Jacques VEDRINE

Prof. Dr. Jacques VEDRINE

Sorbonne Université, Faculté des Sciences et Ingénierie, Laboratoire de Réactivité de Surface, UMR-CNRS 7197, 4 place Jussieu, F-75252 Paris, France
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Research Focus & Metrics

Academic Career Length

19Years (2008-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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10 November 2017 in Catalysts
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Journal Article
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Jacques VEDRINEJacques VEDRINE
Jacques VEDRINE
This review article contains a reminder of the fundamentals of heterogeneous catalysis and a description of the main domains of heterogeneous catalysis and main families of metal oxide catalysts, which cover acid-base reactions, selective partial oxidation reactions, total oxidation reactions, depollution, biomass conversion, green chemistry and photocatalysis. Metal oxide catalysts are essential components in most refining and petrochemical processes. These catalysts are also critical to improving environmental quality. This paper attempts to review the major current industrial applications of supported and unsupported metal oxide catalysts. Viewpoints for understanding the catalysts’ action are given, while applications and several case studies from academia and industry are given. Emphases are on catalyst description from synthesis to reaction conditions, on main industrial applications in the different domains and on views for the future, mainly regulated by environmental issues. Following a review of the major types of metal oxide catalysts and the processes that use these catalysts, this paper considers current and prospective major applications, where recent advances in the science of metal oxide catalysts have major economic and environmental impacts.

13 September 2013 in Catalysis Reviews
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Journal Article
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EDE.G. Derouane
E.G. Derouane
Jacques VEDRINEJacques VEDRINE
Jacques VEDRINE
RPR. Ramos Pinto
R. Ramos Pinto
PBPedro Miguel Ramos Borges
Pedro Miguel Ramos Borges
LCLuis Costa
Luis Costa
FRF. Ramôa Ribeiro
F. Ramôa Ribeiro
In this article, we considered all aspects of acidity (nature of acid sites, strength, density, etc.) in solid catalysts and in zeolites in particular. After reminding the definition of acidity in liquid and solid acids, we emphasized acidity characterization by the most used physical techniques, such as Hammett's indicator titration, microcalorimetry of adsorbed probe molecules (ammonia, pyridine or other amines for acidity characterization and CO2 or SO2 for basicity characterization), ammonia or any amine thermodesorption, IR spectroscopy of hydroxyl groups and of several probe molecules adsorbed (ammonia, pyridine, piperidine, amines, CO, H2, etc.), MAS-NMR of 27Al, 29Si, 1H elements and of 1H, 13C, 31P, etc. of adsorbed probe molecules, and model catalytic reactions. Modeling the way the acid features of zeolites influence the catalytic activity of these catalysts toward acid-catalyzed reactions (relation between ammonia desorption activation energy values and catalytic activities, reaction mechanism, and kinetics) completes the general analysis of acidity and zeolite chemistry.


22 March 2015 in Research on Chemical Intermediates
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Jacques VEDRINEJacques VEDRINE
Jacques VEDRINE

31 March 2015 in Molecules
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IFIoana Fechete
Ioana Fechete
Jacques VEDRINEJacques VEDRINE
Jacques VEDRINE
This review summarizes the importance of nanoporous materials and their fascinating structural properties with respect to the catalytic and photocatalytic reduction of CO2 to methane, toward achieving a sustainable energy supply. The importance of catalysis as a bridge step for advanced energy systems and the associated environmental issues are stressed. A deep understanding of the fundamentals of these nanoporous solids is necessary to improve the design and efficiency of CO2 methanation. The role of the support dominates the design in terms of developing an efficient methanation catalyst, specifically with respect to ensuring enhanced metal dispersion and a long catalyst lifetime. Nanoporous materials provide the best supports for Ni, Ru, Rh, Co, Fe particles because they can prevent sintering and deactivation through coking, which otherwise blocks the metal surface as carbon accumulates. This review concludes with the major challenges facing the CO2 methanation by nanoporous materials for fuel applications.

29 January 2016 in Catalysts
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Jacques VEDRINEJacques VEDRINE
Jacques VEDRINE
This paper presents an overview of heterogeneous partial (amm)oxidation and oxidative dehydrogenation (ODH) of hydrocarbons. The review has been voluntarily restricted to metal oxide-type catalysts, as the partial oxidation field is very broad and the number of catalysts is quite high. The main factors of solid catalysts for such reactions, designated by Grasselli as the “seven pillars”, and playing a determining role in catalytic properties, are considered to be, namely: isolation of active sites (known to be composed of ensembles of atoms), Me–O bond strength, crystalline structure, redox features, phase cooperation, multi-functionality and the nature of the surface oxygen species. Other important features and physical and chemical properties of solid catalysts, more or less related to the seven pillars, are also emphasized, including reaction sensitivity to metal oxide structure, epitaxial contact between an active phase and a second phase or its support, synergy effect between several phases, acid-base aspects, electron transfer ability, catalyst preparation and activation and reaction atmospheres, etc. Some examples are presented to illustrate the importance of these key factors. They include light alkanes (C1–C4) oxidation, ethane oxidation to ethylene and acetic acid on MoVTe(Sb)Nb-O and Nb doped NiO, propene oxidation to acrolein on BiMoCoFe-O systems, propane (amm)oxidation to (acrylonitrile) acrylic acid on MoVTe(Sb)Nb-O mixed oxides, butane oxidation to maleic anhydride on VPO: (VO)2P2O7-based catalyst, and isobutyric acid ODH to methacrylic acid on Fe hydroxyl phosphates. It is shown that active sites are composed of ensembles of atoms whose size and chemical composition depend on the reactants to be transformed (their chemical and size features) and the reaction mechanism, often of Mars and van Krevelen type. An important aspect is the fact that surface composition and surface crystalline structure vary with reaction on stream until reaching steady state, which makes characterisation of active and selective surface sites quite difficult. The use of oxidants other than O2, such as H2O2, N2O or CO2, is also briefly discussed. Based on such analysis and recent discoveries and process developments, our perspective is given.