Effect of side-chain structure on hydrothermolysis of lignin model compounds

Li, 2015, Catalytic transformation of lignin for the production of chemicals and fuels, Chem. Rev., 115, 11559, 10.1021/acs.chemrev.5b00155 Zeng, 2015, Biomimetic fenton-catalyzed lignin depolymerization to high-value aromatics and dicarboxylic acids, ChemSusChem, 8, 861, 10.1002/cssc.201403128 Ouyang, 2016, Effect of solvent on hydrothermal oxidation depolymerization of lignin for the production of monophenolic compounds, Fuel Process. Technol., 144, 181, 10.1016/j.fuproc.2015.12.019 Singh, 2014, Hydrothermal conversion of lignin to substituted phenols and aromatic ethers, Bioresour. Technol., 165, 319, 10.1016/j.biortech.2014.02.076 Zakzeski, 2010, The catalytic valorization of lignin for the production of renewable chemicals, Chem. Rev., 110, 3552, 10.1021/cr900354u Farag, 2014, Lumped approach in kinetic modeling of microwave pyrolysis of kraft lignin, Energy Fuel, 28, 1406, 10.1021/ef4023493 Azarpira, 2014, Catalytic alkaline oxidation of lignin and its model compounds: a pathway to aromatic biochemical, Bioenerg. Res., 7, 78, 10.1007/s12155-013-9348-x Sarkanen, 1971 Deuss, 2015, Aromatic monomers by in situ conversion of reactive intermediates in the acid-catalyzed depolymerization of lignin, J. Am. Chem. Soc., 137, 7456, 10.1021/jacs.5b03693 Long, 2015, Efficient valorization of lignin depolymerization products in the present of NixMg1xO, Appl. Energy, 157, 540, 10.1016/j.apenergy.2015.04.011 Beste, 2008, Computational prediction of α/β selectivities in the pyrolysis of oxygen-substituted phenethyl phenyl ethers, J. Phys. Chem. A, 112, 4982, 10.1021/jp800767j Kawamoto, 2008, Different pyrolytic cleavage mechanisms of β-ether bond depending on the side-chain structure of lignin dimers, J. Anal. Appl. Pyrolysis, 81, 88, 10.1016/j.jaap.2007.09.006 Li, 2016, Effects of oxygen-containing substituents on pyrolysis characteristics of β-O-4 type model compounds, J. Anal. Appl. Pyrolysis, 120, 52, 10.1016/j.jaap.2016.04.009 Rahimi, 2014, Formic-acid-induced depolymerization of oxidized lignin to aromatics, Nature, 515, 249, 10.1038/nature13867 Zhu, 2016, Effect of functional groups on hydrogenolysis of lignin model compounds, Fuel Process. Technol., 154, 132, 10.1016/j.fuproc.2016.08.023 Zhou, 2006, Synthesis of guaiacylglycerol-β-guaiacyl ether-[α-C13], Chem. Res. Appl., 18, 921 Watanabe, 2015, Pyrolytic reactivities of deuterated β-ether-type lignin model dimers, J. Anal. Appl. Pyrolysis, 112, 23, 10.1016/j.jaap.2015.02.028 Liu, 2016, Study on the pyrolysis mechanism of three guaiacyl-type lignin monomeric model compounds, J. Anal. Appl. Pyrolysis, 118, 123, 10.1016/j.jaap.2016.01.007 Rahimi, 2013, Chemoselective metal-free aerobic alcohol oxidation in lignin, J. Am. Chem. Soc., 135, 6415, 10.1021/ja401793n Ye, 2012, Selective production of 4-ethylphenolics from lignin via mild hydrogenolysis, Bioresour. Technol., 118, 648, 10.1016/j.biortech.2012.05.127