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Antiknock properties of furfural derivatives

  • Organic Synthesis and Industrial Organic Chemistry
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Abstract

Preparative amounts of furfuryl alcohol ethers and furfural acetals were prepared from renewable vegetable raw materials. The blending reseach octane numbers of mixing of furan derivatives in straight-run gasoline were estimated: butyl furfuryl ether, 97.8 ± 7; propyl furfuryl ether, 112 ± 6; furfural diethyl acetal, 105 ± 6, furfural ethylene glycol acetal, 108 ± 7; furfurylamine, 194 ± 4. These results demonstrate prospects for using furan derivatives as available biofuels.

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Authors and Affiliations

  1. Institute of Chemistry and Chemical Technology, Siberian Branch, Russian Academy of Sciences, ul. Akademgorodok 50/24, Krasnoyarsk, 660036, Russia

    V. E. Tarabanko, M. Yu. Chernyak & K. L. Kaigorodov

  2. Siberian Federal University, pr. Svobodnyi 79, Krasnoyarsk, 660041, Russia

    V. E. Tarabanko, Yu. N. Bezborodov & N. F. Orlovskaya

  3. Boreskov Institute of Catalysis, Siberian Branch, Russian Academy of Sciences, ul. Akademika Lavrent’eva 5, Novosibirsk, 630090, Russia

    I. L. Simakova

Authors
  1. V. E. Tarabanko
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  2. M. Yu. Chernyak
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  3. I. L. Simakova
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  4. K. L. Kaigorodov
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  5. Yu. N. Bezborodov
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  6. N. F. Orlovskaya
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Corresponding author

Correspondence to V. E. Tarabanko.

Additional information

Original Russian Text © V.E. Tarabanko, M.Yu. Chernyak, I.L. Simakova, K.L. Kaigorodov, Yu.N. Bezborodov, N.F. Orlovskaya, 2015, published in Zhurnal Prikladnoi Khimii, 2015, Vol. 88, No. 11, pp. 1563−1567.

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Tarabanko, V.E., Chernyak, M.Y., Simakova, I.L. et al. Antiknock properties of furfural derivatives. Russ J Appl Chem 88, 1778–1782 (2015). https://doi.org/10.1134/S10704272150110063

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  • DOI: https://doi.org/10.1134/S10704272150110063

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