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Hybrid Organic–Inorganic Anatase as a Bifunctional Catalyst for Enhanced Production of 5‐Hydroxymethylfurfural from Glucose in Water
Author(s) -
Lanziano Carlos A. S.,
Moya Silvia F.,
Barrett Dean. H.,
TeixeiraNeto Erico,
Guirardello Reginaldo,
de Souto da Silva Felipe,
Rinaldi Roberto,
Rodella Cristiane B.
Publication year - 2018
Publication title -
chemsuschem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.412
H-Index - 157
eISSN - 1864-564X
pISSN - 1864-5631
DOI - 10.1002/cssc.201702354
Subject(s) - catalysis , anatase , chemistry , bifunctional , citric acid , lewis acids and bases , calcination , hybrid material , gluconic acid , hydrothermal synthesis , fructose , inorganic chemistry , heterogeneous catalysis , chemical engineering , hydrothermal circulation , organic chemistry , photocatalysis , engineering
Hybrid organic–inorganic anatase (hybrid‐TiO 2 ) is prepared by a facile hydrothermal synthesis method employing citric acid. The synthetic approach results in a high surface‐area nanocrystalline anatase polymorph of TiO 2 . The uncalcined hybrid‐TiO 2 is directly studied as a catalyst for the conversion of glucose into 5‐hydroxymethylfurfural (HMF). In the presence of the hybrid‐TiO 2 , HMF yields up to 45 % at glucose conversions up to 75 % were achieved in water at 130 °C in a monophasic batch reactor. As identified by Ti K‐edge XANES, hybrid‐TiO 2 contains a large fraction of fivefold coordinatively unsaturated Ti IV sites, which act as the Lewis acid catalyst for the conversion of glucose into fructose. As citric acid is anchored in the structure of hybrid‐TiO 2 , carboxylate groups seem to catalyze the sequential conversion of fructose into HMF. The fate of citric acid bound to anatase and the Ti IV Lewis acid sites throughout recycling experiments is also investigated. In a broader context, this contribution outlines the importance of hydrothermal synthesis for the creation of water‐resistant Lewis acid sites for the conversion of sugars. Importantly, the use of the hybrid‐TiO 2 with no calcination step contributes to dramatically decreasing the energy consumption in the catalyst preparation.