How Inter‐ and Intramolecular Reactions Dominate the Formation of Products in Lignin Pyrolysis. Issue 36 (5th June 2017)
- Record Type:
- Journal Article
- Title:
- How Inter‐ and Intramolecular Reactions Dominate the Formation of Products in Lignin Pyrolysis. Issue 36 (5th June 2017)
- Main Title:
- How Inter‐ and Intramolecular Reactions Dominate the Formation of Products in Lignin Pyrolysis
- Authors:
- Custodis, Victoria B. F.
Hemberger, Patrick
van Bokhoven, Jeroen A. - Abstract:
- Abstract: One of the key challenges in renewable chemical production is the conversion of lignin, especially by fast pyrolysis. The complexity of the lignin pyrolysis process has hindered the elucidation of the mechanism, inhibiting further industrial implementation. By combining pyrolysis of model compounds (4‐phenoxyphenol and 2‐methoxy‐phenoxybenzene) with lignin bond characteristics both under vacuum and under realistic pressure conditions, the roles of inter‐ and intramolecular reactions were established. On the one hand, the stable 4‐ O ‐5 ether bond enables, without breaking, C−C bond formation and even directly forms naphthalene depending on the position and type of the substituent. p ‐Benzoquinone intermediates, on the other hand, are highly unstable at ambient pressure and directly decompose into coke and carbon monoxide. The system pressure (radical concentration) plays a crucial role in the dominant reaction mechanism by initiating intramolecular reactions, interfering with intramolecular reactions. H‐transfer and recombination reactions suppress the decarbonylation of phenoxy radicals, thus yielding a very different product distribution. Abstract : Got to split : A key challenge in renewable chemical production is the conversion of lignin, especially by fast pyrolysis. Herein, the roles of inter‐ and intramolecular reactions were established by studying the pyrolysis of model compounds with lignin bond characteristics both under vacuum and under realisticAbstract: One of the key challenges in renewable chemical production is the conversion of lignin, especially by fast pyrolysis. The complexity of the lignin pyrolysis process has hindered the elucidation of the mechanism, inhibiting further industrial implementation. By combining pyrolysis of model compounds (4‐phenoxyphenol and 2‐methoxy‐phenoxybenzene) with lignin bond characteristics both under vacuum and under realistic pressure conditions, the roles of inter‐ and intramolecular reactions were established. On the one hand, the stable 4‐ O ‐5 ether bond enables, without breaking, C−C bond formation and even directly forms naphthalene depending on the position and type of the substituent. p ‐Benzoquinone intermediates, on the other hand, are highly unstable at ambient pressure and directly decompose into coke and carbon monoxide. The system pressure (radical concentration) plays a crucial role in the dominant reaction mechanism by initiating intramolecular reactions, interfering with intramolecular reactions. H‐transfer and recombination reactions suppress the decarbonylation of phenoxy radicals, thus yielding a very different product distribution. Abstract : Got to split : A key challenge in renewable chemical production is the conversion of lignin, especially by fast pyrolysis. Herein, the roles of inter‐ and intramolecular reactions were established by studying the pyrolysis of model compounds with lignin bond characteristics both under vacuum and under realistic pressure conditions (see scheme). … (more)
- Is Part Of:
- Chemistry. Volume 23:Issue 36(2017)
- Journal:
- Chemistry
- Issue:
- Volume 23:Issue 36(2017)
- Issue Display:
- Volume 23, Issue 36 (2017)
- Year:
- 2017
- Volume:
- 23
- Issue:
- 36
- Issue Sort Value:
- 2017-0023-0036-0000
- Page Start:
- 8658
- Page End:
- 8668
- Publication Date:
- 2017-06-05
- Subjects:
- biomass -- high-temperature chemistry -- radical reactions -- reaction mechanisms -- sustainable chemistry
Chemistry -- Periodicals
540 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3765 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/chem.201700639 ↗
- Languages:
- English
- ISSNs:
- 0947-6539
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3168.860500
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 125.xml