The Disposition of Work Energy Applied to Crystals
- 1 August 1934
- journal article
- research article
- Published by AIP Publishing in The Journal of Chemical Physics
- Vol. 2 (8) , 513-527
- https://doi.org/10.1063/1.1749521
Abstract
The experiments described in this paper were initiated for the purely practical purpose of securing data to be used for an energy balance of the process of comminution of solids. The technologic problem is not considered here but rather the antecedent fundamental and scientific one of attempting to describe the thermodynamic properties of crystals as a function of particle size. It has been customary to ascribe observable variations in the properties of crystalline materials of large or fine particle size to a change of free energy,entropy or heat content resultant from the subdivision. Consideration of the first law of thermodynamics with reference to the application of work energy to crystals allows for only two obvious possibilities: (1) The heat produced in the crystals by the applied work is equal to it, whence no change of intrinsic energy of the material can occur; or (2) part only of the work appears as heat and the intrinsic energy of the crystals must increase. In this latter case, it is supposed that the energy corresponding to the increase of intrinsic energy is ``stored'' in the surficial layers of the crystal particles. We shall offer no apology for approaching the problem of testing these alternatives in a strictly empirical manner and for presenting data which may seem to contradict much of previous theory and experiment concerning the ``surface energy'' of solids. However tempting a review and criticism of previous attempts to measure or theoretically define this quantity might be, the elementary approach represented by our work now seems essential for understanding of the anomalous results, both of ourselves and others. Experimental test based on the first law, as expressed above, obviously could be either by (1) attempting to determine the change of intrinsic energy of fine compared to coarse particles of suitable materials or (2) by comparing the work and heat during the comminution process. Both of these experimental alternatives are described below. Thus we shall first describe experiments upon the heat of solution of fine and coarse calcite, designed to reveal measurable differences of intrinsic energy due to comminution. Further, we have investigated the specific heat at low temperatures of similar samples of calcite, and later of finely drawn wires of copper and aluminum in the annealed compared to the cold‐worked state, referring to that part of the intrinsic energy represented by heat content. Finally, in the case of copper and aluminum, we have adopted the second experimental alternative of comparing the work and heat during a drawing process.Keywords
This publication has 8 references indexed in Scilit:
- The Heat Capacities at Low Temperatures of the Alkaline Earth Carbonates1Journal of the American Chemical Society, 1934
- THE HEAT CAPACITIES OF ARSENIC, ARSENIC TRIOXIDE AND ARSENIC PENTOXIDE AT LOW TEMPERATURES1Journal of the American Chemical Society, 1930
- THE HEAT OF FORMATION OF ZINC OXIDE1Journal of the American Chemical Society, 1930
- Die spezifische Wärme einiger Metalle und Metallegierungen bei tiefen TemperaturenZeitschrift für anorganische und allgemeine Chemie, 1930
- STUDIES ON THE THERMOCHEMISTRY OF THE COMPOUNDS OCCURRING IN THE SYSTEM CaO-Al2O3-SiO2. II. THE HEAT OF SOLUTION OF CALCIUM HYDROXIDE IN HCl·200H2O1Journal of the American Chemical Society, 1930
- LV.The effect of boundary distortion on the surface energy of a crystalJournal of Computers in Education, 1929
- The change in lattice spacing at a crystal boundaryProceedings of the Royal Society of London. Series A, Containing Papers of a Mathematical and Physical Character, 1928
- Travaux du bureau international d’étalons physico-chimiquesJournal de Chimie Physique et de Physico-Chimie Biologique, 1926