William E. Acree, Jr. 2 3.0335e+02 Ambient temperature 5 3.0335 K -2 8.53e-02 Mole fraction - Liquid (1) 3 8.53 1 -1 9.147e-01 Mole fraction - Liquid (2) 4 9.147 1 1 2 3.0735e+02 Ambient temperature 5 3.0735 K -1 1.031e-01 Mole fraction - Liquid (1) 4 1.031 1 -1 8.969e-01 Mole fraction - Liquid (2) 4 8.969 1 2 2 3.1205e+02 Ambient temperature 5 3.1205 K -1 1.274e-01 Mole fraction - Liquid (1) 4 1.274 1 -1 8.726e-01 Mole fraction - Liquid (2) 4 8.726 1 3 2 3.1645e+02 Ambient temperature 5 3.1645 K -1 1.565e-01 Mole fraction - Liquid (1) 4 1.565 1 -1 8.435e-01 Mole fraction - Liquid (2) 4 8.435 1 4 2 3.2095e+02 Ambient temperature 5 3.2095 K -1 1.931e-01 Mole fraction - Liquid (1) 4 1.931 1 -1 8.069e-01 Mole fraction - Liquid (2) 4 8.069 1 5 2 3.2565e+02 Ambient temperature 5 3.2565 K -1 2.421e-01 Mole fraction - Liquid (1) 4 2.421 1 -1 7.579e-01 Mole fraction - Liquid (2) 4 7.579 1 6 2 3.2995e+02 Ambient temperature 5 3.2995 K -1 2.984e-01 Mole fraction - Liquid (1) 4 2.984 1 -1 7.016e-01 Mole fraction - Liquid (2) 4 7.016 1 7 2 3.3465e+02 Ambient temperature 5 3.3465 K -1 3.697e-01 Mole fraction - Liquid (1) 4 3.697 1 -1 6.303e-01 Mole fraction - Liquid (2) 4 6.303 1 8 2 3.3985e+02 Ambient temperature 5 3.3985 K -1 4.645e-01 Mole fraction - Liquid (1) 4 4.645 1 -1 5.355e-01 Mole fraction - Liquid (2) 4 5.355 1 9 2 3.4645e+02 Ambient temperature 5 3.4645 K -1 5.992e-01 Mole fraction - Liquid (1) 4 5.992 1 -1 4.008e-01 Mole fraction - Liquid (2) 4 4.008 1 10 2 3.5445e+02 Ambient temperature 5 3.5445 K -1 7.742e-01 Mole fraction - Liquid (1) 4 7.742 1 -1 2.258e-01 Mole fraction - Liquid (2) 4 2.258 1 11 1 Solubility, Solubility data series Constant temperature bath and a precision thermometer. Mixtures of known concentrations sealed in glass ampoules and placed in constant temperature to equilibrate. Samples were rotated while bath temperature slowly increased. Solubility determined by noting the temperature at which the last trace of solid solute disappeared. The International Union of Pure and Applied Chemistry Choi, P. B.; Williams, C. P.; Buehring, K. G.; McLaughlin, E.; J. Chem. Eng. Data 1985, 30, 403-409. paper https://doi.org/10.1021/je00042a011 83-32-9 1 C12H10 InChI=1S/C12H10/c1-3-9-4-2-6-11-8-7-10(5-1)12(9)11/h1-6H,7-8H2 CWRYPZZKDGJXCA-UHFFFAOYSA-N 154.208 Acenaphthene 99.2%, British Drug Houses, United Kingdom, was recrystallized and then zone refined. 110-82-7 2 C6H12 InChI=1S/C6H12/c1-2-4-6-5-3-1/h1-6H2 XDTMQSROBMDMFD-UHFFFAOYSA-N 84.1595 Cyclohexane Gold Label, 99.9+%, Aldrich Chemical Company, was used as received. Acenaphthene with Cyclohexane