1.81 kg/m3, gas (1.013 bar, 15 °C) 1.745 kg/m3, gas (1.013 bar, 25 °C)613.9 kg/m3, liquid
Melting point
−185.2 °C (−301.4 °F; 88.0 K)
Boiling point
−47.6 °C (−53.7 °F; 225.6 K)
Solubility in water
0.61 g/m3
Magnetic susceptibility (χ)
−31.5·10−6 cm3/mol
Viscosity
8.34 µPa·s at 16.7 °C
Structure
Dipole moment
0.366 D (gas)
Hazards
GHS labelling:[3]
Pictograms
Signal word
Danger
Hazard statements
H220
Precautionary statements
P210, P377, P381, P403
NFPA 704 (fire diamond)
141
Flash point
−108 °C (−162 °F; 165 K)
Safety data sheet (SDS)
External MSDS
Related compounds
Related alkenes;related groups
Ethylene, Isomers of Butylene;Allyl, Propenyl
Related compounds
Propane, PropynePropadiene, 1-Propanol2-Propanol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Yverify (what is YN ?) Infobox references
Chemical compound
Propylene, also known as propene, is an unsaturated organic compound with the chemical formula CH3CH=CH2. 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.[4]
Propylene is a product of combustion from forest fires, cigarette smoke, and motor vehicle and aircraft exhaust.[5] It was discovered in 1850 by A. W. von Hoffmann's student John Williams Reynolds as the only gaseous product of thermal decomposition of amyl alcohol to react with chlorine and bromine.[6]
Production
[edit]
Steam cracking
[edit] Main article: Steam cracking
The dominant technology for producing propylene is steam cracking, using propane as the feedstock. Cracking propane yields a mixture of ethylene, propylene, methane, hydrogen gas, and other related compounds. The yield of propylene is about 15%. The other principal feedstock is naphtha, especially in the Middle East and Asia.[7] Propylene can be separated by fractional distillation from the hydrocarbon mixtures obtained from cracking and other refining processes; refinery-grade propene is about 50 to 70%.[8] In the United States, shale gas is a major source of propane.
Olefin conversion technology
[edit]
In the Phillips triolefin or olefin conversion technology, propylene is interconverted with ethylene and 2-butenes. Rhenium and molybdenum catalysts are used:[9]
The technology is founded on an olefin metathesis reaction discovered at Phillips Petroleum Company.[10][11] Propylene yields of about 90 wt% are achieved.
Main article: Syngas to gasoline plus
Related is the Methanol-to-Olefins/Methanol-to-Propene process. It converts synthesis gas (syngas) to methanol, and then converts the methanol to ethylene and/or propene. The process produces water as a by-product. Synthesis gas is produced from the reformation of natural gas or by the steam-induced reformation of petroleum products such as naphtha, or by gasification of coal or natural gas.
Fluid catalytic cracking
[edit]
High severity fluid catalytic cracking (FCC) uses traditional FCC technology under severe conditions (higher catalyst-to-oil ratios, higher steam injection rates, higher temperatures, etc.) in order to maximize the amount of propene and other light products. A high severity FCC unit is usually fed with gas oils (paraffins) and residues, and produces about 20–25% (by mass) of propene on feedstock together with greater volumes of motor gasoline and distillate byproducts. These high temperature processes are expensive and have a high carbon footprint. For these reasons, alternative routes to propylene continue to attract attention.[12]
Other commercialized methods
[edit]
On-purpose propylene production technologies were developed throughout the twentieth century. Of these, propane dehydrogenation technologies such as the CATOFIN and OLEFLEX processes have become common, although they still make up a minority of the market, with most of the olefin being sourced from the above mentioned cracking technologies. Platinum, chromia, and vanadium catalysts are common in propane dehydrogenation processes.
Market
[edit]
Propene production has remained static at around 35 million tonnes (Europe and North America only) from 2000 to 2008, but it has been increasing in East Asia, most notably Singapore and China.[13] Total world production of propene is currently about half that of ethylene.
Research
[edit]
The use of engineered enzymes has been explored but has not been commercialized.[14]
There is ongoing research into the use of oxygen carrier catalysts for the oxidative dehydrogenation of propane. This poses several advantages, as this reaction mechanism can occur at lower temperatures than conventional dehydrogenation, and may not be equilibrium-limited because oxygen is used to combust the hydrogen by-product.[15]
Uses
[edit]
Propylene is the second most important starting product in the petrochemical industry after ethylene. It is the raw material for a wide variety of products. Polypropylene manufacturers consume nearly two thirds of global production.[16] Polypropylene end uses include films, fibers, containers, packaging, and caps and closures. Propene is also used for the production of chemicals such as propylene oxide, acrylonitrile, cumene, butyraldehyde, and acrylic acid. In the year 2013 about 85 million tonnes of propylene were processed worldwide.[16]
Propylene and benzene are converted to acetone and phenol via the cumene process.
Overview of the cumene process
Propylene is also used to produce isopropyl alcohol (propan-2-ol), acrylonitrile, propylene oxide, and epichlorohydrin.[17] The industrial production of acrylic acid involves the catalytic partial oxidation of propylene.[18] Propylene is an intermediate in the oxidation to acrylic acid.
In industry and workshops, propylene is used as an alternative fuel to acetylene in Oxy-fuel welding and cutting, brazing and heating of metal for the purpose of bending. It has become a standard in BernzOmatic products and others in MAPP substitutes,[19] now that true MAPP gas is no longer available.
Reactions
[edit]
Propylene resembles other alkenes in that it undergoes electrophilic addition reactions relatively easily at room temperature. The relative weakness of its double bond explains its tendency to react with substances that can achieve this transformation. Alkene reactions include:
Polymerization and oligomerization
Oxidation
Halogenation
Hydrohalogenation
Alkylation
Hydration
Hydroformylation
Complexes of transition metals
[edit]
Foundational to hydroformylation, alkene metathesis, and polymerization are metal-propylene complexes, which are intermediates in these processes. Propylene is prochiral, meaning that binding of a reagent (such as a metal electrophile) to the C=C group yields one of two enantiomers.
Polymerization
[edit] See also: Polypropylene
The majority of propylene is used to form polypropylene, a very important commodity thermoplastic, through chain-growth polymerization.[16] In the presence of a suitable catalyst (typically a Ziegler–Natta catalyst), propylene will polymerize. There are multiple ways to achieve this, such as using high pressures to suspending the catalyst in a solution of liquid propylene, or running gaseous propylene through a fluidized bed reactor.[20]
Oligomerization
[edit]
In the presence of catalysts, propylene will form various short oligomers. It can dimerizes to give 2,3-dimethyl-1-butene and/or 2,3-dimethyl-2-butene.[21] or trimerise to form tripropylene.
Environmental safety
[edit]
Propene is a product of combustion from forest fires, cigarette smoke, and motor vehicle and aircraft exhaust.[5] It is an impurity in some heating gases. Observed concentrations have been in the range of 0.1–4.8 parts per billion (ppb) in rural air, 4–10.5 ppb in urban air, and 7–260 ppb in industrial air samples.[8]
In the United States and some European countries a threshold limit value of 500 parts per million (ppm) was established for occupational (8-hour time-weighted average) exposure. It is considered a volatile organic compound (VOC) and emissions are regulated by many governments, but it is not listed by the U.S. Environmental Protection Agency (EPA) as a hazardous air pollutant under the Clean Air Act. With a relatively short half-life, it is not expected to bioaccumulate.[8]
Propene has low acute toxicity from inhalation and is not considered to be carcinogenic. Chronic toxicity studies in mice did not yield significant evidence suggesting adverse effects. Humans briefly exposed to 4,000 ppm did not experience any noticeable effects.[22] Propene is dangerous from its potential to displace oxygen as an asphyxiant gas, and from its high flammability/explosion risk.
Bio-propylene is the bio-based propylene.[23][24] It has been examined, motivated by diverse interests such a carbon footprint. Production from glucose has been considered.[25] More advanced ways of addressing such issues focus on electrification alternatives to steam cracking.
Storage and handling
[edit]
Propene is flammable. Propene is usually stored as liquid under pressure, although it is also possible to store it safely as gas at ambient temperature in approved containers.[26]
Occurrence in nature
[edit]
Propene is detected in the interstellar medium through microwave spectroscopy.[27] On September 30, 2013, NASA announced the detection of small amounts of naturally occurring propene in the atmosphere of Titan using infrared spectroscopy.[28][29][30] The detection was made by a team led by NASA GSFC scientist Conor Nixon using data from the CIRS instrument [31][32] on the Cassini orbiter spacecraft, part of the Cassini-Huygens mission. Its confirmation solved a 32-year old mystery by filling a predicted gap in Titan's detected hydrocarbons, adding the C3H6 species (propene) to the already-detected C3H4 (propyne) and C3H8 (propane).[33]
See also
[edit]
Los Alfaques disaster
Inhalant abuse
2014 Kaohsiung gas explosions
2020 Houston explosion
Titan (moon)
References
[edit]
^"General Principles, Rules, and Conventions". Nomenclature of Organic Chemistry: IUPAC Recommendations and Preferred Names 2013 (Blue Book). Cambridge: The Royal Society of Chemistry. 2014. p. 31. doi:10.1039/9781849733069-00001. ISBN 978-0-85404-182-4.
^Moss, G.P. (web version). "P-14.3 Locants". Nomenclature of Organic Chemistry. IUPAC Recommendations and Preferred Names 2013. London: Queen Mary University. Section P-14.3.4.2 (d). Retrieved 23 August 2024.
^"Propylene". pubchem.ncbi.nlm.nih.gov. Retrieved 14 December 2021.
^"Propylene".
^ abMorgott, David (2018-01-04). "The Human Exposure Potential from Propylene Releases to the Environment". International Journal of Environmental Research and Public Health. 15 (1): 66. doi:10.3390/ijerph15010066. ISSN 1660-4601. PMC 5800165. PMID 29300328.
^Rasmussen, Seth C. (2018), Rasmussen, Seth C. (ed.), "Introduction", Acetylene and Its Polymers: 150+ Years of History, SpringerBriefs in Molecular Science, Cham: Springer International Publishing, pp. 1–19, doi:10.1007/978-3-319-95489-9_1, ISBN 978-3-319-95489-9
^Ashford's Dictionary of Industrial Chemicals, Third edition, 2011, ISBN 978-0-9522674-3-0, pages 7766–9
^ abc"Product Safety Assessment(PSA): Propylene". Dow Chemical Co. Archived from the original on 2013-08-28. Retrieved 2011-07-11.
^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. S2CID 103664623.
^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.
^Lionel Delaude; Alfred F. Noels (2005). "Metathesis". Kirk-Othmer Encyclopedia of Chemical Technology. Weinheim: Wiley-VCH. doi:10.1002/0471238961.metanoel.a01. ISBN 978-0-471-23896-6.
^Schiffer, Zachary J.; Manthiram, Karthish (2017). "Electrification and Decarbonization of the Chemical Industry". Joule. 1 (1): 10–14. Bibcode:2017Joule...1...10S. doi:10.1016/j.joule.2017.07.008. hdl:1721.1/124019. S2CID 117360588.
^Amghizar, Ismaël; Vandewalle, Laurien A.; Van Geem, Kevin M.; Marin, Guy B. (2017). "New Trends in Olefin Production". Engineering. 3 (2): 171–178. Bibcode:2017Engin...3..171A. doi:10.1016/J.ENG.2017.02.006.
^de Guzman, Doris (October 12, 2012). "Global Bioenergies in bio-propylene". Green Chemicals Blog.
^Wu, Tianwei; Yu, Qingbo; Roghair; et al. (2020). "Chemical looping oxidative dehydrogenation of propane: A comparative study of Ga-based, Mo-based, V-based oxygen carriers". Chemical Engineering and Processing - Process Intensification. 157 108137. Bibcode:2020CEPPI.15708137W. doi:10.1016/j.cep.2020.108137. ISSN 0255-2701.
^"Cassini finds ingredient of household plastic on Saturn moon". Spacedaily.com. Retrieved 2013-11-12.
^Nixon, C. A.; Jennings, D. E.; Bézard, B.; Vinatier, S.; Teanby, N. A.; Sung, K.; Ansty, T. M.; Irwin, P. G. J.; Gorius, N.; Cottini, V.; Coustenis, A.; Flasar, F. M. (2013-09-30). "Detection of Propene in Titan's Stratosphere". The Astrophysical Journal. 776 (1): L14. arXiv:1309.4489. Bibcode:2013ApJ...776L..14N. doi:10.1088/2041-8205/776/1/L14. ISSN 2041-8205.
^Flasar, F. M.; Kunde, V. G.; Abbas, M. M.; Achterberg, R. K.; Ade, P.; Barucci, A.; Bézard, B.; Bjoraker, G. L.; Brasunas, J. C. (2004), Russell, Christopher T. (ed.), "Exploring the Saturn System in the Thermal Infrared: The Composite Infrared Spectrometer", The Cassini-Huygens Mission: Orbiter Remote Sensing Investigations, Dordrecht: Springer Netherlands, pp. 169–297, Bibcode:2004chm..book..169F, doi:10.1007/1-4020-3874-7_4, ISBN 978-1-4020-3874-7, retrieved 2025-01-05
^Jennings, D. E.; Flasar, F. M.; Kunde, V. G.; Nixon, C. A.; Segura, M. E.; Romani, P. N.; Gorius, N.; Albright, S.; Brasunas, J. C.; Carlson, R. C.; Mamoutkine, A. A.; Guandique, E.; Kaelberer, M. S.; Aslam, S.; Achterberg, R. K. (2017-06-20). "Composite infrared spectrometer (CIRS) on Cassini". Applied Optics. 56 (18): 5274–5294. Bibcode:2017ApOpt..56.5274J. doi:10.1364/AO.56.005274. ISSN 2155-3165. PMID 29047582.
^Maguire, W. C.; Hanel, R. A.; Jennings, D. E.; Kunde, V. G.; Samuelson, R. E. (August 1981). "C3H8 and C3H4 in Titan's atmosphere". Nature. 292 (5825): 683–686. doi:10.1038/292683a0. ISSN 1476-4687.
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