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HandWiki. Propene. Encyclopedia. Available online: https://encyclopedia.pub/entry/29362 (accessed on 16 September 2026).
HandWiki. Propene. Encyclopedia. Available at: https://encyclopedia.pub/entry/29362. Accessed September 16, 2026.
HandWiki. "Propene" Encyclopedia, https://encyclopedia.pub/entry/29362 (accessed September 16, 2026).
HandWiki. (2022, October 14). Propene. In Encyclopedia. https://encyclopedia.pub/entry/29362
HandWiki. "Propene." Encyclopedia. Web. 14 October, 2022.
Propene
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The content is sourced from: https://handwiki.org/wiki/Chemistry:Propene

Propene, also known as propylene, is an unsaturated organic compound with the chemical formula [math]\ce{ CH3CH=CH2 }[/math]. It has one double bond, and is the second simplest member of the alkene class of hydrocarbons. It is a colorless gas with a faint petroleum-like odor.

alkene propylene propene

References

  1. Giovanni Maggini (2013-04-17). "Technology Economics: Propylene via Propane Dehydrogenation, Part 3". Slideshare.net. http://www.slideshare.net/intratec/technology-economics-propylene-via-propane-dehydrogenation-part-3. 
  2. Ashford’s Dictionary of Industrial Chemicals, Third edition, 2011, ISBN:978-0-9522674-3-0, pages 7766-9
  3. "Product Safety Assessment(PSA): Propylene". Dow Chemical Co.. http://www.dow.com/productsafety/finder/pro.htm. 
  4. Ghashghaee, Mohammad (2018). "Heterogeneous catalysts for gas-phase conversion of ethylene to higher olefins". Rev. Chem. Eng. 34 (5): 595–655. doi:10.1515/revce-2017-0003.  https://dx.doi.org/10.1515%2Frevce-2017-0003
  5. Banks, R. L.; Bailey, G. C. (1964). "Olefin Disproportionation. A New Catalytic Process". Industrial & Engineering Chemistry Product Research and Development 3 (3): 170–173. doi:10.1021/i360011a002.  https://dx.doi.org/10.1021%2Fi360011a002
  6. Lionel Delaude, Alfred F. Noels (2005). Kirk-Othmer Encyclopedia of Chemical Technology. Weinheim: Wiley-VCH. doi:10.1002/0471238961.metanoel.a01. ISBN 978-0471238966.  https://dx.doi.org/10.1002%2F0471238961.metanoel.a01
  7. Schiffer, Zachary J.; Manthiram, Karthish (2017). "Electrification and Decarbonization of the Chemical Industry". Joule 1: 10–14. doi:10.1016/j.joule.2017.07.008.  https://dx.doi.org/10.1016%2Fj.joule.2017.07.008
  8. Amghizar, Ismaël; Vandewalle, Laurien A.; Van Geem, Kevin M.; Marin, Guy B. (2017). "New Trends in Olefin Production". Engineering 3 (2): 171–178. doi:10.1016/J.ENG.2017.02.006.  https://dx.doi.org/10.1016%2FJ.ENG.2017.02.006
  9. de Guzman, Doris (October 12, 2012). "Global Bioenergies in bio-propylene". https://greenchemicalsblog.com/2012/10/12/global-bioenergies-in-bio-propylene. 
  10. "Market Study: Propylene (2nd edition), Ceresana, December 2014". ceresana.com. http://www.ceresana.com/en/market-studies/chemicals/propylene/. 
  11. Budavari, Susan, ed (1996). "8034. Propylene". The Merck Index, Twelfth Edition. New Jersey: Merck & Co.. pp. 1348–1349. 
  12. J.G.L., Fierro (Ed.) (2006). Metal Oxides, Chemistry and Applications. CRC Press. pp. 414–455. 
  13. Naumann d'Alnoncourt, Raoul; Csepei, Lénárd-István; Hävecker, Michael et al. (March 2014). "The reaction network in propane oxidation over phase-pure MoVTeNb M1 oxide catalysts". Journal of Catalysis 311: 369–385. doi:10.1016/j.jcat.2013.12.008.  https://dx.doi.org/10.1016%2Fj.jcat.2013.12.008
  14. Amakawa, Kazuhiko; Kolen'Ko, Yury V.; Villa, Alberto et al. (7 June 2013). "Multifunctionality of Crystalline MoV(TeNb) M1 Oxide Catalysts in Selective Oxidation of Propane and Benzyl Alcohol". ACS Catalysis 3 (6): 1103–1113. doi:10.1021/cs400010q.  https://dx.doi.org/10.1021%2Fcs400010q
  15. Hävecker, Michael; Wrabetz, Sabine; Kröhnert, Jutta et al. (January 2012). "Surface chemistry of phase-pure M1 MoVTeNb oxide during operation in selective oxidation of propane to acrylic acid". Journal of Catalysis 285 (1): 48–60. doi:10.1016/j.jcat.2011.09.012.  https://dx.doi.org/10.1016%2Fj.jcat.2011.09.012
  16. Csepei, Lénárd-István (2011). Kinetic studies of propane oxidation on Mo and V based mixed oxide catalysts. pp. 3–24, 93. doi:10.14279/depositonce-2972.  https://dx.doi.org/10.14279%2Fdepositonce-2972
  17. For example, "MAPP-Pro" http://www.worthingtonindustries.com/getmedia/ff77868e-b526-44ae-9064-e51aaa5ea02f/wc001-map-pro-premium-hand-torch-fuel
  18. Heggs, T. Geoffrey (2011-10-15), Wiley-VCH Verlag GmbH & Co. KGaA, ed. (in en), Polypropylene, Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, pp. o21_o04, doi:10.1002/14356007.o21_o04, ISBN 978-3-527-30673-2, https://onlinelibrary.wiley.com/doi/10.1002/14356007.o21_o04, retrieved 2021-07-09 
  19. PubChem. "Hazardous Substances Data Bank (HSDB) : 175" (in en). https://pubchem.ncbi.nlm.nih.gov/source/hsdb/175#section=Human-Toxicity-Excerpts-(Complete). 
  20. Bio-based drop-in, smart drop-in and dedicated chemicals https://www.roadtobio.eu/uploads/news/2017_October/RoadToBio_Drop-in_paper.pdf
  21. Duurzame bioplastics op basis van hernieuwbare grondstoffen https://www.wur.nl/nl/Onderzoek-Resultaten/Onderzoeksinstituten/food-biobased-research/Oplossingen/Duurzame-bioplastics-op-basis-van-hernieuwbare-grondstoffen.htm
  22. Guzman, Doris de (12 October 2012). "Global Bioenergies in bio-propylene" (in en-US). https://greenchemicalsblog.com/2012/10/12/global-bioenergies-in-bio-propylene/. 
  23. Encyclopedia of Chemical Technology, Fourth edition, 1996, ISBN:0471-52689-4 (v.20), page 261
  24. Marcelino, N.; Cernicharo, J.; Agúndez, M. et al. (2007-08-10). "Discovery of Interstellar Propylene (CH2CHCH3): Missing Links in Interstellar Gas-Phase Chemistry". The Astrophysical Journal (IOP) 665 (2): L127–L130. doi:10.1086/521398. Bibcode: 2007ApJ...665L.127M.  https://dx.doi.org/10.1086%2F521398
  25. "Spacecraft finds propylene on Saturn moon, Titan". UPI.com. 2013-09-30. http://www.upi.com/Science_News/2013/09/30/Cassini-finds-ingredient-of-household-plastic-on-Saturn-moon/UPI-42881380571911/. 
  26. "Cassini finds ingredient of household plastic on Saturn moon". Spacedaily.com. http://www.spacedaily.com/reports/Cassini_finds_ingredient_of_household_plastic_on_Saturn_moon_999.html. 
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