W.Y. Shiu, D. Mackay 1 1.5e+01 Ambient temperature 2 1.5 °C -5 2.14e-05 Mass (1) per 100 g solution 3 2.14 g₁/100 g sln 1 -8 2.56e-08 Mole fraction - Liquid (1) 3 2.56 1 -5 2.14e-05 Relative mass - solution (1) 3 2.14 g₁/100 g sln 1 2.0e+01 Ambient temperature 2 2.0 °C -5 5.5e-05 Mass (1) per 100 g solution 2 5.5 g₁/100 g sln 2 -8 6.6e-08 Mole fraction - Liquid (1) 2 6.6 1 -5 5.5e-05 Relative mass - solution (1) 2 5.5 g₁/100 g sln 1 2.5e+01 Ambient temperature 2 2.5 °C 0 1.84e+00 Mass (1) per 100 g solution 3 1.84 µg(1)/g(2) 3 -7 2.20e-07 Mole fraction - Liquid (1) 3 2.20 1 -4 1.84e-04 Relative mass - solution (1) 3 1.84 g₁/100 g sln 1 Solubility, Solubility data series Saturated solutions was prepared by equilibrating seawater with an excess of hydrocarbon for 24 hrs in a constant temperature gyrotary shaker followed by 12 hr stationary period. A 100 mL-aliquot was extracted three times with n-hexane. The concentrated hexane extract was analyzed by a gas chromatograph equipped with a flame ionization detector to determine the hydrocarbon concentration. The International Union of Pure and Applied Chemistry Rossi, S. S.; Thomas, W. H.; Environ. Sci. Technol. 1981, 15, 715-6. paper https://doi.org/10.1021/es00088a013 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 Acenaphthene: from Aldrich Chemical Co. of 99% purity and doubly distilled from distilled methanol, n-Hexane: doubly distilled in glass, seawater: collected off Scripps Pier and was filtered twice through 0.22 µm membrane and twice extracted with n 7732-18-5 2 H2O InChI=1S/H2O/h1H2 XLYOFNOQVPJJNP-UHFFFAOYSA-N 18.0153 Seawater Acenaphthene with Seawater