Lignin conversion into C4 dicarboxylic acids by catalytic wet peroxide oxidation using titanium silicalite-1

被引:2
|
作者
Vega-Aguilar, Carlos A. [1 ,2 ]
Barreiro, M. Filomena [2 ]
Rodrigues, Alirio E. [1 ]
机构
[1] Univ Porto, Fac Engenharia, Dept Chem Engn, Lab Catalysis & Mat LSRE LCM,Lab Separat & React, Rua Dr. Roberto Frias s n, P-4200465 Porto, Portugal
[2] Inst Politecn Braganca, Ctr Invest Montanha CIMO, Campus Santa Apolonia, P-5300253 Braganca, Portugal
关键词
Lignin; Depolymerisation; Succinic acid; Biorefinery; Hydrogen peroxide; Titanium silicalite-1; HYDROGEN-PEROXIDE; CARBOXYLIC-ACIDS; MALEIC-ACID; DEPOLYMERIZATION; DEACTIVATION; REGENERATION; VALORIZATION; EPOXIDATION; CHEMICALS;
D O I
10.1016/j.indcrop.2021.114155
中图分类号
S2 [农业工程];
学科分类号
0828 ;
摘要
Lignin valorisation towards added-value products has become a relevant topic to consolidate a future circular bioeconomy. In this context lignin oxidation to C-4 dicarboxylic acids (C-4-DCA) by catalytic wet peroxide oxidation is emerging as a value-added strategy, supported by the extensive use of these building blocks in several industrial fields. In this work, lignins from different sources and processes (Indulin AT, Lignol, alkali and E. globulus kraft lignins) were oxidised using H2O2 and titanium silicalite-1 catalyst (TS-1) under different operating conditions (temperature, pH, time, H2O2, and TS-1 load). Indulin AT was the lignin leading to the highest succinic acid yield (11.3 wt%), and TS-1 catalyst enhanced its production four times over the non-catalysed reaction. Malic acid was also produced at high yields, especially for Lignol lignin. The other lignins (E. globulus kraft, and alkali lignins) also produced these C-4 acids but at lower yields. The catalyst remained stable at the used experimental conditions, and showed potential to be reused for several cycles without being deactivated. Overall, the catalytic conversion of lignin to C-4-DCA can help to guide the pathway to renewable chemicals production.
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页数:10
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