• Refine Query
  • Source
  • Publication year
  • to
  • Language
  • 61
  • 38
  • 1
  • 1
  • 1
  • Tagged with
  • 118
  • 45
  • 42
  • 28
  • 28
  • 23
  • 23
  • 22
  • 22
  • 16
  • 16
  • 14
  • 13
  • 13
  • 13
  • About
  • The Global ETD Search service is a free service for researchers to find electronic theses and dissertations. This service is provided by the Networked Digital Library of Theses and Dissertations.
    Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.
101

Evaluation of bark material and granulated active carbon for treatment of perfluoroalkyl substances (PFASs) in wastewater / Utvärdering av bark material och granulerat aktivt kol vid behandling av perfluoralkyla ämnen (PFAS) i avloppsvatten

Skoglund, Oskar January 2017 (has links)
Per- and polyfluoroalkyl substances (PFASs) are a group of artificial chemicals which have been used in a wide area of applications such as surface protection agents in cloths and different industrial applications. It has been found that PFASs are potentially toxic and are frequently found in the environment due to their persistent and mobile properties. Effluents from wastewater treatment plants (WWTPs) have been identified as an important point source of PFASs. Bark, by-product from the paper and wood industry, is a low-cost adsorbent and has the potential to be used as a filter material for PFASs in WWTPs. In this study, the removal of PFASs in wastewater has been investigated using granulated active carbon (GAC) (n = 2) and bark (n = 2) in a pilot scale experiment at Kungsängsverket, Uppsala over a period of five weeks. The specific objects included: i) investigate the influence of flow-rate (10, 30 40 and 60 Ld-1 ) on the removal efficiency of PFASs in the GAC and bark filters, ii) investigate the influence of particle size of bark on the removal efficiency of PFASs and iii) establish what circumstances that potentially promotes removal of PFASs in GAC and bark filters. The results showed that GAC was the most effective method compared to bark, with a reduction of 73-93%, with increasing efficiency under low flow (10-30 L d-1 ) conditions. The removal efficiency of bark was 45% with a particle size of 2-5 mm and under low flow conditions (10-30 L d-1 ), while under high flow conditions (60 L d-1 ) with the same particle size the removal of PFASs was not efficient, instead the total PFAS concentration increased with 40%. In contrast, bark with a particle size of 5-7 mm proved to be not efficient in removing PFASs (removal efficiency = 0%). In general, the removal efficiency increased with smaller particle size of the adsorbent and lower flow rate. The results indicate that bark may be a low-cost alternative in reducing PFASs from wastewater, under certain conditions. / Per- och polyfluroalkyla ämnen (PFAS) är en familj av artificiella fluorerade organiska föreningar som har använts sedan 1950-talet i en rad olika applikationer, såsom impregnering i kläder. Studier har visat att PFAS är potentiellt toxiska och att de förekommer globalt på grund av deras persistenta och mobila egenskaper. Spillvatten från avloppsreningsverk etablerats som en betydande källa för PFAS. Bark, vilket är en biprodukt från pappers- och träindustrin, är ett poröst material vilket möjligen kan användas som adsorbent av PFAS. Denna studie har jämfört effektiviteten hos granulerat aktivt kol (GAC) och bark för att minska PFAS i avloppsvatten. Experimentet var utformat som ett småskaligt kolonn-experiment vid Kungsängsängsverket, Uppsala, och pågick under en fem veckors period. Frågeställningen var att i) studera vilka effekter flödes-hastigheten (10, 30, 40 och 60 L d-1 ) har på reduktionen av PFAS hos GAC och barkfiltren, ii) studera vilka effekter partikelstorleken hos bark har på reduktion av PFAS och iii) redogöra vilka förhållanden som potentiellt gynnar reduktionen av PFAS i GAC och bark filtren. Resultaten visade att GAC var det mest effektiva av de två materialen, med en total reduktion på 73- 93% av PFAS, med ökande effektivitet under låga flödesförhållanden (10-30 L d-1 ). Bark minskade den totala mängden av PFAS med 45% då partikelstorleken var 2-5 mm och under låga flödesförhållanden (10-30 L d-1 ) medan bark med samma partikelstorlek under ökade flödesförhållanden (60 L d-1 ) visade en ökning på 40% av PFAS i det utgående vattnet. Bark med en partikelstorlek på 5-7 mm visade ingen reduktion av PFAS. Generellt visade resultaten att reduktionen av PFAS ökar under låga flödesförhållanden och minskad partikelstorlek. Resultaten visade att bark kan vara ett alternativt material för att minska PFAS i avloppsvatten förutsatt att gynnsamma förhållanden upprätthålls.
102

Evaluation of the Removal Efficiency of Per- and Polyfluoroalkyl Substances in Drinking Water using Nanofiltration Membranes, Active Carbon and Anion Exchange / Utvärdering av reningseffektiviteten av per- och polyfluorerade alkylsubstanser i dricksvatten med nanofiltrering, aktivt kol och jonbytarmassa

Lindegren, Klara January 2015 (has links)
Per- and polyfluoroalkyl substances (PFASs) is a group of man-made, highly persistent chemicals. Due to the specific surface-active attributes of these molecules, applications are numerous and feed an economically important industry. During the last decade, PFASs have been detected globally in the environment, living organisms and tap water. The combination of toxic properties and high bioaccumulative potential, together with the discovery that conventional water treatment methods do not remove PFAS, renders further research on purification methods highly needed.  Three techniques of purifying water from PFASs were examined. Nanofiltration technology (NF) is a membrane filtration technique, which produces a purified product (the permeate) by generating an effluent of high contaminant concentration (the reject water). To decontaminate the reject water, adsorption by granular activated carbon (GAC) or anion exchange (AE) have been proposed. The efficiency of these three technologies was studied at Bäcklösa drinking water treatment plant (DWTP) in Uppsala. A nanofiltration pilot with two 270NF membranes (Dow Filmtech™), connected in series, was used. A high removal efficiency (>90%) was found for all PFASs. Furthermore, it was confirmed that the concentration in the permeate water was a function of the concentration in the incoming raw water; increased PFAS raw water concentration resulted in increased PFAS permeate concentration. Size-exclusion and electrostatic repulsion were deemed important mechanisms. For the comparison of GAC (Filtrasorb 400®) and AE (Purolite® A-600), a column experiment was set up. The perfluoroalkane (-alkyl) sulfonic acids (PFSAs) and perfluorooctanesulfonamide (FOSA) had similar removal efficiencies using both GAC and AE, and the efficiency increased with increasing chain length. AE was found to have a higher average removal efficiency of perfluoroalkyl carboxylic acid (PFCAs) (62-95%) than GAC (49-81%). In conclusion, longer chain length PFASs were removed more effectively than shorter-chained, and the PFSAs and FOSA showed higher removal efficiency compared to the PFCAs. Furthermore, linear isomers were removed more effectively than branched for GAC and AE. In contrast, the opposite was found for the NF membrane, where branched isomers were better retained. / Per- och polyfluorerade alkylsubstanser (PFAS) är en grupp syntetiska, ytterst persistenta kemikalier. På grund av deras ytaktiva egenskaper är de lämpliga för användning i många produkter och tillverkningsprocesser, och är således viktiga för en ekonomiskt betydande industri. Under det senaste årtiondet har PFAS påträffats i miljön, levande organismer och kranvatten världen över.  Kombinationen av toxiska egenskaper, en hög bioackumuleringspotential och upptäckten att konventionella reningsmetoder inte avlägsnar substanserna från vatten, gör att vidare forskning av reningsmetoder för PFAS är mycket angelägen. Tre reningsteknikers förmåga att rena vatten från PFAS undersöktes. Nanofiltrering (NF) är en membranfiltreringsteknik som utöver den renade produkten, permeatet, även framställer en biprodukt av hög föroreningsgrad, rententatet. För att rena rententatet har adsorption till granulärt aktivt kol (GAC) eller jonbytarmassa (AE) föreslagits. Teknikerna utvärderades på Bäcklösa Vattenverk i Uppsala.  Nanofiltreringen undersöktes i en pilotanläggning där två 270NF (Dow Filmtech™) membran var seriekopplade. En hög reningsgrad (>90%) konstaterades för alla typer av PFAS. Vidare visades PFAS-koncentrationen i permeatet vara en funktion av PFAS-koncentrationen i råvattnet; en ökad råvattenkoncentration gav en ökad permeatkoncentration. Storleksseparation och elektrostatisk repulsion befanns vara viktiga mekanismer som påverkade reningsgraden. För att undersöka de mekanismer som påverkar PFAS-adsorption jämfördes GAC (Filtrasorb 400®) och AE (Purolite® A-600) i ett kolonnexperiment. Reningsgraden för GAC och AE av perfluorerade sulfonsyror (PFSA) och perfluorooktan sulfonamider (FOSA) var lika hög och reningseffektiviteten ökade med ökande kolkedjelängd. AE återfanns ha en högre genomsnittlig reningsgrad av perfluorkarboxylsyror (PFCA) (62-95%) än GAC (49-81%). Sammanfattningsvis avlägsnades PFAS av längre kolkedjelängd mer effektivt än kortare kolkedjor, och PFAS med sulfonsyror och sulfonamider som funktionella grupper uppvisade en högre reningsgrad än karboxylsyrorna. Vidare renades linjära isomerer mer effektivt än grenade både genom GAC och AE. Däremot konstaterades det motsatta för NF-membranen, där grenade isomerer renades mer effektivt. / SafeDrink
103

Analytical Method Development of Fluorinated Silanes using Mass Spectrometry

Eklundh Odler, Tea January 2018 (has links)
The aim of this study was to develop an analytical method for fluorinated silanes. Furthermore, as a secondary aim, to explore if there would be possible to detect 1H,1H,2H,2H-perfluorooctyl triethoxysilane (6:2 PTrEtSi) and 1H,1H,2H,2H-perfluorodecyl triethoxysilane (8:2 PTrEtSi) in two different matrices, sludge and cosmetic extract. The method development included experiments using LC-MS, LC-MS/MS, UPC2, GC-MS and APGC-MS/MS and was carried out using standards containing 6:2 PTrEtSi and 8:2 PTrEtSi. The analytical method that worked best for the compounds was GC-MS/MS and an analytical method using APGC-MS/MS was developed for fluorinated silanes. The IDL for 6:2 PTrEtSi was 0.0012 μg/mL and 1.32 μg/mL for 8:2 PTrEtSi. This makes the developed method suitable for high contaminated samples, such as extracts from cosmetic products. It was concluded that a method using LC as the analytical instrument would not work for the two target compounds since they were too reactive with the mobile phase. However, LC could be a good choice for siloxanes, compounds that are formed from hydrolysis and condensation of fluorinated silanes. The samples analyzed in this study were three sludge extracts and one extract from a cosmetic product. 6:2 PTrEtSi was expected to be detected in the cosmetic sample since the compound was stated on the table of contents of the cosmetic product. No detection of 6:2 TrEtSi or 8:2 TrEtSi could be made in either of the samples. The reason for this was suspected to be transformation or degradation of the compounds into other compounds. Therefore, a full scan of the cosmetic sample using LC-MS/MS was included in the experiment as an addition to verify the suspicions that compounds such as siloxanes could have been formed. An interesting peak was discovered with m/z 947 which could be a disiloxane of 6:2 PTrEtSi.
104

Toxicity Studies Of Per- and Polyfluoroalkyl Substances (PFAS)

Shittu, Adenike Rofiyat 02 September 2021 (has links)
No description available.
105

<strong>EVALUATING EFFECTS OF PERFLUORINATED ALKYL SUBSTANCES (PFAS) ON ANURAN LIPID HOMEOSTASIS THROUGH </strong><em><strong>XENOPUS LAEVIS </strong></em><strong>BODY & HEPATIC CONDITION</strong>

Anna Grace Bushong (16612647) 18 July 2023 (has links)
<p> Per- and polyfluoroalkyl substances (PFAS) are a class of persistent environmental contaminants that have become ubiquitous, resulting in widespread exposure among humans and wildlife. Amphibians are regularly exposed in the field, making them susceptible to sublethal effects of PFAS exposure. In amphibians exposed to PFAS, deleterious effects have been observed, including reduction in body condition measured using the scaled mass index (SMI) and degraded hepatic condition, among others. PFAS may dysregulate lipid metabolism by altering signaling cascades regulated by peroxisome proliferator activated receptors (PPAR), but whether changes in energy stores can explain changes in amphibian SMI and/or hepatic condition remain underexplored. Since lipids are a critical energy reserve for anurans, understanding whether lipid metabolism is being perturbed is critical. The central objective of this thesis was to investigate the effect of PFAS on lipid homeostasis in <em>Xenopus laevis </em>tadpoles within the context of a PPAR mechanism of action (MOA), considering apical, molecular, and lipidomic endpoints. I conducted three studies: (a) a study to characterize SMI and the relative expression of the hepatic xPPARα/β/γ during metamorphosis, (b) a pharmaceutical exposure to assess the <em>in vivo</em> effects of xPPARα/β/γ agonism on hepatic gene expression for select downstream targets (<em>apoa5, fabp1, acox1,​ pck1</em>), and (c) a chronic PFAS exposure to investigate the effects of environmentally relevant concentrations (PFOS, PFHxS, PFOA, PFHxA at 0.5 ppb; binary mixture of PFOS:PFHxS at 1 ppb) on lipid homeostasis through apical endpoints (mass, snout vent length, SMI, hepatic condition), relative hepatic gene expression, and Multiple Reaction Monitoring (MRM) profiling of the hepatic lipidome for changes in relative class abundance. In study (a), I identified SMI and hepatic expression of <em>xPPARα/β/γ</em> is dynamic during late metamorphosis, indicating the potential for heightened susceptibility. However, in study (b), pharmaceutical agonists had no effect on <em>X. laevis</em> at high doses. For study (c), I did not observe effects on a majority of apical endpoints, including SMI, but detected a significant sex-specific reduction in hepatic condition for male<em> X. laevis</em> tadpoles exposed to single-chemical perfluorosulfonic acid (PFSA) treatments. For gene expression, I observed a transient downregulation for apolipoprotein-V (<em>apoa5</em>) at Nieuwkoop and Faber (NF) stage 62 for <em>X. laevis</em> tadpoles exposed to single-chemical perfluorocarboxylic acid (PFCA) treatments. Lipid profiling detected transient dysregulation of predominantly membrane lipids in-response to short-chain PFAS treatments at NF 58. Overall, our findings indicate PFAS may exert toxicity during anuran metamorphosis through multiple mechanisms of action (MOA) with sex-specific and developmental-stage specific outcomes.</p>
106

Membranbioreaktorer och deras förmåga att avlägsna prioriterade mikroföroreningar / Mambrane bioreactors and their ability to remove emerging substances of concern

Murad, Hassan January 2018 (has links)
Spridning av läkemedelsrester och andra prioriterade mikroföroreningar i miljön har uppmärksammats och stor oro väckts kring problematiken. Bland observationer som forskare har noterat till följd av antibiotika, hormoner och läkemedel i vattenmiljöer är bland annat bakteriell resistens, könsbyte och sterilitet hos fisk och groddjur. Persistenta föroreningar som per- och polyfluor alkalysyror (PFAS) bryts inte heller ner i naturen och mikroskräppartiklar kan anrikas i vattendrag och orsaka negativa effekter på vattenlevande organismer. Gemensamt för mikroföroreningar är att dessa förekommer oftast i små halter och kan härstamma från olika mänskliga aktiviteter. Avloppsreningsverk (ARV) är inte primärt anpassade för att avskilja mikroföroreningar utan främst för att avlägsna kväve, fosfor och organiskt material. Uppströmsarbete är inte heller tillräckligt effektivt för att avlasta reningsprocessen vilket medför att mängden mikroföroreningar ökar i vattenmiljöer och sätter ytterligare påtryckningar på ARV. Utmaningar som ARV står inför idag med nya mikroföroreningar och förekomsten av dessa i miljön har väckt frågor både nationellt och internationellt. Stockholm Vatten och Avfalls (SVOA) beslut att implementera membranbioreaktor (MBR) på Henriksdals reningsverk av porstorleken 0,04 μm är en åtgärd för att rusta upp inför framtida hydrauliska volymer men även potentiella striktare reningskrav. Fördelen med MBR-processen är att den förhindrar föroreningar som förekommer partikulärt att passera membranen och på så sätt hindras skadliga ämnen att passera reningsprocessen. I dagsläge saknas krav på ARV att rena avloppsvatten från de flesta mikroföroreningar. Det förväntas dock att kommande lagstiftning omfattar läkemedel och andra organiska föroreningar. I detta projekt undersöktes mikroföroreningar i form av läkemedelsrester, antibiotika, hormoner, PFAS och mikroskärp i en MBR-process samt förekomsten av adsorberbara och extraherbara organiska halogener (AOX, EOX) som potentiellt bildas under rengöring av membranen till följd av reningsprocessen. Resultat från detta projekt med MBR-processen visade en generell högre reduktion av prioriterade mikroföroreningar i avloppsvatten än tidigare undersökningar på konventionella ARV, med undantag för några substanser som visade på en liknande sämre reduktion. Läkemedlen diklofenak, oxazepam, citalopram med flera visade på en sämre reduktion och lika så för antibiotikumen clindamycin, claritomycin och erytromycin där reduktionen var negativ och visade på en återkommande trend. Östrogena hormoner reducerades i reningsprocessen och likaså för mikroskräp där 60 partiklar/m3 mikroplast av porstorleken större än 300 μm passerade membranen. Mikroplast av en porstorlek i intervallet mindre än 300 men större än 50 μm passerade 140 partiklar/m3 membranen. För AOX och EOX var halten i MBR-processen typiska och i nivå med tidigare undersökningar genomförda på konventionella ARV. Eftersom membranen inte kan avskilja partiklar på molekylnivå visades sig även att det passerade fortfarande mikroföroreningar som undersöktes. En slutsats från detta projekt är att endast ett få tal ämnen reducerades helt medan majoriteten av de prioriterade mikroföroreningarna reducerades delvis i avloppsvatten. För att kunna reducera dessa prioriterade mikroföroreningar i reningsprocessen ytterligare om striktare reningskrav skulle bli aktuella krävs vidare efterbehandling efter MBR-processen. / Release of pharmaceutical residues and other emerging substances in the environment has been highlighted and raised a great concern regarding the issue. Among observations that scientists have noted as a result of antibiotics, hormones and pharmaceutical residues in the aquatic environment are bacterial resistance, sex change and sterility in fish and batrachians. Persistent pollutants such as perfluorinated-alkylated substances (PFAS) are also not degraded in nature, and microscopic debris particles can be enriched in aquatic systems and cause adverse effects on aquatic organisms. The common aspect with these substances is that they usually occur in small quantities and can derive from different human activities. Wastewater treatment plants (WWTP) are not primarily designed to separate emerging substances of concern (ESOC), but primarily to remove nitrogen, phosphorus and particulate organic matter. Upstream work is also not sufficiently effective to relieve the purification process, which means that the amount of pollutants increases in aquatic environments and puts additional pressure on the WWTP. The challenges facing WWTP today with ESOC and their presence in the environment has raised issues both nationally and internationally. Stockholm Vatten och Avfall (SVOA) decision to implement a membrane bioreactor (MBR) with poresize of 0,04 μm at Henriksdal WWTP is a step to prepare for future hydraulic volumes, but also potentially stricter treatments requirements regarding ESOC. The advantage of the MBR process is that it prevents contaminants that appear to be particulate to pass the membranes and end up in the receiving waters. Today, WWTP are not required to treat wastewater in order to remove pharmaceutical residues, antibiotics, hormones, PFAS or microscopic debris particles. However, it is expected that future legislations will include pharmaceuticals and other organic pollutants. In this project, ESOC such as pharmaceutical residues, antibiotics, hormones, PFAS and microscopic debris in the MBR-process are studied as well as the presence of adsorbable and extractable organic halogens (AOX, EOX) that are possibly formed during the cleaning or maintains of the membranes. Results from this study showed a higher general reduction of the studied ESOCs in wastewater with the MBR-process than previous studies in conventional WWTP, except of some substances that showed a poor reduction. Pharmaceuticals such as diclofenac, oxazepam and citalopram showed a weak reduction as well as the antibiotics clindamycin, clarithromycin and erythromycin where they showed a higher outcome levels than the incoming to the treatment process. Estrogenic hormones were reduced in the purification process as well as microplastics where only 60 particles/m3 of pore size higher than 300 μm passed the membranes. Microplastics of the pore size smaller than 300 and larger than 50 μm were detected to 140 particle/m3 in the effluent water. For AOX and EOX, the level of MBR process showed typical values and were in line with previous studies on conventional ARV. However, since the membranes cannot treat contaminants at molecular level, it was also shown that some ESOC that were studied bypassed the treatment process. A conclusion from this project is that only a few numbers of substances were fully reduced while the majority of ESOCs were partially reduced in wastewater. In order to reduce further ESOCs and in case of stricter treatment were to be applied, additional post-treatment is also needed for the MBR process.
107

Stanovení perfluorovaných sloučenin pomocí separačních metod / Determination of perfluorinated compounds using separation methods

Blažková, Eva January 2010 (has links)
The theoretical part of this diploma thesis consists of current matters regarding the presence of perfluorinated organic compounds in living environment elements. The attention has been focused on perfluoroktanoic acid (PFOA), (PFOS), and (FOSA). Physical-chemical characteristics of these organic pollutants and their toxicological and environmental aspects have been described. Possible ways of the pollutants analytical determination have been specified. The experimental part has explored effects of extraction techniques (sonication, pressurized solvent extraction, solid-phase extraction) used for PFAS separation from seats of fire soil sample. Identification of the analytes have been achieved by liquid chromatography/mass spektrometry.
108

Development and comparison of analytical methods for the determination of PFASs as sum parameters in environmental samples using HR-CS-GFMAS

Simon, Michael Fabian 28 February 2024 (has links)
Im ersten Teil wurde Probenvorbereitungs-Methoden und instrumentelle Methoden zur Organofluor-Bestimmung verglichen, um Vor- und Nachteile bei der Summenparameter-Analytik von per- und polyfluorierten Alkylverbindungen (PFAS) zu identifizieren. Daher wurden Oberflächenwasserproben aus der Spree in Berlin und Industrieabwasserproben mit zwei PFAS-Summenparametern analysiert – dem extrahierbaren (EOF) und dem adsorbierbaren organisch gebundenen Fluor (AOF). Beide PFAS-Summenparameter wurden mit zwei fluorsensitiven Detektionssystemen analysiert – Hochauflösender Kontinuumstrahler-Graphitofen Molekülabsorptionsspektrometrie (HR-CS-GFMAS) und combustion Ionenchromatographie (CIC). HR-CS-GFMAS erwies sich im Vergleich zu CIC als der empfindlichere und schnellere Ansatz mit höherer Präzision. Im zweiten Teil wurde eine neue Methode zur PFAS-Summenparameteranalyse und EOF-Bestimmung in Bodenproben auf Basis von HR-CS-GFMAS entwickelt und optimiert. EOF-Massenanteile wurden bei mehrfacher Extraktion und Nutzung der Festphasenextraktion (SPE) zur Entfernung anorganischen Fluors untersucht. Bei einem Vergleich der optimierten Methode mit und ohne SPE zeigte sich eine drastische Diskriminierung von Organofluor-Verbindungen mittels SPE. Im dritten Teil wurden Organofluor-Massenbilanzen in aquatischen Systemen anhand von Oberflächenwasser- und Schwebstoffproben (SPM) untersucht. SPM-Proben wurden mit vier komplementären Analysemethoden analysiert – target und non-target, direct total oxidizable precursor assay (dTOPA) und EOF. Daher wurden drei Organofluor-Massenbilanzansätze für die räumlich und zeitaufgelöste SPM-Probenanalyse verwendet: (I) Identifizierung von oxidierbaren PFAS-Vorläufer, (II) Identifizierung des Anteils der identifizierten und nicht identifiziertes EOF und (III) PFAS-target, PFAS dTOPA, non-target-Screening und EOF-Analyse, um das nicht identifizierte EOF aus Ansatz (II) weiter zu entschlüsseln. / In the first part, a comparison of sample preparation and instrumental methods for organofluorine determination was used to identify advantages and disadvantages in sum parameter analysis of per- and polyfluoroalkyl substances (PFASs). Therefore, surface water samples from the Spree River in Berlin, Germany and industrial effluent samples were analyzed using two PFAS sum parameters – the extractable (EOF) and adsorbable organically bound fluorine (AOF). Both PFAS sum parameters were analyzed using two fluorine sensitive detection systems – high-resolution-continuum source-graphite furnace molecular absorption spectrometry (HR-CS-GFMAS) and combustion ion chromatography (CIC). HR-CS-GFMAS turned out to be the more sensitive and faster approach accompanied with higher precision compared to CIC. In the second part, a new method for PFAS sum parameter analysis and EOF determination in soil samples based on HR-CS-GFMAS was developed and optimized. EOF mass fractions were investigated upon multiple extraction and utilization of solid phase extraction (SPE) for inorganic fluorine removal. In a comparison of the optimized method with and without SPE, a highly biased discrimination of organofluorines using SPE was shown. In the third part, organofluorine mass balances were investigated in aquatic systems using surface water and suspended particulate matter (SPM) samples. SPM samples were analyzed using 4 complementary analytical methods – target and non-target HRMS, direct total oxidizable precursor assay (dTOPA) and EOF. Therefore, 3 organofluorine mass balance approaches were used for SPM sample analysis in spatial and time resolved manner: (I) Identification of oxidizable PFAS precursors, (II) Identification of the proportion of identified and unidentified EOF and (III) PFAS target, PFAS dTOPA, non-target screening and EOF analysis to further unravel the unidentified EOF from approach (II).
109

Modélisation mécaniste de la bioaccumulation de contaminants organiques (PCB et PFAS) chez les poissons dans le contexte du changement global : application aux juvéniles de sole commune de l’estuaire de la Gironde. / Modelling mechanistic bioaccumulation of organic contaminants (PCBs and PFASs) in fish in the context of global change : application to the Gironde estuary juvenile common sole

Mounier, Florence 28 March 2019 (has links)
Les estuaires sont des écosystèmes aquatiques particulièrement soumis au changement global et notamment à la pollution par de nombreux xénobiotiques pouvant présenter un risque écotoxicologique et sanitaire. En toxicologie environnementale et en évaluation des risques la bioaccumulation est un processus fondamental car elle contrôle les doses internes de toxiques potentiels. Or les flux de contamination et de décontamination des organismes dépendent de processus internes (e.g. nutrition, croissance) eux-mêmes dépendant des conditions environnementales (e.g. température, nourriture) qui peuvent être affectées par le changement global.Dans ce contexte, cette thèse se propose de décrire, dans un cadre de modélisation mécaniste, les processus de bioaccumulation de deux familles de polluants organiques persistants (POP) halogénés potentiellement toxiques et bioaccumulables, aux propriétés physico-chimiques contrastées : les polychlorobiphényles (PCB, composés historiques fortement lipophiles) et les substances perfluorées (PFAS, composés émergents amphiphiles). Ce travail se focalise sur l’estuaire de la Gironde dont la fonction de nourricerie est fondamentale pour de nombreuses espèces de poissons marins dont la sole commune (Solea solea), souvent utilisée comme indicatrice de la qualité des nourriceries côtières et estuariennes.Pour permettre de tenir compte des fluctuations des conditions environnementales sur la bioaccumulation, dans la première partie de ce travail, j’ai développé un modèle de toxicocinétique(TK) couplé avec un modèle mécaniste bioénergétique basé sur la théorie DEB (Dynamic Energy Budget). Ce modèle DEB a été paramétré pour la sole commune et calibré pour chaque sexe (package DEB tool). Il permet de prédire les principales évolutions des fonctions physiologiques d’intérêt en bioaccumulation (ingestion, croissance, reproduction...), tout au long du cycle de vie d’un individu, en fonction de conditions environnementales dynamiques. Le modèle TK développé a été complexifié par l’ajout d’un flux d’élimination de contaminants, non considéré dans les précédents modèles DEB-TK.La calibration des paramètres toxicocinétiques (TK) du modèle, pour 4 congénères de PCB, est basée sur une méthode innovante de prise en compte de la variabilité individuelle d’ingestion, appliquée à une expérimentation de contamination de juvéniles de sole via leur nourriture. Ce travail a montré que même en tenant compte de l’ingestion de chaque poisson, l’assimilation efficace de contaminant était très variable et corrélée aux taux de lipides des individus. Dans une seconde partie, ce modèle a été appliqué aux conditions in situ de l’estuaire de la Gironde. Il a permis de mettre en évidence la forte influence de la composition du régime alimentaire sur la variabilité de l’âge à la maturité sexuelle et de la contamination des soles pour les deux familles de contaminant étudiées. La confrontation des prédictions du modèle aux mesures de contaminants dans les juvéniles de sole de l’estuaire a permis de calibrer les paramètres TK du composé majeur de chaque famille dans l’environnement (CB153 et PFOS). Cette calibration a conduit à deux constats dans le cadre de l’évaluation du risque : (1) un manque de connaissances pour extrapoler les calibrations de paramètres TK en conditions contrôlées vers les conditions naturelles ; (2) la différence d’erreur d’évaluation du risque liée à l’utilisation des mêmes paramètres TK «les plus pessimistes » quels que soient les composés. Enfin, des scenarios prospectifs simples ont été développés pour illustrer ces résultats et les possibles applications du modèle développé.In fine, ces prédictions de la contamination, de la croissance et du développement des soles pourront être reliées, lors de travaux ultérieurs, à des effets potentiels sur les fonctions physiologiques de la sole (modèles DEBtox), et aux conséquences sur la dynamique des populations de soles (e.g.modèles matriciels de population). / Estuarine ecosystems are particularly impacted by global change and, specifically, bychemical pollution from numerous xenobiotics that may be associated to ecotoxicological and health risks. In environmental toxicology and risk assessment, bioaccumulation is a fundamental process as it controls the internal doses of potential toxicants in organisms. However, the contamination and decontamination flows depend on internal processes thatare themselves dependent on environmental conditions (e.g. temperature, food) and thus on the other variables of global change.In this context, this manuscript aims at describing, within a mechanistic modelling framework, the bioaccumulation processes of two families of potentially toxic and bioaccumulable halogenated persistent organic pollutants (POPs) with contrasting physicochemical properties: the polychlorinated biphenyls (PCBs, highly lipophilic historical compounds) and the perfluorinated substances (PFAS, amphiphilic emerging compounds).This work focuses on the Gironde estuary whose nursery function is fundamental for many species of marine fish including the common sole (Solea solea), often used as an indicator of the quality of coastal and estuarine bursary grounds. In order to account for the influence of environmental conditions on bioaccumulation, the first part of this work consisted in developing a toxicokinetic model (TK) coupled with a mechanistic bioenergetic model based on the theory DEB (Dynamic Energy Budget). This DEBmodel has been parameterized for common sole and calibrated for each sex (packageDEBtool). It allows predicting the main evolution of the physiological functions of interest forbioaccumulation (ingestion, growth, reproduction...) throughout the life cycle of an individualaccounting for dynamic environmental conditions. The developed TK model was first calibrated for some PCBs, under controlled conditions, using an innovative method to take into account individual ingestion variability. This work showed that even if the individual ingestion of each fish is accounted for, the effective assimilation of contaminant is very variable and correlated with the lipid levels of the individuals. The application of the model tothe in situ conditions of the Gironde estuary led to identify that, whatever the contaminant family, the composition of the soles diet had a strong influence on the variability of soles contamination and age at sexual maturity. The comparison of model predictions with measurements made in juveniles of the estuary allowed calibrating the TK parameters values for the major compound of each family in the environment (CB153 and PFOS). This calibration led to two observations in the context of a risk assessment: (1) a lack of knowledge to extrapolate calibrations of TK parameters under controlled conditions to natural conditions;(2) the difference in risk assessment error related to the use of the same "worst case" TK parameters regardless of the compounds. Lastly, simple prospective scenarios have beendeveloped to illustrate these results and the possible applications of the model developed.Ultimately, these predictions of soles contamination, growth and development may be related in future work to potential effects on the physiological functions of sole (DEBtox models), and to consequences on soles population dynamics (e.g. matrix population models).
110

Calibration and Application of Passive Sampling in Drinking Water for Perfluoroalkyl Substances / Kalibrering och tillämpning av passiv provtagning i dricksvatten för perfluoroalkylsubstanser

Persson, Caroline January 2015 (has links)
Perfluoroalkyl substances (PFASs) are global environmental contaminants and a need for monitoring levels has arisen due to their persistency and their ability to bioaccumulate. One relatively novel method of monitoring for both long and short time intervals and generating time-weighted average (TWA) concentrations is passive sampling for which no power, maintenance and supervision is required. The polar organic compound integrative sampler (POCIS) with a weak anion exchange (WAX) sorbent and the POCIS with a hydrophilic-lipophilic balance (HLB) adsorbent were calibrated for PFASs in a laboratory uptake experiment, and applied at a drinking water treatment plant (DWTP) in Stockholm, Sweden.   In the calibration study, all of the 14 studied PFASs were taken up by both passive samplers. Two and three out of the 14 studied PFASs had reached equilibrium after 28 days using POCIS WAX (PFBA and PFTeDA) and POCIS HLB (PFBA, PFPeA and PFTeDA), respectively. The sampling rate (Rs), which is the extracted water in liters per day, ranged between 0.003 and 0.10 L day-1 for the POCIS WAX and between 0.00052 and 0.13 L day-1 for the POCIS HLB. In general, Rs increased with increasing perfluorocarbon chain-length (C4 to C8) and for a perfluorocarbon chain-length longer than C8, Rs decreased with increasing perfluorocarbon chain-length (C8 to C13) for both passive samplers. FOSA had the highest Rs-value (0.10 and 0.13 L day-1) for both POCIS WAX and POCIS HLB, respectively. The POCIS WAX had a higher uptake for the short-chained PFASs PFBA (134 ng after 28 days), PFPeA (410 ng) and PFHxA (834 ng), compared to the POCIS HLB (0.5 ng, 58 ng, and 373 ng, respectively). For all other compounds, the accumulated amounts in the POCIS HLB were in the same range as in the POCIS WAX.   The application of the passive samplers at the DWTP showed that both passive samplers could detect ultra-trace (pg to ng L-1) levels of PFASs. A comparison of the TWA concentration showed that the two passive samplers had a good linear correlation (R2 = 0.63), but the TWA concentrations derived by POCIS WAX was approximately 40% higher compared to POCIS HLB. A comparison between the passive samplers and the grab samples did not show a correlation (R2 = 0.24 for POCIS WAX and R2 = 0.10 for POCIS HLB). The application also included a comparison of the removal efficiency in the conventional DWTP and a pilot plant with additional treatments steps of granulated activated carbon (GAC) and nanofiltration (NF). For the full-scale DWTP the average removal efficiency was 32% and high removal efficiency was observed for PFBA (81%). For the pilot plant, the removal efficiency was 100% for all the detected PFASs in the raw water. / Perfluoroalkylsubstanser (PFAS) har blivit uppmärksammade som globala miljöföroreningar, och ett behov av att övervaka dessa ämnens förekomst i miljön har uppkommit på grund av hög persistens i kombination med hög förmåga att bioackumulera. En relativt ny metod för tidsintegrerad provtagning är så kallad passiv provtagning. En adsorbent placeras i fält och ackumulerar PFAS från vattnet. Tillgång till elektricitet behövs inte, och behov av övervakning och underhåll är minimalt. I denna studie kalibrerades en så kallad ’polar organic compound integrative sampler’ (POCIS) för mätning av PFAS genom upptagsexperiment med två olika adsorbenter: en svag anjons adsorbent (WAX) och en hydrofil-lipofil balanserad adsorbent (HLB). Metodiken tillämpades sedan på vatten från ett dricksvattenverk i Stockholm, Sverige.   Upptagsexperimenten utfördes med 14 PFAS och samtliga togs upp av båda adsorbenterna. Två respektive tre av de studerade PFAS uppnådde jämvikt efter 28 dagar för WAX (PFBS och PFTeDA) samt HLB (PFBA, PFPeA och PFTeDA). Upptagshastigheten (Rs), det vill säga den volym som extraheras per dag, varierade mellan 0,003 och 0,1 L dag-1 för WAX och mellan 0,00052 och 0,13 L dag-1 för HLB. Generellt ökade Rs med en ökande längd på kedjan av perfluorerade kol upp till C8, för att sedan avta med ökande kedjelängd. FOSA hade det högsta Rs-värdet (0,10 och 0,13 L dag-1) för både WAX och HLB. WAX hade ett högre upptag (upp till 134, 410 och 834 ng) för PFAS med kort perfluorerad kolkedja (PFBA, PFPeA respektive PFHxA) jämfört med HLB (upp till 0,5, 58, och 373 ng). Den ackumulerade mängden för alla andra PFAS överensstämde väl mellan de båda provtagarna.   Mätning av PFAS halter i dricksvattenverket med hjälp av POCIS WAX och POCIS HLB visade att även PFAS kunde detekteras även vid miljörelevanta halter. En jämförelse mellan de båda passiva provtagarna visade på ett linjärt samband (R2 = 0,63), men där POCIS WAX hade en tendens att överskatta koncentrationen med ca 40%. En jämförelse mellan de passiva provtagarna och traditionell uppsamlingsprovtagning visade på låg överrensstämmelse (R2 = 0.24 för POCIS WAX och 0.10 för POCIS HLB). Vid tillämpningen gjordes även en beräkning för reningseffektiviteten av PFAS i dricksvattenverket och i en pilotanläggning där ytterligare rening med granulerat aktivt kol (GAC) och nanofiltration (NF) används. I dricksvattenverket var den genomsnittliga reningen 32%, med den högsta reningseffektiviteten för PFBA (81%). I pilotanläggningen var reningen 100% för alla upptäckta PFAS i råvattnet.

Page generated in 0.0177 seconds