scholarly journals Facile Synthesis of High Performance Iron Oxide/Carbon Nanocatalysts Derived from the Calcination of Ferrocenium for the Decomposition of Methylene Blue

Catalysts ◽  
2019 ◽  
Vol 9 (11) ◽  
pp. 948 ◽  
Author(s):  
Thinnaphat Poonsawat ◽  
Thanyaphat Techalertmanee ◽  
Peerapong Chumkaeo ◽  
Isti Yunita ◽  
Titiya Meechai ◽  
...  
Keyword(s):  
Methylene Blue ◽  
Catalytic Activity ◽  
Iron Oxide ◽  
Photoelectron Spectroscopy ◽  
High Performance ◽  
Significant Loss ◽  
Paramagnetic Resonance ◽  
X Ray ◽  
Highly Active ◽  
Transmission Electron

Iron oxide/carbon nanocatalysts were successfully synthesized by the calcination of ferrocenium at high temperatures ranging from 500 to 900 °C. Then the synthesized nanocomposites were characterized by XRD (X-Ray Diffraction), TEM (Transmission Electron Microscopy), VSM (Vibrating-Sample Magnetometry), BET (Brunauer-Emmett-Teller surface area measurements), TGA (Thermogravimetric Analysis), XPS (X-Ray Photoelectron Spectroscopy), EPR (Electron Paramagnetic Resonance), and CHN elemental analysis. The prepared nanocatalysts were applied for the decomposition of methylene blue as a model in wastewater treatment. It was unexpected to discover that the prepared nanocatalysts were highly active for the reaction with methylene blue in the dark even though no excess of hydrogen peroxide was added. The nanocatalyst calcined at 800 °C exhibited the rod shape with the best catalytic activity. The nanocatalysts could be reused for 12 times without the significant loss of the catalytic activity.

scholarly journals A Highly Efficient Heterogeneous Catalyst of Bimetal-Organic Frameworks for the Epoxidation of Olefin with H2O2

Molecules ◽  
2020 ◽  
Vol 25 (10) ◽  
pp. 2389
Author(s):  
Fei Wang ◽  
Xiang-Guang Meng ◽  
Yan-Yan Wu ◽  
Hong Huang ◽  
Jing Lv ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Catalytic Activity ◽  
Photoelectron Spectroscopy ◽  
Styrene Oxide ◽  
Significant Loss ◽  
X Ray Diffraction ◽  
X Ray ◽  
Cyclic Olefins ◽  
Transmission Electron ◽  
Copper Component

A series of bimetel organic framework MnxCu1−x-MOF were prepared. The MOFs was characterized and analyzed by powder X-ray diffraction (PXRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). The catalytic activity of the developed catalyst was tested on various olefins by H2O2 as oxidant. The MOFs catalyst exhibits excellent catalytic activity for the epoxidations of various aromatic and cyclic olefins. Particularly, Mn0.1Cu0.9-MOF can achieve 90.2% conversion of styrene with 94.3% selectivity of styrene oxide at 0 °C after reaction 6 h. The MOF exhibited the catalytic activity of inverse temperature effect on epoxidation of styrene. The introduction of copper component can stabilize H2O2 and inhibit its decomposition to a certain extent. The catalyst can be reused at least five cycles without significant loss in activity towards epoxidation.

scholarly journals Novel Carbon Dots Derived from Glycyrrhizae Radix et Rhizoma and Their Anti-Gastric Ulcer Effect

Molecules ◽  
2021 ◽  
Vol 26 (6) ◽  
pp. 1512
Author(s):  
Yuhan Liu ◽  
Meiling Zhang ◽  
Jinjun Cheng ◽  
Yue Zhang ◽  
Hui Kong ◽  
...  
Keyword(s):  
Gastric Ulcer ◽  
Photoelectron Spectroscopy ◽  
Carbon Dots ◽  
High Performance ◽  
Raw264.7 Cells ◽  
Mice Model ◽  
X Ray ◽  
Glycyrrhizae Radix ◽  
Transmission Electron ◽  
High Resolution Tem

Glycyrrhizae Radix et Rhizoma (GRR) is one of the commonly used traditional Chinese medicines in clinical practice, which has been applied to treat digestive system diseases for hundreds of years. GRR is preferred for anti-gastric ulcer, however, the main active compounds are still unknown. In this study, GRR was used as precursor to synthesize carbon dots (CDs) by a environment-friendly one-step pyrolysis process. GRR-CDs were characterized by using transmission electron microscopy, high-resolution TEM, fourier transform infrared, ultraviolet-visible and fluorescence spectroscopy, X-ray photoelectron spectroscopy, X-ray diffraction and high-performance liquid chromatography. In addition, cellular toxicity of GRR-CDs was studied by using CCK-8 in RAW264.7 cells, and the anti-gastric ulcer activity was evaluated and confirmed using mice model of acute alcoholic gastric ulcer. The experiment confirmed that GRR-CDs were the spherical structure with a large number of active groups on the surface and their particle size ranged from 2 to 10 nm. GRR-CDs had no toxicity to RAW264.7 cells at concentration of 19.5 to 5000 μg/mL and could reduce the oxidative damage of gastric mucosa and tissues caused by alcohol, as demonstrated by restoring expression of malondialdehyde, superoxide dismutase and nitric oxide in serum and tissue of mice. The results indicated the explicit anti-ulcer activity of GRR-CDs, which provided a new insights for the research on effective material basis of GRR.

Highly active carbon nanotube–promoted Rh-Mn-Li/SiO2 catalysts for the synthesis of C2+ oxygenates from syngas

2021 ◽  
pp. 174751982098472
Author(s):  
Jun Yu ◽  
Ying Han ◽  
Guoqing Chen ◽  
Xiuzhen Xiao ◽  
Haifang Mao ◽  
...  
Keyword(s):  
Carbon Nanotubes ◽  
Photoelectron Spectroscopy ◽  
Co Hydrogenation ◽  
X Ray ◽  
Highly Active ◽  
Transmission Electron ◽  
Co Insertion ◽  
Temperature Programmed Surface Reaction ◽  
Temperature Programmed ◽  
Oxygenate Synthesis

The effect of carbon nanotubes on the catalytic properties of Rh-Mn-Li/SiO2 catalysts was investigated for CO hydrogenation. The catalysts were comprehensively characterized by means of X-ray power diffraction, N2 sorption, transmission electron microscope, H2–temperature-programmed reduction, CO–temperature-programmed desorption, temperature-programmed surface reaction, and X-ray photoelectron spectroscopy. The results showed that an appropriate amount of carbon nanotubes can be attached to the surface of the SiO2 sphere and can improve the Rh dispersion. Moderate Rh-Mn interaction can be obtained by doping with the appropriate amount of carbon nanotubes, which promotes the formation of strongly adsorbed CO and facilitates the progress of CO insertion, resulting in the increase in the selectivity of C2+ oxygenate synthesis.

scholarly journals Facile Preparation of Rod-like MnO Nanomixtures via Hydrothermal Approach and Highly Efficient Removal of Methylene Blue for Wastewater Treatment

Nanomaterials ◽  
2018 ◽  
Vol 9 (1) ◽  
pp. 10 ◽  
Author(s):  
Yuelong Xu ◽  
Bin Ren ◽  
Ran Wang ◽  
Lihui Zhang ◽  
Tifeng Jiao ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Methylene Blue ◽  
Photoelectron Spectroscopy ◽  
Degradation Mechanism ◽  
Dye Adsorption ◽  
Maximum Adsorption Capacity ◽  
X Ray ◽  
Transmission Electron ◽  
Degradation Ratio ◽  
Hydrothermal Approach

In the present study, nanoscale rod-shaped manganese oxide (MnO) mixtures were successfully prepared from graphitic carbon nitride (C3N4) and potassium permanganate (KMnO4) through a hydrothermal method. The as-prepared MnO nanomixtures exhibited high activity in the adsorption and degradation of methylene blue (MB). The as-synthesized products were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), surface area analysis, X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS). Furthermore, the effects of the dose of MnO nanomixtures, pH of the solution, initial concentration of MB, and the temperature of MB removal in dye adsorption and degradation experiments was investigated. The degradation mechanism of MB upon treatment with MnO nanomixtures and H2O2 was studied and discussed. The results showed that a maximum adsorption capacity of 154 mg g−1 was obtained for a 60 mg L−1 MB solution at pH 9.0 and 25 °C, and the highest MB degradation ratio reached 99.8% under the following optimum conditions: 50 mL of MB solution (20 mg L−1) at room temperature and pH ≈ 8.0 with 7 mg of C, N-doped MnO and 0.5 mL of H2O2.

scholarly journals Ni2P/rGO/NF Nanosheets As a Bifunctional High-Performance Electrocatalyst for Water Splitting

Materials ◽  
2020 ◽  
Vol 13 (3) ◽  
pp. 744 ◽  
Author(s):  
Jinyu Huang ◽  
Feifei Li ◽  
Baozhong Liu ◽  
Peng Zhang
Keyword(s):  
Electron Microscopy ◽  
Water Splitting ◽  
Photoelectron Spectroscopy ◽  
High Performance ◽  
High Efficiency ◽  
Splitting Method ◽  
Bifunctional Catalyst ◽  
Strong Activity ◽  
X Ray ◽  
Transmission Electron

The hydrogen generated via the water splitting method is restricted by the high level of theoretical potential exhibited by the anode. The work focuses on synthesizing a bifunctional catalyst with a high efficiency, that is, a nickel phosphide doped with the reduced graphene oxide nanosheets supported on the Ni foam (Ni2P/rGO/NF), via the hydrothermal approach together with the calcination approach specific to the hydrogen evolution reaction (HER) and the oxygen evolution reaction (OER). The Raman, X-Ray Diffraction (XRD), X-ray Photoelectron Spectroscopy (XPS), Transmission Electron Microscope (TEM), Scanning Electron Microscopy (SEM), High-Resolution Transmission Electron Microscopy (HRTEM), as well as elemental mapping, are adopted to study the composition and morphology possessed by Ni2P/rGO/NF. The electrochemical testing is performed by constructing a parallel two-electrode electrolyzer (Ni2P/rGO/NF||Ni2P/rGO/NF). Ni2P/rGO/NF||Ni2P/rGO/NF needs a voltage of only 1.676 V for driving 10 mA/cm2, which is extremely close to Pt/C/NF||IrO2/NF (1.502 V). It is possible to maintain the current density for no less than 30 hours. It can be demonstrated that Ni2P/rGO/NF||Ni2P/rGO/NF has commercial feasibility, relying on the strong activity and high stability.

scholarly journals Nitrogen-Doped Sponge Ni Fibers as Highly Efficient Electrocatalysts for Oxygen Evolution Reaction

2019 ◽  
Vol 11 (1) ◽  
Author(s):  
Kaili Zhang ◽  
Xinhui Xia ◽  
Shengjue Deng ◽  
Yu Zhong ◽  
Dong Xie ◽  
...  
Keyword(s):  
Oxygen Evolution ◽  
Photoelectron Spectroscopy ◽  
Oxygen Evolution Reaction ◽  
Active Sites ◽  
High Performance ◽  
Active Phase ◽  
X Ray ◽  
Highly Active ◽  
N Doping ◽  
Energy Conversion Devices

Abstract Controllable synthesis of highly active micro/nanostructured metal electrocatalysts for oxygen evolution reaction (OER) is a particularly significant and challenging target. Herein, we report a 3D porous sponge-like Ni material, prepared by a facile hydrothermal method and consisting of cross-linked micro/nanofibers, as an integrated binder-free OER electrocatalyst. To further enhance the electrocatalytic performance, an N-doping strategy is applied to obtain N-doped sponge Ni (N-SN) for the first time, via NH3 annealing. Due to the combination of the unique conductive sponge structure and N doping, the as-obtained N-SN material shows improved conductivity and a higher number of active sites, resulting in enhanced OER performance and excellent stability. Remarkably, N-SN exhibits a low overpotential of 365 mV at 100 mA cm−2 and an extremely small Tafel slope of 33 mV dec−1, as well as superior long-term stability, outperforming unmodified sponge Ni. Importantly, the combination of X-ray photoelectron spectroscopy and near-edge X-ray adsorption fine structure analyses shows that γ-NiOOH is the surface-active phase for OER. Therefore, the combination of conductive sponge structure and N-doping modification opens a new avenue for fabricating new types of high-performance electrodes with application in electrochemical energy conversion devices.

scholarly journals Amino-Modified Silica as Effective Support of the Palladium Catalyst for 4-Nitroaniline Hydrogenation

Catalysts ◽  
2020 ◽  
Vol 10 (4) ◽  
pp. 375
Author(s):  
Adele R. Latypova ◽  
Maxim D. Lebedev ◽  
Evgeniy V. Rumyantsev ◽  
Dmitry V. Filippov ◽  
Olga V. Lefedova ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Catalytic Activity ◽  
Electron Donor ◽  
Photoelectron Spectroscopy ◽  
Functionalized Silica ◽  
Amino Groups ◽  
Modified Silica ◽  
Pulse Technique ◽  
X Ray ◽  
Transmission Electron

The article describes the synthesis of aminoorgano-functionalized silica as a prospective material for catalysis application. The amino groups have electron donor properties which are valuable for the metal chemical state of palladium. Therefore, the presence of electron donor groups is important for increasing catalysts’ stability. The research is devoted to the investigation of silica amino-modified support influence on the activity and stability of palladium species in 4-nitroaniline hydrogenation process. A series of catalysts with different supports such as SiO2, SiO2-C3H6-NH2 (amino-functionalized silica), γ-Al2O3 and activated carbon were studied. The catalytic activity was studied in the hydrogenation of 4-nitroaniline to 1,4-phenylenediamine. The catalysts were characterized by scanning electron microscopy, transmission electron microscopy, X-ray photoelectron spectroscopy, Fourier transform infrared spectroscopy and chemisorption of hydrogen by the pulse technique. The 5 wt.% Pd/SiO2-C3H6-NH2 catalyst exhibited the highest catalytic activity for 4-nitroaniline hydrogenation with 100% conversion and 99% selectivity with respect to 1,4-phenylenediamine.

scholarly journals Optimization of sol-immobilized bimetallic Au–Pd/TiO 2 catalysts: reduction of 4-nitrophenol to 4-aminophenol for wastewater remediation

2020 ◽  
Vol 378 (2176) ◽  
pp. 20200057
Author(s):  
Khaled Alshammari ◽  
Yubiao Niu ◽  
Richard E. Palmer ◽  
Nikolaos Dimitratos
Keyword(s):  
Photoelectron Spectroscopy ◽  
Catalytic Reduction ◽  
Catalytic Performance ◽  
Reducing Agent ◽  
Wastewater Remediation ◽  
X Ray ◽  
Molar Ratios ◽  
Highly Active ◽  
Transmission Electron ◽  
Complementary Techniques

A sol-immobilization method is used to synthesize a series of highly active and stable Au x Pd 1− x /TiO 2 catalysts (where x  = 0, 0.13, 0.25, 0.5, 0.75, 0.87 and 1) for wastewater remediation. The catalytic performance of the materials was evaluated for the catalytic reduction of 4-nitrophenol, a model wastewater contaminant, using NaBH 4 as the reducing agent under mild reaction conditions. Reaction parameters such as substrate/metal and substrate/reducing agent molar ratios, reaction temperature and stirring rate were investigated. Structure-activity correlations were studied using a number of complementary techniques including X-ray powder diffraction, X-ray photoelectron spectroscopy and transmission electron microscopy. The sol-immobilization route provides very small Au–Pd alloyed nanoparticles, with the highest catalytic performance shown by the Au 0.5 Pd 0.5 /TiO 2 catalyst. This article is part of a discussion meeting issue ‘Science to enable the circular economy’.

scholarly journals Новые гетерогенные наноструктурные катализаторы на основе наночастиц переходных металлов и гексагонального нитрида бора

2021 ◽  
Vol 47 (16) ◽  
pp. 10
Author(s):  
А.С. Конопацкий ◽  
К.Л. Фаерштейн ◽  
И.Н. Волков ◽  
Д.В. Лейбо ◽  
В.В. Калинина ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Photoelectron Spectroscopy ◽  
Thermal Activation ◽  
Fept Nanoparticles ◽  
The Novel ◽  
Surface Chemical ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Co Conversion

Structure and catalytic activity of the novel heterostructured FePt/h-BN nanomaterials in carbon monoxide oxidation reaction were studied. Transmission electron microscopy, X-ray photoelectron spectroscopy and X-ray diffraction methods were used for structure and surface chemical composition investigation. Developed materials were demonstrated to have enhanced catalytic activity with 100% CO conversion at 250 °C. Structure ordering in FePt nanoparticles was observed during thermal activation of the material.

scholarly journals Synergistically homogeneous-heterogeneous Fenton catalysis of trace copper ion and g-C3N4 for degradation of organic pollutants

2021 ◽  
Author(s):  
Z. Y. Yao ◽  
G. X. Zhu ◽  
T. L. Lu ◽  
Y. Z. Zhan
Keyword(s):  
Electron Microscopy ◽  
Catalytic Activity ◽  
Metal Ions ◽  
Photoelectron Spectroscopy ◽  
Organic Pollutant ◽  
Copper Ion ◽  
Heterogeneous Fenton ◽  
Paramagnetic Resonance ◽  
X Ray ◽  
Synergistic Catalysis

Abstract Using the bulk g-C3N4 as a precursor, four g-C3N4 nanosheets were further prepared by ultrasonic, thermal, acid, and alkali exfoliation. The structures of these materials were characterized by various techniques such as X-ray powder diffraction, Fourier transform infrared spectroscopy, scanning electron microscopy, energy dispersive X-Ray spectroscopy, transmission electron microscopy, and X-ray photoelectron spectroscopy. The synergistical Fenton catalysis of these materials with Cu2+ was evaluated by using rhodamine B as a simulated organic pollutant. The results showed that there existed a significant synergistical Fenton catalysis between Cu2+ and g-C3N4. This synergistic effect can be observed even when the concentration of Cu2+ was as low as 0.064 mg L−1. The properties of g-C3N4 strongly influenced the catalytic activity of the Cu2+/g-C3N4 system. The coexistent of Cu2+ and the alkali exfoliated g-C3N4 showed the most excellent catalytic activity. Hydroxyl radicals as oxidizing species were confirmed in the Cu2+/g-C3N4 system by electron paramagnetic resonance spectrum. The synergistic catalysis may be attributed to the easier reduction of Cu2+ adsorbed on the g-C3N4. This study provided an excellent Fenton catalytic system, and partly solved the rapid deactivation of heterogeneous Fenton catalysts caused by the leaching of metal ions. HIGHTLIGHTS There exists a significant synergistical Fenton catalysis between trace Cu2+ and g-C3N4. The Cu2+ concentration is lower than the maximum acceptable limit in drinking water. This study partly solved the rapid deactivation caused by the leaching of metal ions. This study reminds researchers to pay attention to the possible synergistic catalysis between leached ions and supports.

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