scholarly journals Preparation of magnetic copper ferrite nanoparticle as peroxymonosulfate activating catalyst for effective degradation of levofloxacin

2021 ◽  
Author(s):  
Jing Zhao ◽  
Pengfei Xiao ◽  
Shuang Han ◽  
Musajan Zulhumar ◽  
Dedong Wu
Keyword(s):  
Photoelectron Spectroscopy ◽  
Ph Value ◽  
Reactive Species ◽  
Activation Mechanism ◽  
Copper Ferrite ◽  
Radical Oxygen Species ◽  
Spinel Type ◽  
Paramagnetic Resonance ◽  
X Ray ◽  
Hydroxy Radicals

Abstract The magnetic CuFe2O4 nanoparticles were successfully synthesized with a coprecipitation method at 500 °C calcination temperature, which were utilized to degrade levofloxacin (LEV) as peroxymonosulfate (PMS) activator. The structure and composition of nanocatalyst were characterized by a series of methods, including Scanning electron microscopy, X-ray photoelectron spectroscopy, Fourier transform infrared spectroscopy, X-ray diffraction, Vibrating sample magnetometer and Thermogravimetric analysis. The effect of the PMS concentration, the catalyst dosage, the LEV initial concentration, the pH value and the inorganic anions on the LEV degradation was also explored. The results revealed that the designed CuFe2O4/PMS system had high activity and excellent stability in the complex conditions. The degradation efficiency of LEV still reached above 80% after four recycles of CuFe2O4 catalyst. The reactive species quenching experiments and electron paramagnetic resonance analysis suggested the existence of superoxide radicals, single oxygen, hydroxy radicals and sulfate radicals, and the first two were dominant radical oxygen species. Based on the mechanism analyses, the efficient degradation of LEV was probably due to the continuous generation of reactive species under the condition of Fe (III)/Fe (II) and Cu (II)/Cu (I) redox cycles. The research provided a reasonable reference for the PMS activation mechanism based spinel-type ferrite catalysis.

scholarly journals Degradation of Acid Red B by Manganese doped iron oxychloride and Permonosulfate: Performance and Inhomogeneous Activation Mechanism

2021 ◽  
Author(s):  
Rong Chen ◽  
Dan Zhao ◽  
Yanmao Dong ◽  
Chengrun Cai ◽  
Yan Yuan ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
Ph Value ◽  
Active Species ◽  
Ion Concentration ◽  
Activation Mechanism ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Initial Ph

Abstract manganese doped iron oxychloride (Mn-FeOCl) was synthesized by partial pyrolysis method. The Mn-FeOCl was used as heterogeneous catalyst to activate permonosulfate (PMS) for the degradation of azo dye acid red B(ARB) for the first time. The Mn-FeOCl was characterized by X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and X-ray diffraction spectroscopy (XRD). The effects of Mn-FeOCl dosage, PMS concentration, initial pH value, Cl ion concentration and humic acid (HA) dosage on the degradation of ARB by Mn-FeOCl/PMS were investigated. Results showed that the ARB was degraded effectively by Mn-FeOCl/PMS. The mineralization rate of ARB reached 42.5%. As the Mn-FeOCl dosage was 0.1g/L, PMS concentration was 1mmol/L, and ARB concentration was 0.05mmol/L, the degradation rate of ARB reached 99.4% in 30 minutes. With the increase of PMS dosage, Mn-FeOCl dosage, Cl− ion concentration and initial pH value, the decolorization effect of ARB increased. The reaction mechanism was analyzed by free radical quenching experiment and XPS. The main active species were determined as ·OH and SO4·− which generated by PMS activation. The SO4·−−was the main active species.

Jellyfish-like few-layer graphene nanoflakes: high paramagnetic response alongside increased interlayer interaction

2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Alexander Ulyanov ◽  
Dmitrii Stolbov ◽  
Serguei Savilov
Keyword(s):  
Photoelectron Spectroscopy ◽  
High Sensitivity ◽  
Paramagnetic Centers ◽  
Interlayer Interaction ◽  
Paramagnetic Resonance ◽  
X Ray ◽  
Graphene Nanoflakes ◽  
Few Layer Graphene ◽  
Electron Paramagnetic ◽  
Hydrocarbon Pyrolysis

Abstract Jellyfish-like graphene nanoflakes (GNF), prepared by hydrocarbon pyrolysis, are studied with electron paramagnetic resonance (EPR) method. The results are supported by X-ray photoelectron spectroscopy (XPS) data. Oxidized (GNFox) and N-doped oxidized (N-GNFox) flakes exhibit an extremely high EPR response associated with a large interlayer interaction which is caused by the structure of nanoflakes and layer edges reached by oxygen. The GNFox and N-GNFox provide the localized and mobile paramagnetic centers which are silent in the pristine (GNF p ) and N-doped (N-GNF) samples. The change in the relative intensity of the line corresponding to delocalized electrons is parallel with the number of radicals in the quaternary N-group. The environment of localized and mobile electrons is different. The results can be important in GNF synthesis and for explanation of their features in applications, especially, in devices with high sensitivity to weak electromagnetic field.

scholarly journals Efficient Removal of Levofloxacin by Activated Persulfate with Magnetic CuFe2O4/MMT-k10 Nanocomposite: Characterization, Response Surface Methodology, and Degradation Mechanism

Water ◽  
2020 ◽  
Vol 12 (12) ◽  
pp. 3583
Author(s):  
Junying Yang ◽  
Minye Huang ◽  
Shengsen Wang ◽  
Xiaoyun Mao ◽  
Yueming Hu ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Response Surface Methodology ◽  
Response Surface ◽  
Photoelectron Spectroscopy ◽  
Degradation Mechanism ◽  
Sol Gel ◽  
Combustion Method ◽  
Copper Ferrite ◽  
X Ray ◽  
Rsm Model

In this study, a magnetic copper ferrite/montmorillonite-k10 nanocomposite (CuFe2O4/MMT-k10) was successfully fabricated by a simple sol-gel combustion method and was characterised by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), the Brunner–Emmett–Teller (BET) method, vibrating sample magnetometer (VSM), and X-ray photoelectron spectroscopy (XPS). For levofloxacin (LVF) degradation, CuFe2O4/MMT-k10 was utilized to activate persulfate (PS). Due to the relative high adsorption capacity of CuFe2O4/MMT-k10, the adsorption feature was considered an enhancement of LVF degradation. In addition, the response surface methodology (RSM) model was established with the parameters of pH, temperature, PS dosage, and CuFe2O4/MMT-k10 dosage as the independent variables to obtain the optimal response for LVF degradation. In cycle experiments, we identified the good stability and reusability of CuFe2O4/MMT-k10. We proposed a potential mechanism of CuFe2O4/MMT-k10 activating PS through free radical quenching tests and XPS analysis. These results reveal that CuFe2O4/MMT-k10 nanocomposite could activate the persulfate, which is an efficient technique for LVF degradation in water.

Mixed Metal Oxide Interfaces: An Experimental and Theoretical Assessment of Secondary Metal Influences in Metal Impregnated Aluminas

1994 ◽  
Vol 368 ◽  
Author(s):  
M. Malaty ◽  
D. Singh ◽  
R. Schaeffer ◽  
S. Jansen ◽  
S. Lawrence
Keyword(s):  
Photoelectron Spectroscopy ◽  
Theoretical Calculations ◽  
Mixed Metal Oxide ◽  
X Ray Diffraction ◽  
Paramagnetic Resonance ◽  
X Ray ◽  
Mixed Metal ◽  
Metal Interactions ◽  
Metal Metal ◽  
Bimetallic System

ABSTRACTStudies of the mixed-metal interface in metal impregnated alumina have indicated the possibility of much metal-metal and metal-substrate interaction. Studies were carried out on NiCu/Al2O3 system which was evaluated to develop a better understanding of the forces that drive modification of the catalytic selectivity of Ni in the presence of Cu. Electron Paramagnetic Resonance (EPR), Powder X-ray Photoelectron Spectroscopy (XPS), X-ray Diffraction (XRD) and theoretical calculations were carried out on this bimetallic system, using Ni,Ag/Al2O3 as a reference as Ni shows negligible electron perturbation on co-adsorbance with Ag onto alumina. XRD results indicate that gross modification of the electronic fields of Ni and Cu are due to direct coupling and intercalation into the alumina matrix. As a result of this phenomena, these materials may form a good base for the development of novel ceramics based on mixed-metal interactions where the intermetallic perturbations are driven by the substrate effects.

scholarly journals Aqueous poly(N-Vinylformamide-co-Vinylamine) as a suitable adhesion promoter for wood veneer/biopolyethylene composite materials

BioResources ◽  
2017 ◽  
Vol 12 (4) ◽  
pp. 8134-8159
Author(s):  
Rico John ◽  
Katja Trommler ◽  
Katja Schreiter ◽  
Carolin Siegel ◽  
Frank Simon ◽  
...  
Keyword(s):  
Composite Materials ◽  
Photoelectron Spectroscopy ◽  
Ph Value ◽  
Structural Parameters ◽  
Degree Of Hydrolysis ◽  
Adhesion Promoter ◽  
Wood Veneer ◽  
X Ray ◽  
Young’S Moduli ◽  
Veneer Surface

Wood veneer/biopolyethylene (bio-PE) biocomposite materials were produced by using poly(N-vinylformamide-co-vinylamine) (PVFA-co-PVAm) copolymers as a phase-mediating reagent. In a preliminary step, PVFA-co-PVAm was adsorbed onto the wood veneer component from aqueous solution. In its adsorbed form, it served as an adhesion promoter and improved the compatibility between both the highly polar wood veneer and weakly polar bio-PE surface. Structural parameters and their effect on the adsorption process, such as the degree of hydrolysis (DH) of poly(N-vinylformamide) (PVFA) (30, 50, and > 90%), the molecular weight of PVFA-co-PVAm (Mw 10,000, 45,000, or 340,000 g/mol), and the pH value (4, 7, and 11) influenced the resulting wetting behavior of the PVFA-co-PVAm-modified wood veneer surface. Thus, the hydrophobizing effect of the PVFA-co-PVAm was clearly detectable because the contact angle with water was considerably increased up to 116° by adsorption of PVFA-co-PVAm 9095 at pH 11. The adsorbed amount of PVFA-co-PVAm was determined by energy-dispersive X-ray (EDX) spectroscopy and X-ray photoelectron spectroscopy (XPS). The PVFA-co-PVAm-coated wood veneers were consolidated with bio-PE in a hot press process. The modified composite materials showed remarkably improved Young’s moduli (552 MPa) and tensile strengths (4.5 MPa) compared to former composite materials produced without PVFA-co-PVAm modification.

scholarly journals Spinel-Type (FeCoCrMnZn)3O4 High-Entropy Oxide: Facile Preparation and Supercapacitor Performance

Materials ◽  
2020 ◽  
Vol 13 (24) ◽  
pp. 5798
Author(s):  
Bingliang Liang ◽  
Yunlong Ai ◽  
Yiliang Wang ◽  
Changhong Liu ◽  
Sheng Ouyang ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
Nickel Foam ◽  
Spinel Type ◽  
X Ray ◽  
High Entropy ◽  
Transmission Electron ◽  
Coating Method ◽  
Potential Applications ◽  
Supercapacitor Performance

High-entropy oxides (HEOs) have attracted more and more attention because of their unique structures and potential applications. In this work, (FeCoCrMnZn)3O4 HEO powders were synthesized via a facile solid-state reaction route. The confirmation of phase composition, the observation of microstructure, and the analysis of crystal structure, distribution of elements, and valences of elements were conducted by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy-dispersive X-ray spectroscopy (EDS), and X-ray photoelectron spectroscopy (XPS), respectively. Furthermore, a (FeCoCrMnZn)3O4/nickel foam ((FeCoCrMnZn)3O4/NF) electrode was prepared via a coating method, followed by the investigation of its supercapacitor performance. The results show that, after calcining (FeCoCrMnZn)3O4 powders at 900 °C for 2 h, a single spinel structure (FCC, Fd-3m, a = 0.8399 nm) was obtained with uniform distribution of Fe, Co, Cr, Mn, and Zn elements, the typical characteristic of a high-entropy oxide. In addition, the mass specific capacitance of the (FeCoCrMnZn)3O4/NF composite electrode was 340.3 F·g−1 (with 1 M KOH as the electrolyte and 1 A·g−1 current density), which indicates that the (FeCoCrMnZn)3O4 HEO can be regarded as a prospective candidate for an electrode material in the field of supercapacitor applications.

scholarly journals Preparation and Characterization of Defective TiO2. The Effect of the Reaction Environment on Titanium Vacancies Formation

Materials ◽  
2020 ◽  
Vol 13 (12) ◽  
pp. 2763
Author(s):  
Zuzanna Bielan ◽  
Szymon Dudziak ◽  
Agnieszka Sulowska ◽  
Daniel Pelczarski ◽  
Jacek Ryl ◽  
...  
Keyword(s):  
Photocatalytic Activity ◽  
Visible Light ◽  
Photoelectron Spectroscopy ◽  
Diffuse Reflectance Spectroscopy ◽  
Hydrothermal Reaction ◽  
High Photocatalytic Activity ◽  
Paramagnetic Resonance ◽  
X Ray ◽  
Light Activity ◽  
Cheap Alternative

Among various methods of improving visible light activity of titanium(IV) oxide, the formation of defects and vacancies (both oxygen and titanium) in the crystal structure of TiO2 is an easy and relatively cheap alternative to improve the photocatalytic activity. In the presented work, visible light active defective TiO2 was obtained by the hydrothermal reaction in the presence of three different oxidizing agents: HIO3, H2O2, and HNO3. Further study on the effect of used oxidant and calcination temperature on the physicochemical and photocatalytic properties of defective TiO2 was performed. Obtained nanostructures were characterized by X-ray diffractometry (XRD), specific surface area (BET) measurements, UV-Vis diffuse reflectance spectroscopy (DR-UV/Vis), photoluminescence spectroscopy (PL), X-ray photoelectron spectroscopy (XPS), and electron paramagnetic resonance (EPR) spectroscopy. Degradation of phenol as a model pollutant was measured in the range of UV-Vis and Vis irradiation, demonstrating a significant increase of photocatalytic activity of defective TiO2 samples above 420 nm, comparing to non-defected TiO2. Correlation of EPR, UV-Vis, PL, and photodegradation results revealed that the optimum concentration of HIO3 to achieve high photocatalytic activity was in the range of 20–50 mol%. Above that dosage, titanium vacancies amount is too high, and the obtained materials’ photoactivity was significantly decreased. Studies on the photocatalytic mechanism using defective TiO2 have also shown that •O2− radical is mainly responsible for pollutant degradation.

Sequestered carbon on clay mineral probed by electron paramagnetic resonance and X-ray photoelectron spectroscopy

2006 ◽  
Vol 295 (1) ◽  
pp. 135-140 ◽  
Author(s):  
Kátia Cylene Lombardi ◽  
Antonio Salvio Mangrich ◽  
Fernando Wypych ◽  
Ubirajara Pereira Rodrigues-Filho ◽  
José L. Guimarães ◽  
...  
Keyword(s):  
Electron Paramagnetic Resonance ◽  
Clay Mineral ◽  
Photoelectron Spectroscopy ◽  
Paramagnetic Resonance ◽  
X Ray ◽  
Electron Paramagnetic

scholarly journals Preparation and Photocatalytic Property of Ag Modified Titanium Dioxide Exposed High Energy Crystal Plane (001)

Coatings ◽  
2020 ◽  
Vol 10 (1) ◽  
pp. 27 ◽  
Author(s):  
Li-Yuan Zhang ◽  
Jia You ◽  
Qian-Wen Li ◽  
Zhi-Hong Dong ◽  
Ya-Jie Zhong ◽  
...  
Keyword(s):  
Methyl Orange ◽  
Absorption Band ◽  
Photoelectron Spectroscopy ◽  
Ph Value ◽  
Photocatalytic Property ◽  
High Energy ◽  
Metal Halide ◽  
Crystal Plane ◽  
X Ray ◽  
Metal Halide Lamp

TiO2 exposed high energy crystal plane (001) was prepared by the sol-gel process using butyl titanate as the titanium source and hydrofluoric acid as the surface control agent. Ag-TiO2 was prepared by depositing Ag on the crystal plane of TiO2 (101) with a metal halide lamp. The surface morphology, interplanar spacing, crystal phase composition, ultraviolet absorption band, element composition, and valence state of the samples were characterized by using field emission scanning electron microscopy (FESEM), transmission electron microscope (TEM), X-ray diffraction (XRD), ultraviolet-visible absorption spectrum (UV-Vis-Abs), and X-ray photoelectron spectroscopy (XPS), respectively. The formation mechanism of high energy crystal plane (001) was discussed, and the photocatalytic activities were evaluated by following degradation of methyl orange. The results show that TiO2 exposed the (001) crystal plane with a ratio of 41.8%, and Ag can be uniformly deposited on the crystal plane of TiO2 (101) by means of metal halide lamp deposition. Under the same conditions, the degradation rate of methyl orange by deposited Ag-TiO2 reaches as much as 93.63% after 60 min using the metal halide lamp (300 W) as an illuminant, 81.89% by non-deposited samples and 75.20% by nano-TiO2, causing a certain blue shift in the light absorption band edge of TiO2. Ag-TiO2 has the best photocatalytic performance at a pH value of 2.

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