Heat capacities of hydrogen large port mordenite (H-LPM), H-LPM + Cu and Na-LPM + Cu samples have been measured in the temperature range 25-500 degreesC before and after treatment at 400 degreesC. The changes in weight of the samples with temperature were also examined by thermogravimetry (TG). A large change in heat capacity of a transition at 133 degreesC appeared for the H-LPM sample before treatment. The measured heat capacity was 3.75 J g(-1) K-1 that exceeds H-LPM + Cu (3.5 J g(-1) K-1) and Na-LPM + Cu (3.27 J g(-1) K-1) samples with transitions at 129 and 146 degreesC, respectively. The transition entropies of the samples before treatment showed almost no changes. However, after treatment, the transition entropies of HLPM, H-LPM + Cu and Na-LPM + Cu samples were 31, 15 and 0.06 kJ g(-1) K-1, respectively. These values indicated that Na+ and Cu2+ exchanged H-LPM influenced the entropy as a result of interaction of these cations with the zeolite framework. This interaction caused a diminishing of the self-diffusion of these ions. This was evidenced by the observed changes in lattice parameters of the H-LPM sample when Na+ and Cu2+ exchange took place, as measured by XRD and FT-IR spectroscopic analysis of the samples, in the range 100-1700 cm(-1). This confirmed that the changes in the lattice modes were related to the increase in the electrostatic interactions between the cations and the zeolite framework. The transition heat capacities of the samples after treatment were found to be in the order: Na-LPM + Cu > H-LPM + Cu > H-LPM.