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Sugar alcohols such as Xylitol and Sorbitol are an abundant and renewable carbon resource obtained from plant-generated sugars and starches or – preferably – the breakdown of (hemi-)cellulose into the soluble sugars Xylose and Glucose. Already established industrial processes currently running at > 2 million tons/year allow the facile conversion of these sugar to the corresponding C5 (xylitol) and C6 (sorbitol) sugar alcohols. The linear carbon-chain structure of these sugar alcohols predisposes them for conversion to the corresponding alpha,omega-diols 1,5-pentane-diol and1,6-hexanediol, which can be directly used in polyesters (fabrics) and polyurethanes (foams) and, with further modification, in polyamides (Nylon) displacing the non-renewable fossil hydrocarbon (i.e., crude oil) based feedstocks. This goal is however contingent on developing new green chemistry that uses a catalytic process to selectively remove the oxygen atoms connected to the internal carbons in the sugar alcohols, while leaving the terminal oxygens in place.
Marcel Schlaf
Imperial College London
Physics
Education
University of Guelph
Globalink Research Award
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