Search

Soil-aquifer processes have proven to work as a natural treatment for the attenuation of numerous contaminants during artificial recharge of groundwater. Nowadays, significant scientific effort is being devoted to understanding the fate of pharmaceuticals in subsurface environments, and to verify if such semipersistent organic micropollutants could also be efficiently removed from water. In this context we carried out a series of batch experiments involving aquifer material, selected drugs (initial concentration of 1 μg/L and 1 mg/L), and denitrifying conditions. Diclofenac and sulfamethoxazole exhibited an unreported and peculiar behavior. Their concentrations consistently dropped in the middle of the tests but recovered toward the end, which suggest a complex effect of denitrifying conditions on aromatic amines. The transformation products Nitro-Diclofenac and 4-Nitro-Sulfamethoxazole were detected in the biotic experiments, while nitrite was present in the water. Their concentrations developed almost opposite to those of their respective parent compounds. We conjecture that this temporal and reversible effect of denitrifying conditions on the studied aromatic amines could have significant environmental implications, and could explain at least partially the wide range of removals in subsurface environments reported in literature for DCF and SMX, as well as some apparent discrepancies on SMX behavior., (Copyright © 2012 Elsevier B.V. All rights reserved.)

The antibiotic sulfonamide drug sulfamethoxazole (SMX) is extensively used in both human and veterinary medicine. Since it cannot be completely eliminated by the typical state-of-the-art wastewater treatment technology, it is frequently detected in the water cycle. SMX, as aromatic amine, can undergo abiotic transformations with the under denitrifying conditions produced nitrogen species nitric oxide (NO) and nitrite (NO(2)(-)). NO and aromatic amines are commonly known to form diazonium cations. Depending on the reaction conditions the diazonium cation disintegrates under cleavage of elementary nitrogen and substitutes its diazo-group by an NO(2)-group or by hydrogen. Following this approach, two transformation products (TPs) of the persistent SMX under denitrifying conditions were hypothesized and synthesized: 4-nitro-N-(5-methylisoxazol-3-yl)-benzenesulfonamide (4-nitro-SMX) and N-(5-methylisoxazol-3-yl)-benzenesulfonamide (desamino-SMX). The synthesized compounds were identified by Nuclear Magnetic Resonance (NMR) spectroscopy and used as reference standards for their confirmation and quantification in denitrifying water/sediment batch experiments and in environmental samples. During the denitrifying degradation experiment SMX was no longer detected after 10 days whereas increasing concentrations of the two TPs were observed. However, at day 87 the SMX concentration recovered to 53 ± 16% of the initial concentration after most of the nitrate was consumed. A retransformation of 4-nitro-SMX to SMX was postulated and confirmed by another anoxic water/sediment test in the absence of nitrate as electron acceptor. Both TPs were also detected in karst spring samples, highlighting the need and benefit of focusing on transformation products in environmental studies. Furthermore, the consideration of the retransformation potential of 4-nitro-SMX can substantially improve the understanding of SMX behavior during processes such as bank filtration and artificial recharge., (Copyright © 2012 Elsevier Ltd. All rights reserved.)

Contamination from untreated wastewater leakage and related bacterial contamination poses a threat to drinking water quality. However, a quantification of the magnitude of leakage is difficult. The objective of this work is to provide a highly sensitive methodology for the estimation of the mass of untreated wastewater entering karst aquifers with rapid recharge. For this purpose a balance approach is adapted. It is based on the mass flow of caffeine in spring water, the load of caffeine in untreated wastewater and the daily water consumption per person in a spring catchment area. Caffeine is a source-specific indicator for wastewater, consumed and discharged in quantities allowing detection in a karst spring. The methodology was applied to estimate the amount of leaking and infiltrating wastewater to a well investigated karst aquifer on a daily basis. The calculated mean volume of untreated wastewater entering the aquifer was found to be 2.2 ± 0.5 m(3) d(-1) (undiluted wastewater). It corresponds to approximately 0.4% of the total amount of wastewater within the spring catchment., (Copyright © 2011 Elsevier Ltd. All rights reserved.)

A multi-residue analytical method based on high-performance liquid chromatographic separation, electrospray ionization with tandem mass spectrometric detection (HPLC/MS-MS) was developed for the simultaneous analysis of 46 basic, neutral and acidic compounds covering a wide range of polarity (logK(OW)<0-5.9). The compound list included selected iodinated contrast media, analgesics, anti-inflammatories, stimulants, beta-blockers, antibiotics, lipid regulators, anti-histamines, psychiatric drugs, herbicides, corrosion inhibitors and the gastric acid regulator pantoprazole. The main feature of the presented method was a simultaneous solid phase extraction (SPE) of all analytes followed by simultaneous separation and detection by HPLC/MS-MS with electrospray ionization in both positive and negative polarization within the same chromatogram. Optimization of electrospray drying gas temperature resulted in using a temperature gradient on the ion source. Six different polymeric sorbents for SPE were compared with respect to recoveries, taking into account the specific surface of each sorbent. Method quantitation limits (MQL) in surface and seawater ranged from 1.2 to 28 ng/L, in wastewater from 5.0 to 160 ng/L, respectively. In order to demonstrate the applicability of the method, river water, treated wastewater and seawater were analyzed., (Copyright © 2010 Elsevier B.V. All rights reserved.)