Sulfophenylcarboxylic Acids Research Articles

Evaluation of the anaerobic biodegradation of linear alkylbenzene sulfonates (LAS) using OECD 308 water/sediment systems.

Linear alkylbenzene sulfonates (LAS) are the most widely used anionic surfactants in household detergents and cleaning products. We have evaluated LAS anaerobic degradation in sediments following OECD 308 guidelines. Four different classes of sediments were collected from non-polluted areas and tested to check the influence of: fine and coarse texture, low and high organic carbon content, and freshwater and marine origin. The concentrations of LAS and possible degradation metabolites in sediment and water phases were monitored by high resolution mass spectrometry over an incubation period of 160 days. LAS removal was between 0 and 63%, depending on the sediment used, and it was accompanied by formation of sulfophenyl carboxylic acids (SPCs). The best results were observed for marine sediments having low organic carbon and silt + clay contents (0.5% and 13%, respectively), whereas degradation was negligible in freshwater sediments. The large differences in degradation observed across the sediments tested were attributed to their physicochemical properties influencing LAS bioavailability and the heterogeneity of microbial communities. Further research is also needed to address some shortcomings observed during the application of the OECD 308 and to ensure that test results obtained with these guidelines model anaerobic biodegradation under realistic environmental conditions.

Distribution of anionic and nonionic surfactants in a sewage-impacted Mediterranean coastal lagoon: Inputs and seasonal variations

In this work we have monitored the seasonal inputs, occurrence and distribution of the world's most widely used surfactants (linear alkylbenzene sulfonates, LAS, nonylphenol polyethoxylates, NPEOs, and alcohol polyethoxylates, AEOs) in Mar Menor lagoon (SE Spain) and its main tributary (El Albujón) for the first time. Concentration of target compounds was determined in both surface waters and sediments after solid phase extraction and pressurized liquid extraction, respectively, followed by liquid chromatography–mass spectrometry (LC–MS). There were significant differences in surfactant fluxes from El Albujón towards Mar Menor depending on the season and the day of the week, with maximum estimated annual inputs being detected for LAS (406kg) and their metabolites, sulfophenyl carboxylic acids (482kg). Average concentrations of surfactants in the lagoon were between 44 and 1665μg/kg in sediment, and between 0.3 and 63μg/L in water. These levels were significantly higher for samples collected near the shore than for those measured inside the lagoon itself. Overall, the occurrence and distribution of surfactants in the system could be explained due to a combination of different sources (surface and groundwater inputs, treated and untreated wastewater effluents, towns, ports, etc.) and simultaneous in-situ physicochemical and biological processes, with an special emphasis on degradation during warmer months.

Occurrence and fate of selected surfactants in seawater at the outfall of the Marseille urban sewerage system

This paper describes an investigation of linear alkylbenzene sulfonates (LAS) and nonylphenol ethoxylates (NPEO) and their metabolites in the vicinity of the Marseille sewage outfall (wastewater treatment plant with a capacity of 1.860 million inhabitant equivalents, Northwestern Mediterranean, southeast of France). This analytical survey describes their occurrence in the subsurface and sea surface layers and investigates their possible fates in this marine environment. The results indicated the presence of LAS in both layers and up to 3 km from the discharge point, whereas the concentration of sulfophenyl carboxylic acids, which are the main metabolites of LAS, was only significant near the sewer outfall and in the surface layer. The NPEO were present only in minor quantities, especially near the discharge point, and no other selected metabolites were detected. The fate of the surfactants in question was then assessed by two types of experiments according to their potential means of degradation under natural conditions. Biodegradation assays were conducted according to a protocol defined by the United States Environmental Protection Agency (''Biodegradability in sea water, 835.3160''), with variations in the substrate input frequencies. Photodegradation experiments were carried out in a solar simulator reactor. These results demonstrated the low photodegradability and rapid primary biodegradation of LAS (with half-life times between 10.3 and 11.5 days) in the coastal area under study, although some LAS metabolites were more recalcitrant to biodegradation in this specific environment, which was also validated by linear alkylbenzene analysis in the two selected sediment stations.

Vertical distribution profiles and diagenetic fate of synthetic surfactants in marine and freshwater sediments

This manuscript deals with the presence and degradation of the most commonly-used surfactants, including anionic (linear alkylbenzene sulfonates, LAS, and alkyl ethoxysulfates, AES) and non-ionic (alcohol polyethoxylates, AEOs, and nonylphenol polyethoxylates, NPEOs) compounds, in sediments and pore water from several aquatic environments (Southwest, Spain). Different vertical distributions were observed according to the respective sources, uses, production volumes and physicochemical properties of each surfactant. Levels of nonionics (up to 10mgkg−1) were twice as high as anionics in industrial areas and harbors, whereas the opposite was found near urban wastewater discharge outlets. Sulfophenyl carboxylic acids (SPCs), LAS degradation products, were identified at anoxic depths at some sampling stations. Their presence was related to in situ anaerobic degradation of LAS in marine sediments, whereas the occurrence of these metabolites in freshwater sediments was attributed to the existence of wastewater sources nearby. No significant changes in the average length of AEO and NPEO ethoxylated chains were observed along the sediment cores, suggesting that their biodegradation was very limited in the sampling area. This may be directly related to their lower bioavailability, as their calculated sediment–pore water distribution coefficients (log Ksw), which showed that non-ionic surfactants examined in this study had greater sorption affinity than the anionic surfactants (e.g., 2.3±0.3 for NPEOs).

Degradation of surface-active compounds in a constructed wetland determined using high performance liquid chromatography and extraction spectrophotometry

Degradation of anionic and nonionic surfactants in a constructed wetland with horizontal subsurface flow was studied using high performance liquid chromatography and extraction spectrophotometry. The ratio of individual homologues of linear alkylbenzene sulfonates (LAS) and the efficiency of their removal were studied. Tridecyl-, dodecyl-, undecyl-, and decylbenzene sulfonates were removed with efficiencies of 92.9%, 84.3%, 64.7%, and 41.1%, respectively. These differences are due to sequential shortening of the alkyl chain in homologues during degradation (the higher homologue can provide the lower one). The formation of sulfophenyl carboxylic acids during ω-oxidation of the alkyl chain followed by successive α- and/or β-oxidation is also a possible mechanism for removal of LAS. Solid phase extraction using Chromabond® HR-P columns was used for preconcentration of the analytes prior to their determination by HPLC. Methylene blue active compounds were determined using extraction spectrophotometry. The average efficiency of their removal was 84.9% in this case. The efficiency of nonionic surfactant removal (98.2%) was significantly higher in comparison to that for anionic surfactants. The concentration of the endocrine disruptor nonylphenol (a product of nonylphenol polyethoxylate surfactant degradation) determined in the profile of the wetland was beneath the limit of detection (0.4 μg/L). The average outflow concentrations of anionic and nonionic surfactants determined by spectrophotometry were 0.54 and 0.021 mg/L, respectively. The average outflow concentrations of decyl- and tridecylbenzene sulfonates determined by HPLC were 0.195 and 0.015 mg/L. Efficiencies of 86.4% and 92.2% were obtained for removal of organic compounds as indicated by chemical and biochemical oxygen demand (CODCr and BOD5). These results demonstrate the suitability of the constructed wetland for degrading surface-active compounds.

Molecular characterization of effluent organic matter identified by ultrahigh resolution mass spectrometry

Effluent dissolved organic matter (EfOM) collected from the secondary-treated wastewater of the Orange County Sanitation District (OCSD) located in Fountain Valley, California, USA was compared to natural organic matter collected from the Suwannee River (SRNOM), Florida using ultrahigh resolution electrospray ionization Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR-MS). Furthermore, the two different treatment processes at OCSD, activated sludge and trickling filter, were separately investigated. The blend of these two effluents was further evaluated after it had passed through the microfiltration process of the Advanced Water Purification Facility (AWPF) at Orange County Water District (OCWD). EfOM contained 872 different m/ z peaks that were unambiguously assigned to exact molecular formulae containing a single sulfur atom and carbon, hydrogen and oxygen atoms (CHOS formulae). In contrast, the SRNOM sample only contained 152 CHOS formulae. The trend in CHO molecular compositions was opposite with 2500 CHO formulae assigned for SRNOM but only about 1000 for EfOM. The CHOS-derived mass peaks with highest abundances in EfOM could be attributed to surfactants such as linear alkyl benzene sulfonates (LAS), their co-products dialkyl tetralin sulfonates (DATS) and their biodegraded metabolites such as sulfophenyl carboxylic acids (SPC). The differences between the treatments were found minor with greater differences between sampling dates than treatment methods used.

Multi-residue method for the analysis of synthetic surfactants and their degradation metabolites in aquatic systems by liquid chromatography–time-of-flight-mass spectrometry

Synthetic surfactants are economically important chemicals, as they are widely used in household cleaning detergents, textiles, paints, polymers and personal care products. In this work we have developed a method capable of the isolation and analysis of the most widely used surfactants (linear alkylbenzene sulfonates, LAS, nonylphenol ethoxylates, NPEO, and alcohol ethoxylates, AEO) and their main degradation products (sulfophenyl carboxylic acids, SPC, nonylphenol ethoxycarboxylates, NPEC, and polyethylene glycols, PEG) in aqueous and solid environmental matrices. First, analytes were extracted by ultrasonic extraction from sediments and suspended solids using methanol at 50 °C as solvent and 3 cycles (30 min per cycle). Clean-up and pre-concentration of the extracts and water samples were carried out by solid-phase extraction (SPE), using Oasis HLB cartridges. Recoveries were generally about 80% for most compounds. Identification and quantification of target compounds were performed by liquid chromatography–time-of-flight-mass spectrometry (LC–ToF-MS), which has been much less used in the field of environmental analysis than other MS techniques. Examples which illustrate the possible advantages of this technique for multi-analyte analysis of target and non-target contaminants in environmental samples are provided. Finally, the methodology developed here was validated by measuring the concentration of surfactants and their metabolites in selected marine sediment and seawater samples collected in Long Island Sound (NY), and in influent and effluent wastewater from Stony Brook treatment plant (NY). This paper presents some of the first data relative to the occurrence of PEG in the environment, especially in sediments where concentrations were generally higher (up to 1490 μg/kg) than those for other classes of targeted surfactants and their metabolites.

Tracking sewage derived contamination in riverine settings by analysis of synthetic surfactants

A study has been made of the presence and reactivity of the most commonly used surfactants, both anionic (linear alkylbenzene sulfonates, LAS, and alkyl ethoxysulfates, AES) and non-ionic (alcohol polyethoxylates, AEOs, and nonylphenol polyethoxylates, NPEOs), in water and surface sediments from the middle stretch of the Guadalete River in SW Spain (12 stations). Average values were between 0.1 and 3.7 mg kg(-1) in sediment, and between 0.2 and 37 μg L(-1) in water. The sorption of surfactants was dominated by hydrophobic mechanisms, so those homologues having longer alkyl chains (e.g. C(18)AEO) showed higher relative percentages and concentrations in sediments compared with water. Local and sharply higher concentrations of these compounds were observed at three sampling stations (7, 9 and 12), indicating the occurrence of wastewater discharges into the river. By analysing the distributions of different surfactant homologues and their metabolites we were able to distinguish between sewage contamination from sources discharging treated and untreated wastewaters. Upstream (stations 1-2), LAS concentrations were below 30 μg L(-1) and the composition of their degradation intermediates (sulfophenyl carboxylic acids, SPCs) (160 μg L(-1)) was dominated by short-chain homologues (C(6)-C(9)SPCs), indicating that the degradation of this surfactant is at an advanced stage. The highest concentration (487 μg L(-1)) of SPCs was detected near the effluent outlet of a sewage treatment plant (STP) (station 12). Sampling stations (7 and 9) affected by untreated wastewater discharges were the only ones showing the presence of the most reactive and biodegradable SPC isomers and homologues (e.g. C(11)SPC). Here, LAS reached the highest concentration values measured (>2 mg L(-1)), and showed a homologue distribution closer to that of commercial mixtures than LAS found at the other stations.

Anaerobic Degradation Pathway of Linear Alkylbenzene Sulfonates (LAS) in Sulfate-Reducing Marine Sediments

Linear alkylbenzene sulfonates (LAS) are among the principal synthetic surfactants used worldwide. Their presence in the environment has been reported in a significant number of studies, and it has been generally assumed that LAS are not biotransformed in the absence of oxygen. However, laboratory experiments performed by our group using anoxic marine sediments have reported LAS degradation percentages that can reach up to 79% in 165 days. Here, we show for the first time the initial reaction metabolites (generated via fumarate addition to the LAS molecules), their biotransformation into sulfophenyl carboxylic acids (SPC), and the progressive degradation of these by successive beta-oxidation reactions. Advanced mass spectrometry has been used to carry out the identification of these compounds. This is the first time that an anaerobic degradation pathway for LAS is described, and these results represent a significant advance in understanding the final fate of these and other similar compounds in anoxic environments.

Aerobic biodegradation of linear alkylbenzene sulfonates and sulfophenylcarboxylic acids for different salinity values by means of continuous assays

Aerobic biodegradation of linear alkylbenzene sulfonates (LAS) and sulfophenylcarboxylic acids (SPCs) in water, at different salinity values, has been studied. Three experiments have been carried out employing a staircase model system with continuous dosage of LAS to the system and using concentrations of LAS of the same order as those detected in littoral waters receiving urban wastewater discharges. LAS biodegradation was observed to be almost complete (showing a great extent), and in all cases exceeds 98.4%. At the very low concentration values of LAS utilized in the experiments, no significant variations in the biodegradation of LAS due to the effect of the different salinity values assayed were observed. The biodegradation intermediates detected for all the cases were sulfophenylcarboxylic acids with carboxylic chains of between five and 13 carbon atoms. The detection of C13-SPC (which is only produced by C13-LAS) confirms the existence of omega-oxidation. The total disappearance of SPCs in all cases indicates that mineralization of LAS at the concentrations tested was complete.

Oxidative stress and histopathology damage related to the metabolism of dodecylbenzene sulfonate in Senegalese sole

Surfactants such as linear alkylbenzene sulfonates (LAS) are widely utilised in the formulation of detergents in commercial products. After use, they pass through waste water treatment plants (WWTP) and are then discharged to aquatic ecosystems, causing risk to aquatic life. The exposure of marine animals to these compounds enhances the production of reactive oxygen species (ROS) with subsequent damage to macromolecules, and produces histological alterations. A flow-through experiment with Senegalese sole ( Solea senegalensis) has been devised with the object of correlating the metabolism of LAS including sulfophenylcarboxylic acids (SPCs) by fish with their antioxidant defence system (generation of oxyradicals) and histopathological damage. The generation of intermediate degradation products (SPCs) by the organism, the histopathological responses, the antioxidant enzymes (catalase (CAT), glutathione peroxidase (GPX), glutathione reductase (GR), and glutathione S-transferase (GST)), as well as other kinds of enzyme such as acid and alkaline phosphatases (AcP, ALP), were measured. SPCs from 5ØC 6 to 11ØC 12 were identified and quantified in fish and water; their concentrations differed depending on the sampling moment. In general, the responses found in the enzymes were slight: a decrease in the enzymatic activity in gills and activation in the digestive tract. The evidence of histopathological damage identified was also small; the organism’s defensive mechanism against pollutants should enable it to recover easily. A direct relationship was established between biotransformation and the generation of SPCs and ROS. In conclusion, the correct functioning of the antioxidant defence system with absence of large variations, the short-term histopathological damage, and the evidence of SPCs indicate an adequate metabolism of 2-phenyl-C 12-linear alkylbenzene sulfonates (2ØC 12LAS) by this specie and non-toxic effects at environmentally realistic levels.

Use of dynamic simulation to assess the behaviour of linear alkyl benzene sulfonates and their biodegradation intermediates (sulfophenylcarboxylic acids) in estuaries

Dynamic laboratory simulation of processes affecting chemical species in their transit through estuaries is a very useful tool to characterize these littoral systems. To date, laboratory studies concerning biodegradation and sorption (onto suspended particulate matter) of LAS in an estuary are scarce. For this reason, a dynamic automated estuarine simulator has been employed to carry out different experiments in order to assess the biodegradability of linear alkyl benzene sulfonates (LAS) and their biodegradation intermediates (sulfophenylcarboxylic acids, SPCs) using environmentally representative LAS concentrations in estuaries by a continuous injection of LAS into the system. During the experiments, a great affinity of LAS for the solid phase has been found, as well as an increased adsorption in line with increased chain length. On the other hand, the presence of SPCs with chain length between 6 and 13 carbon atoms was detected. Accumulation and persistence of medium chain length SPCs (C 6–C 8) along the experiments show that their degradation constitutes the limiting step for the process of LAS mineralization. In the final zone of the simulated estuarine system, the levels of SPCs were below the limits of detection. Thus, the disappearance of SPCs indicated that LAS biodegradation had been completed along the estuary. Similar results have been described for different Iberian littoral ecosystems. Therefore, the simulator employed in this research appears to be a useful tool to anticipate the behaviour of a xenobiotic chemical in its transit through littoral systems with different salinity gradients.

Determination of Sulfophenyl Carboxylic Acids in Agricultural Groundwater Samples by Liquid Chromatography with Fluorescence Detection

We have developed an analytical method to determine six sulfophenyl carboxylic acids (SPC) in agricultural groundwater samples. It involves a solid-phase extraction (SPE) procedure and subsequent separation and determination using liquid chromatography with fluorescence detection (LC–FD).The quantification limits ranged between 0.7 and 1.2 ng ml−1. The proposed method was proved satisfactorily for the detection and determination of these compounds in groundwater samples during a study into the biodegradation of linear alkylbenzene sulfonates (LAS) in an agricultural soil sampled from the irrigated plain to the west of Granada (Spain).

Determination of sulfophenyl carboxylic acids in agricultural groundwater samples by CE with ultraviolet absorption detection

An analytical method for the determination of six sulfophenyl carboxylic acids, namely (p-sulfophenyl)acetic, 2-(p-sulfophenyl)propionic, 2-(p-sulfophenyl)butyric, 3-(p-sulfophenyl)butyric, 4-(p-sulfophenyl)butyric, and 5-(p-sulfophenyl)valerianic acid, in agricultural irrigation water samples was developed. It involves an SPE procedure, an on-line preconcentration normal stacking mode and subsequent separation and determination using CE with UV detection (CE-UV). p-Sulfobenzoic acid was used as internal standard. The compounds were separated with an uncoated capillary and a 25 mM ammonium acetate/acetic acid buffer solution (pH 5.5) with 2-propanol (30% v/v) and 0.75 mM CTAB. Analyses were run at -25 kV, 25 degrees C, and 100 s of hydrodynamic injection with UV detection at 225 nm. Quantification limits found ranged between 4 and 6 ng/mL. The proposed method was validated using a recovery assay. It was satisfactorily used for the determination of these compounds in groundwater samples to track down the biodegradation of linear alkylbenzene sulfonates in an agricultural soil from the fertile plain of Granada (Spain).

Experimental determination of bioconcentration, biotransformation, and elimination of linear alkylbenzene sulfonates in Solea senegalensis

The bioconcentration, biotransformation, and elimination of anionic surfactants, linear alkylbenzene sulfonates (LAS), specifically 2ØC(10) and 2ØC(12) LAS, which are pure isomers from two different homologues, have been characterized in Solea senegalensis using an experimental flow-through system with environmental exposure levels. The LAS and their carboxylated metabolites, sulfophenylcarboxylic acids (SPCs), were analyzed by pressurized liquid extraction, followed by solid-phase extraction, liquid chromatography with fluorescence detection, and mass spectrometry. The bioconcentration factors obtained in the steady state were 17.2 +/- 1.2 L/kg for 2ØC(10) LAS and 386.5 +/- 31.5 L/kg for 2ØC(12) LAS. A kinetic study also was performed with 2ØC(12) LAS, and the rate constants of uptake and elimination were K(1) = 177.04 L/kg d and K(2) = 0.92/d, respectively. The formation of the intermediate degradation products was monitored during the 2ØC(10) LAS experiment, thus allowing, to our knowledge for the first time, the identification and quantification of SPCs from 5ØC(6) to 9ØC(10) in marine organisms and in the depuration water as a result of biotransformation by the organisms, diffusive elimination, and excretion. The elimination percentage of the surfactants is both time- and concentration-dependent, and this suggests the existence of a concentration limit for the surfactant in the fish below which the elimination processes are slow. Overall, LAS are not persistent bioaccumulative compounds at environmental exposure levels.

Monitoring the Primary Biodegradation of Linear Alkylbenzene Sulfonates and Their Coproducts in Anoxic Sediments Using Liquid Chromatography−Mass Spectrometry

An accompanying article has demonstrated the anaerobic degradation of the surfactant linear alkylbenzene sulfonate (LAS) in microcosms filled with marine sediments through the generation of sulfophenylcarboxylic acids (SPCs). A detailed study shows that this process was uniform in the blanks (non-spiked natural sediments) for every LAS homologue during the complete course of the experiment. However, when sediments were spiked with commercial LAS and, therefore, enriched with short-chain homologues, degradation was enhanced for these homologues until their percentages were close to those for non-spiked sediments. The reason is that short-chain homologues are more bioavailable due to their higher solubility and lower sorption capacity. Thus, sorption on sediments was found to be increased with the length of the alkyl chain for LAS homologues, following a linear Freundlich isotherm, whereas the metabolites generated were predominant in solution due to their much higher polarity. Intermediate-chain SPC homologues (C7-C9 SPCs) were the most abundant during the experiment, but a significant increase in the concentration of shorter-chain SPC homologues (C4-C6 SPCs) was detected toward the end. In the case of isomers, the steric effect of the aromatic group implies that LAS primary degradation took place preferentially over external isomers. Therefore, the generation of external isomers of SPCs was predominant during the complete experiment although internal isomers of SPCs became more evident when the degradation process had advanced and external isomers of LAS became scarce. The identity of both types of SPC isomer was confirmed by tandem mass spectrometry. With respect to LAS coproducts, the relative percentage of iso-LAS increased during the complete experiment and removal percentages for dialkyl tetralinsulfonates (<30%) were typically lower that those for LAS (66-79%), although a similar behavior was observed for their homologues in both cases.

Anaerobic Degradation of Linear Alkylbenzene Sulfonates in Coastal Marine Sediments

This research shows for the first time the degradation of linear alkylbenzene sulfonates (LAS) under anaerobic conditions, together with the presence of metabolites and the identification of microorganisms involved in this process. This compound is the most widely used surfactant and its main environmental concern is related to its persistence in the absence of oxygen as LAS accumulates in anaerobic sediments and sewage sludges. Laboratory experiments performed with anoxic marine sediments spiked with 10-50 ppm of LAS demonstrated, however, that its degradation reached 79% in 165 days via the generation of sulfophenyl carboxylic acids (SPCs). Almost all of the added LAS (>99%) was found to be attached to the sediment while the less hydrophobic SPCs were predominant in solution, as their concentration increased progressively up to 3 ppm during the full course of the experiment. Average half-life for LAS has been estimated to be 90 days, although higher values should be expected when the LAS concentration exceeds 20 ppm, due to inhibition of the microbial community. Sulfate-reducing and methanogenic activities proved to be intense during the experiment. Several sulfate-reducing bacteria and firmicutes/clostridia have been identified as possible candidates for effecting this degradation. Our results imply that the persistence of LAS in anoxic compartments, such as marine sediments, should be reconsidered when evaluating its environmental risk.

Testing organic solvents for the extraction from fish of sulfophenylcarboxylic acids, prior to determination by liquid chromatography-mass spectrometry

The present paper describes the use of different solvent mixtures to extract from fish various sulfophenylcarboxylic acids (SPCs of C(6) to C(13)), and their originating compounds, linear alkylbenzene sulfonates (LAS of C(10) to C(13)). The analytical method utilized involves pressurized liquid extraction, followed by preconcentration of the samples, purification by solid-phase extraction, and finally identification and quantification of the target compounds by high-performance liquid chromatography-mass spectrometry using a system equipped with an electrospray interface operating in negative ion mode. The SPCs and LAS were extracted from spiked fish first with hexane to remove interference from fats, then with different mixtures of solvents: dichloromethane followed by methanol; 50:50 dichloromethane-methanol; and 30:70 dichloromethane-methanol. The LAS recoveries obtained with these three extraction options were high (between 68.5 and 80.8%); however, owing to the low percentages obtained for SPC homologues (13.5, 13.1, and 15.9%, respectively), another extraction procedure with methanol was developed in order to increase these recoveries. The percentage of recovery for total SPCs with the methanolic extraction was higher (90.1%), with a standard deviation of 9.9, and the LAS recoveries also increased (99.9%). Detection limits were between 1 and 22 ng g(-1) for LAS, and between 1 and 58 ng g(-1) for SPCs. Quantitation limits were between 4 and 73 ng g(-1) for LAS, and between 2 and 193 ng g(-1) for SPCs. This method has been applied to measure the biotransformation of 2ØC(10) LAS (where Ø is a sulfophenyl group) in fish exposed in a flow-through system, and enabled the separation and identification of SPCs from 5ØC(6) to 9ØC(10).

Presence, biotransformation and effects of sulfophenylcarboxylic acids in the benthic fish Solea senegalensis

The presence of linear alkylbenzene sulfonates (LAS) and their degradation intermediates, sulfophenylcarboxylic acids (SPCs), with concentrations up to 100 ppb has been found in surface waters taken from the estuary of the river Guadalete (Cádiz, SW of Spain). Higher concentrations were found at the sampling site located adjacent to the discharge outlet of a wastewater treatment plant (WWTP). The concentrations decreased downstream to a few ppb as a result of dilution, sorption, and degradation processes, which were taking place along the estuary. Once the presence of both xenobiotics was confirmed in the environment, an in vivo assay was conducted to study their biotransformation and effects in the benthic fish Solea senegalensis. A flow-through system was employed, consisting of an exposure phase (120 h) with environmental levels of the surfactant (200, 500 and 800 μg/L of 2ØC 10LAS), followed by a depuration stage (72 h). The generation of SPCs has been quantified during these phases in both water and fish, with LAS biotransformation shown in all cases. The antioxidant enzymes catalase (CAT), glutathione peroxidase (GPX), glutathione reductase (GR), the phase II enzyme glutathione S-transferase (GST), and the phase III acid and alkaline phosphatases (AcP, ALP) were also estimated and utilized as biomarkers.

Development of a method for the simultaneous analysis of anionic and non-ionic surfactants and their carboxylated metabolites in environmental samples by mixed-mode liquid chromatography–mass spectrometry

A new methodology capable of performing the simultaneous analysis of the main surfactants – linear alkylbenzene sulfonates (LAS), alkyl ethoxysulfates (AES), alkyl sulfates (AS), nonylphenol polyethoxylates (NPEOs) and alcohol polyethoxylates (AEOs) – and their carboxylated metabolites – sulfophenyl carboxylic acids (SPCs) and alkylphenol ethoxycarboxylates (APECs) – in environmental samples has been developed for the first time. Extraction is carried out by solid-phase extraction (SPE) and pressurized liquid extraction (PLE) from water and sediment, respectively. Identification and quantification of the target compounds is performed using a liquid chromatography–mass spectrometry (LC–MS) system equipped with an electrospray interface (ESI) operating in mixed-mode. Optimization of parameters such as pH, ionic strength, temperature and solvents has been carried out in order to obtain recoveries in the range from 70 to 107% for most homologs, while the limits of detection are 0.05–0.5 ng mL −1 in water and 1–10 ng g −1 in sediment. The proposed methodology has been applied for the simultaneous determination of all the target compounds in samples taken from aquatic ecosystems in the SW of Spain. Values for LAS, AS, AES, NPEOs and AEOs are up to 38.7, 3.0, 2.9, 5.0 and 1.2 μg L −1 in waters, and in the ranges of 1.73–12.80, 0.11–0.24, 0.02–0.59, 1.94–2.70 and 0.64–3.64 mg kg −1 in sediments, respectively. The highest concentrations of metabolites found in water are 149.6 μg L −1 of SPCs and 3.9 μg L −1 of APECs.