Ionic and Electrochemical Equilibria

This book is part of a set of books which offers advanced students successive characterization tool phases, the study of all types of phase (liquid, gas and solid, pure or multi-component), process engineering, chemical and electrochemical equilibria, and the properties of surfaces and phases of small sizes. Macroscopic and microscopic models are in turn covered with a constant correlation between the two scales. Particular attention has been paid to the rigor of mathematical developments. This sixth volume is made up of two parts. The first part focuses on the study of ionic equilibria in water or non-aqueous solvents. The following are then discussed in succession: the dissociation of electrolytes, solvents and solvation, acid-base equilibria, formation of complexes, redox equilibria and the problems of precipitation. Part 2 discusses electrochemical thermodynamics, with the study of two groups: electrodes and electrochemical cells. The book concludes with the study of potential-pH diagrams and their generalization in an aqueous or non-aqueous medium.

Autorentext
Michel Soustelle is a chemical engineer and Emeritus Professor at Ecole des Mines de Saint-Etienne in France. He taught chemical kinetics from postgraduate to Master degree level while also carrying out research in this topic.

Inhalt

Preface xi

Notations and Symbols xv

Part 1. Ionic Equilibria 1

Chapter 1. Dissociation of Electrolytes in Solution 3

1.1. Strong electrolytes weak electrolytes 3

1.1.1. Dissolution 3

1.1.2. Solvolysis 4

1.1.3. Melting 4

1.2. Mean concentration and mean activity coefficient of ions 5

1.3. Dissociation coefficient of a weak electrolyte 6

1.4. Conduction of electrical current by electrolytes 9

1.4.1. Transport numbers and electrical conductivity of an electrolyte 9

1.4.2. Equivalent conductivity and limiting equivalent conductivity of an electrolyte 10

1.4.3. Ionic mobility 11

1.4.4. Relation between equivalent conductivity and mobility Kohlrausch's law 14

1.4.5. Apparent dissociation coefficient and equivalent conductivity 16

1.4.6. Variations of equivalent conductivities with the concentrations 16

1.5. Determination of the dissociation coefficient 20

1.5.1. Determination of the dissociation coefficient by the cryometric method 21

1.5.2. Determination of the dissociation coefficient on the basis of the conductivity values 22

1.6. Determination of the number of ions produced by dissociation 23

1.6.1. Use of limiting molar conductivity 23

1.6.2. Use of cryometry 24

1.7. Thermodynamic values relative to the ions 27

1.7.1. The standard molar Gibbs energy of formation of an ion 27

1.7.2. Standard enthalpy of formation of ions 29

1.7.3. Absolute standard molar entropy of an ion 29

1.7.4. Determination of the mean activity of a weak electrolyte on the basis of the dissociation equilibrium 30

Chapter 2. Solvents and Solvation 31

2.1. Solvents 31

2.2. Solvation and structure of the solvated ion 33

2.3. Thermodynamics of solvation 35

2.3.1. Thermodynamic values of solvation 36

2.3.2. Gibbs energy of salvation Born's model 37

2.4. Transfer of a solute from one solvent to another 44

2.5. Mean transfer activity coefficient of solvation of an electrolyte 48

2.6. Experimentally determining the transfer activity coefficient of solvation 49

2.6.1. Determining the activity coefficient of a molecular solute 50

2.6.2. Determination of the mean transfer activity coefficient of a strong electrolyte 51

2.6.3. Evaluation of the individual transfer activity coefficient of an ion 51

2.7. Relation between the constants of the same equilibrium achieved in two different solvents 55

2.7.1. General relation of solvent change on an equilibrium constant 55

2.7.2. Influence of the dielectric constant of the solvent on the equilibrium constant of an ionic reaction 56

Chapter 3. Acid/Base Equilibria 61

3.1. Definition of acids and bases and acidbase reactions 62

3.2. Ion product of an amphiprotic solvent 63

3.3. Relative strengths of acids and bases 64

3.3.1. Definition of the acidity constant of an acid 64

3.3.2. Protic activity in a solvent 67

3.4. Direction of acidbase reactions, and domain of predominance 69

3.5. Leveling effect of a solvent 71

3.6. Modeling of the strength of an acid 75

3.6.1. Model of the strength of an acid 75

3.6.2. Comparison of an acid's behavior in two solvents 78

3.6.3. Construction of activity zones for solvents 81

3.7. Acidity functions and acidity scales 84

3.8. Applications of the acidity function 88

3.8.1. Measuring the pKa of an indicator 89

3.8.2. Measuring the ion products of solvents 89

3.9. Acidity in non-protic molecular solvents 91

3.10. Protolysis in ionic solvents (molten salts) 92

3.11. Other ionic exchanges in solution 93

3.11.1. Ionoscopy 93

3.11.2. Acidity in molten salts: definition given by Lux and Flood 94

3.12. Franklin and Gutmann's solvo-acidity and solvo-basicity 96

3.12.1. Definition of solvo-acidity 96

3.12.2. Solvo-acidity in molecular solvents 96 <p&...