Ethylbenzene occurs naturally in coal tar and petroleum. The dominant application of ethylbenzene is role as an intermediate in the production of polystyrene. Catalytic dehydrogenation of ethylbenzene gives hydrogen and styrene: As of May 2012, greater than 99% of all the ethylbenzene produced is used for this purpose.
Ethylbenzene is produced in on a large scale by combining benzene and ethylene in an acid-catalyzed chemical reaction: 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. Small amounts of ethylbenzene are recovered from the mix of xylenes by superfractioning, an extension of the distillation process. 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 zeolitecatalysts. This offers low benzene-to-ethylene ratios, reducing the size of the required equipment and lowering byproduct production.
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. Eye and throat sensitivity can occur when high level exposure to ethylbenzene in the air occurs. At higher level exposure, ethylbenzene can cause dizziness. Once inside the body, ethylbenzene biodegrades to 1-phenylethanol, acetophenone, phenylglyoxylic acid, mandelic acid, benzoic acid and hippuric acid. Ethylbenzene exposure can be determined by testing for the breakdown products in urine. As of September 2007, the United States Environmental Protection Agency determined that drinking water with a concentration of 30 parts per million 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 limits exposure to workers to an average 100 ppm for an 8-hour workday, a 40-hour workweek. Ethylbenzene is classified as a possible carcinogen by the International Agency for Research on Cancer 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 with all organic compounds, ethylbenzene vapors form an explosive mixture with air. When transporting ethylbenzene, it is classified as a flammable liquid in class 3, Packing Group II.
Environmental effects
Ethylbenzene is found mostly as a vapor in the air since it can easily move from water and soil. A median concentration of 0.62 parts per billion was found in urban air in 1999. 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 the 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. 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. 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. As of 2012, according to the EUDangerous Substances Directive, ethylbenzene is not classified as hazardous to the environment. Ethylbenzene is a constituent of tobacco smoke.
Biodegradation
Certain strains of the fungus Cladophialophora can grow on ethylbenzene. The bacterium "Aromatoleum aromaticum" EbN1 was discovered due to its ability to grow on ethylbenzene.