A exposição ambiental aos poluentes orgânicos persistentes tem recebido amplo destaque na literatura recentemente devido à extensa associação entre o desenvolvimento de doenças metabólicas, obesidade e/ou diabetes mellitus, e a presença destes poluentes, principalmente os organoclorados, como as bifenilas policloradas (PCBs), no organismo. Por outro lado, os mecanismos de ação destes poluentes é controverso devido à elevada quantidade de representantes destas classes, gerando diversidade de protocolos de exposição e escassez de estudos experimentais. Por isto, foi objetivo deste trabalho elucidar os mecanismos de ação tóxica do PCB126, nas doses de 0,1; 1 ou 10 µg/kg de massa corpórea, em ratos Wistar machos, durante quinze dias, expostos por instilação intranasal. O procotolo de exposição empregado foi caracterizado e considerado suficiente para causar toxicidade, uma vez que foram observadas alterações no sistema imune, metabolismo e em parâmetros relacionados à gênese do diabetes mellitus. A caracterização da exposição foi determinada pela quantificação da concentração de PCB126 no fígado e pulmão (CG/MS) e pelo aumento da expressão do receptor aril hidrocarboneto (AhR) no rim, fígado, pulmão e tecido adiposo (Western Blot). O efeito imunossupressor do PCB126 foi evidenciado pelo comprometimento da produção de células na medula óssea e, consequentemente, no número de células totais no sangue circulante. Adicionalmente, foi evidenciada a interferência do poluente na via de ativação mediada por receptores acoplados à proteína G (GPCRs), principalmente em neutrófilos, alterando importantes funções destas células, como a expressão de moléculas de adesão, geração de espécies reativas de oxigênio e migração. Entre as alterações metabólicas observadas, destacamos o aumento dos níveis de triglicerídeos e colesterol sérico, aumento da liberação de ácidos graxos livres; aumento da atividade da enzima hepática gama glutamil transferase; aumento da resistência à insulina e aumento da geração de óxido nítrico pelas ilhotas de Langerhans, dados estes, possivelmente relacionados ao comprometimento das células beta (β) pancreáticas, confirmados pelo aumento da expressão de GLUT4 no tecido adiposo, aumento da concentração de insulina sérica e aumento do estresse oxidativo nas ilhotas de Langerhans. Em conjunto, os dados obtidos destacam importantes alterações causadas pela exposição intranasal ao PCB126, evidenciando a participação do poluente na gênese do diabetes mellitus do tipo II. / The environmental exposure to persistent organic pollutants has been widely highlighted in recent literature due to the extensive association between the development of metabolic diseases, obesity and/or diabetes mellitus, and presence of these pollutants, especially organochlorines such as polychlorinated biphenyls (PCBs) in organism. Moreover, the mechanisms of action of these pollutants are controversial due to the high number of PCBs congeners, diversity of exposure protocols and lack of experimental studies. Therefore, the aim of this study was to elucidate the mechanisms of PCB126\'s toxic action at doses of 0.1; 1 or 10 µg/kg body weight in male Wistar rats exposed by intranasal instillation for 15 days. The established exposure procotol was characterized and considered sufficient to cause toxicity since changes were observed in the immune system, metabolism and in parameters related to the pathogenesis of diabetes mellitus. Characterization of exposure was determined by quantifying the concentration of PCB126 in liver and lung (GC-MS) and by the increased expression of aryl hydrocarbon receptor (AhR) in kidney, liver, lung, and adipose tissue (Western blot). The immunosuppressive effect of PCB126 was evidenced by impairment of cell production in the bone marrow and thus the total number of cells in the circulation. In addition, the interference of the pollutant in the activation pathway mediated by G-protein coupled receptors (GPCRs), in particular in neutrophils, was observed by changing important functions of these cells such as the expression of adhesion molecules, reactive oxygen species generation, and migration. Among the metabolic changes observed, we highlight the increased levels of triglycerides and serum cholesterol, increased release of free fatty acids; increased gamma glutamyl transferase hepatic enzyme activity; increased insulin resistance and increased generation of nitric oxide by the islets of Langerhans, these data possibly related to the impairment of beta cells (β) pancreatic function, suggested by the increased expression of GLUT4 in adipose tissue, increased serum insulin concentration and increased oxidative stress in the islets of Langerhans. Altogether, these results highlight important changes caused by intranasal exposure to PCB126, suggesting participation of the pollutant in the genesis of diabetes mellitus type II.

A exposição ambiental aos poluentes orgânicos persistentes tem recebido amplo destaque na literatura recentemente devido à extensa associação entre o desenvolvimento de doenças metabólicas, obesidade e/ou diabetes mellitus, e a presença destes poluentes, principalmente os organoclorados, como as bifenilas policloradas (PCBs), no organismo. Por outro lado, os mecanismos de ação destes poluentes é controverso devido à elevada quantidade de representantes destas classes, gerando diversidade de protocolos de exposição e escassez de estudos experimentais. Por isto, foi objetivo deste trabalho elucidar os mecanismos de ação tóxica do PCB126, nas doses de 0,1; 1 ou 10 µg/kg de massa corpórea, em ratos Wistar machos, durante quinze dias, expostos por instilação intranasal. O procotolo de exposição empregado foi caracterizado e considerado suficiente para causar toxicidade, uma vez que foram observadas alterações no sistema imune, metabolismo e em parâmetros relacionados à gênese do diabetes mellitus. A caracterização da exposição foi determinada pela quantificação da concentração de PCB126 no fígado e pulmão (CG/MS) e pelo aumento da expressão do receptor aril hidrocarboneto (AhR) no rim, fígado, pulmão e tecido adiposo (Western Blot). O efeito imunossupressor do PCB126 foi evidenciado pelo comprometimento da produção de células na medula óssea e, consequentemente, no número de células totais no sangue circulante. Adicionalmente, foi evidenciada a interferência do poluente na via de ativação mediada por receptores acoplados à proteína G (GPCRs), principalmente em neutrófilos, alterando importantes funções destas células, como a expressão de moléculas de adesão, geração de espécies reativas de oxigênio e migração. Entre as alterações metabólicas observadas, destacamos o aumento dos níveis de triglicerídeos e colesterol sérico, aumento da liberação de ácidos graxos livres; aumento da atividade da enzima hepática gama glutamil transferase; aumento da resistência à insulina e aumento da geração de óxido nítrico pelas ilhotas de Langerhans, dados estes, possivelmente relacionados ao comprometimento das células beta (β) pancreáticas, confirmados pelo aumento da expressão de GLUT4 no tecido adiposo, aumento da concentração de insulina sérica e aumento do estresse oxidativo nas ilhotas de Langerhans. Em conjunto, os dados obtidos destacam importantes alterações causadas pela exposição intranasal ao PCB126, evidenciando a participação do poluente na gênese do diabetes mellitus do tipo II. / The environmental exposure to persistent organic pollutants has been widely highlighted in recent literature due to the extensive association between the development of metabolic diseases, obesity and/or diabetes mellitus, and presence of these pollutants, especially organochlorines such as polychlorinated biphenyls (PCBs) in organism. Moreover, the mechanisms of action of these pollutants are controversial due to the high number of PCBs congeners, diversity of exposure protocols and lack of experimental studies. Therefore, the aim of this study was to elucidate the mechanisms of PCB126\'s toxic action at doses of 0.1; 1 or 10 µg/kg body weight in male Wistar rats exposed by intranasal instillation for 15 days. The established exposure procotol was characterized and considered sufficient to cause toxicity since changes were observed in the immune system, metabolism and in parameters related to the pathogenesis of diabetes mellitus. Characterization of exposure was determined by quantifying the concentration of PCB126 in liver and lung (GC-MS) and by the increased expression of aryl hydrocarbon receptor (AhR) in kidney, liver, lung, and adipose tissue (Western blot). The immunosuppressive effect of PCB126 was evidenced by impairment of cell production in the bone marrow and thus the total number of cells in the circulation. In addition, the interference of the pollutant in the activation pathway mediated by G-protein coupled receptors (GPCRs), in particular in neutrophils, was observed by changing important functions of these cells such as the expression of adhesion molecules, reactive oxygen species generation, and migration. Among the metabolic changes observed, we highlight the increased levels of triglycerides and serum cholesterol, increased release of free fatty acids; increased gamma glutamyl transferase hepatic enzyme activity; increased insulin resistance and increased generation of nitric oxide by the islets of Langerhans, these data possibly related to the impairment of beta cells (β) pancreatic function, suggested by the increased expression of GLUT4 in adipose tissue, increased serum insulin concentration and increased oxidative stress in the islets of Langerhans. Altogether, these results highlight important changes caused by intranasal exposure to PCB126, suggesting participation of the pollutant in the genesis of diabetes mellitus type II.

Type 2 diabetes has reached epidemic proportions in adults and youths. Persistent organic pollutants and endocrine-disrupting chemicals (EDCs), such as pesticides, dioxins, and organochlorines, are omnipresent and persist in the environment with potential for human exposure via contaminated air, waterways, soil, and human food supply. EDCs have been correlated with diabetes incidence and risks. Residential proximity to hazardous waste sites (HWS) has been correlated with increased hospital admission rates for diabetes. The study used a sample population (N = 1,724), ages ≥ 12 years from the 2005-2012 Continuous NHANES and HWS data from the National Priorities List of Superfund Sites. The ecosocial theory of disease distribution, and geocoordinates provided theoretical support. Mann-Whitney U test and binary logistic regression analysis were used to investigate the relationship between residence ≤ 1 mile compared with residence >1 mile from a HWS in NHANES surveyed counties of NJ, PA, NY, and CA on the outcome abnormal A1c ≥ 5.7% while controlling the effect of the moderators: abnormal body mass index (BMI), age, sex, and race/ethnicity on the relationship. Participants with a BMI ≥ 28.95 kg/m2 were 1.8 times and persons ≥ 58 years of age were 2.1 times more likely to have an A1c ≥ 5.7%. Also, non-Hispanic Whites residing >1 mile of a HWS had 82.1 % reduced risk of abnormal A1c compared with the same group residing ≤ 1 mile of a HWS. The results forge opportunities for future studies to consider border distance between residence and HWS. In addition, the results may promote positive social change through diabetes risks education, environmental health education, and practices and raise dialogue about social justice and the geographic distribution of hazardous waste sites.

L’objectif de cette thèse est le diagnostic de l’état de santé de la lagune de Bizerte par une approche multi-marqueurs (chimique, biochimique et morphométrique) et multi-compartiments (sédiment et biote). Pour atteindre cet objectif, les modèles biologiques choisis sont la moule Mytilus galloprovincialis et le poisson gobie Zosterisessor ophiocephalus. Ces deux espèces sont largement répandues dans la lagune de Bizerte et la mer Méditerranée. Dans une première partie et afin d’estimer les niveaux de contamination de la lagune de Bizerte par les polluants organiques persistants (POPs), des analyses chimiques, granulométriques et minéralogiques (COT) de sédiments superficiels ont été réalisées. Par la suite la toxicité potentielle des sédiments a été évaluée par une batterie de bioessais. Dans une troisième partie la biodisponibilité et l’impact écotoxicologique des POPs étudiés ont été évalués par l’accumulation de ces contaminants au niveau des deux organismes indicateurs choisis et l’étude des réponses biologiques associées à travers quelques biomarqueurs tels que la catalase (CAT), l’acide thiobarbiturique (TBARS); l’Ethoxyrésorufine O-dééthylase (EROD); la glutathion-S-transférase (GST) et l'acétylcholinestérase (AChE). Les principaux résultats des analyses chimiques révèlent une contamination générale des sédiments et organismes étudiés par les POPs. Les niveaux de contamination sont fonction de l’espèce et de la station étudiée. La comparaison de nos valeurs avec les données de la littérature a montré que les niveaux de contamination de la lagune sont similaires ou légèrement inférieurs à ceux enregistrés dans des écosystèmes équivalents dans d’autres pays du monde. L’estimation de la toxicité des sédiments au moyen des valeurs guides sédimentaires (ERL, ERM, TEL et PEL) et trois tests biologiques (Microtox®, SOS-Chromotest® et test MELA) ont montré que les sédiments des stations du canal de Bizerte S1 et S3 représentent un danger accru pour les organismes aquatiques. Nos résultats ont montré que les biomarqueurs mesurés chez les deux espèces choisies sont des paramètres sensibles et inductibles permettant de qualifier l’état de santé des organismes et la qualité globale du milieu étudié. Les marqueurs morphométriques contrairement aux marqueurs biochimiques n’ont pas permis de discriminer les différents sites étudiés. Contrairement aux poissons, il a été démontré chez les moules que les facteurs abiotiques ont une influence sur les concentrations en POPs et les réponses des biomarqueurs.Au vu de l’ensemble de ces résultats, il apparaît que cette approche intégrative associant des mesures chimiques et écotoxicologiques représente un bon moyen pour évaluer la qualité de l’environnement notamment dans le cadre de programmes de biosurveillance. / The objective of this thesis was the diagnosis of the health status of the Bizerte lagoon using a multi-marker (chemical, biochemical and morphometric) and multi-compartment approach (sediment and biota). To achieve this objective, the selected biological models were the mussel Mytilus galloprovincialis and the goby fish Zosterisessor ophiocephalus. Both species are widespread in the Bizerte lagoon and the Mediterranean Sea. In a first part and in order to estimate the levels of contamination of the Bizerte lagoon, persistent organic pollutant (POPs), granulometric and mineralogical (TOC) analyses of surficial sediments were carried out. Afterwards, the potential toxicity of sediments was assessed by a battery of bioassays. In a the third part, bioavailability and ecotoxicological impact of POPs studied were assessed by bioaccumulation measurement in these two indicators species, and the study of biological responses associated through a battery of biomarkers such as catalase (CAT), thiobarbituric acid (TBARS); Ethoxyresorufin O-deethylase (EROD); glutathione-S-transferase (GST) and acetylcholinesterase (AChE). The main results of the chemical analyses show a general contamination of sediments and organisms studied by POPs. Contamination levels are dependent on the studied species and stations. Comparing our values with literature data, showed that the levels of contamination of the lagoon are similar or slightly lower than equivalent ecosystems in other parts of the world. Besides, the estimation of sediment toxicity, using sediment guideline values (ERL, ERM, TEL et PEL), as well as bioassays (Microtox®, SOS-Chromotest® and MELA test) showed that stations of canal of Bizerte S1 and S3 were associated with an increased hazard to aquatic organisms. Our results showed that biomarkers measured in both selected species are sensitive and inducible parameters, which allowed to characterize the health status of organisms and global quality of the studied environment. Biochemical but not morphometric markers allowed to discriminate the different studied sites according to chemical risk. Unlike fish, it has been demonstrated in mussels that abiotic factors influence the concentrations of POPs and biomarker responses.Obtained data suggest that integrative approach, combining chemical and ecotoxicological measurements, may represent a good way to asses the quality of the environment, particularly, in the context of biomonitoring programs.

The necessity of cost effective, environmentally friendly technology has become increasingly important to remediate persistent organic pollutants in the environment. The emerging greener ultrasound technology has the potential to serve the remediation industry. In this study, the use of low power, high frequency (HF) ultrasound (1.6 MHz, 145 W/L) has been shown to effectively remediate DDT (90% of 8 mg/L) in water and sand slurries. Addition of iron powder accelerated DDT degradation in the sand slurry under ultrasonication. The potential of HF ultrasound (1.6 MHz, 160 W/L) in degradation of the non-volatile, polar model compound methylene blue (MB) was studied in MB spiked demineralised water and wastewater. A 70 % of 0.4 mg/L of MB was degraded in demineralised water whereas only 54% of MB degraded in MB spiked wastewater. There was a decrease in MB degradation rate with an increase in MB concentration. High power, low frequency (LF) ultrasound (20 kHz, 932 W/L) was used to desorb 400 mg/L of DDT added to three different natural soil slurries at 5, 10, 15 and 20 wt. % each. Each soil slurry was prepared in 0.1% v/v SDS surfactant solution, soaked for 30 min. and heated for another 30 min. at 40 oC before sonication. For the neutral pH soil slurry with higher dissolved organic carbon, the desorption efficiency achieved was over 80% in 30 s sonication. Alkaline soil with higher surface area than neutral soil indicated 60% desorption efficiency while the acidic soil, with the highest surface area and a higher amount of non-soluble organic matter, yielded 30% desorption efficiency under similar desorption conditions. Coconut fibre, used to biosorb the desorbed DDT in the decanted solution, was found to have over 25 g/kg of biosorption capacity for DDT. The surfactant SDS and associated DDT were completely separated from decanted liquid of the desorbed slurry with alum using adsorptive micellar flocculation in 60 min. settling. Acidic pH and molar concentration ratio of Al3+/SDS = 0.5 was used to completely remove the DDT. Using 20 kHz, 1125 W/L of sonication in an 80 mL reactor with air saturated 50 mg/L DDT at 20oC, the DDT removal efficiency achieved was 80% in 20 min. With zero valent iron addition, DDT removal efficiency in 15 min. is 100% with 15 and 22 mg/L of initial DDT concentrations. The settled DDT slurrywas remediated using 20 kHz at 240 W/L achieving DDT removal efficiency of 87% in 15 min. Also LF ultrasound was found to be effective in remediating chloroform (8 mg/L in 60 min) from spiked demineralised water and contaminated groundwater in both batch (120 W/L) and flow cell (6000 W/L) modes. Modeling and simulation of the ultrasonic reactor under 20 kHz ultrasonication was performed for various shape reactors using commercially available software. For almost all reactors, the highest ultrasonic intensity was observed near the transducer???s vibrating area. It was found that the highest acoustic pressure distribution, which is critical to the performance of the reactor, occurred in the conical reactor and flow cell configuration. / Thesis (PhD)--University of South Australia, 2010

The environmental occurrence and behaviour of the brominated flame retardant (BFR) decabromodiphenyl ethane (dbdpe) has only been studied to a limited extent. It is structurally similar to decabromodiphenyl ether (decaBDE), which makes it conceivable that dbdpe may also become an environmental contaminant of concern. A method for environmental analysis and comparative assessments of dbdpe and decaBDE was developed. Both BFRs were studied in: a mass balance of the Henriksdal WWTP in Stockholm (Paper I); an international survey of sewage sludge (Paper II); sediment along a transect from Henriksdal WWTP to the outer archipelago of Stockholm and from isolated Swedish lakes (Paper III); and a benthic food web from the Scheldt estuary (Paper IV). Dbdpe was found in sludge from every country surveyed, indicating that it may be a worldwide concern. The WWTP mass balance showed that virtually all of the BFRs were transferred from wastewater to sludge. A small fraction was emitted via the effluent, confirming emissions to the aquatic environment. In the marine sediment, the BFR levels close to the WWTP outfall were high. They decreased along the transect to low levels in the outer archipelago. The study of lake sediment showed a widespread presence of dbdpe in the Swedish environment and provided evidence that it originates from long range atmospheric transport. In the food web, dbdpe did bioaccumulate to a small extent which was similar to decaBDE. The transfer of the BFRs from sediment to benthic invertebrates was low, while transfer from prey to predator was higher. Biodilution was observed rather than biomagnification. This work suggests that the persistence, the susceptibility to long range atmospheric transport, and the potential for bioaccumulation are similar for dbdpe and the regulated decaBDE that it is replacing. Thus, there is a risk that a problematic environmental pollutant is being replaced with a chemical that is equally problematic. / At the time of the doctoral defense, the following papers were unpublished and had a status as follows: Paper 3: Submitted. Paper 4: Manuscript.

In this study, the Persistent Organic Pollutants (POPs) specifically / 17 Organochlorine Pesticides (OCPs) and 19 Polycyclic Aromatic Hydrocarbons (PAHs) were evaluated in the sediment samples of Balikesir (Ikizcetepeler) Dam Lake. Sixteen sampling points were chosen for determination of concentrations of OCPs and PAHs After ultrasonic bath extraction of the sediment samples GC-MS was used as analytical tool. Extraction efficiencies changes from 63.8 to 87.4% depending on the type of the POPs. Average OCP concentration was found in the range of 3.33-379 &micro / g/kg a, average PAH concentration was found in the range of 3.28-32.9 &micro / g/kg. Pollution maps regarding OCP and PAH distributions were drawn and the correlation between these two pollutant types was investigated. The quality control (QC) and quality assurance tests were applied by the analysis of standard reference materials (SRMs), surrogate standards and analysis replicates.

The necessity of cost effective, environmentally friendly technology has become increasingly important to remediate persistent organic pollutants in the environment. The emerging greener ultrasound technology has the potential to serve the remediation industry. In this study, the use of low power, high frequency (HF) ultrasound (1.6 MHz, 145 W/L) has been shown to effectively remediate DDT (90% of 8 mg/L) in water and sand slurries. Addition of iron powder accelerated DDT degradation in the sand slurry under ultrasonication. The potential of HF ultrasound (1.6 MHz, 160 W/L) in degradation of the non-volatile, polar model compound methylene blue (MB) was studied in MB spiked demineralised water and wastewater. A 70 % of 0.4 mg/L of MB was degraded in demineralised water whereas only 54% of MB degraded in MB spiked wastewater. There was a decrease in MB degradation rate with an increase in MB concentration. High power, low frequency (LF) ultrasound (20 kHz, 932 W/L) was used to desorb 400 mg/L of DDT added to three different natural soil slurries at 5, 10, 15 and 20 wt. % each. Each soil slurry was prepared in 0.1% v/v SDS surfactant solution, soaked for 30 min. and heated for another 30 min. at 40 oC before sonication. For the neutral pH soil slurry with higher dissolved organic carbon, the desorption efficiency achieved was over 80% in 30 s sonication. Alkaline soil with higher surface area than neutral soil indicated 60% desorption efficiency while the acidic soil, with the highest surface area and a higher amount of non-soluble organic matter, yielded 30% desorption efficiency under similar desorption conditions. Coconut fibre, used to biosorb the desorbed DDT in the decanted solution, was found to have over 25 g/kg of biosorption capacity for DDT. The surfactant SDS and associated DDT were completely separated from decanted liquid of the desorbed slurry with alum using adsorptive micellar flocculation in 60 min. settling. Acidic pH and molar concentration ratio of Al3+/SDS = 0.5 was used to completely remove the DDT. Using 20 kHz, 1125 W/L of sonication in an 80 mL reactor with air saturated 50 mg/L DDT at 20oC, the DDT removal efficiency achieved was 80% in 20 min. With zero valent iron addition, DDT removal efficiency in 15 min. is 100% with 15 and 22 mg/L of initial DDT concentrations. The settled DDT slurrywas remediated using 20 kHz at 240 W/L achieving DDT removal efficiency of 87% in 15 min. Also LF ultrasound was found to be effective in remediating chloroform (8 mg/L in 60 min) from spiked demineralised water and contaminated groundwater in both batch (120 W/L) and flow cell (6000 W/L) modes. Modeling and simulation of the ultrasonic reactor under 20 kHz ultrasonication was performed for various shape reactors using commercially available software. For almost all reactors, the highest ultrasonic intensity was observed near the transducer???s vibrating area. It was found that the highest acoustic pressure distribution, which is critical to the performance of the reactor, occurred in the conical reactor and flow cell configuration. / Thesis (PhD)--University of South Australia, 2010

The necessity of cost effective, environmentally friendly technology has become increasingly important to remediate persistent organic pollutants in the environment. The emerging greener ultrasound technology has the potential to serve the remediation industry. In this study, the use of low power, high frequency (HF) ultrasound (1.6 MHz, 145 W/L) has been shown to effectively remediate DDT (90% of 8 mg/L) in water and sand slurries. Addition of iron powder accelerated DDT degradation in the sand slurry under ultrasonication. The potential of HF ultrasound (1.6 MHz, 160 W/L) in degradation of the non-volatile, polar model compound methylene blue (MB) was studied in MB spiked demineralised water and wastewater. A 70 % of 0.4 mg/L of MB was degraded in demineralised water whereas only 54% of MB degraded in MB spiked wastewater. There was a decrease in MB degradation rate with an increase in MB concentration. High power, low frequency (LF) ultrasound (20 kHz, 932 W/L) was used to desorb 400 mg/L of DDT added to three different natural soil slurries at 5, 10, 15 and 20 wt. % each. Each soil slurry was prepared in 0.1% v/v SDS surfactant solution, soaked for 30 min. and heated for another 30 min. at 40 oC before sonication. For the neutral pH soil slurry with higher dissolved organic carbon, the desorption efficiency achieved was over 80% in 30 s sonication. Alkaline soil with higher surface area than neutral soil indicated 60% desorption efficiency while the acidic soil, with the highest surface area and a higher amount of non-soluble organic matter, yielded 30% desorption efficiency under similar desorption conditions. Coconut fibre, used to biosorb the desorbed DDT in the decanted solution, was found to have over 25 g/kg of biosorption capacity for DDT. The surfactant SDS and associated DDT were completely separated from decanted liquid of the desorbed slurry with alum using adsorptive micellar flocculation in 60 min. settling. Acidic pH and molar concentration ratio of Al3+/SDS = 0.5 was used to completely remove the DDT. Using 20 kHz, 1125 W/L of sonication in an 80 mL reactor with air saturated 50 mg/L DDT at 20oC, the DDT removal efficiency achieved was 80% in 20 min. With zero valent iron addition, DDT removal efficiency in 15 min. is 100% with 15 and 22 mg/L of initial DDT concentrations. The settled DDT slurrywas remediated using 20 kHz at 240 W/L achieving DDT removal efficiency of 87% in 15 min. Also LF ultrasound was found to be effective in remediating chloroform (8 mg/L in 60 min) from spiked demineralised water and contaminated groundwater in both batch (120 W/L) and flow cell (6000 W/L) modes. Modeling and simulation of the ultrasonic reactor under 20 kHz ultrasonication was performed for various shape reactors using commercially available software. For almost all reactors, the highest ultrasonic intensity was observed near the transducer???s vibrating area. It was found that the highest acoustic pressure distribution, which is critical to the performance of the reactor, occurred in the conical reactor and flow cell configuration. / Thesis (PhD)--University of South Australia, 2010

La contamination des sols agricoles par la chlordécone menace la durabilité de l’élevage de plein air aux Antilles. Afin de maintenir ce dernier tout en protégeant les consommateurs de denrées animales d’origine terrestre, plusieurs stratégies sont étudiées. Ces travaux de thèse sont focalisés sur l’une d’entre elles qui consiste à séquestrer la chlordécone afin de réduire significativement sa biodisponibilité pour l’animal. La démarche expérimentale a été réalisée par étape, elle s’appuie sur trois piliers : des matières séquestrantes carbonées de type biochar ou charbon activé, l’utilisation de sols artificiels et sur le concept de biodisponibilité relative pour évaluer les performances de séquestration. Les essais conduits avec du charbon activé (à base de noyaux de dattes, de coco ou de lignite) ont montré une séquestration de la chlordécone en milieu aqueux ou chez l’animal, mais pour ce dernier cela ne fonctionne que si la chlordécone et la matrice séquestrante ont eu un temps de contact prolongé (ou maturation) avec l’ingestion par l’animal. Ces résultats montrent l’intérêt d’une séquestration in situ, à savoir directement dans le sol contaminé susceptible d’être ingéré par les animaux. Comme le charbon activé a un coût élevé, des matières carbonées a priori moins coûteuses ont été testées : des biochars à base de diverses essences de bois. Ces biochars produits à deux températures de pyrolyse (500 et 700°C) ont été caractérisés d’un point de vue physique (porosité) et sélectionnés via un test in vitro de disponibilité environnementale. Les tests in vivo (sur porcelets) n’ont pas montré que ces biochars sélectionnés étaient aptes à séquestrer efficacement la chlordécone, puisque la biodisponibilité relative n’était pas différente de un (référence = sol standard sans matière organique). La présence de tourbe dans le sol artificiel ne s’oppose pas au piégeage par les matrices carbonées exogènes. Le test in vitro utilisé et le test in vivo donnent des tendances équivalentes de réduction de la biodisponibilité relative, ce qui est intéressant dans une logique de validation du test in vitro. Ces résultats positifs montrent que la stratégie de séquestration par des matériaux hautement carbonés est possible, requiert des propriétés de microporosité et d’accès aux pores proches de celles d’un charbon activé, mais contingents des conditions expérimentales mises en œuvre ils doivent être poursuivis et validés sur des sols dits naturels / The contamination of agricultural soils by chlordecone threatens the sustainability of outdoor farming in the West Indies. In order to maintain the latter while protecting consumers of terrestrial animal products, several strategies are being studied. This thesis is focused on one of them which consists of sequestering chlordecone in order to significantly reduce its bioavailability for the animal. The experimental approach was carried out in stages, based on three pillars: biochar or activated carbon as sequestering materials, the use of artificial soils and the concept of relative bioavailability to assess sequestration performance. Tests conducted with activated charcoal (based on dates kernels, coconut or lignite) have shown that chlordecone is sequestered in an aqueous medium or in animals, but for the latter it only works if chlordecone and sequestering matrix had a prolonged contact time (or maturation) with ingestion by the animal. These results show the interest of in situ sequestration, ie directly in the contaminated soil likely to be ingested by the animals. As activated charcoal has a high cost, a priori less expensive carbonaceous materials have been tested: biochars based on various wood species. These biochars produced at two pyrolysis temperatures (500 and 700 ° C) were characterized from a physical point of view (porosity) and selected via an in vitro environmental availability test. In vivo tests (on piglets) did not show that these selected biochars were able to effectively sequester chlordecone, since the relative bioavailability was not different from one (reference = standard soil without organic matter). The presence of peat in the artificial soil does not prevent trapping by exogenous carbonaceous matrices. The in vitro test used and the in vivo test give equivalent tendencies to reduce the relative bioavailability, which is interesting in a logic of validation of the in vitro test. These positive results show that the strategy of sequestration by highly carbonaceous materials is possible, requires properties of microporosity and access to pores close to those of an activated carbon, but contingent on the experimental conditions implemented, they must be continued and validated on natural soils