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  2. Poly (2,6-diphenylphenylene oxide) - Wikipedia

    en.wikipedia.org/wiki/Poly(2,6-diphenylphenylene...

    Poly(2,6-diphenylphenylene oxide) is a low bleeding material with a low level of impurities, and has a high thermal stability (up to 350 °C). Before use poly(2,6-diphenylphenylene oxide) should be thermally conditioned with a high purity gas at elevated temperatures to remove any residual components.

  3. Polyphenyl ether - Wikipedia

    en.wikipedia.org/wiki/Polyphenyl_ether

    The simplest member of the phenyl ether family is diphenyl ether (DPE), also called diphenyl oxide, the structure of which is provided in Figure 4. Low molecular weight polyphenyl ethers and thioethers are used in a variety of applications, and include high-vacuum devices, optics, electronics, and in high-temperature and radiation-resistant ...

  4. Diphenyl ether - Wikipedia

    en.wikipedia.org/wiki/Diphenyl_ether

    Diphenyl ether is the organic compound with the formula (C 6 H 5) 2 O. It is a colorless, low-melting solid. It is a colorless, low-melting solid. This, the simplest diaryl ether , has a variety of niche applications.

  5. Poly(p-phenylene oxide) - Wikipedia

    en.wikipedia.org/wiki/Poly(p-phenylene_oxide)

    Poly(p-phenylene oxide) (PPO), poly(p-phenylene ether) (PPE), poly(oxy-2,6-dimethyl-1,4-phenylene), often referred to simply as polyphenylene oxide, is a high-temperature thermoplastic with the general formula (C 8 H 8 O) n. It is rarely used in its pure form due to difficulties in processing.

  6. Polybrominated diphenyl ethers - Wikipedia

    en.wikipedia.org/wiki/Polybrominated_diphenyl_ethers

    Polybrominated diphenyl ethers or PBDEs, are a class of organobromine compounds that are used as flame retardants. Like other brominated flame retardants , PBDEs have been used in a wide array of products, including building materials, electronics, furnishings, motor vehicles, airplanes, plastics, polyurethane foams, [ 1 ] and textiles.

  7. Diphenylamine - Wikipedia

    en.wikipedia.org/wiki/Diphenylamine

    Diphenylamine is produced by the thermal deamination of aniline over oxide catalysts: 2 C 6 H 5 NH 2 → (C 6 H 5) 2 NH + NH 3. It is a weak base, with a K b of 10 −14. With strong acids, it forms salts. For example, treatment with sulfuric acid gives the bisulfate [(C 6 H 5) 2 NH 2] + [HSO 4] − as a white or yellowish powder with m.p. 123 ...

  8. Decabromodiphenyl ether - Wikipedia

    en.wikipedia.org/wiki/Decabromodiphenyl_ether

    Decabromodiphenyl ether (also referred to as decaBDE, DBDE, BDE-209) is a brominated flame retardant which belongs to the group of polybrominated diphenyl ethers (PBDEs). It was commercialised in the 1970s and was initially thought to be safe, [3] [4] but is now recognised as a hazardous and persistent pollutant.

  9. Biphenyl - Wikipedia

    en.wikipedia.org/wiki/Biphenyl

    Biphenyl (also known as diphenyl, phenylbenzene, 1,1′-biphenyl, lemonene [4] or BP) is an organic compound that forms colorless crystals. Particularly in older literature, compounds containing the functional group consisting of biphenyl less one hydrogen (the site at which it is attached) may use the prefixes xenyl or diphenylyl .