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Pickering Interfacial Catalysts for solvent-free biomass transformation: Physicochemical behavior of non-aqueous emulsions

Year: 2014

Journal: JOURNAL OF COLLOID AND INTERFACE SCIENCE, Vol. 427, p 80-90, 20150722

Authors: Fan, Zhaoyu; Tay, Astrid; Pera-Titus, Marc; Zhou, Wen-Juan; Benhabbari, Samy; Feng, Xiaoshuang; Malcouronne, Guillaume; Bonneviot, Laurent; De Campo, Floryan; Wang, Limin; Clacens, Jean-Marc

Organizations: E China Univ Sci & Technol, Key Lab Adv Mat, Shanghai 200237, Peoples R China; E China Univ Sci & Technol, Inst Fine Chem, Shanghai 200237, Peoples R China; CNRS Solvay, Ecoefficient Prod & Proc Lab E2P2L, UMI 3464, Shanghai 201108, Peoples R China; Ecole Normale Super Lyon, CNRS, Chem Lab, UMR 5182, F-69364 Lyon, France

A key challenge in biomass conversion is how to achieve valuable molecules with optimal reactivity in the presence of immiscible reactants. This issue is usually tackled using either organic solvents or surfactants to promote emulsification, making industrial processes expensive and not environmentally friendly. As an alternative, Pickering emulsions using solid particles with tailored designed surface properties can promote phase contact within intrinsically biphasic systems. Here we show that amphiphilic silica nano-particles bearing a proper combination of alkyl and strong acidic surface groups can generate stable Pickering emulsions of the glycerol/dodecanol system in the temperature range of 35-130 degrees C. We also show that such particles can perform as Pickering Interfacial Catalysts for the acid-catalyzed etherification of glycerol with dodecanol at 150 degrees C. Our findings shed light on some key parameters governing emulsion stability and catalytic activity of Pickering interfacial catalytic systems. This understanding is critical to pave the way toward technological solutions for biomass upgrading able to promote eco-efficient reactions between immiscible organic reagents with neither use of solvents nor surfactants. (C) 2013 Elsevier Inc. All rights reserved.