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  2. Bisphenol A - Wikipedia

    en.wikipedia.org/wiki/Bisphenol_A

    Bisphenol A (BPA) is a chemical compound primarily used in the manufacturing of various plastics. It is a colourless solid which is soluble in most common organic solvents , but has very poor solubility in water.

  3. Bisphenol - Wikipedia

    en.wikipedia.org/wiki/Bisphenol

    Exceptions include bisphenol S, P, and M. "Bisphenol" is a common name; the letter following denotes the variant, which depends on the additional substituents. Bisphenol A is the most popular representative of the group, with millions of metric tons produced globally in the past decade, often simply called "bisphenol".

  4. Health effects of Bisphenol A - Wikipedia

    en.wikipedia.org/wiki/Health_effects_of_Bisphenol_A

    Epoxy resins derived from bisphenol A are used as coatings on the inside of almost all food and beverage cans; [13] however, due to BPA health concerns, in Japan epoxy coating was mostly replaced by PET film. [14] Bisphenol A is a preferred color developer in carbonless copy paper and thermal point of sale receipt paper.

  5. Bisphenol-A bis(diphenyl phosphate) - Wikipedia

    en.wikipedia.org/wiki/Bisphenol-A_bis(diphenyl...

    Bisphenol A diphenyl phosphate is a halogen-free flame retardant used plastics. It is used in polymer blends of engineering plastics, such as PPO/HIPS and PC/ABS, [1] which are commonly used to make casing for electrical items like TVs, computers and home appliances. It is formed by the transesterification of bisphenol A with triphenyl phosphate.

  6. Polycarbonate - Wikipedia

    en.wikipedia.org/wiki/Polycarbonate

    The main polycarbonate material is produced by the reaction of bisphenol A (BPA) and phosgene COCl 2. The overall reaction can be written as follows: The first step of the synthesis involves treatment of bisphenol A with sodium hydroxide, which deprotonates the hydroxyl groups of the bisphenol A. [6] (HOC 6 H 4) 2 CMe 2 + 2 NaOH → Na 2 (OC 6 ...

  7. Aleksandr Dianin - Wikipedia

    en.wikipedia.org/wiki/Aleksandr_Dianin

    Aleksandr Pavlovich Dianin (Russian: Александр Павлович Дианин; 20 April 1851 – 6 December 1918) was a Russian chemist from Saint Petersburg.He carried out studies on phenols and discovered a phenol derivative now known as bisphenol A [1] [2] and the accordingly named Dianin's compound. [3]

  8. Bisphenol A diglycidyl ether - Wikipedia

    en.wikipedia.org/wiki/Bisphenol_A_diglycidyl_ether

    Bisphenol A diglycidyl ether slowly hydrolyzes to 2,2-bis[4(2,3-dihydroxypropoxy)phenyl)propane (bis-HPPP). Similarly, DGEBA reacts with acrylic acid to give vinyl ester resins . The reaction results in opening of the epoxide ring, generating unsaturated esters at each terminus of the molecule.

  9. Polysulfone - Wikipedia

    en.wikipedia.org/wiki/Polysulfone

    DCDPS is the precursor to polymers known as Udel (from bisphenol A), PES, and Radel R. Udel is a high-performance amorphous sulfone polymer that can molded into a variety of different shapes. It is both rigid and temperature-resistant, and has applications in everything from plumbing pipes, to printer cartridges, to automobile fuses.