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  2. Nylon 6 - Wikipedia

    en.wikipedia.org/wiki/Nylon_6

    Caprolactam molecule used to synthesize Nylon 6 by ring opening polymerization. Nylon 6 or polycaprolactam is a polymer, in particular semicrystalline polyamide.Unlike most other nylons, nylon 6 is not a condensation polymer, but instead is formed by ring-opening polymerization; this makes it a special case in the comparison between condensation and addition polymers.

  3. Caprolactam - Wikipedia

    en.wikipedia.org/wiki/Caprolactam

    Nylon 6 is widely used in fibers and plastics. In situ anionic polymerization is employed for cast nylon production where conversion from ε-caprolactam to Nylon 6 takes place inside a mold. In conjunction with endless fiber processing the term thermoplastic resin transfer molding (T-RTM) is often used.

  4. Ring-opening polymerization - Wikipedia

    en.wikipedia.org/wiki/Ring-opening_polymerization

    A polymerization in which a cyclic monomer yields a monomeric unit which is acyclic or contains fewer cycles than the monomer. Note: If monomer is polycyclic, the opening of a single ring is sufficient to classify the reaction as ring-opening polymerization. Modified from the earlier definition. [1] [2]

  5. Nylon rope trick - Wikipedia

    en.wikipedia.org/wiki/Nylon_Rope_Trick

    Acid Chloride Preparative Route for Nylon-6,10, which is often used in the nylon rope trick. The nylon rope trick is a scientific demonstration that illustrates some of the fundamental chemical principles of step-growth polymerization and provides students and other observers with a hands-on demonstration of the preparation of a synthetic polymer.

  6. Nylon 66 - Wikipedia

    en.wikipedia.org/wiki/Nylon_66

    Nylon 66 (loosely written nylon 6-6, nylon 6/6, nylon 6,6, or nylon 6:6) is a type of polyamide or nylon. It, and nylon 6 , are the two most common for textile and plastic industries. Nylon 66 is made of two monomers each containing 6 carbon atoms, hexamethylenediamine and adipic acid , which give nylon 66 its name. [ 1 ]

  7. Carothers equation - Wikipedia

    en.wikipedia.org/wiki/Carothers_equation

    The simplest case refers to the formation of a strictly linear polymer by the reaction (usually by condensation) of two monomers in equimolar quantities. An example is the synthesis of nylon-6,6 whose formula is [−NH−(CH 2) 6 −NH−CO−(CH 2) 4 −CO−] n from one mole of hexamethylenediamine, H 2 N(CH 2) 6 NH 2, and one mole of adipic acid, HOOC−(CH 2) 4 −COOH.

  8. Polymerization - Wikipedia

    en.wikipedia.org/wiki/Polymerization

    In polymer chemistry, polymerization (American English), or polymerisation (British English), is a process of reacting monomer molecules together in a chemical reaction to form polymer chains or three-dimensional networks. [1] [2] [3] There are many forms of polymerization [4] and different systems exist to categorize them. IUPAC definition for ...

  9. Chain-growth polymerization - Wikipedia

    en.wikipedia.org/wiki/Chain-growth_polymerization

    Ring-opening polymerization is defined [6] as a polymerization in which a cyclic monomer yields a monomeric unit which is acyclic or contains fewer cycles than the monomer. Generally, the ring-opening polymerization is carried out under mild conditions, and the by-product is less than in the polycondensation reaction.