Literature DB >> 22865539

Production of biobutanediols by the hydrogenolysis of erythritol.

Yasushi Amada1, Hideo Watanabe, Yuichirou Hirai, Yasuteru Kajikawa, Yoshinao Nakagawa, Keiichi Tomishige.   

Abstract

The hydrogenolysis of erythritol using an Ir-ReO(x)/SiO(2) catalyst was performed for the production of butanediols, which are widely used as a raw material of polymers. The activity and selectivity to butanediols on Ir-ReO(x)/SiO(2) was much higher than that on conventional hydrogenolysis catalysts. The maximum selectivity to 1,4- and 1,3-butanediols reached 33 and 12 % at 74 % conversion, respectively. The erythritol conversion and selectivity to butanediols was almost maintained during four repeating tests if small amounts of acid were added to the reaction and the catalyst was calcined again. The reaction kinetics, reactivity trends, and characterization results indicate a direct hydrogenolysis mechanism in which the hydride species on the Ir metal surface attacks the alkoxide species on the 3D ReO(x) clusters. Based on the production of erythritol by the fermentation of glucose and glycerol, erythritol hydrogenolysis may be a promising pathway for the production of biobutanediols.
Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

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Year:  2012        PMID: 22865539     DOI: 10.1002/cssc.201200121

Source DB:  PubMed          Journal:  ChemSusChem        ISSN: 1864-5631            Impact factor:   8.928


  2 in total

1.  Complementary function of two transketolase isoforms from Moniliella megachiliensis in relation to stress response.

Authors:  Hisashi Iwata; Yosuke Kobayashi; Daiki Mizushima; Taisuke Watanabe; Jun Ogihara; Takafumi Kasumi
Journal:  AMB Express       Date:  2017-02-21       Impact factor: 3.298

Review 2.  Erythritol: Another C4 Platform Chemical in Biomass Refinery.

Authors:  Yoshinao Nakagawa; Takafumi Kasumi; Jun Ogihara; Masazumi Tamura; Takashi Arai; Keiichi Tomishige
Journal:  ACS Omega       Date:  2020-02-05
  2 in total

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