Ethylbenzene

Ethylbenzene
Skeletal formula of ethylbenzene
Ball-and-stick model of the ethylbenzene molecule
Names
IUPAC name
Ethylbenzene
Other names
Ethylbenzol; Phenylethane: alpha-Methyltoluene; EB
Identifiers
100-41-4 YesY
3D model (Jmol) Interactive image
Abbreviations EB
1901871
ChEBI CHEBI:16101 YesY
ChEMBL ChEMBL371561 YesY
ChemSpider 7219 YesY
DrugBank DB01722 YesY
ECHA InfoCard 100.002.591
KEGG C07111 YesY
PubChem 7500
RTECS number DA0700000
UNII L5I45M5G0O YesY
Properties
C8H10
Molar mass 106.17 g·mol−1
Appearance colorless liquid
Odor aromatic[1]
Density 0.8665 g/mL
Melting point −95 °C (−139 °F; 178 K)
Boiling point 136 °C (277 °F; 409 K)
0.015 g/100 mL (20 °C)
log P 3.27
Vapor pressure 9.998mmHg
1.495
Viscosity 0.669 cP at 20 °C
0.58 D[2]
Thermochemistry
1.726 J/(gK)
Hazards
Main hazards Flammable
R-phrases R11 R20
S-phrases (S2) S16 S24/25 S29
NFPA 704
Flammability code 3: Liquids and solids that can be ignited under almost all ambient temperature conditions. Flash point between 23 and 38 °C (73 and 100 °F). E.g., gasoline) Health code 2: Intense or continued but not chronic exposure could cause temporary incapacitation or possible residual injury. E.g., chloroform Reactivity code 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g., liquid nitrogen Special hazards (white): no codeNFPA 704 four-colored diamond
3
2
0
Flash point 22.22 °C (72.00 °F; 295.37 K)
430 °C (806 °F; 703 K)
Explosive limits 1%-7.8%
Lethal dose or concentration (LD, LC):
5460 mg/kg
4000 ppm (rat, 4 hr)[3]
US health exposure limits (NIOSH):
PEL (Permissible)
 TWA 100 ppm (435 mg/m3)[1]
REL (Recommended)
 TWA 100 ppm (435 mg/m3) ST 125 ppm (545 mg/m3)[1]
IDLH (Immediate danger)
 800 ppm[1]
Related compounds
styrene, toluene
Related compounds
 benzene
polystyrene
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
YesY verify (what is YesYN ?)
Infobox references

Ethylbenzene is an organic compound with the formula C6H5CH2CH3. It is a highly flammable, colorless liquid with an odor similar to that of gasoline. This monocyclic aromatic hydrocarbon is important in the petrochemical industry as an intermediate in the production of styrene, the precursor to polystyrene, a common plastic material. In 2012, more than 99% of ethylbenzene produced was consumed in the production of styrene. Ethylbenzene is also used to make other chemicals, in fuel, and as a solvent in inks, rubber adhesives, varnishes, and paints. Ethylbenzene exposure can be determined by testing for the breakdown products in urine.

Physical and chemical properties

Ethylbenzene[4] is a colorless liquid that smells similar to gasoline with a sweet aroma, evaporates quickly and is highly flammable. It has a characteristic odor with an odor threshold at 2.3 ppm and a melting point of −95 °C (−139 °F) and a boiling point of 136 °C (277 °F).[5] It is classified as a monocyclic aromatic hydrocarbon since it is a compound that contains one aromatic ring.[4][6]

Occurrence and applications

Ethylbenzene occurs naturally in coal tar and petroleum, although this is not the main source of this compound.[7]

The dominant application of ethylbenzene is role as an intermediate in the production of polystyrene. Catalytic dehydrogenation of ethylbenzene gives hydrogen and styrene:

C
6H
5CH
2CH
3 → C6H5CH=CH2 + H
2

As of May 2012, greater than 99% of all the ethylbenzene produced is used for this purpose.

Niche uses

Ethylbenzene is added to gasoline as an anti-knock agent, meaning it reduces engine knocking and increase the octane rating. Ethylbenzene is often found in other manufactured products, including pesticides, cellulose acetate, synthetic rubber, paints, and inks.[7] Used in the recovery of natural gas, ethylbenzene may be injected into the ground.

Production

Ethylbenzene is produced in on a large scale by combining benzene (C
6H
6) and ethylene (C
2H
4) in an acid-catalyzed chemical reaction:

C
6H
6 + C
2H
4 → C
6H
5CH
2CH
3

In 2012, more than 99% of ethylbenzene was produced in this way. Thus, manufacturers of ethylbenzene are the major buyers of benzene, claiming more than half of total output.[8]

Small amounts of ethylbenzene are recovered from the mix of xylenes by superfractioning, an extension of the distillation process.[4]

In the 1980s a zeolite-based process using vapor phase alkylation, offered a higher purity and yield. Then a liquid phase process was introduced using zeolite catalysts. This offers low benzene-to-ethylene ratios, reducing the size of the required equipment and lowering byproduct production.[9]

Approximately 24,700,000 tons were produced in 1999.[10]

Health effects

The acute toxicity of ethylbenzene is low, with an LD50 of about 4 grams per kilogram of body weight. The longer term toxicity and carcinogenicity is ambiguous.[10] Eye and throat sensitivity can occur when high level exposure to ethylbenzene in the air occurs. At higher level exposure, ethylbenzene can cause dizziness.[7] Once inside the body, ethylbenzene biodegrades to 1-phenylethanol, acetophenone, phenylglyoxylic acid, mandelic acid, benzoic acid and hippuric acid.[10]

As of September 2007, the United States Environmental Protection Agency (EPA) determined that drinking water with concentration of 30 parts per million (ppm) for one day or 3 ppm for ten days is not expected to have any adverse effect in children. Lifetime exposure of 0.7 ppm ethylbenzene is not expected to have any adverse effect either. The U.S. Occupational Safety and Health Administration (OSHA) limits exposure to workers to an average 100 ppm for an 8-hour work day, a 40-hour workweek.[7]

Ethylbenzene is classified as a possible carcinogen by the International Agency for Research on Cancer (IARC) however, the EPA has not determined ethylbenzene to be a carcinogen. The National Toxicology Program conducted an inhalation study in rats and mice. Exposure to ethylbenzene resulted in an increased incidence of kidney and testicular tumors in male rats, and trends of increased kidney tumors in female rats, lung tumors in male mice, and liver tumors in female mice.

As for all organic compounds, ethylbenzene vapors form an explosive mixture with air.[4] When transporting ethylbenzene, it is classified as a flammable liquid in class 3, Packing Group II.[4]

Environmental effects

Ethylbenzene is found mostly as a vapor in the air since it can easily move from water and soil.[7] A median concentration of 0.62 parts per billion (ppb) was found in urban air in 1999.[5] A study conducted in 2012 found that in country air the median concentration was found to be 0.01 ppb and indoors the median concentration was 1.0 ppb. It can also be released into the air through the burning of coal, gas, and oil. The use of ethylbenzene in industry contributes to ethylbenzene vapor in the air. After about three days in the air with the help of sunlight, other chemicals break down ethylbenzene into chemicals that can be found in smog.[7] Since it does not readily bind to soil it can also easily move into groundwater. In surface water, it breaks down when it reacts with chemicals naturally found in water.[11] Generally, ethylbenzene is not found in drinking water, however it can be found in residential drinking water wells if the wells are near waste sites, underground fuel storage tanks that are leaking, or landfills.[7]

As of 2012, according to the EU Dangerous Substances Directive, ethylbenzene is not classified as hazardous to the environment.[4]

Biodegradation

Certain strands of the fungus Cladophialophora can grow on ethylbenzene.[12] The bacterium "Aromatoleum aromaticum" EbN1 was discovered due to its ability to grow on ethylbenzene.[13]

References

  1. 1 2 3 4 "NIOSH Pocket Guide to Chemical Hazards #0264". National Institute for Occupational Safety and Health (NIOSH).
  2. ↑ Lange's Handbook of Chemistry (15th ed.). 1999.
  3. ↑ "Ethyl benzene". Immediately Dangerous to Life and Health. National Institute for Occupational Safety and Health (NIOSH).
  4. 1 2 3 4 5 6 "ETHYLBENZENE : ENVIRONMENTAL, HEALTH & SAFETY GUIDELINES". CEFIC. Retrieved 14 February 2013.
  5. 1 2 "Technology Transfer Network Air Toxics Web Site: Ethylbenzene". US Environmental Protection Agency. Retrieved 13 February 2013.
  6. ↑ --, William H. Brown ... [et al.]. (2009). Organic Chemistry. (5th ed. . ed.). Belmont, CA: Brooks/Cole Cengage Learning. pp. 56, 208. ISBN 9780495388579.
  7. 1 2 3 4 5 6 7 "Ethylbenzene" (PDF). Agency for Toxic Substances and Disease Registry. Retrieved 12 February 2013.
  8. ↑ Market Study Benzene, published by Ceresana, July 2011
  9. ↑ "Ethylbenzene (EB) Production and Manufacturing Process". PIERS. Retrieved 14 February 2013.
  10. 1 2 3 Vincent A.Welch, Kevin J. Fallon, Heinz-Peter Gelbke “Ethylbenzene” Ullmann’s Encyclopedia of Industrial Chemistry, Wiley-VCH, Weinheim, 2005. doi:10.1002/14356007.a10_035.pub2
  11. ↑ "Ethylbenzene". eco-usa.net. Retrieved 12 February 2013.
  12. ↑ Francesc X. PRENAFETA-BOLDU; Andrea KUHN; Dion M. A. M. LUYKX; Heidrun ANKE; Johan W. van GROENESTIJN; Jan A. M. de BONT (April 2001). "Isolation and characterisation of fungi growing on volatile aromatic hydrocarbons as their sole carbon and energy source". 105 (4): 477–484.
  13. ↑ Rabus, R.; Widdel, F. (1995). "Anaerobic degradation of ethylbenzene and other aromatic hydrocarbons by new denitrifying bacteria". Archives of microbiology. 163 (2): 96–103. PMID 7710331.

External links

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