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The science-fiction film The Abyss (1989) depicted an experimental liquid-breathing system, in which the use of highly oxygenated Fluorinert enabled a diver to descend to great depths. While several rats were shown actually breathing Fluorinert, scenes depicting actor Ed Harris using the fluid-breathing apparatus were simulated.
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 ...
At these pressures, most fluorocarbon liquids require about 70 mL/kg minute-ventilation volumes of liquid (about 5 L/min for a 70 kg adult) to remove enough CO 2 for normal resting metabolism. [51] This is a great deal of fluid to move, particularly as liquids are more viscous and denser than gases, (for example water is about 850 times the ...
Because of the reduced intermolecular van der Waals interactions, fluorocarbon-based compounds are sometimes used as lubricants or are highly volatile. Fluorocarbon liquids have medical applications as oxygen carriers. [citation needed] The structure of organofluorine compounds can be distinctive.
The table is sortable by each of the following refrigerant properties (scroll right or reduce magnification to view more properties): Type/prefix (see legends); ASHRAE number
Fluorocarbon gases are generally greenhouse gases with global-warming potentials (GWPs) of about 100 to 10,000; sulfur hexafluoride has a value of around 20,000. [288] An outlier is HFO-1234yf which is a new type of refrigerant called a Hydrofluoroolefin (HFO) and has attracted global demand due to its GWP of less than 1 compared to 1,430 for ...
1594 kg/m 3 (liquid, 101.3 kPa at boiling point) [2] ... It is a simple fluorocarbon with a n-butane skeleton and all the hydrogen atoms replaced with fluorine atoms.
Fluorotelomers are fluorocarbon-based oligomers, or telomers, synthesized by telomerization. [1] Some fluorotelomers and fluorotelomer-based compounds are a source of environmentally persistent perfluorinated carboxylic acids such as PFOA and PFNA, while others are under extended investigation.
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