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Chemical structure of Nafion, a fluoropolymer used in fuel cells and many other applications [155] The carbon–fluorine bond is organic chemistry's strongest, [156] and gives stability to organofluorines. [157] It is almost non-existent in nature, but is used in artificial compounds.
It is the principal industrial source of fluorine, often in the form of hydrofluoric acid, and is an important feedstock in the preparation of many important compounds including pharmaceuticals and polymers such as polytetrafluoroethylene (PTFE). HF is also widely used in the petrochemical industry as a component of superacids.
The main uses of fluoride, in terms of volume, are in the production of cryolite, Na 3 AlF 6. It is used in aluminium smelting. Formerly, it was mined, but now it is derived from hydrogen fluoride. Fluorite is used on a large scale to separate slag in steel-making. Mined fluorite (CaF 2) is a commodity chemical used in steel-making.
Fluorine has several distinctive differences from all other substituents encountered in organic molecules. As a result, the physical and chemical properties of organofluorines can be distinctive in comparison to other organohalogens. The carbon–fluorine bond is one of the strongest in organic chemistry (an average bond energy around 480 kJ ...
Fluorine is often added to drug molecules during drug design, as even a single atom can greatly change the chemical properties of the molecule in desirable ways. Because of the considerable stability of the carbon–fluorine bond , many drugs are fluorinated to delay their metabolism , which is the chemical process in which the drugs are turned ...
Fluorine forms compounds with all elements except neon and helium. In particular, it forms binary compounds , named fluorides , with all said elements except argon . All of the elements up to einsteinium , element 99, have been checked except for astatine and francium , [ 24 ] and fluorine is also known to form compounds with mendelevium ...
While different PFAS have different chemical structures, all PFAS have at least one common trait: the presence of carbon-fluorine bonds, which are among the strongest bonds in chemistry.
The halogens (/ ˈ h æ l ə dʒ ə n, ˈ h eɪ-,-l oʊ-,-ˌ dʒ ɛ n / [1] [2] [3]) are a group in the periodic table consisting of six chemically related elements: fluorine (F), chlorine (Cl), bromine (Br), iodine (I), and the radioactive elements astatine (At) and tennessine (Ts), though some authors [4] would exclude tennessine as its chemistry is unknown and is theoretically expected to ...