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OXIDATIVE DEGRADATION OF LIGNIN BY PHOTOCHEMICAL AND CHEMICAL RADICAL GENERATING SYSTEMS
Author(s) -
Gold Michael H.,
Kutsuki Hidetoshi,
Morgan Meredith A.
Publication year - 1983
Publication title -
photochemistry and photobiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.818
H-Index - 131
eISSN - 1751-1097
pISSN - 0031-8655
DOI - 10.1111/j.1751-1097.1983.tb03595.x
Subject(s) - lignin , chemistry , degradation (telecommunications) , reagent , hydroxyl radical , hydrogen peroxide , photochemistry , biopolymer , ring (chemistry) , sephadex , oxidative phosphorylation , organic chemistry , radical , polymer , biochemistry , telecommunications , computer science , enzyme
— Oxidation of specifically radiolabeled 14 C‐lignins by UV/H 2 0 2 . Fenton's reagent, photosesitizing riboflavin. UV‐ and γ‐irradiation was examined. In the presence of UV/H 2 O 2 , a hydroxyl radical (·OH) generating system. 14 C‐methoxy. 2‐[ 14 C‐sidechain] and 14 C‐ring labeled lignin were rapidly and extensively degraded as measured by gel filtration of the reaction products on Sephadex LH‐20. This suggested that exposure to OH leads to rapid, nonspecific lignin degradation. Rapid degradation of 14C‐methoxy, 2‐[ 14 C‐sidechain] and 14 C‐ring labeled lignin also occurred in the presence of the ·OH generating system, Fenton's reagent, confirming the primary role of ·OH in these reactions. Photosensitizing riboflavin, also capable of effecting transformation of organic compounds via Type I hydrogen radical abstractions, caused extensive oxidative degradation of 14 C‐methoxy labeled lignin and significant degradation of 2‐( 14 C‐sidechain] and 14 C‐ring labeled lignin. In addition, UV‐ and γ‐irradiation caused slower but extensive degradation of the polymers, probably via radical type mechanisms. All of these results indicate that ·OH as well as organic radical generating systems are effective agents for the purpose of degrading this heterogeneous, optically inactive and random biopolymer.