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Production of jet and diesel fuel range alkanes from waste hemicellulose-derived aqueous solutions
Open accessAbstract
In this paper we report a novel four-step process for the production of jet and diesel fuel range alkanes from hemicellulose extracts derived from northeastern hardwood trees. The extract is representative of a byproduct that could be produced by wood-processing industries such as biomass boilers or pulp mills in the northeastern U.S. The hemicellulose extract tested in this study contained mainly xylose oligomers (21.2 g/l xylose after the acid hydrolysis) as well as 0.31 g/l glucose, 0.91 g/l arabinose, 0.2 g/l lactic acid, 2.39 g/l acetic acid, 0.31 g/l formic acid, and other minor products. The first step in this process is an acid-catalyzed biphasic dehydration to produce furfural in yields up to 87%. The furfural is extracted from the aqueous solution into a tetrahydrofuran (THF) phase which is then fed into an aldol condensation step. The furfural-acetone-furfural (F-Ac-F) dimer is produced in this step by reaction of furfural with acetone in yields up to 96% for the F-Ac-F dimer. The F-Ac-F dimer is then subject to a low-temperature hydrogenation to form the hydrogenated dimer (H-FAF) at 110–130 °C and 800 psig with a 5 wt% Ru/C catalyst. Finally the H-FAF undergoes hydrodeoxygenation to make jet and diesel fuel range alkanes, primarily C13 and C12, in yields up to 91%. The theoretical yield for this process is 0.61 kg of alkane per kg of dry xylose derived from the hemicellulose extract. Experimentally we were able to obtain 76% of the theoretical yield for the overall process. We estimate that jet and diesel fuel range alkanes can be produced from between $2.06/gal to $4.39/gal depending on the feed xylose concentration, the size of the biorefinery, and the overall yield. Sensitivity analysis shows that the prices of raw materials, the organic-to-aqueous mass ratio in the biphasic dehydration, and the feed xylose concentration in the hemicellulose extract significantly affect the product cost.
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Cites
Huber, G. W., O’Connor, P., & Corma, A. (2007) · Applied Catalysis A: General · doi:10.1016/j.apcata.2007.07.002 · Cited by 637
Self-citation
Cited by
Catalytic co-pyrolysis of lignocellulosic biomass with polymers: a critical review
Zhang, X., Lei, H., Chen, S., & Wu, J. (2016) · Green Chemistry · doi:10.1039/c6gc00911e · Cited by 497
Integration of chemical catalysis with extractive fermentation to produce fuels
Anbarasan, P., Baer, Z. C., Sreekumar, S., Gross, E., Binder, J. B., Blanch, H. W., Clark, D. S., & Toste, F. D. (2012) · Nature · doi:10.1038/nature11594 · Cited by 385
Atsonios, K., Kougioumtzis, M.-A., D. Panopoulos, K., & Kakaras, E. (2015) · Applied Energy · doi:10.1016/j.apenergy.2014.10.056 · Cited by 198
Zhang, X., Lei, H., Zhu, L., Qian, M., Zhu, X., Wu, J., & Chen, S. (2016) · Applied Energy · doi:10.1016/j.apenergy.2016.04.071 · Cited by 178
Wang, C., Zhang, X., Liu, Q., Zhang, Q., Chen, L., & Ma, L. (2020) · Fuel Processing Technology · doi:10.1016/j.fuproc.2020.106485 · Cited by 157
Metadata
- Authors
- Xing, R., Subrahmanyam, A. V., Olcay, H., Qi, W., van Walsum, G. P., Pendse, H., & Huber, G. W.
- Venue
- Green Chemistry
- Publisher
- Royal Society of Chemistry (RSC)
- Published
- 2010
- Volume
- 12
- Issue
- 11
- Pages
- 1933
- ISSN
- 1463-9262 (ISSN-L)
- 1463-9270
- OpenAlex
- W2127997815
- Cited by
- 346
- References
- 1
- FWCI
- 12.74
- Type
- journal article
- Language
- en
- Open access
- green
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