Pressure Photoionization Research Articles

Studying the fragmentation mechanism of selected components present in crude oil by collision-induced dissociation mass spectrometry.

Structural characterization of individual compounds in very complex mixtures is difficult to achieve. One important step in structural elucidation is understanding the mass spectrometric fragmentation mechanisms of the compounds present in such mixtures. Here, different individual compounds presumed to be present in a complex crude oil mixture have been synthesized and structurally characterized by tandem mass spectrometry (MS/MS) studies. Model compounds with different aromatic cores and various substitutents were synthesized. Major effort has been put into producing isomerically pure compounds to better understand the fragmentation pattern. Each synthesized compound has been subjected to MSn studies using either a triple quadrupole or a linear ion trap mass spectrometer with electrospray or atmospheric pressure photoionization. The results are used to analyze individual compounds from a complex vacuum gas oil (VGO). The synthesized compounds and a chromatographically simplified vacuum gas oil were used for structural analysis. The major fragmentation mechanism is the benzylic cleavage of the aliphatic side chain. Each side chain can be separately removed from the aromatic core by using MSn methods. At the end of a series of fragmentations, the base aromatic core structure remains and can be chararcterized. By defining the fragmentation mechanism in complex oil samples it was possible to structurally characterize individual compounds present in a chromatographically simplified VGO. The compounds consist of an aromatic core with aliphatic side chains. Cleavage of all side chains can be achieved by MSn measurements, allowing characterization of the remaining core structure.

Application of Dopant-Assisted Atmospheric Pressure Photoionisation HPLC-MS Method for the Sensitive Determination of Polycyclic Aromatic Hydrocarbons in Dark Chocolate.

Multiple food research studies have shown that the polycyclic aromatic hydrocarbon (PAHs) are frequently found in processed cocoa products and chocolate. In a present study a method based on dopant-assisted atmospheric pressure photoionisation (DA-APPI) combined with a liquid chromatography/high-resolution mass spectrometer (HPLC-HRMS) for high-sensitivity analysis of four EU marker PAHs in dark chocolate samples was developed and fully validated according to the performance criteria set in EU guidelines. PAHs detection was achieved by HRMS in positive electrospray ionization mode with toluene used as a dopant to enhance the ionization efficiency of non-polar PAHs. The on-column instrument detection limits ranged from 0.8 to 1.2 pg for all four marker compounds. The method detection limits ranged from 0.016 to 0.024 μg kg-1 expressed on fat basis. The elaborated method was successfully applied to the analysis of four EU marker PAHs in dark chocolate samples. The presence of benzo[a]anthracene, benzo[b]fluoranthene and chrysene revealed at detectable levels in 100% of the samples, while benzo[a]pyrene was revealed in 77% of the samples, with its content ranging from 0.08 to 2.90 μg kg-1 fat.

Analysis of Petroleum Products by Gel Permeation Chromatography Coupled Online with Inductively Coupled Plasma Mass Spectrometry and Offline with Fourier Transform Ion Cyclotron Resonance Mass Spectrometry

We have examined the aggregation behavior of a typical atmospheric residue feedstock by gel permeation chromatography (GPC). The size profiles for compounds containing sulfur, vanadium, and nickel were determined online from elemental detection by inductively coupled plasma (ICP) mass spectrometry. Four fractions that vary in aggregation state were analyzed by positive atmospheric pressure photoionization (APPI) 9.4 T Fourier transform ion cyclotron resonance mass spectrometry (APPI FT-ICR MS). Results showed an inverse relationship between fraction aggregate size and monomer ion yield and revealed that aggregation tendency did not correlate with higher polar or aromatic species abundance. Aggregation in the atmospheric residue more closely correlated with increased relative abundance of larger and more aliphatic compounds. The molecular composition of the GPC aggregate fractions suggests that nonpolar intermolecular forces between saturated, long-chain alkyl substituents contribute more to aggregation th...

Comparing Crude Oils with Different API Gravities on a Molecular Level Using Mass Spectrometric Analysis. Part 2: Resins and Asphaltenes

The combination of fractionation methods for crude oils, such as saturate, aromatic, resin and asphaltene (SARA) fractionation, in combination with analysis by Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR MS) has been used for reducing the complexity and improving the characterization of crude oils. We have used the FT-ICR MS techniques in conjunction with electrospray ionization (ESI(±)) and atmospheric pressure photoionization (APPI(+)) to find trends between MS data of SARA fractions of crude oils with different American Petroleum Institute (API) gravities from the Sergipe-Alagoas basin (Brazil), focusing on the resin and asphaltene fractions. For the first time, an adaptation of the SARA fractionation has been performed to obtain a second resin fraction, which presented compounds with an intermediate aromaticity level between the first resins and asphaltene fraction. Both the first and second resin and the asphaltene fractions were studied on a molecular level using multiple ionization techniques and FT-ICR MS to find a direct relationship between the API gravities of a heavy, medium and light crude oil. For the FT-ICR MS data and the API gravities an aromaticity tendency was found. The data show that the use of SARA fractionation with FT-ICR MS offers a tool for comprehensive characterization of individual fractions and selective chemical characterization of the components in crude oils.

Comparing Crude Oils with Different API Gravities on a Molecular Level Using Mass Spectrometric Analysis. Part 1: Whole Crude Oil

Different ionization techniques based on different principles have been applied for the direct mass spectrometric (MS) analysis of crude oils providing composition profiles. Such profiles have been used to infer a number of crude oil properties. We have tested the ability of two major atmospheric pressure ionization techniques, electrospray ionization (ESI(±)) and atmospheric pressure photoionization (APPI(+)), in conjunction with Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR MS). The ultrahigh resolution and accuracy measurements of FT-ICR MS allow for the correlation of mass spectrometric (MS) data with crude oil American Petroleum Institute (API) gravities, which is a major quality parameter used to guide crude oil refining, and represents a value of the density of a crude oil. The double bond equivalent (DBE) distribution as a function of the classes of constituents, as well as the carbon numbers as measured by the carbon number distributions, were examined to correlate the API gravities of heavy, medium, and light crude oils with molecular FT-ICR MS data. An aromaticity tendency was found to directly correlate the FT-ICR MS data with API gravities, regardless of the ionization technique used. This means that an analysis on the molecular level can explain the differences between a heavy and a light crude oil on the basis of the aromaticity of the compounds in different classes. This tendency of FT-ICR MS with all three techniques, namely, ESI(+), ESI(−), and APPI(+), indicates that the molecular composition of the constituents of crude oils is directly associated with API gravity.

Molecular Characterization of Ketones in a Petroleum Source Rock

A comprehensive investigation of oil composition is important for the petroleum industry as well as the understanding of natural science. Ketones commonly exist in petroleum; however, as a result of the low concentrations and limitations inherent in the analytical technique, the molecular composition of these compounds is rarely studied. In this study, ketones in a source rock were characterized by gas chromatography–mass spectrometry, Fourier transform ion cyclotron resonance mass spectrometry, and Orbitrap mass spectrometry. Ketones were derivatized with the Girard T reagent under weakly acidic conditions to enhance their detectability by electrospray ionization mass spectrometry (ESI MS) analysis. Atmospheric pressure photoionization mass spectrometry (APPI MS) was also used for the molecular characterization of ketones without chemical derivatization. The characterization techniques were complementary to each other, and the results were consistent in general. The chemical derivatization followed by po...

Comprehensive Molecular Characterization of Atmospheric Brown Carbon by High Resolution Mass Spectrometry with Electrospray and Atmospheric Pressure Photoionization.

Light-absorbing components of atmospheric organic aerosols, which are collectively termed "brown carbon" (BrC), are ubiquitous in the atmosphere. They affect absorption of solar radiation by aerosols in the atmosphere and human health as some of them have been identified as potential toxins. Understanding the sources, formation, atmospheric evolution, and environmental effects of BrC requires molecular identification and characterization of light-absorption properties of BrC chromophores. Identification of BrC components is challenging due to the complexity of atmospheric aerosols. In this study, we employ two complementary ionization techniques, atmospheric pressure photo ionization (APPI) and electrospray ionization (ESI), to obtain broad coverage of both polar and nonpolar BrC components using high-resolution mass spectrometry (HRMS). These techniques are combined with chromatographic separation of BrC compounds with high performance liquid chromatography (HPLC), characterization of their light absorption with a photodiode array (PDA) detector, and chemical composition with HRMS. We demonstrate that this approach enables more comprehensive characterization of BrC in biomass burning organic aerosols (BBOAs) emitted from test burns of sage brush biofuel. In particular, we found that nonpolar BrC chromophores such as PAHs are only detected using positive mode APPI. Meanwhile, negative mode ESI results in detection of polar compounds such as nitroaromatics, aromatic acids, and phenols. For the BrC material examined in this study, over 40% of the solvent-extractable BrC light absorption is attributed to water insoluble, nonpolar to semipolar compounds such as PAHs and their derivatives, which require APPI for their identification. In contrast, the polar, water-soluble BrC compounds, which are detected in ESI, account for less than 30% of light absorption by BrC.

Characterization of aromatic hydrocarbons and sulfur heterocycles in Saudi Arabian heavy crude oil by gel permeation chromatography and ultrahigh resolution mass spectrometry

The characterization of petroleum crude oil samples remains an overwhelming task for any single analytical technique. Additionally, the compositional complexity of crude oil typically increases with increase in sulfur content and decrease in API gravity. In the present investigation we employed gel permeation chromatography (GPC) for separating Arabian Heavy crude oil into clearly defined fractions, and atmospheric pressure photo ionization Fourier transform-ion cyclotron resonance mass spectrometry (APPI FT-ICR MS) for elucidating the structural commonalities through in-depth characterization of the fractions. The work involved the development of a GPC method by the selection of suitable columns, mobile phase, and optimization of separation conditions. Toluene was found to be suitable as a mobile phase for the analysis of nonpolar aromatic compounds as well as compatible with the subsequent APPI FT-ICR MS measurement. The GPC fractionated aromatic compounds based on the number of carbon atoms in alkyl chains. Compounds with a higher number of carbon atoms in their alkyl chains elute earlier in the GPC separation. This observation was true for aromatic hydrocarbons (HC), mono-sulfur (S1) and di-sulfur (S2) containing compounds. Using respective planar aromatic cores as parent structures, we systematically calculated the average number of alkyl carbon atoms present in each GPC fraction. The average number of alkyl carbon atoms were found to be 36, 27, 17, 9 and 5 in successive GPC fractions (from early to late elution), with only two alkyl carbon atoms overlap between successive fractions.

Complementary Ionization Techniques for the Analysis of Scotch Whisky by High Resolution Mass Spectrometry.

Fourier transform mass spectrometry (FTMS) is widely used to characterize the chemical complexity of mixtures, such as natural organic matter (NOM), petroleum, and agri-food products (including Scotch whisky). Although electrospray ionization (ESI) is by far the most widely used ionization source in these studies, other ionization techniques are available and may offer complementary information. In a recent study, we found matrix free laser desorption/ionization (LDI) to be effective for the analysis of Suwannee river fulvic acid (SRFA), and to provide complementary chemical insights. In this study, LDI along with atmospheric pressure photoionization (APPI) and atmospheric pressure chemical ionization (APCI) were compared to ESI for the analysis of Scotch whisky. High mass accuracy (54 ppb, mean) allowed for the assignment of 86% of peaks, with 3993 unique molecular formulas identified from four representative samples analyzed. All four ionization techniques, performed in negative mode, identified thousands of formulas. Many were unique to each ionization source, while 699 formulas were common to all techniques. Ions were identified in both deprotonated and radical anion forms. Our study highlights the importance of a multi-ionization source approach; we recommend that analysis of complex mixtures, especially novel ones, should not be limited solely to ESI.

Advances in Asphaltene Petroleomics. Part 3. Dominance of Island or Archipelago Structural Motif Is Sample Dependent

Asphaltene structure is one of the most controversial topics in petroleum chemistry. The controversy is centered on the organization of aromatic cores within asphaltene molecules (single aromatic core, island and multiple aromatic core, archipelago) and specifically the inconsistency between the island model and the composition of the products derived from asphaltene pyrolysis/thermal cracking. Such products are consistent with the coexistence of island and archipelago asphaltene structural motifs. However, the archipelago model continues to lack the widespread acceptance of the petroleum community, in part due to mass spectrometry results in support of the island model. In the first and second part of this series, we demonstrated that the disproportionally high atmospheric pressure photoionization (APPI) ionization efficiency (monomer ion yield) of island species is due to weak nanoaggregation of large aromatic cores which do not extensively aggregate in toluene, whereas more archipelago-dominant fractio...

Photochemical conversion of toluene in simulated atmospheric matrix and characterization of large molecular weight products by +APPI FT-ICR MS

The lack of kinetic parameters of VOC photochemical conversion especially in the presence of NO and O3, and product information, will result in the incomplete understanding for the occurrence of haze. In the present study, the photochemical conversion of toluene, one of most significant hydrocarbons of VOCs, in toluene, toluene/NO, toluene/O3 and reaction systems was assessed for up to 4 days in a smog chamber at 278 K and 308 K. The results indicated that the addition of NO and O3 promoted the conversion of toluene. The first-order kinetic rate constants of toluene assessed in the toluene reaction system at 278 K and 308 K were 0.12 and 0.19 day−1, respectively. The second-order kinetic rate constants of toluene assessed in the toluene/NO were 0.1 × 10−13 cm3 molecule−1 day−1 (at 278 K) and 0.9 × 10−13 cm3 molecule−1 day−1 (at 308 K), and those in the toluene/O3 reaction systems were 0.06 × 10−12 cm3 molecule−1 day−1 (at 278 K) and 0.11 × 10−12 cm3 molecule−1 day−1 (at 308 K). The small difference of second-order kinetic rate constants between 278 K and 308 K obtained for the toluene/O3 system when compared with the toluene/NO system indicated the reduced reaction sensitivity of O3 to the temperature. Several dozens of large molecule products containing up to O6 heteroatoms were identified by positive ion atmospheric pressure photoionization (+APPI) coupled with Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR MS), with double bond equivalents up to 18, and carbon numbers ranging within 12–38, respectively. The findings presented herein may provide a new train of thought for the photochemical reaction process of toluene and its conversion in ambient air.

Aromatic formulas in ambient PM2.5 samples from Hong Kong determined using FT-ICR ultrahigh-resolution mass spectrometry.

Many aromatic compounds (e.g., polycyclic aromatic hydrocarbons (PAHs)) found in atmospheric aerosols are toxic and exist in both unsubstituted and substituted forms. Previous studies have mainly concentrated on investigating unsubstituted PAHs, leaving the substituted compounds largely uncharacterized. This study focuses on detection of both unsubstituted and substituted aromatics in ambient aerosol samples using ultrahigh-resolution mass spectrometry. Aerosol samples collected from roadside, urban, and suburban sites in Hong Kong were characterized by Fourier-transform ion cyclotron resonance mass spectrometry (FT-ICR-MS) coupled with atmospheric pressure photoionization (APPI) or electrospray ionization (ESI). In the APPI+ mode, 166 aromatic CH formulas (i.e., formulas containing C and H only and with a double bond equivalent (DBE) of 4 or higher) were determined through molecular formula calculations based on an accurate m/z determination. Among the determined aromatic CH formulas, 141 are possible alkylated monocyclic aromatic hydrocarbon (MAH) or PAH formulas, and account for ≥ 45% of the total intensity by aromatic CH+ formulas. Both APPI+ and ESI+ are effective in detecting nitroaromatics (i.e., CHO2N1 formulas and DBE ≥ 5). The two ionization modes provide complementary formula coverage, with formulas determined by APPI+ extending to higher DBE and those by ESI+ covering higher carbon numbers. Alkylated nitrobenzene compounds are the most abundant among nitroaromatics, and they, together with alkylated nitro-PAHs, account for > 80% of the total intensity of aromatic CHO2N+ formulas, indicating the importance of these compounds in real aerosol samples. Aromatic CHN+ and CHO+ formulas are also determined, confirming the atmospheric presence of some previously reported O- and N-containing aromatic compounds and revealing new possible formulas. The determination of aromatic organic formulas in this study provides useful guidance for future quantitative analysis of hazardous aromatic compounds. Future work is needed to determine the abundance and to study the toxicity of alkylated MAHs and PAHs outside the 16 US EPA priority PAH compounds. Graphical abstract.

Finding a relationship between the composition and the emulsifying character of asphaltenes through FTICR-MS

In this work, n-heptane insoluble fractions (asphaltenes) from six crude oils were analyzed by means of Fourier-transform ion cyclotron resonance mass spectrometry (FTICR MS) using both positive Atmospheric Pressure Photo Ionization (+) APPI and negative Electro- Spray Ionization (-) ESI in order to understand their water-oil emulsion stabilization capability on a molecular level basis. Through (+) APPI it was possible to obtain an overview of samples composition. By sorting as nitrogen sulfur and oxygen containing compounds, it was possible to compositionally distinguish the asphaltenes. Through (-) ESI, several differences were also observed by grouping the classes as oxygen (NxOy+NxOySz+Oy+OySz) and non oxygen containing classes (Nx+NxSz). The interactions of these two groups of compounds must be considered in order to understand the water-oil emulsion stability. It implies that the cores where nitrogen and sulfur are part may interact via π-π stacking, while the oxygen containing compounds may interact either via hydrogen bonding or via dipole forces with the aromatic aggregates (highly polarizable), forming potentially surface active aggregates. Thus, the rate between these two families of compounds may determine the surfactant character of asphaltenes at the water-oil interface. Bearing this in mind, an emulsion stability coefficient was proposed based on the relative abundances of some families of compounds detected by (-) ESI-FTICR-MS to explain the crude oils’ tendency to form emulsions.

Negative-ion atmospheric pressure ionisation of semi-volatile fluorinated compounds for ultra-high-performance liquid chromatography tandem mass spectrometry analysis.

In this work, the feasibility of negative-ion atmospheric pressure chemical ionisation (APCI) and atmospheric pressure photoionisation (APPI) for ultra-high-performance liquid chromatography tandem mass spectrometry (UHPLC-MS/MS) determination of fluorotelomer alcohols (FTOHs), fluorinated octanesulfonamides (FOSAs) and fluorinated octanesulfonamido-ethanols (FOSEs) was evaluated. The study of the effect of mobile phase composition on the atmospheric pressure ionisation of these compounds indicated that methanol/water mixtures provided the best responses in APCI, while acetonitrile/water with a post-column addition of toluene as dopant was the most appropriated mixture in APPI. Under the optimal working conditions, most of the target compounds produced the ion [M-H]- as base peak, although in-source collision-induced dissociation fragment ions in APCI and APPI andsuperoxide adduct ions [M+O2]-• in APPI were also present. These ions proved to be more useful as precursor ions for MS/MS determination than the adduct ions generated in electrospray. Although the UHPLC-APCI-MS/MS method allowed the determination of these semi-volatile compounds at low concentration levels, the analysis by UHPLC-APPI-MS/MS provided the lowest limits of detection and it was applied to the analysis of water samples in combination with solid-phase extraction. Quality parameters demonstrated the good performance of the proposed method, providing low method limits of detection (0.3-6ngL-1), good precision (RSD % < 5%) and an accurate quantification (relative error % < 14%). Among the river water samples analysed by the developed method, 4:2 FTOH and N-EtFOSA were determined at 30 and 780ngL-1, respectively.

Carotenoids: Experimental Ionization Energies and Capacity at Inhibiting Lipid Peroxidation in a Chemical Model of Dietary Oxidative Stress.

Carotenoids are important natural pigments and micronutrients contributing to health prevention by several mechanisms, including their electron-donating (antioxidant) activity. In this work, a large series of carotenoids, including 11 carotenes and 14 xanthophylls, have been investigated by wavelength-resolved atmospheric pressure photoionization mass spectrometry (DISCO line of SOLEIL synchrotron), thus allowing the experimental determination of their ionization energy (IE) for the first time. On the other hand, the carotenoids have been also investigated for their ability to inhibit the heme iron-induced peroxidation of linoleic acid in mildly acidic micelles, a simple but relevant chemical model of oxidative stress in the gastric compartment. Thus, the carotenoids can be easily classified from IC50 concentrations deduced from the time dependence of the lipid hydroperoxide concentration. With a selection of two carotenes and three xanthophylls a quantitative analysis is also provided to extract stoichio-kinetic parameters. The influence of the carotenoid structure (number of conjugated carbon-carbon double bonds, presence of terminal six-membered rings, hydroxyl, keto, and/or epoxy groups) on the IE, IC50, and stoichio-kinetic parameters is discussed in details. The data show that the antioxidant activity of carotenes is well correlated to their electron-donating capacity, which itself largely depends on the length of the conjugated polyene chain. By contrast, the IE of xanthophylls is poorly correlated to the polyene chain length because of the strong, and sometimes unexpected, electronic effects of the O-atoms. Although IE remains an approximate predictor of the antioxidant activity of xanthophylls, other factors (interaction with the aqueous phase, competing radical-scavenging mechanisms, the residual activity of the antioxidant's oxidation products) probably play a significant role.

Splitless hyphenation of SFC with MS by APCI, APPI, and ESI exemplified by steroids as model compounds

A systematic evaluation of splitless hyphenation of supercritical fluid chromatography (SFC) with mass spectrometry (MS) was performed using different techniques for ambient pressure ionization. Interfaces commonly known from HPLC-MS/MS, i.e. electrospray ionization (ESI), atmospheric pressure chemical ionization (APCI), and atmospheric pressure photo ionization (APPI), were tested for their suitability in SFC-MS/MS. A triple quadrupole MS was used for data evaluation in a targeted multi-analyte design using endogenous steroids as model compounds. Individual optimization of the ionization parameters was performed in multi-dimensional design for best support of ionization in all three techniques. A post-column make-up was used to avoid analyte precipitation in the transfer capillary but also to support ionization independently from mobile phase composition. Buffer choice and concentration as well as temperature were found crucial in ESI and APCI. Best results for the multi-analyte method were obtained in both techniques using ammonium fluoride as make-up buffer. Instead of buffer solutions different organic solvents were used as dopants in APPI to support ionization. The mobile phase constituent isopropanol was already found to support ionization in APPI, however, for many analytes the addition of toluene resulted in superior results in terms of intensity. Comparing the optimized methods in terms of limit of detection (LOD), limit of quantification (LOQ), and sensitivity (slope of calibration curve) ESI was the best choice for the multiple analyte design. Only a few analytes resulted in a different optimum ionization, if focused on separately. In terms of linear dynamic range, APCI and APPI proved superior to ESI, where calibration over the whole range of concentrations (from LOD up to 5000 pg ∗ μL−1) required quadratic regression.

Solvent composition dependent signal reduction of molecular ions generated from aromatic compounds in (+) atmospheric pressure photoionization mass spectrometry.

The ionization process is essential for successful mass spectrometric (MS) analysis because of its influence on selectivity and sensitivity. In particular, certain solvents reduce the ionization of the analyte, thereby reducing the overall sensitivity in atmospheric pressure photoionization (APPI). Since the sensitivity varies greatly depending on the solvents, a fundamental understanding of the mechanism is required. Standard solutions were analyzed using a (+)-APPI Q Exactive ion trap mass spectrometer (Thermo Scientific). Each solution was infused directly into the APPI source at a flow rate of 100μL/min and the APPI source temperature was 300°C. Other operating mass spectrometric parameters were maintained under the same conditions. Quantum mechanical calculations were carried out using the Gaussian 09 suite program. Density functional theory was used to calculate the reaction enthalpies (∆H) of the reactions between toluene and other solvents. The experimental and theoretical results showed good agreement. The abundances of analyte ions were well correlated with the calculated ∆H values. Therefore, the results strongly support the suggested signal reduction mechanism. In addition, linear correlations between the abundance of toluene and analyte molecular ions were observed, which also supports the suggested mechanism. A solvent composition dependent signal reduction mechanism was suggested and evaluated for the (+)-APPI-MS analysis of polyaromatic hydrocarbons (PAHs) generating mainly molecular ions. Overall, the evidence provided in this work suggests that reactions between solvent cluster(s) and toluene molecular ions are responsible for the observed reductions in signal.

Predicting the glass transition temperature and viscosity of secondary organic material using molecular composition

Abstract. Secondary organic aerosol (SOA) accounts for a large fraction of submicron particles in the atmosphere. SOA can occur in amorphous solid or semi-solid phase states depending on chemical composition, relative humidity (RH), and temperature. The phase transition between amorphous solid and semi-solid states occurs at the glass transition temperature (Tg). We have recently developed a method to estimate Tg of pure compounds containing carbon, hydrogen, and oxygen atoms (CHO compounds) with molar mass less than 450 g mol−1 based on their molar mass and atomic O : C ratio. In this study, we refine and extend this method for CH and CHO compounds with molar mass up to ∼ 1100 g mol−1 using the number of carbon, hydrogen, and oxygen atoms. We predict viscosity from the Tg-scaled Arrhenius plot of fragility (viscosity vs. Tg∕T) as a function of the fragility parameter D. We compiled D values of organic compounds from the literature and found that D approaches a lower limit of ∼ 10 (±1.7) as the molar mass increases. We estimated the viscosity of α-pinene and isoprene SOA as a function of RH by accounting for the hygroscopic growth of SOA and applying the Gordon–Taylor mixing rule, reproducing previously published experimental measurements very well. Sensitivity studies were conducted to evaluate impacts of Tg, D, the hygroscopicity parameter (κ), and the Gordon–Taylor constant on viscosity predictions. The viscosity of toluene SOA was predicted using the elemental composition obtained by high-resolution mass spectrometry (HRMS), resulting in a good agreement with the measured viscosity. We also estimated the viscosity of biomass burning particles using the chemical composition measured by HRMS with two different ionization techniques: electrospray ionization (ESI) and atmospheric pressure photoionization (APPI). Due to differences in detected organic compounds and signal intensity, predicted viscosities at low RH based on ESI and APPI measurements differ by 2–5 orders of magnitude. Complementary measurements of viscosity and chemical composition are desired to further constrain RH-dependent viscosity in future studies.

Insight into the molecular distribution of soluble components from Dayan lignite through mass spectrometers with four ionization methods

Dayan lignite (DL) was subjected to thermal dissolution sequentially with cyclohexane, acetone and methanol to obtain three filtrates. The filtrates were characterized by Fourier transform infrared spectroscopy, gas chromatography/mass spectrometry (GC/MS), and time-of-flight mass spectrometry (TOF-MS) equipped with atmospheric pressure photoionization (APPI), electrospray ionization (ESI) or direct analysis in real time (DART) to understand the structural features of DL. Aliphatic hydrocarbons, furans and alcohols were enriched in the filtrate of cyclohexane, acetone and methanol, respectively, according to the data of GC/MS. One ring aromatics was also identified by GC/MS as major species in the three filtrates. Both GC/MS and APPI-MS can well analyze compounds with low polarity, but APPI-TOF-MS in this work successfully characterized polycyclic aromatics and extended the measurement range (molecular weight and ring size) of GC/MS. ESI-TOF-MS is suitable to analyze polar compounds in coal. Data from ESI-TOF-MS indicated that heteroatom compounds including non-aromatics and aromatics with 1-2 rings are the major polar components in DL. As an ambient MS ionization method, DART shortened the analysis time without sample pretreatment and more aromatics over 4 rings were identified by DART-TOF-MS. Characterization of the complex coal filtrates with multiple mass spectrometers provided a full view of the molecular information of DL.

Applicability of low-flow atmospheric pressure chemical ionization and photoionization mass spectrometry with a microfabricated nebulizer for neutral lipids.

Mass spectrometry with atmospheric pressure chemical ionization (APCI) or photoionization (APPI) is widely used for neutral lipids involved in many fundamental processes in living organisms. Commercial APCI and APPI sources operate at high flow rates compatible with conventional high-performance liquid chromatography (HPLC). However, lipid analysis is often limited by a small amount of sample, which requires low flow rate separations like capillary or micro-HPLC. Therefore, APCI and APPI suitable for microliter-per-minute flow rates need to be developed and applied for neutral lipids. A micro-APCI/APPI source with a heated chip nebulizer was assembled and mounted on a Thermo ion trap instrument. The ion source operated in APCI, APPI or dual mode was optimized for low microliter-per-minute sample flow rates. The source performance was investigated for squalene, wax esters, fatty acid methyl esters, triacylglycerols, and cholesterol. The ion source behaved as a mass-flow-sensitive detector. Direct infusion of methyl oleate showed superior analytical figures of merit when compared with high-flow ion sources. A detection limit of 200pmol/mL and a linear dynamic range spanning three orders of magnitude were measured for micro-APCI. The mass spectra of most lipids differed from high flow rate spectra. Unlike micro-APCI, micro-APPI spectra were complicated by odd-electron species. Dual APCI/APPI mode did not show any benefits for neutral lipids. Applications for lipid samples were demonstrated. Micro-APCI-MS is a useful detection technique for neutral lipids at microliter-per-minute flow rates. It offers high sensitivity and high quality of spectra in direct infusion mode and promises successful utilization in capillary and micro-HPLC applications.