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  2. Perfluorohexane - Wikipedia

    en.wikipedia.org/wiki/Perfluorohexane

    Perfluorohexane (C 6 F 14), or tetradecafluorohexane, is a fluorocarbon. It is a derivative of hexane in which all the hydrogen atoms are replaced by fluorine atoms. It is used in one formulation of the electronic cooling liquid/insulator Fluorinert for low-temperature applications due to its low boiling point of 56 °C and freezing point of ...

  3. Fluorinert - Wikipedia

    en.wikipedia.org/wiki/Fluorinert

    Perfluorohexane is used for low-temperature heat-transfer applications due to its 56 °C (133 °F) boiling point. Another example is FC-75 , perfluoro(2-butyl-tetrahydrofurane). There are 3M fluids that can handle up to 215 °C (419 °F), such as FC-70 ( perfluorotripentylamine ).

  4. List of refrigerants - Wikipedia

    en.wikipedia.org/wiki/List_of_refrigerants

    Net global warming potential, GWP, over a 100-year time horizon (normalized to be 1 for R-744, carbon dioxide) Occupational exposure limit/permissible exposure limit in parts per million (volume per volume) over a time-weighted average (TWA) concentration for a normal eight-hour work day and a 40-hour work week

  5. Fluorinated gases - Wikipedia

    en.wikipedia.org/wiki/Fluorinated_gases

    For example, refrigeration and air conditioning systems are increasingly utilized by humans within a warming environment. [4] Likewise, expansions of electrical infrastructure, as driven by the alternatives to fossil fuels, has led to rising demand for SF 6 . [ 5 ]

  6. R-410A - Wikipedia

    en.wikipedia.org/wiki/R-410A

    However, like methane, R-410A has a global warming potential (GWP) that is appreciably worse than CO 2 (GWP = 1) for the time it persists. R-410A is a mixture of 50% HFC-32 and 50% HFC-125. HFC-32 has a 4.9 year lifetime and a 100-year GWP of 675 and HFC-125 has a 29-year lifetime and a 100-year GWP of 3500.

  7. Fluorocarbon - Wikipedia

    en.wikipedia.org/wiki/Fluorocarbon

    The process proceeds at low voltage (5 – 6 V) so that free fluorine is not liberated. The choice of substrate is restricted as ideally it should be soluble in hydrogen fluoride. Ethers and tertiary amines are typically employed. To make perfluorohexane, trihexylamine is used, for example: N(C 6 H 13) 3 + 45 HF → 3 C 6 F 14 + NF 3 + 42 H 2

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