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@PHDTHESIS{Jestel:807408,
author = {Jestel, Tim Alexander},
othercontributors = {Spieß, Antje Christine and Jupke, Andreas and Schwaneberg,
Ulrich},
title = {{A}dvanced chromatographic methods for lignin
characterization},
school = {RWTH Aachen University},
type = {Dissertation},
address = {Düren},
publisher = {Shaker Verlag},
reportid = {RWTH-2020-11334},
isbn = {978-3-8440-7676-9},
series = {Berichte aus der Verfahrenstechnik},
pages = {XV, 158 Seiten : Illustrationen, Diagramme},
year = {2020},
note = {Deutsche und englische Zusammenfassung; Dissertation, RWTH
Aachen University, 2020},
abstract = {Recent biorefineries employ renewable resources such as
lignocellulosic biomass for sustainable production of fuels
and chemicals. Efficient lignocellulose valorization
processes usually include thermochemical or electrochemical
lignin degradation. However, complex product mixtures and
low yields of target products are challenges in lignin
degradation. Furthermore, a qualitative and quantitative
assessment of lignin degradation processes is often not
possible, due to the lack of suitable analytical methods.
This work aims at improving and developing new
chromatographic methods for the analysis of lignin in
biorefineries and lignin valorizationprocesses. For the
analysis of lignin in raw lignocellulosic biomass, an
existing method based on high performance anion exchange
chromatography coupled to pulsed amperometric detection was
extended by the ability to detect lignin derived aldehydes
and alcohols that act as fermentation inhibitors. Gel
permeation chromatography (GPC) is the standard technique to
monitor the lignin molecular weight during lignin removal
and degradation. Here, secondary separation effects such as
column interactions and lignin association were reduced by
the addition of additives to GPC eluents. Liquid
chromatography electrospray ionization quadrupole
time-of-flight mass spectrometry (LC-ESI-Q-ToF-MS) was used
to elucidate the underlying mechanism of lignocellulose
treatment with laccases in combination with the mediator
1-hydroxybenzotriazole (HBT). Lignin surface modification by
HBT grafting led to reduced unspecific cellulase adsorption
and thus, increased glucose yields. Furthermore, Kraft
lignin was electrochemically depolymerized to produce
valuable degradation products such as carboxylic acids that
were detected and quantified by LC-ESI-Q-ToF-MS. To enable a
more facilitated analysis of complex lignin degradation
processes, GPC and LC-ESI-Q-ToF-MS were coupled. With the
help of the new method, the lignin molecular weight as well
as lignin degradation products could be determined in a
single step without labor intensive sample preparation and
dilution steps. Overall, the importance of efficient and
accurate analytical methods for lignin analysis during the
whole biorefinery process chain was highlighted in this
work. By refining existing analytical techniques and
coupling of methods, first important steps were successfully
taken for a facilitated and comprehensive lignin analysis.
Especially, the coupling of different analytical methods has
great potential to combine their respective advantages,
thereby providing a better understanding of lignin
chemistry.},
cin = {420110},
ddc = {620},
cid = {$I:(DE-82)420110_20140620$},
typ = {PUB:(DE-HGF)11 / PUB:(DE-HGF)3},
url = {https://publications.rwth-aachen.de/record/807408},
}