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Phase Diagrams and Thermodynamic Properties of Binary Organic Systems Based on 1.2 1.30. 1. 4Odiaminobenzene or Benzidine

By Sangster, James

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Book Id: WPLBN0000659588
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Reproduction Date: 2005

Title: Phase Diagrams and Thermodynamic Properties of Binary Organic Systems Based on 1.2 1.30. 1. 4Odiaminobenzene or Benzidine  
Author: Sangster, James
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Language: English
Subject: Technology., Reference materials, Technology and literature
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Sangster, B. J. (n.d.). Phase Diagrams and Thermodynamic Properties of Binary Organic Systems Based on 1.2 1.30. 1. 4Odiaminobenzene or Benzidine. Retrieved from http://www.gutenberg.us/


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Technical Reference Publication

Table of Contents
Contents 1. Introduction ............................. 2 . Critique of Experimental Methods ........... 2.1. Thermal Analysis ..................... 2.2. Thaw-Melt Method ................... 2.3. Microthermal Method ................. 3 . Computer-coupled Themodynamicfphase Dia- gram Analysis ........................... 3.1. Thermodynamics ..................... 3.2. Limiting Slopes of Liquidus Lines And Solid Solubility ........................... 3.3. Optimization Procedure ................ 4 . Principles of the Evaluation Procedure ....... 4.1. General Phase Diagram Considerations ... 4.2. Weighting of Phase Diagram Data ....... 4.3. Status of the Calculated Results ......... 5 . Properties of the Pure Substances ........... 5.1. The Diamino Compounds .............. 5.2. Phenol and Substituted Phenols ......... 5.3. Di- and Trihydroxybenzenes ............ 5.4. Naphthols ........................... 5.5. Remaining Compounds ................ 5.6. Experimental Melting Points and Purity of Substances .......................... 6 . These Evaluations ........................ 6.1. Systems with 1,2-Diaminobenzene . ...... 6.1.1. Dihydroxybenzenes as Second Component ..................... 12-dhb (a) + 1, 2-dab (b) .......... 13-dhb (a) + 1, 2-dab (b) .......... 1, 4-dhb (a) + 1, 2-dab (b) .......... 6.1.2.Naphthols as Second Component ... 1-n (a) + 1, 2-dab (b) ............. 2-n (a) + 1. 2.dab (b) ............. 6.1.3. Phenol and Substituted Phenols as Second Component ................. P (a) + 1. Zdab (b) ............... 2-np (a) + 1. 2.dab (b) ............ 3-np (a) + 1. Zdab (b) ............ 4-np (a) + 1. Zdab (b) ............ 2. 4.dnp (a) + 1. Zdab (b) .......... 6.1.4. Other Compounds as Second Component .................... Ba (a) + 1. Zdab (b) .............. Benz (a) + 1. Zdab (b) ............ 6.2. Systems with 1.3.Diaminobenzene. ...... 6.2.1. Dihydroxybenzenes as Second Component ..................... 1. 2.dhb (a) + 13-dab (b) .......... 1.3.dhb (a) + 1.3.dab (b) ........... 1-4-dhb (a) + 1. 3.dab (b) .......... 6.2.2. Naphthols as Second Component ... I -n (a) + 1. 3.dab (b) ............. 2-n (a) + 1. 3.dab (b) ............. 6.2.3.Phenols and Substituted Phenols as Second Component .............. P (a) + 1. 3.dat.1 (b) ............... 2-np (a) + 1. 3.dab (b) ............ 3-np (a) + 1. 3.dab (b) ............ 4-np (a) + 1. 3dab (b) ............ 2. 4.dnp (a) + 19-dab (b) .......... 6.2.4. Other Compounds as Second Component .................... Benz (a) + 13-dab (b) ............ 6.3. Systems with 1. 4.Diaminobenzene ....... 6.3.1. Dihydroxybenzenes as Second Component .................... 317 01994 by the U.S. Secretary of Commerce on behalf of the United States . . ...... This copyright is assigned to the American Institute of Physics and the 1 ZDHB (A) + 1 .&DAB (B) 317 American Chemical Society. 1. 3.DHB (A) + 1+ DAB (B) ...... 318 Reprints available from ACS; see Reprints List at back of issue . 1. 4.DHB (A) + 1.C DAB (B) .....

 
 



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