Photocatalytic Degradation of Oxytetracycline by Photosensitive Materials and Toxicological Analysis by Caenorhabditis elegans

2019 ◽  
Vol 19 (11) ◽  
pp. 6924-6932 ◽  
Author(s):  
Qiaojie Yu ◽  
Tong Ouyang ◽  
Kefu Zhou ◽  
Changtang Chang
Keyword(s):  
Caenorhabditis Elegans ◽  
High Performance ◽  
Diffuse Reflectance Spectroscopy ◽  
Toxicity Testing ◽  
Degradation Process ◽  
Favorable Result ◽  
X Ray Diffraction ◽  
Transmission Electron ◽  
Initial Ph ◽  
One Step

This study explored a facile one-step hydrothermal method of preparing a high-performance photocatalyst, namely, graphene-TiO2, for oxytetracycline (OTC) removal. The nanocomposites were characterized by Fourier transform infrared (FT-IR) spectroscopy, transmission electron microscopy, UV-Vis diffuse reflectance spectroscopy and X-ray diffraction (XRD). The photocatalytic properties of different graphene loading types and various OTC initial concentrations, temperatures, and initial pH values were investigated. Results showed that the material with 10% graphene content exhibited the best performance and removal efficiency (beyond 99%) of OTC within 180 min at 35 °C and pH 5.5. The effects of different reactive oxygen species scavengers on photodegradation and the contributions were evaluated, and a possible reaction mechanism was proposed. Caenorhabditis elegans was used for toxicity testing during the entire degradation process and achieved a favorable result.

scholarly journals Facile Synthesis of Uniform Mesoporous Nb2O5 Micro-Flowers for Enhancing Photodegradation of Methyl Orange

Materials ◽  
2021 ◽  
Vol 14 (14) ◽  
pp. 3783
Author(s):  
Jian-Qing Qiu ◽  
Huan-Qing Xie ◽  
Ya-Hao Wang ◽  
Lan Yu ◽  
Fang-Yuan Wang ◽  
...  
Keyword(s):  
Methyl Orange ◽  
Active Sites ◽  
High Performance ◽  
Diffuse Reflectance Spectroscopy ◽  
X Ray Diffraction ◽  
Flower Structure ◽  
Electron Microscopies ◽  
Bet Method ◽  
One Step ◽  
Catalytic Active Sites

The removal of organic pollutants using green environmental photocatalytic degradation techniques urgently need high-performance catalysts. In this work, a facile one-step hydrothermal technique has been successfully applied to synthesize a Nb2O5 photocatalyst with uniform micro-flower structure for the degradation of methyl orange (MO) under UV irradiation. These nanocatalysts are characterized by transmission and scanning electron microscopies (TEM and SEM), X-ray diffraction (XRD), Brunauer–Emmett–Teller (BET) method, and UV-Vis diffuse reflectance spectroscopy (DRS). It is found that the prepared Nb2O5 micro-flowers presents a good crystal phases and consist of 3D hierarchical nanosheets with 400–500 nm in diameter. The surface area is as large as 48.6 m2 g−1. Importantly, the Nb2O5 micro-flowers exhibit superior catalytic activity up to 99.9% for the photodegradation of MO within 20 mins, which is about 60-fold and 4-fold larger than that of without catalysts (W/O) and commercial TiO2 (P25) sample, respectively. This excellent performance may be attributed to 3D porous structure with abundant catalytic active sites.

Facile hydrothermal synthesis of ternary CeO2–SnO2/rGO nanocomposite for supercapacitor application

2020 ◽  
Vol 13 (02) ◽  
pp. 2051005 ◽  
Author(s):  
Godlaveeti Sreenivasa Kumar ◽  
Somala Adinarayana Reddy ◽  
Hussen Maseed ◽  
Nagireddy Ramamanohar Reddy
Keyword(s):  
Electron Microscope ◽  
Specific Capacitance ◽  
High Performance ◽  
High Specific Capacitance ◽  
Energy Storage And Conversion ◽  
X Ray Diffraction ◽  
X Ray ◽  
Supercapacitor Application ◽  
Transmission Electron ◽  
One Step

In this work, we present the synthesis of a ternary CeO2–SnO2/rGO nanocomposite by using a facile one-step hydrothermal method. The as-synthesized composite was structural, chemical, morphological, elemental information studied by using different characterization techniques X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy and field emission scanning electron microscope (FESEM), energy dispersive X-ray spectroscopy (EDAX) and transmission electron microscope (TEM). The CeO2–SnO2/rGO exhibited an excellent specific capacitance of 156[Formula: see text]F[Formula: see text][Formula: see text] at 0.5[Formula: see text]A/g in the presence of 3 M KOH solution. The synergic effect of CeO2, SnO2 and graphene composite coated on Ni foam endowed a high specific capacitance than their individual compounds. This work suggests that the novel ternary composite is a promising candidate for the high performance electrochemical energy storage and conversion systems.

Controllable one-step synthesis of ZnO nanostructures using molybdophosphoric acid

2014 ◽  
Vol 68 (4) ◽  
Author(s):  
Hamed Rashidi ◽  
Ali Ahmadpour ◽  
Fatemeh Bamoharram ◽  
Seyed Zebarjad ◽  
Majid Heravi ◽  
...  
Keyword(s):  
Photocatalytic Degradation ◽  
High Performance ◽  
Hydrothermal Reaction ◽  
Hexagonal Phase ◽  
Zno Nanostructures ◽  
Molybdophosphoric Acid ◽  
X Ray Diffraction ◽  
Experimental Conditions ◽  
Transmission Electron ◽  
One Step

AbstractZnO nanostructures were synthesised in a hydrothermal reaction of zinc acetate in the presence of molybdophosphoric acid (H3[PMo12O40]) as well as its vanadium-substituted acid (H4[PMo11VO40]) at various times, temperatures, and concentrations. The ZnO nanostructures were characterised by X-ray diffraction, transmission electron microscopy, and Fourier transform infrared spectroscopy. The results demonstrated that the synthesised products are crystalline with a zincite hexagonal phase. Various ZnO nanostructures, such as nanoparticles, microrods, and nanosheets, were produced by changing the experimental conditions. The photocatalytic degradation of methyl orange was also investigated using the ZnO nanoparticles thus prepared. These particles exhibited high performance in the photocatalytic degradation of MO and almost 100 % decolourisation occurred within only 20 min.

Photocatalytic Performance of BiOCl Nanosheets Composite with Graphene

2014 ◽  
Vol 496-500 ◽  
pp. 297-300 ◽  
Author(s):  
Bi Tao Liu ◽  
Liang Liang Tian ◽  
Ling Ling Peng
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Photocatalytic Performance ◽  
Diffuse Reflectance Spectroscopy ◽  
Hydrothermal Reaction ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
One Step ◽  
High Migration

A series of composites of the high photoactivity of {001} facets exposed BiOCl and grapheme sheets (GS) were synthesized via a one-step hydrothermal reaction. The obtained BiOCl/GS photocatalysts were characterized by X-ray diffraction (XRD), Raman spectroscopy, scanning electron microscopy, transmission electron microscopy (TEM), Ultraviolet-visible (UV-Vis) diffuse reflectance spectroscopy. The as-prepared BiOCl/GS photocatalyst showed enhanced photocatalytic activity for the degradation of methyl orange (MO) under UV and visible light (λ > 400 nm). The enhanced photocatalytic activity could be attributed to oxygen vacancies of the {001} facets of BiOCl/GS and the high migration efficiency of photo-induced electrons, which could suppress the charge recombination effectively.

scholarly journals Photocatalytic Degradation of Selected Pharmaceuticals Using g-C3N4 and TiO2 Nanomaterials

Nanomaterials ◽  
2019 ◽  
Vol 9 (9) ◽  
pp. 1194 ◽  
Author(s):  
Smýkalová ◽  
Sokolová ◽  
Foniok ◽  
Matějka ◽  
Praus
Keyword(s):  
Photocatalytic Degradation ◽  
High Performance ◽  
Diffuse Reflectance Spectroscopy ◽  
Attenuated Total Reflection ◽  
Aqueous Environment ◽  
X Ray Diffraction ◽  
Mass Detection ◽  
Fourier Transformed Infrared Spectroscopy ◽  
Transmission Electron ◽  
Tio2 Nanomaterials

Exfoliated graphitic carbon nitride (g-C3N4) and two commercially available nanomaterials from titanium dioxide (P25 and CG300) were tested for the photocatalytic degradation of paracetamol (PAR), ibuprofen (IBU), and diclofenac (DIC). Prior to photocatalytic experiments, the nanomaterials were characterized by common methods, such as X-ray diffraction (XRD), UV–VIS diffuse reflectance spectroscopy (DRS), Fourier transformed infrared spectroscopy in attenuated total reflection mode (FTIR–ATR), transmission electron microscopy (TEM), physisorption of nitrogen, and dynamic vapor adsorption (DVS) of water. The sizes and specific surface area (SSA) of the TiO2 nanoparticles were 6 nm and 300 m2·g−1 for CG300 and 21 nm and 50 m2·g−1 for P25. The SSA of g-C3N4 was 140 m2·g−1. All photocatalytic experiments were performed under UV (368 nm), as well as VIS (446 nm) irradiation. TiO2 P25 was the most active photocatalyst under UV irradiation and g-C3N4 was the most active one under VIS irradiation. Photodegradation yields were evaluated by means of high performance liquid chromatography (HPLC) and reaction intermediates were identified using gas chromatography with mass detection (GC–MS). Paracetamol and ibuprofen were totally removed but the intermediates of diclofenac were observed even after 6 h of irradiation. Some intermediates, such as carbazole-1-acetic acid, 2,6-dichloraniline, and hydroxylated derivates of diclofenac were identified. This study showed that g-C3N4 is a promising photocatalyst for the degradation of pharmaceuticals in an aqueous environment, under visible light.

scholarly journals Photodegradation of Methyl Orange Using Magnetically Recoverable AgBr@Ag3PO4/Fe3O4Photocatalyst under Visible Light

2014 ◽  
Vol 2014 ◽  
pp. 1-6 ◽  
Author(s):  
Zhen Wang ◽  
Lu Yin ◽  
Ziwen Chen ◽  
Guowang Zhou ◽  
Huixiang Shi
Keyword(s):  
Photocatalytic Activity ◽  
Methyl Orange ◽  
Visible Light ◽  
High Performance ◽  
Diffuse Reflectance Spectroscopy ◽  
X Ray Diffraction ◽  
Electron Hole ◽  
Transmission Electron ◽  
Activity Enhancement ◽  
Matching Band

A novel magnetically recoverable AgBr@Ag3PO4/Fe3O4hybrid was prepared by a simple deposition-precipitation approach and characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), and UV-Vis diffuse reflectance spectroscopy (DRS). The results revealed that the photocatalytic activity and stability of AgBr@Ag3PO4/Fe3O4composite toward decomposition of methyl orange (MO) dye were superior to those of pure Ag3PO4under visible light irradiation. The photocatalytic activity enhancement of AgBr@Ag3PO4/Fe3O4is closely related to the efficient separation of electron-hole pairs derived from the matching band potentials between Ag3PO4and AgBr, as well as the good conductivity of Fe3O4. Moreover, the photocatalyst could be easily separated by applying an external magnetic field due to its magnetic property. The quenching effects of different scavengers proved that active h+and played the major role for the MO degradation. This work would provide new insight for the construction of visible light responsible photocatalysts with high performance, good stability, and recoverability.

scholarly journals Platinum-Decorated TiO2: One Step Fast Monometallic Impregnation and Plasma Effect on Nanoparticles

2021 ◽  
Vol 6 (1) ◽  
pp. 4
Author(s):  
Rudy Trejo-Tzab ◽  
Alejandro Avila-Ortega ◽  
Patricia Quintana-Owen ◽  
Ricardo Rangel ◽  
Mayra Angélica Álvarez-Lemus
Keyword(s):  
Platinum Nanoparticles ◽  
Photoelectron Spectroscopy ◽  
Diffuse Reflectance Spectroscopy ◽  
Plasma Discharge ◽  
Nitrogen Plasma ◽  
X Ray Diffraction ◽  
Discharge System ◽  
X Ray ◽  
Transmission Electron ◽  
One Step

In the present work, N-TiO2−x/Pt was synthesized using a homemade nitrogen plasma (AC) discharge system. The overall procedure use of low-power nitrogen plasma (100 watts) with 1 and 2 h of plasma discharge to successfully impregnate platinum nanoparticles on P25 titanium dioxide. The obtained samples were characterized using X-ray diffraction (XRD), UV–Vis diffuse reflectance spectroscopy (DRS), X-ray photoelectron spectroscopy (XPS), and high-resolution transmission electron microscopy (HRTEM). The results reveal the incorporation of metallic Pt up to 2.9% on the surface of TiO2 by increasing the duration of plasma discharge by up to two hours with a constant power of 100 watts. Likewise, the incorporation of nitrogen atoms into a lattice crystal was also favored, confirming a direct relationship between the amount of Pt and nitrogen atoms introduced in TiO2 as a function of the duration of plasma treatment. By characterizing nanoparticles loaded on a N-TiO2−x/Pt surface, we show that joined platinum nanoparticles have two different patterns, and the boundary between these two regions coalesces. The results demonstrate that the use of nitrogen plasma to impregnate platinum nanoparticles on the surface of TiO2 to obtain N-TiO2−x/Pt allows wide and relevant physics and chemistry applications.

Structural, Morphological, Magnetic and Self-Heating Studies of One-Step Polyol Synthesized Manganese Ferrite (MnFe2O4) Nanoparticles

2019 ◽  
Vol 19 (01) ◽  
pp. 1950003
Author(s):  
P. R. Ghutepatil ◽  
S. H. Pawar
Keyword(s):  
Room Temperature ◽  
Synthesis Method ◽  
Average Crystallite Size ◽  
Superparamagnetic Nanoparticles ◽  
Polyol Synthesis ◽  
X Ray Diffraction ◽  
Self Heating ◽  
Transmission Electron ◽  
One Step ◽  
Mnfe2o4 Nanoparticles

In this paper, uniform and superparamagnetic nanoparticles have been prepared using one-step polyol synthesis method. Structural, morphological and magnetic properties of obtained MnFe2O4 nanoparticles have been investigated by using X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), field emission scanning electron microscope (FE-SEM), transmission electron microscopy (TEM), vibrating sample magnetometry (VSM) and thermogravimetric analysis (TGA) techniques. Structural investigation showed that the average crystallite size of obtained nanoparticles was about 10[Formula: see text]nm. Magnetic study revealed that the nanoparticles were superparamagnetic at room temperature with magnetization 67[Formula: see text]emu/g at room temperature. The self-heating characteristics of synthesized MnFe2O4 nanoparticles were studied by applying external AC magnetic field of 167.6 to 335.2[Formula: see text]Oe at a fixed frequency of 265[Formula: see text]kHz. The SAR values of MnFe2O4 nanoparticles were calculated for 2, 5, 10[Formula: see text]mg[Formula: see text]mL[Formula: see text] concentrations and it is observed that the threshold hyperthermia temperature is achieved for all concentrations.

One Step Synthesis and Characterization of Zirconia-Graphene Composites

2012 ◽  
Vol 600 ◽  
pp. 174-177 ◽  
Author(s):  
Jian Fei Xia ◽  
Zong Hua Wang ◽  
Yan Zhi Xia ◽  
Fei Fei Zhang ◽  
Fu Qiang Zhu ◽  
...  
Keyword(s):  
Synthesis And Characterization ◽  
Two Dimensional ◽  
X Ray Diffraction ◽  
X Ray ◽  
Graphene Composite ◽  
Transmission Electron ◽  
One Step ◽  
Ft Ir ◽  
Xrd Techniques

Zirconia-graphene composite (ZrO2-G) has been successfully synthesized via decomposition of ZrOCl2•6H2O in a water-isopropanol system with dispersed graphene oxide (GO) utilizing Na2S as a precursor could enable the occurrence of the deposition of Zr4+ and the deoxygenation of GO at the same time. Transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FT-IR) and X-ray diffraction (XRD) techniques were used to characterize the samples. It was found that graphene were fully coated with ZrO2, and the ZrO2 existing in tetragonal phase, which resulted in the formation of two-dimensional composite.

scholarly journals Carbon-coated titania nanostructured particles: Continuous, one-step flame-synthesis

2003 ◽  
Vol 18 (11) ◽  
pp. 2670-2676 ◽  
Author(s):  
Hendrik K. Kammler ◽  
Sotiris E. Pratsinis
Keyword(s):  
Crystal Size ◽  
Nitrogen Adsorption ◽  
Titanium Tetraisopropoxide ◽  
X Ray Diffraction ◽  
Composite Powders ◽  
Nanostructured Particles ◽  
Carbon Particles ◽  
Transmission Electron ◽  
Carbon Coated ◽  
One Step

Concurrent synthesis of titania-carbon nanoparticles (up to 52 wt.% in C) was studied in a diffusion flame aerosol reactor by combustion of titanium tetraisopropoxide and acetylene. These graphitically layered carbon-coated titania particles were characterized by high-resolution transmission electron microscopy (HRTEM), with elemental mapping of C and Ti, x-ray diffraction (XRD), and nitrogen adsorption [Brunauer-Emmett-Teller (BET)]. The specific surface area of the powder was controlled by the acetylene flow rate from 29 to 62 m2/g as the rutile content decreased from 68 to 17 wt.%. Light blue titania suboxides formed at low acetylene flow rates. The average XRD crystal size of TiO2 decreased steadily with increasing carbon content of the composite powders, while the average BET primary particle size calculated from nitrogen adsorption decreased first and then approached a constant value. The latter is attributed to the formation of individual carbon particles next to carbon-coated titania particles as observed by HRTEM and electron spectroscopic imaging.

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