scholarly journals Furfural Oxidation on Gold Supported on MnO2: Influence of the Support Structure on the Catalytic Performances

2018 ◽  
Vol 8 (8) ◽  
pp. 1246 ◽  
Author(s):  
Camila Palombo Ferraz ◽  
Anderson Gabriel Marques Da Silva ◽  
Thenner Silva Rodrigues ◽  
Pedro Henrique Cury Camargo ◽  
Sébastien Paul ◽  
...  

A series of catalysts consisting of gold nanoparticles supported on MnO2 presenting different morphologies were synthesized and tested in the base-free oxidation of furfural. Ultra-small Au particles (less than 3 nm) were deposited on low (commercial MnO2) and high (NF, nanoflowers and NW, nanowires MnO2) surface area supports. High activity was observed for Au/MnO2-NF material with very high selectivity to furoic acid. The X-ray photoelectron spectroscopy (XPS) study confirmed the presence of a significant amount of highly active Auδ+ species on the surface of the Au/MnO2-NF catalyst. These species seem to be responsible for the high activity in oxidation of furfural under mild conditions (air as oxidant, 110 °C).

2021 ◽  
pp. 174751982098472
Author(s):  
Jun Yu ◽  
Ying Han ◽  
Guoqing Chen ◽  
Xiuzhen Xiao ◽  
Haifang Mao ◽  
...  

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.


2019 ◽  
Vol 11 (1) ◽  
Author(s):  
Kaili Zhang ◽  
Xinhui Xia ◽  
Shengjue Deng ◽  
Yu Zhong ◽  
Dong Xie ◽  
...  

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.


Molecules ◽  
2019 ◽  
Vol 24 (15) ◽  
pp. 2695 ◽  
Author(s):  
Mhadmhan ◽  
Marquez-Medina ◽  
Romero ◽  
Reubroycharoen ◽  
Luque

We have successfully incorporated iron species into mesoporous aluminosilicates (AlSBA15) using a simple mechanochemical milling method. The catalysts were characterized by nitrogen physisorption, inductively coupled plasma mass spectrometry (ICP-MS), pyridine (PY) and 2,6-dimethylpyridine (DMPY) pulse chromatography titration, powder X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and scanning electron microscopy with energy-dispersive X-ray spectroscopy (SEM-EDX). The catalysts were tested in the N-alkylation reaction of aniline with benzyl alcohol for imine production. According to the results, the iron sources, acidity of catalyst and reaction conditions were important factors influencing the reaction. The catalyst showed excellent catalytic performance, achieving 97% of aniline conversion and 96% of imine selectivity under optimized conditions.


Author(s):  
Khaled Alshammari ◽  
Yubiao Niu ◽  
Richard E. Palmer ◽  
Nikolaos Dimitratos

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’.


2010 ◽  
Vol 152-153 ◽  
pp. 484-488
Author(s):  
Yu Gui Tao ◽  
Hao Gu ◽  
Yan Qiu Xu ◽  
Lian Bin Ye ◽  
Qi Jin Wang

Pb(II)-imprinted chitosan/TiO2 hybrid film (LIHF) was synthesized through a two-step process. The selectivity of LIHF was studied via competitive adsorption experiment. The LIHF shows higher selectivity to Pb (II) ion than Cu (II) and Zn (II) ions. X-ray photoelectron spectroscopy(XPS) was used to characterize the as-obtained samples. XPS results showed that the nitrogen atom and the Pb (II) were concerned for coordination. The evidences for the imprinting process and the recognition of Pb (II) with LIHF were provided.


2000 ◽  
Vol 108 (1253) ◽  
pp. 61-64 ◽  
Author(s):  
Masahiro OZAWA ◽  
Yoichiro FURUKAWA ◽  
Mitsushige OGAWA ◽  
Kei ISOZAKI

2017 ◽  
Vol 58 (6) ◽  
pp. 1152-1159 ◽  
Author(s):  
A. I. Stadnichenko ◽  
V. V. Murav’ev ◽  
V. A. Svetlichnyi ◽  
A. I. Boronin

1992 ◽  
Vol 271 ◽  
Author(s):  
G. Granozzi ◽  
A. Glisenti ◽  
R. Bertoncello ◽  
G. D. Soraru

ABSTRACTThe nitridation process of a polytitanocarbosilane, leading to the formation of a Si-Ti-N-O ceramics, has been investigated mainly by means of X-ray photoelectron spectroscopy (XPS). Ti2p spectra collected on samples fired at various stages of the transformation process clearly shown that Ti-N bonds of TiOxNy mixed units start to form at 500 °C. By increasing the firing temperature, the Ti2p peak shifts toward values typical of titanium nitride ceramics, so indicating the progressive nitrogen enrichment of the mixed units up to the formation of a TiN phase.


RSC Advances ◽  
2016 ◽  
Vol 6 (15) ◽  
pp. 12627-12637 ◽  
Author(s):  
Yaovi Holade ◽  
Christine Canaff ◽  
Suzie Poulin ◽  
Têko W. Napporn ◽  
Karine Servat ◽  
...  

The nature of the reduction agent changes drastically the palladium nanomaterials chemical stability, which subsequently alters earnestly their catalytic performances.


2007 ◽  
Vol 14 (04) ◽  
pp. 725-728
Author(s):  
XIQI FENG ◽  
WEIFENG LI ◽  
WENLIANG ZHU

Lead tungstate ( PbWO 4) (PWO) crystals doped with high concentration trivalent rare earth ions have demonstrated to be a promising Cherenkov radiator material and also a potential material for optoelectronic application. In this paper, the doping mechanisms of the trivalent ions ( La 3+, Nd 3+, and Gd 3+) in the PWO host were studied using X-ray photoelectron spectroscopy (XPS), and the results were consistent with those of computer simulation. It was found that when heavily doped, La 3+ may substitute for the W sites as well as the Pb sites for self-compensation by forming La dimers or small aggregates. However, the doping mechanism of heavily doped PWO: Nd 3+ and PWO: Gd 3+ might be different from that of heavily doped PWO: La 3+ crystals.


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