FeNiCeOx ternary catalyst prepared by ultrasonic impregnation method for diclofenac removal in Fenton-like system

Abstract FeNiCeOx was firstly prepared by ultrasonic impregnation method and used to remove diclofenac in a Fenton-like system. The catalytic activity was improved successfully by doping Ni into FeCeOx. The diclofenac removal efficiency reached 97.9% after 30 min reaction. The surface morphology and properties of FeNiCeOx were characterized by Brunauer-Emmett-Teller (BET), scanning electron microscopy (SEM), X-ray diffraction (XRD), high-resolution transmission electron microscopy (HRTEM), Raman and X-ray photoelectron spectroscopy (XPS) analyses. FeNiCeOx in this paper had larger specific surface area than those prepared by other methods, which was attributed to the cavitation effect and hot-spot effect during the ultrasonic synthesis process. Low crystallinity of Fe2O3 and NiO showed by characterization could lead to high interaction of Fe and Ni ions with support of CeO2. They substituted Ce in CeO2, caused lattice contraction and formed more oxygen vacancies, which favoured the catalytic reaction. Meanwhile, Fe and Ce ions both had redox cycles of Fe3+/Fe2+ and Ce4+/Ce3+, which facilitated the electron transfer in the reaction. The synergistic effect among Fe, Ni and Ce might lead to better catalytic performance of FeNiCeOx than any binary metal oxides constituted from the above three elements. Finally, the potential mechanism of diclofenac removal in FeNiCeOx-H2O2 system is proposed.

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Influence of Sulfur-Containing Sodium Salt Poisoned V2O5–WO3/TiO2 Catalysts on SO2–SO3 Conversion and NO Removal

Catalysts ◽

10.3390/catal8110541 ◽

2018 ◽

Vol 8 (11) ◽

pp. 541 ◽

Cited By ~ 3

Author(s):

Haiping Xiao ◽

Chaozong Dou ◽

Hao Shi ◽

Jinlin Ge ◽

Li Cai

Keyword(s):

Photoelectron Spectroscopy ◽

No Reduction ◽

Catalytic Performance ◽

Acid Sites ◽

Impregnation Method ◽

So2 Oxidation ◽

Sodium Salts ◽

X Ray ◽

Temperature Programmed ◽

Physical Features

A series of poisoned catalysts with various forms and contents of sodium salts (Na2SO4 and Na2S2O7) were prepared using the wet impregnation method. The influence of sodium salts poisoned catalysts on SO2 oxidation and NO reduction was investigated. The chemical and physical features of the catalysts were characterized via NH3-temperature programmed desorption (NH3-TPD), H2-temperature programmed reduction (H2-TPR), X-ray photoelectron spectroscopy (XPS), Brunauer–Emmett–Teller (BET), X-ray diffraction (XRD), and Fourier Transform Infrared Spectroscopy (FT-IR). The results showed that sodium salts poisoned catalysts led to a decrease in the denitration efficiency. The 3.6% Na2SO4 poisoned catalyst was the most severely deactivated with denitration efficiency of only 50.97% at 350 °C. The introduction of SO42− and S2O72− created new Brønsted acid sites, which facilitated the adsorption of NH3 and NO reduction. The sodium salts poisoned catalysts significantly increased the conversion of SO2–SO3. 3.6%Na2S2O7 poisoned catalyst had the strongest effect on SO2 oxidation and the catalyst achieved a maximum SO2–SO3-conversion of 1.44% at 410 °C. Characterization results showed sodium salts poisoned catalysts consumed the active ingredient and lowered the V4+/V5+ ratio, which suppressed catalytic performance. However, they increased the content of chemically adsorbed oxygen and the strength of V5+=O bonds, which promoted SO2 oxidation.

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Synthesis of Hollow Flower-Like Fe3O4/MnO2/Mn3O4 Magnetically Separable Microspheres with Valence Heterostructure for Dye Degradation

Catalysts ◽

10.3390/catal9070589 ◽

2019 ◽

Vol 9 (7) ◽

pp. 589 ◽

Cited By ~ 4

Author(s):

Mingliang Ma ◽

Yuying Yang ◽

Yan Chen ◽

Fei Wu ◽

Wenting Li ◽

...

Keyword(s):

Electron Microscopy ◽

Visible Light ◽

Photoelectron Spectroscopy ◽

Organic Contaminants ◽

Dye Degradation ◽

Catalytic Performance ◽

X Ray ◽

Composite Microspheres ◽

Magnetically Separable ◽

Mno2 Nanosheet

In this manuscript, hollow flower-like ferric oxide/manganese dioxide/trimanganese tetraoxide (Fe3O4/MnO2/Mn3O4) magnetically separable microspheres were prepared by combining a simple hydrothermal method and reduction method. As the MnO2 nanoflower working as precursor was partially reduced, Mn3O4 nanoparticles were in situ grown from the MnO2 nanosheet. The composite microspheres were characterized in detail by employing scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Brunauer–Emmett–Teller (BET), vibration sample magnetometer (VSM) and UV–visible spectrophotometer (UV–vis). Under visible light conditions, the test for degrading rhodamine B (RhB) was used to verify the photocatalytic activity of the photocatalyst. The results showed that the efficiency of the Fe3O4/MnO2/Mn3O4 photocatalyst in visible light for 130 min is 94.5%. The catalytic activity of photocatalyst far exceeded that of the Fe3O4/MnO2 component, and after four cycles, the catalytic performance of the catalyst remained at 78.4%. The superior properties of the photocatalyst came from improved surface area, enhanced light absorption, and efficient charge separation of the MnO2/Mn3O4 heterostructure. This study constructed a green and efficient valence heterostructure composite that created a promising photocatalyst for degrading organic contaminants in aqueous environments.

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Preparation of pod-shaped TiO 2 and Ag@TiO 2 nano burst tubes and their photocatalytic activity

Royal Society Open Science ◽

10.1098/rsos.191019 ◽

2019 ◽

Vol 6 (9) ◽

pp. 191019 ◽

Cited By ~ 2

Author(s):

Shang Wang ◽

Zhaolian Han ◽

Tingting Di ◽

Rui Li ◽

Siyuan Liu ◽

...

Keyword(s):

Electron Microscopy ◽

Photocatalytic Activity ◽

Oxalic Acid ◽

Ultraviolet Light ◽

Photoelectron Spectroscopy ◽

Degradation Process ◽

Catalytic Performance ◽

Tetrabutyl Titanate ◽

Order Kinetic ◽

X Ray

The pod-shaped TiO 2 nano burst tubes (TiO 2 NBTs) were prepared by the combination of electrospinning and impregnation calcination with oxalic acid (H 2 C 2 O 4 ), polystyrene (PS) and tetrabutyl titanate. The silver nanoparticles (AgNPs) were loaded onto the surface of TiO 2 NBTs by ultraviolet light reduction method to prepare pod-shaped Ag@TiO 2 NBTs. In this work, we analysed the effect of the amount of oxalic acid on the cracking degree of TiO 2 NBTs; the effect of the concentration of AgNO 3 solution on the particle size and loading of AgNPs on the surface of TiO 2 NBTs. Scanning electron microscopy and transmission electron microscopy investigated the surface morphology of samples. X-ray diffraction and X-ray photoelectron spectroscopy characterized the structure and composition of samples. Rhodamine B (RhB) solution was used to evaluate the photocatalytic activity of pod-shaped TiO 2 NBTs and Ag@TiO 2 NBTs. The results showed that TiO 2 NBTs degraded 91.0% of RhB under ultraviolet light, Ag@TiO 2 NBTs degraded 95.5% under visible light for 75 and 60 min, respectively. The degradation process of both samples was consistent with the Langmuir–Hinshelwood first-order kinetic equation. Therefore, the catalytic performance of the sample is: Ag@TiO 2 NBTs > TiO 2 NBTs > TiO 2 nanotubes.

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Recyclable Heterogeneous Fe-Mo Nanocatalyst: Application in Solvent Free Synthesis of β-enaminones

Current Organocatalysis ◽

10.2174/2213337206666190415125053 ◽

2019 ◽

Vol 6 (3) ◽

pp. 238-247

Author(s):

Swapnil R. Bankar

Keyword(s):

Electron Microscopy ◽

Photoelectron Spectroscopy ◽

Significant Loss ◽

Solvent Free ◽

Catalyst Loading ◽

Spectroscopic Techniques ◽

Impregnation Method ◽

Molybdenum Catalyst ◽

X Ray ◽

Solvent Free Condition

Background: In recent years, green organic transformation has become a challenge for a chemist in areas like social sector, health, and environment. Literature survey revealed that a nano magnetite supported heterogeneous catalysis is an emergent field with huge application in chemical synthesis. Objective: In the present article, the aim was to develop a simple and facile method to carry organic reaction under benign media. So, the focus was on the synthesis of nano-magnetite supported molybdenum catalyst and its application in β-enaminones synthesis. Methods: Magnetically recyclable heterogeneous ferrite-molybdenum catalyst was prepared by simple impregnation method. The synthesized nanocatalyst Fe-Mo was well analysed by spectroscopic techniques like X-ray diffraction analysis, X-ray photoelectron spectroscopy, transmission electron microscopy, field-emission gun scanning electron microscopy and vibrating-sample magnetometry. The functionalized nanocatalyst Fe-Mo was employed in the synthesis of β-enaminones under solvent free condition. Results: The competency of synthesized nanocatalyst-Fe-Mo was observed to be good for the synthesis of β-enaminones derivatives under microwave irradiation and gave excellent yield (86-96%) of the product. The catalyst was recycled for more than five consecutive runs without significant loss in its activity. Conclusion: In the present research article, synthesis of highly active, magnetically recyclable Fe- Mo nanocatalyst was obtained from easily available precursor. The MNP was stable under investigated conditions and effective in β-enaminones synthesis. The simple eco-friendly method, low catalyst loading, short transformation time, and reusability of the catalyst thoroughly follow the sustainable protocol.

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MoSe2-GO/rGO Composite Catalyst for Hydrogen Evolution Reaction

Polymers ◽

10.3390/polym10121309 ◽

2018 ◽

Vol 10 (12) ◽

pp. 1309 ◽

Cited By ~ 15

Author(s):

Wenwu Guo ◽

Quyet Le ◽

Amirhossein Hasani ◽

Tae Lee ◽

Ho Jang ◽

...

Keyword(s):

Electron Microscopy ◽

Graphene Oxide ◽

Hydrogen Evolution ◽

Hydrogen Evolution Reaction ◽

Photoelectron Spectroscopy ◽

Transition Metal Dichalcogenides ◽

Catalytic Performance ◽

Composite Catalyst ◽

X Ray ◽

Molybdenum Selenide

There has been considerable research to engineer composites of transition metal dichalcogenides with other materials to improve their catalytic performance. In this work, we present a modified solution-processed method for the formation of molybdenum selenide (MoSe2) nanosheets and a facile method of structuring composites with graphene oxide (GO) or reduced graphene oxide (rGO) at different ratios to prevent aggregation of the MoSe2 nanosheets and hence improve their electrocatalytic hydrogen evolution reaction performance. The prepared GO, rGO, and MoSe2 nanosheets were characterized by X-ray powder diffraction, Raman spectroscopy, X-ray photoelectron spectroscopy, transmission electron microscopy, energy-dispersive X-ray spectroscopy, and scanning electron microscopy. The electrocatalytic performance results showed that the pure MoSe2 nanosheets exhibited a somewhat high Tafel slope of 80 mV/dec, whereas the MoSe2-GO and MoSe2-rGO composites showed lower Tafel slopes of 57 and 67 mV/dec at ratios of 6:4 and 4:6, respectively. We attribute the improved catalytic effects to the better contact and faster carrier transfer between the edge of MoSe2 and the electrode due to the addition of GO or rGO.

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

10.21203/rs.3.rs-627855/v1 ◽

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.

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Platinum Reduction Study on Pt/C Electro-catalysts for PEMFC

Journal of New Materials for Electrochemical Systems ◽

10.14447/jnmes.v16i3.1 ◽

2013 ◽

Vol 16 (3) ◽

pp. 141-145

Author(s):

M.L. Hernandez-Pichardo ◽

R. Gonzalez-Huerta ◽

P. del Angel ◽

E. Palacios-Gonzalez ◽

M. Tufiño-Velazquez ◽

...

Keyword(s):

Electron Microscopy ◽

Photoelectron Spectroscopy ◽

Uv Light ◽

Reducing Agents ◽

Impregnation Method ◽

X Ray Diffraction ◽

X Ray ◽

Synthesis Conditions ◽

Platinum Species ◽

Scanning Electron

Platinum reduction on Pt/C catalysts was studied on samples prepared by the impregnation method using different Pt precursors and reducing agents such as ethanol, sodium borohydride and ethanol-UV light (photo-assisted reduction), in order to compare the efficiency of the different reducing agents. The influence of the reduction level of the platinum species on the electrochemical behavior of these catalysts has been determined. The catalysts were characterized by X-Ray Diffraction (XRD), Scanning Electron Microscopy (SEM), X-ray photoelectron spectroscopy (XPS) and linear and cyclic voltammetry. The results show that the reduction level depends mainly on the platinum precursor. Moreover, it was found that the higher electrochemical activity was found using catalysts reduced with ethanol, whereas by using NaBH4 as the reducing agent, the total reduction of the platinum precursor is very difficult in same synthesis conditions. The analysis of the XPS results shows that samples reduced with ethanol presented the lower PtOx/Pt reduction ratio.

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Microstructural of Cr/MWCNT Composites and its Catalysis in Synthesis of Biodiesel

Advanced Materials Research ◽

10.4028/www.scientific.net/amr.455-456.1053 ◽

2012 ◽

Vol 455-456 ◽

pp. 1053-1059

Author(s):

Xue Hai Fan ◽

Guo Min Xiao

Keyword(s):

Electron Microscopy ◽

Potassium Dichromate ◽

Catalytic Performance ◽

Impregnation Method ◽

X Ray Diffraction ◽

X Ray ◽

Transmission Electron ◽

Multi Walled Carbon Nanotubes ◽

Ft Ir ◽

Walled Carbon Nanotubes

Multi-walled carbon nanotubes (MWCNTs), potassium dichromate (K2Cr2O7) and sulphuric acid were used for the preparation of Cr/MWCNT composite by impregnation method. The composites were comprehensively characterized by transmission electron microscopy （TEM），energy dispersive X-ray analysis (EDX), infrared spectroscopy (FT-IR), X-ray diffraction (XRD) and thermal gravity analysis (TGA). Due to its unique electrical and structural properties, this composite was applied to the synthesis of biodiesel (FAME) as a catalyst, showing effectively catalytic performance.

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Facet-Dependent Reactivity of Fe2O3/CeO2 Nanocomposites: Effect of Ceria Morphology on CO Oxidation

Catalysts ◽

10.3390/catal9040371 ◽

2019 ◽

Vol 9 (4) ◽

pp. 371 ◽

Cited By ~ 16

Author(s):

Maria Lykaki ◽

Sofia Stefa ◽

Sόnia Carabineiro ◽

Pavlos Pandis ◽

Vassilis Stathopoulos ◽

...

Keyword(s):

Electron Microscopy ◽

Co Oxidation ◽

Photoelectron Spectroscopy ◽

Rational Design ◽

Mixed Oxides ◽

Specific Activity ◽

Catalytic Performance ◽

Catalytic Systems ◽

X Ray ◽

Full Characterization

Ceria has been widely studied either as catalyst itself or support of various active phases in many catalytic reactions, due to its unique redox and surface properties in conjunction to its lower cost, compared to noble metal-based catalytic systems. The rational design of catalytic materials, through appropriate tailoring of the particles’ shape and size, in order to acquire highly efficient nanocatalysts, is of major significance. Iron is considered to be one of the cheapest transition metals while its interaction with ceria support and their shape-dependent catalytic activity has not been fully investigated. In this work, we report on ceria nanostructures morphological effects (cubes, polyhedra, rods) on the textural, structural, surface, redox properties and, consequently, on the CO oxidation performance of the iron-ceria mixed oxides (Fe2O3/CeO2). A full characterization study involving N2 adsorption at –196 °C, X-ray diffraction (XRD), transmission electron microscopy (TEM), scanning electron microscopy-energy dispersive X-ray spectroscopy (SEM-EDS), temperature programmed reduction (TPR), and X-ray photoelectron spectroscopy (XPS) was performed. The results clearly revealed the key role of support morphology on the physicochemical properties and the catalytic behavior of the iron-ceria binary system, with the rod-shaped sample exhibiting the highest catalytic performance, both in terms of conversion and specific activity, due to its improved reducibility and oxygen mobility, along with its abundance in Fe2+ species.

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Effect of Ce-modified Fe/ZSM-5 zeolite for selective catalytic reduction of NOx by ammonia

E3S Web of Conferences ◽

10.1051/e3sconf/202021803032 ◽

2020 ◽

Vol 218 ◽

pp. 03032

Author(s):

Chenxi Li ◽

Fanwei Meng ◽

Qing Ye

Keyword(s):

Selective Catalytic Reduction ◽

Photoelectron Spectroscopy ◽

Catalytic Reduction ◽

Catalytic Performance ◽

Acid Sites ◽

Impregnation Method ◽

Adsorption Ability ◽

In Situ Drifts ◽

X Ray

A series of xCe-Fe/ZSM-5 (x = 0, 0.25, 0.5 wt%) samples were prepared by the impregnation method, and the catalytic activity was evaluated by the selective catalytic reduction of NOx with ammonia (NH3-SCR). The physicochemical properties of prepared samples were characterized by various techniques such as X-ray diffraction (XRD), Brunner-Emmet-Teller (BET) measurement, hydrogen temperatureprogrammed reduction (H2-TPR), X-ray photoelectron spectroscopy (XPS), ammonia temperatureprogrammed desorption (NH3-TPD) and in situ diffuse reflectance infrared Fourier transform spectroscopy (in situ DRIFTS). XRD and BET results demonstrated that Ce and Fe species were uniform dispersed on the surface of the ZSM-5 zeolite and the micropore structure of ZSM-5 was still maintained. H2-TPR analysis indicated that the doping of Ce created more isolated Ce4+ and Fe3+ on the surface of catalysts, and the abundant Ce4+ and Fe3+ could enhance the reduction ability of catalysts. XPS analysis suggested that the doping of Ce could generate more oxygen vacancies, thereby increasing the number of chemisorption oxygen. According to the in-situ DRIFTS and NH3-TPD results, Ce species provided more acidic sites, which is beneficial to the NH3 adsorption ability of ZSM-5 zeolite. Additionally, the abundant chemisorption oxygen, medium and strong Brønsted acid sites, excellent NH3 adsorption ability and outstanding reduction property are beneficial to the NH3-SCR reaction. Among all prepared samples, the 0.25Ce-Fe/ZSM-5 sample possessed the widest reaction temperature window and the best catalytic performance (NO conversion over 98% at 350-450 °C), which was associated with the abundant acid sites and remarkable adsorption ability of NH3, outstanding redox ability and abundant chemisorption oxygen after the doping of Ce.

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