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The F-gas Regulation adopts an approach based on containment and recovery of F-gases as well as imposing obligations on reporting, training and labeling on those using F-gases. On 26 September 2011, the Commission issued a report on the application, effects and adequacy of the Regulation, drawing from the results of an analytical study it ...
According to ASHRAE standard 34, the R-number of a chemical refrigerant is assigned systematically according to its molecular structure and has between two and four digits. If there are carbon -carbon multiple bonds , there are four digits in all: the number of these bonds is the first digit and the number of carbon atoms minus one (C-1) is next.
The structure of organofluorine compounds can be distinctive. As shown below, perfluorinated aliphatic compounds tend to segregate from hydrocarbons. This "like dissolves like effect" is related to the usefulness of fluorous phases and the use of PFOA in processing of fluoropolymers.
A special numbering system is to be used for fluorinated alkanes, prefixed with Freon-, R-, CFC- and HCFC-, where the rightmost value indicates the number of fluorine atoms, the next value to the left is the number of hydrogen atoms plus 1, and the next value to the left is the number of carbon atoms less one (zeroes are not stated), and the ...
Animation showing the crystal structure of beta-fluorine. Molecules on the faces of the unit cell have rotations constrained to a plane. At room temperature, fluorine is a gas of diatomic molecules, [5] pale yellow when pure (sometimes described as yellow-green). [42] It has a characteristic halogen-like pungent and biting odor detectable at 20 ...
Perfluoroalkanes are very stable because of the strength of the carbon–fluorine bond, one of the strongest in organic chemistry. [4] Its strength is a result of the electronegativity of fluorine imparting partial ionic character through partial charges on the carbon and fluorine atoms, which shorten and strengthen the bond (compared to carbon-hydrogen bonds) through favorable covalent ...
Consequently, the solid state of fluorine is more similar to that of oxygen [6] [7] or the noble gases than to those of the heavier halogens. [citation needed] Animation showing the crystal structure of beta-fluorine. [8] Low-temperature fluorine phases. Fluorine solidifies at −220 °C (−363 °F) [5] into a cubic structure
Halocarbon compounds are chemical compounds in which one or more carbon atoms are linked by covalent bonds with one or more halogen atoms (fluorine, chlorine, bromine or iodine – group 17) resulting in the formation of organofluorine compounds, organochlorine compounds, organobromine compounds, and organoiodine compounds.