scholarly journals Ruling Factors in Cinnamaldehyde Hydrogenation: Activity and Selectivity of Pt-Mo Catalysts

Nanomaterials ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 362
Author(s):  
Marta Stucchi ◽  
Maela Manzoli ◽  
Filippo Bossola ◽  
Alberto Villa ◽  
Laura Prati
Keyword(s):  
Photoelectron Spectroscopy ◽  
Pt Nanoparticles ◽  
Carbon Support ◽  
Catalytic Performance ◽  
Acid Sites ◽  
Hydrogenation Catalysts ◽  
Cinnamaldehyde Hydrogenation ◽  
Transmission Electron ◽  
Heat Treated ◽  
Heating Treatment

To obtain selective hydrogenation catalysts with low noble metal content, two carbon-supported Mo-Pt bimetallic catalysts have been synthesized from two different molybdenum precursors, i.e., Na2MoO4 and (NH4)6Mo7O24. The results obtained by X-ray photoelectron spectroscopy (XPS) and transmission electron microscopy (TEM) combined with the presence and strength of acid sites clarified the different catalytic behavior toward cinnamaldehyde hydrogenation. After impregnating the carbon support with Mo precursors, each sample was used either as is or treated at 400 °C in N2 flow, as support for Pt nanoparticles (NPs). The heating treatment before Pt deposition had a positive effect on the catalytic performance. Indeed, TEM analyses showed very homogeneously dispersed Pt NPs only when they were deposited on the heat-treated Mo/C supports, and XPS analyses revealed an increase in both the exposure and reduction of Pt, which was probably tuned by different MoO3/MoO2 ratios. Moreover, the different acid properties of the catalysts resulted in different selectivity.

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

Catalysts ◽  
2018 ◽  
Vol 8 (11) ◽  
pp. 541 ◽  
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.

Carbon Supported Pt+Os Catalysts for Methanol Oxidation

2002 ◽  
Vol 57 (2) ◽  
pp. 193-201 ◽  
Author(s):  
Gülsün Gökağaç ◽  
Brendan J. Kennedy
Keyword(s):  
Methanol Oxidation ◽  
Photoelectron Spectroscopy ◽  
Surface Composition ◽  
Carbon Support ◽  
Methanol Oxidation Reaction ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Metal Metal ◽  
Metal Support

11% Pt/C, 10% Pt + 1%Os/C, 9% Pt + 2%Os/C, 8% Pt + 3%Os/C, 7% Pt + 4%Os/C, 6% Pt + 5%Os/C and 5%Pt + 6% Os/C catalysts have been prepared for methanol oxidation reaction. Transmission electron microscopy, X-ray photoelectron spectroscopy, X-ray diffraction and cyclic voltammetry have been used to understand the nature of the species present in these catalysts. 7% Pt + 4% Os/C was the most active catalyst, while 8% Pt + 3% Os/C was the least active one. It is found that the metal particle size and distribution on the carbon support, the surface composition and the oxidation states of the metal particles, the metal-metal and metal support interactions are important parameters to define the activity of the catalyst.

Synthesis of Novel g-C3N4/NH2-MIL-88B(Fe) Composite Photocatalysis for Efficient Ciprofloxacin Degradation Under Simulated Sunlight Irradiation

NANO ◽  
2021 ◽  
pp. 2150063
Author(s):  
Jungang Yi ◽  
Kun Wu ◽  
Huadong Wu ◽  
Jia Guo ◽  
Linfeng Zhang ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Adsorption Property ◽  
Catalytic Performance ◽  
Step Method ◽  
Area Formula ◽  
Aquatic Life ◽  
X Ray ◽  
Transmission Electron ◽  
Uniform Dispersion ◽  
Composite Photocatalysts

The presence of the antibiotics in the wastewater has posed a huge risk to aquatic life and human health. It is a great significance to develop an effective technology to treat the antibiotics-containing wastewater. In this study, a series of g-C3N4/NH2-MIL-88B(Fe) composite photocatalysts are synthesized through a simple one-step method. The structure and optical properties of prepared photocatalysts are detected by X-ray diffraction (XRD), field emission scanning electron microscope (FESEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), UV–Vis absorption spectra (UV–Vis DRS), photoluminescence (PL) spectroscopy and transient photocurrent techniques, respectively. FESEM and TEM show that MOF is uniformly dispersed in petaloid g-C3N4. The uniform dispersion of Fe-MOFs in the heterojunction composites increases the specific surface area ([Formula: see text] of g-C3N4, which results in a great adsorption property for the nanocomposite. The capture experiment shows that [Formula: see text]O[Formula: see text] and h[Formula: see text] are the main active substances in ciprofloxacin (CIP) degradation. These prepared composite photocatalysts exhibit excellent CIP photodegradation activity under visibly light irradiation with an apparent rate constant of 0.0127[Formula: see text]min[Formula: see text] (3.74 times as the rate of single component). The remarkable catalytic performance can be ascribed to the fact that the g-C3N4/NH2-MIL-88B(Fe) heterojunction inhibits the recombination of photoinduced electron–hole pairs and improved the visible light absorption.

scholarly journals Capping Agent Effect on Pd-Supported Nanoparticles in the Hydrogenation of Furfural

Catalysts ◽  
2019 ◽  
Vol 10 (1) ◽  
pp. 11 ◽  
Author(s):  
Shahram Alijani ◽  
Sofia Capelli ◽  
Stefano Cattaneo ◽  
Marco Schiavoni ◽  
Claudio Evangelisti ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Active Sites ◽  
Catalytic Performance ◽  
Shielding Effect ◽  
Capping Agents ◽  
X Ray ◽  
Supported Nanoparticles ◽  
Liquid Phase Hydrogenation ◽  
Diallyldimethylammonium Chloride ◽  
Transmission Electron

The catalytic performance of a series of 1 wt % Pd/C catalysts prepared by the sol-immobilization method has been studied in the liquid-phase hydrogenation of furfural. The temperature range studied was 25–75 °C, keeping the H2 pressure constant at 5 bar. The effect of the catalyst preparation using different capping agents containing oxygen or nitrogen groups was assessed. Polyvinyl alcohol (PVA), polyvinylpyrrolidone (PVP), and poly (diallyldimethylammonium chloride) (PDDA) were chosen. The catalysts were characterized by ultraviolet-visible spectroscopy (UV-Vis), Fourier transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM), and X-ray photoelectron spectroscopy (XPS). The characterization data suggest that the different capping agents affected the initial activity of the catalysts by adjusting the available Pd surface sites, without producing a significant change in the Pd particle size. The different activity of the three catalysts followed the trend: PdPVA/C > PdPDDA/C > PdPVP/C. In terms of selectivity to furfuryl alcohol, the opposite trend has been observed: PdPVP/C > PdPDDA/C > PdPVA/C. The different reactivity has been ascribed to the different shielding effect of the three ligands used; they influence the adsorption of the reactant on Pd active sites.

scholarly journals Catalytic Dehydrogenation of Methylcyclohexane by Pt Nanoparticles Supported on Nitrogen doped Carbon

2020 ◽  
Vol 194 ◽  
pp. 01030
Author(s):  
Jian Wang ◽  
Shiguang Fan ◽  
Xuan Xu ◽  
Huiru Yun ◽  
He Liu ◽  
...  
Keyword(s):  
Surface Area ◽  
Pt Nanoparticles ◽  
Catalytic Performance ◽  
Support Surface ◽  
Catalytic Dehydrogenation ◽  
Nitrogen Doped ◽  
Surface Areas ◽  
Transmission Electron ◽  
Methylcyclohexane Dehydrogenation ◽  
Nitrogen Doped Carbon

Pt nanoparticles supported on nitrogen doped carbon (Pt/CN) catalysts with different surface areas were obtained and characterized by transmission electron microscope （TEM） and brunner-emmet-teller （BET）. The characterized results showed that Pt nanoparticles dispersed uniformly on the support surface, and the surface area of the Pt/CN catalyst increased with the increase of annealing temperature. Subsequently, the catalytic performance of Pt/CN catalysts for methylcyclohexane dehydrogenation was studied. The activity of Pt/CN catalysts in methylcyclohexane dehydrogenation increased with the increase of the surface area, Pt/CN-1000 catalyst has the largest surface area and the highest catalytic activity, with the methylcyclohexane conversion of 99% and the TOF value of 424.78 h-1 at 180 ℃ for 150 minutes.

scholarly journals Verification Study of Nanostructure Evolution with Heating Treatment between Thin and Thick Fullerene-Like Hydrogen Carbon Films

Coatings ◽  
2019 ◽  
Vol 9 (2) ◽  
pp. 82 ◽  
Author(s):  
Zhaolong Wang ◽  
Kaixiong Gao ◽  
Bin Zhang ◽  
Zhenbin Gong ◽  
Xiaoli Wei ◽  
...  
Keyword(s):  
Thin Films ◽  
Photoelectron Spectroscopy ◽  
Thick Films ◽  
Carbon Films ◽  
Good Choice ◽  
Xps Spectra ◽  
Si Substrates ◽  
Transmission Electron ◽  
Original Films ◽  
Heating Treatment

Fullerene-like hydrogen carbon films with a thin film grown on a NaCl substrate are usually employed to show the nanostructure of films (usually of hundred nanometers thick grown on Si substrates) under high resolution transmission electron microscopy (HRTEM) tests because it is easier floated off, where dependability and reasonability has never been seriously contested. Thus, in this paper, thin and thick hydrogen carbon films have been deposited on NaCl (thin films) and Si (thick films) substrates and annealed under room temperature to 500 °C, of which nanostructures have been investigated by HRTEM, Raman spectroscopy, and X-ray photoelectron spectroscopy, to verify the dependability and reasonability of the NaCl method. The results showed heating induced graphitization but with hydrogen content nearly unchanged. HRTEM results revealed that under annealing of 200, 250, and 300 °C, the curved graphene structures gradually increase in films. However, beyond 400 °C, onions structures are present. However, both Raman and XPS spectra show us that after annealed treatment, for original films, both thin and thick films have the near sp2 bonding content and size, but with the annealing temperature increase, sp2 bonding content increases more quickly for thick FL-C:H films due to the higher internal stress compared to thin films. In one word, the NaCl method used for nanostructure detection for films might be a good choice for an easier and quicker analysis, but it is still insufficient, because the heating effect induced by plasma cannot be ignored.

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’.

Electroless Synthesis of 1.4 nm Pd and Pt Nanoparticles on Self-Assembled Rosette Nanotubes

2011 ◽  
Vol 1301 ◽  
Author(s):  
Rahul Chhabra ◽  
Hicham Fenniri
Keyword(s):  
Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
Pt Nanoparticles ◽  
Hierarchical Organization ◽  
X Ray ◽  
Force Microscopy ◽  
Rosette Nanotubes ◽  
Atomic Force ◽  
Transmission Electron ◽  
Self Assembled

ABSTRACTElectroless synthesis and hierarchical organization of 1.4 nm Pd and Pt nanoparticles (NPs) on self-assembled Rosette Nanotubes (RNTs) is described. The nucleated NPs are nearly monodisperse and reveal supramolecular organizations guided by RNT templates. Interestingly, the narrow size distribution is attributable to unique templating behavior of RNTs. The resulting metal NP-RNT composites were characterized by Atomic Force Microscopy (AFM), Scanning Electron Microscopy (SEM) and Transmission Electron Microscopy (TEM). X-ray Photoelectron Spectroscopy (XPS) was also performed to confirm the nature and composition of RNT-templated NPs.

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.

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