Abstract
Lignocellulosic biomass offers a renewable carbon source which can be anaerobically digested to produce short-chain carboxylic acids. Here, we assess fuel properties of oxygenates accessible from catalytic upgrading of these acids a priori for their potential to serve as diesel bioblendstocks. Ethers derived from C2 and C4 carboxylic acids are identified as advantaged fuel candidates with significantly improved ignition quality (>56% cetane number increase) and reduced sooting (>86% yield sooting index reduction) when compared to commercial petrodiesel. The prescreening process informed conversion pathway selection toward a C11 branched ether, 4-butoxyheptane, which showed promise for fuel performance and health- and safety-related attributes. A continuous, solvent-free production process was then developed using metal oxide acidic catalysts to provide improved thermal stability, water tolerance, and yields. Liter-scale production of 4- butoxyheptane enabled fuel property testing to confirm predicted fuel properties, while incorporation into petrodiesel at 20 vol % demonstrated 10% improvement in ignition quality and 20% reduction in intrinsic sooting tendency. Storage stability of the pure bioblendstock and 20 vol % blend was confirmed with a common fuel antioxidant, as was compatibility with elastomeric components within existing engine and fueling infrastructure. Technoeconomic analysis of the conversion process identified major cost drivers to guide further research and development. Life-cycle analysis determined the potential to reduce greenhouse gas emissions by 50 to 271% relative to petrodiesel, depending on treatment of coproducts.
Original language | English |
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Pages (from-to) | 26421-26430 |
Number of pages | 10 |
Journal | Proceedings of the National Academy of Sciences of the United States of America |
Volume | 116 |
Issue number | 52 |
DOIs | |
State | Published - Dec 26 2019 |
Funding
ACKNOWLEDGMENTS. We thank Jon Luecke, J. Hunter Mack, Anne K. Starace, and Jessica L. Olstad for their contributions. A portion of this research was conducted as part of the Co-Optimization of Fuels & Engines (Co-Optima) project sponsored by the US Department of Energy – Office of Energy Efficiency and Renewable Energy, Bioenergy Technologies and Vehicle Technologies Offices. Work at the National Renewable Energy Laboratory was performed under Contract DE347AC36-99GO10337. Part of this work was also supported by Co-Optima through Program Award DE-EE0007983. P.A.C.’s participation was supported by an NSF Research Experiences for Undergraduates supplement to Grant CBET 1604983. The views expressed in the article do not necessarily represent the views of the US Department of Energy or the US Government. The US Government retains and the publisher, by accepting the article for publication, acknowledges that the US Government retains a nonexclusive, paid-up, irrevocable, worldwide license to publish or reproduce the published form of this work, or allow others to do so, for US Government purposes.
Funders | Funder number |
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NSF Research Experiences | CBET 1604983 |
Vehicle Technologies Offices | DE-EE0007983 |
Office of Energy Efficiency and Renewable Energy |
Keywords
- Biofuel
- Biooxygenate
- Life-cycle analysis
- Solvent-free
- Technoeconomic analysis