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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. Its competition with nylon 6,6 and the example it set ...
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 ]
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 ...
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.
List of some addition polymers and their uses ; Polymer Abbreviation Properties Uses Low-density polyethylene: LDPE: Chemically inert, flexible, insulator: Squeeze bottles, toys, flexible pipes, insulation cover (electric wires), six-pack rings, etc.
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 ...
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]
Alternatively, more explicit structure-based nomenclature can be used when the polymer structure is proven. Where there is no confusion, some traditional names are also acceptable. Whatever method is used, all polymer names have the prefix poly, followed by enclosing marks around the rest of the name. The marks are used in the order: {[( )]}.