scholarly journals Synthesis and Catalytic Performance of Ni/SiO2for Hydrogenation of 2-Methylfuran to 2-Methyltetrahydrofuran

2015 ◽  
Vol 2015 ◽  
pp. 1-6 ◽  
Author(s):  
Fu Ding ◽  
Yajing Zhang ◽  
Guijin Yuan ◽  
Kangjun Wang ◽  
Ileana Dragutan ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Sol Gel ◽  
Catalytic Performance ◽  
Bet Surface Area ◽  
X Ray Diffraction ◽  
X Ray ◽  
Ni Content ◽  
Transmission Electron ◽  
Temperature Programmed ◽  
Ni Species

A series of Ni/SiO2catalysts with different Ni content were prepared by sol-gel method for application in the synthesis of 2-methyltetrahydrofuran (2-MTHF) by hydrogenation of 2-methylfuran (2-MF). The catalyst structure was investigated by X-ray diffraction (XRD), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), and temperature programmed reduction (TPR). It is found that structures and catalytic performance of the catalysts were highly affected by the Ni content. The catalyst with a 25% Ni content had an appropriate size of the Ni species and larger BET surface area and produced a higher 2-MF conversion with enhanced selectivity in 2-MTHF.

FeYO3@rGO nanocomposites: Synthesis, characterization and application in photooxidative degradation of atrazine under visible light

2021 ◽  
Vol 11 (5) ◽  
pp. 706-716
Author(s):  
Nada D. Al-Khthami ◽  
Tariq Altalhi ◽  
Mohammed Alsawat ◽  
Mohamed S. Amin ◽  
Yousef G. Alghamdi ◽  
...  
Keyword(s):  
Visible Light ◽  
Photoelectron Spectroscopy ◽  
Sol Gel ◽  
Bandgap Energy ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Reduced Graphene ◽  
Structural Surface ◽  
Adsorption Desorption

Different organic pollutants have been remediated photo catalytically by applying perovskite photocatalysts. Atrazine (ATR) is a pesticide commonly detected as a pollutant in drinking, surface and ground water. Herein, FeYO3@rGO heterojunction was synthesized and applied for photooxidation decomposition of ATR. First, FeYO 3nanoparticles (NPs) were prepared via routine sol-gel. After that, FeYO3 NPs were successfully incorporated with different percentages (5, 10, 15 and 20 wt.%) of reduced graphene oxide (rGO) in the synthesis of novel FeYO3@rGO photocatalyst. Morphological, structural, surface, optoelectrical and optical characteristics of constructed materials were identified via X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Transmission electron microscopy (TEM), adsorption/desorption isotherms, diffusive reflectance (DR) spectra, and photoluminescence response (PL). Furthermore, photocatalytic achievement of the constructed materials was evaluated via photooxidative degradation of ATR. Various investigations affirmed the usefulness of rGO incorporation on the advancement of formed photocatalysts. Actually, novel nanocomposite containing rGO (15 wt.%) possessed diminished bandgap energy, as well as magnified visible light absorption. Furthermore, such nanocomposite presented exceptional photocatalytic achievement when exposed to visible light as ATR was perfectly photooxidized over finite amount (1.6 g · L-1) from the optimized photocatalyst when illuminated for 30 min. The advanced photocatalytic performance of constructed heterojunctions could be accredited mainly to depressed recombination amid induced charges. The constructed FeYO3@rGO nanocomposite is labelled as efficient photocatalyst for remediation of herbicides from aquatic environments.

scholarly journals Microwave-assisted preparation of ZnS and ZnSe nanocrystals with different morphologies for photodegradation process of organic dyes

2019 ◽  
Author(s):  
Katarzyna Matras-Postolek ◽  
A. Zaba ◽  
S. Sovinska ◽  
D. Bogdal
Keyword(s):  
Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
Organic Dyes ◽  
Zinc Sulphide ◽  
Conventional Heating ◽  
Bet Surface Area ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Vis Spectroscopy

Zinc sulphide (ZnS) and zinc selenide (ZnSe) and manganese-doped and un-doped with different morphologies from 1D do 3D microflowers were successfully fabricated in only a few minutes by solvothermal reactions under microwave irradiation. In order to compare the effect of microwave heating on the properties of obtained  nanocrystals, additionally the synthesis under conventional heating was conducted additionally in similar conditions. The obtained nanocrystals were systematically characterized in terms of structural and optical properties using X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), diffuse reflectance UV-Vis spectroscopy (DR UV-Vis), Fourier-transform infrared spectroscopy (FT-IR), photoluminescence spectroscopy (PL), X-ray photoelectron spectroscopy (XPS) and Brunauer-Emmett-Teller (BET) surface area analysis. The photocatalytic activity of ZnSe, ZnS, ZnS:Mn and ZnSe:Mn nanocrystals with different morphologies was evaluated by the degradation of methyl orange (MO) and Rhodamine 6G (R6G), respectively. The results show that Mn doped NCs samples had higher coefficient of degradation of organic dyes under ultraviolet irradiation (UV).

scholarly journals Bulk Versus Surface Modification of Alumina with Mn and Ce Based Oxides for CH4 Catalytic Combustion

Materials ◽  
2019 ◽  
Vol 12 (11) ◽  
pp. 1771 ◽  
Author(s):  
Stefan Neatu ◽  
Mihaela M. Trandafir ◽  
Adelina Stănoiu ◽  
Ovidiu G. Florea ◽  
Cristian E. Simion ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Catalytic Combustion ◽  
Mixed Oxides ◽  
Sol Gel ◽  
Nitrogen Adsorption ◽  
X Ray Diffraction ◽  
X Ray ◽  
Temperature Programmed ◽  
Catalytic Combustion Of Methane ◽  
Adsorption Desorption

This study presents the synthesis and characterization of lanthanum-modified alumina supported cerium–manganese mixed oxides, which were prepared by three different methods (coprecipitation, impregnation and citrate-based sol-gel method) followed by calcination at 500 °C. The physicochemical properties of the synthesized materials were investigated by various characterization techniques, namely: nitrogen adsorption-desorption isotherms, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM) and H2–temperature programmed reduction (TPR). This experimental study demonstrated that the role of the catalytic surface is much more important than the bulk one. Indeed, the incipient impregnation of CeO2–MnOx catalyst, supported on an optimized amount of 4 wt.% La2O3–Al2O3, provided the best results of the catalytic combustion of methane on our catalytic micro-convertors. This is mainly due to: (i) the highest pore size dimensions according to the Brunauer-Emmett-Teller (BET) investigations, (ii) the highest amount of Mn4+ or/and Ce4+ on the surface as revealed by XPS, (iii) the presence of a mixed phase (Ce2MnO6) as shown by X-ray diffraction; and (iv) a higher reducibility of Mn4+ or/and Ce4+ species as displayed by H2–TPR and therefore more reactive oxygen species.

scholarly journals Preparation and Characterization of Rh/MgSNTs Catalyst for Hydroformylation of Vinyl Acetate: The Rh0 was Obtained by Calcination

Catalysts ◽  
2019 ◽  
Vol 9 (3) ◽  
pp. 215 ◽  
Author(s):  
Penghe Su ◽  
Ya Chen ◽  
Xiaotong Liu ◽  
Hongyuan Chuai ◽  
Hongchi Liu ◽  
...  
Keyword(s):  
Vinyl Acetate ◽  
Atomic Emission ◽  
Catalytic Performance ◽  
Bet Surface Area ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Atomic Emission Spectrometer ◽  
Calcination Method

A simple and practical Rh-catalyzed hydroformylation of vinyl acetate has been synthesized via impregnation-calcination method using silicate nanotubes (MgSNTs) as the supporter. The Rh0 (zero valent state of rhodium) was obtained by calcination. The influence of calcination temperature on catalytic performance of the catalysts was investigated in detail. The catalysts were characterized in detail by X-ray diffraction (XRD), transmission electron microscopy (TEM), X-ray photoelectron spectrometer (XPS), atomic emission spectrometer (ICP), and Brunauer–Emmett–Teller (BET) surface-area analyzers. The Rh/MgSNTs(a2) catalyst shows excellent catalytic activity, selectivity and superior cyclicity. The catalyst could be easily recovered by phase separation and was used up to four times.

scholarly journals Nanosized V-Ce Oxides Supported on TiO2 as a Superior Catalyst for the Selective Catalytic Reduction of NO

Catalysts ◽  
2020 ◽  
Vol 10 (2) ◽  
pp. 202
Author(s):  
Long Lu ◽  
Xueman Wang ◽  
Chunhua Hu ◽  
Ying Liu ◽  
Xiongbo Chen ◽  
...  
Keyword(s):  
Low Temperature ◽  
Selective Catalytic Reduction ◽  
Photoelectron Spectroscopy ◽  
Catalytic Reduction ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Redox Capacity ◽  
Scr Of No ◽  
Temperature Programmed

Nanosized V-Ce oxides supported on TiO2 (VCT) were prepared and utilized in the low-temperature selective catalytic reduction (SCR) of NO with NH3. Compared with the other V-Ce oxides-based catalysts supported on Al2O3, ZrO2, and ZSM-5, VCT showed the best SCR activity in a low-temperature range. The NOx conversion of 90% could be achieved at 220 °C. Characterizations including X-ray diffraction (XRD), scanning election micrograph (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), temperature-programmed desorption with NH3 (NH3-TPD), and temperature-programmed reduction with H2 (H2-TPR) showed that V1.05Ce1/TiO2 exhibited a good dispersion of V2O5, enrichment of surface Ce3+ and chemical-absorbed oxygen, and excellent redox capacity and acidity, which resulted in the best SCR performance at low temperature.

scholarly journals Ultrasound enhanced heterogeneous activation of peroxymonosulfate by a Co-NiOx catalyst

2017 ◽  
Vol 76 (6) ◽  
pp. 1436-1446 ◽  
Author(s):  
Chenmo Wei ◽  
Jing Zhang ◽  
Yongli Zhang ◽  
Gucheng Zhang ◽  
Peng Zhou ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Sol Gel ◽  
Maximum Efficiency ◽  
Acid Orange 7 ◽  
X Ray Diffraction ◽  
X Ray ◽  
Surface Hydroxyl ◽  
Transmission Electron ◽  
Initial Ph ◽  
Reactive Oxidant

Sulfate radical-based advanced oxidation processes have had considerable attention due to the highly oxidizing function of sulfate radicals (SO4−·) resulting in acceleration of organic pollutants degradation in aqueous environments. A Co-Ni mixed oxide nanocatalyst, which was prepared by the sol-gel method, was employed to activate peroxymonosulfate (PMS, HSO5−) to produce SO4−· with Acid Orange 7 (AO7) selected as a radical probe. The catalyst was characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FT-IR) and transmission electron microscopy (TEM). The characterization results indicated that the ingredient of the catalyst had been changed and the amount of surface hydroxyl increased significantly with the addition of Ni. Therefore, it proved that Co-NiOx catalyst was more effective than CoOx to activate PMS. Moreover, ultrasound (US) can increase the degradation rate of AO7 and US/Co-NiOx/PMS system. This study also focused on some synthesis parameters and the system reached the maximum efficiency under the condition when [PMS] = 0.4 mM, [catalyst] = 0.28 g/L, Pus = 200 W. The AO7 removal in these systems follows first order kinetics. Last but not least, quenching studies was conducted which indicated that the amount of hydroxyl radicals (·OH) increases with the increase of initial pH and SO4−· was the primary reactive oxidant for AO7 degradation.

scholarly journals Generalized Methodology for Inserting Metal Heteroatoms into the Layered Zeolite Precursor RUB-36 by Interlayer Expansion

Crystals ◽  
2020 ◽  
Vol 10 (6) ◽  
pp. 530 ◽  
Author(s):  
Chaoqun Bian ◽  
Xiao Wang ◽  
Lan Yu ◽  
Fen Zhang ◽  
Jie Zhang ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Inductively Coupled Plasma ◽  
Catalytic Performance ◽  
X Ray Diffraction ◽  
Zeolite Sample ◽  
X Ray ◽  
Inductively Coupled ◽  
Temperature Programmed ◽  
First Time ◽  
N2 Sorption

The incorporation of metal heteroatoms into zeolites is an effective modification strategy for enhancing their catalytic performance. Herein, for the first time we report a generalized methodology for inserting metal heteroatoms (such as Sn, Fe, Zn, and Co) into the layered zeolite precursor RUB-36 via interlayer expansion by using the corresponding metal acetylacetate salt. Through this generalized methodology, Sn-JHP-1, Fe-JHP-1, Zn-JHP-1 and Co-JHP-1 zeolites could be successfully prepared by the reaction of RUB-36 and corresponding metal acetylacetate salt at 180 °C for 24 h in the presence of HCl solution. As a typical example, Sn-JHP-1 and calcined Sn-JHP-1 (Sn-JHP-2) zeolite is well characterized by the X-ray diffraction (XRD), diffuse reflectance ultraviolet-visible (UV-Vis), inductively coupled plasma (ICP), N2 sorption, temperature-programmed-desorption of ammonia (NH3-TPD) and X-ray photoelectron spectroscopy (XPS) techniques, which confirm the expansion of adjacent interlayers and thus the incorporation of isolated Sn sites within the zeolite structure. Notably, the obtained Sn-JHP-2 zeolite sample shows enhanced catalytic performance in the conversion of glucose to levulinic acid (LA) reaction.

scholarly journals Preparation of g-C3N4/MoS2 Composite Material and Its Visible Light Catalytic Performance

2021 ◽  
Author(s):  
Yu Fan ◽  
Yan-ning Yang ◽  
Chen Ding
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Visible Light ◽  
Photoelectron Spectroscopy ◽  
Photogenerated Electron ◽  
Catalytic Performance ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Calcination Method

Abstract The g-C3N4 nanosheet was prepared by calcination method, the MoS2 nanosheet was prepared by hydrothermal method. The g-C3N4/MoS2 composites were prepared by ultrasonic composite in anhydrous ethanol. X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), ultraviolet-visible spectroscopy (UV-Vis), and photoluminescence (PL) techniques were used to characterize the materials. The photocatalytic degradation of Rhodamine B (Rh B) by g-C3N4/MoS2 composites with different mass ratios was investigated under visible light. The results show that a small amount of MoS2 combined with g-C3N4 can significantly improve photocatalytic activity. The g-C3N4/MoS2 composite with a mass ratio of 1:8 has the highest photocatalytic activity, and the degradation rate of Rh B increases from 50% to 99.6%. The main reason is that MoS2 and g-C3N4 have a matching band structure. The separation rate of photogenerated electron-hole pairs is enhanced. So the g-C3N4/MoS2 composite can improve the photocatalytic activity. The photocatalytic mechanism was proposed through the active matter capture experiment.

scholarly journals Improved Visible Light Photocatalytic Activity for TiO2Nanomaterials by Codoping with Zinc and Sulfur

2015 ◽  
Vol 2015 ◽  
pp. 1-8 ◽  
Author(s):  
Qianzhi Xu ◽  
Xiuying Wang ◽  
Xiaoli Dong ◽  
Chun Ma ◽  
Xiufang Zhang ◽  
...  
Keyword(s):  
Photocatalytic Activity ◽  
Visible Light ◽  
Photoelectron Spectroscopy ◽  
Diffuse Reflectance Spectroscopy ◽  
Sol Gel ◽  
X Ray Diffraction ◽  
Sunlight Irradiation ◽  
X Ray ◽  
Transmission Electron ◽  
Photoinduced Charge

S/Zn codoped TiO2nanomaterials were synthesized by a sol-gel method. X-ray diffraction, UV-vis diffuse reflectance spectroscopy, transmission electron microscopy, photoluminescence spectroscopy, and X-ray photoelectron spectroscopy were used to characterize the morphology, structure, and optical properties of the prepared samples. The introduction of Zn and S resulted in significant red shift of absorption edge for TiO2-based nanomaterials. The photocatalytic activity was evaluated by degrading reactive brilliant red X-3B solution under simulated sunlight irradiation. The results showed S/Zn codoped TiO2exhibited higher photocatalytic activity than pure TiO2and commercial P25, due to the photosynergistic effect of obvious visible light absorption, efficient separation of photoinduced charge carriers, and large surface area. Moreover, the content of Zn and S in the composites played important roles in photocatalytic activity of TiO2-based nanomaterials.

scholarly journals Evolution of Copper Supported on Fe3O4 Nanorods for WGS Reaction

Catalysts ◽  
2018 ◽  
Vol 8 (10) ◽  
pp. 415 ◽  
Author(s):  
Lingjuan Ma ◽  
Hongbin Ma ◽  
Dawei Han ◽  
Mingyue Qiu ◽  
Yafei Guan ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Ambient Pressure ◽  
Phase Evolution ◽  
Precipitation Method ◽  
X Ray Diffraction ◽  
X Ray ◽  
In Situ Xrd ◽  
Wgs Reaction ◽  
Transmission Electron ◽  
Temperature Programmed

Rod-shaped Cu1Fe9Ox precursor was successfully prepared through an aqueous precipitation method. The shape and phase composition were characterized by X-ray diffraction (XRD) and transmission electron microscopy (TEM). It was found that Cu1Fe9Ox is composed of CuFe2O4 and Fe2O3. The reduction performance of Cu1Fe9Ox was studied by in situ XRD and H2 temperature-programmed reduction (H2-TPR). Cu/Fe3O4 nanorod catalyst is obtained through the controllable reduction of Cu1Fe9Ox nanorod, and the formed Cu/Fe3O4 nanorod catalyst does not have low-temperature water gas shift (WGS) activity, but exhibits high-temperature WGS reaction activity. Ambient pressure X-ray photoelectron spectroscopy (AP-XPS) studies showed that the main species of copper is Cu+ during the WGS reaction. The interaction between Cu and Fe3O4 rod and phase evolution of Cu species are quite different from Cu/Fe3O4 nanoparticles.

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