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Aqueous acidic hydrogen peroxide as an efficient medium for tungsten insertion into MCM-41 mesoporous molecular sieves with high metal dispersion

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TLDR
In this article, two sets of WOx/SiO2-MCM-41 precatalysts (A and B) were prepared and compared, and the results suggest that the novel preparation method (route A) has a marked effect on the dispersion of the WOx species on and into the silica matrix.
Abstract
Two sets of WOx/SiO2-MCM-41 precatalysts (A and B) were prepared and compared. Tungsten-containing MCM-41 mesoporous molecular sieves have been synthesized with tetraethyl orthosilicate and tungsten precursors, tungstic acid, 'H2WO4', or sodium tungstate, in the presence of cetyltrimethylammonium chloride (CTMACl) micelles as template in aqueous acid solution. In route A, H2O2 was added to avoid the formation of iso- (or hetero-) polyoxometalates in the counter-ion-mediated S+X−I+ pathway with oxo–peroxo species [S+ = quaternary ammonium ion surfactant, in this paper cetyltrimethylammonium (CTMA+), X− = Cl− and/or anionic peroxo species, I+ = inorganic silicate precursor generating silanols or their protonated forms]. This procedure is compared with methods involving or generating polyoxometalates without peroxo moieties (route B) to determine whether the metal loading and/or dispersion is improved by H2O2. The native materials were calcined in air (1 K min−1, isothermal at 920 K for 4 h) in order to decompose the organic template. The resulting molecular sieves have been characterized by chemical analysis, powder X-ray diffraction, UV-visible diffuse reflectance spectroscopy, nitrogen sorption isotherms, TEM and EDX analysis, and Raman spectrometry. High incorporation levels ((Si∶W)exp molar ratio ≈30∶1) with a nearly homogeneous distribution of the dopants can be obtained only by route A. The spectral differences between the materials are correlated with their catalytic reactivities for cyclooctene epoxidation with an anhydrous H2O2/t-BuOH mixture at room temperature. The results suggest that the novel preparation method (route A) has a marked effect on the dispersion of the WOx species on and into the silica matrix.

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Transition-metal complexes for liquid-phase catalytic oxidation: some aspects of industrial reactions and of emerging technologies

TL;DR: In this paper, the similarities and specificities of the transformation of cyclohexane into adipic acid (via the formation and isolation of the cycloshexanol-cyclohexanone mixture) and of the process for the preparation of terephthalic acid by oxidation of p-xylene are analysed from a prospective viewpoint.
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Direct Synthesis of Ordered Macroporous Silica Materials Functionalized with Polyoxometalate Clusters

TL;DR: In this paper, 3D ordered macroporous (3DOM) materials functionalized with highly dispersed polyoxometalate clusters have been prepared via direct synthesis, and the products were characterized by IR, solid-state 29Si and 13C NMR, scanning electron microscopy (SEM) and X-ray energy-dispersive spectroscopy, and chemical analysis.
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The utilization of rice husk silica as a catalyst: Review and recent progress

TL;DR: In this article, the authors report the recent development and utilization of silica from rice husk (RH) for the immobilization of transition metals and organic moieties and use 3-(Chloropropyl)triethoxy-silane (CPTES) as a bridge to link the organic mixtures to the silica matrix.
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Synthesis, characterization, and catalytic function of novel highly dispersed tungsten oxide catalysts on mesoporous silica

TL;DR: The physical and chemical properties of tungsten oxide supported on SBA-15 mesoporous silica prepared by a controlled grafting process through atomic layer deposition (ALD) were studied using complementary characterization methods as discussed by the authors.
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From polyoxometalates to polyoxoperoxometalates and back again; potential applications

TL;DR: In this article, a short review of the development of catalysts for epoxidations and for carbon-carbon bond cleavage is presented, focusing on fully inorganic systems, some with the dimeric moiety [M2O2(μ-O2)2(O2 )2], (M = V, Mo, W) which have more scope than those containing organic ligands or supports.
References
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Journal ArticleDOI

Reporting physisorption data for gas/solid systems with special reference to the determination of surface area and porosity (Recommendations 1984)

TL;DR: Mise au point comportant des definitions generales et la terminologie, la methodologie utilisee, les procedes experimentaux, les interpretations des donnees d'adsorption, les determinations de l'aire superficielle, and les donnes sur la mesoporosite et la microporosite.
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Ordered mesoporous molecular sieves synthesized by a liquid-crystal template mechanism

TL;DR: In this paper, the synthesis of mesoporous inorganic solids from calcination of aluminosilicate gels in the presence of surfactants is described, in which the silicate material forms inorganic walls between ordered surfactant micelles.
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A new family of mesoporous molecular sieves prepared with liquid crystal templates

TL;DR: In this paper, the synthesis, characterization, and proposed mechanism of formation of a new family of silicatelaluminosilicate mesoporous molecular sieves designated as M41S is described.
Journal ArticleDOI

Infrared and Raman study of WO3 tungsten trioxides and WO3, xH2O tungsten trioxide tydrates

TL;DR: In this article, the infrared and Raman spectra of powder samples of WO3 (monoclinic and hexagonal) and XH 2 O (x = 1,2, 1 3 ) have been recorded and the most characteristic vibrations are discussed with reference to the available structural data.
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