Glass transition temperature nylon

Qiana, introduced by Du Pont in 1968 but later withdrawn from the market, was made from bis(4-aminocyclohexyl)methane and dodecanedioic acid. This diamine exists in several cis—trans and trans—trans isomeric forms that influence fiber properties such as shrinkage. The product offered silk-like hand and luster, dimensional stabiUty, and wrinkle resistance similar to polyester. The yam melted at 280°C, had a high wet glass-transition temperature of - 85° C and a density of 1.03 g/cm, the last was lower than that of nylon-6 and nylon-6,6. Qiana requited a carrier for effective dyeing (see Dye carriers). 

As is commonly the case with crystalline polymers the glass transition temperature is of only secondary significance with the aliphatic polyamide homopolymers. There is even considerable uncertainty as to the numerical values. Rigorously dried polymers appear to have TgS of about 50°C, these figures dropping towards 0°C as water is absorbed. At room temperature nylon 66 containing the usual amounts of absorbed water appears to be slightly above the T ... 

The glass transition temperatures of the nylons appear to be below room temperature so that the materials have a measure of flexibility in spite of their high crystallinity under general conditions of service. The polymers have fairly sharply defined melting points and above this temperature the homopolymers have low melt viscosities. Some thermal properties of the nylons are given in Table 18.4. 

Among the spectrum of melt-spinnable fibers such as polyolefins and nylons, PET stands at the upper end in terms of crystalline melt temperature and glass transition temperature. This provides superior dimensional stability for applications where moderately elevated temperatures are encountered, e.g. in automobile tires or in home laundering and drying of garments. The high thermal stability results from the aromatic rings that hinder the mobility of the polymer chain. 

The glass transition temperature Tt of aliphatic nylons is low (40 to 70 C) and is not affected to any great extent by composition. However, the Tm is inversely related to the number of methylene groups present In the... 

The model PBZT/ABPBI molecular composite system is limited since the rod and the matrix do not possess glass transition temperatures for subsequent post form consolidation. In an effort to improve the processability for molecular composites, thermoplastics were used as the host matrix. Processing from acidic solvents requires the thermoplastic host to be soluble and stable in meth-anesulfonic add. Thermoplastic matrices were investigated including both amorphous and semicrystalline nylons [71,72], polyphenylquinoxaline (PPQ) [73] and polyetheretherketone (PEEK) [74], Table 5 shows the mechanical properties obtained for various processed PBZT thermoplastic molecular composite systems. As an example, the PBZT/Nylon systems showed 50-300% improvement over uniaxially aligned chopped fiber composite of comparable compositions. However, the thermally-induced phase separation during consol-... 

It is accomplished usually by just stretching when the fibers are produced. They can also be stretched by a set of heated rolls where each of their rotating speeds (rpm) are increased. A fiber or thread of nylon 6/6, that is an unoriented glassy polymer, has a modulus of elasticity of about 2,000 MPa (300,000 psi). Above the Tg (glass transition temperature) its elastic modulus drops even lower, because small stresses will readily straighten the kinked molecular chains (Chapter 1). However, once it is extended and has its molecules oriented in the direction of the stress, larger stresses are required to produce added strain. The elastic modulus significantly increases. 

Like nylon, polyester fibers are made from linear-condensation polymers by melt spinning, followed by drawing. Similar to nylon, the drawing treatment involves a stretch ratio of 5. The drawing of polyester fiber is done above its glass transition temperature of 80°C. 

---