Condensed-Phase Membrane Introduction Mass Spectrometry (CP-MIMS)
We have pioneered the use of mass spectrometry coupled to membrane interfaces to study intrinsic molecular and material properties at low permeant concentrations and in multi-component mixtures. This contribution opens significant new capacity in the study of mass transport in semi-permeable membranes. Furthermore, understanding the factors that limit membrane transport has directly contributed to the evolution of an important MIMS variant (known as Condensed Phase MIMS or CP-MIMS) in our group. This invention, protected by Canada, US and worldwide (PCT) patents, uses a liquid (condensed) acceptor phase for analyte transfer. CP-MIMS has already had a significant impact on the field of environmental chemistry, opening new territory by widening the analyte range to include low volatility targets of concern such as polyaromatic hydrocarbons (PAHs), pesticides, surfactants and drugs, leading to substantial progress and new applications.
The characterization of this technique was followed up with a paper that described improved performance characteristics for thinner membranes and their application to pharmaceutical compounds and naphthenic acids. This was the first paper to establish a semi-quantitative rapid screening method for multiple naphthenic acid isomer classes directly in complex oil sands process water samples using an immersion probe designed in our group. The impact of CP-MIMS is substantial, enabling the chemical determination of a much broader range of environmentally and biologically important chemicals of concern, attracting the interest of industries in the energy sector, regulators and analytical service providers. In-situ reaction monitoring by dynamic chemical systems by MIMS Our group has employed the continuous real-time capabilities of MIMS to investigate the transformation of organic compounds directly in aqueous solution. We published the first example of an in-situ sampling platform to extract rate constants by simultaneously monitoring the degradation of individual gasoline components by tandem MS techniques at parts per trillion levels. We have extended this work to monitor the kinetics of photosensitized halogenation reactions of trace halocarbon contaminants directly in natural waters containing dissolved organic matter as well as the formation kinetics of volatile and non-volatile disinfection by-products. We have applied this approach to monitor dynamic changes in both the distribution and quantity of naphthenic acids in oil sands processed waters under the influence of ultraviolet light and adsorbents. The sensitivity and selectivity afforded by tandem MS strategies coupled to the direct measurement of reaction kinetics in complex samples without laborious and time-consuming handling has significantly improved our ability to follow natural and industrial processes, including remediation and treatment efforts. Our work in this area is important to the field of environmental organic chemistry, enabling kinetic studies of chemical transformations directly in environmental media. This contribution addresses a long-standing problem in the investigation of environmental transformations- that of extrapolating measurements made in-silico under controlled conditions to environmental systems, such as lakes, estuaries and tailings ponds.
Field portable MS systems with real-time geospatial mapping
Development and application of small MS for portable scenarios is an active paradigm shift in which the AERL is a key player. Our early work mobilized bench top systems, temporally and spatially quantifying air toxics, using MS/MS, online internal standards and off-line data analysis. Taking the lab to the sample has been a logical progression for our research. Our group developed the first prototype ruggedized membrane introduction ion-trap mass spectrometer capable of tandem mass spectrometry experiments on a mobile platform. This has resulted in substantial improvements in our ability to directly measure VOC/SVOCs in both air and water, during stationary and mobile deployments. The ability to detect a wide variety of analyte classes ranging from low to high volatility makes in field/in situ instrumentation more versatile, allowing superior environmental monitoring and rapid bioanalytical screening. To date, we have developed a leading edge technological solution, and we are proposing further improvements in this area to confront the direct, in-field/in-situ measurement of important target analytes in complex and dirty samples, such as naphthenic acids in oil sands extraction and processing wastes or drugs and metabolites in small volume bio-fluid samples.
We subsequently added adaptive feedback and real-time, cloud based data storage and analysis. Interactive results in the Google Earth™ web environment enabled, for the first time, rapid access to quantitative field MS measurements in an intuitive format. The time series data can be viewed in real-time and/or interrogated later providing unprecedented data sets that can be linked to sources, human exposure and health effects. This significant development removes delays between sampling/analysis and informed, results-based decisions. Rapid response is key in critical events such as spills or accidents, and allows intelligent, adaptive decisions for field sampling (site selection, prescreening) prior to off-line lab, based measurements. MIMS provides ‘real-time’, free analyte concentrations, and temporal concentration changes (e.g. moving emission plumes) can be measured, recording transient events that may have significant health implications. Our leadership in this area has helped to inspire academics and industry to develop MIMS monitoring systems capable of direct, in-field monitoring. Real-time, cloud based data handling is now becoming more common for field measurements by MS and other methods. This pioneering work has the potential to revolutionize environmental assessments and source apportionment studies and has attracted considerable attention from both industrial users and public agencies. This work represents a significant milestone in the evolution of environmental analysis from the lab to the field. This research was funded by Statoil Hydro, Norway.
Membrane Interface Design Development
MIMS membranes perform a direct, online, non-exhaustive extraction of permeating analytes, obviating contamination, dilution and recovery losses associated with off-line sample preparation, while simultaneously rejecting the bulk sample matrix and allowing sample remeasurement. Our research group aims to improve MIMS membrane transport, develop small volume, microfluidic based interfaces and couple them with flexible ionization approaches.We have used several interface variants for continuous, online sampling systems, exploiting hollow fibre membranes in robust flow cell geometries and direct insertion/immersion probes. Micro to nano flow scale MIMS systems based on hollow fibre membranes will be further developed because of their easy incorporation with conventional (HPLC) fluid handling. Microfluidics adoption is a better approach, enabling new applications for very small samples (blood spots, cerebrospinal fluids) and in situ diagnostics. Stereolithographic 3D printing will be used to make miniature, sheet membrane based, microfluidic MIMS interface systems.
Better understanding membrane transport behavior and the increased selectivity/selectivity it affords opens new territory. Small sample measurements with simple, one use interfaces and multiplexed, automated microfluidic systems will elevate MIMS to a realistic alternative for high throughput, direct environmental and bioanalytical screening with continuous measurement capabilities.
Correlation of HPLC-HRMS separation and speciation of naphthenic acids to direct sampling, on-line membrane introduction mass spectrometry techniques
Napthenic Acids (NAs), a by-product of crude oil refining from oil sands deposits, are a major contaminant of oil sands process water (OSPW) and are toxic to fish and other organisms. Membrane introduction mass spectrometry (MIMS) has been demonstrated as an analytical method capable of rapidly screening NAs directly in samples with very little or no sample preparation. A polydimethylsiloxane (PDMS) polymer membrane is used as an interface between the sample and mass spectrometer. In acidic solution, protonated NAs are transferred into a methanol acceptor phase coupled to an atmospheric pressure ion source. Used in conjunction with HRMS and multiple ionization modes, MIMS can provide accurate mass data, and allow for compound class and/or molecular formula assignment directly from contaminated samples, without sample clean up or chromatographic separation. The overarching research question motivating this work is to determine if MIMS techniques can adequately differentiate the composition and quantity of NA mixtures in a series of variously impacted natural and OSPW water samples. This project is funded by Environment Canada.