The gelation of xanthan-locust bean gum (LBG) mixtures has been invest
igated. It has been observed that, over the ionic strength range chose
n, the melting temperatures of the gels (T(g)) remains constant, where
as the order-disorder transition temperature (T(m)) for xanthan alone
increases with increasing ionic strength. The preparation temperature
(T(p)) of the mixed gels is known to affect gelation. Studies have bee
n made on the effect of T(p) relative to T(g) and T(m) on gelation. It
has been observed that gelation occurs at all T(p), even when T(p) <
T(m). At a given ionic strength, increasing T(p) leads to an increase
in the measured storage modulus (G') which closely follows the degree
of disordering of the xanthan molecules. Similarly, for a fixed T(p),
increasing the ionic strength stabilises the ordered xanthan conformat
ion and is found to reduce the measured storage modulus (G'). These re
sults are discussed in the light of the current models for mixed-biopo
lymer gelation.