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  2. Reversible addition−fragmentation chain-transfer polymerization

    en.wikipedia.org/wiki/Reversible_addition%E2%88...

    Initiation: The reaction is started by a free-radical source which may be a decomposing radical initiator such as AIBN. In the example in Figure 5, the initiator decomposes to form two fragments (I•) which react with a single monomer molecule to yield a propagating (i.e. growing) polymeric radical of length 1, denoted P 1 •.

  3. Fenton's reagent - Wikipedia

    en.wikipedia.org/wiki/Fenton's_reagent

    The free radicals generated by this process engage in secondary reactions. For example, the hydroxyl is a powerful, non-selective oxidant. [6] Oxidation of an organic compound by Fenton's reagent is rapid and exothermic and results in the oxidation of contaminants to primarily carbon dioxide and water.

  4. Mixed radix - Wikipedia

    en.wikipedia.org/wiki/Mixed_radix

    Mixed-radix numbers of the same base can be manipulated using a generalization of manual arithmetic algorithms. Conversion of values from one mixed base to another is easily accomplished by first converting the place values of the one system into the other, and then applying the digits from the one system against these.

  5. Free-radical addition - Wikipedia

    en.wikipedia.org/wiki/Free-radical_addition

    Chain propagation: A radical reacts with a non-radical to produce a new radical species; Chain termination: Two radicals react with each other to create a non-radical species; In a free-radical addition, there are two chain propagation steps. In one, the adding radical attaches to a multiply-bonded precursor to give a radical with lesser bond ...

  6. Polymer stabilizer - Wikipedia

    en.wikipedia.org/wiki/Polymer_stabilizer

    The ability of hindered amine light stabilizers (HALS or HAS) to scavenge radicals produced by weathering, may be explained by the formation of aminoxyl radicals through a process known as the Denisov Cycle. The aminoxyl radical (N-O•) combines with free radicals in polymers: N-O• + R• → N-O-R

  7. Elimination reaction of free radicals - Wikipedia

    en.wikipedia.org/wiki/Elimination_reaction_of...

    Radicals can undergo a disproportionation reaction through a radical elimination mechanism (See Fig. 1). Here a radical abstracts a hydrogen atom from another same radical to form two non-radical species: an alkane and an alkene. Radicals can also undergo an elimination reaction to generate a new radical as the leaving group.

  8. Radical (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Radical_(chemistry)

    The hydroxyl radical, Lewis structure shown, contains one unpaired electron. Lewis dot structure of a Hydroxide ion compared to a hydroxyl radical. In chemistry, a radical, also known as a free radical, is an atom, molecule, or ion that has at least one unpaired valence electron.

  9. Kinetic chain length - Wikipedia

    en.wikipedia.org/wiki/Kinetic_chain_length

    Termination by disproportionation occurs when an atom is transferred from one polymer free radical to another. The atom is usually hydrogen, and this results in two polymer chains. With this type of termination and no chain transfer, the number average degree of polymerization (DP n) is then equal to the average kinetic chain length: