Ari L. Horvath 1 1.0e+01 Ambient temperature 2 1.0 °C -5 9.9e-05 Relative mass - solution (1) 2 9.9 g₁/g₂ 1 -3 9.9e-03 Percent mass fraction (1) 2 9.9 1 -5 1.076e-05 Mole fraction - Liquid (1) 4 1.076 1 1 2.0e+01 Ambient temperature 2 2.0 °C -4 1.36e-04 Relative mass - solution (1) 3 1.36 g₁/g₂ 2 -2 1.36e-02 Percent mass fraction (1) 3 1.36 1 -5 1.467e-05 Mole fraction - Liquid (1) 4 1.467 1 1 3.0e+01 Ambient temperature 2 3.0 °C -4 1.16e-04 Relative mass - solution (1) 3 1.16 g₁/g₂ 3 -2 1.16e-02 Percent mass fraction (1) 3 1.16 1 -5 1.260e-05 Mole fraction - Liquid (1) 4 1.260 1 1 Solubility, Solubility data series 250 cm³ bottles were filled with distilled and deionized water and sealed. A measured volume of tetrachloroethene was injected into the bottles through each septum using a microliter syringe. Tetrachloroethene was in excess of the anticipated solubility limit. The bottles were shaken for one hour with a wrist-action shaker and allowed to equilibrate for about three weeks. Samples were then injected into a gas chromatograph equipped with a Carbopack column and a FID detector.The GC was response was compared with the calibration plots. The International Union of Pure and Applied Chemistry Howe, G. B.; Mullins, M. E.; Rogers, T. N.; AFESC Tyndall Air Force Base, Report ESL-TR-86-66, Vol. 1, Florida, Sept. 1987, 86 pp. (AD-A188 571). report 127-18-4 1 C2Cl4 InChI=1S/C2Cl4/c3-1(4)2(5)6 CYTYCFOTNPOANT-UHFFFAOYSA-N 165.833 Tetrachloroethene Probably a commercial reagent at least 99% pure, used as received. 7732-18-5 2 H2O InChI=1S/H2O/h1H2 XLYOFNOQVPJJNP-UHFFFAOYSA-N 18.0153 Water Distilled deionized. Tetrachloroethene with Water