- Alkali[6]
- Aluminum Powder[6]
- Oxide[3]
- Lubricant[6]
- Other Ore[1]
- Chemical Auxiliary Agent[6]
- Other Organic Chemical[6]
- Other Rubber Raw Materials[4]
- Organic Acid[6]
- Alcohol & Hydroxybenzene & Ether[3]
- Aldehyde & Ketone & Chinone[3]
- Hydrocarbon & Derivatives[4]
- Amine[1]
- Chemical Reagents[6]
- Other Chemicals[1]
- Ceiling Lights[2]
- Chandeliers & Pendant Lights[1]
- Perlite[4]
- Dried Fruit[1]
- Flanges[6]
- Contact Person : Ms. Lee Sara
- Company Name : Tianjin Okeyou International Trade Co., Ltd.
- Tel : 86-22-28231369
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Perchloroethylene:
Uses
Tetrachloroethylene is an excellent solvent for organic materials. Otherwise it is volatile, highly stable, and nonflammable. For these reasons, it is widely used in dry cleaning. Usually as a mixture with other chlorocarbons, 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.
Production
Michael Faraday first synthesized tetrachloroethene in 1821 by thermal decomposition of hexachloroethane.
C2Cl6 → C2Cl4 + Cl2Most tetrachloroethene is produced by high temperature chlorinolysis of light hydrocarbons. The method is related to Faraday's discovery since hexachloroethane is generated and thermally decomposes.[1] Side products include carbon tetrachloride, hydrogen chloride, and hexachlorobutadiene.
Several other methods have been developed. When 1,2-dichloroethane is heated to 400 °C with chlorine, tetrachloroethene is produced by the chemical reaction:
ClCH2CH2Cl + 3 Cl2 → Cl2C=CCl2 + 4 HClThis reaction can be catalyzed by a mixture of potassium chloride and aluminium chloride or by activated carbon. Trichloroethylene is a major byproduct, which is separated by distillation.
Health and safety
The International Agency for Research on Cancer has classified tetrachloroethene as a Group 2A carcinogen, which means that it is probably carcinogenic to humans.[3] Like many chlorinated hydrocarbons, tetrachloroethene is a central nervous system depressant and can enter the body through respiratory or dermal exposure.[4] Tetrachloroethene dissolve fats from the skin, potentially resulting in skin irritation.
Tetrachloroethene is a common soil contaminant. 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 are more difficult than for oil spills. Recent research has focused on the in place remediation of soil and ground water pollution by tetrachloroethylene. Instead of excavation or extraction for above-ground treatment or disposal, tetrachloroethylene contamination has been successfully remediated by chemical treatment or bioremediation. Bioremediation has been successful under anaerobic conditions by reductive dechlorination by Dehalococcoides sp. and under aerobic conditions by cometabolism by Pseudomonas sp. [5][6]
Animal studies and a study of 99 twins by Dr. Samuel Goldman and researchers at the Parkinson's Institute in Sunnyvale, California determined there is a "lot of circumstantial evidence" that exposure to Tetrachloroethlene increases the risk of developing Parkinson's disease ninefold. Larger population studies are planned.
Tetrachloroethylene PCE