The Salting-out of Liquid Nitroaromatic Compounds at Temperatures between 5 and 41 º C

1. Solubility of Nitroaromatic Compounds in Seawater Solutions · Salt lowers the solubility of NB, 2-NT, and 3-NT as shown in Figure 4. · Modeled using Setschenow equation: log (Sw/S) = Ks′ I Sw - solute solubility in pure water S - solute solubility in the salt solution Ks’ - the salting-out parameter I - ionic strength of solution Ks′ values for all four nitroaromatic compounds do not vary significantly with temperature (Table 2) and compare well with other nitroaromatic compounds (0.08 to 0.16 L/mol)1 Table 2. Salting-out Coefficients for NB, 2-NT, and 3-NT at Various Temperatures SE: Standard error NB 2 - NT 3 - NT T Ks’ SE T Ks’ SE T Ks’ SE ( º C ) ( L·mol-1) ( º C ) ( L·mol-1) ( º C ) ( L·mol-1) 5.0 0.13 0.001 4.7 0.15 0.004 20.8 0.12 0.005 20.9 0.15 0.010 20.9 0.14 0.009 30.6 0.12 0.011 30.7 0.14 0.002 30.8 0.14 0.003 35.6 0.12 0.007 35.5 0.14 0.010 35.5 0.13 0.007 40.3 0.12 0.002 40.3 0.14 0.005 40.3 0.14 0.013 2500 2000 Nitrobenzene 1500 [Nitroaromatic] (mg/L) 1000 2-Nitrotoluene 500 3-Nitrotoluene 0 270 280 290 300 310 320 Temperature (K) The Salting-out of Liquid Nitroaromatic Compounds at Temperatures between 5 and 41 ºC D. J. Luning Prak(prak@usna.edu) and D. W. O’Sullivan U.S. Naval Academy, Chemistry Department, 572M Holloway Road, Annapolis, MD 21402. Abstract This work was done in support of a 3-year project, funded by SERDP (ER 1431), that seeks to quantify the factors (salinity, dissolved organic matter, sunlight conditions) that affect the transformation of nitrogenous compounds in marine systems. Since most of the transformations occur in the aqueous phase, measurements were made of the solubility of nitroaromatic compounds at temperatures ranging from 5 to 41 °C and salinity values ranging from pure water to 100% seawater (33.1 g salt/kg seawater). The solubility of the nitroaromatic compounds in seawater was lower than that in pure water due to the presence of the salts. The average salting-out coefficients for nitrobenzene, 2-nitrotoluene, and 3-nitrotoluene were 0.12, 0.14, and 0.14 L·mol-1, respectively, which are consistent with measurements for other nitroaromatic compounds. The solubility of these compounds increased with temperature, but the salting-out coefficients did not show any significant variation with temperature over the range examined. Nitroaromatic Compound Analysis Agilent 1100 Series High Performance Liquid Chromatograph (Fig. 2) · C-18 column; Platinum, 100 Ǻ, 3 mm,53 mm by 7 mm, Alltech · variable wavelength detector set to 254 nm · Samples (10 mL for 2-NT, 3-NT, 4 mLfor NB) injected into an eluent (50 % MeOH in water) · Isocratic separation with a flow rate of 0.75 mL/min. Introduction Nitroaromatic compounds can enter and pollute the aquatic environment through the improper handling practices and the corrosion of underwater unexploded ordnance casings. The impact of this pollution source on the aquatic systems depends on the capacity of the aquatic system to transform these pollutants into less harmful species. Since most of these transformations occur in the aqueous phase, aqueous solubility is a key variable in modeling these transformations. The goal of this work was to quantify the influence of temperature and salinity on the solubility of several nitroaromatic compounds. Figure 2: HPLC Solubility of NB, 3-NT, and 2-NT in Fresh Water Systems · Increasing temperature increases solubility of all three nitroaromatic compounds as shown in Figure 3. · Modeled using: c = a exp (b T) c – concentration (mg/L) T – temperature in Kelvin a,b fitting parameters “b” values in Table 1 for liquid 2-NT (0.0124 T-1) and 3-NT (0.00885 T-1) are lower are lower than those of solid 4-NT1, 0.0310 ± 0.0021 K-1Figure 3. Nitroaromatic solubility increases astemperature increases Table 1. Temperature Coefficients for NB, 2-NT, and 3-NT Equilibration Experiments Liquid nitrobenzene (NB), 2-nitrotoluene (2-NT), or 3-nitrotoluene (3-NT) was pipetted into 14-mL glass vials containing 12 mL of aqueous solution. The vials were: · shaken on a reciprocal shaker or Labquake tube shaker (Fig. 1) for more than 24 hrs · placed in a temperature-control room, on lab bench, or in an incubator (temperature ± 0.7 ºC) · allowed to settled before sampling Figure 4. The solubility of all three nitroaromatic compounds decreases as salinity increases and as temperature decreases, 100% was 34 ppt seawater. • Conclusions ►Solubility of nitroaromatic compounds increases with temperature. ►The average salting-out coefficients are 0.12, 0.14, and 0.014 L/mol for NB, 2-NT, and 3-NT, respectively. The values do not vary significantly with temperature. NB 2 - - NT 3 - - NT a a b b a a b b a a b b – – 1 1 – – 1 1 – – 1 1 (mg/L) ( K ( K (mg/L) ( K ( K (mg/L) ( K ( K ) ) ) ) ) ) 116 0.00961 15.7 0.0124 36.4 0.00885 (81,166) ( ( ± ± 0.00120) (10.5, 23.5) ( ( ± ± 0.0020) (20.4, 65.0) ( ( ± ± 0.00136) Support for this work was provided by the SERDP Office grant ER-1431, and Naval Academy Research Council. Reference: (1) Luning Prak, D. J.; O’Sullivan, D. W., 2007, “Solubility of 4-Nitrotoluene, 2,6-Dinitrotoluene, 2,3-Dinitroluene, and 1,3,5-Trinitrobenzene in Pure Water and Seawater,” Journal of Chemical Engineering Data, 52 (6), 2446-2450. Values in parentheses represent the 95% confidence interval. Figure 1: Labquake tube shaker