Effect of Hydrogen Bonds on the Thermodynamic Behavior of Liquid Water

Peter H. Poole, Francesco Sciortino, Tor Grande, H. Eugene Stanley, and C. Austen Angell
Phys. Rev. Lett. 73, 1632 – Published 19 September 1994
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Abstract

We propose an extension of the van der Waals equation which is designed to incorporate, in an approximate fashion, the effects of the network of hydrogen bonds that exist in liquid water. The resulting model qualitatively predicts the unique thermodynamic properties of water, including those of the deeply supercooled states. It also reconciles two proposals for the phase behavior of supercooled and stretched water and provides a thermodynamic origin for the observed polymorphism of the amorphous solid form of water.

  • Received 28 April 1994

DOI:https://doi.org/10.1103/PhysRevLett.73.1632

©1994 American Physical Society

Authors & Affiliations

Peter H. Poole1, Francesco Sciortino2, Tor Grande1,3, H. Eugene Stanley4, and C. Austen Angell1

  • 1Department of Chemistry, Arizona State University, Tempe, Arizona 85287
  • 2Dipartimento di Fisica, Università "La Sapienza," Piazzale Aldo Moro, 00185 Roma, Italy
  • 3Department of Inorganic Chemistry, Norwegian Institute of Technology, N-7034 Trondheim, Norway
  • 4Center for Polymer Studies and Physics Department, Boston University, Boston, Massachusetts 02215

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Vol. 73, Iss. 12 — 19 September 1994

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