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  2. 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 ...

  3. Photo-oxidation of polymers - Wikipedia

    en.wikipedia.org/wiki/Photo-oxidation_of_polymers

    The type I reaction dominates, which cause chain scission at the carbonyl unit to give a range of products. [1] [38] Type II Norrish reactions are less common but give rise to acetaldehyde by way of vinyl alcohol esters. [36] This has an exceedingly low odour and taste threshold and can cause an off-taste in bottled water. [39]

  4. Polymer devolatilization - Wikipedia

    en.wikipedia.org/wiki/Polymer_devolatilization

    When exiting a reactor after a polymerization reaction, many polymers still contain undesired low-molecular weight components. These component may make the product unusable for further processing (for example, a polymer solution cannot directly be used for plastics processing), may be toxic, may cause bad sensory properties such as an unpleasant smell or worsen the properties of the polymer.

  5. Polymerization - Wikipedia

    en.wikipedia.org/wiki/Polymerization

    For example, polyester chains grow by reaction of alcohol and carboxylic acid groups to form ester links with loss of water. However, there are exceptions; for example polyurethanes are step-growth polymers formed from isocyanate and alcohol bifunctional monomers) without loss of water or other volatile molecules, and are classified as addition ...

  6. Carbonate ester - Wikipedia

    en.wikipedia.org/wiki/Carbonate_ester

    Carbonate esters can be converted to other carbonates by transesterification. A more nucleophilic alcohol will displace a less nucleophilic alcohol. In other words, aliphatic alcohols will displace phenols from aryl carbonates. If the departing alcohol is more volatile, the equilibrium may be driven by distilling that off. [2] [3]

  7. Aldol condensation - Wikipedia

    en.wikipedia.org/wiki/Aldol_condensation

    The first part of this reaction is an Aldol reaction, the second part a dehydration—an elimination reaction (Involves removal of a water molecule or an alcohol molecule). ). Dehydration may be accompanied by decarboxylation when an activated carboxyl group is pres

  8. Emulsion polymerization - Wikipedia

    en.wikipedia.org/wiki/Emulsion_polymerization

    The continuous water phase is an excellent conductor of heat, enabling fast polymerization rates without loss of temperature control. Since polymer molecules are contained within the particles, the viscosity of the reaction medium remains close to that of water and is not dependent on molecular weight.

  9. Condensation polymer - Wikipedia

    en.wikipedia.org/wiki/Condensation_polymer

    One important class of condensation polymers are polyamides. [4] They arise from the reaction of carboxylic acid and an amine. Examples include nylons and proteins.When prepared from amino-carboxylic acids, e.g. amino acids, the stoichiometry of the polymerization includes co-formation of water: