Propene

Propene

Names
Preferred IUPAC name Propene[1]
Identifiers
CAS Number	115-07-1 Y
3D model (JSmol)	Interactive image Interactive image
ChEBI	CHEBI:16052 Y
ChEMBL	ChEMBL117213 Y
ChemSpider	7954 Y
KEGG	C11505 Y
PubChem CID	8252
RTECS number	UC6740000
UNII	AUG1H506LY Y
UN number	1077 In Liquefied petroleum gas: 1075
InChI InChI=1S/C3H6/c1-3-2/h3H,1H2,2H3 Y Key: QQONPFPTGQHPMA-UHFFFAOYSA-N Y InChI=1/C3H6/c1-3-2/h3H,1H2,2H3 Key: QQONPFPTGQHPMA-UHFFFAOYAA
SMILES C=CC CC=C
Properties
Chemical formula	C3H6
Molar mass	42.081 g·mol−1
Appearance	Colorless gas
Density	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
Safety data sheet	External MSDS
EU classification (DSD) (outdated)
R-phrases (outdated)	12
S-phrases (outdated)	9-16-33
NFPA 704 (fire diamond)	4 1 1
Flash point	−108 °C (−162 °F; 165 K)
Related compounds
Related alkenes; related groups	Ethylene, Isomers of Butylene; Allyl, Propenyl
Related compounds	Propane, Propyne Propadiene, 1-Propanol 2-Propanol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Y verify (what is YN ?)
Infobox references

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.^[2]

Production

Steam cracking

Main page: Chemistry:Steam cracking

The dominant technology for producing propylene is steam cracking. The same technology is applied to ethane to ethylene. These two conversions are the #2 and #1 processes in the chemical industry, as judged by their scale.^[3] In this process, propane undergoes dehydrogenation. The by-product is hydrogen:

CH₃CH₂CH₃ → CH₃CH=CH₂ + H₂

The yield of propene is about 85 m%. By-products are usually used as fuel for the propane dehydrogenation reaction. Steam cracking is one of the most energy-intensive industrial processes.

The feedstock is naphtha or propane, especially in the Middle East, where there is an abundance of propane from oil/gas operations.^[4] Propene can be separated by fractional distillation from hydrocarbon mixtures obtained from cracking and other refining processes; refinery-grade propene is about 50 to 70%.^[5] In the United States, shale gas is a major source of propane.

Olefin conversion technology

In the Phillips Triolefin or Olefin conversion technology propylene is interconverted with ethylene and 2-butenes. Rhenium and molybdenum catalysts are used:^[6]

CH₂=CH₂ + CH₃CH=CHCH₃ → 2 CH₂=CHCH₃

The technology is founded on an olefin metathesis reaction discovered at Phillips Petroleum Company.^[7][8] Propene yields of about 90 wt% are achieved.

Main page: Physics: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 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.

Fluid catalytic cracking

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 m% 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.^[9]

Market and research

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.^[10] Total world production of propene is currently about half that of ethylene.

The use of engineered enzymes has been explored but is of no commercial value.^[11]

Uses

Propene 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.^[12] Polypropylene end uses include films, fibers, containers, packaging, and caps and closures. Propene is also used for the production of important chemicals such as propylene oxide, acrylonitrile, cumene, butyraldehyde, and acrylic acid. In the year 2013 about 85 million tonnes of propene were processed worldwide.^[12]

Propene and benzene are converted to acetone and phenol via the cumene process.

Propene is also used to produce isopropanol (propan-2-ol), acrylonitrile, propylene oxide, and epichlorohydrin.^[13] The industrial production of acrylic acid involves the catalytic partial oxidation of propene.^[14] Propene is also an intermediate in the one-step propane selective oxidation to acrylic acid.^{[15][16][17][18]} In industry and workshops, propene 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

Propene resembles other alkenes in that it undergoes 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: 1) polymerization, 2) oxidation, 3) halogenation and hydrohalogenation, 4) alkylation, 5) hydration, 6) oligomerization, and 7) hydroformylation.

Complexes of transition metals

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

The majority of propene is used to form polypropylene, a very important commodity thermoplastic, through chain-growth polymerization.^[12] In the presence of a suitable catalyst (typically a Ziegler–Natta catalyst), propene will polymerize. There are multiple ways to achieve this, such as using high pressures to suspending the catalyst in a solution of liquid propene, or running gaseous propene through a fluidized bed reactor.^[20]

Combustion

Propene burns in a similar fashion to other alkenes. In the presence of sufficient or excess oxygen, propene burns to form water and carbon dioxide.

2 C₃H₆ + 9 O₂ → 6 CO₂ + 6 H₂O

Environmental safety

Propene is a product of combustion from forest fires, cigarette smoke, and motor vehicle and aircraft exhaust. 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.^[5]

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.^[5]

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.^[21] 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.^[22][23] It has been examined, motivated by diverse interests such a carbon footprint. Production from glucose has been considered.^[24] More advance ways of addressing such issues focus on electrification alternatives to steam cracking.

Storage and handling

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.^[25]

Occurrence in nature

Propene is detected in the interstellar medium through microwave spectroscopy.^[26] On September 30, 2013, NASA also announced that the Cassini orbiter spacecraft, part of the Cassini-Huygens mission, had discovered small amounts of naturally occurring propene in the atmosphere of Titan using spectroscopy.^[27][28]

See also

• Los Alfaques Disaster
• Inhalant abuse
• 2014 Kaohsiung gas explosions
• 2020 Houston explosion

References

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