preface to fifteenth edition

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TABLE 11.59 Type K Thermocouples: Nickel-Chromium Alloy vs. Nickel-Aluminum Alloy Thermoelectric voltage in millivolts; reference junction at 0C. C 0 10 20 30 40 50 60 70 80 90 200 5.891 6.035 6.158 6.262 6.344 6.404 6.441 6.458 100 3.553 3.852 4.138 4.410 4.669 4.912 5.141 5.354 5.550 5.730 0 0.000 0.392 0.777 1.156 1.517 1.889 2.243 2.586 2.920 3.242 0 0.000 0.397 0.798 1.203 1.611 2.022 2.436 2.850 3.266 3.681 100 4.095 4.508 4.919 5.327 5.733 6.137 6.539 6.939 7.338 7.737 200 8.137 8.537 8.938 9.341 9.745 10.151 10.560 10.969 11.381 11.793 300 12.207 12.623 13.039 13.456 13.874 14.292 14.712 15.132 15.552 15.974 400 16.395 16.818 17.241 17.664 18.088 18.513 18.839 19.363 19.788 20.214 500 20.640 21.066 21.493 21.919 22.346 22.772 23.198 23.624 24.050 24.476 600 24.902 25.327 25.751 26.176 26.599 27.022 27.445 27.867 28.288 28.709 700 29.128 29.547 29.965 30.383 30.799 31.214 31.629 32.042 32.455 32.866 800 33.277 33.686 34.095 34.502 34.909 35.314 35.718 36.121 36.524 36.925 900 37.325 37.724 38.122 38.519 38.915 39.310 39.703 40.096 40.488 40.879 1000 41.269 41.657 42.045 42.432 42.817 43.202 43.585 43.968 44.349 44.729 1100 45.108 45.486 45.863 46.238 46.612 46.985 47.356 47.726 48.095 48.462 1200 48.828 49.129 49.555 49.916 50.276 50.633 50.990 51.344 51.697 52.049 1300 52.398 52.747 53.093 53.439 53.782 54.125 54.466 54.807 11.145
TABLE 11.60 Type N Thermocouples: Nickel–14.2% Chromium–1.4% Silicon Alloy vs. Nickel–4.4% Silicon–0.1% Magnesium Alloy Thermoelectric voltage in millivolts; reference junction at 0C. C 0 10 20 30 40 50 60 70 80 90 200 3.990 4.083 4.162 4.227 4.277 4.313 4.336 4.345 100 2.407 2.612 2.807 2.994 3.170 3.336 3.491 3.634 3.766 3.884 0 0.000 0.260 0.518 0.772 1.023 1.268 1.509 1.744 1.972 2.193 0 0.000 0.261 0.525 0.793 1.064 1.339 1.619 1.902 2.188 2.479 100 2.774 3.072 3.374 3.679 3.988 4.301 4.617 4.936 5.258 5.584 200 5.912 6.243 6.577 6.914 7.254 7.596 7.940 8.287 8.636 8.987 300 9.340 9.695 10.053 10.412 10.772 11.135 11.499 11.865 12.233 12.602 400 12.972 13.344 13.717 14.091 14.467 14.844 15.222 15.601 15.981 16.362 500 16.744 17.127 17.511 17.896 18.282 18.668 19.055 19.443 19.831 20.220 600 20.609 20.999 21.390 21.781 22.172 22.564 22.956 23.348 23.740 24.133 700 24.526 24.919 25.312 25.705 26.098 26.491 26.885 27.278 27.671 28.063 800 28.456 28.849 29.241 29.633 30.025 30.417 30.808 31.199 31.590 31.980 900 32.370 32.760 33.149 33.538 33.926 34.315 34.702 35.089 35.476 35.862 1000 36.248 36.633 37.018 37.402 37.786 38.169 38.552 38.934 39.315 39.696 1100 40.076 40.456 40.835 41.213 41.590 41.966 42.342 42.717 43.091 43.464 1200 43.836 44.207 44.577 44.947 45.315 45.682 46.048 46.413 46.777 47.140 1300 47.502 11.146
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LANGE'S HANDBOOK OF CHEMISTRY John
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Grateful acknowledgment is hereby m
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PREFACE TO FIFTEENTH EDITION This n
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PREFACE TO FIFTEENTH EDITION ix inv
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xii PREFACE TO FOURTEENTH EDITION l
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PREFACE TO FIRST EDITION This book
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For the detailed contents of any se
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1.2 SECTION 1 is derived from the G
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1.4 SECTION 1 rather than methylide
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1.6 SECTION 1 Styrene Toluene Xylen
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1.8 SECTION 1 TABLE 1.2 Fused Polyc
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1.10 SECTION 1 1.1.1.6 Bridged Hydr
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1.12 SECTION 1 TABLE 1.4 Suffixes f
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1.14 SECTION 1 TABLE 1.5 Trivial Na
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1.16 SECTION 1 TABLE 1.6 Trivial Na
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1.18 SECTION 1 Selection of the pri
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1.20 SECTION 1 attached to one anot
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1.22 SECTION 1 When side chains of
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1.24 SECTION 1 heterocyclic structu
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1.26 SECTION 1 Bivalent radicals of
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1.28 SECTION 1 Complex linear polya
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1.30 SECTION 1 TABLE 1.11 Names of
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1.32 SECTION 1 hydroxyamino- to the
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1.34 SECTION 1 may be named (1) by
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1.36 SECTION 1 Examples are methyl
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1.38 SECTION 1 tuted acid, respecti
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1.40 SECTION 1 FIGURE 1.2 Newman pr
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1.42 SECTION 1 from the ring are kn
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1.44 SECTION 1 FIGURE 1.11 Two isom
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1.46 SECTION 1 Chiral Center. The c
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1.48 SECTION 1 FIGURE 1.15 Isomers
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1.50 SECTION 1 entries to bring tog
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1.52 SECTION 1 TABLE 1.13 Names and
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1.60 SECTION 1 TABLE 1.14 Empirical
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2.2 SECTION 2 2.3.6 Student’s Dis
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2.4 SECTION 2 TABLE 2.1 Fundamental
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2.6 SECTION 2 TABLE 2.1 Fundamental
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2.8 SECTION 2 TABLE 2.2 Physical an
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2.10 SECTION 2 TABLE 2.2 Physical a
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2.24 SECTION 2 TABLE 2.3 Mathematic
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2.26 SECTION 2 TABLE 2.6 Abbreviati
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2.36 SECTION 2 TABLE 2.7 Conversion
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2.54 SECTION 2 TABLE 2.8 Temperatur
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2.66 SECTION 2 2.1.1 Conversion of
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2.68 SECTION 2 Oleometer. A hydrome
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2.70 SECTION 2 Example 3. 25 1.2500
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2.72 SECTION 2 TABLE 2.9 Barometer
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2.74 SECTION 2 TABLE 2.9 Barometer
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2.76 SECTION 2 TABLE 2.10 Barometri
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2.78 SECTION 2 TABLE 2.12 Reduction
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2.80 SECTION 2 TABLE 2.12 Reduction
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2.82 SECTION 2 TABLE 2.13 Viscosity
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2.84 SECTION 2 TABLE 2.14 Conversio
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2.86 SECTION 2 TABLE 2.15 Hydromete
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2.88 SECTION 2 TABLE 2.17 Correctio
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2.90 SECTION 2 TABLE 2.18 Pressure
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2.96 SECTION 2 TABLE 2.20 Values of
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2.98 SECTION 2 TABLE 2.21 Transmitt
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2.100 SECTION 2 TABLE 2.21 Transmit
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2.102 SECTION 2 2.2 MATHEMATICAL TA
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2.104 SECTION 2 TABLE 2.23 Derivati
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2.106 SECTION 2 TABLE 2.24 Integral
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2.108 SECTION 2 TABLE 2.24 Integral
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2.110 SECTION 2 Regular Polygon of
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2.112 SECTION 2 A h[0.4(y y ) 1.
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2.114 SECTION 2 2.2.3.1 Signs of th
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2.116 SECTION 2 x2 x3 x4 x5 ln(1 x
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2.118 SECTION 2 2.3.2 Errors in Qua
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2.120 SECTION 2 The breadth or spre
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2.122 SECTION 2 TABLE 2.26b Areas U
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2.124 SECTION 2 The distribution of
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2.126 SECTION 2 Should there be mor
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2.128 SECTION 2 Example 10 Six samp
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2.130 SECTION 2 2.3.9 The F Statist
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TABLE 2.29 F Distribution (Continue
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2.134 SECTION 2 mathematical treatm
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2.136 SECTION 2 The confidence limi
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2.138 SECTION 2 situation where rel
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3.2 SECTION 3 The alphabetical orde
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3.4 SECTION 3 When it is required t
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3.6 SECTION 3 PO phosphoryl SeO sel
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3.8 SECTION 3 3.1.5 Acids 3.1.5.1 A
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3.10 SECTION 3 3.1.6.6 Multiplicati
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3.12 SECTION 3 3.2 PHYSICAL PROPERT
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TABLE 3.2 Physical Constants of Ino
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3.62 SECTION 3 TABLE 3.3 Synonyms a
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SECTION 4 PROPERTIES OF ATOMS, RADI
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4.3 Fermium Fm 100 [Rn] 5f 12 7s 2
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Silver (argentum) Ag 47 [Kr] 4d 10
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PROPERTIES OF ATOMS,RADICALS,AND BO
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PROPERTIES OF ATOMS, RADICALS, AND
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SECTION 5 PHYSICAL PROPERTIES 5.1 S
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PHYSICAL PROPERTIES 5.3 5.1 SOLUBIL
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TABLE 5.1 Solubility of Gases in Wa
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TABLE 5.1 Solubility of Gases in Wa
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TABLE 5.2 Solubilities of Inorganic
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formateBa(CHO 2 ) 2 26.2 28.0 29.9
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(III) sulfateCe 2 (SO 4 ) 3 ·9H 2
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iodidePbI 2 0.044 0.056 0.069 0.090
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Nickel sulfateNiSO 4 ·6H 2 O (pale
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Praseodymium bromatePr(BrO 3 ) 3 55
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formate NaCHO 2 43.9 62.5 81.2 102
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Uranyl nitrate UO 2 (NO 3 ) 2 98 10
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PHYSICAL PROPERTIES 5.25 TABLE 5.3
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PHYSICAL PROPERTIES 5.57 5.3 BOILIN
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TABLE 5.12 Ternary Azeotropic Mixtu
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TABLE 5.12 Ternary Azeotropic Mixtu
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PHYSICAL PROPERTIES 5.83 5.4 FREEZI
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PHYSICAL PROPERTIES 5.87 5.5 DENSIT
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PHYSICAL PROPERTIES 5.89 dt Dt P
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PHYSICAL PROPERTIES 5.135 5.6.1 Ref
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PHYSICAL PROPERTIES 5.137 where the
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PHYSICAL PROPERTIES 5.139 5.7 COMBU
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Temperature, C Substance 40 20 0 20
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PHYSICAL PROPERTIES 5.171 This equa
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SECTION 6 THERMODYNAMIC PROPERTIES
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THERMODYNAMICPROPERTIES 6.3 6.1.1.2
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THERMODYNAMICPROPERTIES 6.5 A gener
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THERMODYNAMICPROPERTIES 6.7 TABLE 6
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THERMODYNAMICPROPERTIES 6.9 TABLE 6
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THERMODYNAMICPROPERTIES 6.11 TABLE
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THERMODYNAMIC PROPERTIES 6.21 TABLE
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THERMODYNAMIC PROPERTIES 6.101 TABL
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THERMODYNAMIC PROPERTIES 6.143 The
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SECTION 7 SPECTROSCOPY 7.1 X-RAY ME
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SPECTROSCOPY 7.3 TABLE 7.1 Waveleng
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SPECTROSCOPY 7.9 TABLE 7.3 Critical
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SPECTROSCOPY 7.11 TABLE 7.4 X-Ray E
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SPECTROSCOPY 7.13 Emission line K 1
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SPECTROSCOPY 7.15 TABLE 7.7 Analyzi
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SPECTROSCOPY 7.17 TABLE 7.8 Mass Ab
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SPECTROSCOPY 7.19 TABLE 7.9 Electro
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SPECTROSCOPY 7.21 TABLE 7.11 Absorp
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SPECTROSCOPY 7.23 TABLE 7.13 Solven
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SPECTROSCOPY 7.25 7.3 FLUORESCENCE
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SPECTROSCOPY 7.27 TABLE 7.16 Fluore
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SPECTROSCOPY 7.29 TABLE 7.18 Detect
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SPECTROSCOPY 7.35 TABLE 7.19 Sensit
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SPECTROSCOPY 7.37 TABLE 7.19 Sensit
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SPECTROSCOPY 7.39 In terms of m ,
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SPECTROSCOPY 7.41 The ionization co
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SPECTROSCOPY 7.67 TABLE 7.28 Infrar
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7.69
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SPECTROSCOPY 7.71 7.6 RAMAN SPECTRO
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SPECTROSCOPY 7.73 TABLE 7.30 Raman
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SPECTROSCOPY 7.89 7.7 NUCLEAR MAGNE
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SPECTROSCOPY 7.91 TABLE 7.41 Nuclea
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SPECTROSCOPY 7.93 TABLE 7.42 Proton
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SPECTROSCOPY 7.95 TABLE 7.44 Estima
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SPECTROSCOPY 7.97 TABLE 7.46 Proton
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SPECTROSCOPY 7.99 TABLE 7.48 Solven
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SPECTROSCOPY 7.101 TABLE 7.49 Carbo
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SPECTROSCOPY 7.103 TABLE 7.51 Effec
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SPECTROSCOPY 7.107 TABLE 7.56 One-B
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SPECTROSCOPY 7.113 TABLE 7.63 Nitro
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SPECTROSCOPY 7.115 TABLE 7.64 Nitro
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SPECTROSCOPY 7.117 TABLE 7.69 Fluor
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SPECTROSCOPY 7.119 TABLE 7.72 Silic
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SPECTROSCOPY 7.121 TABLE 7.73 Phosp
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SPECTROSCOPY 7.123 TABLE 7.74 Phosp
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SPECTROSCOPY 7.125 when z 3 and y
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SPECTROSCOPY 7.127 Masses 19 and 31
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SPECTROSCOPY 7.129 TABLE 7.76 Conde
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SECTION 8 ELECTROLYTES, ELECTROMOTI
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ELECTROLYTES, EMF, AND CHEMICAL EQU
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TABLE 8.7 Proton Transfer Reactions
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TABLE 8.7 Proton Transfer Reactions
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TABLE 8.9 Selected Equilibrium Cons
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8.75 3-tert-Butylbenzoic acid (0) 4
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4-Hydroxyproline (1) 1.900 1C 1.850
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N-Propionylglycine (1) 3.728 3.723
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TABLE 8.14 National Bureau of Stand
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1 part 0.1% neutral red in alc. * V
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3,3-Dimethoxybenzidine dihydrochlor
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TABLE 8.35 Equivalent Conductivitie
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KCl 127.3 124.4 122.4 115.8 112.0 1
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NaIO 3 75.2 72.6 70.9 64.4 60.5 1
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9.2 SECTION 9 9.1 LINEAR FREE ENERG
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9.4 SECTION 9 TABLE 9.1 Hammett and
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9.6 SECTION 9 TABLE 9.1 Hammett and
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9.8 SECTION 9 TABLE 9.3 pK a and Rh
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10.2 SECTION 10 10.4.6 Polyacrylate
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10.4 SECTION 10 10.2 ADDITIVES TO P
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10.6 SECTION 10 injection molding.
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10.8 SECTION 10 10.3 FORMULAS AND K
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10.10 SECTION 10 Key properties of
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10.12 SECTION 10 10.3.8 Fluorocarbo
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10.14 SECTION 10 10.3.11 Phenolics
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10.16 SECTION 10 The resin has the
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10.18 SECTION 10 10.3.19 Polyuretha
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10.20 SECTION 10 10.3.22 Sulfones B
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TABLE 10.2 Properties of Commercial
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10.58 SECTION 10 10.4 FORMULAS AND
Page 1078 and 1079:
10.60 SECTION 10 10.4.8 Polychlorop
Page 1080 and 1081:
10.62 SECTION 10 Styrene-butadiene
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10.5 CHEMICAL RESISTANCE TABLE 10.4
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10.6 GAS PERMEABILITY TABLE 10.5 Ga
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TABLE 10.5 Gas Permeability Constan
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TABLE 10.7 Constants ofFats and Oil
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TABLE 10.8 Constants ofWaxes Wax Me
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SECTION 11 PRACTICAL LABORATORY INF
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11.4 SECTION 11 TABLE 11.2 Molecula
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11.6 SECTION 11 A saturated aqueous
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11.8 SECTION 11 TABLE 11.6 Relative
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11.10 SECTION 11 11.3 BOILING POINT
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11.12 SECTION 11 TABLE 11.8 Organic
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11.14 SECTION 11 TABLE 11.9 Molecul
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11.4 SEPARATION METHODS TABLE 11.11
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11.18 SECTION 11 TABLE 11.12 Solven
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11.20 SECTION 11 TABLE 11.12 Solven
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TABLE 11.13 McReynolds’ Constants
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TABLE 11.13 McReynolds’ Constants
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11.26 SECTION 11 11.4.1 McReynolds
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11.28 SECTION 11 11.4.2.2 Partition
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11.30 SECTION 11 FIGURE 11.2 Band a
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11.32 SECTION 11 11.4.3 Ion-Exchang
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11.34 SECTION 11 TABLE 11.16 Guide
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11.36 SECTION 11 TABLE 11.16 Guide
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11.38 SECTION 11 TABLE 11.18 Relati
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11.40 SECTION 11 distribution coeff
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11.42 SECTION 11 TABLE 11.19 Gravim
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11.68 SECTION 11 TABLE 11.20 Elemen
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11.70 SECTION 11 TABLE 11.22 Common
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11.72 SECTION 11 TABLE 11.25 Tolera
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11.74 SECTION 11 TABLE 11.26 Heatin
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11.76 SECTION 11 TABLE 11.28 Titrim
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11.84 SECTION 11 appears becomes le
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11.86 SECTION 11 TABLE 11.29 Equati
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11.88 SECTION 11 TABLE 11.29 Equati
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11.90 SECTION 11 The more stable th
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11.92 SECTION 11 11.6.6.2.5 Buffer
Page 1185 and 1186: 11.94 SECTION 11 TABLE 11.30 Standa
Page 1187 and 1188: TABLE 11.32 Properties and Applicat
Page 1189 and 1190: 11.98 SECTION 11 TABLE 11.36 Maskin
Page 1191 and 1192: 11.100 SECTION 11 TABLE 11.37 Anion
Page 1193 and 1194: 11.102 SECTION 11 TABLE 11.39 Amino
Page 1195 and 1196: 11.104 SECTION 11 TABLE 11.44 Facto
Page 1197 and 1198: 11.106 SECTION 11 11.7 LABORATORY S
Page 1199 and 1200: 11.108 SECTION 11 TABLE 11.48 Stand
Page 1201 and 1202: 11.110 SECTION 11 Alizarin yellow G
Page 1203 and 1204: 11.112 SECTION 11 Bromchlorophenol
Page 1205 and 1206: 11.114 SECTION 11 p-Ethoxychrysoidi
Page 1207 and 1208: 11.116 SECTION 11 Mercurous nitrate
Page 1209 and 1210: 11.118 SECTION 11 Potassium carbona
Page 1211 and 1212: 11.120 SECTION 11 until the ammoniu
Page 1213 and 1214: 11.122 SECTION 11 TABLE 11.49 TLV C
Page 1221 and 1222: 11.130 SECTION 11 TABLE 11.50 Chemi
Page 1229 and 1230: 11.138 SECTION 11 of water which is
Page 1231 and 1232: TABLE 11.55 Thermoelectric Values i
Page 1233 and 1234: TABLE 11.56 Type B Thermocouples: P
Page 1235: TABLE 11.58 Type J Thermocouples: I
Page 1239 and 1240: TABLE 11.62 Type S Thermocouples: P
Page 1241 and 1242: 11.150 SECTION 11 11.11 CORRECTION
Page 1243 and 1244: Index Terms Links 2 Acid-base indic
Page 1245 and 1246: Index Terms Links 4 Alkynes, nomenc
Page 1247 and 1248: Index Terms Links 6 Aurintricarboxy
Page 1249 and 1250: Index Terms Links 8 Boron-11 chemic
Page 1251 and 1252: Index Terms Links 10 Cellulose acet
Page 1253 and 1254: Index Terms Links 12 Collective ino
Page 1255 and 1256: Index Terms Links 14 Degree Fahrenh
Page 1257 and 1258: Index Terms Links 16 Electrical res
Page 1259 and 1260: Index Terms Links 18 Equivalent wei
Page 1261 and 1262: Index Terms Links 20 Fluorocarbon p
Page 1263 and 1264: Index Terms Links 22 Halogenated hy
Page 1265 and 1266: Index Terms Links 24 Impact strengt
Page 1267 and 1268: Index Terms Links 26 Kα 1 lines, m
Page 1269 and 1270: Index Terms Links 28 Melmine phenol
Page 1271 and 1272: Index Terms Links 30 Neon-neon bond
Page 1273 and 1274: Index Terms Links 32 One-tailed tes
Page 1275 and 1276: Index Terms Links 34 Physical chemi
Page 1277 and 1278: Index Terms Links 36 Polyolefin the
Page 1279 and 1280: Index Terms Links 38 Pyridine: bina
Page 1281 and 1282: Index Terms Links 40 Rho values: fo
Page 1283 and 1284: Index Terms Links 42 Single-bond ra
Page 1285 and 1286: Index Terms Links 44 Stereoisomers
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Index Terms Links 46 Tension, aqueo
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Index Terms Links 48 Triethylenetet
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Index Terms Links 50 Water (Cont.)
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