Effect of orientation, anisotropy, and water on the relaxation behavior of nylon 6 from 4.2 to 300°K

• Published in: Journal of polymer science. Part A-2, Polymer physics Polymer physics, 1972-07, Vol.10 (7), p.1305-1319
• Main Authors: Papir, Yoram S., Kapur, Sudhir, Rogers, Charles E., Baer, Eric
• Format: Article
• Language: English
• ISSN: 0449-2978; 1542-9377
• DOI: 10.1002/pol.1972.160100710

The relaxation behavior of nylon 6 from 4.2 to 300°K was investigated as a function of orientation, anisotropy and moisture content by using an inverted free‐oscillating torsion pendulum. Three new relaxations, δ at 53°K, ϵ below 4.2°K, and ζ at 20°K, were discovered. The characteristics of these new relaxations strongly depend on the orientation anisotropy, and concentration of adsorbed water in the specimens. The results suggest that the mechanism of the γ process is associated with the motions of both the polar and methylene units. The mechanism of the β relaxation is postulated to originate with motions of both non‐hydrogen‐bonded polar groups and polymer—water complex units. The behavior of the α peak is consistent with the hypothesis that it originates with the rupture of interchain hydrogen bonding due to the motions of long‐chain segments in the amorphous regions. Finally, the data strongly support the proposition that two types of water, tightly bound and loosely bound, exist in nylon 6.