“…The technique is based on the measurement of sample deformation under very low load as the temperature is increased and two main modes of deformation, defined by the probe/sample contact area and the applied load, can be performed: (i) expansion, when low forces are applied to large contact areas, and (ii) penetration, with small contact areas and high forces. [1][2][3][4][5] In general, a combination of expansion/penetration is observed. TMA has been used successfully for the measurement of several properties of polymers, such as the glass transition temperature, 1,3,4 softening temperature, 1,2,4 thermal expansion coefficient, 1,2,6 degree of crosslinking 1,2,7 and the average number of degrees of freedom of polymer segments between crosslinks.…”