Bifunctional heterogeneous catalysts from biomass and waste polysaccharides for the conversion of CO2 into cyclic carbonates. Issue 2 (9th December 2022)

• Record Type: Journal Article
• Authors: Parodi, Adriano; Vagnoni, Martina; Frontali, Lucia; Albonetti, Cristiano; De Giorgio, Francesca; Mezzi, Alessio; Petri, Elisabetta; Samorì, Chiara; Soavi, Francesca; Ruani, Giampiero; Galletti, Paola
• Is Part Of: Journal of materials chemistry. Volume 11:Issue 2(2023)
• Page Start: 775
• Page End: 788
• Publication Date: 2022-12-09
• Subjects: Materials -- Research -- Periodicals; Chemistry, Analytic -- Periodicals; Environmental sciences -- Research -- Periodicals; 543.0284
• DOI: 10.1039/d2ta05906a
• Languages: English
• ISSNs: 2050-7488

Abstract

Abstract : A four-step method was applied to biomass and waste polysaccharides, obtaining char-based bifunctional catalysts active in CO2 conversion into cyclic carbonates. Abstract : A four-step methodology for the valorization of polysaccharide-based materials into bifunctional heterogeneous catalysts, active in the conversion of CO2 and epoxides into cyclic carbonates, is presented. The synthesis protocol consists of (i) pyrolysis of the starting material to produce biochar; (ii) oxidation to increase the number of –OH and –COOH functionalities; (iii) anchoring of (3-aminopropyl)triethoxysilane (APTES) on the surface of the oxidized biochar; (iv) quaternarization of the amine groups into alkylammonium iodide salts. The versatility of the method was demonstrated by applying the same protocol to six different polysaccharidic materials and wastes: six catalysts with no appreciable differences in terms of chemical composition and catalytic activity were obtained. The bifunctionality given by –OH and ammonium iodide groups was confirmed by several analyses performed on the catalysts. An extensive characterization (elemental analysis composition, FTIR, Raman, SEM, XPS and porosimetry) was done on all the functionalized biochars for every synthetic step. The catalysts were widely investigated in their activity for the conversion of CO2 and epoxides into cyclic carbonates, demonstrating to be effective under mild conditions (3 bar of CO2 ; 70 °C; 7 h). TONs and TOFs were calculated for each catalyst and condition. Yields up to 96%, with >99% selectivity, were obtained for terminal epoxides. The recyclability of the bifunctional heterogeneous catalysts was also confirmed over five cycles.