Aromatic nylon properties

Properties Nylon 6/9, molding and extrusion Nylon 6/12 Nylon 11, molding and extrusion Nylon 12, molding and extrusion Aromatic nylon (aramid), molded and unfilled Poly(amide- imide), unfilled... 

Nylon-4,6 was developed by DSM Engineering Plastics in 1990 and sold under the trade name Stanyl giving a nylon that has a higher heat and chemical resistance for the automotive industry and in electrical applications. It has a of 295°C and can be made more crystalline than nylon-6,6. A number of other nylons, such as the aromatic nylons and aramids, are strong and can operate at high temperatures, and they have good flame-resistant properties. 

The process uses Ultramid T (a crystalline, semi-aromatic Nylon 6/6T), a special BASF compound which incorporates 30% glass fibre and other properties to facilitate the initiation of metal deposition and metal adhesion. The final result, after incorporating a special laser-sensitive metal complex, was Ultramid T KR4380 LS. This polymer has the high melting point of 295 "C and is equally suitable... 

Uses. The principal use of adiponitrile is for hydrogenation to hexamethylene diamine leading to nylon-6,6. However, as a result of BASE s new adiponitrile-to-caprolactam process, a significant fraction of ADN produced may find its way into nylon-6 production. Adipoquanamine, which is prepared by the reaction of adiponitrile with dicyandiamide [461-58-5] (cyanoguanidine), may have uses in melamine—urea amino resins (qv) (see "Benzonitrile, Uses"). Its typical Hquid nitrile properties suggest its use as an extractant for aromatic hydrocarbons. 

Reduced and partially reduced azepines are more common. Perhydroazepine (hexamethylenimine) was first prepared in 1905 and chemically it behaves as a typical secondary amine (B-67MI51600). Its 2-oxo derivative (caprolactam) is a bulk chemical and is of great industrial importance as an intermediate in the manufacture of nylon. Many oxo and dioxo derivatives of azepines and benzazepines have been prepared, often with difficulty, in a mainly fruitless search for aromatic properties in these azatropone and benz-azatropone systems (see Section 5.16.3.1.2). 

The fiftieth anniversary of the announcement of nylon as the first synthetic organic textile fiber by the Du Pont Co. on October 27,1938 was celebrated as a significant event by the textile industry in 1988 (1,2). The announcement was the culmination of the fundamental research efforts of W. H. Carothers and his team at Du Pont (3). Carothers synthesized diamines from C2 to C18 in order for them to react with a variety of aliphatic dicarboxylic acids to make polyamides for evaluation as fibers (4—10). Alicyclic and aromatic diamines and dicarboxylic acids were also included. Nylon-6,6 was ultimately selected for scale-up and development because of its favorable melting point ( 260° C), best balance of properties, and lower manufacturing cost. The pilot plant for nylon-6,6 was completed in Wilmington, Delaware, in July, 1938, and a product was introduced on the market as Exton brisdes for Dr. West s toothbrushes (2). The first nylon filament plant was built in 1939 at Seaford, Delaware, and nylon stockings went on sale on October 24,1939 only to residents of Wilmington, and then nationally, on May 15, 1940 (2). 

Uses. The principal use of adiponitrile is for hydrogenation to hexamethylene diamine leading to nylon-6,6. Adipoquanamine, prepared by the reaction of adiponitrile with dicyandiamide (cyanoguanidine), has typical liquid nitrile properties that suggest its use as an extractant for aromatic hydrocarbons. 

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