcining Zn[Formula: see text]-adsorbed Mg(OH)2 precursor, as evidenced by X-ray diffraction, UV-visible, X-ray photoelectron spectroscopy analyses, etc. The surface modification of magnesium oxide (MgO) sheet-like adsorbents by Zn–Mg–O alloys generates photocatalytic activity for the degradation removal of cationic dye Rhodamine B and anionic dye methyl orange under UV light irradiation. These findings provide a route to chemically controlled synthesis of new and highly robust MgO–ZnxMg[Formula: see text]O materials for water purification. The endowed photocatalysis function of MgO makes it be easily recovered via photodegradation of adsorbed dyes rather than high-temperature calcination, thus extending the applications of MgO in dye wastewater treatment.

Ultrasonic-hydrothermal Synthesis and Characterization of Mesoporous Anatase TiO2 Microspheres

2011 ◽  
Vol 239-242 ◽  
pp. 2323-2326 ◽  
Author(s):  
Hai Bin Li ◽  
Shu Guang Chen ◽  
Wei Ming Lu ◽  
Qi Cheng Liu
Keyword(s):  
Diffuse Reflectance Spectroscopy ◽  
Tetrabutyl Titanate ◽  
X Ray Diffraction ◽  
Structure Directing Agent ◽  
X Ray ◽  
Transmission Electron ◽  
Uv Visible ◽  
Average Size ◽  
Adsorption Desorption

Mesoporous TiO2 microspheres with a combination of large surface and high crystallinity were fabricated by an ultrasonic-hydrothermal method with Octadecylamine as a structure-directing agent and tetrabutyl titanate as a precursor. The mesoporous materials were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), N2 adsorption–desorption measurements, and UV–visible diffuse reflectance spectroscopy (UV-vis). Low-angle XRD and TEM images indicated that the disordered wormhole-like mesoporous architecture of TiO2 microspheres with diameters of about 200-400 nm were actually formed by agglomerization of nanoparticles with an average size of about 10nm. The analysis from N2 adsorption–desorption isotherms showed that the surface area of mesoporous sample was 204.7 m2g-1, with a pore size of 4.3 nm and pore volume of 0.263 cm3g-1 after calcined at 673 K.

scholarly journals Europium-Doped Y2O3-Coated Diatomite Nanomaterials: Hydrothermal Synthesis, Characterization, Optical Study with Enhanced Photocatalytic Performance

Inorganics ◽  
2021 ◽  
Vol 9 (12) ◽  
pp. 88
Author(s):  
Younes Hanifehpour ◽  
Mehdi Abdolmaleki ◽  
Sang Woo Joo
Keyword(s):  
Photoelectron Spectroscopy ◽  
Diffuse Reflectance ◽  
Photocatalytic Performance ◽  
Diffuse Reflectance Spectroscopy ◽  
Cubic Phase ◽  
Ultrasonic Power ◽  
X Ray Diffraction ◽  
X Ray ◽  
Reactive Blue 19 ◽  
Bet Specific Surface Area

Eu-doped Y2O3 coated diatomite nanostructures with variable Eu3+ contents were synthesized by a facile hydrothermal technique. The products were characterized by means of energy dispersive X-ray photoelectron spectroscopy (EDX), scanning electron microscopy (SEM), powder X-ray diffraction (PXRD), Brunauer–Emmett–Teller (BET), UV-vis diffuse reflectance spectroscopy, and photoluminescence spectroscopy techniques. As claimed by PXRD, the particles were crystallized excellently and attributed to the cubic phase of Y2O3. The influence of substitution of Eu3+ ions into Y2O3 lattice caused a redshift in the absorbance and a decrease in the bandgap of as-prepared coated compounds. The pore volume and BET specific surface area of Eu-doped Y2O3-coated diatomite is greater than uncoated biosilica. The sonophotocata-lytic activities of as-synthesized specimens were evaluated for the degradation of Reactive Blue 19. The effect of various specifications such as ultrasonic power, catalyst amount, and primary dye concentration was explored.

Investigation of CO2 Adsorption on Triethylenetetramine Modified Adsorbents of TETA(n)/Zr-TSCD

2020 ◽  
Vol 73 (11) ◽  
pp. 1051
Author(s):  
Fan-Ming Yang ◽  
Min Liao ◽  
Chang-Hua Long ◽  
Jian-Bin Fu ◽  
Xiao-Yan Zhu
Keyword(s):  
Adsorption Capacity ◽  
Photoelectron Spectroscopy ◽  
Diffuse Reflectance Spectroscopy ◽  
Absorption Capacity ◽  
X Ray Diffraction ◽  
X Ray ◽  
Energy Dispersion Spectrum ◽  
New Type ◽  
Modified Adsorbents ◽  
Adsorption Desorption

In the present study, a new type of material of Zr-TSCD was first synthesized and modified with different amounts of triethylenetetramine (TETA). The properties of the adsorbents were characterised with X-ray diffraction, UV-vis diffuse reflectance spectroscopy, FT-IR spectroscopy, X-ray photoelectron spectroscopy, Raman spectroscopy, N2 adsorption–desorption, energy dispersion spectrum, and thermogravimetric analysis. The results suggested that Zr-TSCD (TSCD=Na3C6H5O7·2H2O) was successfully synthesized through the coordination of Zr atoms from ZrOCl2·8H2O and O species in –COO– groups. After functionalization with TETA, the structure of Zr-TSCD was preserved and the adsorption capacity of CO2 was enhanced dramatically. At 75°C, TETA(30)/Zr-TSCD achieved a maximum absorption capacity of 175.1mg g−1 in a stream of 10mL min−1 CO2. The adsorption capacity ratio of CO2/N2, CO2/O2, and CO2/SO2 was 10.5, 7.4, and 1.2, respectively. In addition, the adsorption capacity of CO2 remained stable during 10 adsorption–desorption cycles.

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