The influence of mercury(II) on the extraction efficiency of herbicides from water

In this work, the effect of Hg(II) on the extraction efficiency of triazine and phenylurea herbicides from water samples was tested. The results showed that in the presence of Hg(II), the recoveries of the s-triazine herbicides (except hexazinon) from styrene divinylbenzene (SDVB) cartridges were significantly reduced using acetonitrile as the elution solvent, whereas acidified methanol quantitatively eluted all the herbicides. Consequently, the loss in the recoveries was not due to degradation of the compounds but rather due to irreversible adsorption onto the resin. The adsorption is probably due to ternary complex formation between the compounds, Hg(II) and the polymeric resin. The chemical structure and the basicity of the compounds affected their interaction with Hg(II). When using octadecyl (C18) cartridges, only atraton was affected. Mercury did not affect the liquid-liquid extraction of the herbicides. The findings suggest that acidic methanol is a suitable elution solvent of s-triazines from mercury-loaded water samples. © 2006 Taylor & Francis

Determination of the antifouling booster biocides irgarol 1051 and diuron and their metabolites in seawater by high performance liquid chromatography-diode array detector

A method for the simultaneous determination of two antifouling booster biocides, diuron (1-(3,4 dichlorophenyl) 3,3 dimethyl urea) and irgarol 1051 (2-methylthio-4-tert-butylamino-6-cyclopropylamino-s-triazine), and their metabolites, DCPMU (1-(3,4 dichlorophenyl)-3 methyl urea), DCPU (1-(3,4 dichlorophenyl) urea), DCA (3,4 dichloroaniline) and M1 (2-methylthio-4-tert- butylamino-s-triazine) in seawater by high performance liquid chromatography-diode array detector (HPLC-DAD) was developed. The optimization of the extraction procedure included the type of sorbent and the type of the organic solvent for the elution. Optimization of the liquid chromatography (LC) separation was also performed and the robustness of the developed separation was tested, in respect to the effect of three factors (column temperature, flow rate and initial strength of acetonitrile) on the retention times, peak resolution and peak area of the six compounds. The optimized procedure included off-line extraction of these compounds from seawater samples using C18 solid phase extraction (SPE) cartridges. The inter-day precision of the developed procedure was less than 14% (as R.S.D.s) for all the tested compounds. Satisfactory recoveries (higher than 82%) were obtained for all substances, except for DCA, for which low recovery was obtained (30.5%). The limits of detection (LODs) of the substances varied between 0.005 (DCPMU) and 0.026 (M1) μg L -1. © 2004 Elsevier B.V. All rights reserved

Evaluation of the pollution of the surface waters of Greece from the priority compounds of List II, 76/464/EEC Directive, and other toxic compounds

The pollution of the surface waters of Greece from the priority compounds of 76/464/EEC Directive was evaluated. The occurrence of 92 toxic compounds, 64 of which belong to priority compounds of List II, candidates for List I, of 76/464/EEC Directive, was studied in surface waters and wastewater through the developed network of 62 sampling stations, which covers the whole Greek territory. The analytical determination was performed by Purge and Trap-Gas chromatography-Mass spectrometry for volatile and semivolatile organic compounds (VOCs), Gas Chromatography-Electron Capture Detection for organochlorine insecticides, Gas Chromatography-Nitrogen Phosphorous Detection for organophosphorous insecticides, High Performance Liquid Chromatography-Photodiode Array Detection for herbicides, and Electrothermal Atomic Absorption Spectrophotometry and Inductively Coupled Plasma-Atomic Emission Spectrometry (ICP-AES) for metals and the toluene extractable organotin compounds. The concentrations of VOCs and insecticides detected in the surface waters of Greece were very low, whereas the concentrations of herbicides and metals ranged generally at moderate levels. VOCs were detected almost exclusively in the rivers and very rarely in the lakes, while the frequency of occurrence of insecticides, herbicides and metals was similar for rivers and lakes. Water quality objectives (WQO) and emission limit values (ELV) have been laid down in national legal framework for a number of compounds detected in the samples, in order to safeguard the quality of surface waters from any future deterioration. © 2004 Elsevier Ltd. All rights reserved

Evaluation of the pollution of the surface waters of Greece from the priority compounds of List II, 76/464/EEC Directive, and other toxic compounds

The pollution of the surface waters of Greece from the priority compounds of 76/464/EEC Directive was evaluated. The occurrence of 92 toxic compounds, 64 of which belong to priority compounds of List II, candidates for List I, of 76/464/EEC Directive, was studied in surface waters and wastewater through the developed network of 62 sampling stations, which covers the whole Greek territory. The analytical determination was performed by Purge and Trap-Gas chromatography-Mass spectrometry for volatile and semivolatile organic compounds (VOCs), Gas Chromatography-Electron Capture Detection for organochlorine insecticides, Gas Chromatography-Nitrogen Phosphorous Detection for organophosphorous insecticides, High Performance Liquid Chromatography-Photodiode Array Detection for herbicides, and Electrothermal Atomic Absorption Spectrophotometry and Inductively Coupled Plasma-Atomic Emission Spectrometry (ICP-AES) for metals and the toluene extractable organotin compounds. The concentrations of VOCs and insecticides detected in the surface waters of Greece were very low, whereas the concentrations of herbicides and metals ranged generally at moderate levels. VOCs were detected almost exclusively in the rivers and very rarely in the lakes, while the frequency of occurrence of insecticides, herbicides and metals was similar for rivers and lakes. Water quality objectives (WQO) and emission limit values (ELV) have been laid down in national legal framework for a number of compounds detected in the samples, in order to safeguard the quality of surface waters from any future deterioration. © 2004 Elsevier Ltd. All rights reserved

Transformation products in the life cycle impact assessment of chemicals

Contains fulltext : 83769.pdf (publisher's version ) (Closed access)5 p

Mixture toxicity of three photosystem II inhibitors (atrazine, isoproturon, and diuron) toward photosynthesis of freshwater phytoplankton studied in outdoor mesocosms

Mixture toxicity of three herbicides with the same mode of action was studied in a long-term outdoor mesocosm study. Photosynthetic activity of phytoplankton as the direct target site of the herbicides was chosen as physiological response parameter. The three photosystem II (PSII) inhibitors atrazine, isoproturon, and diuron were applied as 30% hazardous concentrations (HC30), which we derived from species sensitivity distributions calculated on the basis of EC50 growth inhibition data. The respective herbicide mixture comprised 1/3 of the HC30 of each herbicide. Short-term laboratory experiments revealed that the HC30 values corresponded to EC40 values when regarding photosynthetic activity as the response parameter. In the outdoor mesocosm experiment, effects of atrazine, isoproturon, diuron and their mixture on the photosynthetic activity of phytoplankton were investigated during a five-week period with constant exposure and a subsequent five-month postexposure period when the herbicides dissipated. The results demonstrated that mixture effects determined at the beginning of constant exposure can be described by concentration addition since the mixture elicited a phytotoxic effect comparable to the single herbicides. Declining effects on photosynthetic activity during the experiment might be explained by both a decrease in water herbicide concentrations and by the induction of community tolerance