Degradation of the Cellulosic Key Chromophore 5,8-Dihydroxy-[1,4]-naphthoquinone by Hydrogen Peroxide under Alkaline Conditions

被引:9
|
作者
Zwirchmayr, Nele Sophie [1 ]
Hosoya, Takashi [1 ]
Henniges, Ute [1 ]
Gille, Lars [2 ]
Bacher, Markus [1 ]
Furtmueller, Paul [1 ]
Rosenau, Thomas [1 ]
机构
[1] Univ Nat Resources & Life Sci, Dept Chem, Muthgasse 18, A-1190 Vienna, Austria
[2] Univ Vet Med Vienna, Dept Biomed Sci, Vet Pl 1, A-1210 Vienna, Austria
来源
JOURNAL OF ORGANIC CHEMISTRY | 2017年 / 82卷 / 21期
关键词
RESIDUAL CHROMOPHORES; IDENTIFICATION; 2,5-DIHYDROXY-1,4-BENZOQUINONE; EPR;
D O I
10.1021/acs.joc.7b01827
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
5,8-Dihydroxy-[1,4]-naphthoquinone (DHNQ) is one of the key chromophores in cellulosic materials. Its almost ubiquitous presence in cellulosic materials makes it a target molecule of the pulp and paper industry's bleaching efforts. In the presented study, DHNQ was treated with hydrogen peroxide under alkaline conditions at pH 10, resembling the conditions of industrial hydrogen peroxide bleaching (I) stage). The reaction mechanism, reaction intermediates, and final degradation products were analyzed by UV/vis, NMR, GC-MS, and EPR. The degradation reaction yielded C-1-C-4 carboxylic acids as the final products. Highly relevant for pulp bleaching are the findings on intermediates of the reaction, as two of them, 2,5-dihydroxy-[1,4]-benzoquinone (DHBQ) and 1,4,5,8-naphthalenetetrone, are potent chromophores themselves. While DHBQ is one of the three key cellulosic chromophores and its degradation by H2O2 is well-established, the second intermediate, 1,4,5,8-naphthalenetetrone, is reported for the first time in the context of cellulose discoloration.
引用
收藏
页码:11558 / 11565
页数:8
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