A previous method based upon Liquid Chromatography (HPLC) with fluorometric detection for determining linear aklylbenzenesulfonates (LAS) in aqueous environmental samples has been modified for extending it to the monitoring of dialkyltetralinsulfonates (DATS). DATS are reaction byproducts of LAS surfactant synthesis. 10, 100, 200, 1000 ml of respectively untreated sewage, treated one, riverwater and groundwater samples have been extracted by a 0.5-g Graphitized Carbon Black (GCB) cartridge. After sample extraction, co-extracted basic, neutral and weakly acidic compounds have been washed out by a formic acid containing solvent system. DATS and LAS have been then reextracted by passing through the cartridge a basified organic eluant mixture. After solvent removal and residue reconstitution by a suitable solvent system, the subfractionation of the analytes have been achieved by chromatographing them on a C-8 reverse-phase HPLC column. Recovery studies have shown that DATS have been quantitatively extracted by the GCB cartridge. By this procedure, the concentrations in water of DATS entering and leaving two sewage treatment plants in Rome have been monthly monitored over 1 year. With respect to LAS, the higher resistance to biodegradation of DATS has been demonstrated by comparative biodegradation tests. Analysis of a sewage-contaminated groundwater sample has shown that, although DAIS are minor components in LAS formulations, the concentration of the former was even higher than that of the latter, with C-10 DATS being the most abundant species.

Simultaneous determination of alkylbenzenesulfonates and dialkyltetralinsulfonates in water by liquid chromatography / Carlo, Crescenzi; DI CORCIA, Antonio; Enrico, Marchiori; Samperi, Roberto; Antonio, Marcomini. - In: WATER RESEARCH. - ISSN 0043-1354. - STAMPA. - 30:3(1996), pp. 722-730. [10.1016/0043-1354(95)00209-x]

Simultaneous determination of alkylbenzenesulfonates and dialkyltetralinsulfonates in water by liquid chromatography

DI CORCIA, Antonio;SAMPERI, Roberto;
1996

Abstract

A previous method based upon Liquid Chromatography (HPLC) with fluorometric detection for determining linear aklylbenzenesulfonates (LAS) in aqueous environmental samples has been modified for extending it to the monitoring of dialkyltetralinsulfonates (DATS). DATS are reaction byproducts of LAS surfactant synthesis. 10, 100, 200, 1000 ml of respectively untreated sewage, treated one, riverwater and groundwater samples have been extracted by a 0.5-g Graphitized Carbon Black (GCB) cartridge. After sample extraction, co-extracted basic, neutral and weakly acidic compounds have been washed out by a formic acid containing solvent system. DATS and LAS have been then reextracted by passing through the cartridge a basified organic eluant mixture. After solvent removal and residue reconstitution by a suitable solvent system, the subfractionation of the analytes have been achieved by chromatographing them on a C-8 reverse-phase HPLC column. Recovery studies have shown that DATS have been quantitatively extracted by the GCB cartridge. By this procedure, the concentrations in water of DATS entering and leaving two sewage treatment plants in Rome have been monthly monitored over 1 year. With respect to LAS, the higher resistance to biodegradation of DATS has been demonstrated by comparative biodegradation tests. Analysis of a sewage-contaminated groundwater sample has shown that, although DAIS are minor components in LAS formulations, the concentration of the former was even higher than that of the latter, with C-10 DATS being the most abundant species.
1996
ground water; liquid chromatography; river water; surfactant; water contamination
01 Pubblicazione su rivista::01a Articolo in rivista
Simultaneous determination of alkylbenzenesulfonates and dialkyltetralinsulfonates in water by liquid chromatography / Carlo, Crescenzi; DI CORCIA, Antonio; Enrico, Marchiori; Samperi, Roberto; Antonio, Marcomini. - In: WATER RESEARCH. - ISSN 0043-1354. - STAMPA. - 30:3(1996), pp. 722-730. [10.1016/0043-1354(95)00209-x]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/34064
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