Depolymerization of cellouronic acid during TEMPO-mediated oxidation

被引:165
作者
Shibata, I [1 ]
Isogai, A [1 ]
机构
[1] Univ Tokyo, Grad Sch Agr & Life Sci, Dept Biomat Sci, Bunkyo Ku, Tokyo 1138657, Japan
基金
日本学术振兴会;
关键词
cellouronic acid; Nitroxide; Oxidation; TEMPO;
D O I
10.1023/A:1024051514026
中图分类号
TB3 [工程材料学]; TS [轻工业、手工业、生活服务业];
学科分类号
0805 ; 080502 ; 0822 ;
摘要
The mechanism of partial depolymerization of cellouronic acid (beta-1,4-linked polyglucuronic acid sodium salt) during 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO)-mediated oxidation of cellulose was studied by treating cellouronic acid with one reagent or a combination of TEMPO-NaBr-NaClO under various conditions. Although NaClO, NaBrO and an alkali at pH 11 brought about partial depolymerization of cellouronic acid, the use of these reagents themselves did not seem to be the primary reason for depolymerization. On the other hand, when all the reagents, i.e. TEMPO-NaBr-NaClO, were applied to cellouronic acid at pH 11, a remarkable decrease in weight-average degree of polymerization (DPw) from 430 to ca. 20 was observed within the initial 10 min. Probably hydroxyl radicals formed from NaBrO and TEMPO at pH 10 - 11 cause the depolymerization during the oxidation. Some radical scavengers were then used for the TEMPO-mediated oxidation of cellulose in order to suppress the depolymerization. Although the addition of crotonic acid under certain conditions gave cellouronic acid having higher DPw, none of the radical scavengers examined so far could completely prevent the depolymerization. When regenerated celluloses having higher DP were used as the starting materials, cellouronic acids having DPw of more than 1000 were obtained, although they still had large low-molecular-weight fractions.
引用
收藏
页码:151 / 158
页数:8
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