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  2. Polymerization - Wikipedia

    en.wikipedia.org/wiki/Polymerization

    Polymerization that is not sufficiently moderated and proceeds at a fast rate can be very hazardous. This phenomenon is known as autoacceleration , and can cause fires and explosions. Step-growth vs. chain-growth polymerization

  3. Autoacceleration - Wikipedia

    en.wikipedia.org/wiki/Autoacceleration

    Autoacceleration of the overall rate of a free-radical polymerization system has been noted in many bulk polymerization systems. The polymerization of methyl methacrylate, for example, deviates strongly from classical mechanism behavior around 20% conversion; in this region the conversion and molecular mass of the polymer produced increases rapidly.

  4. Hazardous Materials Identification System - Wikipedia

    en.wikipedia.org/wiki/Hazardous_Materials...

    Materials that may form explosive mixtures with water and are capable of detonation or explosive reaction in the presence of a strong initiating source. Materials may polymerize, decompose, self-react, or undergo other chemical change at normal temperature and pressure with moderate risk of explosion (e.g., ammonium nitrate). 2.

  5. Ziegler–Natta catalyst - Wikipedia

    en.wikipedia.org/wiki/Ziegler–Natta_catalyst

    The polymerization reaction of alkenes occurs similarly to the reactions in metallocene catalysts: L n Ti–CH 2 −CHR–polymer + CH 2 =CHR → L n Ti–CH 2-CHR–CH 2 −CHR–polymer. The two chain termination reactions occur quite rarely in Ziegler–Natta catalysis and the formed polymers have a too high molecular weight to be of ...

  6. Polyurethane - Wikipedia

    en.wikipedia.org/wiki/Polyurethane

    The most common application of polyurethane is as solid foams, which requires the presence of a gas, or blowing agent, during the polymerization step. This is commonly achieved by adding small amounts of water, which reacts with isocyanates to form CO 2 gas and an amine, via an unstable carbamic acid group.

  7. Alkylation unit - Wikipedia

    en.wikipedia.org/wiki/Alkylation_unit

    Polymerization reactions also have a higher rate of production of acid soluble oils, resulting in higher acid consumption. Temperature; Typically, alkylation is carried out in the neighborhood of 20 °C. Higher reaction temperatures dramatically favor polymerization reactions that will dilute the acid.

  8. Polymerisation inhibitor - Wikipedia

    en.wikipedia.org/wiki/Polymerisation_inhibitor

    In polymer chemistry, polymerisation inhibitors (US: polymerization inhibitors) are chemical compounds added to monomers to prevent their self-polymerisation. Unsaturated monomers such as acrylates , vinyl chloride , butadiene and styrene require inhibitors for both processing and safe transport and storage.

  9. Buchner ring expansion - Wikipedia

    en.wikipedia.org/wiki/Buchner_ring_expansion

    Buchner's first synthesis of cycloheptatriene derivatives in 1885 used photolysis and thermal conditions to generate the carbene. A procedure for preparation of the hazardous starting material needed for carbene generation in the Buchner reaction, ethyl-diazoacetate, is available in Organic Syntheses. [12]