Naphthenic acids (NA) are a highly complex mixture of aliphatic carboxylic acids that may contain multiple rings and unsaturated double bonds, and are a subset of the naphthenic acid fraction components (NAFC), which can contain heteroatoms, unsaturations, and aromatic structures. Mono-carboxylated NAs can be classically represented by CnH2n+zO2 where z is a negative integer representing the hydrogen deficiency. NAs and NAFCs are components of the acid extractable organics (AEO) frequently associated with increased toxicity and observed at elevated concentrations in oil sands process waters (OSPW). Numerous chromatographic and mass spectrometry techniques have recently emerged to probe the composition and concentrations of these components. This thesis reports the use of a capillary hollow fiber polydimethylsiloxane (PDMS) membrane mounted on a probe interface that can be immersed directly into an aqueous sample. A methanol acceptor phase passing through the lumen transports analyte to an electrospray ionization source and a triple quadrupole mass spectrometer. This technique, termed condensed phase membrane introduction mass spectrometry (CP-MIMS), allows for rapid screening of m/z profiles and on-line quantification of NAs in complex samples within minutes. This thesis reports parametric studies of several model carboxylic acids and a standard naphthenic acid mixture (Merichem) involving the effect of sample pH on membrane transport and acceptor phase pH on ionization enhancement. Several quantitative strategies are explored including the use of an internal standard in the acceptor phase to correct for ionization suppression and variations in instrument sensitivity, and the use of selected ion monitoring (SIM) experiments to increase analytical sensitivity and potentially target specific NA isomer classes for quantitation. Analytical performance measures such as the linear dynamic range (1-2300 ppb [NA]T as Merichem), sensitivity (~1 ppb [NA]T as Merichem detection limit), precision (~20 %RSD for replicates of a single OSPW) and accuracy are reported. Quantitative results for various OSPW samples in the ppb to ppm range are reported as equivalents of several surrogates, including 1-pyrenebutyric acid (PyBA), Merichem, and a large-volume extract of northern Alberta OSPWs. The variety of quantitation strategies allows results to be compared with several other published methods. CP-MIMS results for three mid-range northern Alberta OSPWs are compared to analysis by Environment Canada with an average -21% bias. Results for five archived OSPWs spanning a wider concentration are compared to data from AXYS Analytical, with an average -49% bias. Applications of CP-MIMS as an in-situ monitor of removal efficiencies of NAs on adsorbents and real-time mass profile changes are also presented, along with some interpretation of the resulting high-resolution kinetic data to obtain decay constants. Using the targeted SIM method, adsorption decay can be followed in real-time for various isomer classes within the Merichem mixture, and kinetic data extracted to obtain decay constants for each. CP-MIMS is also used to characterize adsorption behavior for two activated biochars, including % removals for various loadings of each when added to stirred Merichem solutions. Preliminary multi-loading experiments are conducted with one biochar, and the ability of CP-MIMS to characterize adsorbent behavior by constructing adsorption isotherm plots is demonstrated. / Graduate

The typical strategy for atmospheric analysis of volatile organic compounds (VOCs), is to collect discrete samples which are then transported to a laboratory for analysis. This method has limited spatial and temporal resolution, and can be both costly and time consuming. To overcome these limitations, a mobile monitoring platform was developed for real-time quantitative chemical analysis. This work describes the development of membrane introduction mass spectrometer and identi es the necessary requirements to make a reliable and e ective instrument for in-situ chemical analysis. These include, the integration of a membrane interface with a miniaturized mass spectrometer, development of a data management strategy, reducing the e ects of isobaric interferences and employing an internal standard for quantitative measurements. Furthermore, the negative e ects of environmental variables, such as the Earth's magnetic eld, were examined and e ectively eliminated. In addition, this work demonstrates quantitative mapping of atmospheric VOCs in real-time, which allows rapid identi cation of chemical plumes and therefore, areas of potential concern. Both lab and eld-based comparisons of iv membrane introduction mass spectrometer data and traditional whole air sampling canister data were undertaken. The primary eld site was near Ft. McMurray, AB where baseline data was collected around a steam assisted gravity drainage (SAGD) facility and surrounding public roads. Monitoring for fugitive emissions at this facility and surrounding bitumen mining and processing operations is demonstrated. Field data were also obtained, near an industrial site in Ft.Saskatchewan, AB, that demonstrate the e cacy of an adaptive sampling strategy. Finally, chemical ionization was investigated as a soft ionization strategy to improve chemical selectivity for the analysis of complex hydrocarbon mixtures. The development of an in-line liquid chemical ionization reagent delivery system is presented and proposed as an e ective strategy for eliminating interferences arising from biogenic terpenes and alkyl aromatics. In all, this thesis presents the design and implementation of a mobile membrane introduction mass spectrometer for atmospheric chemical analysis. Results that improve performance and demonstrate the novelty of the data-type are provided, along with avenues for future development. / Graduate / 0486 / 0799 / 0608

Over the last few decades, membrane introduction mass spectrometry (MIMS) has been established as a robust tool for the on-line continuous monitoring of trace gases and volatile organic compounds. However, the range of amenable anlaytes has been limited by the need for molecules to pervaporate into a gaseous acceptor phase, or high vacuum environment of a mass spectrometer. This thesis expands the range of amenable analytes for MIMS to include larger, less volatile molecules (e.g., 200 to 500 Da), such as pharmaceuticals, persistent organic pollutants, and small biomolecules. This was achieved through the use of a liquid|membrane|liquid interface. We distinguish the technique from conventional MIMS, which uses a gaseous acceptor phase, by inserting the prefix ‘condensed phase’ to emphasize the use of a solvent acceptor phase – thus yielding CP-MIMS. An initial flow-cell interface with a methanol acceptor phase was characterized, yielding detection limits for model analytes in pptr to ppb, and analyte response times from 1-10 minutes. The flow cell interface was miniaturized into an immersion style CP-MIMS probe (~2 cm), which allowed for analysis of smaller volume samples and improved membrane washing capabilities. Comparable detection limits were observed for the immersion probe, however, it was noticed that significant analyte depletion was observed for samples under 2 mL. In addition, each of the developed membrane interfaces were observed to suffer from ionization suppression effects from complex samples when paired with ESI. Several strategies for mitigating ionization suppression using CP-MIMS are presented, including the use of a continuously infused internal standard present within the acceptor solvent. The developed CP-MIMS system was challenged with the analysis of naphthenic acids (a complex mixture of aliphatic carboxylic acids) directly in contaminated real-world samples. The method used negative ESI to rapidly screen and mass profile aqueous samples for naphthenic acids (as [M-H]-), with sample duty cycles ~20 min. However, it was found that Negative ESI did not differentiate hydroxylated and carboxylated analytes, and both species contributed signal to the total naphthenic acid concentration. To increase method specificity for carboxylic acids, barium ion chemistry was used in conjunction with positive ion tandem mass spectrometry. Common product ions were used to quantify carboxylated analytes, while a qualifier ion was used to confirm the functionality. The increased selectivity afforded by the barium ion chemistry was at the cost of a modest increase in detection limits. CP-MIMS has been established as a technique capable of the direct analysis of real-world samples, and shows promise as a rapid screening method for amenable environmental contaminants and/or biomolecules. / Graduate / 0486 / 0485 / kyle.duncan@viu.ca

Condensed phase membrane introduction mass spectrometry (CP-MIMS) is a direct, in situ analysis technique that is well suited to persistent organic pollutants, pesticides, and other small molecules. In CP-MIMS, neutral analytes permeate a hollow fibre membrane, typically polydimethylsiloxane (PDMS), driven by a concentration gradient. Analytes are subsequently dissolved by a liquid (condensed) solvent acceptor phase that is continuously flowed through the membrane lumen, which finally entrains the analytes to a mass spectrometer for detection. The membrane rejects charged and particulate matrix components, therefore eliminating sample cleanup that is otherwise necessary for conventional (i.e., chromatographic) techniques. However, larger analytes may suffer from relatively lengthy response times and lower sensitivity. A heptane cosolvent was therefore doped into the PDMS membrane, resulting in a polymer inclusion membrane (PIM). Through a system coupling CP-MIMS to electrospray ionization (ESI), the use of a PIM for model compounds resulted in faster response (~3×) and improved sensitivity (~3.5×, parts per trillion level detection limits). While effective for the demonstration of the PIM, pairing ESI with CP-MIMS represents an inherent incongruity: ESI is effective for polar, hydrophilic analytes, whereas CP-MIMS (i.e., PDMS membranes) is effective for hydrophobic analytes. CP-MIMS was therefore coupled with liquid electron ionization (LEI) as a more suitable ionization strategy. In LEI, the post-membrane solvent flow is entrained at nanolitre per minute flowrates to a LEI source, where the liquid is sequentially nebulized, vaporized, and ionized. The CP-MIMS-LEI coupling was optimized for the measurements of polycyclic aromatic hydrocarbon (PAH) isomer classes from aqueous samples, demonstrating low ng/L detection limits and response times (≤1.6 min). CP-MIMS-LEI was also applied to PAH isomer classes from soil samples, demonstrating rapid sample throughput (15 samples/hr) and low μg/kg detection limits, and additionally was quantitatively comparable to conventional techniques. A similar CP-MIMS-LEI system was applied to online monitoring of catalytic oxidation and alkylation reactions, demonstrating quantitative, real-time results for harsh, complex organic reaction mixtures. A significant analytical improvement was conducted by intentionally exploiting the already present liquid acceptor phase as an in situ means of providing liquid chemical ionization (CI) reagents for improved analyte sensitivity and selectivity (i.e., CP-MIMS-LEI/CI). Acetonitrile and diethyl ether were used as a combination acceptor phase/CI reagent system (i.e., proton transfer reagents) for the direct analysis of bis(2-ethylhexyl)phthalate from house dust (6 mg/kg detection limit). CP-MIMS-LEI/CI was then applied to PAHs from soils. Using methanol and dichloromethane combination acceptor phase/CI reagents, CP-MIMS-LEI/CI was shown to quantify and resolve PAH isomers from direct soil analyses via diagnostic PAH adduct ions: [M+CH2Cl+CH3OH-HCl]+ or [M+CHCl2-HCl]+. Using these selective ions, CP-MIMS-LEI/CI was again shown to be rapid (15 soils/hr), sensitive (ng/g detection limits) and quantitatively comparable to gas chromatography-MS for PAH measurements (average percent difference of -9% across 9 PAHs in 8 soil samples). The results across this thesis present a compelling argument for direct, quantitative screening from complex samples using CP-MIMS-LEI/CI, particularly given the simple workflow and short analytical duty cycle. / Graduate

Anthropogenic emissions into the troposphere can impact air quality, leading to poorer health outcomes in the affected areas. Volatile organic compounds (VOCs) are a group of chemical compounds, including some which are toxic, that are precursors in the formation of ground-level ozone and secondary organic aerosols. VOCs have a variety of sources, and the distribution of atmospheric VOCs differs significantly over time and space. Historically, the large number of chemical species present at low concentrations (parts-per-trillion to parts-per-billion by volume) have made VOCs difficult to measure in ambient air. However, with improvements in analytical instrumentation, these measurements are becoming more common place. Direct mass spectrometry (MS), such as membrane introduction mass spectrometry (MIMS) and proton-transfer reaction time-of-flight mass spectrometry (PTR-ToF-MS) facilitate real-time, continuous measurements of VOCs in air, with full scan mass spectral data capturing changes in chemical composition with high temporal resolution. Operated on-road, mobilized direct MS has been used for quantitative mapping of VOCs at the neighborhood scale, but identifying VOC sources based on the observed mixture of molecules in the full scan MS dataset has yet to be explored. This dissertation describes the use of chemometric techniques to interrogate full scan MS data, and the progression from discriminating VOC samples of known chemical composition based on full scan MIMS data through to the apportionment of VOC sources measured continuously with a PTR-ToF-MS system operating in a moving vehicle. Lab‐constructed VOC samples of known chemical composition and concentration demonstrated the use of principal component analysis (PCA) to discriminate, and k-nearest neighbours to classify, samples based on normalized full scan MIMS data. Furthermore, multivariate curve resolution-alternating least squares (MCR-ALS) was used to resolve mixtures into molecular component contributions. PCA was also used to discriminate ‘real-world’ VOC mixtures (e.g., woodsmoke VOCs, headspace above aqueous hydrocarbon samples) of unknown chemical composition measured by MIMS. Using vehicle mounted MIMS and PTR-ToF-MS systems, full scan MS data of ambient atmospheric VOCs were collected and PCA was applied to the normalized full scan MS data. A supervised analysis performed PCA on samples collected near known VOC sources, while an unsupervised analysis using PCA followed by cluster analysis was used to identify groups in a continuous, time series PTR-ToF-MS dataset measured between Nanaimo and Crofton, British Columbia (BC). In both the supervised and unsupervised analysis, samples impacted by emissions from different sources (e.g., internal combustion engines, sawmills, composting facilities, pulp mills) were discriminated. With PCA, samples were discriminated based on differences in the observed full scan MS data, however real-world samples are often impacted by multiple VOC sources. MCR-weighted ALS (MCR-WALS) was applied to the continuous, time series PTR-ToF-MS data from three field campaigns on Vancouver Island, BC for source apportionment. Variable selection based on signal-to-noise ratios was used to reduce the mass list while retaining the observed m/z that capture changes in the mixture of VOCs measured, improving model results, and reducing computation time. Both point (e.g., anthropogenic hydrocarbon emissions, pulp mill emissions) and diffuse (e.g., VOCs from forest fire smoke) VOC sources were identified in the data, and were apportioned to determine their contributions to the measured samples. The data analyzed captured fine scale changes in the ambient VOCs present in the air, and geospatial maps of each individual source, and of the source apportionment were used to visualize the distribution of VOC sources across the sampling area. This work represents the first use of MCR-WALS to identify and apportion ambient VOC sources based on continuous PTR-ToF-MS data measured from a moving vehicle. The methods described can be applied to larger scale field campaigns for the source apportionment of VOCs across multiple days to capture diurnal and seasonal variations. Identifying spatial and temporal trends in the sources of VOCs at the regional scale can help to identify pollution ‘hot spots’ and inform evidence-based public policy for improving air quality. / Graduate / 2022-08-17