Gas chromatography coupled to time-of-flight mass spectrometry using parallel electron and chemical ionization with permeation tube facilitated reagent ion control for material emission analysis.

RATIONALE: Volatile organic compounds (VOCs) emitted by an artificial leather part for car interiors are determined using GC-MS (gas chromatograph coupled to a mass spectrometer) using simultaneous electron and chemical ionization (EI&CI). A device for swift reagent ion switching in CI mode between consecutive runs is presented. METHODS: VOCs emitted from the investigated material were sampled onto Tenax® absorption tubes using micro emission chambers and subsequently injected into the GC through thermal desorption. The detector was a time-of-flight mass spectrometer (TOFMS) simultaneously operating in EI and CI modes during a single chromatographic run. A custom permeation tube setup allowed for swift selection between various reagent ions in CI mode, e.g., [N2 H]+ , [H3 O]+ , [(H2 O)2 H]+ , and [NH4 ]+ . RESULTS: Different reagent ions are swiftly selectable between single GC runs without hardware changes. Differences in precursor ion survival yields and the selectivity of the various reactants were carefully assessed. Several examples for the improved identification of unknown compounds with the available complementary and comprehensive EI&CI data set are demonstrated for a relevant material emission application. CONCLUSION: The presented technique provides additional value to the standard GC-EI/MS procedure commonly used for material emission characterization. It allows for a non-targeted analysis approach with moderate analysis time.

Parallel Operation of Electron Ionization and Chemical Ionization for GC-MS Using a Single TOF Mass Analyzer.

This work describes a novel mass spectrometer coupled to gas chromatography (GC-MS) that simultaneously displays the mass spectral information of electron (EI)- and chemical ionization (CI)-generated ion populations for a single chromatographic peak. After GC separation, the eluent is equally split and supplied in parallel to an EI and a novel CI source, both operating continuously. Precise switching of the ion optics provides the exact timing to consecutively extract the respective ion population from both sources and transfer them into a time-of-flight (TOF) mass analyzer. This technique enables the acquisition of complementary information from both ion populations (EI and CI) within a single chromatographic run and with sufficient data points to retain the chromatographic fidelity. The carefully designed GC transfer setup, fast ion optical switching, and synchronized TOF data acquisition system provide an automatic and straightforward spectral alignment of two ion populations. With an eluent split ratio of about 50% between the two ion sources, instrument detection limits of <40 fg on the column (octafluoronaphthalene) for the EI and <2 pg (benzophenone) for the CI source were obtained. The system performance and the additional analytical value for compound identification are demonstrated by means of different common GC standard mixtures and a commercial perfume sample of unknown composition.

Observation of charged droplets from electrospray ionization (ESI) plumes in API mass spectrometers.

Electrospray ionization (ESI) generates bare analyte ions from charged droplets, which result from spraying a liquid in a strong electric field. Experimental observations available in the literature suggest that at least a significant fraction of the initially generated droplets remain large, have long lifetimes, and can thus aspirate into the inlet system of an atmospheric pressure ionization mass spectrometer (API-MS). We report on the observation of fragment signatures from charged droplets penetrating deeply the vacuum stages of three commercial mass spectrometer systems with largely different ion source and spray configurations. Charged droplets can pass through the ion source and pressure reduction stages and even into the mass analyzer region. Since droplet signatures were found in all investigated instruments, the incorporation of charged droplets is considered a general phenomenon occurring with common spray conditions in ESI sources.

Computational analysis of the proton-bound acetonitrile dimer, (ACN)2 H.

RATIONALE: In atmospheric pressure ionization mass spectrometry the theoretical thermodynamic treatment of proton-bound cluster stabilities helps us to understand the prevailing chemical processes. However, such calculations are rather challenging because low-barrier internal rotations and strong anharmonicity of the hydrogen bonds cause the breakdown of the usually applied harmonic approximation. Even the implemented anharmonic treatment in standard ab initio software failed in the case of (ACN)2 H+ . METHODS: For a case study of the proton-bound acetonitrile dimer, (ACN)2 H+ , we scan the potential energy surface (PES) for the internal rotation and the proton movement in all three spatial directions. We correct the partition functions by treating the internal rotation as a free rotor and by solving the nuclear Schrödinger equation explicitly for the proton movement. An additional PES scan for the dissociation surface further improves the understanding of the cluster behavior. RESULTS: The internal rotation is essentially barrier free (V0 = 2.6 × 10-6 eV) and the proton's movement between the two nitrogen atoms follows a quartic rather than quadratic potential. As a figure of merit we calculate the free dissociation enthalpy of the dimer. Our description significantly improves the standard results from about 118.3 kJ/mol to 99.6 kJ/mol, compared with the experimentally determined value of 92.2 kJ/mol. The dissociation surface reveals strong crosstalk between modes and is essentially responsible for the observed errors. CONCLUSIONS: The presented corrections to the partition functions significantly improve their accuracy and are rather easy to implement. In addition, this work stresses the importance of alternative theoretical methods for proton-bound cluster systems besides the standard harmonic approximations.

Non-targeted and targeted analysis of oxylipins in combination with charge-switch derivatization by ion mobility high-resolution mass spectrometry.

Eicosanoids and other oxylipins play an important role in mediating inflammation as well as other biological processes. For the investigation of their biological role(s), comprehensive analytical methods are necessary, which are able to provide reliable identification and quantification of these compounds in biological matrices. Using charge-switch derivatization with AMPP (N-(4-aminomethylphenyl)pyridinium chloride) in combination with liquid chromatography ion mobility quadrupole time-of-flight mass spectrometry (LC-IM-QTOF-MS), we developed a non-target approach to analyze oxylipins in plasma, serum, and cells. The developed workflow makes use of an ion mobility resolved fragmentation to pinpoint derivatized molecules based on the cleavage of AMPP, which yields two specific fragment ions. This allows a reliable identification of known and unknown eicosanoids and other oxylipins. We characterized the workflow using 52 different oxylipins and investigated their fragmentation patterns and ion mobilities. Limits of detection ranged between 0.2 and 10.0 nM (1.0-50 pg on column), which is comparable with other state-of-the-art methods using LC triple quadrupole (QqQ) MS. Moreover, we applied this strategy to analyze oxylipins in different biologically relevant matrices, as cultured cells, human plasma, and serum. Graphical abstract.

Ion-Trap Mass Spectrometric Analysis of Bisphenol A Interactions With Titanium Dioxide Nanoparticles and Milk Proteins.

Quantitative analysis of endocrine-disrupting molecules such as bisphenol A (BPA) in freshwater to determine their widespread occurrence in environmental resources has been challenged by various adsorption and desorption processes. In this work, ion trap mass spectrometry (ITMS) analysis of BPA was aimed at studying its molecular interactions with titanium dioxide (TiO2) nanoparticles and milk whey proteins. Addition of sodium formate prevented TiO2 nanoparticles from sedimentation while enhancing the electrospray ionization (ESI) efficiency to produce an abundance of [BPA + Na]+ ions at m/z 251.0. More importantly, the ESI-ITMS instrument could operate properly during a direct infusion of nanoparticles up to 500 µg/mL without clogging the intake capillary. Milk protein adsorption of BPA could decrease the [BPA + Na]+ peak intensity significantly unless the proteins were partially removed by curdling to produce whey, which allowed BPA desorption during ESI for quantitative analysis by ITMS.

Study of Brake Wear Particle Emissions: Impact of Braking and Cruising Conditions.

A novel measurement setup is designed, constructed, and validated by theoretical simulations and by experiments enabling sensitive and loss-free brake particle emission investigations. With the goal to simulate realistic driving, a 3 h subsection of the Los Angeles City Traffic (LACT) cycle is selected as test cycle. The tests are performed with the front brake of a midsize passenger vehicle under both static laboratory and more dynamic realistic conditions that include parasitic drag and vehicle brake temperatures (advanced vehicle simulations). A PM10 emission factor of around 4.6 mg km-1 brake-1 is determined. During five cycle runs the emission factor in terms of particle number decreases by 1 order of magnitude. This decrease is accompanied by a shift of the critical brake temperature Tcrit, at which ultrafine particle emissions occur, from 140 to 170 °C. Investigations with advanced vehicle simulations generate brake temperatures below Tcrit and consequently do not show ultrafine particle emissions above background level. A particle number emission factor of approximately 4.9 × 1010 km-1 brake-1 is estimated for realistic vehicle brake temperatures. Particle formation during cruising is clearly identified. The brake drag is estimated to contribute about 34% to the total airborne particle mass emission.

Recent developments in atmospheric pressure photoionization-mass spectrometry.

Recent developments in atmospheric pressure photoionization (APPI), which is one of the three most important ionization techniques in liquid chromatography-mass spectrometry, are reviewed. The emphasis is on the practical aspects of APPI analysis, its combination with different separation techniques, novel instrumental developments - especially in gas chromatography and ambient mass spectrometry - and the applications that have appeared in 2009-2014. © 2015 Wiley Periodicals, Inc. Mass Spec Rev 36:423-449, 2017.

Pathways in the Degradation of Geminal Diazides.

The degradation of geminal diazides is described. We show that diazido acetates are converted into tetrazoles through the treatment with bases. The reaction of dichloro ketones with azide anions provides acyl azides, through in situ formation of diazido ketones. We present experimental and theoretical evidence that both fragmentations may involve the generation of acyl cyanide intermediates. The controlled degradation of terminal alkynes into amides (by loss of one carbon) or ureas (by loss of two carbons) is also shown.

Development of an ion activation stage for atmospheric pressure ionization sources.

RATIONALE: The ion-molecule chemistry in typical atmospheric pressure ion sources is essentially thermodynamically controlled. Methods relying on gas-phase protonation reactions, e.g. atmospheric pressure chemical ionization (APCI), thus suffer from the low reactivity of the equilibrated reagent ion population, which is mostly [H + (H2O)n](+). Reagent ion activation to yield reactive species such as H3O(+) is largely uncontrolled in commercial API mass spectrometers. METHODS: The ion activation stage (IAS) is realized as an ion 'tunnel' device. The 30-electrode geometry has an octagonal cross section and an inner diameter of 10 mm. The tunnel is mounted in a vacuum chamber, which directly attaches to the first pumping stage of API mass spectrometers. The effluent from a typical inlet capillary is expanding into the IAS. Reagent ions are generated at atmospheric pressure. Mass spectrometric analysis is performed with quadrupole and time-of-flight instruments. RESULTS: The performance of the IAS is demonstrated by the controlled activation of the initially equilibrated proton-bound water cluster system. It is shown that a gradual increase in the RF voltage amplitude applied to the electrode structure leads to a reproducible shift of the cluster distribution along with clearly discernible protonation thresholds of selected analytes. Increasing the radiofrequency (RF) voltage from zero to maximum values does not change the average ion residence time within the IAS. CONCLUSIONS: We have developed an IAS for operation in the intermediate (1-10 mbar) regime in the ion transfer region of API mass spectrometers. This stage is fully compatible with the recently introduced cAPCI method, which relies on the operation of a liquid point electrode generating very clean and stable thermal distributions of [H + (H2O)n] clusters. The IAS allows controlled ion activation by increasing the ion temperature, which is demonstrated by selective analyte protonation.

Capillary atmospheric pressure chemical ionization using liquid point electrodes.

RATIONALE: Atmospheric pressure chemical ionization (APCI) sources operated with point to plane DC discharges ('Coronas') frequently suffer from point electrode degradation and potentially lead to oxidation and/or fragmentation of the generated analyte ions. It is postulated that these adverse effects are caused by the interaction of these ions with the discharge chemistry as well as en route to the mass analyzer region. METHODS: The corona discharge metal point electrode is replaced by the conically shaped liquid effluent evolving from a fused-silica capillary, which is analogous but not identical to the Taylor cone formation in electrospray ionization. The liquid consisting of either pure water or water containing 0.1 %V formic acid is fed via a nano-flow delivery stage at typical flow rates between 1-800 µL/h. The liquid flow is continuously replenishing the surface of the point electrode. The source is directly coupled to the inlet capillary of appropriate mass spectrometers, e.g., the Bruker Daltonics and Agilent varieties. RESULTS: The actively pumped liquid flow is supplying a constant amount of the reagent gas (H2O) to the corona region in the 20 ppmV to 30 %V range, leading to controlled, very stable operation of the source. The typical light emission observed for corona discharges is in very close proximity to the aqueous surface. Analyte protonation is the dominating ionization pathway. The degree of primary analyte fragmentation is extremely low. CONCLUSIONS: We have developed a novel atmospheric pressure chemical ionization source designed for the hyphenation of nano-flow liquid chromatography and gas chromatography with atmospheric pressure ionization mass spectrometry. The proposed reaction mechanism including the electrochemistry occurring in the source along with formation of protonated analyte molecules via collision-induced dissociation (CID) is in full accord with the experimental results. The system exhibits an extremely stable performance over prolonged operation times, sole generation of protonated molecules, and low degree of analyte ion fragmentation.

High-Resolution Electron Ionization Mass Spectrometry of Stannane: Deconvolution of Superimposed Fragmentation Patterns.

In a pulsed laser plasma driven extreme ultraviolet (EUV) light, tin droplets undergo evaporation, eventually depositing on different surfaces. The removal of surface bound tin is commonly achieved with a hydrogen plasma, resulting in the formation of stannane (SnH4). The mechanisms leading to the formation and decomposition of stannane remain incompletely understood. To analyze these mechanisms mass spectrometrically, a reference is crucial, necessitating a high-resolution and thoroughly characterized mass spectrum of stannane. In this paper, a high-resolution 70 eV electron ionization (EI) mass spectrum of stannane is presented. The mass spectrum comprises all ten natural isotopes of the stannane fragments generated through EI. Utilizing the custom analysis program RASP, the relative distribution of fragments is calculated from the isotopically superimposed mass signals, offering crucial insights into the occurring processes. Furthermore, the dependence of fragment formation on ion source pressure and temperature was determined.

IDSimF: An Open-Source Framework for the Simulation of Molecular Ion Dynamics in Mass Spectrometry and Ion Mobility Spectrometry.

The development of mass spectrometric and ion mobility devices heavily depends on a comprehensive understanding of the behavior of ions within such systems. Therefore, numerical modeling of ion paths helps to optimize and verify existing devices, and contributes to the development of innovative ion optical systems and multipole geometries. This Article introduces IDSimF (Ion Dynamics Simulation Framework), an open-source simulation tool tailored to the nonrelativistic dynamics of molecular ions in mass and ion mobility spectrometry applications. Addressing limitations in existing software packages, as for example SIMION, OpenFOAM, and COMSOL, IDSimF offers a specialized platform for simulating ion trajectories in electric fields. IDSimF efficiently accounts for space charge effects and considers various ion-neutral collision models while handling chemical kinetics. The framework is highly modular with reduced user input configuration complexity and aims to support simulation efforts in development and optimization of in mass spectrometers.

Observation of Large, Charged Droplet Signatures within the High-Vacuum Region of a Commercial Electrospray TOF-MS.

Electrospray ionization (ESI) is one of the most prominent atmospheric pressure ionization techniques in modern mass spectrometry. It generates charged droplets from an analyte-containing solution as an initial step in the ionization process. Textbooks and the majority of the articles assume the entire droplet evaporation and release of bare analyte ions within the ionization chamber. However, non-mass-spectrometry-related literature and recent reports demonstrate droplet observation in regions of the vacuum systems of a variety of mass spectrometers. In this work, we report on the observation of large droplet fragments within the orthogonal acceleration stage of a Bruker micrOTOF by connecting an oscilloscope to an auxiliary ion current detector downstream of the acceleration stage. Moreover, we detected fragment debris even with the MCP TOF detector by evaluating individual TOF spectra. Droplet fragments appear as pronounced and intensive pulses of the ion current. This observation is clearly connected to ESI, as other atmospheric pressure ionization methods do not show this behavior. The recorded droplet signatures show clear dependencies on the ion source and transfer stage parameters. The existence of large and highly charged droplets may adversely affect or at least impact the analytical performance of the instrument due to space charge or complex heterogeneous chemical reactions. Furthermore, the penetration of large charged aggregates into the vacuum system explains the reported surface contamination after multipole stages. This contamination of critical components leads to substantially higher maintenance efforts.

Carbon disulfide as a dopant in photon-induced chemical ionization mass spectrometry.

RATIONALE: The addition of a dopant to an Atmospheric Pressure PhotoIonization (APPI) source of a mass spectrometer has been shown to enhance the degree of analyte ionization. A series of different dopants has been successfully utilized; however, there has been very little published on the characteristics of a good dopant. We have proposed carbon disulfide (CS2) as a novel new dopant based on its absorption cross-section for the VUV photon's energy used and its unique gas-phase ion chemistry, notably the fact that it does not contain a proton. METHODS: The ability of CS2 to enhance the ionization effectiveness of APPI was tested by using a group of compounds that have different proton affinities (PAs) and electron affinities (EAs). These results were compared to results obtained using the commonly used dopants, toluene and anisole. Particular attention was paid to the formation of [M](+) ions relative to [M+H](+) ions. Mass spectra were collected using a Waters Quattro Premier liquid chromatography/tandem mass spectrometry (LC/MS/MS) system equipped with a commercial Photomate™ photoionization source. RESULTS: The results show that CS2 increases the ionization efficiency of most of the analytes studied in this work comparably to toluene and anisole. CS2 promotes both ionization routes of [M](+) and [M+H](+). In addition, due to the higher ionization energy (IE) of CS2 (10.01) compared to the IEs of toluene (8.83) and anisole (8.20), CS2 can enhance the ionization efficiency of analytes that cannot be enhanced with toluene and anisole. CONCLUSIONS: We have determined that CS2 is a viable dopant for use in APPI sources. For some analytes, significant [M+H](+) ion signals are observed; therefore, the donated proton must come from either water clusters or solvents. In addition, CS2 promotes the ionization of analytes with low PAs and higher IEs than that of toluene and anisole.

Generation of ion-bound solvent clusters as reactant ions in dopant-assisted APPI and APLI.

We provide experimental and theoretical evidence that the primary ionization process in the dopant-assisted varieties of the atmospheric pressure ionization methods atmospheric pressure photoionization and atmospheric pressure laser ionization in typical liquid chromatography-mass spectrometry settings is--as suggested in the literature--dopant radical cation formation. However, instead of direct dopant radical cation-analyte interaction--the broadly accepted subsequent step in the reaction cascade leading to protonated analyte molecules--rapid thermal equilibration with ion source background water or liquid chromatography solvents through dopant ion-molecule cluster formation occurs. Fast intracluster chemistry then leads to almost instantaneous proton-bound water/solvent cluster generation. These clusters interact either directly with analytes by ligand switching or association reactions, respectively, or further downstream in the intermediate-pressure regions in the ion transfer stages of the mass spectrometer via electrical-field-driven collisional decomposition reactions finally leading to the predominantly observed bare protonated analyte molecules [M + H](+).

Molecular Dynamics-Based Modeling of Ion-Neutral Collisions in an Open Ion Trajectory Simulation Framework.

Ion mobility spectrometry (IMS) and ion mobility mass spectrometry (IMS-MS) methods have become increasingly popular and are important analytical techniques to determine information about the structural parameters of gas-phase analytes. The accurate description of the interaction between molecular ions and neutral background gas particles is an essential part of high-quality simulations of such modern mass- and ion-mobility-spectrometric systems. Established ion-neutral collision models (Hard-sphere collision modeling and statistical diffusion simulations) in common ion-trajectory simulation systems like SIMION use strongly simplified assumptions and are thus limited in their predictive ability. In contrast, collision cross-section (CCS) modeling programs (e.g., MOBCAL, IMoS, and Colloidoscope) allow high-quality ion mobility predictions for low-field equilibrium conditions using explicit scattering processes with a molecular dynamics-based trajectory method but cannot be used for nonequilibrium collision modeling in an ion trajectory simulation. This work presents an extension to the open-source Ion Dynamics Simulation Framework (IDSimF), which allows the simulation of ion dynamics under arbitrary and even nonequilibrium conditions. It was extended by an advanced collision model employing the molecular dynamics trajectory method for a detailed microscopic description of ion-neutral collisions within ion-trajectory simulations. We used drift tube ion mobility spectrometry (DT-IMS) to validate the predictive abilities of the model and to estimate the runtime requirements for productive simulations. Simulated high-field ion mobilities for small ion systems in a drift tube IMS are compared to experimental values from the literature and an implementation of a hard-sphere model in IDSimF for helium and argon as background gas particles. Significant improvements in ion mobility predictions using the molecular dynamics trajectory approach are obtained with deviations of only a few percent from experimental values. Therefore, the established and publicly available MD collision model will serve as foundation for nonequilibrium ion dynamics simulations and the development of improved ion dynamics modeling methods.

Comparison of direct and alternating current vacuum ultraviolet lamps in atmospheric pressure photoionization.

A direct current induced vacuum ultraviolet (dc-VUV) krypton discharge lamp and an alternating current, radio frequency (rf) induced VUV lamp that are essentially similar to lamps in commercial atmospheric pressure photoionization (APPI) ion sources were compared. The emission distributions along the diameter of the lamp exit window were measured, and they showed that the beam of the rf lamp is much wider than that of the dc lamp. Thus, the rf lamp has larger efficient ionization area, and it also emits more photons than the dc lamp. The ionization efficiencies of the lamps were compared using identical spray geometries with both lamps in microchip APPI mass spectrometry (µAPPI-MS) and desorption atmospheric pressure photoionization-mass spectrometry (DAPPI-MS). A comprehensive view on the ionization was gained by studying six different µAPPI solvent compositions, five DAPPI spray solvents, and completely solvent-free DAPPI. The observed reactant ions for each solvent composition were very similar with both lamps except for toluene, which showed a higher amount of solvent originating oxidation products with the rf lamp than with the dc lamp in µAPPI. Moreover, the same analyte ions were detected with both lamps, and thus, the ionization mechanisms with both lamps are similar. The rf lamp showed a higher ionization efficiency than the dc lamp in all experiments. The difference between the lamp ionization efficiencies was greatest when high ionization energy (IE) solvent compositions (IEs above 10 eV), i.e., hexane, methanol, and methanol/water, (1:1 v:v) were used. The higher ionization efficiency of the rf lamp is likely due to the larger area of high intensity light emission, and the resulting larger efficient ionization area and higher amount of photons emitted. These result in higher solvent reactant ion production, which in turn enables more efficient analyte ion production.

The role of ion-bound cluster formation in negative ion mass spectrometry.

RATIONALE: The ionization mechanisms operative in negative ion atmospheric pressure mass spectrometry are far from being properly understood. In an excess of oxygen superoxide (O(2)(-)) is generally the primary charge-carrying species that is generated. However, subsequent reactions leading to the finally detected ion signals remain obscure. METHODS: Since adiabatic expansion induced cluster growth and collision-induced dissociation (CID) processes rendered a representative sampling of ion distributions present in the source difficult, a custom-built thermally sampling time-of-flight mass spectrometer was used for the investigations. Using atmospheric pressure laser ionization of toluene as the reagent gas, high yields of thermal electrons were observed, but only negligible amounts of by-products. Ab initio calculations for individual ion/molecule reaction pathways were performed. RESULTS: Electron capture by molecular oxygen resulted in the formation of subsequent superoxide water clusters as well as distinct analyte-adduct ions. By adjusting the extent of CID within the ion optical stages of the mass spectrometer, the cluster distribution changes to smaller cluster sizes and the analyte signals strongly shifted towards M(-) or [M-H](-). The observed superoxide water cluster distribution was close to thermal. The theoretical results confirmed the experimental findings. CONCLUSIONS: In negative atmospheric pressure mass spectrometry the water concentration in the ion source (determining the ionization efficiency) and the CID energy provided through electrical fields (determining the ion distribution) are primary, critical parameters for the observed overall ionization mechanism and efficiency.

Kinetic study of gas-phase reactions of OH and NO3 radicals and O3 with iso-butyl and tert-butyl vinyl ethers.

Using a relative rate technique, kinetic studies on the gas-phase reactions of OH radicals, ozone, and NO(3) radicals with iso-butyl vinyl ether (iBVE) and tert-butyl vinyl ether (tBVE) have been performed in a 405 L Duran glass chamber at (298 ± 3) K and atmospheric pressure (750 ± 10 Torr) in synthetic air using in situ FTIR spectroscopy to monitor the reactants. The following rate coefficients (in units of cm(3) molecule(-1) s(-1)) have been obtained: (1.08 ± 0.23) × 10(-10) and (1.25 ± 0.32) × 10(-10) for the reactions of OH with iBVE and tBVE, respectively; (2.85 ± 0.62) × 10(-16) and (5.30 ± 1.07) × 10(-16) for the ozonolysis of iBVE and tBVE, respectively; and (1.99 ± 0.56) × 10(-12) and (4.81 ± 1.01) × 10(-12) for the reactions of NO(3) with iBVE and tBVE, respectively. The rate coefficients for the NO(3) reactions are first-time determinations. The measured rate coefficients are compared with estimates using current structure activity relationship (SAR) methods and the effects of the alkoxy group on the gas-phase reactivity of the alkyl vinyl ethers toward the oxidants are compared and discussed. In addition, estimates of the tropospheric lifetimes of iBVE and tBVE with respect to their reactions with OH, ozone, and NO(3) for typical OH radical, ozone, and NO(3) radical concentrations are made, and their relevance for the environmental fate of compounds is considered.