Poly(ethylene glycols) (PEGs) and related menu- and dicarboxylated forms constitute one of the most abundant classes of contaminants in natural waters. Because of the Jack of efficient analytical methods, only one study has been devoted to estimate levels of these analyses in some river waters. The present method involves analyse extraction from 50 mL of raw sewage, 100 mL of treated sewage, 500 mL of river water and seawater, and 2000 mL of groundwater by a 0.5-g Carbograph 4 cartridge. Isolation of acidic analyses from co-extracted neutral ones was accomplished by differential elution. During removal of the HCl-acidified CH2Cl2/CH3OH eluent mixture, carboxylated PEGs were purposely allowed to convert into their methyl esters. This offered the advantage of analyzing for all the species of interest using the same instrumental arrangement. Extracts were analyzed by liquid chromatography/electrospray/mass spectrometry operated in the positive-ion mode. For species with ethoxy chain lengths ≤4, analyte recoveries were better than 83%, while lower homologues were poorly recovered, and thus, they were not considered when analyzing environmental aqueous samples. Under full- scan conditions, analyses in real water samples could be quantified at few tens of nanograms per liter, while data acquisition in the selected ion monitoring mode afforded limits of quantification of 0.1-0.3 ng/L. Analyses of influents and effluents of activated sludge wastewater treatment facilities showed that even high molecular mass PEGs, so far considered rather resistant to biodegradation, were very efficiently removed from sewages. The ubiquitous nature of PEG-type compounds was evidenced by the fact that they were detected at parts per trillion levels in marine waters 16 nautical miles from the italian coast and in five groundwaters samples collected from subsurface depths ranging between 60 and 208 m. The levels of polyethylene glycols (PEGs) and related mono- and di-carboxylated forms in some river waters were estimated using liquid chromatography/electrospray/mass spectrometry operated in the positive mode. Acidic analytes were isolated from co-extracted neutral ones using differential elution. Carboxylated PEGs were converted into their methyl esters which allowed the analysis for all the species of interest using the same instrumental arrangements. Under full-scan conditions, analytes in real water samples can be quantified at few tens of nanograms per liter, while data acquisition in the selected ion monitoring mode afforded limits of quantification of 0.1-0.3 ng/L.

Detection of Poly(Ethylene Glycols) and Related Acidic Forms in Environmental Waters by Liquid Chromatography Electrospray Mass Spectrometry / Crescenzi, C.; DI CORCIA, Antonio; Marcomini, A.; Samperi, Roberto. - In: ENVIRONMENTAL SCIENCE & TECHNOLOGY. - ISSN 0013-936X. - STAMPA. - 31:9(1997), pp. 2679-2685. [10.1021/es9700966]

Detection of Poly(Ethylene Glycols) and Related Acidic Forms in Environmental Waters by Liquid Chromatography Electrospray Mass Spectrometry

DI CORCIA, Antonio;SAMPERI, Roberto
1997

Abstract

Poly(ethylene glycols) (PEGs) and related menu- and dicarboxylated forms constitute one of the most abundant classes of contaminants in natural waters. Because of the Jack of efficient analytical methods, only one study has been devoted to estimate levels of these analyses in some river waters. The present method involves analyse extraction from 50 mL of raw sewage, 100 mL of treated sewage, 500 mL of river water and seawater, and 2000 mL of groundwater by a 0.5-g Carbograph 4 cartridge. Isolation of acidic analyses from co-extracted neutral ones was accomplished by differential elution. During removal of the HCl-acidified CH2Cl2/CH3OH eluent mixture, carboxylated PEGs were purposely allowed to convert into their methyl esters. This offered the advantage of analyzing for all the species of interest using the same instrumental arrangement. Extracts were analyzed by liquid chromatography/electrospray/mass spectrometry operated in the positive-ion mode. For species with ethoxy chain lengths ≤4, analyte recoveries were better than 83%, while lower homologues were poorly recovered, and thus, they were not considered when analyzing environmental aqueous samples. Under full- scan conditions, analyses in real water samples could be quantified at few tens of nanograms per liter, while data acquisition in the selected ion monitoring mode afforded limits of quantification of 0.1-0.3 ng/L. Analyses of influents and effluents of activated sludge wastewater treatment facilities showed that even high molecular mass PEGs, so far considered rather resistant to biodegradation, were very efficiently removed from sewages. The ubiquitous nature of PEG-type compounds was evidenced by the fact that they were detected at parts per trillion levels in marine waters 16 nautical miles from the italian coast and in five groundwaters samples collected from subsurface depths ranging between 60 and 208 m. The levels of polyethylene glycols (PEGs) and related mono- and di-carboxylated forms in some river waters were estimated using liquid chromatography/electrospray/mass spectrometry operated in the positive mode. Acidic analytes were isolated from co-extracted neutral ones using differential elution. Carboxylated PEGs were converted into their methyl esters which allowed the analysis for all the species of interest using the same instrumental arrangements. Under full-scan conditions, analytes in real water samples can be quantified at few tens of nanograms per liter, while data acquisition in the selected ion monitoring mode afforded limits of quantification of 0.1-0.3 ng/L.
1997
Liquid chromatography, Mass spectrometry, Polyethylene glycols, Rivers, Seawater, water analysis, Water pollution
01 Pubblicazione su rivista::01a Articolo in rivista
Detection of Poly(Ethylene Glycols) and Related Acidic Forms in Environmental Waters by Liquid Chromatography Electrospray Mass Spectrometry / Crescenzi, C.; DI CORCIA, Antonio; Marcomini, A.; Samperi, Roberto. - In: ENVIRONMENTAL SCIENCE & TECHNOLOGY. - ISSN 0013-936X. - STAMPA. - 31:9(1997), pp. 2679-2685. [10.1021/es9700966]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/245184
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