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1.
Bull Environ Contam Toxicol ; 91(5): 503-9, 2013 Nov.
Article in English | MEDLINE | ID: mdl-24008278

ABSTRACT

Contamination of water sources by pesticides is one of the most critical environmental problems. The present work is designed to address the occurrence of 67 pesticides in the Lebanese waters. Chemical analysis was performed by a solid-phase extraction followed by a gas chromatography-mass spectrometry using programmed temperature vaporization injection. In drinking water and groundwater samples, organochlorine and organophosphate pesticides were frequently detected with a maximal sum concentration of up to 31.8 ng L(-1). High pesticide ecotoxicological risk was noticed in many surface waters, while this risk was driven mainly by diazinon, chlorpyrifos, fenpropathrin and bifenthrin insecticides.


Subject(s)
Environmental Monitoring , Pesticide Residues/analysis , Water Pollutants, Chemical/analysis , Water Resources/analysis , Fresh Water/chemistry , Lebanon , Organophosphorus Compounds/analysis , Solid Phase Extraction , Water Resources/statistics & numerical data
2.
J Agric Food Chem ; 59(14): 7592-600, 2011 Jul 27.
Article in English | MEDLINE | ID: mdl-21476566

ABSTRACT

A fast and reliable method for the determination of polycyclic aromatic hydrocarbons (PAHs) in water samples by solid-phase extraction (SPE) using centrifugation has been developed and optimized. A silica-based C18 cartridge was used; parameters affecting the extraction procedure such as type and volume of the elution solvent, breakthrough volume of the percolated water sample, drying of the sorbent, and evaporation of the elute have been studied. The innovation of this work was the examination of the use of a centrifugation technique in both the drying and elution steps. When combined with centrifugation, the volume of the elution solvent was reduced to 1 mL and the time for sorbent drying decreased also to 10 min under vacuum. Under optimal conditions, recoveries for the 16 U.S. EPA PAHs were between 70 and 85% and the relative standard deviation varied between 1 and 14%. Surrogate standard recoveries were similarly between 61 and 94% with a relative standard deviation between 2 and 15%. The simplicity of the described method, use of less of organic solvent, short procedure time, and good recoveries demonstrate the advantages of this environmentally friendly approach for routine analysis of numerous samples.


Subject(s)
Centrifugation/methods , Polycyclic Aromatic Hydrocarbons/isolation & purification , Solid Phase Extraction/methods , Water Pollutants, Chemical/isolation & purification , Chromatography, High Pressure Liquid , Polycyclic Aromatic Hydrocarbons/analysis , Water Pollutants, Chemical/analysis
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