Design of Multicationic Copper‐Bearing Layered Double Hydroxides for Catalytic Application in Biorefinery

Author:

Awan Iqra Zubair123ORCID,Ho Phuoc Hoang14ORCID,Beltrami Giada5ORCID,Gimello Olinda1ORCID,Cacciaguerra Thomas1,Gaudin Pierrick1ORCID,Tanchoux Nathalie1ORCID,Albonetti Stefania2ORCID,Martucci Annalisa5ORCID,Cavani Fabrizio2ORCID,Tichit Didier1ORCID,Di Renzo Francesco1

Affiliation:

1. ICGM University of Montpellier-CNRS-ENSCM 1919 Route de Mende 34090 Montpellier France

2. Department of Industrial Chemistry “Toso Montanari” Alma Mater Studiorum Università di Bologna Viale Risorgimento, 4 40136 Bologna Italy

3. Department of Chemistry Lahore Garrison University Main Campus, Sector-C, DHA Phase VI 54000 Lahore Pakistan

4. Competence Centre for Catalysis Chalmers University of Technology Kemivägen 4 SE.412 96 Gothenburg Sweden

5. Dipartimento di Fisica e Scienze della Terra Università degli Studi di Ferrara Via Saragat, 1 44100 Ferrara Italy

Abstract

AbstractEthanol has been used as a renewable hydrogen‐donor in the conversion of a lignin model molecule in subcritical conditions. Noble metal‐free porous mixed oxides, obtained by activation of Cu−Ni−Al and Cu−Ni−Fe layered double hydroxide (LDH) precursors, have been used as heterogeneous catalysts for Meerwein‐Ponndorf‐Verley (MPV) hydrogen transfer and further hydrogenation by ethanol dehydrogenation products. Both the Cu/(Cu+Ni) ratio and the nature of the trivalent cation (Al or Fe) affect the activity of the catalysts, as well as the selectivity towards the different steps of the hydrogenation reactions and the cleavage of lignin‐like phenylether bonds. Accounting for the peculiar behaviour of Cu2+ and M(III) cations in the synthesis of LDHs, the coprecipitation of the precursors has been monitored by titration experiments. Structural and textural properties of the catalysts are closely related to the composition of the LDH precursors.

Publisher

Wiley

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

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