Refine
Document Type
- Doctoral Thesis (9)
Has Fulltext
- yes (9)
Is part of the Bibliography
- no (9)
Keywords
- Kernresonanzspektroskopie (1)
- Mikroplastik (1)
- NMR (1)
- biofiltration (1)
- micropollutants (1)
- ozonation (1)
- soil aquifer treatment (1)
- trace organic chemicals (1)
- transformation products (1)
- wastewater treatment plant (1)
Identifizierung und Quantifizierung von Mikroplastik mittels quantitativer ¹H-NMR Spektroskopie
(2021)
Plastic, and so microplastics (MP), are globally present and represent an increasingly significant problem for the environment. In order to understand the distribution and impact of MP it is important to identify and quantify MP over a wide range of sizes and to ensure comparability of studies. However, comparability of studies is made difficult or even impossible by different MP concentration data. There still is a great need for research in the field of size-independent, quantitative analysis of MP in environmental samples, especially with regard to mass-based MP concentration information. Therefore, this thesis aims to utilize quantitative ¹H-NMR spectroscopy (qNMR) as an alternative method in MP analysis. The qNMR method is a size-independent, mass-based method which can be used as an alternative for MP analysis and has potential for routine analysis. The proof-of-concept was demonstrated for LDPE, PET and PS particles (Chapter 2). Additionally, PVC, PA, and ABS particles were tested to cover the most important polymer types for MP-analysis (Chapter 3). Moreover, using PET, PVC and PS as examples it was examined whether the qNMR method can also be transferred to the more cost-effective NoD method (Chapter 4). Results of method validation of both methods (1D and NoD) show that quantification using the qNMR method is not only possible in principle, but also shows high accuracy (88.0-110 %) and detection limits (1 – 84 µg) that lie within the environmentally relevant range. Furthermore, it was examined whether not only high-field instruments are suitable for MP analysis, but also benchtop devices (low-field instruments), which are much more cost-effective in purchase and maintenance. Increasing measurement times for PET and PS to 30 min and for PVC to 140 min, the lower measuring frequency especially concerning resolving capacity could be compensated (Chapter 4). To address the question of potential matrix effects of environmental samples, matrix effects and recovery rates of sample preparation procedures, which have been developed specifically for the application of the qNMR method were investigated using PET fibers as an example (Chapter 5). It could be shown that environmental matrices do not interfere with the quantitative analysis of MP using qNMR methods. Specific sample preparation methods developed for qNMR analysis can be used with recovery rates > 80 % for different environmental matrices (Chapter 5). Finally, first orienting investigations for the simultaneous determination of several polymer types in one sample are reported (Chapter 6).
Water scarcity is already an omnipresent problem in many parts of the world, especially in sub-Saharan Africa. The dry years 2018 and 2019 showed that also in Germany water resources are finite. Projections and predictions for the next decades indicate that renewal rates of existing water resources will decline due the growing influence of climate change, but that water extraction rates will increase due to population growth. It is therefore important to find alternative and sustainable methods to make optimal use of the water resources currently available. For this reason, the reuse of treated wastewater for irrigation and recharge purposes has become one focus of scientific research in this field. However, it must be taken into account that wastewater contains so-called micropollutants, i.e., substances of anthropogenic origin. These are, e.g., pharmaceuticals, pesticides and industrial chemicals which enter the wastewater, but also metabolites that are formed in the human body from pharmaceuticals or personal care products. Through the treatment in wastewater treatment plants (WWTPs) as well as through chemical, biological and physical processes in the soil passage during the reuse of water, these micropollutants are transformed to new substances, known as transformation products (TPs), which further broaden the number of contaminants that can be detected within the whole water cycle.
Despite the fact that the presence of human metabolites and environmental TPs in untreated and treated wastewater has been known for a many years, they are rarely included in common routine analysis methods. Therefore, a first goal of this thesis was the development of an analysis method based on liquid chromatography - tandem mass spectrometry (LC-MS/MS) that contains a broad spectrum of frequently detected micropollutants including their known metabolites and TPs. The developed multi-residue analysis method contained a total of 80 precursor micropollutants and 74 metabolites and TPs of different substance classes. The method was validated for the analysis of different water matrices (WWTP influent and effluent, surface water and groundwater from a bank filtration site). The influence of the MS parameters on the quality of the analysis data was studied. Despite the high number of analytes, a sufficient number of datapoints per peak was maintained, ensuring a high sensitivity and precision as well as a good recovery for all matrices. The selection of the analytes proved to be relevant as 95% of the selected micropollutants were detected in at least one sample. Several micropollutants were quantified that were not in the focus of other current multi-residue analysis methods (e.g. oxypurinol). The relevance of including metabolites and TPs was demonstrated by the frequent detection of, e.g., clopidogrel acid and valsartan acid at higher concentrations than their precursors, the latter even being detected in samples of bank filtrate water.
By the integration of metabolites, which are produced in the body by biological processes, and biological and chemical TPs, the multi-residue analysis method is also suitable for elucidating degradation mechanisms in treatment systems for water reuse that, e.g., use a soil passage for further treatment. In the second part of the thesis, samples from two treatment systems based on natural processes were analysed: a pilot-scale above-ground sequential biofiltration system (SBF) and a full-scale soil aquifer treatment (SAT) site. In the SBF system mainly biological degradation was observed, which was clearly demonstrated by the detection of biological TPs after the treatment. The efficiency of the degradation was improved by an intermediate aeration, which created oxic conditions in the upper layer of the following soil passage. In the SAT system a combination of biodegradation and sorption processes occurred. By the different behaviour of some biodegradable micropollutants compared to the SBF system, the influence of redox conditions and microbial community was observed. An advantage of the SAT system over the SBF system was found in the sorption capacity of the natural soil. Especially positively charged micropollutants showed attenuation due to ionic interactions with negatively charged soil particles. Based on the physicochemical properties at ambient pH, the degree of removal in the investigated systems and the occurrence in the source water, a selection of process-based indicator substances was proposed.
Within the first two parts of this thesis a micropollutant was frequently detected at elevated concentrations in WWTPs effluents, which was not previously in the focus of environmental research: the antidiabetic drug sitagliptin (STG). STG showed low degradability in biological systems and thus it was investigated to what extend chemical treatment by ozonation can ensure attenuation of it. STG contains an aliphatic primary amine as the principal point of attack for the ozone molecule. There is only limited information about the behaviour of this functional group during ozonation and thus, STG served as an example for other micropollutants containing aliphatic primary amines. A pH-dependent degradation kinetic was observed due to the protonation of the primary amine at lower pH values. At pH values in the range 6 - 8, which is typical for the environment and in WWTPs, STG showed degradation kinetics in the range of 103 M-1s-1 and thus belongs to the group of readily degradable substances. However, complete degradation can only be expected at significantly higher pH values (> 9). The transformation of the primary amine moiety into a nitro group was observed as the major degradation mechanism for STG during ozonation. Other mechanisms involved the formation of a diketone, bond breakages and the formation of trifluoroacetic acid (TFA). Investigations at a pilot-scale ozonation plant using the effluent of a biological degradation of a municipal WWTP as source water confirmed the results of the laboratory studies: STG could not be removed completely even at high ozone doses and the nitro compound was formed as the main TP and remained stable during further ozonation and subsequent biological treatment. It can therefore be assumed that under realistic conditions both a residual concentration of STG and the formed main TP as well as other stable TPs such as TFA can be detected in the effluents of a WWTP consisting of conventional biological treatment followed by ozonation and subsequent biological polishing steps.
The present study deals with the synthesis of N-phenacylpyridinium salts and their use as photoinitiators for epoxy resins. The use and suitability of phenacyl salts as photoinitiators for epoxy resins has already been described in previous studies. The individual impact of the specific components on the rate constants of epoxy reaction has not been investigated in detail. Based on the structure of N-phenacylpyridinium salt the substances described in the present study were varied due to the exchange of counter ion and different substituents. Investigating the impact of the specific substituent with focus on the reaction of epoxy groups there is a dependence found for three main factors. First, depending on whether to use a phenyl or methyl group as substituent there was found an impact on the process of photolysis. Furthermore, concerning the dependences on the pyridine derivative and the counter ion, it was found that pyridine derivatives with electron withdrawing groups and counter ions, which can build strong acids, accelerate the rate constants of the epoxy reaction. Vice versa, pyridine derivatives with electron donating groups and counter ions, which can form weaker acids, decrease the rate constants.
The determined rate constants and the formulation of substances discussed in the present thesis in an adhesive formulation show the suitability of selected substances as photoinitiators for the polymerization of epoxy resins.
Die Biopolyester Cutin und Suberin stellen hydrophobe Grenzbarrieren dar, die sich im Laufe der Evolution der Landpflanzen entwickelt haben. Cutin bildet den Hauptbestandteil der Cuticula, die den Pflanzen Schutz vor unkontrollierter Transpiration bietet. Die Einlagerung von Suberin in die Zellwände definierter Zellen des Wurzelgewebes ermöglicht eine kontrollierte Aufnahme von Wasser und Nährstoffen. Zu den wichtigsten monomeren Bestandteilen dieser biologischen Polyester gehören langkettige α,ω-Dicarbonsäuren und ω-Hydroxycarbonsäuren. Bisher wurde der mikrobielle Abbau der Makromoleküle unzureichend erforscht. Zur Entschlüsselung der Zersetzung ist es notwendig, den Kreislauf der monomeren Bestandteile im Boden zu betrachten. Hierzu eignen sich vor allem Experimente mit positionsspezifisch ¹³C -markierten α,ω-Dicarbonsäuren und ω-Hydroxycarbonsäuren, die in der vorliegenden Arbeit erstmals synthetisch zugänglich gemacht wurden. Die Synthesen umfassten Dicarbonsäuren der geradzahligen Kettenlängen C12 bis C30, deren Carboxygruppen ¹³C -markiert sind. Ebenfalls wurde die Synthese von ω-Hydroxycarbonsäuren der Kettenlängen C14, C18, C22 und C30 mit ¹³C-Markierung an der Carboxygruppe realisiert. Weitere Zielverbindungen waren ω-Hydroxycarbonsäuren der Kettenlängen C14, C15, C18, C22 und C30, deren terminales hydroxyliertes Kohlenstoffatom mit ¹³C markiert ist. Im Rahmen der durchgeführten Arbeit gelang es, alle 19 Zielcarbonsäuren erfolgreich in hohen Ausbeuten und Reinheiten darzustellen. Die Synthese der isotopenmarkierten Verbindungen erforderte die Entwicklung spezieller auf die jeweiligen Zielsubstanzen individuell angepasster Syntheserouten, die den Einbau des Kohlenstoffisotops ¹³C ermöglichten. Für alle Zielverbindungen erfolgte die Einführung des ¹³C durch die Verwendung von ¹³C -markiertem Kaliumcyanid (99 at%). Wegen der hohen Kosten des ¹³C -markierten Ausgangsstoffes wurden alle Reaktionen zunächst unter der Verwendung analoger unmarkierter Edukte optimiert. Der letzte Teil der Arbeit bestand in der Ausführung eines Inkubationsexperimentes mit den ¹³C -markierten α,ω-Dicarbonsäuren der Kettenlängen C12, C18, C22 und C30. Mittels Phospholipidfettsäure-Analyse konnte gezeigt werden, dass die ¹³C -Dicarbonsäuren zu unterschiedlichen Anteilen von verschiedenen Mikroorganismengruppen zum Aufbau von Phospholipidfettsäuren verwendet wurden. Außerdem konnte durch die Anreicherung des CO2 mit dem Isotop ¹³C nachgewiesen werden, dass die ¹³C -markierten Fettsäuren von den Mikroorganismen zur Energiegewinnung abgebaut wurden. Für zukünftige Arbeiten wäre es interessant, Ausschnitte der Cutin- und Suberinstruktur nachzubilden. Durch die Veresterung der ¹³C -markierten α,ω-Dicarbonsäuren und der ¹³C -markierten ω-Hydroxycarbonsäuren untereinander oder mit Alkoholen könnten Dimere und Oligomere hergestellt werden.
During the development phase of plastic components, simulations are being used to an increasing extent. Against the background of product requirements and the inevitable necessity of conserving resources, the expanded use of simulation tools is an essential part of the solution. Among available methods, but so far underutilized with respect to real-life processes, is the molecular dynamics simulation. By the use of this method it is possible to visualize the physical processes occurring on the microscopic level, as e.g. those that arise during plastics processing. This thesis examines how boundary conditions, which mimic the extrusion blow molding process, affect the behavior of polyethylene on the microscopic level. A mesoscopic model (coarse-graining) is applied to describe the polymer. Initially, this model is verified by determining material properties. The uniaxial tensile test is modeled on the micro-scale to identify parameters such as the elastic modulus, yield stress, and Poisson’s ratio. Additionally, thermal properties, particularly those characterizing the crystallization behavior, are identified. The objective of these investigations is the microscopic observation and quantification of effects that occur during dynamic stretching and crystallization processes. The calculated properties show good agreement with the experimental data, especially regarding the thermal parameters. Qualitatively, the stress-strain behavior is reproduced in alignment with experimentally observed results. However, the short time scale of the simulation models leads to micromechanical behavior that is more extreme than what is monitored on a macroscopic level. By extending the simulation models, biaxial stretching processes are simulated. These stretching processes resemble the situation during the inflation of the parison in the extrusion blow molding process. The examination of various cooling conditions, particularly by the use of mold constraints, is another focus of the investigations. The analysis of the biaxially stretched simulations reveals that disentanglement processes during stretching dominate the further development of polymer systems. It is possible to quantify the dynamics of crystallization processes depending on the degree of stretching and cooling conditions through various parameters (distribution of entanglement points, local orientations). The results indicate that coarse-grained molecular dynamics simulations are able to significantly enhance the micromechanical understanding of local events occurring during plastic processing.
Die vorliegende Doktorarbeit hatte zum Ziel zu prüfen, ob Emulsionspolymere auf Acrylatbasis als neuartige Photokatalysatoren bzw. Katalysatoren genutzt werden können.
Auf Grund der Beschaffenheit und der Eigenschaften von Emulsionspolymeren ist davon auszugehen, dass die Nutzung selbiger als Katalysatoren eine neue Art einer chemischen Katalyse ermöglicht. So sollen die Vorteile der heterogenen und homogenen Katalyse vereint und die jeweiligen Nachteile minimiert werden. Als besonders erfolgversprechend hat sich während der praktischen Arbeit die Nutzung von Emulsionspolymeren als Photokatalysatoren herausgestellt.
Die Anbindung der photokatalytisch aktiven Moleküle an/in den Polymerstrang soll kovalent erfolgen. Deshalb war ein erstes Teilziel dieser Arbeit prototypische Katalysatormoleküle zu synthetisieren, die über einen Acrylat-Substituenten verfügen, der in einer radikalischen Polymerisationsreaktion reagieren kann. Als Photokatalysatoren wurden Ruthenium- Polypyridin-Komplexe ausgewählt, die sowohl für eine inter- als auch intramolekulare Photokatalyse zur Herstellung von Wasserstoff aus Wasser geeignet sind. Für organokatalytische Zwecke wurde ein L-Prolin-Derivat synthetisiert, welches jedoch nicht auf seine Polymerisierbarkeit getestet wurde.
In einem ersten Schritt wurden die prototypischen 2,2’-Bipyridin-Liganden synthetisiert. Dabei konnte eine verbesserte Synthesemethode für 4-Brom-2,2’-bipyridin ausgearbeitet werden. Die Funktionalisierung erfolgte letztendlich durch eine Horner-Wadsworth-Emmons-Reaktion, die anschließend an eine Eintopfsynthese zur Darstellung von 4-Formyl-2,2’-biypridin erfolgte. Die prototypischen Photokatalysatoren zeigten mäßige Erfolge (TON: 37-136, 6h, 10% H2O, 470 nm) in Bezug auf die photokatalytische Wasserstoffproduktion, sodass an dieser Stelle eine Verbesserung der entsprechenden katalytischen Systeme erfolgen sollte.
Die Polymerisationsreaktion konnte für zwei intermolekulare Photokatalysatoren und zwei intramolekulare Photokatalysatoren durchgeführt werden. Dabei fiel auf, dass die intermolekularen Photokatalysatoren besser polymerisieren als die intramolekularen Photokatalysatoren. Es wird angenommen, dass dies mit der Löslichkeit der Substanzen im Monomer Ethylmethacrylat zusammen hängt.
Die photokatalytisch funktionalisierten Emulsionspolymere zeigten eine ähnliche photokatalytische Aktivität (TON: 9-101, 6h, 10% H2O, 470 nm) wie die jeweiligen Ausgangsstoffe selbst. Es konnte jedoch bewiesen werden, dass Emulsionspolymere als Photokatalysatoren genutzt werden können, wenn auch noch weitere Arbeiten zur Optimierung der Systeme nötig sind.
Microplastics (MP), i.e., plastic particles < 5 mm, are perceived as a threatening envi-
ronmental and human health issue. Growing public interest in this class of contaminants
requires standardized and harmonized methods for their quantification. While an abun-
dance of analytical methods (both particle-based and mass-based) for the detection of
microplastics is available, existing studies on the quantity of MP in the environment lack
comparability. Therefore, the aim of this work was to establish a fast, reliable screen-
ing method for the quantification of the most common synthetic polymers in complex
environmental samples.
This was accomplished by a two-step pressurized liquid extraction (PLE) followed by
analysis via pyrolysis coupled to gas chromatography and mass spectrometry (Py–GC–
MS). In the first extraction step, a large part of the organic matrix was removed with
methanol at 100 ∘C and 100 bar, followed by a second step with tetrahydrofuran at
185 ∘C and 100 bar to extract the polymers that were subsequently adsorbed to silica
gel and measured with Py–GC–MS. With the developed method, limits of quantification
in an environmentally relevant concentration range of 7–8 μg g−1 for the most common
thermoplastic polymers polyethylene (PE), polypropylene (PP), and polystyrene (PS)
were achieved.
In order to improve the robustness of the method, poly(styrene-d5) (PSd5) was initially
applied as internal standard. However, further analyses revealed a deuterium–hydrogen
exchange during Py–GC–MS measurement, which was catalyzed by the inorganic ma-
trix. This effect was thereupon systematically investigated and poly(4-fluorostyrene) was
established as a new, stable internal standard.
While the developed method enabled the quantification of PE, PP, and PS, several other
polymers had to be excluded. In particular, the quantification of poly(ethylene tereph-
thalate) (PET) proved challenging via Py–GC–MS. A variety of catalytic effects by the
inorganic matrix was revealed and systematically investigated, e.g., changes in pyrolysis
product distribution. Several different sample preparation approaches failed to resolve
these issues. PLE led to a depolymerization of PET which was also catalyzed by the
inorganic sample matrix.
After further optimization and reduction of false positives, the developed method has
the potential to be included in future standardized procedures for MP quantification. It
provides a fast, robust analysis of MP in complex samples, while also considering widely overlooked matrix effects. Potential quantification approaches for other polymers that are
not included in the developed method (e.g., tire wear particles, paint particles) are also
discussed in this thesis.
The production and use of polymeric materials have been increasing continuously for
years. At the same time, the entry of microplastics (MP) – tiny particles resulting from the
wear and tear of these materials – into our environment is growing as well. By now,
awareness of MP has reached broad sections of the population and also research and
development on this field are similarly becoming increasingly important. However,
insufficient standardization and the lack of suitable analytical methods still make
recording and tracking of MP difficult, so that it remains largely unregulated. Mass-based
analytical methods are particularly advantageous for the establishment of legal
regulations. Apart from thermogravimetric methods, however, there are currently few
alternatives in this field. In this context, the use of nuclear magnetic resonance
spectroscopy (NMR), previously only qualitatively applied to MP, has now also been
examined for its quantitative benefits. This work deals with the current state of
quantitative NMR spectroscopy (qNMR) and tests possibilities for optimization and further
development for this purpose. Initially, the reduction of sample volumes and thus
minimized effort and measurement time of the method will be examined by combining
different polymer types into simultaneously measurable groups, as well as the suitability
of homopolymer calibrations for the detection of copolymers. Existing restrictions during
measurement will be adopted, and thus extractive procedures for sample preparation are
implemented. Finally, the influence of real environmental samples will be assessed, and
measures to reduce interfering factors will be taken in to account. As a result, the method
encompasses at least six polymer types, from PMMA, PS, BR, and PVC to PA and PET, as
well as separate approaches for polymers such as PAN and LDPE. A modular sample
preparation protocol, including extractive fractionation into measurement groups and a
chemical digestion method for matrix reduction, will be established and expanded to
include options for diffusion measurement and application to low-field instruments.
Practical application will be presented using real-world examples, such as freshwater
biofilms, as well as the use for quality control of certified reference materials.
Furthermore, initial insights into future development possibilities, like for the detection of
tire abrasion, will be provided.
The presence of synthetic chemicals in the environment can affect both ecosystems and
human health. In particular, the increasing contamination of the aquatic environment by
complex mixtures of anthropogenic trace substances has become a major global concern.
Once released into the environment, these compounds can undergo diverse
transformation processes to form a wide range of transformation products (TPs), which
are commonly unknown. Transformation inevitably alters the pattern of contamination and
exposure, as new substances are formed with frequently different physicochemical
properties, environmental behavior and toxicity in comparison to their precursor
compounds. For instance, TPs can exhibit significantly greater persistence and mobility in
the aquatic environment, posing a threat to both aquatic ecosystems and drinking water
resources. Therefore, TPs need to be considered in the risk assessment and authorization
process of chemicals. However, due to a combination of predictive, analytical, and
regulatory challenges, TPs currently remain largely unrecognized and unregulated. By
addressing these challenges, this thesis comprehensively characterizes the entry paths,
occurrence, fate, and (eco)toxicological relevance of selected TPs in the aquatic system in
Germany. These TPs have been largely overlooked in environmental studies and aquatic
monitoring programs for decades, despite their precursors being produced and used in
large quantities on a global scale.
The highly persistent and mobile substance trifluoroacetate (TFA) has garnered
significant attention in recent years due to its diverse sources, widespread occurrence in
the aquatic environment, and the lack of economically viable options to remove TFA from
contaminated waters. One of the most frequently discussed diffuse sources is the
formation of TFA in the atmosphere through the oxidation of volatile precursors and its
subsequent scavenging from the atmosphere by wet deposition. Despite the previously
reported occurrence of TFA in precipitation, the lack of recent and comprehensive data
has severely limited the understanding of the significance of wet deposition as a source of
TFA to the (aquatic) environment. Thus, in the present work, a nationwide field monitoring
campaign covering all precipitation events over a one-year sampling period was
conducted at eight sites across Germany. Samples were analyzed for TFA using ion
exchange chromatography (IC) coupled to negative-ion electrospray tandem mass
spectrometry (ESI-MS/MS). Of the analyzed samples, 16% exhibited TFA concentrations
≥ 1 μg/L. The precipitation-weighted average TFA concentration of 0.34 μg/L highlighted
that wet deposition alone is responsible for approximately 0.3 to 0.4 μg/L of TFA in
surface waters in Germany. The annual wet deposition fluxes ranged from 91 to
400 μg/m², with the highest fluxes observed in densely populated regions. The annual wet
deposition of TFA for Germany during the observation period was estimated to be 68 t.
The sampling revealed a pronounced seasonality, with the highest concentrations and wet
deposition fluxes of TFA observed in summer. Pearson correlation analyses indicated that
the transformation of TFA precursors in the troposphere is enhanced in summer due to
elevated concentrations of photochemically generated oxidants, primarily •OH, which
ultimately results in increased atmospheric TFA deposition. Overall, the study provided the
first published data on TFA in precipitation in Germany since 1995/96. The derived data
serves as a benchmark for future studies. In addition, it allows for the establishment of
mass balances and can be used to develop models to predict the loads of TFA entering
the aquatic environment from multiple sources.
The lack of robust historical data on the wet deposition fluxes of TFA also impeded long-
term trend analyses. Specifically, a postulated increase in atmospheric formation and
deposition of TFA due to substantial emission increases of numerous volatile TFA
precursors in recent decades remained unquantified. To address this knowledge gap,
archived plant samples were analyzed to evaluate the long-term temporal trends in the
atmospheric deposition of TFA in Germany. A robust and highly sensitive analytical
method for TFA in plant matrices was developed and validated. The method
encompassed a three-step sequential extraction procedure followed by the analysis of the
diluted sample extracts using IC-ESI-MS/MS. Subsequently, archived leaf samples of
various tree species and sampling sites from the German Environmental Specimen Bank
(observation period: 1989−2020) were analyzed for TFA. Statistical analysis revealed
significant (p < 0.05) positive trends in TFA concentrations in plant leaves, which is likely
the result of both phytoaccumulation and increasing emissions of gaseous TFA precursors
over the observation period. The concentrations increased by factors of up to 12 from
1989 to 2020. The highest concentrations (up to ∼1,000 μg/kg dry weight) were found in
Lombardy poplar leaves. Overall, the study presents the first trend analysis of TFA in biota
and raises awareness of the escalating atmospheric deposition of TFA over the past three
decades.
Sulfamate has previously been identified as a TP of the artificial sweeteners cyclamate
and acesulfame in wastewater and drinking water treatment. The preliminary results
indicated that sulfamate concentrations in wastewater treatment plant (WWTP) effluent
are substantially higher than those of other wastewater-borne contaminants. However,
despite its high global production and usage, no information was available on the sources,
occurrence, and environmental significance of sulfamate in the aquatic system in
Germany. To close this knowledge gap, a quantitative monitoring approach of different
urban water cycle compartments was conducted. Target analysis based on IC-ESI-MS/MS
revealed exceptionally high concentrations of sulfamate in wastewater (up to 1,900 μg/L),
surface water (up to 580 μg/L), and finished drinking water (up to 140 μg/L) in Germany.
Considering the limited data on short-term ecotoxicity, approximately 30% of the
sulfamate concentrations detected in groundwater and surface water samples exceeded
the derived predicted no-effect concentration (PNEC) of sulfamate. Therefore, the
potential impact of sulfamate on the aquatic ecosystem in Germany cannot be excluded.
Municipal WWTP effluent was identified as the primary source of sulfamate for the aquatic
system, as its concentrations correlated positively (r > 0.77) with the municipal wastewater
tracer carbamazepine in samples from different waterbodies. Ozonation and activated
sludge experiments demonstrated that sulfamate can be formed through chemical and
biological degradation of various precursors containing a sulfonamide group.
Nevertheless, the transformation of precursors to sulfamate in WWTPs and receiving
waters was found to be quantitatively insignificant, due to the substantial direct use of
sulfamic acid as a descaling agent in domestic and industrial applications. Laboratory
batch experiments, in conjunction with the findings from the sampling conducted at full-
scale waterworks, demonstrated that the commonly applied drinking water treatment
techniques, including ozonation and activated carbon filtration, are largely ineffective in
removing sulfamate. Bank filtration was identified as the only option to efficiently eliminate
sulfamate from contaminated raw water resources (removal: 62% to 99%). Overall, the
study presents the first comprehensive analysis of sulfamate in the urban water cycle and
suggests that there may be other high production volume inorganic chemicals that are
currently overlooked in environmental studies and monitoring programs.
Despite pantoprazole (PPZ) being one of the most widely prescribed human
pharmaceuticals globally, consistently low concentrations of this proton-pump inhibitor in
environmental water samples have been documented. This can be attributed to the
extensive metabolism of PPZ within the human body, with only minor amounts of the
parent compound being excreted. Since environmental monitoring and risk assessment
for regulatory purposes focus on the parent substances of pharmaceuticals, it was
assumed that the current environmental exposure associated with the use of PPZ is
considerably underestimated. In the presented thesis, 4′-O-demethyl-PPZ sulfide (M1)
was identified as the most relevant PPZ metabolite for environmental analysis. This was
achieved by applying reversed-phase high-performance liquid chromatography (RP-
HPLC) coupled to high-resolution mass spectrometry (HRMS) to urine samples of a PPZ
user, as well as to municipal wastewater. M1, which had not been investigated in previous
monitoring studies, was found to be ubiquitous in WWTP influent and effluent (max.:
3 μg/L, detention frequency: 100%) as well as in surface water (max.: 1.2 μg/L; detection
frequency: 97%) in Germany. Its average surface water concentration was approximately
30 times higher than that of the parent compound PPZ. Moreover, quantitative structure-
toxicity relationship (QSTR) modeling indicated a lower preliminary freshwater PNEC for
M1 (4.8 μg/L) compared to PPZ (28 μg/L). The analysis of archived suspended particulate
matter (SPM) samples from the Rhine at Koblenz revealed that the concentrations of M1
increased significantly from 2005 to 2015 and were positively correlated with the
prescription volume of PPZ. Conventional biological wastewater treatment was found to
be insufficient to remove M1 (average removal: 22%). Laboratory-scale experiments and
the analysis of samples taken after different treatment steps of an advanced full-scale
WWTP demonstrated that post-treatment with activated carbon as well as ozonation can
significantly improve the removal of M1 and PPZ during wastewater treatment, thereby
reducing their release to the aquatic environment. During ozonation, a rapid oxidation of
M1 was observed, accompanied by the formation of several ozonation products, which
were proposed for the first time. The identity of the main ozonation TPs of M1 was
confirmed through the synthesis of reference compounds. Their detection in samples
collected after the ozonation step of a full-scale WWTP demonstrated the transferability of
the laboratory-scale ozonation experiments. M1 was found to be sufficiently removed from
contaminated source waters (max. raw water concentration: 0.25 μg/L) by bank filtration
under different redox conditions (removal ≥ 80 %) and by other commonly applied
purification processes in drinking water production. In summary, this study revealed that
the environmental exposure and risk associated with the use of PPZ have been previously
underestimated, which likely extends to other human pharmaceuticals. Therefore, these
findings call for more sophisticated approaches to environmental monitoring and risk
assessment of pharmaceuticals that take TPs into account.
This thesis provides an in-depth understanding of the entry paths, occurrence, fate, and
environmental significance of selected TPs in the aquatic system in Germany. It
significantly advances our understanding of the introduction of TFA into the water cycle,
by characterizing the source of wet deposition and elucidating long-term temporal trends
of atmospherically deposited TFA. Additionally, the thesis gives comprehensive insights
into the formation, behavior, removability, and potential (eco)toxicological risks of
sulfamate, PPZ and its TPs. The thesis addresses key challenges in assessing and
integrating TPs into chemical management and presents solutions to overcome these
challenges. Finally, it highlights the urgent need for increased focus on TPs in research,
aquatic monitoring, and regulation to safeguard the environment and human health.