Handbook of Solvents - George Wypych - ChemTech - Ventech!

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A ab initio 39,424,426,430,455,470,485,655,661, 711 abiotic attenuation 1579 degradation 1175 process 1151 absorbance 343 absorption capacity 1635 acceptor number 566 acetaldehyde 1131 acetic acid 9,506,829 acetone 341-342,640,829,847,849,854,881,906, 959,1149,1508 acetonitrile 2,13 acetophenone 819 acid/base character 580 interaction 3,565,570,584,683,689 properties 617 acidic groups 348 acidity 585,806,1053 acids 574 acoustic dissipation 364 wave admittance analysis 342 acrylics 848 acrylonitrile 787 activated carbon 1509,1513,1543,1634 service life 1531 activation energy 778,807 theory 362 activity coefficient 177,282 at infinite dilution 164 adhesion 14,339,570 adhesives 581,847,849,851,1638 anaerobic 847 chemically reactive 847 polychloroprene 849 pressure-sensitive 851 UV-curable 847 adsorbent 1509 inner surface area 1510 adsorption 570,1151 capacity 1510 enthalpy 1509 fundamentals 1509 heat 1526 isotherm 1510 kinetics 1509,1511 preferential 274 adsorption-desorption 1160 adsorptive power 1510 aerosolization 354 aerospace 852,1640 AFM 569,706 agar 710 aggregate mass 689 vesicular 690 aggregates 506,580,697 aggregation 565,570,578,689,697 agitation speed 798 agriculture 1640 air 1149 contaminants, standard 925 velocity 1526 airflow 353-354 airways 1082 Alagona approach 444 alcohol consumption 1396 alcohols 127,137,806,828,880 alkahest 7 alkalinity 1053 alkanes 127 N-alkylpyridinium 1468 allergic effects 1319 potential 1320 Allerhand-Schleyer scale 588 p-allylanisole 826 allylation 811 altitude 1191 alumina 1513 aluminum stearate 693 amine 510 aminoacids 23 ammonia 16 amobarbital 286 amorphous phase 351 structure 348 amphiphiles 691 amphotericity 577 n-amyl acetate 848-849 n-amyl ketone 849 analytical ultracentrifuge 186 anemia 1376 Index
1658 Index anhydrous form 282 aniline 9 point 102,1056 anisole 819 annealing 254 anthraquinone 701 antifungal properties 881 antigens 1361 antiparallel orientation 12 Antoine equation 389 apolar 875,884 approximation, two-body 37 aprotic 762-763,798,811,813,829 aquifer 1572 Arrhenius description 573 asphalt 855 processing 1640 association heteromolecular 505-507 number 692,689 self 350 asthma 1328 atomic surface tension 482 ATP 866 attenuation capacity 1163 autoignition temperature 1054 automotive 851 finishing 1641 industry 958 maintenance 1641 painting operations 1641 autoprotolysis 524 Axilrod-Teller term 453 B bacteria Gram-positive 862 solvent-tolerant 859 Bader charges 444 barbituric acid 286 Barker-Henderson approach 749 barotropic effect 1425 barrier properties 693 basicity 585 bathochromic shift 590,592,602 battery electrolytes 1472 Beer law 353 Benard cells 412 benzene 1,39,105,127,342,697-698,812,817, 829,848,882,952,957,1127,1133,1334 exposure 1365 benzonitrile 794 benzyl alcohol 778,854 benzyl cyanide 815 BET 1510 binding energy 754 binodal 131,148,184,191-192,400,408 bioavailability 1130 biocatalysis 875 biodegradation 1151 first-order 1153 potential 1054 bi<strong>of</strong>ilm 1624 biological membrane 866,870 monitoring 1080 biomarker 1375 bioreactor 1624 biosphere 856 biotic process 1151 biotransformation 859,1133,1618 biphenyls 287,301 bleaching 344 blends 184,694 blistering 956 blisters 1131 Blodgett-Langmuir film 496 blood 1081 blue shift 639 blush resistor 956 boiling point 1055 temperature 15 Boltzmann factor 476,655 bond covalent 16 energy 16 intermolecular 345 strength 849 Bondi approach 126 Bootstrap model 791 Born approach 482 equation 769 formula 677 model 769 radius 771 term 652 theory 133,738 Born-Kirkwood-Onsager expansion 665 Born-Oppenheimer approximation 422 Bose-Einstein statistics 429 boson 429 boundary condition 312 surface 419 Brannon-Peppas equation 348 breakdown voltage 1059 breakthrough time 342,1631,1633,1635 breath monitoring 1079 breathing 1634 Brillouin theorem 659 Bristow-Watson method 246 bromine index 1055
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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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970 David Randall 14.19.2.2 Water b
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972 David Randall Hydrophobic subst
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974 David Randall 50-60% glutaric,
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976 George Wypych Figure 14.20.1. D
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978 Michel Bauer, Christine Barthé
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998 An Li This discussion is intend
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1000 An Li Trade Name Cosolvent vol
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1002 An Li Figure 14.21.2.1. Effect
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1004 An Li partial derivative ∂(l
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1006 An Li Equation [14.21.2.8] can
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1008 An Li Figure 14.21.2.2a. Devia
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1010 An Li Figure 14.21.2.2c. Devia
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1012 An Li f 0.1 0.2 0.4 0.6 0.8 0.
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1014 An Li estimated from the log K
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1016 George Wypych 72 K. Brololm, a
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1018 George Wypych Figure 14.22.2.
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1020 George Wypych New technology i
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1022 George Wypych Table 14.23.1. R
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1026 Mohamed Serageldin, Dave Reeve
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1050 George Wypych Table 14.32.5. T
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1052 George Wypych The traditional
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1054 George Wypych The acidity of b
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1056 George Wypych except water whi
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1058 George Wypych solution is 2.73
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1060 George Wypych presence of igni
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1062 George Wypych method of determ
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1064 George Wypych used. A thermal
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1066 George Wypych 15.1.26 REFRACTI
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1068 George Wypych Table 15.1.1. Ty
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1070 George Wypych Wexcluded solven
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1072 George Wypych 25 ASTM D 2108-9
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1074 George Wypych 68 ASTM D 3844-9
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1076 George Wypych BS 506-2.84. Met
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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
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1084 Myrto Petreas lection at the a
Page 1113 and 1114:
1086 Myrto Petreas and legal reperc
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1088 Myrto Petreas • The solvent
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1090 Myrto Petreas of time after ex
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1092 Myrto Petreas even after log-l
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1094 Myrto Petreas 26 M Petreas, J
Page 1123 and 1124:
1096 James L. Botsford In Europe ma
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1098 James L. Botsford Figure 15.2.
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1100 James L. Botsford cussed. Neit
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1102 James L. Botsford n Ave. Var.
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1104 James L. Botsford (Calleja et
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1106 James L. Botsford Table 15.2.2
Page 1135 and 1136:
1108 James L. Botsford the test is
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1110 James L. Botsford Table 15.2.2
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1112 James L. Botsford Geiger, D. L
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1114 Christine Barthélémy, Michel
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1126 George Wypych n-heptane molecu
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1128 George Wypych MEK P PA Fat-fre
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1130 Michel Bauer, Christine Barth
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17 Environmental Impact of Solvents
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17.1 The environmental fate and mov
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Page 1185 and 1186:
Page 1187 and 1188:
Page 1189 and 1190:
17.2 Fate-based management 1163 dat
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17.2 Fate-based management 1165 bre
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17.2 Fate-based management 1167 gra
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17.3 Environmental fate of glycol e
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Page 1199 and 1200:
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17.4 Organic solvent impacts on tro
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Page 1221 and 1222:
Page 1223 and 1224:
Page 1225 and 1226:
Page 1227 and 1228:
18 Concentration of Solvents in Var
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18.1 Measurement and estimation of
Page 1231 and 1232:
Page 1233 and 1234:
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Page 1237 and 1238:
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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
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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
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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
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Page 1299 and 1300:
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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
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1302 Carlos M. Nu�ez For comparis
Page 1329 and 1330:
1304 Carlos M. Nu�ez tives. Four
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1306 Carlos M. Nu�ez • Program
Page 1333 and 1334:
1308 Carlos M. Nu�ez 31 Federal R
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1310 Carlos M. Nu�ez HSWA Hazardo
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Page 1339 and 1340:
20 Toxic Effects of Solvent Exposur
Page 1341 and 1342:
20.1 Toxicokinetics, toxicodynamics
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Page 1347 and 1348:
Page 1349 and 1350:
Page 1351 and 1352:
20.2 Cognitive and psychosocial out
Page 1353 and 1354:
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Page 1357 and 1358:
20.3 Pregnancy outcome following so
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20.4 Industrial solvents and kidney
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Page 1387 and 1388:
20.5 Lymphohematopoietic study of w
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Page 1395 and 1396:
Page 1397 and 1398:
Page 1399 and 1400:
20.6 Chromosomal aberrations 1375 2
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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
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21.1 Supercritical solvents 1435 wh
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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
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21.1 Supercritical solvents 1447 Re
Page 1473 and 1474:
21.1 Supercritical solvents 1449 ta
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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
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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
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21.2 Ionic liquids 1473 these alloy
Page 1499 and 1500:
21.2 Ionic liquids 1475 ( ) ln = K
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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
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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
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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
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1512 Klaus-Dirk Henning point the a
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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
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1524 Klaus-Dirk Henning • activit
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1526 Klaus-Dirk Henning adsorption
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Page 1557 and 1558:
1534 Klaus-Dirk Henning vent conden
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1542 Klaus-Dirk Henning 12 H. Krill
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1544 Isao Kimura Table 22.2.1. Appl
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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
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1552 Isao Kimura • Difficult in d
Page 1577 and 1578:
1554 Isao Kimura Figure 22.2.12. Fl
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1556 Denis Kargol Figure 22.3.1. So
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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
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1566 K. A. Magrini, et al. On the l
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1568 K. A. Magrini, et al. ating te
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1570 K. A. Magrini, et al. Cummings
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1572 Hanadi S. Rifai, Charles J. Ne
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Page 1625 and 1626: 1602 Hanadi S. Rifai, Charles J. Ne
Page 1641 and 1642: 1618 Barry J. Spargo, James G. Muel
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: 1652 George Wypych 75 M Solinas, T
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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