4.8 Article

Oxidation of Lignin Using Aqueous Polyoxometalates in the Presence of Alcohols

Journal

CHEMSUSCHEM
Volume 1, Issue 8-9, Pages 763-769

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/cssc.200800050

Keywords

alcohols; lignin; oxidation; polyoxometalates; reactive intermediates

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A novel approach has been developed in order to use Kraft lignin as a renewable resource for the production of chemicals. The concept is based on the use of polyoxometalates as reversible oxidants and on the use of radical scavengers, which prevent lignin fragments from repolymerizing. The oxidation of Kraft lignin, which is a potential source of functionalized phenols, by H(3)PMo(12)O(40) in water yields a relatively small amount of monomeric species detected by GC-MS. The addition of methanol to the reaction resulted in on increase in the yield of monomeric products by a factor of up to 15. Vanillin and methyl vanillate are the main products obtained, in a maximum yield of 5 wt% based on dry Kraft lignin. Methanol plays a decisive role in the prevention of repolymerization by reducing lignin-lignin condensation reactions. Furthermore, it is proposed that methanol generates small amounts of (center dot)CH(3) and CH(3)O(center dot) radicals through the acid-catalyzed formation of dimethyl ether which couple with lignin fragments.

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