Fact sheet: Acenaphthene

From: Public Services and Procurement Canada

Discover a list of a contaminant's important chemical properties, how it will react in the environment, main sources of contamination related, and a brief overview of health and safety issues.

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General information

CAS number

83-32-9

Molecular formula

C12H10

Formula weight

154.2 g/mol

Family

Polycyclic aromatic hydrocarbons (PAH)

Properties (at room temperature where applicable)

Compound properties list
ParameterValueComment
Melting/boiling point 93 °CSolid
Relative density1.18 g/cm3Sinks in water
Vapour pressure0.002 mm HgVery low volatility
Vapour density0N/A
Solubility in water4 mg/LLow solubility
Henry's law constant1 x 10-4 atm·m3/molModerate volatilization when dissolved
log Koc (Depending on soil or sediment characteristics)3.5 - 5.8*Strong adsorption to organic matter

Environmental behaviour

At 20 0C, acenaphthene is a solid with very low volatility. Characterized by low solubility, it will volatilize moderately once dissolved and adsorbs strongly to organic matter. When present in soil, this compound will undergo light volatilize and solubilize slowly. Once dissolved, it will either enter into the groundwater table or migrate towards a waterway, where it will be diluted before partially volatilizing. Fragments of acenaphthene can also be carried into a waterway and deposited at the bottom where they will dissolve slowly. Once the source has been removed, the adsorbed acenaphthene will take a very long time to disappear, liberating contamination in either the gaseous or dissolved state. The resulting plumes (gaseous or dissolved) will be relatively small in size.

Health and safety

Acenaphthene should be handled with care as it is toxic.

Principal resources

Acenaphthene is a polycyclic aromatic hydrocarbon (PAH). PAHs are a group of organic compounds that contain two or more benzene rings in their structure. There are more than 100 different PAHs that generally occur as complex mixtures (example, combustion by-products such as soot). Incomplete combustion of fuels in engines, during coal coking, or when wood is burning (forest fires, wood stoves) produces PAHs. PAHs are also constituents of petroleum and coal, and they are more present in some of their derivatives like tars and asphalt. The wood preservative industry (example, creosote), aluminum smelters using Soderberg electrodes, and hazardous waste disposal sites are further contributors of anthropogenic PAHs to the environment.

Acenaphthene may be obtained from coal tar and petroleum refining, or by passing ethylene and benzene or naphthalene through a red-hot tube. Acenaphthene has been used as an intermediate in the production of dyes, pharmaceuticals, photographic chemicals, insecticides, fungicides, plastics and plant growth hormones, and in chemical, biochemical, or cancer research. Acenaphthene is also likely to be found mixed with other PAHs in commercial products like coal tar, coal tar pitch, creosote, bitumen and asphalt. Coal tar is used as a fuel in the steel industry, distilled to give coal tar pitch and creosote, and has been used in the clinical treatment of skin disorders such as eczema and dermatitis. Coal tar pitch is used primarily as a binder for aluminum smelting electrodes, but is also used in roofing, surface coatings, and a variety of other applications. Creosote is used to preserve wood for railroad ties, marine pilings and telephone poles. Some creosote products are also used as a fuel in steel production. Bitumen and asphalt are used for paving roads, for sound- and water-proofing, and coating pipes.

References

Polycyclic Aromatic Hydrocarbons (PAHs). U.S. Department of Health and Human Services, Public Health Service, Georgia, USA. (Viewed December 2013)

Canadian Council of Ministers of the Environment. 1999. Canadian Water Quality Guidelines for the Protection of Aquatic Life: Polycyclic Aromatic Hydrocarbons (PAHs). In: Canadian Environmental Quality Guidelines. Canadian Council of Ministers of the Environment, Manitoba, Canada. (Viewed December 2013).

Montgomery, John H. 2007. Groundwater Chemicals, Desk Reference, Fourth Edition, CRC Press, Taylor and Francis Group, Florida, USA.

National Toxicology Program. 2005. Report on Carcinogens, Twelfth Edition: Substance Profile of Polycyclic Aromatic Hydrocarbons. U.S. Department of Health and Human Services, Public Health Services, USA.(PDF, 256KB) (Viewed December 2013)

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