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  2. Polycarbonate - Wikipedia

    en.wikipedia.org/wiki/Polycarbonate

    Polycarbonate is mainly used for electronic applications that capitalize on its collective safety features. A good electrical insulator with heat-resistant and flame-retardant properties, it is used in products associated with power systems and telecommunications hardware. It can serve as a dielectric in high-stability capacitors. [6]

  3. Polycarbonate (functional group) - Wikipedia

    en.wikipedia.org/wiki/Polycarbonate_(functional...

    A polycarbonate is an oxocarbon dianion consisting of a chain of carbonate units, where successive carbonyl groups are directly linked to each other by shared additional oxygen atoms. That is, they are the conjugate bases of polycarbonic acids , the conceptual anhydrides of carbonic acid , or polymers of carbon dioxide .

  4. Plastic - Wikipedia

    en.wikipedia.org/wiki/Plastic

    The development of plastics has evolved from the use of naturally plastic materials (e.g., gums and shellac) to the use of the chemical modification of those materials (e.g., natural rubber, cellulose, collagen, and milk proteins), and finally to completely synthetic plastics (e.g., bakelite, epoxy, and PVC).

  5. Twinwall plastic - Wikipedia

    en.wikipedia.org/wiki/Twinwall_plastic

    Twinwall plastic most commonly refers to two exterior plastic sheets that are connected with a plastic support layer to create parallel channels. This design adds both impact toughness and the ability to support weight. Twinwall plastic may also be used to describe a pipe that has a smooth interior with exterior air filled ridges. [3]

  6. Category:Polycarbonates - Wikipedia

    en.wikipedia.org/wiki/Category:Polycarbonates

    Polycarbonate e-passport; Polypropylene carbonate This page was last edited on 21 November 2024, at 13:30 (UTC). Text is available under the Creative Commons ...

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  8. Fluorocarbon - Wikipedia

    en.wikipedia.org/wiki/Fluorocarbon

    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 ...

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