Photodegradation is a major degradation mechanism for many environmental contaminants, both in indoor environments as well as in outdoor environments, and many of the contaminants are persistent and toxic. However, there is a lack of knowledge about the exact degradation process for many of them. It is important to not only monitor and study environmental contaminants that are commonly found. But it is also important to be able to identify their degradation products, however, due to lack of standards there is a difficulty to conduct identification. There is also the drawback with most spectral libraries used for identification being recorded at low resolution, when new instruments are being developed for using high resolution. This makes it challenging to identify compounds with spectral peaks that differ only slightly in their mass-to-charge ratio (m/z). Thus, the aim of this study was to determine potential degradation products from different compounds commonly found in indoor environments and then add these findings to a spectral library for high resolution mass spectrometry. This was conducted by first exposing the standards to ultraviolet (UV) light, and then the chemical analysis was performed using a gas chromatography coupled with a high resolution mass spectrometer. All data was then processed in different software in order to determine potential products. Many of the compounds did not indicate any degradation using the experimental settings, and for some not even the parent compound could be identified. In total, four potential degradation products were found in this study; degradation products were identified for hexabromobenzene (HBB) with penta-, tetra-, and tribromobenzene, as well as one potential product for 2-ethylhexyl-2,3,4,5-tetrabromobenzoate (EHTBB).

No description available.

No description available.

Although wastewater treatment plants are a line of defense in minimizing indiscriminate output of microconstituents to natural waters, we do not possess a fundamental understanding of the mechanisms involved in microconstituent removal during wastewater treatment. With this in mind, experiments were designed to investigate the factors that can influence the fate of four microconstituents, carbamazepine (CBZ), 17alpha-ethinylestradiol (EE2), iopromide (IOP), and trimethoprim (TMP), during biological suspended culture treatment. Specifically, the role that various ecological members of biological treatment systems play in biotransforming these compounds was evaluated. Sorption assays were performed with inactivated biomass samples (ammonia oxidizing bacteria (AOB), laboratory enriched heterotrophic cultures free of active nitrifiers with low (Ox⁻) or high (Ox⁺) oxygenase activity, and a nitrifying activated sludge (NAS) from a full-scale wastewater treatment plant) to determine whether partitioning dictates removal of individual microconstituents. No microconstituents sorbed to the AOB culture. Neither CBZ nor IOP sorbed to Ox⁻, Ox⁺ and NAS cultures; however, EE2 and TMP sorbed to the Ox⁻, Ox⁺ and NAS biomass. Sorption was positively influenced by the presence of exopolymeric substances (EPS) associated with the cultures. The protein content of EPS affected EE2 and TMP sorption more appreciably than the polysaccharide content of EPS. Further experiments were performed to investigate microconstituent biodegradation by AOBs, Ox⁻ and Ox⁺ cultures. The influence of growth state and oxygenase activity on biotransformation by each culture was also evaluated. Results indicate that EE2 was the only microconstituent that was amenable to biotransformation by batch cultured AOB and heterotrophic cultures. EE2 was biotransformed but not mineralized by AOB chemostat and batch cultures. TMP was not transformed by AOB batch or chemostat cultures; however both EE2 and TMP were transformed by Ox⁻ and Ox⁺ chemostat cultures. Radiolabeled studies showed that EE2 was mineralized by this culture. Kinetically, AOBs dominated EE2 transformation to monohydroxylated metabolites; however, both Ox⁻ and Ox⁺ cultures further degraded and mineralized EE2 and metabolites generated by AOBs. These results indicate that biotransformation of EE2 by NAS may be limited by heterotrophic activity whereas TMP fate may be a function of heterotrophic activity only. Oxygenase activity did not limit EE2 or TMP biotransformation in chemostat cultures. Subsequent experiments that were performed to identify the factors that influence heterotrophic degradation of EE2 and TMP indicated that the presence of readily biodegradable substrates slows EE2 and TMP biotransformation. The impact of slowly biodegradable substrates like EPS on EE2 and TMP degradation was unclear. These results suggest that EE2 and TMP are most amenable to biodegradation in bioreactors where endogenous conditions dominate. / Ph. D.

De nombreuses familles de polluants organiques en provenance de différentes sources se retrouvent dans les milieux aquatiques continentaux et littoraux. Ces molécules, dont les lipophiles et les persistantes, sont souvent présentes à l'état de trace dans la fraction dissoute. L'utilisation de compartiments concentrateurs comme les sédiments rend alors plus accessible l'évaluation des concentrations ambiantes du milieu. L'objectif de la thèse a été d'évaluer l'exposition en zones côtières aux différentes familles de contaminants organiques « émergents » incluant les filtres UV, les alkylphénols et les alkylphénols polyéthoxylés, ainsi que « persistants-classiques » incluant les hydrocarbures aromatiques polycycliques et les polychlorobiphényles dans les sédiments et, éventuellement, dans les eaux. Un important effort de recherche a été accordé à l'étude des variations spatiales et temporelles des contaminants sélectionnés dans les sédiments, permettant ainsi l'acquisition d'un premier jeu de données nationales (libanais) représentatif pour ces familles de contaminants.Trois rivières en Méditerranée orientale et leur environnement côtier ont été pris comme cas d'étude en plus de la côte d'une petite ville et ses sites portuaires qui ont été sélectionnés afin de compléter l'étude en milieu côtier. Un premier aperçu des niveaux de ces contaminants hydrophobes dans les zones côtières recevant des apports typiques de la Méditerranée orientale est ainsi fourni. Les résultats des analyses chimiques ont clairement montré l'impact des rejets des effluents non traités dans les zones côtières via les entrées des rivières et les déversements directs le long de la côte, en absence des activités récréatives (pour les filtres UV) et de rejets industriels (pour les alkylphénols et les alkylphénols polyéthoxylés). Les zones de transition peuvent être à l'origine de la contamination de l'environnement côtier des trois rivières par ces polluants émergents en absence des apports marins. Des concentrations élevées en hydrocarbures aromatiques polycycliques et en polychlorobiphényles ont été mesurées dans les sédiments prélevés en milieu côtier. Cette contamination a persisté des années après la marée noire qui a envahi la côte Est-Méditerranéenne en 2006. Nos résultats globaux indiquent que les concentrations mesurées dans les sédiments des trois rivières étudiées et du littoral peuvent être classées parmi les niveaux les plus élevés détectés dans le pourtour du bassin méditerranéen et pouvant induire des effets toxiques chez le biota aquatique.Ce travail peut être d'une importance primordiale pour la région Est-Méditerranéenne, et plus particulièrement pour le Liban, un pays qui, malgré d'être parmi les signataires de la convention de Barcelone pour la protection de la mer Méditerranée et qui est, par la suite, impliqué dans la surveillance de la qualité de son milieu marin, souffre jusqu'à présent des rejets de différents types d'effluents non traités le long de ces côtes en absence des stations d'épuration. / Many organic pollutants issued from different sources are present into freshwater and coastal waters. Since these lipophilic contaminants are present at trace levels in water, accumulator compartments such as sediments can be used to assess their concentration in aquatic systems. The objective of the thesis was to assess the exposure in coastal areas to the various families of organic contaminants namely "emerging pollutants" including UV filters, alkylphenols, alkylphenol polyethoxylates, and "persistent pollutants" including polycyclic aromatic hydrocarbons and polychlorinated biphenyls in sediments and water. A major research effort has been given to the investigation spatial and temporal dynamics of the selected pollutants in sediment, allowing the acquisition of a first set of national data (Lebanese).Three rivers and their coastal environment in the eastern Mediterranean have been taken as a case study in addition to the small coastal city that was selected to complete the study in the coastal environment. A first overview of the levels of these hydrophobic contaminants in coastal areas receiving typical eastern Mediterranean inputs is thus provided. The results of chemical analyzes have clearly shown the impact of discharges of untreated effluents into coastal areas via inputs from rivers and direct discharges along the coast, without recreational activities (for UV filters) and industrial effluents discharges (for alkylphenols and alkylphenol polyethoxylates). Transition zones may act like a source of contamination of the three rivers coastal environment in the absence of marine inputs. Elevated concentrations of polycyclic aromatic hydrocarbons and polychlorinated biphenyls were measured in sediments in coastal environments. This contamination has persisted for years after the oil spill that has invaded the Mediterranean coast in 2006. Our overall results indicate that concentrations in sediments of the three studied rivers and the coastline can be classified among the highest levels detected in the Mediterranean basin and may induce toxic effects in aquatic biota.This work may be of paramount importance for the East-Mediterranean region, and particularly for Lebanon, a country which, despite being a signatory to the Barcelona Convention for the Protection of the Mediterranean Sea and is, subsequently involved in monitoring the quality of its marine environment, suffers far different types of discharges of untreated effluent along its coast in the absence of wastewater treatment plants.

Contaminated land is a widespread, global issue affecting millions of people. Atrazine is a commonly used herbicide which often contaminates groundwater and drinking water supplies and is associated with adverse health outcomes. Biochar is the solid product of pyrolysis and is associated with several environmental benefits. It may be an effective remediation tool when used as a soil amendment. This thesis investigates the mechanisms through which biochar can immobilise atrazine, and the implications of the mechanisms for remediating contaminated land. Nine biochar samples were obtained from the United Kingdom Biochar Research Centre , which were produced from softwood pellets (SWP), wheat straw pellets (WSP), miscanthus straw pellets (MSP), rice husk (RH) and oil seed rape (OSR) each at pyrolysis temperatures of 550°C and 700°C (excluding OSR at 700°C). The sorption mechanisms controlling atrazine sorption to these biochars were determined through various characterisation methods and batch sorption experiments. The sorption tests showed that sorption to each of the standard biochars occurs via multiple simultaneously occurring mechanisms, which are each promoted under certain conditions. Studies investigating sorption kinetics, isotherms and interactions with humic acids showed that for all biochars in this study, pore filling was a significant process through which atrazine is transported to adsorption sites, although poor intraparticle diffusion for softwood and oil seed rape biochars can prevent efficient transport. Wheat straw and rice husk biochars showed effective pore diffusion, resulting in high sorption capacities. Partitioning was associated with poor remediation outcomes and was significant to softwood biochars, although adsorption dominated overall sorption for all other biochars. pH was shown to significantly influence the occurrence of various sorption mechanisms. At low pH values, most biochars showed evidence of electrostatic repulsion between positive atrazine species and the positively charged biochar surface. At intermediate pH values, all biochars showed strong hydrogen bonding between H+ groups on the surface of the biochar and atrazine. A meta-analysis of previous relevant studies provided further evidence for hydrogen bonding of atrazine to biochar and showed that hydrophobic effects likely play little role in adsorption after accounting for the effects of surface area. Varying contributions of π-π EDA interactions, hydrogen bonding involving biochar O- groups, and interactions with ash minerals resulted in different sorption profiles for each biochar at high pH values. In order to further determine the mechanisms controlling sorption at high pH, surface compositions of SWP550, RH700 and OSR550 biochars were modified using hydrofluoric acid. Modification with hydrofluoric acid successfully removed the ash contents of rice husk and oil seed rape biochars and reduced atrazine removal at high pH values. This suggested that the ash fraction increases atrazine removal at high pH through complexation or catalytic hydrolysis. The roles of the various mechanisms are related to remediation outcomes in a novel manner allowing for the improved design of biochar for environmental remediation.

O lodo de esgoto, também denominado biossólido, depois de tratado adequadamente, constitui fonte de matéria orgânica, micro e macro-nutrientes para o crescimento das plantas. A aplicação do lodo de esgoto no solo pode trazer benefícios tais como: distribuição em áreas para produção agrícola, recuperação de solos perdidos por erosão, aplicação em áreas de reflorestamento. Os lodos de esgotos, entretanto, são resíduos que contem patógenos, metais pesados, e poluentes orgânicos, entre estes os compostos orgânicos voláteis (COVs). A resolução CONAMA nº 375 em vigor no Brasil, assim como as regulamentações de outros países, não exigem valores limites para alguns COVs considerados prioritários. Uma base de dados sobre COVs em lodos de esgoto é necessário para estabelecer valores limites nos lodos usados para fins agrícolas. O presente trabalho evidenciou a presença de COVs em concentrações significativas nas amostras de lodo coletadas nas Estações de Tratamento de Esgoto (ETE) na Região Metropolitana de São Paulo (RMSP), Jundiaí, Vinhedo e Americana. Na ETE da RMSP foram encontrados vários COVs em concentrações significativas. Dentre os COVs identificados, apenas 1,4-diclorobenzeno e naftaleno apresentam valores permitidos em solo agrícola (390 e 120 µmg/kg, respectivamente) e valores de concentrações muito acima desses limites foram encontrados para as amostras de lodo da ETE de RMSP (845 a 2037 e 901 a 5670 µmg/kg, respectivamente). Os resultados obtidos neste trabalho, embora não forneçam dados suficientes para uma imediata tomada de decisão, permitem fornecer subsídios técnicos para iniciar uma base de dados sobre COVs em lodo de esgoto que, futuramente, utilizando-se metodologias adequadas, será útil para se realizar uma revisão das regulamentações vigentes para lodo de esgoto com finalidade agrícola. / The sewage sludge also entitled biosolid, after adequate treatment, is source of organic matter, micro and macronutrients for plants growth. The application of sewage sludge in soil may provide some benefits like: distribution in areas for agricultural production, recovery of degraded soil by erosion, application in areas of reforestation. However, sewage sludges are residues that contain phatogens, heavy metals, organic pollutants, such as volatile organic compounds (VOCs). The current resolution in Brazil (CONAMA nº 375), as well as regulations from other countries do not establish acceptable levels for some priority VOCs. It is necessary to establish data a base related to VOCs in sewage sludge for agricultural use to be able to present acceptable levels of them. The present work reports the presence of VOCs at significant levels in sewage sludge samples collected at sewage treatment stations (ETE) in the Metropolitan Region of São Paulo city (RMSP), Jundiaí, Vinhedo and Americana. Among VOCs identified, only 1,4 dichlorobenzene and naphthalene are regulated for use in agricultural soil (390 and 120 µg/kg, respectively) and levels found for sewage sludge samples from RMSPETE were higher than those regulated limits (845 to 2037 and 901 to 5670 µg/kg, respectively). Although results obtained in this study do not provide enough data for an immediate decision, results will be useful to start a data base regarding to VOCs in iv sewage sludge for agricultural use that, using adequate methodologies, will permit a review of current regulations on VOCs for agricultural use.

Du fait du coût élevé de certains matériaux adsorbants d’intérêt pour le traitement de la micropollution organique, l’étude a porté sur la régénération de matériaux adsorbants de type zéolithes hydrophobes et monolithe de carbone dans le cas de l’adsorption du bisphénol A et du diclofénac comme micropolluants réfractaires. Des procédés d’oxydation avancée impliquant des espèces radicalaires HO• (réaction de Fenton, électro-Fenton) et SO₄• – (activation de persulfate par voie thermique) ont été utilisés pour assurer la régénération des matériaux par désorption et dégradation oxydative des polluants fixés. La production de radicaux HO• au sein de la phase aqueuse circulant au niveau de l’adsorbant n’est pas suffisamment efficace pour sa régénération. Il a donc été envisagé de générer les radicaux au plus près des molécules adsorbées. Au cours de ce travail, une méthode sensible d’analyse par polarographie de H₂O₂ a été développée et validée pour le suivi des expériences avec les procédés mettant en jeu la réaction de Fenton. Pour différentes zéolithes, le catalyseur de la réaction de Fenton à base de fer a été incorporé préalablement dans la zéolithe. Pour le monolithe de carbone, les propriétés de conduction du matériau ont été mises à profit en l’utilisant comme cathode pour l’application du procédé électro-Fenton permettant de produire les radicaux HO• directement au sein du matériau. Cela a conduit à améliorer les performances de la régénération avec toutefois une diminution de son efficacité au cours de cycles successifs adsorption/régénération. / The elimination of organic micropollutants often requires the use of adsorption processes among the water treatments. The aim of our study is to regenerate two expensive materials (hydrophobic zeolites and carbon monoliths) to increase their life expectancy and decrease their investing cost. Two organic contaminants were targeted : diclofenac and bisphenol A, which are refractory pollutants. Advanced oxidation processes involve radical species, HO• (Fenton and electro-Fenton reactions) and SO₄• – (thermal activation of persulfate ion). These oxidants were used to decompose the adsorbed pollutants and thus regenerate the adsorbents. The HO• production, within the core of aqueous phase, did not reach satisfactory regeneration, and a loss of adsorption capacity was observed. Furthermore, during this study, a sensitive polarographic analytical method was developed and validated for the quantification of H₂O₂ in the aqueous phase. This method was used to follow in situ the Fenton reaction. The location of the catalyst in a closer vicinity of the adsorbed species was then optimized and the iron catalyst was impregnated in the host, prior to the adsorption, on different types of hydrophobic zeolites. Concerning carbon monolith, the electro-Fenton process was carried out using the material as the cathode thanks to its electrical conductivity. Consequently, HO• are produced in the porosity of monolith. This latter property enhanced the degradation of adsorbed solutes. The overall performances were increased compared to the homogeneous Fenton process. Nonetheless, a decrease of the adsorption capacities with adsorption-regeneration cycles was observed.

Conselho Nacional de Desenvolvimento Científico e Tecnológico / The presence of organic contaminants in the environment and in food have become a major concern due to the harmful effects to living organisms. Such contaminants may be pesticides used in agriculture for the control of pests, transformation products formed in the environment or through chemical processes, such as water treatment, and more recently pharmaceuticals and personal care products. Therefore, it is necessary to use sample preparation procedures and detection systems able to detect a variety of organic contaminants in trace level present in complex matrices, such as food and environmental samples. Thus, this study aims to: (1) address the use of high resolution mass spectrometry (HRMS) for the identification and quantification of organic contaminants in fish fillet using two acquisition data modes (full scan and all ions MS/MS) and to optimize QuEChERS method as sample preparation (PAPER 1); (2) present a second quantitative application of the use of QuEChERS method and HRMS for fruit samples (apple, pear and grape) in full scan mode, as well as to apply the proposed method for commercial fruit samples (PAPER 2) and (3) optimize and use QuEChERS method for extracting ionophore antimicrobials in poultry litter, followed by its quantification by LC-MS/MS and identification of transformation products by LC-QToF/MS after three different composting processes (PAPER 3). The three papers presented the importance of sample preparation optimization, QuEChERS, in order to obtain proper recovery of organic contaminants, besides to minimize the matrix effects caused by interferences in the extract. As the use of HRMS, which proved to be a very effective analytical tool for combining high resolution and mass accuracy, for identification and quantification of target organic contaminants, transformation products and metabolites in complex matrices using a rapid chromatographic run. / A presença de contaminantes orgânicos no meio ambiente e em alimentos têm se tornado uma grande preocupação devido aos efeitos nocivos aos seres vivos. Tais contaminantes podem ser desde agrotóxicos empregados na agricultura para o controle de pragas, produtos de transformação formados no meio ambiente ou através de processos químicos, como o tratamento de água, e mais recentemente fármacos e produtos de cuidado pessoal. Com isso, tem-se a necessidade de empregar procedimentos de preparo de amostra e sistemas de detecção capazes de detectar uma variedade de contaminantes orgânicos em nível de traços presentes em matrizes complexas como alimentos e amostras ambientais. Portanto, o presente trabalho tem como objetivos: (1) abordar o emprego da espectrometria de massas de alta resolução (HRMS) para a identificação e quantificação de contaminantes orgânicos em filé de peixe utilizando dois modos de aquisição de dados (full scan e all ions MS/MS) e otimizar o método QuEChERS para o preparo da amostra (ARTIGO 1); (2) apresentar uma segunda aplicação quantitativa do uso de QuEChERS e HRMS para amostras de frutas (maçã, pera e uva) no modo full scan, bem como aplicar o método proposto em amostras reais de frutas (ARTIGO 2) e (3) otimizar e empregar o método QuEChERS para a extração de antimicrobianos ionóforos em cama de frango, seguido de quantificação por LC-MS/MS e identificação de produtos de transformação por LC-QToF/MS após três diferentes processos de compostagem (ARTIGO 3). Os três artigos apresentados abordam a importância da otimização do procedimento de preparo de amostra, QuEChERS, a fim de obter recuperação adequada de contaminantes orgânicos, além de minimizar os efeitos de matriz causados pelos interferentes presentes no extrato. Assim como o uso de HRMS, a qual demonstrou ser uma ferramenta analítica bastante eficiente, por combinar alta resolução e exatidão de massa, para identificação e quantificação de contaminantes orgânicos alvo, produtos de transformação e metabólitos em matrizes complexas utilizando uma análise cromatográfica rápida.

O lodo de esgoto, também denominado biossólido, depois de tratado adequadamente, constitui fonte de matéria orgânica, micro e macro-nutrientes para o crescimento das plantas. A aplicação do lodo de esgoto no solo pode trazer benefícios tais como: distribuição em áreas para produção agrícola, recuperação de solos perdidos por erosão, aplicação em áreas de reflorestamento. Os lodos de esgotos, entretanto, são resíduos que contem patógenos, metais pesados, e poluentes orgânicos, entre estes os compostos orgânicos voláteis (COVs). A resolução CONAMA nº 375 em vigor no Brasil, assim como as regulamentações de outros países, não exigem valores limites para alguns COVs considerados prioritários. Uma base de dados sobre COVs em lodos de esgoto é necessário para estabelecer valores limites nos lodos usados para fins agrícolas. O presente trabalho evidenciou a presença de COVs em concentrações significativas nas amostras de lodo coletadas nas Estações de Tratamento de Esgoto (ETE) na Região Metropolitana de São Paulo (RMSP), Jundiaí, Vinhedo e Americana. Na ETE da RMSP foram encontrados vários COVs em concentrações significativas. Dentre os COVs identificados, apenas 1,4-diclorobenzeno e naftaleno apresentam valores permitidos em solo agrícola (390 e 120 µmg/kg, respectivamente) e valores de concentrações muito acima desses limites foram encontrados para as amostras de lodo da ETE de RMSP (845 a 2037 e 901 a 5670 µmg/kg, respectivamente). Os resultados obtidos neste trabalho, embora não forneçam dados suficientes para uma imediata tomada de decisão, permitem fornecer subsídios técnicos para iniciar uma base de dados sobre COVs em lodo de esgoto que, futuramente, utilizando-se metodologias adequadas, será útil para se realizar uma revisão das regulamentações vigentes para lodo de esgoto com finalidade agrícola. / The sewage sludge also entitled biosolid, after adequate treatment, is source of organic matter, micro and macronutrients for plants growth. The application of sewage sludge in soil may provide some benefits like: distribution in areas for agricultural production, recovery of degraded soil by erosion, application in areas of reforestation. However, sewage sludges are residues that contain phatogens, heavy metals, organic pollutants, such as volatile organic compounds (VOCs). The current resolution in Brazil (CONAMA nº 375), as well as regulations from other countries do not establish acceptable levels for some priority VOCs. It is necessary to establish data a base related to VOCs in sewage sludge for agricultural use to be able to present acceptable levels of them. The present work reports the presence of VOCs at significant levels in sewage sludge samples collected at sewage treatment stations (ETE) in the Metropolitan Region of São Paulo city (RMSP), Jundiaí, Vinhedo and Americana. Among VOCs identified, only 1,4 dichlorobenzene and naphthalene are regulated for use in agricultural soil (390 and 120 µg/kg, respectively) and levels found for sewage sludge samples from RMSPETE were higher than those regulated limits (845 to 2037 and 901 to 5670 µg/kg, respectively). Although results obtained in this study do not provide enough data for an immediate decision, results will be useful to start a data base regarding to VOCs in iv sewage sludge for agricultural use that, using adequate methodologies, will permit a review of current regulations on VOCs for agricultural use.