Issue 7, 2015

Temperature-induced amorphisation of hexagonal ice

Abstract

We systematically studied the competition between polymorphic transformations and amorphisation of hexagonal ice on isobaric heating from 77 K to 155–170 K at pressures between 0.50 and 1.00 GPa. This competition is analysed here systematically by in situ dilatometry and ex situ X-ray diffraction and calorimetry. Volume vs. temperature curves were analysed using a novel fitting approach in order to understand the underlying mechanism. Hexagonal ice undergoes solid-state-transformation to ice IX/III at 0.50 and 0.60 GPa and to a mixture of ices IX/III and IV at 0.70 and 0.80 GPa. Possibly a tiny fraction of amorphous intermediate is transiently formed in this pressure range. At 0.85 GPa the amorphisation process becomes competitive, and leads to very high-density amorphous ice (VHDA) as by-product. At 0.90 and 0.95 GPa VHDA is the main product and at 1.00 GPa only VHDA is found. This represents the first observation of temperature-induced amorphisation (TIA) for hexagonal ice using diffraction methods. Our analysis suggests TIA to be a first-order phase transition which, by contrast to pressure-induced amorphisation (PIA), does not involve a precursor process. We suggest interpreting TIA as thermodynamic melting of ice followed by immediate vitrification rather than as mechanical collapse of hexagonal ice. The activation energies for amorphisation and polymorphic transformation are equal at ∼0.75 GPa. At 1.00 GPa the activation energy for amorphisation of hexagonal ice is lower by about 6 kJ mol−1 than the activation energy for polymorphic transitions.

Graphical abstract: Temperature-induced amorphisation of hexagonal ice

Article information

Article type
Paper
Submitted
01 Dec 2014
Accepted
13 Jan 2015
First published
13 Jan 2015
This article is Open Access
Creative Commons BY-NC license

Phys. Chem. Chem. Phys., 2015,17, 5403-5412

Author version available

Temperature-induced amorphisation of hexagonal ice

P. H. Handle and T. Loerting, Phys. Chem. Chem. Phys., 2015, 17, 5403 DOI: 10.1039/C4CP05587J

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