Optimization of Solid State Urea Clathrate Formation as a Chemical Separation Method Coupled to Compound Specific Stable Carbon Isotope Analysis

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Optimization of Solid State Urea Clathrate Formation as a Chemical Separation Method Coupled to Compound Specific Stable Carbon Isotope Analysis Márton Novák a, Csaba Kirchkeszner a, Dóra Palya a, Zsolt Bodai a, Zoltán Nyiri a, Norbert Magyar b, József Kovács b, Tamás Rikker c, Zsuzsanna Eke a,c * a, Eötvös Loránd University, Joint Research and Training Laboratory on Separation Techniques (EKOL), 1/A, Pázmány Péter sétány, Budapest 1117, Hungary b, Eötvös Loránd University, Department of Physical and Applied Geology, 1/C, Pázmány Péter sétány, Budapest 1117, Hungary c, Wessling International Research and Educational Center, 56, Fóti út, Budapest 1047, Hungary

Supporting Information Characterization of the water samples Table S1. Basic water quality parameters of the tested water samples: DW: Distilled Water; TW: Tap Water; RW: River Water; IWW 1-3: Industrial Wastewater 1-3; CF: Confined Water; GW 1-2: Groundwater 1-2. The concentration of NH4 + was not determined in samples IWW 1-3 because of the disturbance of hydrogen sulfide. The Electrical Conductivity (EC) was referred to 20 C. The dissolved O2 and the O2 saturation was not determined for samples GW 1, GW 2 and CW samples. DW TW RW IWW 1 IWW 2 IWW 3 CW GW 1 GW 2 ph 5.45 7.66 7.62 7.25 6.92 6.73 6.65 6.52 6.72 EC / µs cm -1 3 448 375 553 1054 1285 1325 916 1157 O2 / mg L -1 6.3 5.3 6.4 3.4 1.6 2.0 - - - Oxygen saturation / % 93 73 84 49 23 29 - - - CODCr / mg L -1 O2 blank <1 23 75 144 181 2 5 5 NH4 + / mg L -1 blank <0.01 0.1 n.d.* n.d.* n.d.* <0.01 <0.01 <0.01 NO3 - / mg L -1 blank 15.1 20.3 11.5 10.2 9.0 4.3 62.8 83.4 NO2 - / mg L -1 blank <0.02 0.029 0.021 <0.02 <0.02 <0.02 0.22 0.39 PO4 3- / mg L -1 blank <0.1 0.6 1.4 5.8 10.6 0.1 0.3 0.5 Water quality parameters were determined using the following instruments. ph was measured with WTW ProfiLine ph 3110 portable ph meter with SenTix 41 ph electrodes. Electrical conductivity was determined with HANNA HI 98303 DiST3 ECtester with automated temperature compensation (20 C). Dissolved oxygen and oxygen saturation was measured with WTW ProfiLine Oxi 3205 portable dissolved oxygen meter with DurOx 325 membrane covered galvanic dissolved oxygen sensor. Ammonium ion, nitrite ion, nitrate ion and reactive orthophosphate ion concentration were measured with an MN PF-11 filter photometer. The ph, electrical conductivity, dissolved oxygen and oxygen saturation were determined by electroanalytical methods on the spot of sampling. The concentration of ammonium ion was measured by photometric phenate method at 720 nm. The concentration of nitrite ion was determined photometrically. Nitrite produces diazonium salt with sulphanilamide. This product reacts with N-(1-naphtyl)-ethylenediamine to form an intensive red-violet azo dye. The intensity of developed colour was measured at 520 nm. The concentration of nitrate ion was determined photometrically with 2,6- dimethylphenol in sulphuric-phosphoric acid mixture. In acidic solution nitrate ions react with 2,6-dimethylphenol to form 4-nitro-2,6-dimethylphenol. Measurements were performed at 470 nm. Reactive orthophosphate was determined by photometric molybdenum blue method at 720 nm. Chemical oxygen demand (COD) was determined in a strong acidic solution of potassium dichromate in the presence of silver sulphate and mercury(ii) sulphate. At a temperature of 148 C, after two hours, the dichromate ion was reduced to chromium(iii) ion. After this digestion the amount of residual dichromate ion was determined photometrically at 380 nm.

The m/z 44 chromatograms of the purified n-alkane solutions from the different water samples and the contaminating diesel fuel Figure S1. m/z 44 chromatogram of the purified n-alkane solution from distilled water Figure S2. m/z 44 chromatogram of the purified n-alkane solution from the tap water

Figure S3. m/z 44 chromatogram of the purified n-alkane solution from river water Figure S4. m/z 44 chromatogram of the purified n-alkane solution from industrial wastewater sample 1.

Figure S5. m/z 44 chromatogram of the purified n-alkane solution from industrial wastewater sample 2. Figure S6. m/z 44 chromatogram of the purified n-alkane solution from industrial wastewater sample 3.

Figure S7. m/z 44 chromatogram of the purified n-alkane solution from confined water Figure S8. m/z 44 chromatogram of the purified n-alkane solution from groundwater sample 1.

Figure S9. m/z 44 chromatogram of the purified n-alkane solution from groundwater sample 2. Figure S10. m/z 44 chromatogram of the purified n-alkane solution from contaminating diesel fuel.