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  2. Polymer stabilizer - Wikipedia

    en.wikipedia.org/wiki/Polymer_stabilizer

    The aminoxyl radical (N-O•) combines with free radicals in polymers: N-O• + R• → N-O-R Although they are traditionally considered as light stabilizers, they can also stabilize thermal degradation. Even though HALS are extremely effective in polyolefins, polyethylene and polyurethane, they are ineffective in polyvinyl chloride (PVC). It ...

  3. Emulsion stabilization using polyelectrolytes - Wikipedia

    en.wikipedia.org/wiki/Emulsion_stabilization...

    Polymers become charged through the dissociation of the monomer side groups. If more monomer side groups are dissociated, the polymer has a higher charge. In turn, the charge of the polymer classifies the polyelectrolyte, which can be positive (cationic) or negative (anionic).

  4. Hindered amine light stabilizers - Wikipedia

    en.wikipedia.org/wiki/Hindered_amine_light...

    Hindered amine light stabilizers (HALS) are chemical compounds containing an amine functional group that are used as stabilizers in plastics and polymers. [1] These compounds are typically derivatives of tetramethylpiperidine and are primarily used to protect the polymers from the effects of photo-oxidation; as opposed to other forms of polymer degradation such as ozonolysis.

  5. Suspension polymerization - Wikipedia

    en.wikipedia.org/wiki/Suspension_polymerization

    Polymerization in which polymer is formed in monomer, or monomer-solvent droplets in a continuous phase that is a nonsolvent for both the monomer and the formed polymer. Note 1: In suspension polymerization, the initiator is located mainly in the monomer phase. Note 2: Monomer or monomer-solvent droplets in suspension polymerization have

  6. Polymerisation inhibitor - Wikipedia

    en.wikipedia.org/wiki/Polymerisation_inhibitor

    Styrene, for example, is distilled at temperatures above 100 °C whereupon it undergoes thermal polymerisation at a rate of ~2% per hour. [1] This polymerisation is undesirable, as it can foul the fractionating tower; it is also typically exothermic, which can lead to a runaway reaction and potential explosion if left unchecked.

  7. Thermostability - Wikipedia

    en.wikipedia.org/wiki/Thermostability

    Crystal structure of β-glucosidase from Thermotoga neapolitana (PDB: 5IDI).Thermostable protein, active at 80°C and with unfolding temperature of 101°C. [1]In materials science and molecular biology, thermostability is the ability of a substance to resist irreversible change in its chemical or physical structure, often by resisting decomposition or polymerization, at a high relative ...

  8. Reversible addition−fragmentation chain-transfer polymerization

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

    Specific materials and their applications include polymer-protein and polymer-drug conjugates, mediation of enzyme activity, molecular recognition processes and polymeric micelles which can deliver a drug to a specific site in the body. [19] RAFT has also been used to graft polymer chains onto polymeric surfaces, for example, polymeric ...

  9. Thermal degradation of polymers - Wikipedia

    en.wikipedia.org/.../Thermal_degradation_of_polymers

    Although thermal degradation is defined as an oxygen free process it is difficult in practise to completely exclude oxygen. Where this is the case thermal oxidation is to be expected, leading to the formation of free radicals by way of hydroperoxides. These may then participate in thermal degradation reactions, accelerating the rate of breakdown.