 | |
| Names | |
|---|---|
| IUPAC name Poly[imino(1,6-dioxohexamethylene) iminohexamethylene] | |
| Systematic IUPAC name Poly(azanediyladipoylazanediylhexane-1,6-diyl) | |
| Other names Poly(hexamethylene adipamide),Poly(N,N'-hexamethyleneadipinediamide), Maranyl, Ultramid, Zytel, Akromid, Durethan, Frianyl, Vydyne | |
| Identifiers | |
| ChemSpider |
|
| ECHA InfoCard | 100.130.739 |
| Properties | |
| (C12H22N2O2)n | |
| Density | 1.140 g/ml (Zytel) |
| Melting point | 264 °C (507 °F) |
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa). | |
Nylon 66 (loosely writtennylon 6-6,nylon 6/6,nylon 6,6, ornylon 6:6) is a type ofpolyamide ornylon. It, andnylon 6, are the two most common for textile and plastic industries. Nylon 66 is made of two monomers each containing 6 carbon atoms,hexamethylenediamine andadipic acid, which give nylon 66 its name.[1] Aside from its superior physical characteristics, nylon 66 is attractive because its precursors are inexpensive.
Nylon 66 is synthesized bypolycondensation of hexamethylenediamine and adipic acid.Equivalent amounts of hexamethylenediamine and adipic acid are combined in water. In the original implementation, the resultingammonium/carboxylate salt was isolated and then heated either in batches or continuously to induce polycondensation.[2]
Removing water drives the reaction toward polymerization through the formation of amide bonds from the acid and amine functions. Alternatively, the polymerization is conducted on a concentrated aqueous mixture formed of hexamethylenediamine and adipic acid.[3]
It can either be extruded and granulated at this point or directly spun into fibers by extrusion through aspinneret (a small metal plate with fine holes) and cooling to form filaments.
In 2011 worldwide production was two million tons. At that time, fibers consumed just over half of production and engineering resins the rest. It is not used in film applications as it cannot be biaxially oriented.[4] Fiber markets represented 55% of the 2010 demand with engineering thermoplastics being the remainder.[5]
Nylon 66 is frequently used when high mechanical strength, rigidity, good stability under heat and/or chemical resistance are required.[6] It is used in fibers for textiles and carpets and molded parts. For textiles, fibers are sold under various brands, for exampleNilit brands or theCordura brand for luggage, but it is also used in airbags, apparel, and for carpet fibres under the Ultron brand. Nylon 66 lends itself well to make 3D structural objects, mostly byinjection molding. It has broad use in automotive applications; these include "under the hood" parts such asradiator end tanks, rocker covers, air intake manifolds, and oil pans,[7] as well as numerous other structural parts such as hinges,[8] and ball bearing cages. Other applications include electro-insulating elements, pipes, profiles, various machine parts,zip ties, conveyor belts, hoses, polymer-framed weapons, and the outer layer ofturnout blankets.[9] Nylon 66 is also a popularguitar nut material.[10]
Nylon 66, especiallyglass fiber reinforced grades, can be effectively fire retardant with halogen-free products. Phosphorus-based flame retardant systems are used in thesefire-safe polymers and are based onaluminium diethyl phosphinate and synergists. They are designed to meetUL 94 flammability tests as well as Glow Wire Ignition Tests (GWIT), Glow Wire Flammability Test (GWFI) andComparative Tracking Index (CTI). Its main applications are in the electrical and electronics (E&E) industry.
