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Cited by 232

The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.

Oxidative Depolymerization of Lignin in Ionic Liquids

Stärk, Kerstin, Taccardi, Nicola, Bösmann, Andreas, Wasserscheid, Peter·2010·ChemSusChem

Abstract

Beech lignin was oxidatively cleaved in ionic liquids to give phenols, unsaturated propylaromatics, and aromatic aldehydes. A multiparallel batch reactor system was used to screen different ionic liquids and metal catalysts. Mn(NO 3)2 in 1‐ethyl‐3‐methylimidazolium trifluoromethanesulfonate [EMIM][CF 3 SO 3] proved to be the most effective reaction system. A larger scale batch reaction with this system in a 300 mL autoclave (11 g lignin starting material) resulted in a maximum conversion of 66.3 % (24 h at 100 °C, 84×10 5 Pa air). By adjusting the reaction conditions and catalyst loading, the selectivity of the process could be shifted from syringaldehyde as the predominant product to 2,6‐dimethoxy‐1,4‐benzoquinone (DMBQ). Surprisingly, the latter could be isolated as a pure substance in 11.5 wt % overall yield by a simple extraction/crystallization process.

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Metadata

Authors
Stärk, K., Taccardi, N., Bösmann, A., & Wasserscheid, P.
Venue
ChemSusChem
Publisher
Wiley
Published
2010-06-11
Volume
3
Issue
6
Pages
719-723
ISSN
  • 1864-5631 (ISSN-L)
  • 1864-564X
OpenAlex
W2003257483
Cited by
232
References
2
FWCI
5.83
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Oxidative Depolymerization of Lignin in Ionic Liquids. https://app.cochat.ai/papers/10.1002/cssc.200900242
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Stärk, K., Taccardi, N., Bösmann, A., & Wasserscheid, P. (2010). Oxidative Depolymerization of Lignin in Ionic Liquids. ChemSusChem. https://doi.org/10.1002/cssc.200900242

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