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Перфторэтен структурированное изображение

Перфторэтен

  • английское имяTetrafluoroethylene
  • CAS №116-14-3
  • CBNumberCB6225793
  • ФормулаC2F4
  • мольный вес100.01
  • EINECS204-126-9
  • номер MDLMFCD00039272
  • файл Mol116-14-3.mol
химическое свойство
Температура плавления -142°C
Температура кипения -76.3°C
плотность 1.1507
показатель преломления 1.2420 (estimate)
Растворимость в воде 110mg/L at 28℃
Диэлектрическая постоянная 1.9(Ambient)
Стабильность Stable. Reactive when heated.
LogP 1.21 at 20℃
Справочник по базе данных CAS 116-14-3(CAS DataBase Reference)
Непрямые добавки, используемые в веществах, контактирующих с пищевыми продуктами TETRAFLUOROETHENE
Рейтинг продуктов питания EWG 2
FDA UNII OMW63Z518S
Предложение 65 Список Tetrafluoroethylene
МАИР 2A (Vol. 19, Sup 7, 71, 110) 2017
Справочник по химии NIST Ethene, tetrafluoro-(116-14-3)
Система регистрации веществ EPA Tetrafluoroethene (116-14-3)
Заявления об опасности и безопасности
Коды опасности C,F
Заявления о рисках 11
Заявления о безопасности 16-36/37/39-45
РИДАДР 1081
Примечание об опасности Corrosive/Flammable
Класс опасности 2.1
Банк данных об опасных веществах 116-14-3(Hazardous Substances Data)
Токсичность LC50 (4 hr) in rats, mice, hamsters, guinea pigs (ppm): 37500-45000, 35000, 28500, 28000 (Kennedy)
NFPA 704:
4
2 3

рисовальное письмо(GHS)

  • рисовальное письмо(GHS)

    GHS hazard pictograms

  • сигнальный язык

    опасность

  • вредная бумага

    H350:Может вызывать раковые заболевания.

Перфторэтен MSDS

Перфторэтен химические свойства, назначение, производство

Описание

Tetrafluoroethylene is a synthetic, colorless, flammable gas that is insoluble in water. Tetrafluoroethylene is used primarily in the synthesis of polytetrafluoroethylene resins. It is also used as a monomer in the synthesis of copolymers and as a propellant for food product aerosols. When heated to decomposition, tetrafluoroethylene emits highly toxic fluorocarbon fumes. The primary route of human exposure to this compound is inhalation. Acute inhalation exposure to tetrafluoroethylene may result in irritation of the respiratory tract and buildup of fluid in the lungs (pulmonary edema). Contact with this gas can cause eye irritation. This chemical is reasonably anticipated to be a human carcinogen. (NCI05)

Химические свойства

Tetrafluoroethylene is a colorless, flammable gas. Heavier than air. insoluble in water. soluble in acetone.

Использование

In manufacture of polymers and synthesis of fluorinated refrigerants, dielectric media and solvents. In vinyl polymerization, cycloalkylation and addition reactions.

Подготовка

Tetrafluoroethylene (TFE) is manufactured from chloroform. 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
2CHClF2 → 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.

прикладной

The main use of tetrafluoroethylene is in the manufacture of polytetrafluoroethylene (PTFE) that is used as nonstick coatings on cookware, membranes for clothing that are both waterproof and breathable, electrical-wire casing, fire- and chemical-resistant tubing, and plumbing thread seal tape.The most widely known PTFE formulation is sold under the brand name of Teflon®. PTFE was discovered by DuPont Co. in 1938.

Определение

Tetrafluoroethene is a fluorocarbon. It is a gaseous organic compound (a fluorocarbon and a haloalkene) used to make the plastic polytetrafluoroethene (PTFE).

Общее описание

Tetrafluoroethylene, stabilized appears as a colorless odorless gas. Easily ignited. Vapors are heavier than air. May asphyxiate by the displacement of air. May violently polymerize under prolonged exposure to fire or heat, violently rupturing the container. Under prolonged exposure to fire or heat the containers may rupture violently and rocket. Water insoluble.

Реакции воздуха и воды

Flammable. Forms polymeric peroxides that are explosive [Bretherick 1979 p. 164].

Профиль реактивности

Tetrafluoroethylene reacts with air (oxygen) to form polymeric peroxides that are explosive [Bretherick 1979 p. 164]. Probably susceptible to similar reactions with a number of oxidizing agents.May polymerize violently (inhibitor tends to prevent this reaction). May react violently with aluminum. Contamination of a tetrafluoroethylene gas supply system led to a reaction between the inhibitor, limonene, and the contaminant, iodine pentafluoride. This initiated an explosive polymerization event [MCA Case History No. 1520].

Опасность

Flammable, dangerous fire risk. Kidney and liver damage; kidney and liver cancer. Possible carcinogen.

Угроза здоровью

Inhalation causes irritation of respiratory system. Contact with eyes causes slight irritation.

Профиль безопасности

Confirmed carcinogen. Mildly toxic by inhalation. Can act as an asphyxiant and may have other toxic properties. The gas is flammable when exposed to heat or flame. The inhibited monomer will explode if igntted. Explosive in the form of vapor when exposed to heat or flame. Will explode at pressures above 2.7 bar if limonene inhbitor is not added. Iodine pentafluoride depletes the limonene inhbitor and then causes explosive polymerization of the monomer. Mixtures with hexafluoropropene and air form an explosive peroxide. Reacts violently with SO3; air; dfluoromethylene dihypofluorite; loxygen difluoride; iodine pentafluoride; oxygen. When heated to decomposition it emits highly toxic fumes of F-. See also FLUORIDES.

Возможный контакт

A potential danger to those involved in the production of TFE and the manufacture of fluorocarbon polymers.

Канцерогенность

Tetrafluoroethylene is reasonably anticipated to be a human carcinogen based on sufficient evidence of carcinogenicity from studies in experimental animals (NTP 1997).

Несовместимости

Reacts with air. Hazardous polymerization may occur unless inhibited. Will explode at pressures above 2.7 bar if terpene inhibitor is not added. Inhibited monomer can decompose explosively in fire, under pressure, or upon contact with materials with which it can react exothermically. Violent reaction with oxygen, oxidizers, sulfur trioxide; halogen compounds.

Утилизация отходов

Return refillable compressed gas cylinders to supplier. Nonrefillable cylinders should be disposed of in accordance with local, state and federal regulations. Allow remaining gas to vent slowly into atmosphere in an unconfined area or exhaust hood. Refillable-type cylinders should be returned to original supplier with any valve caps and outlet plugs secured and valve protection caps in place.

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