The fragilities (T(g)-normalized temperature dependence of alpha-relaxation times) of 33 glass-forming liquids and polymers are compared for isobaric, mP, and isochoric, mV, conditions. We find that the two quantities are linearly correlated: mP = (37+/-3) + (0.84+/-0.05)mV. This result has obvious and important consequences, since the ratio mV/mP is a measure of the relative degree to which temperature and density control the dynamics. Moreover, we show that the fragility itself is a consequence of the relative interplay of temperature and density effects near T(g). Specifically, strong behavior reflects a substantial contribution from density (jammed dynamics), while the relaxation of fragile liquids is more thermally activated. Drawing on the scaling law log(tau) = I(T upsilon(gamma)), a physical interpretation of this result in terms of the intermolecular potential is offered.
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Casalini et al. (2005) studied this question.
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