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  4. Lignin oxidation and depolymerisation in ionic liquids
 
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Lignin oxidation and depolymerisation in ionic liquids
File(s)
Lignin oxidation TW corrected.docx (5.27 MB)
Accepted version
Author(s)
Prado, R
Brandt, A
Erdocia, X
Hallet, J
Welton, T
more
Type
Journal Article
Abstract
The depolymerisation of lignin directly in the black liquor was studied, comparing two ionic liquids as extracting solvents (butylimidazolium hydrogen sulphate and triethylammonium hydrogen sulphate), under oxidising conditions. H2O2 was chosen as the oxidant agent. It was observed that lignins derived from butylimidazolium hydrogen sulphate were more susceptible to degradation. The main degradation products found in the extracted oils were aromatic acids, such as vanillic acid, benzoic acid and 1,2-benzenedicarboxylic acid.
Date Issued
2015-09-21
Date Acceptance
2015-09-21
Citation
Green Chemistry, 2015, 18 (3), pp.834-841
URI
http://hdl.handle.net/10044/1/30642
DOI
https://www.dx.doi.org/10.1039/c5gc01950h
ISSN
1463-9262
Publisher
Royal Society of Chemistry
Start Page
834
End Page
841
Journal / Book Title
Green Chemistry
Volume
18
Issue
3
Copyright Statement
© The Royal Society of Chemistry 2015
Sponsor
Engineering & Physical Science Research Council (E
Imperial College Trust
Engineering & Physical Science Research Council (EPSRC)
Grant Number
EP/K503733/1
N/A
EP/K014676/1
Subjects
Science & Technology
Physical Sciences
Chemistry, Multidisciplinary
Chemistry
ORGANOSOLV LIGNIN
CHEMICALS
BIOMASS
ALCOHOL
Publication Status
Published
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