Controllable oxidative depolymerization of lignin to produce aromatic aldehydes and generate electricity under mild conditions with direct biomass fuel cells as flexible reactors

被引:5
作者
Gao, Daihong [1 ,2 ]
Ouyang, Denghao [1 ,2 ]
Zhao, Xuebing [1 ,2 ]
机构
[1] Tsinghua Univ, Key Lab Ind Biocatalysis, Minist Educ, Beijing 100084, Peoples R China
[2] Tsinghua Univ, Inst Appl Chem, Dept Chem Engn, Beijing 100084, Peoples R China
基金
中国国家自然科学基金;
关键词
Lignin; Direct biomass fuel cell; Oxidative depolymerization; Aromatic aldehydes; Electron transfer; ELECTROCHEMICAL OXIDATION; ALKALINE-HYDROLYSIS; ANODIC DEGRADATION; PBO2; ELECTRODE; CONVERSION; PERFORMANCE; CHEMICALS; HYDROGEN; ELECTROCATALYST; FABRICATION;
D O I
10.1016/j.cej.2023.147874
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Lignin was oxidized and depolymerized by a direct biomass fuel cell (DBFC) for electricity generation and production of aromatic aldehydes. The yield of aromatic aldehydes could be easily controlled by changing the anodic catalyst, cathodic oxidants and external loading. Cobalt and (VO2)2SO4 were screened as the most suitable anodic catalyst and cathodic oxidant, respectively. A maximum power density of 199.8 mW/cm2 was obtained under the optimized conditions for electricity generation; however, the yield of the aromatic aldehydes was greatly dependent on the type of lignin used, reaction conditions and the external loading (output voltage) of the DBFC. At a lignin concentration of 0.5 g/L, aromatic aldehydes yield of 7.8 % was obtained at an output voltage of 0.9 V. The formation of aromatic aldehydes was mainly caused by cleavage of beta-O-4 linkage and oxidation of side chains by the hydroxyl radicals formed via oxidation of OH- by Co3+ on the anode.
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页数:13
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共 67 条
  • [1] Oxidative depolymerization of lignins for producing aromatics: variation of botanical origin and extraction methods
    Almada, Cedric Cabral
    Kazachenko, Aleksandr
    Fongarland, Pascal
    Perez, Denilson Da Silva
    Kuznetsov, Boris N.
    Djakovitch, Laurent
    [J]. BIOMASS CONVERSION AND BIOREFINERY, 2022, 12 (09) : 3795 - 3808
  • [2] Mediated Fuel Cells: Soluble Redox Mediators and Their Applications to Electrochemical Reduction of O2 and Oxidation of H2, Alcohols, Biomass, and Complex Fuels
    Anson, Colin W.
    Stahl, Shannon S.
    [J]. CHEMICAL REVIEWS, 2020, 120 (08) : 3749 - 3786
  • [3] Lignin structure in Buxus sempervirens reaction wood
    Bailleres, H
    Castan, M
    Monties, B
    Pollet, B
    Lapierre, C
    [J]. PHYTOCHEMISTRY, 1997, 44 (01) : 35 - 39
  • [4] Breiner M, 2021, GREEN CHEM, V23, P6449, DOI [10.1039/d1gc01995c, 10.1039/D1GC01995C]
  • [5] Electrochemical conversion of corn stover lignin to biomass-based chemicals between Cu/Ni-Mo-Co cathode and Pb/PbO2 anode in alkali solution
    Cai, Pan
    Fan, Hongxian
    Cao, Shuo
    Qi, Jian
    Zhang, Songmei
    Li, Gang
    [J]. ELECTROCHIMICA ACTA, 2018, 264 : 128 - 139
  • [6] Electrochemical oxidation behavior of Mg-Li-Al-Ce-Zn and Mg-Li-Al-Ce-Zn-Mn in sodium chloride solution
    Cao, Dianxue
    Wu, Lin
    Wang, Guiling
    Lv, Yanzhuo
    [J]. JOURNAL OF POWER SOURCES, 2008, 183 (02) : 799 - 804
  • [7] Fabrication and enhanced electrocatalytic activity of 3D highly ordered macroporous PbO2 electrode for recalcitrant pollutant incineration
    Chai, Shouning
    Zhao, Guohua
    Wang, Yujing
    Zhang, Ya-nan
    Wang, Yanbin
    Jin, Yefei
    Huang, Xiaofeng
    [J]. APPLIED CATALYSIS B-ENVIRONMENTAL, 2014, 147 : 275 - 286
  • [8] Alkaline hydrolysis of nonphenolic beta-O-4 lignin model dimers: Further studies of the substituent effect on the leaving phenoxide
    Collier, WE
    Fisher, TH
    Ingram, LL
    Harris, AL
    Schultz, TP
    [J]. HOLZFORSCHUNG, 1996, 50 (05) : 420 - 424
  • [9] Added-Value Chemicals from Lignin Oxidation
    Costa, Carina A. Esteves
    Vega-Aguilar, Carlos A.
    Rodrigues, Alirio E.
    [J]. MOLECULES, 2021, 26 (15):
  • [10] Alkaline hydrolysis of nonphenolic α-carbonyl β-0-4 lignin dimers substituted on the leaving phenoxide ring:: Comparison with benzylic hydroxyl analogues
    Criss, DL
    Fisher, TH
    Schultz, TP
    [J]. HOLZFORSCHUNG, 1998, 52 (01) : 57 - 60