Noémie Perret

ORCID: 0000-0003-4976-5189
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Research Areas
  • Catalysis and Hydrodesulfurization Studies
  • Catalysis for Biomass Conversion
  • Catalytic Processes in Materials Science
  • Nanomaterials for catalytic reactions
  • Catalysts for Methane Reforming
  • Asymmetric Hydrogenation and Catalysis
  • Oxidative Organic Chemistry Reactions
  • Biofuel production and bioconversion
  • Catalysis and Oxidation Reactions
  • Lignin and Wood Chemistry
  • Carbon dioxide utilization in catalysis
  • Electrocatalysts for Energy Conversion
  • MXene and MAX Phase Materials
  • Process Optimization and Integration
  • Ammonia Synthesis and Nitrogen Reduction
  • Polyoxometalates: Synthesis and Applications
  • Chemical Synthesis and Reactions
  • Metal and Thin Film Mechanics
  • Mesoporous Materials and Catalysis
  • Crystallization and Solubility Studies
  • X-ray Diffraction in Crystallography
  • Advanced Nanomaterials in Catalysis
  • Copper-based nanomaterials and applications
  • Metal-Organic Frameworks: Synthesis and Applications
  • Environmental remediation with nanomaterials

Université Claude Bernard Lyon 1
2017-2025

Centre National de la Recherche Scientifique
2017-2025

Institut de Recherches sur la Catalyse et l'Environnement de Lyon
2016-2025

Centre d'Etudes et de Recherches pour l'Intensification du Traitement du Diabète
2019-2024

Forum Réfugiés - Cosi
2017-2020

Heriot-Watt University
2009-2019

Service de Santé de la Jeunesse
2019

Maison des Sciences de l'Homme Lyon St-Étienne
2019

Clinique Claude-Bernard
2019

University of Liverpool
2015-2017

Abstract The catalytic response of Ni on Al 2 O 3 obtained from Ni–Al layered double hydroxides was studied for the liquid‐phase hydrogenation hydroxymethyl furfural to tetrahydrofuran‐2,5‐diyldimethanol (THFDM) in water. successive calcination and reduction precursors caused removal interlayer hydroxyl carbonate groups 2+ 0 . Four reduced mixed oxide catalysts were obtained, consisting different amount metal contents (47–68 wt %) an Al‐rich amorphous component. activity linked content...

10.1002/cssc.201501225 article EN ChemSusChem 2016-02-12

The production of cyclopentanone derivatives from 5-hydroxymethylfurfural using non-noble metal based catalysts is reported for the first time.

10.1039/c7gc00315c article EN Green Chemistry 2017-01-01

Au–Pt and Au–Pd bimetallic catalysts were prepared over various supports using different preparation methods compared in the base-free selective aerobic catalytic oxidation of glucose to glucaric acid. The method catalysts, support material for nanoparticles, metal molar ratios have a strong influence on activity maximum yield Au–Pt/ZrO2 catalyst with ratio Au/Pt = 1 provides 50% acid at complete conversion gluconic 100 °C, under 40 bar air, glucose/metal 80. was stable upon sequential...

10.1021/acs.iecr.7b01571 article EN Industrial & Engineering Chemistry Research 2017-06-06

The catalytic gas phase hydrogenation of m-dinitrobenzene (1 atm, 423 K) over laboratory synthesised mol%) Au supported on Al2O3, TiO2, Fe2O3 and CeO2 a reference Au/TiO2 (World Gold Council) has been investigated. catalysts were prepared by deposition-precipitation (DP) impregnation (IMP), where the former route generated smaller (surface area weighted) mean particle sizes (1.5–2.8 nm) compared with IMP synthesis (3.5–9.0 nm). have characterized in terms temperature programmed reduction...

10.1039/c1cy00051a article EN Catalysis Science & Technology 2011-01-01

Direct cation-exchange of a homogeneous organometallic cationic molecular catalyst inside the pores an anionic MOF is conclusively demonstrated.

10.1039/c5sc03494a article EN cc-by-nc Chemical Science 2015-12-09

Abstract Bimetallic Rh‐ReO x (Re/Rh molar ratio 0.4–0.5) catalysts supported on TiO 2 and ZrO were prepared by the successive impregnation of dried calcined unreduced Rh catalysts. Their catalytic performances evaluated in hydrogenolysis erythritol to butanetriols (BTO) butanediols (BDO) aqueous solution at 150–240 °C under 30–120 bar H . The activity depended nature support, highest selectivity BTO BDO 80 % conversion was 37 29 %, respectively, presence 3.7 wt %Rh‐3.5 %ReO /ZrO 200 120 bar....

10.1002/cctc.201700260 article EN ChemCatChem 2017-02-27

The hydrogenolysis of tetrahydrofurfuryl alcohol was studied in aqueous phase over a range bifunctional catalysts based on Rh and an oxophilic promoter (Re, W, Mo) supported ZrO2. structures the were characterised employing powder XRD, Raman spectroscopy TEM analysis. degrees reduction evaluated by H2-TPR XPS analyses. metallic properties assessed CO chemisorption. For first time, acidic calorimetric measurements 2-phenyl-ethylamine adsorption heat. combination sites Brønsted (linked to...

10.1016/j.jcat.2024.115305 article EN cc-by-nc-nd Journal of Catalysis 2024-01-21

The catalytic continuous gas phase hydrogenation of p-chloronitrobenzene (P=1 atm;T=423 K) has been investigated over a series oxide (Al2O3, TiO2, Fe2O3 and CeO2) supported Au (1 mol %) catalysts. application two catalyst synthesis routes,i.e. impregnation (IMP) deposition-precipitation (DP), considered where the DP route generated smaller mean particle sizes (1.5-2.8 nm) compared with IMP preparation (3.5-9.0 nm). catalysts have characterised in terms H2 chemisorption BET area measurements...

10.1007/bf03214922 article EN cc-by-nc Gold Bulletin 2009-06-01

A temperature programmed treatment of MoO3 in flowing N2 + H2 has been employed to prepare β-phase molybdenum nitride (β-Mo2N) which used promote, for the first time, catalytic hydrogenation p-chloronitrobenzene. The reduction/nitridation synthesis steps have monitored situ and starting oxide, reaction intermediates product identified characterized by powder X-ray diffraction (XRD), diffuse reflectance UV-Vis (DRS UV-Vis), elemental analysis, scanning electron microscopy (SEM) BET/pore...

10.1039/c0cy00011f article EN Catalysis Science & Technology 2011-01-01

The use of nonreducible (Al2O3) and reducible (Ce0.62Zr0.38O2, CZ) carriers to support nanoscale Au has been studied in gas phase p-chloronitrobenzene hydrogenation. Reaction over Au/Al2O3 generated p-chloroaniline as the sole product, whereas Au/CZ catalyzed nitro-group reduction dechlorination aniline. A parallel/consecutive kinetic model applied quantify selectivity for Au/CZ. Catalyst characterization included temperature programmed (TPR)/desorption (TPD), XPS, HAADF-STEM, CO...

10.1021/jp3093836 article EN The Journal of Physical Chemistry C 2012-12-18

The hydrogenolysis reaction of biomass-derived xylitol to glycols and glycerol has been carried out in different water/organic solvent mixtures over a bifunctional Ru/MnO/C catalyst under alkaline-free conditions at 60 bar H2 200 °C. In pure water, the retro-aldol takes place. However, decarbonylation epimerization are dominant reactions produce C4 C5 alditols, which limits overall selectivity (30%). When 90:10 vol % water/1,4-dioxane water/2-PrOH solutions used as solvents, product...

10.1021/acssuschemeng.7b04424 article EN ACS Sustainable Chemistry & Engineering 2018-02-05

Understanding platinum (Pt) speciation on catalysts is crucial for the design of atom-efficient materials and optimized formulations. The adsorption carbon monoxide (CO) as a probe molecule widely used to reveal Pt dispersion structures, yet assignment IR bands not straightforward, hindering determination nature surface sites or ensemble involved. CO was studied here over zirconia-supported catalyst. Specific at interface between support were highlighted, giving rise an unusual band around...

10.1021/acs.inorgchem.9b00774 article EN Inorganic Chemistry 2019-06-04

Catalysts based on molybdenum carbide or nitride nanoparticles (2-5 nm) supported titania were prepared by wet-impregnation followed a thermal treatment under alkane (methane ethane)/hydrogen nitrogen/hydrogen mixture, respectively. The samples characterized elemental analysis, volumetric adsorption of nitrogen, X-ray diffraction, and transmission electron microscopy. They evaluated for the hydrogenation CO2 in 2-3 MPa 200-300 °C ranges with gas-phase flow fixed bed reactor. CO, methane,...

10.3389/fchem.2020.00452 article EN cc-by Frontiers in Chemistry 2020-06-09
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