William E. Acree, Jr.
2
2.732e+02
Ambient temperature
4
2.732
$\pu{K}$
-3
8.2e-03
Mole fraction - Liquid (1)
2
8.2
1
-1
9.918e-01
Mole fraction - Liquid (2)
4
9.918
1
1
2
2.841e+02
Ambient temperature
4
2.841
$\pu{K}$
-3
8.6e-03
Mole fraction - Liquid (1)
2
8.6
1
-1
9.914e-01
Mole fraction - Liquid (2)
4
9.914
1
2
2
3.053e+02
Ambient temperature
4
3.053
$\pu{K}$
-2
1.56e-02
Mole fraction - Liquid (1)
3
1.56
1
-1
9.844e-01
Mole fraction - Liquid (2)
4
9.844
1
3
2
3.202e+02
Ambient temperature
4
3.202
$\pu{K}$
-2
2.19e-02
Mole fraction - Liquid (1)
3
2.19
1
-1
9.781e-01
Mole fraction - Liquid (2)
4
9.781
1
4
2
3.434e+02
Ambient temperature
4
3.434
$\pu{K}$
-2
7.52e-02
Mole fraction - Liquid (1)
3
7.52
1
-1
9.248e-01
Mole fraction - Liquid (2)
4
9.248
1
5
1
Solubility, Solubility data series
Experimental procedure only marginally described by author.<br>Excess solute and solvent were equilibrated in a constant temperature water bath for between 10-30 minutes. Saturated solution was withdrawn through a coarse filter and analyzed by specific gravity. Author noted that evaporation to dryness and weighing the residue was subject to too much decomposition.
The International Union of Pure and Applied Chemistry
Speyers, C. L.; Am. J. Sci. 1902, 14, 293-302.
paper
https://doi.org/10.2475/ajs.s4-14.82.293
85-01-8
1
C14H10
InChI=1S/C14H10/c1-3-7-13-11(5-1)9-10-12-6-2-4-8-14(12)13/h1-10H
YNPNZTXNASCQKK-UHFFFAOYSA-N
178.229
Phenanthrene
Purity not given, Kahlbaum, was recrystallized from toluene to a melting point temperature of 100.4°C.
64-17-5
2
C2H6O
InChI=1S/C2H6O/c1-2-3/h3H,2H2,1H3
LFQSCWFLJHTTHZ-UHFFFAOYSA-N
46.0684
Ethanol
Marked absolute, from Eimer and Amend and Chas. Cooper and Co., dried over calcium oxide and distilled before use.
Phenanthrene with Ethanol
Solubility data from IUPAC SDS Volume 59 (page ?) - Phenanthrene with Ethanol