Oxidative conversion of lignin and lignin model compounds catalyzed by CeO2-supported Pd nanoparticles. Issue 11 (8th September 2015)
- Record Type:
- Journal Article
- Title:
- Oxidative conversion of lignin and lignin model compounds catalyzed by CeO2-supported Pd nanoparticles. Issue 11 (8th September 2015)
- Main Title:
- Oxidative conversion of lignin and lignin model compounds catalyzed by CeO2-supported Pd nanoparticles
- Authors:
- Deng, Weiping
Zhang, Hongxi
Wu, Xuejiao
Li, Rongsheng
Zhang, Qinghong
Wang, Ye - Abstract:
- Abstract : Pd/CeO2 efficiently catalyzes the oxidative conversion of 2-phenoxy-1-phenylethanol, a lignin model compound with a β-O-4 linkage, in methanol, producing monomeric aromatics. Abstract : The oxidative transformation of lignin into aromatic compounds is an attractive route for chemical utilization of lignocellulosic biomass. Unlike hydrogenolysis, no consumption of expensive hydrogen is required for the oxidative transformation. However, only limited success has been achieved for the oxidative conversion of lignin. Here, we report that cerium oxide-supported palladium nanoparticles (Pd/CeO2 ) can efficiently catalyze the one-pot oxidative conversion of 2-phenoxy-1-phenylethanol, a lignin model compound containing a β-O-4 bond and a Cα -hydroxyl group, in methanol in the presence of O2, producing phenol, acetophenone and methyl benzoate as the major products. Pd nanoparticles played a pivotal role in the oxidation of a Cα -hydroxyl group into a Cα -ketonic group, which was crucial for the transformation of the model compound. The presence of the Cα -ketonic group activated the β-O-4 bond, which was subsequently cleaved over the Pd/CeO2 catalyst, affording phenol and acetophenone. At the same time, the Cα –Cβ bond also underwent oxidative cleavage catalyzed by CeO2, producing benzoic acid and further methyl benzoate. The Pd/CeO2 catalyst could also catalyze the oxidative conversion of organosolv lignin under mild conditions (458 K), producing vanillin, guaiacol andAbstract : Pd/CeO2 efficiently catalyzes the oxidative conversion of 2-phenoxy-1-phenylethanol, a lignin model compound with a β-O-4 linkage, in methanol, producing monomeric aromatics. Abstract : The oxidative transformation of lignin into aromatic compounds is an attractive route for chemical utilization of lignocellulosic biomass. Unlike hydrogenolysis, no consumption of expensive hydrogen is required for the oxidative transformation. However, only limited success has been achieved for the oxidative conversion of lignin. Here, we report that cerium oxide-supported palladium nanoparticles (Pd/CeO2 ) can efficiently catalyze the one-pot oxidative conversion of 2-phenoxy-1-phenylethanol, a lignin model compound containing a β-O-4 bond and a Cα -hydroxyl group, in methanol in the presence of O2, producing phenol, acetophenone and methyl benzoate as the major products. Pd nanoparticles played a pivotal role in the oxidation of a Cα -hydroxyl group into a Cα -ketonic group, which was crucial for the transformation of the model compound. The presence of the Cα -ketonic group activated the β-O-4 bond, which was subsequently cleaved over the Pd/CeO2 catalyst, affording phenol and acetophenone. At the same time, the Cα –Cβ bond also underwent oxidative cleavage catalyzed by CeO2, producing benzoic acid and further methyl benzoate. The Pd/CeO2 catalyst could also catalyze the oxidative conversion of organosolv lignin under mild conditions (458 K), producing vanillin, guaiacol and 4-hydroxybenzaldehyde. … (more)
- Is Part Of:
- Green chemistry. Volume 17:Issue 11(2015)
- Journal:
- Green chemistry
- Issue:
- Volume 17:Issue 11(2015)
- Issue Display:
- Volume 17, Issue 11 (2015)
- Year:
- 2015
- Volume:
- 17
- Issue:
- 11
- Issue Sort Value:
- 2015-0017-0011-0000
- Page Start:
- 5009
- Page End:
- 5018
- Publication Date:
- 2015-09-08
- Subjects:
- Environmental chemistry -- Industrial applications -- Periodicals
Environmental management -- Periodicals
660 - Journal URLs:
- http://www.rsc.org/ ↗
http://pubs.rsc.org/en/journals/journalissues/gc#issueid=gc016010&type=current&issnprint=1463-9262 ↗ - DOI:
- 10.1039/c5gc01473e ↗
- Languages:
- English
- ISSNs:
- 1463-9262
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4214.935500
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 536.xml