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3. Catalytic Applications in the Production of Hydrotreated Vegetable Oil (HVO) as a Renewable Fuel: A Review.

Author

Mussa, Nur-Sultan, Toshtay, Kainaubek, and Capron, Mickael

Subjects
TRANSITION metal catalysts, VEGETABLE oils, ALTERNATIVE fuels, PRECIOUS metals, TRANSITION metals
Abstract

The significance and challenges of hydrotreatment processes for vegetable oils have recently become apparent, encompassing various reactions like decarbonylation, decarboxylation, and hydrogenation. Heterogeneous noble or transition metal catalysts play a crucial role in these reactions, offering high selectivity in removing oxygen and yielding desired hydrocarbons. Notably, both sulphided and non-sulphided catalysts exhibit effectiveness, with the latter gaining attention due to health and toxicity concerns associated with sulphiding agents. Nickel-based catalysts, such as NiP and NiC, demonstrate specific properties and tendencies in deoxygenation reactions, while palladium supported on activated carbon catalysts shows superior activity in hydrodeoxygenation. Comparisons between the performances of different catalysts in various hydrotreatment processes underscore the need for tailored approaches. Transition metal phosphides (TMP) emerge as promising catalysts due to their cost-effectiveness and environmental friendliness. Ultimately, there is an ongoing pursuit of efficient catalysts and the importance of further advancements in catalysis for the future of vegetable oil hydrotreatment. [ABSTRACT FROM AUTHOR]

Published
2024
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7. Preparation and isolation of mono-Nb substituted Keggin-type phosphomolybdic acid and its application as an oxidation catalyst for isobutylaldehyde and Wacker-type oxidation.

Author

Matono, Takashi, Ueno, Shinsuke, Kato, Yuki, Umehara, Naoya, Lang, Zhongling, Li, Yangguang, Ninomiya, Wataru, Elhallal, Maher, Gonzales-Yañez, Edgar Osiris, Capron, Mickael, Ishikawa, Satoshi, Ueda, Wataru, Sano, Tsuneji, and Sadakane, Masahiro

Subjects
PHOSPHOMOLYBDIC acid, CATALYTIC activity, OXIDATION, POTASSIUM salts, CATALYSTS, PALLADIUM catalysts, FREEZE-drying, PHENYL ethers
Abstract

The potassium and proton mixed salt of mono-Nb substituted Keggin-type phosphomolybdate, KH3[PMo11NbO40], was isolated in a pure form by reacting Keggin-type phosphomolybdic acid (H3[PMo12O40]) and potassium hexaniobate (K8Nb6O19) in water, followed by freeze-drying. The all protonic form, H4[PMo11NbO40], was isolated via proton exchange with H-resin and subsequent freeze-drying. The most crucial factor to isolate KH3[PMo11NbO40] and H4[PMo11NbO40] in pure forms is the evaporation of water using the freeze-drying method. Using a similar procedure, the potassium salt of the di-Nb substituted compound K5[PMo10Nb2O40] was isolated. H4[PMo11NbO40] exhibited high catalytic activity for oxidizing isobutylaldehyde to methacrolein and moderate catalytic activity for the Wacker-type oxidation of allyl phenyl ether when combined with Pd(OAc)2. [ABSTRACT FROM AUTHOR]

Published
2023
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8. Valorisation of Light Alcohols ex-Biomass: Some Examples

Author

Tavera, C. P., Thavornprasert, K.-A., Deng, J., Pomalaza, G., Borowiek, A., Elroz Soraya Zaid, A., Aparicio, J., Ordomsky, Vitaly, Araque Marin, Marcia-Carolina, Skrzynska, E., Dumeignil, Franck, Capron, Mickael, Unité de Catalyse et Chimie du Solide - UMR 8181 (UCCS), and Université d'Artois (UA)-Centrale Lille-Institut de Chimie du CNRS (INC)-Université de Lille-Centre National de la Recherche Scientifique (CNRS)

Subjects
[CHIM]Chemical Sciences
Abstract

International audience

Published
2023

20. Glycerol Valorization in Liquid Phase for the Production of Glycolic Acid

Author

Capron, Mickael, Gonzales, E. O., Patricia Tavera Ruiz, C., Zaïd, S., Girardon, Jean-Sébastien, Skrzynska, E., Dumeignil, Franck, Aparicio, J., Unité de Catalyse et Chimie du Solide - UMR 8181 (UCCS), and Université d'Artois (UA)-Centrale Lille-Institut de Chimie du CNRS (INC)-Université de Lille-Centre National de la Recherche Scientifique (CNRS)

Subjects
[CHIM]Chemical Sciences
Abstract

International audience

Published
2022

22. Halogenated Ti3C2 MXenes Prepared by Microwave Molten Salt for Hg0 Photo‐Oxidation.

Author

Xie, Cheng, Xu, Lei, Peng, Jinhui, Zhang, Libo, Wang, Xueqian, Deng, Jianying, Capron, Mickael, and Ordomsky, Vitaly

Subjects
ELECTRON work function, FUSED salts, CONDUCTION bands, MICROWAVES, BAND gaps
Abstract

Ti3C2 MXenes with different halogen modifications are prepared rapidly and efficiently by microwave molten salt method, and the MXene surface functional group modification is successfully achieved to address the problems of low purity, complex functional groups, and uncontrollable energy band structure of MXenes obtained by traditional liquid phase etching. Among them, the modification of the iodine (I) functional group onto the surface of Ti3C2 changes the energy band structure and band gap, resulting in easier photoexcitation and more photogenerated carriers. The increased Fermi energy is closer to the conduction band, the decreased surface work function weakens the electron confinement ability. The photogenerated carriers can migrate to the surface of the material more easily with extended lifetime, so the activity of the catalyst is improved. Further, for gaseous monomeric mercury (Hg0) photo‐oxidative removal, Ti3C2‐I2 exhibits 85.5% efficiency of Hg0 photo‐oxidative removal under visible light. Based on the experimental characterization and density functional theory calculations, a mechanism for the photo‐oxidative removal of Hg° from Ti3C2‐I2 MXene is proposed, which provides a valuable strategy for studying Ti3C2 MXenes in the field of photocatalysis. [ABSTRACT FROM AUTHOR]

Published
2023
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29. Carbon-based catalysts for Fischer–Tropsch synthesis

Author

Ordomsky, Vitaly, Wang, Qiyan, Zhou, Wen-Juan, Heyte, Svetlana, Thuriot-Roukos, Joëlle, Marinova, Maya, Addad, Ahmed, Rouzière, Stéphan, Simon, Pardis, Capron, Mickael, Zhang, Linjie, Grimaud, Alexis, Schwiedernoch, Renate, Hernández, Willinton Yesid, Naghavi, Negar, Pedrolo, Débora, Schwaab, Marcio, Marcilio, Nilson, Khodakov, Andrei, Santos, Sara, Urbina-Blanco, César, Zhou, Wenjuan, Yang, Yong, Joelle, Thuriot-Roukos, Ersen, Ovidiu, Baaziz, Walid, Safonova, Olga, Saeys, Mark, Gu, Bang, Peron, Deizi, Barrios, Alan, Virginie, Mirella, La Fontaine, Camille, Briois, Valérie, Vorokhta, Mykhailo, Šmíd, Břetislav, Moldovan, Simona, Koneti, Siddardha, Gambu, Thobani, Hernández, Willinton, Impéror-Clerc, Marianne, Vovk, Evgeny, Wu, Dan, Nuns, Nicolas, Palčić, Ana, Jaén, Sara Navarro, Cai, Mengdie, Liu, Chong, Pidko, Evgeny, Valtchev, Valentin, Yan, Zhen, Zhang, Songwei, Li, Jerry Pui Ho, Zhao, Jingpeng, Yuan, Biao, He, Tao, Yu, Yi, Li, Tao, Hu, Di, Chen, Yanping, Wei, Jiatong, Duyar, Melis, Liu, Jian, Dalian Institute of Chemical Physics - Chinese Academy of Sciences, University of Surrey (UNIS), Unité de Catalyse et Chimie du Solide - UMR 8181 (UCCS), Université d'Artois (UA)-Centrale Lille-Institut de Chimie du CNRS (INC)-Université de Lille-Centre National de la Recherche Scientifique (CNRS), ANR-16-CE06-0013,NANO4FuT,Synthèse des carburants alternatifs et des molécules plateforme sur nanoréacteurs(2016), CNRS, Centrale Lille, ENSCL, Univ. Artois, Université de Lille, Unité de Catalyse et Chimie du Solide (UCCS) - UMR 8181, Ordomsky, Vitaly, Centrale Lille Institut (CLIL)-Université d'Artois (UA)-Centrale Lille-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Université de Lille, Eco-Efficient Products &Processes Laboratory (E2PL2), Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)-RHODIA, Laboratoire de Chimie - UMR5182 (LC), Centre National de la Recherche Scientifique (CNRS)-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-École normale supérieure - Lyon (ENS Lyon)-Institut de Chimie du CNRS (INC), Institut Michel Eugène Chevreul - FR 2638 (IMEC), Université d'Artois (UA)-Institut de Chimie du CNRS (INC)-Université de Lille-Centre National de la Recherche Scientifique (CNRS)-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE)-Centrale Lille Institut (CLIL), Unité Matériaux et Transformations - UMR 8207 (UMET), Institut de Chimie du CNRS (INC)-Institut National de la Recherche Agronomique (INRA)-Centre National de la Recherche Scientifique (CNRS)-Université de Lille-Ecole Nationale Supérieure de Chimie de Lille (ENSCL), Laboratoire de Physique des Solides (LPS), Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS), Chimie du solide et de l'énergie (CSE), Collège de France (CdF (institution))-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Solvay (France), Instituto Federal do Rio Grande do Sul (IFRS), Institut de Physique et Chimie des Matériaux de Strasbourg (IPCMS), Université de Strasbourg (UNISTRA)-Matériaux et nanosciences d'Alsace (FMNGE), Institut de Chimie du CNRS (INC)-Université de Strasbourg (UNISTRA)-Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Université de Strasbourg (UNISTRA)-Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Centre National de la Recherche Scientifique (CNRS)-Réseau nanophotonique et optique, Centre National de la Recherche Scientifique (CNRS)-Université de Strasbourg (UNISTRA)-Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Centre National de la Recherche Scientifique (CNRS)-Université de Strasbourg (UNISTRA), Institut de chimie et procédés pour l'énergie, l'environnement et la santé (ICPEES), Institut de Chimie du CNRS (INC)-Université de Strasbourg (UNISTRA)-Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Université de Strasbourg (UNISTRA)-Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Centre National de la Recherche Scientifique (CNRS), Paul Scherrer Institute (PSI), Synchrotron SOLEIL (SSOLEIL), Centre National de la Recherche Scientifique (CNRS), Charles University [Prague] (CU), Groupe de physique des matériaux (GPM), Centre National de la Recherche Scientifique (CNRS)-Institut national des sciences appliquées Rouen Normandie (INSA Rouen Normandie), Institut National des Sciences Appliquées (INSA)-Normandie Université (NU)-Institut National des Sciences Appliquées (INSA)-Normandie Université (NU)-Université de Rouen Normandie (UNIROUEN), Normandie Université (NU), Ruđer Bošković Institute (IRB), Delft University of Technology (TU Delft), Laboratoire catalyse et spectrochimie (LCS), Centre National de la Recherche Scientifique (CNRS)-École Nationale Supérieure d'Ingénieurs de Caen (ENSICAEN), Normandie Université (NU)-Normandie Université (NU)-Institut de Chimie du CNRS (INC)-Université de Caen Normandie (UNICAEN), ShanghaiTech University [Shanghai], Beihang University (BUAA), School of Physics Science and Engineering, Tongji University, Université de Strasbourg (UNISTRA)-Centre National de la Recherche Scientifique (CNRS)-Matériaux et nanosciences d'Alsace (FMNGE), Institut de Chimie du CNRS (INC)-Université de Strasbourg (UNISTRA)-Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Université de Strasbourg (UNISTRA)-Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Réseau nanophotonique et optique, Université de Strasbourg (UNISTRA)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)-Matériaux et nanosciences d'Alsace (FMNGE), Institut de Chimie du CNRS (INC)-Université de Strasbourg (UNISTRA)-Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Université de Strasbourg (UNISTRA)-Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Université d'Artois (UA)-Centrale Lille-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Université de Lille, Eco-Efficient Products & Processes Laboratory (E2P2L), RHODIA-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS), and Centre National de la Recherche Scientifique (CNRS)-Collège de France (CdF (institution))-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)

Subjects
Materials science, chemistry.chemical_element, 02 engineering and technology, Carbon nanotube, 010402 general chemistry, 01 natural sciences, 7. Clean energy, law.invention, Catalysis, law, [CHIM] Chemical Sciences, medicine, [CHIM]Chemical Sciences, Coal, Gasoline, Carbon nanofiber, business.industry, Fischer–Tropsch process, General Chemistry, 021001 nanoscience & nanotechnology, 0104 chemical sciences, Chemical engineering, chemistry, 0210 nano-technology, business, Carbon, Activated carbon, medicine.drug
Abstract

International audience; Fischer-Tropsch synthesis (FTS) is an essential approach to convert coal, biomass, and shale gas into fuels and chemicals, such as lower olefins, gasoline, diesel, and so on. In recent years, there has been increasing motivation to deploy FTS at commercial scales which has been boosting the discovery of high performance catalysts. In particular, the importance of support in modulating the activity of metals has been recognized and carbonaceous materials have attracted attention as supports for FTS. In this review, we summarised the substantial progress in the preparation of carbon-based catalysts for FTS by applying activated carbon (AC), carbon nanotubes (CNTs), carbon nanofibers (CNFs), carbon spheres (CSs), and metal-organic frameworks (MOFs) derived carbonaceous materials as supports. A general assessment of carbon-based catalysts for FTS, concerning the support and metal properties, activity and products selectivity, and their interactions is systematically discussed. Finally, current challenges and future trends in the development of carbon-based catalysts for commercial utilization in FTS are proposed.

Published
2021

31. Valorisation de la Biomasse : Catalyse & ‘Bio-Raffineries’, l’exemple du concept EuroBioRef

Author

Pomalaza, Guillaume, Capron, Mickael, Dumeignil, Franck, Unité de Catalyse et Chimie du Solide - UMR 8181 (UCCS), Centrale Lille Institut (CLIL)-Université d'Artois (UA)-Centrale Lille-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Université de Lille, Université de Lille, LillOA, and Université d'Artois (UA)-Centrale Lille-Institut de Chimie du CNRS (INC)-Université de Lille-Centre National de la Recherche Scientifique (CNRS)

Subjects
[CHIM.CATA] Chemical Sciences/Catalysis, [CHIM.CATA]Chemical Sciences/Catalysis, ComputingMilieux_MISCELLANEOUS
Abstract

National audience

Published
2020

32. METHOD FOR OXIDATION OF ALCOHOL

Author

Ordomsky, Vitaly, Zhao, Jingpeng, Hernández, Willinton Yesid, Capron, Mickael, Unité de Catalyse et Chimie du Solide - UMR 8181 (UCCS), Centrale Lille Institut (CLIL)-Université d'Artois (UA)-Centrale Lille-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Université de Lille, Solvay (France), and Université d'Artois (UA)-Centrale Lille-Institut de Chimie du CNRS (INC)-Université de Lille-Centre National de la Recherche Scientifique (CNRS)

Subjects
[CHIM]Chemical Sciences
Published
2019

33. Procédé d'oxydation d'alcool

Author

Zhao, Jingpeng, V., Ordomsky, Hernández, Willinton Yesid, Zhou, Wen-Juan, Capron, Mickael, Streiff, Stéphane, Unité de Catalyse et Chimie du Solide - UMR 8181 (UCCS), and Université d'Artois (UA)-Centrale Lille-Institut de Chimie du CNRS (INC)-Université de Lille-Centre National de la Recherche Scientifique (CNRS)

Subjects
[CHIM.CATA]Chemical Sciences/Catalysis
Abstract

Disclosed is a method for the oxidation of an alcohol comprising contacting the alcohol with O 2 in the presence of a catalyst. Furthermore disclosed is the use of free metallic ruthenium nanoparticles as catalyst for the oxidation of an alcohol with O 2. Additionally, disclosed is a method of preparing metallic ruthenium nanoparticles of controllable size.; L'invention concerne un procédé d'oxydation d'un alcool consistant à mettre en contact un alcool avec du O 2 en présence d'un catalyseur. L'invention concerne en outre l'utilisation de nanoparticules de ruthénium métalliques libres en tant que catalyseur pour l'oxydation d'un alcool avec O 2. De plus, l'invention concerne un procédé de préparation de nanoparticules métalliques de ruthénium de taille apte à être contrôlée.

Published
2019

34. Oxydation sélective d'alcools

Author

Zhao, Jingpeng, V., Ordomsky, Hernandez, Willinton Yesid, Zhou, Wen-Juan, Capron, Mickael, Streiff, Stéphane, Unité de Catalyse et Chimie du Solide - UMR 8181 (UCCS), and Université d'Artois (UA)-Centrale Lille-Institut de Chimie du CNRS (INC)-Université de Lille-Centre National de la Recherche Scientifique (CNRS)

Subjects
[CHIM.CATA]Chemical Sciences/Catalysis
Abstract

Disclosed is a catalyst system exhibiting high activity and selectivity in the oxidation of alcohols to aldehydes or ketones using molecular oxygen as a terminal oxidant. Such catalyst system comprises quinone-type compound and is particularly useful for, but not limited to, the oxidation of primary or secondary aliphatic and aromatic alcohols to the respective aldehydes or ketones. Also disclosed is a process for oxidizing said alcohols to the respective aldehydes or ketones.; L'invention concerne un système catalyseur présentant une activité et une sélectivité élevées dans l'oxydation d'alcools en aldéhydes ou cétones à l'aide d'oxygène moléculaire en tant qu'oxydant terminal. Un tel système de catalyseur comprend un composé de type quinone et est particulièrement utile pour, mais sans y être limité, l'oxydation d'alcools aliphatiques et aromatiques primaires ou secondaires en aldéhydes ou cétones respectifs. L'invention concerne également un procédé d'oxydation desdits alcools en aldéhydes ou cétones respectifs.

Published
2019

38. Selective Oxidation of Alcohols to Carbonyl Compounds over Small Size Colloidal Ru Nanoparticles

Author

V., Ordomsky, Ordomskiy, Vitaly, Zhao, Jingpeng, Hernández, Willinton, Zhou, Wenjuan, Yang, Yong, Vovk, Evgeny, Capron, Mickael, Ordomsky, Vitaly, Eco-Efficient Products &Processes Laboratory (E2PL2), Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)-RHODIA, Unité de Catalyse et Chimie du Solide - UMR 8181 (UCCS), Centrale Lille Institut (CLIL)-Université d'Artois (UA)-Centrale Lille-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Université de Lille, Centre National de la Recherche Scientifique (CNRS), Faculty of Animal Husbandry and Veterinary Medicine, Shenyang Agricultural University, Eco-Efficient Products & Processes Laboratory (E2P2L), RHODIA-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS), and Université d'Artois (UA)-Centrale Lille-Institut de Chimie du CNRS (INC)-Université de Lille-Centre National de la Recherche Scientifique (CNRS)

Subjects
chemistry.chemical_classification, 010405 organic chemistry, Chemistry, Organic Chemistry, chemistry.chemical_element, Nanoparticle, [CHIM.CATA]Chemical Sciences/Catalysis, 010402 general chemistry, Photochemistry, 01 natural sciences, Aldehyde, Catalysis, 0104 chemical sciences, Ruthenium, Inorganic Chemistry, Colloid, X-ray photoelectron spectroscopy, Alcohol oxidation, Physical and Theoretical Chemistry, Selectivity, ComputingMilieux_MISCELLANEOUS
Abstract

The selective oxidation of alcohols to corresponding aldehydes is one of the most challenging problems in modern chemistry due to over-oxidation of these products further into corresponding acids and esters. Herein, we report an efficient and eco-friendly method for selective oxidation of aliphatic, unsaturated and aromatic alcohols to aldehydes (>90 %) using small size (2 nm) non-supported colloidal Ru nanoparticles. The selectivity rapidly decreases with increase of the size of nanoparticles (from 2 to 10 nm) or after their deposition over support. X-ray photoelectron spectroscopy suggests that this catalytic performance can be attributed to high content Ru-O species on the surface of small size Ru nanoparticles, which undergo reduction with formation of water and aldehyde and easy oxidation cycles during the reaction according to the Mars-van Krevelen mechanism. The presence of surface oxide layer over small size Ru nanoparticles suppresses over-oxidation of aldehydes to acids.

Published
2019

39. Metallic Ru Size Effect in Selective Oxidation of Alcohols to Carbonyl Compounds

Author

Zhao, Jingpeng, V., Ordomsky, Capron, Mickael, Enciso, Yecid, Zhou, Wenjuan, Unité de Catalyse et Chimie du Solide - UMR 8181 (UCCS), Université d'Artois (UA)-Centrale Lille-Institut de Chimie du CNRS (INC)-Université de Lille-Centre National de la Recherche Scientifique (CNRS), and Centrale Lille Institut (CLIL)-Université d'Artois (UA)-Centrale Lille-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Université de Lille

Subjects
[CHIM.CATA]Chemical Sciences/Catalysis, ComputingMilieux_MISCELLANEOUS
Abstract

International audience

Published
2019

40. Production of glycolic acid from liquid phase glycerol oxidation: Comparison of batch and continuous process

Author

Tavera Ruiz, Claudia, Capron, Mickael, Skrzyńska, Elżbieta, Dumeignil, Franck, Unité de Catalyse et Chimie du Solide - UMR 8181 (UCCS), Centrale Lille Institut (CLIL)-Université d'Artois (UA)-Centrale Lille-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Université de Lille, and Université d'Artois (UA)-Centrale Lille-Institut de Chimie du CNRS (INC)-Université de Lille-Centre National de la Recherche Scientifique (CNRS)

Subjects
[CHIM.CATA]Chemical Sciences/Catalysis, ComputingMilieux_MISCELLANEOUS
Abstract

International audience

Published
2019

41. Esterification of glycolic acid with propanol, butanol and octanolover homogeneous and heterogeneous catalyst

Author

Aparicio, Juliana, Nikitine, Clemence, Mutschler, Carole, Araque Marin, Marcia-Carolina, Fongarland, Pascal, Capron, Mickael, Unité de Catalyse et Chimie du Solide - UMR 8181 (UCCS), Centrale Lille Institut (CLIL)-Université d'Artois (UA)-Centrale Lille-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Université de Lille, and Université d'Artois (UA)-Centrale Lille-Institut de Chimie du CNRS (INC)-Université de Lille-Centre National de la Recherche Scientifique (CNRS)

Subjects
[CHIM.CATA]Chemical Sciences/Catalysis, ComputingMilieux_MISCELLANEOUS
Abstract

International audience

Published
2019

42. Liquid phase glycerol oxidation: Choice of the catalysts and the ad-hoc reaction conditions for the right target molecule

Author

El Roz, Ayman, Tavera Ruiz, Claudia, Zaid, Soraya, Skrzyńska, Elżbieta, Dumeignil, Franck, Capron, Mickael, Unité de Catalyse et Chimie du Solide - UMR 8181 (UCCS), Université d'Artois (UA)-Centrale Lille-Institut de Chimie du CNRS (INC)-Université de Lille-Centre National de la Recherche Scientifique (CNRS), and Centrale Lille Institut (CLIL)-Université d'Artois (UA)-Centrale Lille-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Université de Lille

Subjects
[CHIM.CATA]Chemical Sciences/Catalysis, ComputingMilieux_MISCELLANEOUS
Abstract

International audience

Published
2019

43. Kinetic Study and Modeling of Glycerol Oxidation on a Commercial Supported Gold Catalyst

Author

Pomolaza, Guillaume, Capron, Mickael, Dumeignil, Franck, Unité de Catalyse et Chimie du Solide - UMR 8181 (UCCS), Centrale Lille Institut (CLIL)-Université d'Artois (UA)-Centrale Lille-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Université de Lille, and Université d'Artois (UA)-Centrale Lille-Institut de Chimie du CNRS (INC)-Université de Lille-Centre National de la Recherche Scientifique (CNRS)

Subjects
[CHIM.CATA]Chemical Sciences/Catalysis, ComputingMilieux_MISCELLANEOUS
Abstract

International audience

Published
2019

44. Hybrid Catalysis: Combining Bio- and Chemo-Catalysis for Biosourced Substrates Upgrading

Author

Dumeignil, Franck, Gimbernat, Alexandra, Guehl, Marie, Capron, Mickael, Lopes Ferreira, Nicolas, Froidevaux, Rénato, Girardon, Jean-Sébastien, Dhulster, Pascal, Delcroix, Damien, Unité de Catalyse et Chimie du Solide - UMR 8181 (UCCS), Université d'Artois (UA)-Centrale Lille-Institut de Chimie du CNRS (INC)-Université de Lille-Centre National de la Recherche Scientifique (CNRS), Institut Charles Viollette (ICV) - EA 7394 (ICV), Université d'Artois (UA)-Institut National de la Recherche Agronomique (INRA)-Université du Littoral Côte d'Opale (ULCO)-Institut Supérieur d'Agriculture-Université de Lille, and IFP Energies nouvelles (IFPEN)

Subjects
[CHIM.CATA]Chemical Sciences/Catalysis, ComputingMilieux_MISCELLANEOUS
Abstract

National audience

Published
2019

45. Hybrid Catalysis: Novel Concept for Upgrading Biosourced Substrates

Author

Dumeignil, Franck, Gimbernat, Alexandra, Guehl, Marie, Capron, Mickael, Lopes Ferreira, Nicolas, Froidevaux, Rénato, Girardon, Jean-Sébastien, Dhulster, Pascal, Delcroix, Damien, Unité de Catalyse et Chimie du Solide - UMR 8181 (UCCS), Université d'Artois (UA)-Centrale Lille-Institut de Chimie du CNRS (INC)-Université de Lille-Centre National de la Recherche Scientifique (CNRS), Institut Charles Viollette (ICV) - EA 7394 (ICV), Université d'Artois (UA)-Institut National de la Recherche Agronomique (INRA)-Université du Littoral Côte d'Opale (ULCO)-Institut Supérieur d'Agriculture-Université de Lille, IFP Energies nouvelles (IFPEN), and Centrale Lille Institut (CLIL)-Université d'Artois (UA)-Centrale Lille-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Université de Lille

Subjects
[CHIM.CATA]Chemical Sciences/Catalysis, ComputingMilieux_MISCELLANEOUS
Abstract

International audience

Published
2019

47. Hybrid Catalysis as an Innovative Way for Upgrading Biosourced Substrates

Author

Pomalaza, Guillaume, Capron, Mickael, Dumeignil, Franck, Unité de Catalyse et Chimie du Solide - UMR 8181 (UCCS), and Université d'Artois (UA)-Centrale Lille-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Université de Lille

Subjects
[CHIM.CATA]Chemical Sciences/Catalysis, ComputingMilieux_MISCELLANEOUS
Abstract

International audience

Published
2018

48. Hybrid Catalysis as an Innovative Way for Upgrading Biosourced Substrates

Author

Dumeignil, Franck, Gimbernat, Alexandra, Guehl, Marie, Capron, Mickael, Lopes Ferreira, Nicolas, Froidevaux, Rénato, Girardon, Jean-Sébastien, Dhulster, Pascal, Delcroix, Damien, Unité de Catalyse et Chimie du Solide - UMR 8181 (UCCS), Université d'Artois (UA)-Centrale Lille-Institut de Chimie du CNRS (INC)-Université de Lille-Centre National de la Recherche Scientifique (CNRS), Institut Charles Viollette (ICV) - EA 7394 (ICV), Université d'Artois (UA)-Institut National de la Recherche Agronomique (INRA)-Université du Littoral Côte d'Opale (ULCO)-Institut Supérieur d'Agriculture-Université de Lille, and IFP Energies nouvelles (IFPEN)

Subjects
[CHIM.CATA]Chemical Sciences/Catalysis, ComputingMilieux_MISCELLANEOUS
Abstract

International audience

Published
2018

49. Hybrid catalysis as the next challenge in biorefineries: concept and examples

Author

Dumeignil, Franck, Gimbernat, Alexandra, Guehl, Marie, Capron, Mickael, Lopes Ferreira, Nicolas, Froidevaux, Rénato, Girardon, Jean-Sébastien, Dhulster, Pascal, Delcroix, Damien, Unité de Catalyse et Chimie du Solide - UMR 8181 (UCCS), Université d'Artois (UA)-Centrale Lille-Institut de Chimie du CNRS (INC)-Université de Lille-Centre National de la Recherche Scientifique (CNRS), Institut Charles Viollette (ICV) - EA 7394 (ICV), Université d'Artois (UA)-Institut National de la Recherche Agronomique (INRA)-Université du Littoral Côte d'Opale (ULCO)-Institut Supérieur d'Agriculture-Université de Lille, and IFP Energies nouvelles (IFPEN)

Subjects
[CHIM.CATA]Chemical Sciences/Catalysis, ComputingMilieux_MISCELLANEOUS
Abstract

International audience

Published
2018

50. Catalytic Deoxydehydration of Glycerol to Allyl Alcohol – a Promising Pathway to a High-Versatile Platform Molecule

Author

Pomalaza, Guillaume, Capron, Mickael, Dumeignil, Franck, Unité de Catalyse et Chimie du Solide - UMR 8181 (UCCS), Centrale Lille Institut (CLIL)-Université d'Artois (UA)-Centrale Lille-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Université de Lille, and Université d'Artois (UA)-Centrale Lille-Institut de Chimie du CNRS (INC)-Université de Lille-Centre National de la Recherche Scientifique (CNRS)

Subjects
[CHIM.CATA]Chemical Sciences/Catalysis, ComputingMilieux_MISCELLANEOUS
Abstract

International audience

Published
2018

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