In situ Observation of Radicals and Molecular Products During Lignin Pyrolysis

被引:81
作者
Baehrle, Christian [1 ]
Custodis, Victoria [2 ]
Jeschke, Gunnar [3 ]
van Bokhoven, Jeroen A. [2 ,4 ]
Vogel, Frederic [1 ]
机构
[1] Paul Scherrer Inst, Res Dept Gen Energy, CH-5232 Villigen, PSI, Switzerland
[2] ETH, Inst Chem & Bioengn, CH-8093 Zurich, Switzerland
[3] ETH, EPR Res Grp, CH-8093 Zurich, Switzerland
[4] Paul Scherrer Inst, Lab Catalysis & Sustainable Chem, CH-5232 Villigen, PSI, Switzerland
基金
瑞士国家科学基金会;
关键词
EPR spectroscopy; gas chromatography; lignin; pyrolysis; radicals; ELECTRON-PARAMAGNETIC-RESONANCE; STABLE FREE RADICALS; MILLED-WOOD LIGNIN; SCAVENGING ACTIVITY; MAGNETIC-RESONANCE; MASS-SPECTROMETRY; MODEL COMPOUNDS; HUMIC ACIDS; CELLULOSE; SPECTROSCOPY;
D O I
10.1002/cssc.201400079
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Lignin pyrolysis is a promising method for the sustainable production of phenolic compounds from biomass. However, detailed knowledge about the radicals involved in this process and their influence on the molecular products is missing. Herein, we report on the pyrolysis of hard-and softwood Klason lignins under inert gas conditions in a temperature range between 350-550 degrees C. During the pyrolysis process, the formed radicals were detected by in situ high-temperature electron paramagnetic resonance spectroscopy. The overall formation of volatile products during lignin pyrolysis was determined using thermogravimetric analysis. The volatile molecular products were characterized and quantified using GC-MS analysis. Major differences were observed between hardwood and softwood lignins. Hardwood lignins form more radicals and volatile products than softwood lignins at temperatures from 350 to 450 degrees C. In the late stages of the pyrolysis process at 550 degrees C radical quenching reactions become dominant in hardwood lignins. We identified the disproportionation of two semiquinone radicals to quinone and hydroquinone species as the most likely quenching reaction. Our results show that both the pyrolysis temperature and the type of lignin source have a major influence on radical formation and the molecular products during the depolymerization of lignin.
引用
收藏
页码:2022 / 2029
页数:8
相关论文
共 49 条
[1]   Production of monomeric phenols by thermochemical conversion of biomass: a review [J].
Amen-Chen, C ;
Pakdel, H ;
Roy, C .
BIORESOURCE TECHNOLOGY, 2001, 79 (03) :277-299
[2]   FREE-RADICAL FORMATION IN LIGNIN DURING PYROLYSIS [J].
AVNI, E ;
SUIB, SL ;
COUGHLIN, RW .
HOLZFORSCHUNG, 1985, 39 (01) :33-40
[3]   FOSSIL-FUELS AND SYNTHETIC-POLYMERS - ISOTHERMAL PYROLYSIS KINETICS AS INDICATION OF STRUCTURAL RESEMBLANCE [J].
BAR, H ;
IKAN, R ;
AIZENSHTAT, Z .
JOURNAL OF ANALYTICAL AND APPLIED PYROLYSIS, 1988, 14 (01) :73-79
[4]   Lignin biosynthesis [J].
Boerjan, W ;
Ralph, J ;
Baucher, M .
ANNUAL REVIEW OF PLANT BIOLOGY, 2003, 54 :519-546
[5]   Determination of the substituent effect on the O-H bond dissociation enthalpies of phenolic antioxidants by the EPR radical equilibration technique [J].
Brigati, G ;
Lucarini, M ;
Mugnaini, V ;
Pedulli, GF .
JOURNAL OF ORGANIC CHEMISTRY, 2002, 67 (14) :4828-4832
[6]   PYROLYSIS MECHANISMS OF LIGNIN - SURFACE-IMMOBILIZED MODEL-COMPOUND INVESTIGATION OF ACID-CATALYZED AND FREE-RADICAL REACTION PATHWAYS [J].
BRITT, PF ;
BUCHANAN, AC ;
THOMAS, KB ;
LEE, SK .
JOURNAL OF ANALYTICAL AND APPLIED PYROLYSIS, 1995, 33 :1-19
[7]   Flash vacuum pyrolysis of methoxy-substituted lignin model compounds [J].
Britt, PF ;
Buchanan, AC ;
Cooney, MJ ;
Martineau, DR .
JOURNAL OF ORGANIC CHEMISTRY, 2000, 65 (05) :1376-1389
[8]   A comprehensive approach for quantitative lignin characterization by NMR spectroscopy [J].
Capanema, EA ;
Balakshin, MY ;
Kadla, JF .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2004, 52 (07) :1850-1860
[9]   Quantitative characterization of a hardwood milled wood lignin by nuclear magnetic resonance spectroscopy [J].
Capanema, EA ;
Balakshin, MY ;
Kadla, JF .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2005, 53 (25) :9639-9649
[10]   Kinetics and reaction chemistry for slow pyrolysis of enzymatic hydrolysis lignin and organosolv extracted lignin derived from maplewood [J].
Cho, Joungmo ;
Chu, Sheng ;
Dauenhauer, Paul J. ;
Huber, George W. .
GREEN CHEMISTRY, 2012, 14 (02) :428-439