Depolymerization of Lignin in Wood with Molecular Hydrogen Iodide

نویسنده

  • Sergey M. Shevchenko
چکیده

Depolymerization of lignin in wood with hydrogen iodide in a nonpolar solvent is a selective, high-yield reaction that releases a diiodide of potential synthetic value into the solution. Finely milled wood (Douglas-fir, spruce, aspen, and sugarcane), was suspended in CDCl3 and treated with dry hydrogen iodide in a NMR tube. The yields and composition of the chloroform-soluble monomeric lignin depolymerization products, 1,3-diiodo-1-(4-hydroxyaryl)propanes, originated from guaiacyl (G), syringyl (S) and 4-hydroxyphenyl (H) units were assessed on a semi-quantitative basis. 1,3-Diiodoguaiacylpropane was the only product obtained from softwood whereas hardwood and grassy materials gave the mixtures of two (G, S) and three (G, S, H) products, respectively. This finding opens new avenues in utilization of wood wastes.

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تاریخ انتشار 2003