scholarly journals Achieving the enhanced photocatalytic degradation of ceftriaxone sodium using CdS-g-C3N4 nanocomposite under visible light irradiation: RSM modeling and optimization

2021 ◽  
Author(s):  
Naime AttariKhasraghi ◽  
Karim Zare ◽  
Ali Mehrizad ◽  
Nasser Modirshahla ◽  
Mohammad Ali Behnajady
Keyword(s):  
Electron Microscopy ◽  
Visible Light ◽  
Photocatalytic Degradation ◽  
Visible Light Irradiation ◽  
Irradiation Time ◽  
Energy Levels ◽  
Light Irradiation ◽  
X Ray ◽  
Ceftriaxone Sodium ◽  
Operational Variables

Abstract In this research, the cadmium sulfide - graphite carbon nitride (CdS-g-C3N4) nanocomposite was synthesized and characterized by X-ray diffraction (XRD), Field emission scanning electron microscopy (FESEM), energy-dispersive X-ray spectrometer (EDX), and transmission electron microscopy (TEM) techniques. The photocatalytic activity of as-prepared nanocomposite was evaluated in the degradation of ceftriaxone sodium (CTX) antibiotic from aqueous solution under visible light irradiation. The influence of the operational variables such as the amount of photocatalyst (g/L), initial CTX concentration (mg/L), pH, and irradiation time (min) on the photodegradation process was investigated and optimized using response surface methodology (RSM) - central composite design (CCD) model. The maximum degradation percentage (92.55 %) was obtained in the optimal condition, including 0.06 g/L of CdS-g-C3N4 photocatalyst, 15 mg/L of CTX, pH= 10.5, and irradiation time = 81 min. The efficient photocatalytic performance of CdS-g-C3N4 nanocomposite is due to the appropriate alignment of energy levels between the CdS and g-C3N4, which synergistically impact the charge separation and the degradation efficiency of CTX. The kinetics of the photocatalytic degradation process was well described by Langmuir-Hinshelwood’s pseudo-first-order model (kapp = 0.0336 min-1).

scholarly journals Photocatalytic degradation of deoxynivalenol over dendritic-like α-Fe2O3 under visible light irradiation

Toxins ◽  
2019 ◽  
Vol 11 (2) ◽  
pp. 105 ◽  
Author(s):  
Huiting Wang ◽  
Jin Mao ◽  
Zhaowei Zhang ◽  
Qi Zhang ◽  
Liangxiao Zhang ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Visible Light ◽  
Photocatalytic Degradation ◽  
Visible Light Irradiation ◽  
Photoelectron Spectroscopy ◽  
High Performance ◽  
Synthesis Method ◽  
Light Irradiation ◽  
Trichothecene Mycotoxin ◽  
X Ray

Deoxynivalenol (DON) is a secondary metabolite produced by Fusarium, which is a trichothecene mycotoxin. As the main mycotoxin with high toxicity, wheat, barley, corn and their products are susceptible to contamination of DON. Due to the stability of this mycotoxin, traditional methods for DON reduction often require a strong oxidant, high temperature and high pressure with more energy consumption. Therefore, exploring green, efficient and environmentally friendly ways to degrade or reduce DON is a meaningful and challenging issue. Herein, a dendritic-like α-Fe2O3 was successfully prepared using a facile hydrothermal synthesis method at 160 °C, which was systematically characterized by X-ray diffraction (XRD), high-resolution transmission electron microscopy (HRTEM), scanning electron microscopy (SEM), and X-ray photoelectron spectroscopy (XPS). It was found that dendritic-like α-Fe2O3 showed superior activity for the photocatalytic degradation of DON in aqueous solution under visible light irradiation (λ > 420 nm) and 90.3% DON (initial concentration of 4.0 μg/mL) could be reduced in 2 h. Most of all, the main possible intermediate products were proposed through high performance liquid chromatography-mass spectrometry (HPLC-MS) after the photocatalytic treatment. This work not only provides a green and promising way to mitigate mycotoxin contamination but also may present useful information for future studies.

Ag2O/ZnO Heterostructures with Enhanced Photocatalytic Activity

2021 ◽  
Vol 1035 ◽  
pp. 1043-1049
Author(s):  
Di Xiang ◽  
Chang Long Shao
Keyword(s):  
Electron Microscopy ◽  
Visible Light ◽  
Visible Light Irradiation ◽  
Environmental Remediation ◽  
Organic Dyes ◽  
Light Irradiation ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
P Type

A simple route has been developed for the synthesis of Ag2O/ZnO heterostructures and the samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy dispersive X-ray spectroscopy (EDS) and photoluminescence (PL) spectroscopy analysis. Considering the porous structure of Ag2O/ZnO, the photocatalytic degradation for the organic dyes, such as eosin red (ER), methyl orange (MO), methylene blue (MB) and rhodamine B (RhB), under visible light irradiation was investigated in detail. Noticeably, Ag2O/ZnO just took 40 min to degrade 96 % MB. The rate of degradation using the Ag2O/ZnO heterostructures was 2.3 times faster than that of the bare porous ZnO nanospheres under visible light irradiation due to that the recombination of the photogenerated charge was inhibited greatly in the p-type Ag2O and n-type ZnO semiconductor. So the Ag2O/ZnO heterostuctures showed the potential application on environmental remediation.

scholarly journals Perovskite-type LaFeO3: Photoelectrochemical Properties and Photocatalytic Degradation of Organic Pollutants Under Visible Light Irradiation

Catalysts ◽  
2019 ◽  
Vol 9 (4) ◽  
pp. 342 ◽  
Author(s):  
Mohammed Ismael ◽  
Michael Wark
Keyword(s):  
Visible Light ◽  
Photocatalytic Degradation ◽  
Visible Light Irradiation ◽  
Metal Ion ◽  
Electrochemical Impedance ◽  
Diffuse Reflectance Spectroscopy ◽  
Light Irradiation ◽  
Complexing Agent ◽  
X Ray ◽  
Perovskite Type

Perovskite-type oxides lanthanum ferrite (LaFeO3) photocatalysts were successfully prepared by a facile and cost-effective sol-gel method using La(NO)3 and Fe(NO)3 as metal ion precursors and citric acid as a complexing agent at different calcination temperatures. The properties of the resulting LaFeO3 samples were characterized by powder X-ray diffraction (XRD), energy dispersive X-ray spectroscopy (EDXS), UV-Vis diffuse reflectance spectroscopy (DRS), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectra (IR), transmission electron microscopy (TEM), N2 adsorption/desorption and photoelectrochemical tests. The photoactivity of the LaFeO3 samples was tested by monitoring the photocatalytic degradation of Rhodamine B (RhB) and 4-chlorophenol (4-CP) under visible light irradiation, the highest photocatalytic activity was found for LaFeO3 calcined at 700 °C, which attributed to the relatively highest surface area (10.6 m2/g). In addition, it was found from trapping experiments that the reactive species for degradation were superoxide radical ions (O2−) and holes (h+). Photocurrent measurements and electrochemical impedance spectroscopy (EIS) proved the higher photo-induced charge carrier transfer and separation efficiency of the LaFeO3 sample calcined at 700 °C compared to that that calcined at 900 °C. Band positions of LaFeO3 were estimated using the Mott-Schottky plots, which showed that H2 evolution was not likely.

Preparation of BiXY(2-X)O3 and its Photocatalytic Degradation of Molasses Fermentation Wastewater under Visible-Light Irradiation

2011 ◽  
Vol 287-290 ◽  
pp. 1640-1645 ◽  
Author(s):  
Min Guang Fan ◽  
Zu Zeng Qin ◽  
Zi Li Liu ◽  
Tong Ming Su
Keyword(s):  
Photocatalytic Activity ◽  
Visible Light ◽  
Photocatalytic Degradation ◽  
Visible Light Irradiation ◽  
Photoelectron Spectroscopy ◽  
Diffuse Reflectance ◽  
Diffuse Reflectance Spectroscopy ◽  
Active Oxygen Species ◽  
Light Irradiation ◽  
X Ray

A series of BixY(2-x)O3photocatalysts were successfully prepared by a solid-state reaction and were subsequently characterized by powder X-ray diffraction, UV-vis diffuse reflectance spectroscopy, and X-ray photoelectron spectroscopy (XPS). The UV-vis diffuse reflectance spectra revealed that the BixY(2-x)O3samples absorbed light in the visible-light range (400-800 nm). The XPS results indicated that active oxygen species were generated on the Bi1.8Y0.2O3surface, which displayed a higher photocatalytic activity. When using photocatalytic degradation molasses fermentation wastewater as a model reaction, the Bi1.8Y0.2O3showed higher photocatalytic activity in comparison to Bi0.2Y1.8O3under visible-light irradiation.

A simple method to synthesise Ag-doped TiO2 photocatalysts with different Ag0:Ag2O atomic ratios for enhancing visible-light photocatalytic activity

2017 ◽  
Vol 41 (8) ◽  
pp. 475-483 ◽  
Author(s):  
C. Chen ◽  
X. F. Lei ◽  
M. Z. Xue
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Visible Light ◽  
Visible Light Irradiation ◽  
Light Absorption ◽  
Separation Efficiency ◽  
Visible Region ◽  
Light Irradiation ◽  
Electron Hole ◽  
X Ray

Pure anatase TiO2 photocatalysts with different Ag contents were prepared via a simple sol-gel method. The as-prepared anatase Ag-doped TiO2 photocatalysts were characterised by X-ray diffraction, transmission electron microscopy, UV-Vis diffuse reflectance spectra, photoluminescence spectroscopy, X-ray photoelectron spectroscopy, thermal gravity and differential thermal analysis, scanning electron microscopy and N2 adsorption–desorption measurements (BET). Compared with pure TiO2, Ag-doped anatase TiO2 photocatalysts exhibited not only increases in light absorption in the visible region, the separation efficiency of electron–hole pairs and surface area, but also inhibition of the titania phase transition from anatase to rutile. Photoreduction results showed that Ag-doped anatase TiO2 photocatalysts have greatly improved photocatalytic activity, compared with pure TiO2, and the reduction of Cr(VI) under visible light irradiation was much higher than that of pure TiO2. The optimum Ag content was 1.0 mol%, which led to the complete reduction of Cr(VI) under visible light irradiation (λ > 420 nm) for 4 h. The enhanced photocatalytic activity was attributed to the synergic effect of the pure anatase structure, and the increased light absorption in the visible region, separation efficiency of electron–hole pairs and atomic ratio of Ag0:Ag2O.

A Comparative Study on the Role of Precursors of Graphitic Carbon Nitrides for the Photocatalytic Degradation of Direct Red 81

2014 ◽  
Vol 807 ◽  
pp. 101-113 ◽  
Author(s):  
J. Theerthagiri ◽  
R.A. Senthil ◽  
J. Madhavan ◽  
B. Neppolian
Keyword(s):  
Particle Size ◽  
Photocatalytic Activity ◽  
Visible Light ◽  
Photocatalytic Degradation ◽  
Visible Light Irradiation ◽  
Carbon Nitride ◽  
Light Irradiation ◽  
X Ray Diffraction ◽  
X Ray ◽  
Carbon Nitrides

The graphitic carbon nitride (g-C3N4) materials have been synthesized from nitrogen rich precursors such as urea and thiourea by directly heating at 520 °C for 2 h. The as-synthesized carbon nitride samples were characterized by x-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), ultraviolet-visible (UV-vis) absorption spectroscopy, photoluminescence (PL) and particle size analysis. The photoelectrochemical measurements were performed using several on-off cycles under visible-light irradiation. The x-ray diffraction peak is broader which indicates the fine powder nature of the synthesized materials. The estimated crystallite size of carbon nitrides synthesized from urea (U-CN) and thiourea (T-CN) are 4.0 and 4.4 nm respectively. The particle size of U-CN and T-CN were analysed by particle size analyser and were found to be 57.3 and 273.3 nm respectively. The photocatalytic activity for the degradation of the textile dye namely, direct red-81 (DR81) using these carbon nitrides were carried out under visible light irradiation. In the present investigation, a comparison study on the carbon nitrides synthesized from cheap precursors such as urea and thiourea for the degradation of DR81 has been carried out. The results inferred that U-CN exhibited higher photocatalytic activity than T-CN. The photoelectrochemical studies confirmed that the (e--h+) charge carrier separation is more efficient in U-CN than that of T-CN and therefore showed high photocatalytic degradation. Further, the smaller particle size of U-CN is also responsible for the observed degradation trend.

scholarly journals Gemini surfactant assisted synthesis of mesoporous Mn/Mg bimetal doped TiO2 nanomaterial: Characterization and photocatalytic activity studies under visible light irradiation

2021 ◽  
Author(s):  
Sankara Rao Miditana ◽  
Siva Rao Tirukkovalluri ◽  
Imandi Manga Raju ◽  
Shaik Abdul Alim ◽  
Genji Jaishree ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Visible Light ◽  
Surface Area ◽  
Visible Light Irradiation ◽  
Gemini Surfactant ◽  
Light Irradiation ◽  
Methyl Red ◽  
X Ray ◽  
Ft Ir

Abstract The present work mainly aimed to synthesize different weight percentages (0.25-1.00 wt%) of Manganese (Mn2+) and Magnesium (Mg2+) bimetal ions doped TiO2 nanomaterial assisted with different weight percentages (5-15 wt%) of Gemini surfactant (GS) using sol-gel method. The bimetal doped and undoped TiO2 photocatalysts were characterized by X-ray Diffraction, Scanning Electron Microscopy, Energy Dispersive X-ray Spectroscopy, Fourier Transform Infrared Spectroscopy (FT-IR), UV-Visible Diffused Reflectance Spectroscopy, Transmission Electron Microscopy, Brunauer-Emmett-Teller surface area analyzer, and Photoluminescence Spectroscopy. Characterization results revealed that mesoporous multi-particle anatase TiO2 nanoparticles with a narrowed band gap, small particle size, and high surface area were formed due to the combined effect of Mn2+/Mg2+ bimetal ions doping and effective encapsulation of GS over the initially formed TiO2 nanoparticles. The surface elemental composition of the 0.25 wt% Mn2+ and 1.00 wt% Mg2+ bimetal doped TiO2 in the presence of 10 wt% of GS (after calcination) revealed the presence of both the metal dopants Mn2+ and Mg2+ along with the Ti and O and their chemical interactions were further confirmed by FT-IR results. The photocatalytic activity of these catalysts was assessed by the degradation of Methyl Red using visible light irradiation. To understand the effect of different reaction parameters on the photocatalytic activity of the nanocatalysts such as the dopant concentration, surfactant concentration, catalyst dosage, solution pH, and initial dye concentrations were investigated and optimized to achieve the best performance. The photoluminescence results conclude that OH radicals are the crucial reactive species responsible for oxidative photocatalytic degradation of Methyl Red.

scholarly journals Design and fabrication of Ag3VO4/g-C3N4 heterostructure photocatalyst for enhanced visible light degradation of various organic pollutants

2021 ◽  
Author(s):  
N Sujatha ◽  
M Meenachi ◽  
S Mohammed Harshulkhanb ◽  
H.H Hegazy
Keyword(s):  
Electron Microscopy ◽  
Visible Light ◽  
Visible Light Irradiation ◽  
Photoelectron Spectroscopy ◽  
Diffuse Reflectance Spectroscopy ◽  
Light Irradiation ◽  
X Rays ◽  
Hydrothermal Route ◽  
X Ray ◽  
Visible Light Degradation

Abstract In later years, numerous viable photocatalysts have been created in order to illuminate the issues of natural toxins. In this work, heterostructured photocatalysts Ag3VO4/g-C3N4 were prepared by effortless hydrothermal route in order to anchor Ag3VO4 on the surface of the g-C3N4 nanosheets. The prepared samples were fairly characterized using X-ray diffraction (XRD), Energy dispersive analysis of X-rays (EDAX), Scanning electron microscopy (SEM), Transmission electron microscopy (TEM), UV-vis diffuse reflectance spectroscopy (UV-DRS), photoluminescence, and X-ray photoelectron spectroscopy (XPS) techniques. The photocatalytic activity of the samples was evaluated by degrading malachite green (MG) and 2,4 dimethyl phenol (DMP) in aqueous solution under visible light irradiation. Compared with Ag3VO4 and g-C3N4, the heterojuncted photocatalyst 50 wt% Ag3VO4/g-C3N4 exhibits the best activity such as high degradation efficiency (99%), high apparent constant (0.0923 min− 1) and long term stability towards DMP under visible light irradiation. The development of a phase scheme heterojunction between Ag3VO4 and g-C3N4 improved the photocatalytic efficiency of Ag3VO4/g-C3N4 composites. Furthermore, the porous structure of g-C3N4 and the effect of Ag surface plasmon resonance (SPR) speed up the isolation and transfer of electron-hole pairs, reducing the likelihood of recombination.

scholarly journals Synthesis, characterization of Ag-doped CdS-WO2 nanocomposite and effects of photocatalytic degradation in RhB under visible light irradiation

2022 ◽  
Author(s):  
G. Roshini ◽  
V. Sathish ◽  
S. Manigandan ◽  
A. Tamilarasi ◽  
E. Priyanka
Keyword(s):  
Visible Light ◽  
Visible Light Irradiation ◽  
Photocatalytic Performance ◽  
Irradiation Time ◽  
Light Irradiation ◽  
X Ray Diffraction ◽  
X Ray ◽  
Ft Ir ◽  
Ft Ir Spectroscopy

Abstract In this paper, the highly stable Ag/CdS-WO2 nanocomposite was fabricated by a facile and capping agent-free hydrothermal technique. The fabricated Ag doped CdS-WO2 nanocomposite were characterized by powder X-ray diffraction (XRD), Fourier transform infrared (FT-IR) spectroscopy and UV-vis diffuse reflectance (DRS) spectroscopy. The photocatalytic performance of synthesized photocatalysts was evaluated for the photodegradation of rhodamine B (Rh B) under visible light irradiation (VLI). The parameters used for the optimization of the photocatalyst were pH, catalyst dose, oxidant dose, and irradiation time. Based on this, a possible reaction mechanism for the enhancement of photocatalytic activity of Ag/CdS-WO2 has been proposed. Hence, we have a tendency to believe it might be a promising material that may be used for the photodegradation of organic pollutants present in wastewater.

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