Structural characterization of organic aerosol using Fourier transform ion cyclotron resonance mass spectrometry: aromaticity equivalent approach.

RATIONALE: A challenge of atmospheric particulate matter (PM) analysis is the understanding of the sources and chemistry of complex organic aerosols, especially the water-soluble organic compounds (WSOC) fraction, a key component of atmospheric fine PM (PM(2.5)). The sources of WSOC are not well understood and, thus, the molecular characterization of WSOC is important because it provides insight into aerosol sources and the underlying mechanisms of secondary organic aerosols formation and transformation. METHODS: In this study, molecular characterization of WSOC was achieved using Fourier transform ion cyclotron resonance mass spectrometry. The aromaticity equivalent (X(c)), a new parameter calculated from the assigned molecular formula, is introduced to improve the identification and characterization of aromatic and condensed aromatic compounds in WSOC. Diesel PM (DPM) and atmospheric PM samples were used to study the applicability of the proposed method. RESULTS: Threshold values of X(c) ≥2.5000 and X(c) ≥2.7143 are proposed as unambiguous minimum criteria for the presence of aromatics and condensed aromatics, respectively. By using these criteria, 36% of precursors were defined as aromatics and condensed aromatics in the DPM. For comparison, 21% of aromatic and condensed aromatic compounds were defined using the Aromaticity Index (AI) classification. The lower estimates by the AI approach are probably due to the failure to recognize aromatics and condensed aromatics with longer alkyl chains. The estimated aromatic and condensed aromatic fractions in the atmospheric aerosol samples collected in an industrial area affected by biomass burning events were 51.2 and 50.0%, respectively. CONCLUSIONS: The advantage of employing this parameter is that X(c) would have a constant value for each proposed core structure regardless of the degree of alkylation, and thus visual representation and structural interpretations of the spectra become advantageous for characterizing and comparing complex samples. In addition, the proposed parameter complements the AI classification and identification of aromatic and condensed aromatic structures in complex matrices.

Effect of industrialization on the differences in sources and composition of ambient PM2.5 in two Southern Ontario locations.

PM2.5 was sampled over a seven-year period (2013-2019) at two locations ∼50 km apart in Southern Ontario (concurrently for five years: 2015-2019). One is a heavily industrialized site (Hamilton), while the other was a rural site (Simcoe). To assess the impact of industrialization on the composition and sources of PM affecting air quality in these two locations, positive matrix factorization coupled with dispersion normalization (DN-PMF) was used to identify six and eight factors at Simcoe and Hamilton, respectively. The Simcoe factors in order of diminishing PM mass contribution were: particulate sulphate (pSO4), secondary organic aerosol (SOA), crustal matter, particulate nitrate (pNO3), biomass burning, and vehicular emissions. At Hamilton, the effects of industrialization were observed by the ∼36% higher average ambient PM2.5 concentration for the study period as well as the presence of factors unique to metallurgy, i.e., coking and steelmaking, compared to Simcoe. The coking and steelmaking factors contributed ∼15% to the PM mass at Hamilton. Seasonal variants of appropriate nonparametric trend tests with the associated slopes (Sen's) were used to assess statistically significant changes in the factor contributions to PM2.5 over time. Specifically at Hamilton, a significant decline in PM contributions was noted for coking (-0.03 µg/m³/yr or -4.1%/yr) while steelmaking showed no statistically significant decline over the study period. Other factors at Hamilton that showed statistically significant declines over the study period were: pSO4 (-0.27 µg/m³/yr or -12.6%/yr), biomass burning (-0.05 µg/m³/yr or -9.02%/yr), crustal matter (-0.03 µg/m³/yr or -5.28%/yr). These factors mainly accounted for the significant decline in PM2.5 over the study period (-0.35 µg/m³/yr or -4.24%/yr). This work shows the importance of long-term monitoring in assessing the unique contributions and temporal changes of industrialization on air quality in Ontario and similarly affected locations.

Identification of weak and strong organic acids in atmospheric aerosols by capillary electrophoresis/mass spectrometry and ultra-high-resolution Fourier transform ion cyclotron resonance mass spectrometry.

A novel approach using a combination of capillary electrophoresis/mass spectrometry (CE/MS) and off-line Fourier transform ion cyclotron resonance mass spectrometry (FTICR-MS) revealed the structural details of acidic constituents of atmospheric organic aerosol. Both techniques utilized electrospray ionization (ESI), a soft ionization method, to facilitate the analysis of complex mixtures of organic compounds. CE/ESI-MS using an UltraTrol LN-precoated capillary and acidic background electrolytes at different pH values (2.5 and 4.7) was used to differentiate between weak (carboxylic) and strong (sulfonic) organic acids. On the basis of the electrophoretic mobility, m/z constraints from CE/ESI(-)-MS, and elemental composition information retrieved from off-line FTICR-MS, a variety of aliphatic and aromatic carboxylic acids (CHO-bearing molecules), nitrogen-containing carboxylic acids (CHON-bearing molecules), organosulfates (CHOS-bearing molecules), and (nitrooxy)organosulfates (CHONS-bearing molecules) were tentatively identified in the Oasis-HLB-extracted urban PM(2.5) (particulate matter with an aerodynamic diameter of <2.5 µm). The chemical known/unknown structures of detected compounds were confirmed by the semiempirical Offord model (effective mobility linearly correlated to Z/M(2/3)). The majorities of the identified compounds are products of atmospheric reactions and are known contributors to secondary organic aerosols.

Insights into Elemental Composition and Sources of Fine and Coarse Particulate Matter in Dense Traffic Areas in Toronto and Vancouver, Canada.

Traffic is a significant pollution source in cities and has caused various health and environmental concerns worldwide. Therefore, an improved understanding of traffic impacts on particle concentrations and their components could help mitigate air pollution. In this study, the characteristics and sources of trace elements in PM2.5 (fine), and PM10-2.5 (coarse), were investigated in dense traffic areas in Toronto and Vancouver, Canada, from 2015-2017. At nearby urban background sites, 24-h integrated PM samples were also concurrently collected. The PM2.5 and PM10-2.5 masses, and a number of elements (i.e., Fe, Ba, Cu, Sb, Zn, Cr), showed clear increases at each near-road site, related to the traffic emissions resulting from resuspension and/or abrasion sources. The trace elements showed a clear partitioning trend between PM2.5 and PM10-2.5, thus reflecting the origin of some of these elements. The application of positive matrix factorization (PMF) to the combined fine and coarse metal data (86 total), with 24 observations at each site, was used to determine the contribution of different sources to the total metal concentrations in fine and coarse PM. Four major sources were identified by the PMF model, including two traffic non-exhaust (crustal/road dust, brake/tire wear) sources, along with regional and local industrial sources. Source apportionment indicated that the resuspended crustal/road dust factor was the dominant contributor to the total coarse-bound trace element (i.e., Fe, Ti, Ba, Cu, Zn, Sb, Cr) concentrations produced by vehicular exhaust and non-exhaust traffic-related processes that have been deposited onto the surface. The second non-exhaust factor related to brake/tire wear abrasion accounted for a considerable portion of the fine and coarse elemental (i.e., Ba, Fe, Cu, Zn, Sb) mass at both near-road sites. Regional and local industry contributed mostly to the fine elemental (i.e., S, As, Se, Cd, Pb) concentrations. Overall, the results show that non-exhaust traffic-related processes were major contributors to the various redox-active metal species (i.e., Fe, Cu) in both PM fractions. In addition, a substantial proportion of these metals in PM2.5 was water-soluble, which is an important contributor to the formation of reactive oxygen species and, thus, may lead to oxidative damage to cells in the human body. It appears that controlling traffic non-exhaust-related metals emissions, in the absence of significant point sources in the area, could have a pronounced effect on the redox activity of PM, with broad implications for the protection of public health.

Characterization of benzene polycarboxylic acids and polar nitroaromatic compounds in atmospheric aerosols using UPLC-MS/MS.

The molecular characterization of water-soluble organic compounds (WSOC), a large fraction of the organic mass found in the atmospheric aerosols, is important to better understand emissions and atmospheric processes influencing the particulate pollution in most urban areas. This study deals with the development of a routine method using ultrahigh pressure liquid chromatography-electrospray ionization-triple quadrupole mass spectrometry (UPLC-ESI-MS/MS) for rapid analysis of primary and secondary organic compounds distributed among three classes: (i) benzene polycarboxylic acids; (ii) nitroaromatic acids and (iii) nitrophenols in ambient particles. Using an UPLC HSS T3 column with a mobile phase consisting of formic acid/acetonitrile under gradient elution, all target analytes were eluted within a total time of 12 min. Although some targeted analytes with different m/z were not resolved, a quantitation of these compounds was carried by distinct multiple reaction monitoring (MRM) transitions. Quality parameters of the method were established. The method was proven to be sensitive with limits of detection ranged from 0.02 to 0.89 ng/mL. Together with a simple sample preparation and the use of labeled internal standards, the method was confirmed to be robust and reliable to determine a large number of organic tracers in atmospheric particulate matter samples. The analytical procedure was also applied to assess the abundance and characteristics of target analytes in PM2.5 emitted from diesel and gasoline-powered engines, and Urban Dust and Diesel Particulate Matter Standard Reference Materials (SRM 1649b and SRM 1650b, respectively). The obtained results suggest that trimellitic, 4-hydroxyphthalic and 4-nitrophthalic acids may be used as potential tracers for diesel engine emissions. Clear differences in distribution of target species were observed between urban PM2.5 affected by the traffic and biomass burning emissions.

CE-MS: a useful tool for the identification of water-soluble polar organics in air and vehicular emitted particulate matter.

A CE-ESI/quadrupole-MS method using an ammonium acetate-based BGE (pH 4.7) was developed for the determination of isomeric benzoic acids in atmospheric aerosols and vehicular emission. UltraTrol LN was employed as the pre-coating polymer to suppress the EOF (0.3 x 10(-9) m2 V(-1) s(-1)) and achieve a baseline separation of the studied acids. Good repeatability for migration time (RSD < 1%, N = 10) was obtained without coating regeneration. The high pre-coating stability allowed coupling of CE to MS without ion suppression in the MS. In scanning mode and using field-amplified sample injection with electrokinetic injection (-5 kV for 60 s), LODs (S/N = 3) ranged from 2.5 to 6 microg/L for standard target analytes prepared in DI water. In the presence of 100 mg/L of sulfate (added to simulate a sample matrix), LODs ranged from 8 to 90 microg/L. Several isomeric aromatic acids could be separated in atmospheric and diesel-engine-emitted particulate matter extracts based on their different acidities. Additional measurements with a flow infusion ESI Fourier transform ion cyclotron resonance MS were used for further structural information acquisition on the unknown compounds and allowed their formula to be proposed.

Investigation of isomeric structures in a commercial mixture of naphthenic acids using ultrahigh pressure liquid chromatography coupled to hybrid traveling wave ion mobility-time of flight mass spectrometry.

The separation of isomeric naphthenic acids (NAs) is of high importance to obtain more detailed and therefore useful information to understand their fate, transport, toxicity and potential removal treatment methodologies. In the current study, the capabilities of the ultrahigh pressure liquid chromatography/traveling wave ion mobility-time of flight mass spectrometry (UPLC/TWIM-TOF-MS) to separate and study different isomeric structures of NAs were investigated. Fifty seven standard compounds belonging to different chemical families of classical NAs were analyzed to obtain their experimental drift times in addition to chromatographic retention time and mass-to-charge information (m/z). These acyclic and cyclic molecules yielded ions with collision cross section (CCS) values ranging from 110 to 210 Å2. The feasibility of the UPLC/TWIM-TOF-MS method to provide a higher degree of confidence in the identification of isomeric structures was evaluated by analyzing the commercial (Sigma-Aldrich) NAs mixture. Identification and structure confirmation of several alicyclic compounds of similar m/z in the NAs mixture were possible by this method. For instance, the presence of previously tentatively identified compounds by the ultrahigh pressure liquid chromatography/quadrupole time of flight mass spectrometry (UPLC/QTOF-MS), such as 4-tert-butylcyclohexanoic acid, 4-dicyclohexylacetic acid or 3,5-dimethyladamantane-1-carboxylic acid, was confirmed. Combining ion mobility separation with UPLC/TOF-MS gives a higher level of selectivity to the overall method by selective interrogation of specific retention time, mass-to-charge and mobility regions. However, there are cases where it is not possible to resolve many similar molecules such as acyclic isomeric compounds in commercial NAs mixture by this technique. This was likely due to the very small CCS area differences among the structural isomeric species. Considerable improvements in the ion mobility resolution and separation will be required for this technique to be able to resolve isomeric species with slight differences in physicochemical properties (e.g., size and structure).

Application of ultrahigh-performance liquid chromatography-quadrupole time-of-flight mass spectrometry for the characterization of organic aerosol: Searching for naphthenic acids.

Naphthenic acids (NAs) are naturally occurring constituents of hydrocarbon deposits (petroleum, oil sands bitumen, and crude oils), and present in any facilities that extract, process or use crude oil or bitumen for manufacturing. In the Athabasca oil sands region (AOSR) of Alberta, Canada, this diverse group of saturated acyclic, monocyclic, and polycyclic carboxylic acids is present in bitumen and in tailing ponds. Little is known about the occurrence of residual oil sands derived organic material, including NAs, in atmospheric particulate matter (PM). This work describes the optimization of an ultrahigh-performance liquid chromatography-quadrupole time-of-flight mass spectrometry (UPLC/QTOF-MS) method to characterize and identify classical NAs in atmospheric PM. Under the optimum conditions, analysis of the Sigma-Aldrich technical NA STD Mix showed the absence of saturated fatty acids, while branched and cyclic NAs isomers with carbon number ranged between 10 and 30, and Z families between 0 and -12 were detected. Higher molecular weight NAs representing compounds with carbon number ranging between 30 and 40 were identified in the analyzed PM samples collected in AOSR. In contrast, isomeric branched acyclic NAs were not detected in the background (PM-R) samples collected far from AOSR. Except for fatty acids (Z=0), other Z homologues were also not detectable or present at very low concentration in the analysed PM-R samples. Preliminary examination of NA profiles showed that the composition of NAs in PM collected in close proximity to surface mining operations is predominantly "refractory" high molecular weight branched NAs, differing from that collected closer to upgraders and tailings ponds. It is suspected that dust released from the mine faces and dry tailings in the AOSR are sources of NAs to atmosphere. Further samples should be examined to confirm findings. This preliminary study presents, to our knowledge, the first direct identification of branched acyclic and cyclic NAs in atmospheric PM.

Development of a hydrophilic interaction liquid chromatography-mass spectrometry method for detection and quantification of urea thermal decomposition by-products in emission from diesel engine employing selective catalytic reduction technology.

The use of urea based selective catalytic reduction (SCR) technology for the reduction of NOx from the exhaust of diesel-powered vehicles has the potential to emit at least six thermal decomposition by-products, ammonia, and unreacted urea from the tailpipe. These compounds may include: biuret, dicyandiamine, cyanuric acid, ammelide, ammeline and melamine. In the present study, a simple, sensitive and reliable hydrophilic interaction liquid chromatography (HILIC)-electrospray ionization (ESI)/mass spectrometry (MS) method without complex sample pre-treatment was developed for identification and determination of urea decomposition by-products in diesel exhaust. Gradient separation was performed on a SeQuant ZIC-HILIC column with a highly polar zwitterionic stationary phase, and using a mobile phase consisting of acetonitrile (eluent A) and 15 mM ammonium formate (pH 6; eluent B). Detection and quantification were performed using a quadrupole ESI/MS operated simultaneously in negative and positive mode. With 10 µL injection volume, LODs for all target analytes were in the range of 0.2-3 µg/L. The method showed a good inter-day precision of retention time (RSD<0.5%) and peak area (RSD<3%). Satisfactory extraction recoveries from spiked blanks ranged between 96 and 98%. Analyses of samples collected during transient chassis dynamometer tests of a bus engine equipped with a diesel particulate filter (DPF) and urea based SCR technology showed the presence of five target analytes with cyanuric acid and ammelide the most abundant compounds in the exhaust.

Recent advances in CE and CEC of pollutants.

Recent advances in CE and CEC separation, detection and sample preparation/preconcentration methodologies, for the determination of a variety of compounds having current or potential environmental relevance, have been overviewed. The reviewed literature has illustrated the wide range of CE applications available, indicating a continuing interest in CE and CEC in the environmental field. New developments in chip-based CE systems are also discussed.

Semipermanent capillary coatings in mixed organic-water solvents for CE.

This report describes the creation of semipermanent capillary coatings that are compatible with organic-water solvent systems in CE. The coatings are created by simply rinsing the fused-silica capillary with long double-chain cationic surfactants, such as dimethyl-ditetradecyl ammonium bromide (2C(14)DAB), dihexadecyldimethyl ammonium bromide (2C(16)DAB), and dimethyldioctadecyl ammonium bromide (2C(18)DAB). These surfactants generate semipermanent bilayer coatings on the capillary surface, which display a high degree of stability in buffers containing up to 60% v/v of organic solvents, such as methanol and ACN. The coating stability increases with increasing hydrophobicity of the surfactant, i.e., with increasing chain length. For instance, the EOF changes by only 1.2% in a 2C(18)DAB-coated capillary after 130 capillary volumes of rinsing with 60% v/v methanol containing buffer. The bilayer coatings allow separations to be performed without the need to regenerate the coating between runs or to maintain the EOF modifier in the run buffer. Rapid separations (<2 min) of anions and basic drugs with migration time reproducibility of less than 0.5% RSD and efficiencies of 0.4-0.6 million plates/m are obtained. In addition, selectivity changes for small anions and cationic drugs are also observed when the organic solvent content is adjusted.

Off-line coupling of preparative capillary zone electrophoresis with microwave-assisted acid hydrolysis and matrix-assisted laser desorption ionization mass spectrometry for protein sequencing.

An off-line coupling of capillary electrophoresis (CE) with microwave-assisted acid hydrolysis/matrix-assisted laser desorption ionization mass spectrometry (MAAH/MALDI) has been developed for protein identification and characterization. Preparative scale protein separations enable collection of 10-50 pmol of purified cytochrome c for subsequent sequencing using MAAH/MALDI. To reduce protein adsorption onto the silica surface, the cationic surfactant-based coatings, dimethylditetradecylammonium bromide and dimethyldioctadecylammonium bromide, are employed. The choice of the buffer conditions is critical for both the preparative CE and MAAH/MALDI method. The use of high buffer concentrations (100 mM Bis-tris) reduces electromigration dispersion, but suppressed MALDI ionization such that a peptide sequence coverage of only 80% was achieved at a sample loading of 40 g L(-1) of each cytochrome c. By reducing the buffer concentration to 25 mM Bis-tris, the sequence coverage increased to 95% at a sample loading of 40 g L(-1).

Preparative capillary zone electrophoresis using a dynamic coated wide-bore capillary.

Preparative capillary zone electrophoresis separations of cytochrome c from bovine and horse heart are performed efficiently in a surfactant-coated capillary. The surfactant, dimethylditetradecylammonium bromide (2C(14)DAB), effectively eliminated protein adsorption from the capillary surface, such that symmetrical peaks with efficiencies of 0.7 million plates/m were observed in 50-microm id capillaries when low concentrations of protein were injected. At protein concentrations greater than 1 g/L, electromigration dispersion became the dominant source of band broadening and the peak shape distorted to triangular fronting. Matching of the mobility of the buffer co-ion to that of the cytochrome c resulted in dramatic improvements in the efficiency and peak shape. Using 100 mM bis(2-hydroxyethyl)imino-tris(hydroxymethyl)methane phosphate buffer at pH 7.0 with a 100-microm id capillary, the maximum sample loading capacity in a single run was 160 pmol (2.0 microg) of each protein.

Enhanced stability self-assembled coatings for protein separations by capillary zone electrophoresis through the use of long-chained surfactants.

Semipermanent coatings were generated within fused-silica capillaries by flushing the capillary with a 0.1 mM solution of the double-chained cationic surfactants didodecyldimethylammonium bromide, dimethylditetradecylammonium bromide (2C(14)DAB), dihexadecyldimethylammonium bromide, and dimethyldioctadecylammonium bromide (2C(18)DAB) and the triple-chained surfactant tridodecylmethylammonium iodide. All of these coatings were semipermanent, whereby the coating remained intact after the unadsorbed surfactant was removed from the capillary. The separation efficiencies for four model cationic proteins ranged from 1.2 to 1.4 million plates/m for the 2C(14)DAB coating to 0.3-0.4 million plates/m for the 2C(18)DAB coatings. The stability of the coating increased with increasing hydrophobicity of the surfactant (i.e., increasing chain length and decreasing cmc). Over 60 successive separations were performed on a 2C(18)DAB-coated capillary over 12 days, without any regeneration of the coating. The migration times varied by less than 2.3% over this period with no loss in efficiency.

Factors affecting the temporal stability of semipermanent bilayer coatings in capillary electrophoresis prepared using double-chained surfactants.

Surfactants such as didodecyldimethylammonium bromide (DDAB) adsorb onto fused-silica capillaries to form semipermanent bilayer coatings. However, such coatings must be regenerated between runs to maintain efficiency and reproducibility. In this paper, chemical and physical factors affecting the stability of DDAB coatings are investigated. Chemical factors such as ionic strength and the nature of the buffer anion (e.g., from acetate to phosphate), which decrease the critical micelle concentration of DDAB, improve the coating stability. Increasing buffer pH also increases the coating stability. Finally, reducing the capillary diameter and reducing the volume of buffer flushed through the capillary enhance the coating stability. Using 50 mM acetate, pH 5.0, in a 25-microm-i.d. capillary, cationic proteins were separated with efficiencies of 1.05 million plates/m and a run-to-run migration time reproducibility of 0.6-0.8% RSD for 10 successive runs without regeneration of the DDAB coating between runs.