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  2. Autoxidation - Wikipedia

    en.wikipedia.org/wiki/Autoxidation

    The common mechanism is a free radical chain reaction, where the addition of oxygen gives rise to hydroperoxides and their associated peroxy radicals (ROO•). [5] Typically, an induction period is seen at the start where there is little activity; this is followed by a gradually accelerating take-up of oxygen, giving an autocatalytic reaction ...

  3. Photo-oxidation of polymers - Wikipedia

    en.wikipedia.org/wiki/Photo-oxidation_of_polymers

    Photo-oxidation is a form of photodegradation and begins with formation of free radicals on the polymer chain, which then react with oxygen in chain reactions. For many polymers the general autoxidation mechanism is a reasonable approximation of the underlying chemistry.

  4. Acrylic acid - Wikipedia

    en.wikipedia.org/wiki/Acrylic_acid

    Acrylic acid undergoes the typical reactions of a carboxylic acid. When reacted with an alcohol, it forms the corresponding ester. The esters and salts of acrylic acid are collectively known as acrylates (or propenoates). The most common alkyl esters of acrylic acid are methyl, butyl, ethyl, and 2-ethylhexyl acrylate.

  5. Polymer stabilizer - Wikipedia

    en.wikipedia.org/wiki/Polymer_stabilizer

    Under these conditions reactions with oxygen occur much more rapidly. Once initiated, autoxidation can be autocatalytic . [ 6 ] As such, even though efforts are usually made to reduce oxygen levels, total exclusion is often not achievable and even exceedingly low concentrations of oxygen can be sufficient to initiate degradation.

  6. Polymerisation inhibitor - Wikipedia

    en.wikipedia.org/wiki/Polymerisation_inhibitor

    In the simplest example oxygen can be used as it exists naturally in its triplet state (i.e. it is a diradical). This is referred to as air inhibition and is a diffusion-controlled reaction with rates typically in the order of 10 7 –10 9 mol −1 s −1, [3] the resulting peroxy radicals (ROO•) are less reactive towards polymerisation ...

  7. α,β-Unsaturated carbonyl compound - Wikipedia

    en.wikipedia.org/wiki/Α,β-Unsaturated_carbonyl...

    An α,β-unsaturated acid is a type of α,β-unsaturated carbonyl compound that consists of an alkene conjugated to a carboxylic acid. [3] The simplest example is acrylic acid (CH 2 =CHCO 2 H). These compounds are prone to polymerization, giving rise to the large area of polyacrylate plastics. Acrylate polymers are derived from but do not ...

  8. The hidden dangers of acrylic nails and why you might ... - AOL

    www.aol.com/lifestyle/2015-10-22-the-hidden...

    Photo: Getty 1. The hard-to-clean area underneath your nail may cause your nails to be extra sensitive, especially if an MMA-based acrylic (Methyl Methacrylate) is used. Though they've been banned ...

  9. Methyl acrylate - Wikipedia

    en.wikipedia.org/wiki/Methyl_acrylate

    Methyl acrylate is an organic compound, more accurately the methyl ester of acrylic acid. It is a colourless liquid with a characteristic acrid odor. It is mainly produced to make acrylate fiber, which is used to weave synthetic carpets. [6] It is also a reagent in the synthesis of various pharmaceutical intermediates.