scholarly journals Growth Mechanism of Sea Urchin ZnO Nanostructures in Aqueous Solutions and Their Photocatalytic Activity for the Degradation of Organic Dyes

ACS Omega ◽  
2019 ◽  
Vol 4 (9) ◽  
pp. 14013-14020 ◽  
Author(s):  
Hiran D. Kiriarachchi ◽  
Khaled M. Abouzeid ◽  
Longli Bo ◽  
M. Samy El-Shall
Keyword(s):  
Photocatalytic Activity ◽  
Aqueous Solutions ◽  
Sea Urchin ◽  
Growth Mechanism ◽  
Organic Dyes ◽  
Zno Nanostructures

Highly efficient photocatalytic degradation of organic dyes by Cu doped ZnO nanostructures

2015 ◽  
Vol 17 (38) ◽  
pp. 25172-25181 ◽  
Author(s):  
Sini Kuriakose ◽  
Biswarup Satpati ◽  
Satyabrata Mohapatra
Keyword(s):  
Methylene Blue ◽  
Photocatalytic Activity ◽  
Methyl Orange ◽  
Photocatalytic Degradation ◽  
Organic Dyes ◽  
Zno Nanostructures ◽  
Highly Efficient ◽  
Doped Zno

Cu doped ZnO nanostructures exhibit highly efficient sunlight driven photocatalytic activity for degradation of methylene blue and methyl orange dyes.

scholarly journals Zirconium-Doped Chromium IV Oxide Nanocomposites: Synthesis, Characterization, and Photocatalysis towards the Degradation of Organic Dyes

Catalysts ◽  
2021 ◽  
Vol 11 (1) ◽  
pp. 117
Author(s):  
Zahir Muhammad ◽  
Farman Ali ◽  
Muhammad Sajjad ◽  
Nisar Ali ◽  
Muhammad Bilal ◽  
...  
Keyword(s):  
Methylene Blue ◽  
Photocatalytic Activity ◽  
Methyl Orange ◽  
Solid State ◽  
Room Temperature ◽  
Organic Dyes ◽  
Uv Light ◽  
Heterogeneous Photocatalysis ◽  
Ft Ir ◽  
Complete Mineralization

Degradation of organic dyes and their byproducts by heterogeneous photocatalysts is an essential process, as these dyes can be potentially discharged in wastewater and threaten aquatic and xerophyte life. Therefore, their complete mineralization into nontoxic components (water and salt) is necessary through the process of heterogeneous photocatalysis. In this study, Zr/CrO2 (Zirconium-doped chromium IV oxide) nanocomposite-based photocatalysts with different compositions (1, 3, 5, 7 & 9 wt.%) were prepared by an environmentally friendly, solid-state reaction at room temperature. The as-prepared samples were calcined under air at 450 °C in a furnace for a specific period of time. The synthesis of Zr/CrO2 photocatalysts was confirmed by various techniques, including XRD, SEM, EDX, FT-IR, UV-Vis, and BET. The photocatalytic properties of all samples were tested towards the degradation of methylene blue and methyl orange organic dyes under UV light. The results revealed a concentration-dependent photocatalytic activity of photocatalysts, which increased the amount of dopant (up to 5 wt.%). However, the degradation efficiency of the catalysts decreased upon further increasing the amount of dopant due to the recombination of holes and photoexcited electrons.

Photocatalytic Activity of Fe-Doped ZnO/Montmorillonite Nanocomposite for Degradation of Malachite Green

2015 ◽  
Vol 827 ◽  
pp. 19-24 ◽  
Author(s):  
Nur Afifah ◽  
Nadia Febiana Djaja ◽  
Rosari Saleh
Keyword(s):  
Photocatalytic Activity ◽  
Malachite Green ◽  
Organic Dyes ◽  
Uv Light ◽  
Precipitation Method ◽  
X Ray Diffraction ◽  
X Ray ◽  
Spin Resonance ◽  
Doped Zno ◽  
Co Precipitation

In this study, the photocatalytic activity of pure Fe- doped ZnO and Fe- doped ZnO/Montmorillonite nanocomposite has been investigated for the degradation of malachite green under UV light irradiation. Both photocatalysts were synthesized using co-precipitation method and characterized by X-ray diffraction, energy dispersive X-ray spectroscopy, Fourier-transform infrared absorption, and electron spin resonance. The results showed that the photocatalytic efficiency is better in the presence of montmorillonite compared to pure Fe- doped ZnO. To detect the possible reactive species involved in degradation of organic dyes control experiments with introducing scavengers into the solution of organic dyes were carried out. It is found that electron plays an important role in the degradation of malachite green.

Facile Preparation of P-25 Films Dip-Coated Nickel Foam and High Photocatalytic Activity for the Degradation of Quinoline and Industrial Wastewater

2011 ◽  
Vol 9 (1) ◽  
Author(s):  
Suiyi Zhu ◽  
Xia Yang ◽  
Gu-Ning Wang ◽  
Lei-Lei Zhang ◽  
He-Feng Zhu ◽  
...  
Keyword(s):  
Photocatalytic Activity ◽  
Aqueous Solutions ◽  
Specific Surface ◽  
Continuous Flow ◽  
Industrial Wastewater ◽  
Nickel Foam ◽  
High Photocatalytic Activity ◽  
Photocatalytic Reactor ◽  
X Ray ◽  
Three Phase

A kind of P-25 TiO2 films coated nickel foam was synthesized by a facile dip-coating/calcination route, and used to fabricate a continuous-flow three-phase photocatalytic reactor. The morphology, crystal phase structure, surface composition and specific surface area of P-25 films coated nickel foam were investigated by field emission scanning electron microscope (FE-SEM), X-ray diffractometer (XRD), X-ray photoelectron spectroscopy (XPS) and nitrogen adsorption-desorption measurements, respectively. The results indicated that the coated/ calcined P-25 films had the porous surface structure fabricated by nano-sized titanium dioxide consisted of two crystal phases and incorporated with a NiO interlayer. The increase of P-25 contents enhanced the specific surface area; however, 20 percent of initial P-25 sol would result in visible large cracks because of too high P-25 content and consequently cause the peeling of films. The photocatalytic activities of nickel foam with different coating amounts of P-25 for the degradation of quinoline aqueous solutions were investigated with a continuous-flow three-phase photocatalytic reactor based on the P-25 films coated nickel foam. The results suggested that nickel foam coated with 10 percent of P-25 sol had an optimal photocatalytic activity for the degradation of quinoline aqueous solutions. The continuous-flow three-phase photocatalytic reactor fabricated with P-25 films coated nickel foam with an optimal P-25 coating amount shows high photocatalytic activity and stability for the degradation of quinoline aqueous solutions and industrial wastewater. The treated industrial wastewater meets the international discharge standard.

SHAPE EVOLUTION IN ONE-DIMENSIONAL ZnO NANOSTRUCTURES GROWN FROM ZnO NANOPOWDER SOURCE: VAPOR–LIQUID–SOLID VERSUS VAPOR–SOLID GROWTH MECHANISMS

2011 ◽  
Vol 10 (01n02) ◽  
pp. 75-79 ◽  
Author(s):  
SOUMEN DHARA ◽  
P. K. GIRI
Keyword(s):  
Growth Mechanism ◽  
Growth Temperature ◽  
Shape Evolution ◽  
Zno Nanostructures ◽  
Growth Mechanisms ◽  
Vapor Liquid Solid ◽  
One Dimensional ◽  
Zno Nanopowder ◽  
Simultaneous Growth ◽  
Vapor Liquid

Here we report on the growth and evolution of ZnO nanowires grown from ZnO nanopowder as a source material using a horizontal muffle furnace. The shape evolution has been studied with variation in growth temperature and zinc vapor pressure. The structural analysis on these nanostructures shows c-axis oriented aligned growth. Scanning electron microscopy imaging of these nanostructures revealed the shape evolution from nanowires to nanoribbons and then to nanorods as the growth temperature increases from 650°C to 870°C. At 650°C, only vertical nanowires have been observed and with increase in growth temperature nanowires transform to nanoribbons and then to nanorods at 870°C. And we also observed simultaneous growth of nanorods and nanoribbons under a specific growth condition. We believe that these nanowires and nanorods were formed by vapor–liquid–solid growth mechanism (catalyst-mediated growth), whereas nanoribbons were grown by vapor–solid growth mechanism (without the aid of a metal catalyst). We observed simultaneous occurrence of vapor–liquid–solid and vapor–solid growth mechanisms at a particular growth temperature. These ZnO nanowires exhibit bound exciton related UV emission at ~379 nm, and defect-emission band in the visible region. Possible growth mechanism, shape evolution, and simultaneous growth of two types of one-dimensional ZnO nanostructures under the same growth condition are discussed.

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