Bio-based benzene, toluene, xylenes(BTX) can be produced starting from biomasses via several different routes, as shown in Figure 2.1 [1]. Main pathways include (i) pyrolysis or catalytic pyrolysis of lignocellulose fractions; (ii) aqueousphase reforming (APR) of aqueous carbohydrate solutions, followed by catalytic transformations; (iii) Diels–Alder reactions between furanic compounds, the latter having been obtained from monosaccharides, and ethylene; this approach has several variants, with either differently functionalized furanics or dienofile compounds; and (iv) dimerization and dehydrocyclization of bioisobutanol. The latter two pathways are aimed at the synthesis of p-xylene, whereas the former two produce mixtures of aromatics, which can be either fractionated to single compounds or used as a blend for fuels. The reaction involving the Diels–Alder reaction is not discussed here, being dealt with in the chapter devoted to reactions for C–C bond formation
Cavani, F., Albonetti, S., Basile, F. (2016). Aromatics from Biomasses: Technological Options for Chemocatalytic Transformations. Weinheim : Wiley-VCH Verlag GmbH & Co. KGaA. [10.1002/9783527698202.ch2].
Aromatics from Biomasses: Technological Options for Chemocatalytic Transformations
CAVANI, FABRIZIO;ALBONETTI, STEFANIA;BASILE, FRANCESCO
2016
Abstract
Bio-based benzene, toluene, xylenes(BTX) can be produced starting from biomasses via several different routes, as shown in Figure 2.1 [1]. Main pathways include (i) pyrolysis or catalytic pyrolysis of lignocellulose fractions; (ii) aqueousphase reforming (APR) of aqueous carbohydrate solutions, followed by catalytic transformations; (iii) Diels–Alder reactions between furanic compounds, the latter having been obtained from monosaccharides, and ethylene; this approach has several variants, with either differently functionalized furanics or dienofile compounds; and (iv) dimerization and dehydrocyclization of bioisobutanol. The latter two pathways are aimed at the synthesis of p-xylene, whereas the former two produce mixtures of aromatics, which can be either fractionated to single compounds or used as a blend for fuels. The reaction involving the Diels–Alder reaction is not discussed here, being dealt with in the chapter devoted to reactions for C–C bond formationI documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.