Modeling of Liquid Phases. (Record no. 51441)
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| fixed length control field | 10907nam a22004813i 4500 |
| 001 - CONTROL NUMBER | |
| control field | EBC2057223 |
| 003 - CONTROL NUMBER IDENTIFIER | |
| control field | MiAaPQ |
| 005 - DATE AND TIME OF LATEST TRANSACTION | |
| control field | 20240729123644.0 |
| 006 - FIXED-LENGTH DATA ELEMENTS--ADDITIONAL MATERIAL CHARACTERISTICS | |
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| 007 - PHYSICAL DESCRIPTION FIXED FIELD--GENERAL INFORMATION | |
| fixed length control field | cr cnu|||||||| |
| 008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION | |
| fixed length control field | 240724s2015 xx o ||||0 eng d |
| 020 ## - INTERNATIONAL STANDARD BOOK NUMBER | |
| International Standard Book Number | 9781119178491 |
| Qualifying information | (electronic bk.) |
| 020 ## - INTERNATIONAL STANDARD BOOK NUMBER | |
| Canceled/invalid ISBN | 9781848218659 |
| 035 ## - SYSTEM CONTROL NUMBER | |
| System control number | (MiAaPQ)EBC2057223 |
| 035 ## - SYSTEM CONTROL NUMBER | |
| System control number | (Au-PeEL)EBL2057223 |
| 035 ## - SYSTEM CONTROL NUMBER | |
| System control number | (CaPaEBR)ebr11086793 |
| 035 ## - SYSTEM CONTROL NUMBER | |
| System control number | (CaONFJC)MIL820177 |
| 035 ## - SYSTEM CONTROL NUMBER | |
| System control number | (OCoLC)939554533 |
| 040 ## - CATALOGING SOURCE | |
| Original cataloging agency | MiAaPQ |
| Language of cataloging | eng |
| Description conventions | rda |
| -- | pn |
| Transcribing agency | MiAaPQ |
| Modifying agency | MiAaPQ |
| 050 #4 - LIBRARY OF CONGRESS CALL NUMBER | |
| Classification number | QD923 .S384 2015 |
| 082 0# - DEWEY DECIMAL CLASSIFICATION NUMBER | |
| Classification number | 541.3630151 |
| 100 1# - MAIN ENTRY--PERSONAL NAME | |
| Personal name | Soustelle, Michel. |
| 245 10 - TITLE STATEMENT | |
| Title | Modeling of Liquid Phases. |
| 250 ## - EDITION STATEMENT | |
| Edition statement | 1st ed. |
| 264 #1 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE | |
| Place of production, publication, distribution, manufacture | Newark : |
| Name of producer, publisher, distributor, manufacturer | John Wiley & Sons, Incorporated, |
| Date of production, publication, distribution, manufacture, or copyright notice | 2015. |
| 264 #4 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE | |
| Date of production, publication, distribution, manufacture, or copyright notice | ©2015. |
| 300 ## - PHYSICAL DESCRIPTION | |
| Extent | 1 online resource (261 pages) |
| 336 ## - CONTENT TYPE | |
| Content type term | text |
| Content type code | txt |
| Source | rdacontent |
| 337 ## - MEDIA TYPE | |
| Media type term | computer |
| Media type code | c |
| Source | rdamedia |
| 338 ## - CARRIER TYPE | |
| Carrier type term | online resource |
| Carrier type code | cr |
| Source | rdacarrier |
| 505 0# - FORMATTED CONTENTS NOTE | |
| Formatted contents note | Cover -- Title Page -- Copyright -- Contents -- Preface -- Notations and Symbols -- 1: Pure Liquids -- 1.1. Macroscopic modeling of liquids -- 1.2. Distribution of molecules in a liquid -- 1.2.1. Molecular structure of a non-associated liquid -- 1.2.2. The radial distribution function -- 1.2.3 The curve representative of the radial distribution function -- 1.2.4. Calculation of the macroscopic thermodynamic values -- 1.3. Models extrapolated from gases or solids -- 1.3.1. Guggenheim's smoothed potential model -- 1.3.2. Mie's harmonic oscillator model -- 1.3.3. Determination of the free volume on the basis of the dilation and the compressibility -- 1.4. Lennard-Jones and Devonshire cellular model -- 1.5. Cellular and vacancies model -- 1.6. Eyring's semi-microscopic formulation of the vacancy model -- 1.7. Comparison between the different microscopic models and experimental results -- 2: Macroscopic Modeling of Liquid Molecular Solutions -- 2.1. Macroscopic modeling of the Margules expansion -- 2.2. General representation of a solution with several components -- 2.3. Macroscopic modeling of the Wagner expansions -- 2.3.1. Definition of the Wagner interaction coefficients -- 2.3.2. Example of a ternary solution: experimental determination of Wagner's interaction coefficients -- 2.4. Dilute ideal solutions -- 2.4.1. Thermodynamic definition of a dilute ideal solution -- 2.4.2. Activity coefficients of a component with a pure-substance reference -- 2.4.3. Excess Gibbs energy of an ideal dilute solution -- 2.4.4. Enthalpy of mixing for an ideal dilute solution -- 2.4.5. Excess entropy of a dilute ideal solution -- 2.4.6. Molar heat capacity of an ideal dilute solution at constant pressure -- 2.5. Associated solutions -- 2.5.1. Example of the study of an associated solution -- 2.5.2. Relations between the chemical potentials of the associated solution. |
| 505 8# - FORMATTED CONTENTS NOTE | |
| Formatted contents note | 2.5.3. Calculating the extent of the equilibrium in an associated solution -- 2.5.4. Calculating the activity coefficients in an associated solution -- 2.5.5. Definition of a regular solution -- 2.5.6. Strictly-regular solutions -- 2.5.7. Macroscopic modeling of strictly-regular binary solutions -- 2.5.8. Extension of the model of a strictly-regular solution to solutions with more than two components -- 2.6. Athermic solutions -- 2.6.1. Thermodynamic definition of an athermic solution -- 2.6.2. Variation of the activity coefficients with temperature in an athermic solution -- 2.6.3. Molar entropy and Gibbs energy of mixing for an athermic solution -- 2.6.4. Molar heat capacity of an athermic solution -- 3: Microscopic Modeling of Liquid Molecular Solutions -- 3.1. Models of binary solutions with molecules of similar dimensions -- 3.1.1. The microscopic model of a perfect solution -- 3.1.2. Microscopic description of strictly-regular solutions -- 3.1.3. Microscopic modeling of an ideal dilute solution -- 3.2. The concept of local composition -- 3.2.1. The concept of local composition in a solution -- 3.2.2. Energy balance of the mixture -- 3.2.3. Warren and Cowley's order parameter -- 3.2.4. Model of Fowler & -- Guggenheim's quasi-chemical solution -- 3.3. The quasi-chemical method of modeling solutions -- 3.4. Difference of the molar volumes: the combination term -- 3.4.1. Combinatorial excess entropy -- 3.4.2. Flory's athermic solution model -- 3.4.3. Staverman's corrective factor -- 3.4.3.1. The concept of structural parameters -- 3.4.3.2. Staverman's model -- 3.5. Combination of the different concepts: the UNIQUAC model -- 3.6. The concept of contribution of groups: the UNIFAC model -- 3.6.1. The concept of the contribution of groups -- 3.6.2. The UNIFAC model -- 3.6.3. The modified UNIFAC model (Dortmund). |
| 505 8# - FORMATTED CONTENTS NOTE | |
| Formatted contents note | 3.6.4. Use of the UNIFAC system in the UNIQUAC model -- 4: Ionic Solutions -- 4.1. Reference state, unit of composition and activity coefficients of ionic solutions -- 4.2. Debye and Hückel's electrostatic model -- 4.2.1. Presentation of the problem -- 4.2.2. Notations -- 4.2.3. Poisson's equation -- 4.2.4. Electrical potential due to the ionic atmosphere -- 4.2.5. Debye and Hückel's hypotheses -- 4.2.5.1. Hypothesis 1: shape of the ions and nature of the medium -- 4.2.5.2. Hypothesis 2: pairwise interactions -- 4.2.5.3. Hypothesis 3: Boltzmann distribution -- 4.2.5.4. Hypothesis 4: relation between < -- Ψ(r)> -- k and ε kj -- 4.2.5.5. Hypothesis 5: primacy of thermal agitation -- 4.2.6. Debye and Hückel's solution for the potential due to the ionic atmosphere -- 4.2.7. Charge and radius of the ionic atmosphere of an ion -- 4.2.8. Excess Helmholtz energy and excess Gibbs energy due to charges -- 4.2.9. Activity coefficients of the ions and mean activity coefficient of the solution -- 4.2.10. Self-consistency of Debye and Hückel's model -- 4.2.10.1. Thermodynamic criteria -- 4.2.10.2. Electrostatic criteria -- 4.2.11. Switching from concentrations to molalities -- 4.2.12. Debye and Hückel's law: validity and comparison with experimental data -- 4.2.13. Debye and Hückel's limit law -- 4.2.14. Extensions of Debye and Hückel's law -- 4.3. Pitzer's model -- 4.4. UNIQUAC model extended to ionic solutions -- 5: Determination of the Activity of a Component of a Solution -- 5.1. Calculation of an activity coefficient when we know other coefficients -- 5.1.1. Calculation of the activity of a component when we know that of the other components in the solution -- 5.1.2. Determination of the activity of a component at one temperature if we know its activity at another temperature. |
| 505 8# - FORMATTED CONTENTS NOTE | |
| Formatted contents note | 5.2. Determination of the activity on the basis of the measured vapor pressure -- 5.2.1. Measurement by the direct method -- 5.2.2. Method using the vaporization constant in reference II -- 5.3. Measurement of the activity of the solvent of the basis of the colligative properties -- 5.3.1. Use of measuring of the depression of the boiling point - ebullioscopy -- 5.3.2. Use of measuring of the depression of the freezing point - cryoscopy -- 5.3.3. Use of the measurement of osmotic pressure -- 5.4. Measuring the activity on the basis of solubility measurements -- 5.4.1. Measuring the solubilities in molecular solutions -- 5.4.2. Measuring the solubilities in ionic solutions -- 5.5. Measuring the activity by measuring the distribution of a solute between two immiscible solvents -- 5.6. Activity in a conductive solution -- 5.6.1. Measuring the activity in a strong electrolyte -- 5.6.1.1. Measuring the absolute activity of an ion -- 5.6.1.2. Measurement of the mean activity coefficient of a strong electrolyte -- 5.6.2. Determination of the mean activity of a weak electrolyte on the basis of the dissociation equilibrium -- Appendices -- Appendix 1: Statistical Methods of Numerical Simulation -- A.1.1. The physical bases of simulation -- A.1.2. Construction of the sample -- A.1.2.1. Truncation of the potential function -- A.1.2.2. Limitation of edge effects -- A.1.2.2.1. Periodic boundary condition -- A.1.2.2.2. Minimum-image convention -- A.1.2.3. Estimation of the duration of the calculation -- A.1.3. The main calculation methods -- A.1.3.1. The Monte-Carlo method -- A.1.3.2. The molecular dynamics method -- Appendix 2: Reminders of the Properties of Solutions -- A.2.1. Values attached to solutions -- A.2.2. Peculiar values and mixing values -- A.2.2.1. Definitions -- A.2.3. Characterization of the imperfection of a real solution. |
| 505 8# - FORMATTED CONTENTS NOTE | |
| Formatted contents note | A.2.4. Activity coefficients -- A.2.5. Activity coefficients and reference states -- A.2.5.1. Relation between the activity coefficients of the components of a solution -- A.2.5.2. Influence of the different variables on the activity coefficients -- A.2.5.2.1. Temperature -- A.2.5.2.2. Influence of the composition on the activity coefficients -- A.2.6. Excess values -- A.2.7. Ionic solutions -- A.2.7.1. Composition of an ionic solution and reference state -- A.2.7.2. Chemical potential of an ion -- A.2.7.3. Relation between the activities of the ions and the overall activity of the solutes -- A.2.7.4. Mean concentration and mean activity coefficient of the ions -- A.2.7.5. Activity coefficient of an individual ion -- A.2.7.6. Concept of ionic strength -- Appendix 3: Reminders on Statistical Thermodynamics -- A.3.1. The three statistical distributions -- A.3.1.1. Maxwell-Boltzmann statistics -- A.3.1.2. Bose-Einstein quantum statistics -- A.3.1.3. Fermi-Dirac quantum statistics -- A.3.1.4. Classic limit case -- A.3.2. Partition functions of a molecule object -- A.3.2.1. Definition -- A.3.2.2. Independence of the energies -- A.3.2.3. Partial molecular partition functions, relating to the different motions -- A.3.2.3.1. Translation -- A.3.2.3.2. Rotation with moment of inertia I -- A.3.2.3.3. Vibration of frequency ν -- A.3.3. Canonical partition function -- A.3.3.1. Canonical ensemble -- A.3.3.2. Canonical partition functions -- A.3.3.3. Canonical partition function and molecular partition functions -- A.3.3.3.1. Case of collections of discernible molecules -- A.3.3.3.2. Case of collections of indiscernible molecules -- A.3.4. Interactions between molecules -- A.3.5. Canonical partition functions and thermodynamic functions -- A.3.6. Equilibrium constants in the liquid phase and partition functions -- Bibliography -- Index. |
| 588 ## - SOURCE OF DESCRIPTION NOTE | |
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| 590 ## - LOCAL NOTE (RLIN) | |
| Local note | Electronic reproduction. Ann Arbor, Michigan : ProQuest Ebook Central, 2024. Available via World Wide Web. Access may be limited to ProQuest Ebook Central affiliated libraries. |
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| Topical term or geographic name entry element | Science. |
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| Relationship information | Print version: |
| Main entry heading | Soustelle, Michel |
| Title | Modeling of Liquid Phases |
| Place, publisher, and date of publication | Newark : John Wiley & Sons, Incorporated,c2015 |
| International Standard Book Number | 9781848218659 |
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