THE RHEOLOGY OF GELS
1980; Wiley; Volume: 11; Issue: 4 Linguagem: Inglês
10.1111/j.1745-4603.1980.tb01312.x
ISSN1745-4603
Autores Tópico(s)Polysaccharides and Plant Cell Walls
ResumoABSTRACT The following aspects of the rheological behavior of polysaccharide and protein gels are discussed with particular emphasis on recent investigations: (1) Viscoelasticity of gels; (2) Validity of rubber elasticity theory; (3) Rupture strength of gels; and (4) Single‐point measurements of gel strength. It is concluded that in contrast to most food materials gels show linear viscoelastic behavior up to strains of the order of 0.1. Results obtained from creep and stress relaxation experiments would suggest that noncovalent crosslinks in gels move or break when the gel is stressed. Activation energies associated with crosslink breakage have been estimated from the temperature dependence of viscoelastic parameters. For gelatin and polysaccharide gels energies ranging from 5–65 Kcals/mole have been reported. The stiff and extended nature of polysaccharide chains make it unlikely that polysaccharide gels obey rubber elasticity theory, though it is possible that this theory holds for gelatin gels and also for ovalbumin gels in 6 M urea. It is emphasized that the rupture strength of a gel is not necessarily related to its elastic modulus and therefore ‘single point’ measurements of ‘gel strength’ based on rupture tests will not always rank a series of gels in the same order as tests which involve small deformations without rupture. One of the reasons for this is that the elastic modulus and rupture strength depend in different ways on the primary molecular weight of the polymer from which the gel is formed.
Referência(s)