Handbook of Solvents - George Wypych - ChemTech - Ventech!

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15.1 Standard methods of solvent analysis 1071 10 ASTM D 850-93. Standard test method for distillation of industrial aromatic hydrocarbons and related materials. BS 7392-90. Method for determination of distillation characteristics of petroleum products (ISO 3405). ISO 918-83. Volatile organic liquids for industrial use - Determination of distillation characteristics. ISO 3405-88. Petroleum products - Determination of distillation characteristics. ISO 4626-80. Volatile organic liquids - determination of boiling range of organic solvents used as raw materials. JIS K 2254-98. Petroleum products - Determination of distillation characteristics. 11 ASTM D 1078-97. Standard test method for distillation range of volatile organic liquids. BS 4591-90. Method of determination of distillation characteristics of organic liquids (other than petroleum products) (ISO 918). JIS K 0066-92. Test methods for distillation of chemical products. 12 ASTM D 3272-98. Standard practice for vacuum distillation of solvents from solvent-reducible paints for analysis. 13 ASTM D 5399-95. Standard test method for boiling point distribution of hydrocarbon solvents by gas chromatography. ISO 3924-99. Petroleum products - Determination of boiling range distribution - Gas chromatography method. 14 ASTM D 5776-98. Standard method for bromine index of aromatic hydrocarbons by electrometric titration. ISO 3839-96. Petroleum products - Determination of bromine number of distillates and aliphatic olefins - Electrometric method. JIS K 2605-96. Petroleum distillates and commercial aliphatic olefins - Determination of bromine number - Electrometric method. 15 ASTM D 1492-96. Standard test method for bromine index of aromatic hydrocarbons by coulometric titration. 16 ASTM D 240-97. Standard test method for heat of combustion of liquid hydrocarbon fuels by bomb calorimeter. BS 7420-91. Guide for determination of calorific values of solid, liquid and gaseous fuels (including definitions). DIN 5499-72. Gross and net Calorific values. Terms. DIN 51900-1-89. Determination of gross calorific value of solid and liquid fuels by the bomb calorimeter and calculation of net calorific value. Part 1: Principles, apparatus, methods. DIN 51900-2-77. Testing of solid and liquid fuels. Determination of gross calorific value by bomb calorimeter and calculation of net calorific value. Method of using isothermal water jacket. DIN 51900-3-77. Testing of solid and liquid fuels. Determination of gross calorific value by bomb calorimeter and calculation of net calorific value. Method of using adiabatic jacket. JIS K 2279-93. Crude petroleum and petroleum products - Determination and estimation of heat of combustion. 17 ASTM D 1405-95a. Standard test method for estimation of net heat of combustion of aviation fuels. 18 ASTM D 5468-95. Standard test method for gross calorific value of waste materials. 19 ASTM D 5468-95. Standard test method for gross calorific and ash value of waste materials. 20 ASTM F 1105-95. Standard test method for preparing aircraft cleaning compounds, liquid-type, temperature sensitive, or solvent-based, for storage stability testing. 21 ASTM D 3698-92. Standard practices for solvent vapor degreasing operations. 22 ASTM D 4579-96. Standard practice for handling an acid degreaser or still. 23 ASTM D 848-97. Standard test method for acid wash color of industrial aromatic hydrocarbons. ISO 5274-79. Aromatic hydrocarbons - Acid wash test. ISO 755-3-81. Butan-1-ol for industrial use - Methods of test - Part 3: Sulfuric acid color test. JIS K 0072-98. Testing method of color after treatment with sulfuric acid. 24 ASTM D 1686-96. Standard test method for color of solid aromatic hydrocarbons and related materials in the molten state (platinum-cobalt scale). BS 5339-76. Method of measurement of color in Hazen units (platinum-cobalt scale) of liquid chemical products (ISO 2211). ISO 2211-73. Liquid chemical products - Measurement of color in Hazen units (platinum-cobalt scale). ISO 6271-97. Clear liquids - Estimation of color by the platinum-cobalt scale. JIS K 0071-98. Testing methods for color of chemical products - Part 1. Estimation of color in Hazen units (platinum-cobalt scale).
1072 George Wypych 25 ASTM D 2108-97. Standard test method for color of halogenated organic solvents and their admixtures (platinum-cobalt scale). 26 ASTM D 5386-93b. Standard test method for color of liquids using tristimulus colorimetry. 27 ASTM D 3316-96. Standard test method for stability of perchloroethylene with copper. 28 ASTM D 849-97. Standard test method for copper strip corrosion by industrial aromatic hydrocarbons. ISO 2160-98. Petroleum products - Corrosiveness of copper - Copper strip test. JIS K 2513-91. Petroleum products - Corrosiveness to copper - Copper strip test. SFS-EN ISO 2160. Petroleum products. Corrosiveness to copper. Copper strip test. 29 ASTM D 2943-96. Standard test method for aluminum scratch of 1,1,1-trichloroethane to determine stability. 30 ASTM D 1217-98. Standard test method for density and relative density (specific gravity) of liquids by Bingham pycnometer. 31 ASTM D 891-95. Standard test method for specific gravity, apparent, of liquid industrial chemicals. BS 4522-88. Method for determination of absolute density at 20 o C of liquid chemical products for industrial use (ISO 758). JIS K 0061-92. Test methods for density and relative density of chemical products. 32 ASTM D 2111-95. Standard test methods for specific gravity of halogenated organic solvents and their admixtures. 33 ASTM D 1555-95. Standard test method for calculation of volume and weight of industrial aromatic hydrocarbons. 34 ASTM D 1555M-95. Standard test method for calculation of volume and weight of industrial aromatic hydrocarbons (metric). ISO 5281-80. Aromatic hydrocarbons - Benzene, xylene and toluene - Determination of density at 20 o C. SFS 3773-76. Determination of density of liquids at 20 o C. 35 ASTM D 1720-96. Standard test method for dilution ratio of active solvents in cellulose nitrate solutions. 36 ASTM D 5062-96. Standard test method for resin solution dilutability by volumetric/gravimetric determination. 37 ASTM D 1476-96. Standard test method for heptane miscibility of lacquer solvents 38 ASTM D 1722-94. Standard test method for water miscibility of water-soluble solvents. 39 ASTM D 5226-98. Standard practice for dissolving polymer materials. 40 ASTM D 2257-96. Standard test method for extractable mater in textiles. 41 ASTM F 58-96. Standard test method for measuring specific resistivity of electronic grade solvents. JIS C 0052-95. Environmental testing procedure of electronic and electrical resistance to solvents. 42 ASTM D 4308-95. Standard test method for electrical conductivity of liquid hydrocarbons by precision meter. 43 ASTM D 1816-97. Standard test method for dielectric breakdown voltage of insulating oils of petroleum origin using VDE electrodes. 44 ASTM D 3300-94. Standard test method for dielectric breakdown voltage of insulating oils of petroleum origin under impulse conditions. 45 ASTM F 791-96. Standard test method for stress crazing of transparent plastics. 46 ASTM D 4508-98. Standard test method for chip impact strength of plastics. 47 ASTM D 1901-95. Standard test method for relative evaporation time of halogenated organic solvents and their admixtures. DIN 53170-91. Solvents for paints and similar coating materials. Determination of the evaporation rate. 48 ASTM E 1232-96. Standard test method for temperature limit of flammability of chemicals. 49 ASTM E 681-98. Test method for concentration limits of flammability of chemicals. BS 6713-3-86. Explosion protection systems. Method for determination of explosion indices of fuel/air mixtures other than dust/air and gas/air mixtures (ISO 6184-3). 50 ASTM D 3828-97. Standard test method for flash point by small scale closed tester. AS/NZS 2106.0-99. Methods for determination of flash point of flammable liquids (closed cup) - General. AS/NZS 2106.1-99. Methods for the determination of the flash point of flammable liquids (closed cup) - Abel closed cup method. 51 ASTM D 1310-97. Standard test method for flash point and fire point of liquids by tag open-cup apparatus. 52 ASTM D 56-97a. Standard test method for flash point by tag closed tester. 53 ASTM D 92-97. Standard test method for flash and fire points by Cleveland open cup. ISO 2592-73. Petroleum product - Determination of flash and fire points - Cleveland open cup method.
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HANDBOOK OF SOLVENTS George Wypych,
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Preface Although the chemical indus
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Preface xxix contain or to have use
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1654 Acknowledgments 10.3 Solvent e
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Table of Contents Preface .........
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Table of contents iii 4.3 Polar sol
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Table of contents v 7.2.1.1 Rheolog
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Table of contents vii 9.4.4 Solvent
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Table of contents ix 12.2.2.1 Chemi
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Table of contents xi 14.4.3.1 Intro
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Table of contents xiii 14.19 Paints
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Table of contents xv 15.1.20 Gas ch
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Table of contents xvii 17.2.2 Movem
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Table of contents xix 18.4.7 Dry cl
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Table of contents xxi 20.7.1 Introd
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Table of contents xxiii 21.4.1.3 Pr
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Table of contents xxv 23.2.1.3 Sour
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2 Christian Reichardt aliphatic nit
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4 Christian Reichardt the knowledge
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2 Fundamental Principles Governing
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2.1 Solvent effects on chemical sys
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2.2 Molecular design of solvents 37
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2.3 Basic physical and chemical pro
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66 George Wypych Aprotic/Protic Ter
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68 George Wypych Biodegradability T
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70 George Wypych Figure 3.2.1. Sche
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72 George Wypych Figure 3.3.4. Simp
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74 George Wypych Synthetic routes a
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76 George Wypych Property minimum V
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96 Tilman Hahn, Konrad Botzenhart,
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General Principles Governing Dissol
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4.1 Simple solvent characteristics
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4.2 Effect of system variables on s
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4.3 Polar solvation dynamics 133 tr
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4.3 Polar solvation dynamics 135 Fo
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4.3 Polar solvation dynamics 137 at
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4.3 Polar solvation dynamics 139 li
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4.3 Polar solvation dynamics 141 Fi
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4.3 Polar solvation dynamics 143 Fi
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4.3 Polar solvation dynamics 145 ta
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4.4 Measurement of solvent activity
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Solubility of Selected Systems and
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5.1 Solubility parameters 245 ln P
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5.1 Solubility parameters 247 Accep
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5.1 Solubility parameters 249 media
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5.1 Solubility parameters 251 Polym
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5.2 Prediction of solubility parame
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5.3 Methods of calculation of solub
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5.4 Mixed solvents - polymer solubi
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5.5 The phenomenological theory of
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306 E. Ya. Denisyuk, V. V. Tereshat
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318 V V Tereshatov, V Yu. Senichev,
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328 Vasiliy V. Tereshatov, Valery Y
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340 George Wypych where: τM the mo
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342 George Wypych ξ 0.55 0.5 0.45
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344 George Wypych Self-diffusion co
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346 George Wypych Temperature, K 31
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348 George Wypych Diffusion distanc
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350 George Wypych • evaporation-i
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352 George Wypych Water volume frac
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354 George Wypych Diffusion coeffic
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356 Semyon Levitsky, Zinoviy Shulma
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386 Seung Su Kim, Jae Chun Hyun 7.3
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388 Seung Su Kim, Jae Chun Hyun rat
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390 Seung Su Kim, Jae Chun Hyun The
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392 Seung Su Kim, Jae Chun Hyun whe
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394 Seung Su Kim, Jae Chun Hyun beg
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396 Seung Su Kim, Jae Chun Hyun 7.3
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398 Seung Su Kim, Jae Chun Hyun Fig
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404 Seung Su Kim, Jae Chun Hyun sol
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406 Seung Su Kim, Jae Chun Hyun Tab
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408 Seung Su Kim, Jae Chun Hyun and
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410 Seung Su Kim, Jae Chun Hyun to
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412 Seung Su Kim, Jae Chun Hyun The
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414 Seung Su Kim, Jae Chun Hyun cau
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416 Seung Su Kim, Jae Chun Hyun Nu
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Interactions in Solvents and Soluti
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8.2 Basic simplifications of quantu
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8.2 Basic simplifications of quantu
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8.4 Two-body interaction energy 425
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8.5 Three- and many-body interactio
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8.6 The variety of interaction pote
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8.6 The variety of interaction pote
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8.7 Theoretical and computing model
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8.8 Practical applications of model
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8.9 Liquid surfaces 493 to study th
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8.9 Liquid surfaces 495 The potenti
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8.9 Liquid surfaces 497 out of equi
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8.9 Liquid surfaces 499 tions) of t
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8 Interactions in solvents and solu
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8 Interactions in solvents and solu
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9 Mixed Solvents Y. Y. Fialkov, V.
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9.2 Chemical interaction between co
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9.2 Chemical interaction between co
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9.3 Physical properties of mixed so
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9.4 Mixed solvent influence on the
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9.5 The mixed solvent effect on the
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9 Mixed solvents 563 22 Minkin V.,
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10 Acid-base Interactions 10.1 GENE
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10.1 General concept of acid-base i
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10.1 General concept of acid-base i
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10.2 Effect of polymer/solvent acid
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10.3 Solvent effects based on pure
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10.4 Acid-base equilibria in ionic
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11 Electronic and Electrical Effect
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11.1 Theoretical treatment of solve
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11.2 Dielectric solvent effects 681
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12 Other Properties of Solvents, So
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12.1 Rheological properties, aggreg
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12.2 Chain conformations of polysac
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738 Roland Schmid Figure 13.1.1. Re
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740 Roland Schmid HB interactions,
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742 Roland Schmid AN = -133.8 - 0.0
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744 Roland Schmid ated by the macro
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746 Roland Schmid turns out, polar
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748 Roland Schmid Packing density
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750 Roland Schmid tween calculated
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752 Roland Schmid over the solute-s
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754 Roland Schmid of the empirical
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756 Roland Schmid From X-ray and ne
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758 Roland Schmid Table 13.1.5. Sol
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760 Roland Schmid ΔG = ΔG + ΔG [
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762 Roland Schmid very recent paper
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764 Roland Schmid Solvent ΔvH/RT
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766 Roland Schmid E r = E i + E s [
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768 Roland Schmid from the explicit
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770 Roland Schmid sequently, there
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772 Roland Schmid simulations. 188-
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774 Roland Schmid 23 N. A. Lewis, Y
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776 Roland Schmid 132 R. R. Dogonad
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778 Michelle L. Coote and Thomas P.
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798 Maw-Ling Wang 13.3 EFFECTS OF O
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800 Maw-Ling Wang [13.3.2] Inverse
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802 Maw-Ling Wang Both cation and a
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804 Maw-Ling Wang Table 13.3.2. Eff
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806 Maw-Ling Wang Table 13.3.3. Ext
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808 Maw-Ling Wang Table 13.3.5. Eff
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810 Maw-Ling Wang reacts with pheno
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812 Maw-Ling Wang Figure 13.3.3. Ef
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814 Maw-Ling Wang the organic solve
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816 Maw-Ling Wang crease. Therefore
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818 Maw-Ling Wang (F) Polymerizatio
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820 Maw-Ling Wang Table 13.3.16. Sy
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822 Maw-Ling Wang 13.3.1.4 Effect o
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824 Maw-Ling Wang Table 13.3.19 Eff
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826 Maw-Ling Wang quaternary salt c
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828 Maw-Ling Wang Table 13.3.24. Ef
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830 Maw-Ling Wang Solvent Dielectri
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832 Maw-Ling Wang ied. 82,83,97,101
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834 Maw-Ling Wang substitution, suc
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836 Maw-Ling Wang (2) the ion excha
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838 Maw-Ling Wang REFERENCES 1 A. A
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840 Maw-Ling Wang 101 D. C. Sherrin
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842 Norio Tsubokawa [13.4.2] PAI is
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844 Norio Tsubokawa Table 13.4.2. I
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846 Norio Tsubokawa more easily tha
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848 George Wypych methyl amyl keton
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850 George Wypych Peel strength, N/
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852 George Wypych 8 P Enenkel, H Ba
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854 George Wypych Table 14.2.2. Tot
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856 M Matsumoto, S Isken, JAMdeBont
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866 Tilman Hahn, Konrad Botzenhart
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872 Tsuneo Yamane 14.4.3 CHOICE OF
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874 Tsuneo Yamane Very trace amount
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876 Tsuneo Yamane It has been shown
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878 Tsuneo Yamane [ ( kcat Km) ( kc
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880 George Wypych 11 A. Zaks, in En
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882 George Wypych rected towards im
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884 Kaspar D. Hasenclever than 55°
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886 Kaspar D. Hasenclever The same
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888 Kaspar D. Hasenclever Figure 14
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890 Kaspar D. Hasenclever Computer
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892 Kaspar D. Hasenclever • Solve
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894 Martin Hanek, Norbert Löw, And
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920 George Wypych 20 N. L�w, EPP
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922 George Wypych Table 14.9.2. Rep
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924 Phillip J. Wakelyn, Peter J. Wa
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950 George Wypych 14.11 GROUND TRAN
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952 George Wypych Figure 14.13.1. S
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956 George Wypych more to show that
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958 George Wypych Table 14.16.1. Re
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Page 991 and 992:
Page 993 and 994:
Page 995 and 996:
Page 997 and 998:
970 David Randall 14.19.2.2 Water b
Page 999 and 1000:
972 David Randall Hydrophobic subst
Page 1001 and 1002:
974 David Randall 50-60% glutaric,
Page 1003 and 1004:
976 George Wypych Figure 14.20.1. D
Page 1005 and 1006:
978 Michel Bauer, Christine Barthé
Page 1007 and 1008:
Page 1009 and 1010:
Page 1011 and 1012:
Page 1013 and 1014:
Page 1015 and 1016:
Page 1017 and 1018:
Page 1019 and 1020:
Page 1021 and 1022:
Page 1023 and 1024:
Page 1025 and 1026:
998 An Li This discussion is intend
Page 1027 and 1028:
1000 An Li Trade Name Cosolvent vol
Page 1029 and 1030:
1002 An Li Figure 14.21.2.1. Effect
Page 1031 and 1032:
1004 An Li partial derivative ∂(l
Page 1033 and 1034:
1006 An Li Equation [14.21.2.8] can
Page 1035 and 1036:
1008 An Li Figure 14.21.2.2a. Devia
Page 1037 and 1038:
1010 An Li Figure 14.21.2.2c. Devia
Page 1039 and 1040:
1012 An Li f 0.1 0.2 0.4 0.6 0.8 0.
Page 1041 and 1042:
1014 An Li estimated from the log K
Page 1043 and 1044:
1016 George Wypych 72 K. Brololm, a
Page 1045 and 1046:
1018 George Wypych Figure 14.22.2.
Page 1047 and 1048: 1020 George Wypych New technology i
Page 1049 and 1050: 1022 George Wypych Table 14.23.1. R
Page 1053 and 1054: 1026 Mohamed Serageldin, Dave Reeve
Page 1077 and 1078: 1050 George Wypych Table 14.32.5. T
Page 1079 and 1080: 1052 George Wypych The traditional
Page 1081 and 1082: 1054 George Wypych The acidity of b
Page 1083 and 1084: 1056 George Wypych except water whi
Page 1085 and 1086: 1058 George Wypych solution is 2.73
Page 1087 and 1088: 1060 George Wypych presence of igni
Page 1089 and 1090: 1062 George Wypych method of determ
Page 1091 and 1092: 1064 George Wypych used. A thermal
Page 1093 and 1094: 1066 George Wypych 15.1.26 REFRACTI
Page 1095 and 1096: 1068 George Wypych Table 15.1.1. Ty
Page 1097: 1070 George Wypych Wexcluded solven
Page 1101 and 1102: 1074 George Wypych 68 ASTM D 3844-9
Page 1103 and 1104: 1076 George Wypych BS 506-2.84. Met
Page 1105 and 1106: 1078 Myrto Petreas 15.2 SPECIAL MET
Page 1107 and 1108: 1080 Myrto Petreas In short, biolog
Page 1109 and 1110: 1082 Myrto Petreas cients of some i
Page 1111 and 1112: 1084 Myrto Petreas lection at the a
Page 1113 and 1114: 1086 Myrto Petreas and legal reperc
Page 1115 and 1116: 1088 Myrto Petreas • The solvent
Page 1117 and 1118: 1090 Myrto Petreas of time after ex
Page 1119 and 1120: 1092 Myrto Petreas even after log-l
Page 1121 and 1122: 1094 Myrto Petreas 26 M Petreas, J
Page 1123 and 1124: 1096 James L. Botsford In Europe ma
Page 1125 and 1126: 1098 James L. Botsford Figure 15.2.
Page 1127 and 1128: 1100 James L. Botsford cussed. Neit
Page 1129 and 1130: 1102 James L. Botsford n Ave. Var.
Page 1131 and 1132: 1104 James L. Botsford (Calleja et
Page 1133 and 1134: 1106 James L. Botsford Table 15.2.2
Page 1135 and 1136: 1108 James L. Botsford the test is
Page 1137 and 1138: 1110 James L. Botsford Table 15.2.2
Page 1139 and 1140: 1112 James L. Botsford Geiger, D. L
Page 1141 and 1142: 1114 Christine Barthélémy, Michel
Page 1149 and 1150:
1122 Christine Barthélémy, Michel
Page 1151 and 1152:
1124 Christine Barthélémy, Michel
Page 1153 and 1154:
1126 George Wypych n-heptane molecu
Page 1155 and 1156:
1128 George Wypych MEK P PA Fat-fre
Page 1157 and 1158:
1130 Michel Bauer, Christine Barth
Page 1159 and 1160:
Page 1161 and 1162:
Page 1163 and 1164:
Page 1165 and 1166:
Page 1167 and 1168:
Page 1169 and 1170:
Page 1171 and 1172:
Page 1173 and 1174:
Page 1175 and 1176:
17 Environmental Impact of Solvents
Page 1177 and 1178:
17.1 The environmental fate and mov
Page 1179 and 1180:
Page 1181 and 1182:
Page 1183 and 1184:
Page 1185 and 1186:
Page 1187 and 1188:
Page 1189 and 1190:
17.2 Fate-based management 1163 dat
Page 1191 and 1192:
17.2 Fate-based management 1165 bre
Page 1193 and 1194:
17.2 Fate-based management 1167 gra
Page 1195 and 1196:
17.3 Environmental fate of glycol e
Page 1197 and 1198:
Page 1199 and 1200:
Page 1201 and 1202:
Page 1203 and 1204:
Page 1205 and 1206:
Page 1207 and 1208:
Page 1209 and 1210:
Page 1211 and 1212:
Page 1213 and 1214:
Page 1215 and 1216:
17.4 Organic solvent impacts on tro
Page 1217 and 1218:
Page 1219 and 1220:
Page 1221 and 1222:
Page 1223 and 1224:
Page 1225 and 1226:
Page 1227 and 1228:
18 Concentration of Solvents in Var
Page 1229 and 1230:
18.1 Measurement and estimation of
Page 1231 and 1232:
Page 1233 and 1234:
Page 1235 and 1236:
Page 1237 and 1238:
Page 1239 and 1240:
Page 1241 and 1242:
Page 1243 and 1244:
Page 1245 and 1246:
Page 1247 and 1248:
Page 1249 and 1250:
Page 1251 and 1252:
Page 1253 and 1254:
18.2 Prediction of organic solvents
Page 1255 and 1256:
Page 1257 and 1258:
Page 1259 and 1260:
Page 1261 and 1262:
18.3 Indoor air pollution by solven
Page 1263 and 1264:
Page 1265 and 1266:
Page 1267 and 1268:
Page 1269 and 1270:
Page 1271 and 1272:
Page 1273 and 1274:
Page 1275 and 1276:
Page 1277 and 1278:
18.4 Solvent uses with exposure ris
Page 1279 and 1280:
Page 1281 and 1282:
Page 1283 and 1284:
Page 1285 and 1286:
Page 1287 and 1288:
Page 1289 and 1290:
Page 1291 and 1292:
Page 1293 and 1294:
1268 Carlos M. Nu�ez ter or habit
Page 1295 and 1296:
1270 Carlos M. Nu�ez CAS No. Chem
Page 1297 and 1298:
Page 1299 and 1300:
Page 1301 and 1302:
Page 1303 and 1304:
Page 1305 and 1306:
Page 1307 and 1308:
1282 Carlos M. Nu�ez tronic circu
Page 1309 and 1310:
1284 Carlos M. Nu�ez EPA Region 6
Page 1311 and 1312:
1286 Carlos M. Nu�ez i.e., entire
Page 1313 and 1314:
1288 Carlos M. Nu�ez Table 19.6.
Page 1315 and 1316:
1290 Carlos M. Nu�ez Schedule Sou
Page 1317 and 1318:
1292 Carlos M. Nu�ez The CAA prov
Page 1319 and 1320:
1294 Carlos M. Nu�ez CWA to estab
Page 1321 and 1322:
1296 Carlos M. Nu�ez amended to i
Page 1323 and 1324:
1298 Carlos M. Nu�ez Figure 19.5.
Page 1325 and 1326:
1300 Carlos M. Nu�ez environmenta
Page 1327 and 1328:
1302 Carlos M. Nu�ez For comparis
Page 1329 and 1330:
1304 Carlos M. Nu�ez tives. Four
Page 1331 and 1332:
1306 Carlos M. Nu�ez • Program
Page 1333 and 1334:
1308 Carlos M. Nu�ez 31 Federal R
Page 1335 and 1336:
1310 Carlos M. Nu�ez HSWA Hazardo
Page 1337 and 1338:
Page 1339 and 1340:
20 Toxic Effects of Solvent Exposur
Page 1341 and 1342:
20.1 Toxicokinetics, toxicodynamics
Page 1343 and 1344:
Page 1345 and 1346:
Page 1347 and 1348:
Page 1349 and 1350:
Page 1351 and 1352:
20.2 Cognitive and psychosocial out
Page 1353 and 1354:
Page 1355 and 1356:
Page 1357 and 1358:
20.3 Pregnancy outcome following so
Page 1359 and 1360:
Page 1361 and 1362:
Page 1363 and 1364:
Page 1365 and 1366:
Page 1367 and 1368:
Page 1369 and 1370:
Page 1371 and 1372:
Page 1373 and 1374:
Page 1375 and 1376:
Page 1377 and 1378:
Page 1379 and 1380:
20.4 Industrial solvents and kidney
Page 1381 and 1382:
Page 1383 and 1384:
Page 1385 and 1386:
Page 1387 and 1388:
20.5 Lymphohematopoietic study of w
Page 1389 and 1390:
Page 1391 and 1392:
Page 1393 and 1394:
Page 1395 and 1396:
Page 1397 and 1398:
Page 1399 and 1400:
20.6 Chromosomal aberrations 1375 2
Page 1401 and 1402:
20.6 Chromosomal aberrations 1377 p
Page 1403 and 1404:
20.7 Hepatotoxicity 1379 8 Mitelman
Page 1405 and 1406:
20.7 Hepatotoxicity 1381 to convert
Page 1407 and 1408:
20.7 Hepatotoxicity 1383 Table 20.7
Page 1409 and 1410:
20.7 Hepatotoxicity 1385 toxicity o
Page 1411 and 1412:
20.7 Hepatotoxicity 1387 early pote
Page 1413 and 1414:
20.7 Hepatotoxicity 1389 vents. It
Page 1415 and 1416:
20.7 Hepatotoxicity 1391 19 Slater
Page 1417 and 1418:
20.8 Solvents and the liver 1393 20
Page 1419 and 1420:
20.8 Solvents and the liver 1395 Cu
Page 1421 and 1422:
20.8 Solvents and the liver 1397 th
Page 1423 and 1424:
20.8 Solvents and the liver 1399 cu
Page 1425 and 1426:
Page 1427 and 1428:
Page 1429 and 1430:
20.9 Toxicity of environmental solv
Page 1431 and 1432:
Page 1433 and 1434:
Page 1435 and 1436:
Page 1437 and 1438:
Page 1439 and 1440:
Page 1441 and 1442:
Page 1443 and 1444:
21 Substitution of Solvents by Safe
Page 1445 and 1446:
21.1 Supercritical solvents 1421 So
Page 1447 and 1448:
21.1 Supercritical solvents 1423 Fi
Page 1449 and 1450:
Page 1451 and 1452:
Page 1453 and 1454:
21.1 Supercritical solvents 1429 K
Page 1455 and 1456:
21.1 Supercritical solvents 1431 ai
Page 1457 and 1458:
21.1 Supercritical solvents 1433 Th
Page 1459 and 1460:
21.1 Supercritical solvents 1435 wh
Page 1461 and 1462:
21.1 Supercritical solvents 1437 *
Page 1463 and 1464:
21.1 Supercritical solvents 1439 In
Page 1465 and 1466:
21.1 Supercritical solvents 1441 21
Page 1467 and 1468:
21.1 Supercritical solvents 1443 Ta
Page 1469 and 1470:
21.1 Supercritical solvents 1445 Re
Page 1471 and 1472:
21.1 Supercritical solvents 1447 Re
Page 1473 and 1474:
21.1 Supercritical solvents 1449 ta
Page 1475 and 1476:
Page 1477 and 1478:
Page 1479 and 1480:
Page 1481 and 1482:
Page 1483 and 1484:
21.2 Ionic liquids 1459 85 M. Polia
Page 1485 and 1486:
21.2 Ionic liquids 1461 be used. Th
Page 1487 and 1488:
21.2 Ionic liquids 1463 Figure 21.2
Page 1489 and 1490:
21.2 Ionic liquids 1465 Table 21.2.
Page 1491 and 1492:
21.2 Ionic liquids 1467 been utiliz
Page 1493 and 1494:
21.2 Ionic liquids 1469 One specifi
Page 1495 and 1496:
21.2 Ionic liquids 1471 lustrates t
Page 1497 and 1498:
21.2 Ionic liquids 1473 these alloy
Page 1499 and 1500:
21.2 Ionic liquids 1475 ( ) ln = K
Page 1501 and 1502:
21.2 Ionic liquids 1477 According t
Page 1503 and 1504:
21.2 Ionic liquids 1479 Acidic melt
Page 1505 and 1506:
21.2 Ionic liquids 1481 21 C.L. Hus
Page 1507 and 1508:
21.2 Ionic liquids 1483 110 G.P. Li
Page 1509 and 1510:
21.3 Oxide solubilities in ionic me
Page 1511 and 1512:
Page 1513 and 1514:
Page 1515 and 1516:
Page 1517 and 1518:
Page 1519 and 1520:
Page 1521 and 1522:
21.4 Alternative cleaning technolog
Page 1523 and 1524:
Page 1525 and 1526:
Page 1527 and 1528:
Page 1529 and 1530:
Page 1531 and 1532:
1508 Klaus-Dirk Henning Application
Page 1533 and 1534:
1510 Klaus-Dirk Henning 22.1.2.2 Ad
Page 1535 and 1536:
1512 Klaus-Dirk Henning point the a
Page 1537 and 1538:
1514 Klaus-Dirk Henning Figure 22.1
Page 1539 and 1540:
Page 1541 and 1542:
1518 Klaus-Dirk Henning Table 22.1.
Page 1543 and 1544:
Page 1545 and 1546:
1522 Klaus-Dirk Henning Regeneratio
Page 1547 and 1548:
1524 Klaus-Dirk Henning • activit
Page 1549 and 1550:
1526 Klaus-Dirk Henning adsorption
Page 1551 and 1552:
Page 1553 and 1554:
Page 1555 and 1556:
Page 1557 and 1558:
1534 Klaus-Dirk Henning vent conden
Page 1559 and 1560:
Page 1561 and 1562:
Page 1563 and 1564:
Page 1565 and 1566:
1542 Klaus-Dirk Henning 12 H. Krill
Page 1567 and 1568:
1544 Isao Kimura Table 22.2.1. Appl
Page 1569 and 1570:
1546 Isao Kimura Table 22.2.2. Typi
Page 1571 and 1572:
1548 Isao Kimura 22.2.4 SOLVENT REC
Page 1573 and 1574:
1550 Isao Kimura Figure 22.2.9. Flo
Page 1575 and 1576:
1552 Isao Kimura • Difficult in d
Page 1577 and 1578:
1554 Isao Kimura Figure 22.2.12. Fl
Page 1579 and 1580:
1556 Denis Kargol Figure 22.3.1. So
Page 1581 and 1582:
1558 Denis Kargol Figure 22.3.4. AS
Page 1583 and 1584:
1560 K. A. Magrini, et al. and Olli
Page 1585 and 1586:
1562 K. A. Magrini, et al. ysis of
Page 1587 and 1588:
1564 K. A. Magrini, et al. Figure 2
Page 1589 and 1590:
1566 K. A. Magrini, et al. On the l
Page 1591 and 1592:
1568 K. A. Magrini, et al. ating te
Page 1593 and 1594:
1570 K. A. Magrini, et al. Cummings
Page 1595 and 1596:
1572 Hanadi S. Rifai, Charles J. Ne
Page 1597 and 1598:
Page 1599 and 1600:
Page 1601 and 1602:
Page 1603 and 1604:
Page 1605 and 1606:
Page 1607 and 1608:
Page 1609 and 1610:
Page 1611 and 1612:
Page 1613 and 1614:
Page 1615 and 1616:
Page 1617 and 1618:
Page 1619 and 1620:
Page 1621 and 1622:
Page 1623 and 1624:
Page 1625 and 1626:
Page 1627 and 1628:
Page 1629 and 1630:
Page 1631 and 1632:
Page 1633 and 1634:
Page 1635 and 1636:
Page 1637 and 1638:
Page 1639 and 1640:
Page 1641 and 1642:
1618 Barry J. Spargo, James G. Muel
Page 1643 and 1644:
Page 1645 and 1646:
Page 1647 and 1648:
Page 1649 and 1650:
Page 1651 and 1652:
Page 1653 and 1654:
Page 1655 and 1656:
1632 George Wypych number of 1 or e
Page 1657 and 1658:
1634 George Wypych In addition to t
Page 1659 and 1660:
1636 George Wypych d diameter of gr
Page 1661 and 1662:
1638 George Wypych wax-containing c
Page 1663 and 1664:
1640 George Wypych product of inven
Page 1665 and 1666:
1642 George Wypych selection of sol
Page 1667 and 1668:
1644 George Wypych fining processes
Page 1669 and 1670:
1646 George Wypych requires several
Page 1671 and 1672:
1648 George Wypych crease color str
Page 1673 and 1674:
1650 George Wypych tion. The patent
Page 1675 and 1676:
1652 George Wypych 75 M Solinas, T
Page 1677 and 1678:
1658 Index anhydrous form 282 anili
Page 1679 and 1680:
1660 Index 1-chlorooctane 826 chlor
Page 1681 and 1682:
1662 Index term 750 dipole moment 1
Page 1683 and 1684:
1664 Index Friedel-Crafts alkylatio
Page 1685 and 1686:
1666 Index method 245 laser 689 lat
Page 1687 and 1688:
1668 Index O octane 127,185 1-octan
Page 1689 and 1690:
1670 Index Prandtl number 392 Praus
Page 1691 and 1692:
1672 Index function 137 preferentia
Page 1693 and 1694:
1674 Index change 350 time scale 33
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