scholarly journals Cu2O nanoparticles for the degradation of methyl parathion

2020 ◽  
Vol 11 ◽  
pp. 1546-1555
Author(s):  
Juan Rizo ◽  
David Díaz ◽  
Benito Reyes-Trejo ◽  
M Josefina Arellano-Jiménez
Keyword(s):  
Photoelectron Spectroscopy ◽  
Methyl Parathion ◽  
Aqueous Suspension ◽  
Hydrolytic Degradation ◽  
Indirect Evidence ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Surface Basicity ◽  
One Step

Methyl parathion (MP) is one of the most neurotoxic pesticides. An inexpensive and reliable one-step degradation method of MP was achieved through an aqueous suspension of copper(I) oxide nanoparticles (NPs). Three different NPs sizes (16, 29 and 45 nm), determined with X-ray diffraction (XRD) and high-resolution transmission electron microscopy (HRTEM), were synthesized using a modified Benedict’s reagent. 1H nuclear magnetic resonance (NMR) results show that the hydrolytic degradation of MP leads to the formation of 4-nitrophenol (4-NPh) as the main product. While the P=S bond of MP becomes P=O, confirmed by 31P NMR. Although Cu2O is a widely known photocatalyst, the degradation of methyl parathion was associated to the surface basicity of Cu2O NPs. Indirect evidence for the basicity of Cu2O NPs was achieved through UV–vis absorption of 4-NPh. Likewise, it was shown that the surface basicity increases with decreasing nanoparticle size. The presence of CuCO3 on the surface of Cu2O, identified using X-ray photoelectron spectroscopy (XPS), passivates its surface and consequently diminishes the degradation of MP.

Activation of persulfate by heterogeneous catalyst ZnCo2O4–RGO for efficient degradation of bisphenol A

2020 ◽  
Vol 98 (12) ◽  
pp. 771-778
Author(s):  
Xin Chang ◽  
Xiangyang Xu ◽  
Zhifeng Gao ◽  
Yingrui Tao ◽  
Yixuan Yin ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Bisphenol A ◽  
Photoelectron Spectroscopy ◽  
X Ray Diffraction ◽  
Reaction Conditions ◽  
X Ray ◽  
Transmission Electron ◽  
Nucleation Sites ◽  
One Step ◽  
Application Potential

A nanocomposite, reduced graphene oxide (RGO) modified ZnCo2O4 (ZnCo2O4–RGO) was synthesized via one-step solvothermal method for activating persulfate (PS) to degrade bisphenol A (BPA). The morphology and structure of the nanocomposite were identified by X-ray diffraction, Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, scanning electron microscopy, and transmission electron microscopy. RGO provides nucleation sites for ZnCo2O4 to grow and inhibits the agglomeration of the nanoparticles. The influence of different reaction conditions on the oxidation of BPA catalyzed by ZnCo2O4–RGO was investigated, including the content of RGO, the dosage of catalyst, the concentration of humic acid (HA), anions in the environment, the reaction temperature, and pH. BPA can be totally degraded within 20 min under optimized reaction conditions. The presence of HA, Cl−, and NO3− only has a slight effect on the oxidation of BPA, whereas the presence of either H2PO4− or HCO3− can greatly inhibit the reaction. ZnCo2O4–RGO shows good cycling stability and practical application potential. A reaction mechanism of the degradation of BPA was also explored.

Aqueous Ferrofluid of Citric Acid Coated Magnetite Particles

2003 ◽  
Vol 789 ◽  
Author(s):  
A. Goodarzi ◽  
Y. Sahoo ◽  
M. T. Swihart ◽  
P. N. Prasad
Keyword(s):  
Citric Acid ◽  
Photoelectron Spectroscopy ◽  
Quantum Interference ◽  
Fluorescent Dyes ◽  
Aqueous Suspension ◽  
Medical Diagnostics ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Magnetite Particles

ABSTRACTMagnetic nanoparticles have found application in medical diagnostics such as magnetic resonance imaging and therapies such as cancer treatment. In these applications, it is imperative to have a biocompatible solvent such as water at optimum pH for possible bio-ingestion. In the present work, a synthetic methodology has been developed to get a well-dispersed and homogeneous aqueous suspension of Fe3O4 nanoparticles in the size range of 8–10 nm. The surface functionalization of the particles is provided by citric acid. The particles have been characterized using transmission electron microscopy, magnetization measurements with a superconducting quantum interference device, FTIR spectroscopy (for surfactant binding sites), thermogravimetric studies (for strength of surfactant binding), and x-ray photoelectron spectroscopy and x-ray diffraction (for composition and phase information). The carboxylate functionality on the surface provides an avenue for further surface modification with fluorescent dyes, hormone linkers etc for possible cell-binding, bioimaging, tracking, and targeting.

scholarly journals One-Step Synthesis of b-N-TiO2/C Nanocomposites with High Visible Light Photocatalytic Activity to Degrade Microcystis aeruginosa

Catalysts ◽  
2020 ◽  
Vol 10 (5) ◽  
pp. 579
Author(s):  
Xu Zhang ◽  
Min Cai ◽  
Naxin Cui ◽  
Guifa Chen ◽  
Guoyan Zou ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Chlorophyll A ◽  
Photoelectron Spectroscopy ◽  
Sol Gel ◽  
X Ray Diffraction ◽  
Paramagnetic Resonance ◽  
X Ray ◽  
Transmission Electron ◽  
One Step

Black TiO2 with doped nitrogen and modified carbon (b-N-TiO2/C) were successfully prepared by sol-gel method in the presence of urea as a source of nitrogen and carbon. The photocatalysts were characterized by field emission scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Raman, electron paramagnetic resonance (EPR), and UV-vis diffuse reflectance spectra (DRS). The doped nitrogen, introduced defects, and modified carbon played a synergistic role in enhancing photocatalytic activity of b-N-TiO2/C for the degradation of chlorophyll-a in algae cells. The sample, with a proper amount of phase composition and oxygen vacancies, showed the highest efficiency to degrade chlorophyll-a, and the addition of H2O2 promoted this photocatalysis degradation. Based on the trapping experiments and electron spin resonance (ESR) signals, a photocatalytic mechanism of b-N-TiO2/C was proposed. In the photocatalytic degradation of chlorophyll-a, the major reactive species were identified as OH and O2−. This research may provide new insights into the photocatalytic inactivation of algae cells by composite photocatalysts.

Graphene/SnO2/Citric Acid Nanocomposites as the Excellent Sorbent for Removal of Crystal Violet and Methylene Blue

2014 ◽  
Vol 1073-1076 ◽  
pp. 990-994
Author(s):  
Jin Ping Song ◽  
Qi Ma ◽  
Shao Min Shuang ◽  
Yong Guo ◽  
Chuan Dong
Keyword(s):  
Citric Acid ◽  
Photoelectron Spectroscopy ◽  
X Ray Diffraction ◽  
Step Method ◽  
Adsorption Ability ◽  
X Ray ◽  
Adsorption Performance ◽  
Transmission Electron ◽  
One Step ◽  
Performance Research

A simple, fast one-step method was used to prepare graphene/SnO2/citric acid (GN/SnO2/CA) nanocomposites. Fourier transform Infrared spectroscopy, UV-vis adsorption spectroscopy, transmission electron microscopy, X-Ray diffraction, Raman spectroscopy and X-ray photoelectron spectroscopy were employed to characterize as-prepared GN/SnO2/CA nanocomposites. Furthermore, in the adsorption performance research, GN/SnO2/CA nanocomposites indeed displayed excellent adsorption ability towards cationic dyes.

Incorporation of Gold Nanoparticles Within Thermoresponsive Microgel Particles: Effect of Crosslinking Density

2008 ◽  
Vol 8 (12) ◽  
pp. 6283-6289
Author(s):  
Yang Dong ◽  
Ying Ma ◽  
Tianyou Zhai ◽  
Yi Zeng ◽  
Hongbing Fu ◽  
...  
Keyword(s):  
Gold Nanoparticles ◽  
Photoelectron Spectroscopy ◽  
Trisodium Citrate ◽  
Crosslinking Density ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Microgel Particles ◽  
One Step ◽  
Ft Ir

Hybrid microgel particles were prepared by one step incubation of poly(N-isopropylacrylamide)-co-poly(acrylic acid) (PNIPAM-co-PAA) and gold nanoparticles (AuNPs). PNIPAM-co-PAA microgel particles were synthesized by surfactant-free emulsion polymerization with different crosslinking densities (4.5 wt.-%, 10 wt.-%, 15 wt.-%, MBA to NIPAM) and AuNPs obtained by trisodium citrate reduction method independently. The effect of crosslinking density of synthesized microgel particles on the loadings of AuNPs was investigated. The results showed that 18±2 nm AuNPs could be well entrapped in the loosely crosslinked (4.5 wt.-%, MBA to NIPAM) PNIPAM-co-PAA microgel particles with high loadings. The final hybrid microgel particles were well characterized by transmission electron microscopy (TEM), UV-vis spectra, X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD) and FT-IR. In particular, the PNIPAM-co-PAA/AuNPs hybrid microgel particles were thermoresponsive and completely reversible with several heating/cooling cycles. Therefore, the PNIPAM-co-PAA/AuNPs hybrid microgel particles allow for combined surface plasmon and thermal switching applications.

Effects of Calcination Temperature on Photoreduction Activity of Cu/TiO2 Nanoparticles

2011 ◽  
Vol 55-57 ◽  
pp. 1648-1652
Author(s):  
Jing Wei ◽  
Xin Tan ◽  
Tao Yu ◽  
Lin Zhao
Keyword(s):  
Calcination Temperature ◽  
Photoelectron Spectroscopy ◽  
Sol Gel ◽  
Chemical Properties ◽  
Titania Nanoparticles ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
One Step ◽  
Doped Titania

A one step sol-gel method was used for preparation of Cu doped titania nanoparticles (NPs). The crystal structures, morphologies and chemical properties were characterized using X-ray diffraction (XRD), transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS). We discussed the calcination temperature effection on the photoreduction activity of Cu/TiO2. When the calcination temperature was 500°C, the synthesized Cu/TiO2 performed the highest photocatalytic activity.

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.

scholarly journals α-Cellulose Fibers of Paper-Waste Origin Surface-Modified with Fe3O4 and Thiolated-Chitosan for Efficacious Immobilization of Laccase

Polymers ◽  
2021 ◽  
Vol 13 (4) ◽  
pp. 581
Author(s):  
Gajanan S. Ghodake ◽  
Surendra K. Shinde ◽  
Ganesh D. Saratale ◽  
Rijuta G. Saratale ◽  
Min Kim ◽  
...  
Keyword(s):  
Enzyme Immobilization ◽  
Photoelectron Spectroscopy ◽  
Cellulose Fibers ◽  
Relative Activity ◽  
Significant Activity ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Laccase Immobilization ◽  
Surface Modified

The utilization of waste-paper-biomass for extraction of important α-cellulose biopolymer, and modification of extracted α-cellulose for application in enzyme immobilization can be extremely vital for green circular bio-economy. Thus, in this study, α-cellulose fibers were super-magnetized (Fe3O4), grafted with chitosan (CTNs), and thiol (-SH) modified for laccase immobilization. The developed material was characterized by high-resolution transmission electron microscopy (HR-TEM), HR-TEM energy dispersive X-ray spectroscopy (HR-TEM-EDS), X-ray diffraction (XRD), vibrating sample magnetometer (VSM), X-ray photoelectron spectroscopy (XPS), and Fourier transform infrared spectroscopy (FT-IR) analyses. Laccase immobilized on α-Cellulose-Fe3O4-CTNs (α-Cellulose-Fe3O4-CTNs-Laccase) gave significant activity recovery (99.16%) and laccase loading potential (169.36 mg/g). The α-Cellulose-Fe3O4-CTNs-Laccase displayed excellent stabilities for temperature, pH, and storage time. The α-Cellulose-Fe3O4-CTNs-Laccase applied in repeated cycles shown remarkable consistency of activity retention for 10 cycles. After the 10th cycle, α-Cellulose-Fe3O4-CTNs possessed 80.65% relative activity. Furthermore, α-Cellulose-Fe3O4-CTNs-Laccase shown excellent degradation of pharmaceutical contaminant sulfamethoxazole (SMX). The SMX degradation by α-Cellulose-Fe3O4-CTNs-Laccase was found optimum at incubation time (20 h), pH (3), temperatures (30 °C), and shaking conditions (200 rpm). Finally, α-Cellulose-Fe3O4-CTNs-Laccase gave repeated degradation of SMX. Thus, this study presents a novel, waste-derived, highly capable, and super-magnetic nanocomposite for enzyme immobilization applications.

scholarly journals Surface Stoichiometry and Depth Profile of Tix-CuyNz Thin Films Deposited by Magnetron Sputtering

Materials ◽  
2021 ◽  
Vol 14 (12) ◽  
pp. 3191
Author(s):  
Arun Kumar Mukhopadhyay ◽  
Avishek Roy ◽  
Gourab Bhattacharjee ◽  
Sadhan Chandra Das ◽  
Abhijit Majumdar ◽  
...  
Keyword(s):  
Magnetron Sputtering ◽  
Photoelectron Spectroscopy ◽  
Film Surface ◽  
Grazing Incidence ◽  
X Ray Diffraction ◽  
X Ray ◽  
Relative Composition ◽  
Transmission Electron ◽  
Deposited Film ◽  
Deposited Films

We report the surface stoichiometry of Tix-CuyNz thin film as a function of film depth. Films are deposited by high power impulse (HiPIMS) and DC magnetron sputtering (DCMS). The composition of Ti, Cu, and N in the deposited film is investigated by X-ray photoelectron spectroscopy (XPS). At a larger depth, the relative composition of Cu and Ti in the film is increased compared to the surface. The amount of adventitious carbon which is present on the film surface strongly decreases with film depth. Deposited films also contain a significant amount of oxygen whose origin is not fully clear. Grazing incidence X-ray diffraction (GIXD) shows a Cu3N phase on the surface, while transmission electron microscopy (TEM) indicates a polycrystalline structure and the presence of a Ti3CuN phase.

scholarly journals Synthesis of Ce1−xPdxO2−δ Solid Solution in Molten Nitrate

Catalysts ◽  
2020 ◽  
Vol 10 (6) ◽  
pp. 640
Author(s):  
Hideaki Sasaki ◽  
Keisuke Sakamoto ◽  
Masami Mori ◽  
Tatsuaki Sakamoto
Keyword(s):  
Electron Microscopy ◽  
Solid Solution ◽  
Solid Solutions ◽  
Photoelectron Spectroscopy ◽  
Synthesis Method ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Co Precipitation ◽  
Ionic States

CeO2-based solid solutions in which Pd partially substitutes for Ce attract considerable attention, owing to their high catalytic performances. In this study, the solid solution (Ce1−xPdxO2−δ) with a high Pd content (x ~ 0.2) was synthesized through co-precipitation under oxidative conditions using molten nitrate, and its structure and thermal decomposition were examined. The characteristics of the solid solution, such as the change in a lattice constant, inhibition of sintering, and ionic states, were examined using X-ray diffraction (XRD), scanning electron microscopy–energy-dispersive X-ray spectroscopy (SEM−EDS), transmission electron microscopy (TEM)−EDS, and X-ray photoelectron spectroscopy (XPS). The synthesis method proposed in this study appears suitable for the easy preparation of CeO2 solid solutions with a high Pd content.

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