Skip to main content
  • 1577 Accesses

Abstract

The objective of statistical physics is to derive the macroscopic (thermodynamic) properties of matter from the laws of mechanics that govern the motion of its microscopic constituents. Note that in this context microscopic may have different meanings. Indeed, although it is common to consider that matter is made of atoms or molecules (something known as the atomic description atomic description), this is not the only possible description. For instance, one might consider from the outset that matter is made of electrons and nuclei (subatomic description subatomic description) that interact through Coulomb forces. Clearly, the derivation of the thermodynamic properties of matter is much more involved when, instead of the atomic description, one uses the subatomic one. The reason is that, in this case, one should analyze successively how electrons and nuclei form atoms, how these atoms constitute molecules, and, finally, how the macroscopic properties of matter may be derived from the molecular description. As a matter of fact, the subject of going from the subatomic description to the atomic one does not truly belong to the realm of statistical physics (rather it belongs to atomic and molecular physics) which usually takes as starting point the atomic and molecular interactions.

There is yet a third description in the thermodynamic study of matter (supramolecular or mesoscopic description), which has sometimes been used to study systems having such a complex molecular architecture that it is very difficult to derive the intermolecular interactions from the atomic interactions. The properties of mesoscopic systems are nevertheless similar to those of atomic systems, but they differ in the relevant length scales: the angstrom in atomic systems (microscopic) and the micron in the supramolecular ones (mesoscopic). In the last few years, there has been a spectacular development of research in mesoscopic systems in what is called soft condensed matter (liquid crystals, colloidal dispersions, polymers, etc.), some examples of which are considered later in this chapter.

Due to the existence of an interaction potential between the constituents of a nonideal system, the latter may be found in different structures or phases whose relative stability depends on the thermodynamic state, such as the pressure and the temperature.When these variables are changed, a phase transition may occur in which the structure of the system changes. These transitions will be studied in Chap. 9. In the present chapter a summary is provided of some common structures of matter.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 39.99
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
Hardcover Book
USD 54.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  1. J. O. Hirschfelder, C. F. Curtiss and R. B. Bird, Molecular Theory of Gases and Liquids, J. Wiley, New York (1954). Contains a detailed presentation of the cell theory.

    MATH  Google Scholar 

  2. T. M. Reed and K. E. Gubbins, Applied Statistical Mechanics , McGraw-Hill Kogakusha Ltd, Tokyo (1973). Discusses the relation between the pair potential and the polarization of the electronic clouds surrounding the atoms.

    Google Scholar 

  3. N. W. Ashcroft and N. D. Mermin, Solid State Physics, Saunders, Philadelphia (1976). Provides a good introduction to the different Bravais lattices.

    Google Scholar 

  4. L. V. Woodcock, Annals of the New York Academy of Sciences , 371, 274 (1981). Discusses the glass phase of hard-sphere systems.

    Google Scholar 

  5. J. P. Hansen and I. R. McDonald, Theory of Simple Fluids, 2nd ed., Academic Press, London (1986). Contains a derivation of the solution of the PY-equations.

    Google Scholar 

  6. P. G. de Gennes and J. Prost, The Physics of Liquid Crystals, Clarendon Press, Oxford (1993). A classic introduction to all the known mesophases.

    Google Scholar 

  7. C. Janot, Quasicrystals, Clarendon Press, Oxford (1994). A first introduction to the non-periodic crystal structures.

    MATH  Google Scholar 

  8. M. Doi, Introduction to Polymer Physics, Clarendon Press, Oxford (1996). Contains an elementary derivation of the Flory–Huggins theory.

    Google Scholar 

Download references

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2008 Marc Baus, Carlos F. Tejero

About this chapter

Cite this chapter

(2008). Phases of Matter. In: Baus, M., Tejero, C.F. (eds) Equilibrium Statistical Physics. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-540-74632-4_8

Download citation

Publish with us

Policies and ethics