Tetrafluoroethylene
You don't need to be Editor-In-Chief to add or edit content to WikiDoc. You can begin to add to or edit text on this WikiDoc page by clicking on the edit button at the top of this page. Next enter or edit the information that you would like to appear here. Once you are done editing, scroll down and click the Save page button at the bottom of the page.
| Tetrafluoroethylene | |
|---|---|
| Image:Tetrafluoroethylene.png Image:Tetrafluoroethylene3D.png | |
| Common name | tetrafluoroethylene |
| Systematic name | tetrafluoroethene |
| Other names | perfluoroethylene TFE |
| Chemical formula | C2F4 |
| Molecular mass | 100.02 g/mol |
| CAS number | [116-14-3] |
| Density | 1.519 g/cm³ at -76 °C |
| Melting point | -142.5 °C |
| Boiling point | -76.3 °C |
| SMILES | FC(F)=C(F)F |
| Disclaimer and references | |
Tetrafluoroethylene (TFE) is a chemical compound composed containing only carbon and fluorine with the molecular formula C2F4. This gaseous species is used primarily in the industrial preparation of polymers. In organic chemistry, tetrafluoroethylene is a potent dienophile.
Properties
TFE is a derivative of ethylene in which each of the four hydrogen atoms have been replaced with fluorine. Tetrafluoroethylene is a colourless, odourless gas. Like all unsaturated fluorocarbons it is susceptible to nucleophilic attack. In air it is prone to form explosive peroxides.[citation needed]
Industrial use
Polymerization of tetrafluoroethylene produces polytetrafluoroethylene (PTFE) polymers such as Teflon. PTFE is one of the three fluorocarbon resins composed wholly of fluorine and carbon. The other resins in this group are perfluoroalkoxy resin (PFA) and fluorinated ethylene propylene (FEP). TFE is also used in the preparation of copolymers such as ETFE.
Manufacture
TFE is manufactured from chloroform.[1] Chloroform is fluorinated by reaction with hydrogen fluoride to produce chlorodifluoromethane (R-22). Pyrolysis of chlorodifluoromethane then yields TFE.
- CHCl3 + 2 HF → CHClF2 + 2 HCl
- 2 CHClF2 → C2F4 + 2 HCl
A laboratory synthesis entails pyrolysis of a PTFE under a vacuum. The PTFE polymer "cracks" and depending on the pressure, produces mainly C2F4.[1]
Safety
LD50(rat, inhalation) = 40000 ppm.[1]
See also
References
External links
it:Tetrafluoroetenesv:Tetrafluoreten
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 .

