The Phase Rule and Its Applications

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THE PHASE RULE CHAPTER I

Title: The Phase Rule and Its Applications

Author: Alexander Findlay

Language: English

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THE PHASE RULE AND ITS APPLICATIONS. By Alex. Findlay, M.A., Ph.D., D.Sc., Lecturer and Demonstrator in Chemistry, University of Birmingham. With 134 Figures in the Text. Crown 8vo. 5s.

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LONGMANS, GREEN, AND CO.
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THE PHASE RULE

AND ITS APPLICATIONS

BY

ALEX. FINDLAY, M.A., Ph.D., D.Sc.

LECTURER ON PHYSICAL CHEMISTRY, UNIVERSITY OF BIRMINGHAM

WITH ONE HUNDRED AND THIRTY-FOUR FIGURES
IN THE TEXT

THIRD IMPRESSION

LONGMANS, GREEN, AND CO.

39 PATERNOSTER ROW, LONDON
NEW YORK, BOMBAY, AND CALCUTTA
1908

All rights reserved



DEDICATED

TO

FRANCIS ROBERT JAPP, LL.D., F.R.S.

PROFESSOR OF CHEMISTRY, UNIVERSITY OF ABERDEEN,

IN GRATITUDE FOR EARLY TRAINING

AND ADVICE



PREFACE TO THE SECOND EDITION.

During the two years which have elapsed since the first edition of this book appeared, the study of chemical equilibria has been prosecuted with considerable activity, and valuable additions have been made to our knowledge in several departments of this subject. In view of the scope of the present work, it has been, of course, impossible to incorporate all that has been done; but several new sections have been inserted, notably those on the study of basic salts; the interpretation of cooling curves, and the determination of the composition of solid phases without analysis; the equilibria between iron, carbon monoxide, and carbon dioxide, which are of importance in connection with the processes occurring in the blast furnace; and the Phase Rule study of the ammonia-soda process. I have also incorporated a short section on the reciprocal salt-pair barium carbonate—potassium sulphate, which had been written for the German edition of this book by the late Professor W. Meyerhoffer. The section on the iron-carbon alloys, which in the first edition was somewhat unsatisfactory, has been rewritten.

A. F.

September, 1906.



PREFACE

Although we are indebted to the late Professor Willard Gibbs for the first enunciation of the Phase Rule, it was not till 1887 that its practical applicability to the study of Chemical Equilibria was made apparent. In that year Roozeboom disclosed the great generalization, which for upwards of ten years had remained hidden and unknown save to a very few, by stripping from it the garb of abstract Mathematics in which it had been clothed by its first discoverer. The Phase Rule was thus made generally accessible; and its adoption by Roozeboom as the basis of classification of the different cases of chemical equilibrium then known established its value, not only as a means of co-ordinating the large number of isolated cases of equilibrium and of giving a deeper insight into the relationships existing between the different systems, but also as a guide in the investigation of unknown systems.

While the revelation of the principle embedded in the Phase Rule is primarily due to Roozeboom, it should not be forgotten that, some years previously, van't Hoff, in ignorance of the work of Willard Gibbs, had enunciated his "law of the incompatibility of condensed systems," which in some respects coincides with the Phase Rule; and it is only owing to the more general applicability of the latter that the very important generalization of van't Hoff has been somewhat lost sight of.

The exposition of the Phase Rule and its applications given in the following pages has been made entirely non-mathematical, the desire having been to explain as clearly as possible the principles underlying the Phase Rule, and to illustrate their application to the classification and investigation of equilibria, by means of a number of cases actually studied. While it has been sought to make the treatment sufficiently elementary to be understood by the student just commencing the study of chemical equilibria, an attempt has been made to advance his knowledge to such a stage as to enable him to study with profit the larger works on the subject, and to follow with intelligence the course of investigation in this department of Physical Chemistry. It is also hoped that the volume may be of use, not only to the student of Physical Chemistry, or of the other branches of that science, but also to the student of Metallurgy and of Geology, for whom an acquaintance with at least the principles of the Phase Rule is becoming increasingly important.

In writing the following account of the Phase Rule, it is scarcely necessary to say that I have been greatly indebted to the larger works on Chemical Equilibria by Ostwald ("Lehrbuch"), Roozeboom ("Die Heterogenen Gleichgewichte"), and Bancroft ("The Phase Rule"); and in the case of the first-named, to the inspiration also of personal teaching. My indebtedness to these and other authors I have indicated in the following pages.

In conclusion, I would express my thanks to Sir William Ramsay, whose guidance and counsel have been constantly at my disposal; and to my colleagues, Dr. T. Slater Price and Dr. A. McKenzie, for their friendly criticism and advice. To Messrs. J. N. Friend, M.Sc., and W. E. S. Turner, B.Sc., I am also indebted for their assistance in reading the proof-sheets.

A. F.

November, 1903.



CONTENTS

PAGE
CHAPTER I
Introduction 1
General, I. Homogeneous and heterogeneous equilibrium, 5. Real and apparent equilibrium, 5.
CHAPTER II
The Phase Rule 7
Phases, 8. Components, 10. Degree of freedom. Variability of a system, 14. The Phase Rule, 16. Classification of systems according to the Phase Rule, 17. Deduction of the Phase Rule, 18.
CHAPTER III
Typical Systems of One Component 21
A. Water. Equilibrium between liquid and vapour. Vaporization curve, 21. Upper limit of vaporization curve, 23. Sublimation curve of ice, 24. Equilibrium between ice and water. Curve of fusion, 25. Equilibrium between ice, water, and vapour. The triple point, 27. Bivariant systems of water, 29. Supercooled water. Metastable state, 30. Other systems of the substance water, 32. B. Sulphur, 33. Polymorphism, 33. Sulphur, 34. Triple point—Rhombic and monoclinic sulphur and vapour. Transition point, 34. Condensed systems, 36. Suspended transformation, 37. Transition curve—Rhombic and monoclinic sulphur, 37. Triple point—Monoclinic sulphur, liquid, and vapour. Melting point of monoclinic sulphur, 38. Triple point—Rhombic and monoclinic sulphur and liquid, 38. Triple point—Rhombic sulphur, liquid, and vapour. Metastable triple point, 38. Fusion curve of rhombic sulphur, 39. Bivariant systems, 39. C. Tin, 41. Transition point, 41. Enantiotropy and monotropy, 44. D. Phosphorus, 46. Enantiotropy combined with monotropy, 51. E. Liquid Crystals, 51. Phenomena observed, 51. Nature of liquid crystals, 52. Equilibrium relations in the case of liquid crystals, 53.
CHAPTER IV
General Summary 55
Triple point, 55. Theorems of van't Hoff and of Le Chatelier, 57. Changes at the triple point, 58. Triple point solid—solid—vapour, 62. Sublimation and vaporization curves, 63. Fusion curve—Transition curve, 66. Suspended transformation. Metastable equilibria, 69. Velocity of transformation, 70. Law of successive reactions, 73.
CHAPTER V
Systems of Two Components—Phenomena of Dissociation 76
Different systems of two components, 77. Phenomena of Dissociation. Bivariant systems, 79. Univariant systems, 80. Ammonia compounds of metal chlorides, 82. Salts with water of crystallization, 85. Efflorescence, 86. Indefiniteness of the vapour pressure of a hydrate, 87. Suspended transformation, 89. Range of existence of hydrates, 90. Constancy of vapour pressure and the formation of compounds, 90. Measurement of the vapour pressure of hydrates, 91.
CHAPTER VI
Solutions 92
Definition, 92. Solutions of Gases in Liquids, 93. Solutions of Liquids in Liquids, 95. Partial or limited miscibility, 96. Phenol and water, 97. Methylethylketone and water, 100. Triethylamine and water, 101. General form of concentration-temperature curve, 101. Pressure-concentration diagram, 102. Complete miscibility, 104. Pressure-concentration diagram, 104.
CHAPTER VII
Solutions of Solids in Liquids, only One of the Components being Volatile 106
General, 106. The saturated solution, 108. Form of the solubility curve, 108. A. Anhydrous Salt and Water. The solubility curve, 111. Suspended transformation and supersaturation, 113. Solubility curve at higher temperatures, 114. (1) Complete miscibility of the fused components. Ice as solid phase, 116. Cryohydrates, 117. Changes at the quadruple point, 119. Freezing mixtures, 120. (2) Partial miscibility of the fused components. Supersaturation, 124. Pressure-temperature diagram, 126. Vapour pressure of solid—solution—vapour, 126. Other univariant systems, 127. Bivariant systems, 129. Deliquescence, 130. Separation of salt on evaporation, 130. General summary, 131.
CHAPTER VIII
Solutions of Solids in Liquids, only One of the Components being Volatile 133
B. Hydrated Salt and Water, (1) The compounds formed do not have a definite melting point. Concentration-temperature diagram, 133. Sodium sulphate and water, 134. Suspended transformation, 137. Dehydration by means of anhydrous sodium sulphate, 138. Pressure-temperature diagram, 138. (2) The compounds formed have a definite melting point. Solubility curve of calcium chloride hexahydrate, 145. Pressure-temperature diagram, 149. The indifferent point, 150. The hydrates of ferric chloride, 151. Suspended transformation, 155. Evaporation of solutions at constant temperature, 155. Inevaporable solutions, 157. Illustration, 158.
CHAPTER IX
Equilibria between Two Volatile Components 161
General, 161. Iodine and chlorine, 161. Concentration-temperature diagram, 162. Pressure-temperature diagram, 165. Bivariant systems, 167. Sulphur dioxide and water, 169. Pressure-temperature diagram, 170. Bivariant systems, 173.
CHAPTER X
Solid Solutions. Mixed Crystals 175
General, 175. Solution of gases in solids, 176. Palladium and hydrogen, 178. Solutions of solids in solids. Mixed crystals, 180. Formation of mixed crystals of isomorphous substances, 182. I. The two components can form an unbroken series of mixed crystals. (a) The freezing points of all mixtures lie between the freezing points of the pure components. Examples, 183. Melting-point curve, 183. (b) The freezing-point curve passes through a maximum. Example, 186. (c) The freezing-point curve passes through a minimum. Example, 188. Fractional crystallization of mixed crystals, 188. II. The two components do not form a continuous series of mixed crystals. (a) The freezing-point curve exhibits a transition point, 190. Example, 190. (b) The freezing-point curve exhibits a eutectic point, 191. Examples, 192. Changes in mixed crystals with the temperature, 192.
CHAPTER XI
Equilibrium between Dynamic Isomerides 195
Temperature-concentration diagram, 196. Transformation of the unstable into the stable form, 201. Examples, 203. Benzaldoximes, 203. Acetaldehyde and paraldehyde, 204.
CHAPTER XII
Summary.Application of the Phase Rule to the Study of Systems of Two Components 207
Summary of the different systems of two components, 208. (1) Organic compounds, 212. (2) Optically active substances, 213. Examples, 216. Transformations, 217. (3) Alloys, 220. Iron—carbon alloys, 223. Determination of the composition of compounds without analysis, 228. Formation of minerals, 232.
CHAPTER XIII
Systems of Three Components 234
General, 234. Graphic representation, 235.
CHAPTER XIV
Solutions of Liquids in Liquids 240
1. The three components form only one pair of partially miscible liquids, 240. Retrograde solubility, 245. The influence of temperature, 247. 2. The three components can form two pairs of partially miscible liquids, 249. 3. The three components form three pairs of partially miscible liquids, 251.
CHAPTER XV
Presence of Solid Phases 253
A. The ternary eutectic point, 253. Formation of compounds, 255. B. Equilibria at higher temperatures. Formation of double salts, 258. Transition point, 258. Vapour pressure. Quintuple point, 261. Solubility curves at the transition point, 264. Decomposition of the double salt by water, 267. Transition interval, 270. Summary, 271.
CHAPTER XVI
Isothermal Curves and the Space Model 272
Non-formation of double salts, 272. Formation of double salt, 273. Transition interval, 277. Isothermal evaporation, 278. Crystallization of double salt from solutions containing excess of one component, 280. Formation of mixed crystals, 281. Application to the characterization of racemates, 282. Representation in space. Space model for carnallite, 284. Summary and numerical data, 287. Ferric chloride—hydrogen chloride—water, 290. Ternary systems, 291. The isothermal curves, 294. Basic Salts, 296. Bi2O3—N2O5—H2O, 298. Basic mercury salts, 301. Indirect determination of the composition of the solid phase, 302.
CHAPTER XVII
Absence of Liquid Phase 305
                                                                                                                                                                                                                                                                                                           

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