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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. 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 ]

  4. Nylon - Wikipedia

    en.wikipedia.org/wiki/Nylon

    Type 6,6 Nylon 101 is the most common commercial grade of nylon, and Nylon 6 is the most common commercial grade of molded nylon. [ 94 ] [ 95 ] For use in tools such as spudgers , nylon is available in glass-filled variants which increase structural and impact strength and rigidity, and molybdenum disulfide -filled variants which increase ...

  5. Zytel - Wikipedia

    en.wikipedia.org/wiki/Zytel

    The Zytel product line is based mostly on nylon 66, but also includes grades based on nylon 6 as a matrix, long chain nylons such as nylon 610 (if based on at least one renewable monomer they are branded Zytel RS), and copolymers including a transparent resin called Zytel 330.

  6. Copolymer - Wikipedia

    en.wikipedia.org/wiki/Copolymer

    A step-growth copolymer -(-A-A-B-B-) n - formed by the condensation of two bifunctional monomers A–A and B–B is in principle a perfectly alternating copolymer of these two monomers, but is usually considered as a homopolymer of the dimeric repeat unit A-A-B-B. [6] An example is nylon 66 with repeat unit -OC-( CH 2) 4-CO-NH-(CH 2) 6-NH ...

  7. 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]

  8. Crystallization of polymers - Wikipedia

    en.wikipedia.org/wiki/Crystallization_of_polymers

    Crystalline areas are generally more densely packed than amorphous areas. This results in a higher density, up to 15% depending on the material. For example, polyamide 6 (nylon) has crystalline density ρ c = 1.24 g/cm 3 and amorphous density ρ a = 1.08 g/cm 3). However, moisture which is often present in the sample does affect this type of ...

  9. Diamine - Wikipedia

    en.wikipedia.org/wiki/Diamine

    Diamines are used as monomers to prepare polyamides, polyimides, and polyureas. The term diamine refers mostly to primary diamines, as those are the most reactive. [1] In terms of quantities produced, 1,6-diaminohexane (a precursor to Nylon 6-6) is most important, followed by ethylenediamine. [2]