Tetrachloroethylene
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| Tetrachloroethylene | |
|---|---|
| Image:Tetrachloroethylene.svg | |
| Image:Tetrachloroethylene-3D-vdW.png | |
| IUPAC name | tetrachloroethene |
| Other names | perchloroethylene perc, PCE |
| Identifiers | |
| CAS number | |
| EINECS number | |
| RTECS number | KX3850000 |
| SMILES | C(=C(Cl)Cl)(Cl)Cl |
| Properties | |
| Molecular formula | C2Cl4 |
| Molar mass | 165.8 g/mol |
| Appearance | Clear, colorless liquid |
| Density | 1.622 g/cm3, liquid |
| Melting point |
−19 °C (254 K) |
| Boiling point |
121.1 °C (394 K) |
| Solubility in water | 0.015 g/100 ml (20 °C) |
| Viscosity | 0.89 cP at 25 °C |
| Hazards | |
| MSDS | External MSDS |
| Main hazards | Harmful (Xn), Dangerous for the environment (N) |
| R-phrases | 40-51/53 |
| S-phrases | 23-36/37-61 |
| Flash point | Not flammable |
| Related Compounds | |
| Related Related Haloforms | tetrabromoethylene tetraiodoethylene |
| Related compounds | trichloroethylene dichloroethene tetrachloroethane |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) Infobox disclaimer and references | |
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Overview
Tetrachloroethylene Cl2C=CCl2 is a manufactured chemical compound that is widely used for the dry cleaning of fabrics and for metal-degreasing. It is also used to make other chemicals and is used in some consumer products.
Other names for tetrachloroethylene include perchloroethylene, perc, PCE, and tetrachloroethene. It is a nonflammable liquid at room temperature. It evaporates easily into the air and has a sharp, sweet odor. Most people can smell tetrachloroethylene when it is present in the air at a concentration of 1 part per million (1 ppm), although some can smell it at even lower levels.
Michael Faraday first synthesized tetrachloroethylene in 1821 by heating hexachloroethane until it decomposed into tetrachloroethylene and chlorine.
Production
Most tetrachloroethylene is produced from ethylene via 1,2-dichloroethane. When 1,2-dichloroethane is heated to 400°C with chlorine, tetrachloroethylene is produced by the chemical reaction
ClCH2CH2Cl + 3 Cl2 → Cl2C=CCl2 + 4 HCl
This reaction can be catalyzed by a mixture of potassium chloride and aluminium chloride, or by activated carbon. Trichloroethylene is a major byproduct of the reaction, and since both are salable commercial chemicals, typical industrial practice is to collect both products and then separate them by distillation.
Tetrachlorethylene can also be made from a mixture of partially chlorinated light hydrocarbons that would otherwise be hazardous waste products of several chemical processes. When these compounds are heated in the presence of excess chlorine, they are converted to a mixture of tetrachloroethylene, carbon tetrachloride, and hydrogen chloride.
Uses
Most applications of tetrachloroethylene use it for its solvent properties. Most organic materials dissolve in tetrachloroethylene. It is the most widely used solvent in dry cleaning. It is also used to degrease metal parts in the automotive and other metalworking industries. It appears in a few consumer products including paint strippers and spot removers.
In the early 20th century, tetrachloroethylene was the most effective available treatment for hookworm.
Tetrachloroethylene is also extensively used as an intermediate in the manufacture of refrigerants such as HFC-134a.
Health and safety
Like many chlorinated hydrocarbons, tetrachloroethylene is a central nervous system depressant, and inhaling its vapors (particularly in closed, poorly ventilated areas) can cause dizziness, headache, sleepiness, confusion, nausea, difficulty in speaking and walking, unconsciousness, and death.
After repeated or extended skin contact, tetrachloroethylene may dissolve fats from the skin, resulting in severe skin irritation in work environments where people have been exposed to high concentrations.
Tetrachloroethylene is a common soil contaminant. Such contamination most often results from spillage, overfilling, or sewer leakage at commercial dry cleaning facilities. Because of the mobility of PCE in groundwater, its toxicity at low levels, and its density (which causes it to sink below the water table), cleanup activities tend to be especially problematic compared to cleanups of oil spills.
In industry, most workers are exposed to levels lower than those causing obvious nervous system effects. The health effects of tetrachloroethylene at levels typically encountered in occupational or environmental exposures have not been well established.
Results from some studies suggest that women who work in dry cleaning industries where exposures to tetrachloroethylene can be quite high may have more menstrual problems and spontaneous abortions than women who are not exposed. However, it is not known if tetrachloroethylene was responsible for these problems because other possible causes were not considered.
Results of animal studies, conducted with amounts much higher than those that most people are exposed to, show that tetrachloroethylene can cause liver and kidney damage. Exposure to very high levels of tetrachloroethylene can be toxic to the unborn pups of pregnant rats and mice. Changes in behavior were observed in the offspring of rats that breathed high levels of the chemical while they were pregnant.
The International Agency for Research on Cancer has classified tetrachloroethylene as a Group 2A carcinogen, which means that it is probably carcinogenic to humans.[1]
Under a high temperature flame such as those produced by a TIG torch or other welding arcs, Phosgene gas is produced. The gas instantly attacks the central nervous system shutting down the ability to breathe. The odour of the converted chemical is similar to almonds and very sweet smelling. Care in welding porous castings recently cleaned with tetrachloroethylene should be taken to allow the solvent to completely evaporate prior to welding.
Contamination at U.S. Marine base
On June 12, 2007, the U.S. Centers for Disease Control and Prevention reported that as many as 75,000 people may have drunk water contaminated with tetrachloroethylene at Camp Lejeune in North Carolina. The affected area is the Tarawa Terrace family housing area, and the contamination lasted from November 1957 through February 1987, the agency said. An off-base dry cleaners leaked a maximum concentration of 200 micrograms per liter of the fluid into a septic system near the housing area's well.[1]
Testing for PCE
One method of testing for tetrachloroethylene exposure is to measure the amount of the chemical in the breath, much the same way breath-alcohol measurements are used to determine the amount of alcohol in the blood.
Because it is stored in the body's fat and slowly released into the bloodstream, tetrachloroethylene can be detected in the breath for weeks following a heavy exposure.
Tetrachloroethylene and trichloroacetic acid (TCA), a breakdown product of tetrachloroethylene, can be detected in the blood. These tests are relatively simple to perform. These tests are not available at most doctors' offices, but can be performed at laboratories with the necessary equipment. Because exposure to other chemicals can produce the same breakdown products in the urine and blood, the tests for breakdown products cannot determine if one has been exposed to tetrachloroethylene or the other chemicals.
Popular culture
- Tetrachloroethylene contamination was used as a plot focus in a story arc of the TV show Ghostwriter.
- It has been featured in an episode of Stargate SG1.
References
External links
- Tetrachloroethylene MSDS
- Australian National Pollutant Inventory (NPI) page
- "Toxic Fumes May Have Made Gunman Snap", by Julian Kesner, New York Daily News, April 20, 2007.
bg:Тетрахлороетен de:Tetrachlorethen fr:Perchloroéthylène id:Tetrakloroetilena nl:Perchloorethyleen ja:テトラクロロエチレンsv:Perkloretylen
Acknowledgement and Attribution Regarding Sources of Content
Some of the initial content on this page may be incorporated in part from copyleft sources in the public domain including wikis such as Wikipedia and AskDrWiki. Drug information for patients came from the The National Library of Medicine. Infectious disease information may have come from the Centers for Disease Control (CDC). Differential Diagnoses are drawn from clinicians as well as an amalgamation of 3 sources: 1.The Disease Database; 2. Kahan, Scott, Smith, Ellen G. In A Page: Signs and Symptoms. Malden, Massachusetts: Blackwell Publishing, 2004:3; 3. Sailer, Christian, Wasner, Susanne. Differential Diagnosis Pocket. Hermosa Beach, CA: Borm Bruckmeir Publishing LLC, 2002:7 .
