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Effects of water on the mechanical properties of gelatin films
Author(s) -
Tanioka Akihiko,
Tazawa Takashi,
Miyasaka Keizo,
Ishikawa Kinzo
Publication year - 1974
Publication title -
biopolymers
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.556
H-Index - 125
eISSN - 1097-0282
pISSN - 0006-3525
DOI - 10.1002/bip.1974.360130410
Subject(s) - gelatin , chemistry , viscoelasticity , shear modulus , thermodynamics , dissolution , polymer chemistry , organic chemistry , physics
The mechanical properties of gelatin films were studied in relation to the effect of water, and compared with those of collagen films. The S‐shaped sorption isotherm was separated into an adsorption curve C 1 and dissolution curve C 2 . From the C 2 curve, the interaction parameter χ 1 of Flory–Huggins' equation was calculated. The χ 1 of gelatin were larger than those of collagen at low relative humidities (RH), while they coincided with each other at high RH. It was found that a composite curve was made by shifting stress relaxation curves obtained at different humidities along the log time axis. The shift factor for the formation of the composite curve was analyzed by Fujita–Kishimoto's equation, which was based on the free volume theory. The parameter β, which expressed the extent of the contribution of sorbed water to the increase in the free volume of the system, was 0.05 in the range of C 2 from 0 to 0.08 (0–65% RH). This value was much smaller than 0.16 for collagen. The value was 0.16 in the range of C 2 higher than 0.08, which was equal to that of the collagen. Dynamic shear modulus G ′, loss modulus G ″, and tan δ were determined as functions of RH. The gelatin film extended more than 100% at 73% RH under the very small stress of about 10 7 dyn/cm 2 . This corresponds to the region where β changes from 0.05 to 0.16, although such a phenomenon was not observed in the collagen film. The wide‐angle X‐ray pattern of extended gelatin was similar to that of renatured collagen fiber.