INCORPORATION OF PARA-CRESOL INTO LIGNINS VIA PEROXIDASE-CATALYZED COPOLYMERIZATION IN NONAQUEOUS MEDIA

被引:45
作者
POPP, JL
KIRK, TK
DORDICK, JS
机构
[1] UNIV IOWA, DEPT CHEM & BIOCHEM ENGN, IOWA CITY, IA 52242 USA
[2] US FOREST SERV, INST MICROBIAL & BIOCHEM TECHNOL, FOREST PROD LAB, MADISON, WI 53705 USA
基金
美国国家科学基金会;
关键词
HORSERADISH PEROXIDASE; LIGNIN; NONAQUEOUS MEDIA; COPOLYMERIZATION; PHENOLIC GRAFTING;
D O I
10.1016/0141-0229(91)90118-T
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Lignin, the second most abundant biopolymer after cellulose, is a low value by-product of agricultural and wood conversion processes, including wood pulp manufacture. Copolymerization with phenols has the potential to convert by-product lignins to higher-value phenolic resins. In this initial investigation, we have studied the use of horseradish peroxidase (HRP) in aqueous dioxane to catalyse the grafting of p-cresol (p-methylphenol) onto milled wood lignin, kraft lignin, and a lignin selectivity o-demethylated by a brown-rot fungus. Advantages of this system are (1) the mild reaction conditions employed and (2) the ability of HRP to function in the dioxane: water solutions which solubilize lignin. The reaction is monitored by gel permeation chromatography using a reaction system of [C-14]-p-cresol with unlabeled lignins. We have found that optimal incorporation of cresol into high-molecular-weight polymer occurs at 50-70% dioxane in water under the conditions used; a maximum incorporation of ca. 4 mol% (e.g., p-cresol incorporated per C-9 lignin unit) was obtained. Blocking the phenolic hydroxyl groups of the lignin inhibits copolymerization, consistent with the proposed mechanism of phenoxy radical copolymerization for this reaction.
引用
收藏
页码:964 / 968
页数:5
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