Electrochemical cross-coupling of biogenic di-acids for sustainable fuel production. Issue 9 (2nd April 2019)
- Record Type:
- Journal Article
- Title:
- Electrochemical cross-coupling of biogenic di-acids for sustainable fuel production. Issue 9 (2nd April 2019)
- Main Title:
- Electrochemical cross-coupling of biogenic di-acids for sustainable fuel production
- Authors:
- Holzhäuser, F. Joschka
Creusen, Guido
Moos, Gilles
Dahmen, Manuel
König, Andrea
Artz, Jens
Palkovits, Stefan
Palkovits, Regina - Abstract:
- Abstract : Tailored electrochemical cross-coupling enables a flexible modular access to bio-fuels starting from biomass derived mono- and di-acids and renewable energy. Abstract : Direct electrocatalytic conversion of bio-derivable acids represents a promising technique for the production of value-added chemicals and tailor-made fuels from lignocellulosic biomass. In the present contribution, we report the electrochemical decarboxylation and cross-coupling of ethyl hydrogen succinate, methyl hydrogen methylsuccinate and methylhexanoic acid with isovaleric acid. The reactions were performed in aqueous solutions or methanol at ambient temperatures, following the principles of green chemistry. High conversions of the starting materials have been obtained with maximum yields between 42 and 61% towards the desired branched alkane products. Besides costly Pt electrodes also (Ru x Ti1− x )O2 on Ti electrodes exhibited a notable activity for cross-Kolbe electrolysis. As some of the products are insoluble in water, easy product isolation and reuse of the reaction solvent is enabled via phase separation. Several side products have been identified to evaluate the efficiency of the reaction and to elucidate the factors influencing the product selectivity. The yielded alkanes and esters were assessed with regard to their potential as fuels for internal combustion engines. While the longer alkanes constitute promising candidates for the compression–ignition engine, the smaller esterAbstract : Tailored electrochemical cross-coupling enables a flexible modular access to bio-fuels starting from biomass derived mono- and di-acids and renewable energy. Abstract : Direct electrocatalytic conversion of bio-derivable acids represents a promising technique for the production of value-added chemicals and tailor-made fuels from lignocellulosic biomass. In the present contribution, we report the electrochemical decarboxylation and cross-coupling of ethyl hydrogen succinate, methyl hydrogen methylsuccinate and methylhexanoic acid with isovaleric acid. The reactions were performed in aqueous solutions or methanol at ambient temperatures, following the principles of green chemistry. High conversions of the starting materials have been obtained with maximum yields between 42 and 61% towards the desired branched alkane products. Besides costly Pt electrodes also (Ru x Ti1− x )O2 on Ti electrodes exhibited a notable activity for cross-Kolbe electrolysis. As some of the products are insoluble in water, easy product isolation and reuse of the reaction solvent is enabled via phase separation. Several side products have been identified to evaluate the efficiency of the reaction and to elucidate the factors influencing the product selectivity. The yielded alkanes and esters were assessed with regard to their potential as fuels for internal combustion engines. While the longer alkanes constitute promising candidates for the compression–ignition engine, the smaller ester represents an interesting option for the spark-ignition engine. … (more)
- Is Part Of:
- Green chemistry. Volume 21:Issue 9(2019)
- Journal:
- Green chemistry
- Issue:
- Volume 21:Issue 9(2019)
- Issue Display:
- Volume 21, Issue 9 (2019)
- Year:
- 2019
- Volume:
- 21
- Issue:
- 9
- Issue Sort Value:
- 2019-0021-0009-0000
- Page Start:
- 2334
- Page End:
- 2344
- Publication Date:
- 2019-04-02
- 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/c8gc03745k ↗
- 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:
- 10407.xml