J Am Oil Chem Soc
Johnson, J. R. (1942) The Perkin reaction and related reactions.
Organic Reactions, 1:210–265.
Julis, J., & Leitner, W. (2012) Synthesis of 1-octanol and 1,1-dioctyl
ether from biomass-derived platform chemicals. Angewandte Che-
mie International Edition, 51:8615–8619.
for soaps. U.S. Patent No. 5,279,759. Plymouth Meeting, PA: Hen-
kel Corporation.
Schaarschmidt, A., Georgeacopol, E., & Herzenberg, J. (1918) Die
isovaleriansäure und ihr abweichendes verhalten bei der Per-
kinschen synthese. Berichte der Deutschen Chemischen Gesell-
schaft, 51:1059–1074.
Selinger, Z., & Lapidot, Y. (1966) Synthesis of fatty acid anhydrides
by reaction with dicyclohexylcarbodiimide. Journal of Lipid
Research, 7:174–175.
Sigma-Aldrich. (2018) Sigma-Aldrich chemical catalog. Milwaukee,
WI: Sigma-Aldrich.
Sonntag, N. O. V., Trowbridge, J. R., & Krems, I. J. (1954) Reactions
of fatty acid chlorides. I. Preparation of fatty acid anhydrides. Jour-
nal of the American Oil Chemists’ Society, 31:151–157.
Stipp, G. K., & Kluesener, B. W. (1995) Fatty acid anhydride pro-
cess. U.S. Patent No. 5,387,705. Cincinatti, OH: Proctor &
Gamble.
Sudholt, A., Cai, L., Heyne, J., Haas, F. M., Pitsch, H., & Dryer, F. L.
(2015) Ignition characteristics of a bio-derived class of saturated
and unsaturated furans for engine applications. Proceedings of the
Combustion Institute, 35:2957–2965.
Wagner, C. R. (1947) Production of alkenylfurans. U.S. Patent
No. 2,431,216. Wilmington, DE: Phillips Petroleum.
Wallace Jr., J. M., & Copenhaver, J. E. (1941) Anhydrides of the nor-
mal aliphatic saturated monobasic acids. Journal of the American
Chemical Society, 63:699–700.
Walters, R. N. (2002) Molar group contributions to the heat of com-
bustion. Fire and Materials, 26:131–145.
Wasfi, B. (2017) Cetane number of biodiesel from karaya oil.
(Dissertation). King Abdullah University of Science and
Technology.
Werpy, T., & Peterson, G. (Eds.) (2004) Top value added chemicals
from biomass, Volume I: Results of screening for potential candi-
date from sugars and synthesis gas. Washington, DC: U.S. Depart-
Wilson, G. R. III (2016) Comparison of ASTM D613 and ASTM
D6890. U.S. Army TARDEC Fuels and Lubricants Research Facil-
Wu, J., Shi, J., Fu, J., Leidl, J. A., Hou, Z., & Lu, X. (2016) Catalytic
decarboxylation of fatty acids to aviation fuels over nickel sup-
ported on activated carbon. Scientific Reports, 6:27820. https://doi.
Xu, W., Xia, Q., Zhang, Y., Guo, Y., Wang, Y., & Lu, G. (2011)
Effective production of octane from biomass derivtives under mild
conditions. ChemSusChem, 4:1758–1761.
Kiefer, T. A. (2013) Energy insecurity: The false promise of liquid
biofuels. Strategic Studies Quarterly, 7:114–151.
Knothe, G. (2008) “Designer” biodiesel: optimizing fatty ester com-
position to improve fuel properties. Energy
1358–1364.
& Fuels, 22:
Knothe, G., Steidley, K. R., Moser, B. R., & Doll, K. M. (2017)
Decarboxylation of fatty acids with triruthenium dodecacarbonyl:
Influence of the compound structure and analysis of the product
mixtures. ACS Omega, 2:6473–6480.
Krafft, F., & Rosiny, W. (1900) Ueber reindarstellung der hochmole-
cularen säureanhydride (CnH2n+1O)2O. Berichte der Deutschen
Chemischen Gesellschaft, 33:3578–3579.
Leitner, W., Klankermayer, J., Pischinger, S., Pitsch, H., & Kohse-
Höinghaus, K. (2017) Advanced biofuels and beyond: Chemistry
solutions for propulsion and production. Angewandte Chemie Inter-
national Edition, 56:5412–5452.
Lipkin, D. (1940) Fuel for compression ignition engines. U.S. Patent
No. 2,221,839. Philadelphia, PA: The Atlantic Refining Company.
Lukes, R. M., & Nelson, L. S. (1956) Concurrent hydrogenation and
hydrolysis of furfuryl alcohol. Journal of Organic Chemistry, 21:
1096–1098.
Miner, C. S., & Brownlee, H. J. (1929) Process of manufacturing fur-
fural. Patent No. 1,735,084. Chicago, IL: Quaker Oats Company.
Mohite, S., Armbruster, U., Richter, M., & Martin, A. (2014) Impact
of chain length of saturated fatty acids during their heterogeneously
catalyzed deoxygenation. Journal of Sustainable Bioenergy Sys-
tems, 4:183–193.
Moureu, C., Dufraisse, C., & Johnson, J. R. (1927) Le furylacétylène.
Annales de Chimie, 7:14–42.
Office of the Assistant Secretary of Defense for Energy, Installations,
and Environment. (2017) Annual energy management and resil-
ience (AEMR) report fiscal year 2016. Washington, DC: Depart-
Papa, D., & Schwenk, E. (1950) Halogenhydroxyarylaliphatic acids.
U.S. Patent No. 2,528,542. Bloomfield, NJ: Schering Corporation.
Park, S. H., & Lee, C. S. (2013) Combustion performance and emis-
sion reduction characteristics of automotive DME engine system.
Progress in Energy and Combustion Science, 39:147–168.
Perkin, W. H. (1886) XXXIII–The formation of acids from aldehydes
by the action of anhydrides and salts, and the formation of ketones
from the compounds resulting from the union of anhydrides and
salts. Journal of the Chemical Society Transactions, 49:317–328.
Pratas, M. J., Freitas, S., Oliveira, M. B., Monteiro, S. C.,
Lima, A. S., & Coutinho, J. A. P. (2010) Densities and viscosities
of fatty acid methyl and ethyl esters. Journal of Chemical & Engi-
neering Data, 55:3983–3990.
Yanowitz, J., Ratcliff, M. A., McCormick, R. L., Taylor, J. D., &
Murphy, M. J. (2017) Compedium of experimental cetane numbers.
National Renewable Energy Laboratory, NRELTP-5400-61693.
Zheng, Z., Badawy, T., Henein, N., & Sattler, E. (2012) Invetigation
of physical and chemical delay periods of different fuels in the igni-
tion quality tester (IQT). U.S. Army TARDEC, Warren,
Rebrovic, L., & Kilbarger, A. C. (1994) Alpha-(p-alkoxybenzylidene)
carboxylic acids as color stabilizers, process, aids, and whiteners
MI.
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