Mobility Spectrometer Research Articles

Field induced displacement reactions with proton bound dimers of organophosphorus compounds in a tandem differential mobility spectrometer.

Endothermic displacement reactions between proton bound dimers of organophosphorus compounds (OPCs) and isopropanol (IPA) were enabled in air at ambient pressure with tandem differential mobility spectrometry (DMS). Proton bound dimers (M2H+) were mobility isolated in purified air with a first DMS stage, mixed with IPA at ≥100 ppm in a middle reactive stage at 106 to 160 Td from a symmetrical 4 MHz waveform, and mobility analyzed in a second DMS stage. Although the enthalpy for displacement of M by IPA in M2H+ is unfavorable by +44 to 50 kJ mol-1, formation of the heterogenous proton bound dimer, MH+(IPA) arises from field induced dissociation of M2H+ to MH+ and addition of IPA. While peak dispersion for M2H+ of OPCs is limited to -2.25 to -0.5 V compensation voltage, peaks for MH+(IPA) were located at -10.5 to -8.25 V through a combination of ion transformation and mobility-based vapor modification. This inaugural use of ion reactions in air at ambient pressure demonstrates that multi-stage sequential processing of ions can improve significantly the analytical performance in a mobility spectrometer.

Determination of chemical warfare agents by low cost differential mobility spectrometry

A low-cost differential mobility spectrometer (DMS) was constructed using polytetrafluoroethylene printed circuit boards with two pairs of gold electrodes. The printed circuit boards were used to construct the drift tube into which the gas samples are introduced by a carrier gas and ionized. The ionized gas moves toward the gold electrode to which an asymmetric voltage is applied. Only the ionized gas with the proper ion mobility leaves the electrode region and reach the detection electrodes to form the ion current. Traces of five chemical warfare agents, including dimethyl methylphosphonate, triethylamine, 2-diisopropylaminoethanol, diethylaminoethanol, and N, N-dimethylethanolamine, were prepared using the permeation tube method and introduced into the sensor. All of the chemicals show characteristic ion peak shifts in the electric field. The limits of detection for the analytes are less than 1 ng/L. The recovery time was less than 10 s and the response time is 2 s. The developed sensor exhibits the ability to detect and distinguish between these chemical warfare agents.

Uncertainty quantifications of calibrating laser-induced incandescence intensity on sooting propensity in a wick-fed diffusion flame burner

Extensive research has been devoted to engineering analysis in the presence of parameter uncertainties. Meanwhile, parameter estimations with uncertainty quantifications facilitate the reduction of bias and physical unrealistic estimates on interpreting model predictions. In this study, the sooting propensity from wick-fed diffusion flames tested by Jet A-1, diesel and their blended fuels are interpreted, with Laser-induced incandescence (LII) diagnosis to quantitative calibrate the soot volume fraction fv. To make the calibration independent of optical properties, the fv is directly inferred from particle size distribution measured in flames by the Differential Mobility Spectrometer 500 (DMS500). Thus, the calibration parameter with its uncertainties is therefore qualified with errors that arise from measurements. This study refers to several methodologies with potential estimates of parameter uncertainties for proper interpretation of fv by LII diagnosis measurement. Bayesian regression method with Gaussian mixture functions are accounted for calibration parameter uncertainties derived from heteroscedastic measurement errors. And the principal component analysis (PCA) assisted statistical approach is responsible for projecting multivariable datasets into low-dimension space, therefore joint probability distribution would be inferred. As a consequence, probability interval from inferred probability distribution of the calibration parameter is associated with degree of uncertainties, which provides better guidance regarding the applicability and uncertainty of LII diagnosis on soot characteristics.

Improved selectivity for the determination of trinitrotoluene through reactive stage tandem ion mobility spectrometry and a quantitative measure of source-based suppression of ionization

A tandem ion mobility spectrometer was used to mobility isolate ions at the drift time for trinitrotoluene (TNT) in a first mobility stage, remove an interfering compound by ion decomposition in a middle reactive stage, and mobility characterize the remaining TNT ions in a second mobility stage. This sequential processing of ions provided decisive detection of TNT in the presence of an interfering peak differing from TNT in reduced mobility coefficient (Ko) by only 0.02 cm2/V. Even though ions of TNT (as M − 1)- and the interfering compound were more than 90% convolved, TNT could be selectively detected with more than 95% decomposition of the interferent at 123 Td to an ion now separated by ΔKo of 0.2 cm2/V from TNT. Ions for TNT were not decomposed in these electric fields though transmission efficiency was decreased by 20% through a wire grid assembly (the reactive stage). Although tandem ion mobility spectrometry with a reactive stage improves selectivity of measurement in the drift time dimension, the chemistry of ion formation in the ion source is affected still by ion suppression. Response to 1 ng TNT was decreased as much as 30% from 200 ng of interferent deposited on sample trap.

Towards a hand-held, fast, and sensitive gas chromatograph-ion mobility spectrometer for detecting volatile compounds

Ion mobility spectrometers can detect gaseous compounds at atmospheric pressure in the range of parts per trillion within a second. Due to their fast response times, high sensitivity, and limited instrumental effort, they are used in a variety of applications, especially as mobile or hand-held devices. However, most real-life samples are gas mixtures, which can pose a challenge for IMS with atmospheric pressure chemical ionization mainly due to competing gas-phase ionization processes. Therefore, we present a miniaturized drift tube IMS coupled to a compact gas chromatograph for pre-separation, built of seven bundled standard GC columns (Rtx-Volatiles, Restek GmbH) with 250 μm ID and 1.07 m in length. Such pre-separation significantly reduces chemical cross sensitivities caused by competing gas-phase ionization processes and adds orthogonality. Our miniaturized GC-IMS system is characterized with alcohols, halocarbons, and ketones as model substances, reaching detection limits down to 70 pptv with IMS averaging times of just 125 ms. It separates test mixtures of ketones and halocarbons within 180 s and 50 s, respectively. The IMS has a short drift length of 40.6 mm and reaches a high resolving power of RP = 68.Graphical abstract

Rapid quantitative determination of blood propofol concentration throughout perioperative period by negative photoionization ion mobility spectrometer with solvent-assisted neutral desorption

Rapid and quantitative determination of blood propofol concentration is important for anesthesiologists to accurately control intraoperative propofol dose, timely monitor physiological statuses of patients and greatly improve the safety of surgery. Herein, a dopant-assisted negative photoionization ion mobility spectrometer with the optimized ionization region structure and the three-way inlet design was developed, increasing the generation ratio of the reactant ions O2−, and improving the ionization efficiency of propofol molecules. Besides, the addition of methanol-anisole solution during injection promoted the neutral desorption of propofol in blood, further improving the detection sensitivity by an order of magnitude, eliminating any sample pretreatment and effectively reducing the single analysis time to less than 1 min compared to the previous article. The dual calibration quantitative method, i.e. the method of calibrating the O2− concentration and the sample concentration changes during the entire process of detecting propofol through the integral value of M·O2− and the maximum signal intensity of O2−, successfully achieved accurate quantification of blood propofol. And the linear calibration curve of propofol was obtained with the range of 0.1–15 ng μL−1 and with the limit of detection of 0.03 ng μL−1, which was fulfilled to conduct propofol determination throughout the perioperative period. Finally, this method was applied to clinically measure the blood propofol concentration in patients newly regained consciousness with concentrations ranging from 0.2 ng μL−1 to 3 ng μL−1, and it turned out that the older patient had the lower propofol concentration in blood.

A portable sensor system for the detection of human volatile compounds against transnational crime

Human smuggling accounts for a significant part of transnational organized crime, creating a growing threat to national and international security and putting at risk the health and lives of the people being smuggled. Early detection and interception of human beings hidden in containers or trucks are therefore of considerable importance, especially at key transportation hubs, such as at international borders and harbors. The major challenge is to provide fast inspection procedures without needing to open sealed trucks and containers. The detection of trace key volatile organic compounds, which includes aldehydes and ketones, emitted by humans can be used to rapidly determine human presence, requiring only several ml of air to be taken from inside a container. In this paper, we describe a prototype portable device for the rapid detection of hidden or entrapped people, employing a combined ion mobility spectrometer and sensor array system for obtaining a volatile signature of human presence. The detection limits of this combined analytical device are sufficiently low for use in sensing ketones and aldehydes being emitted by humans in closed containers. For easy handling by security personnel, a classification algorithm is applied that provides a simple YES or NO decision. With a training dataset of more than 1000 measurements, the algorithm achieved an area under curve of 0.9 for untrained scenarios. The field measurements show that two people need to stay in a car for between 20 and 30 minutes in order for the emitted trace volatile organic compounds to reach concentrations high enough for reliable detection with our analytical device.

Effect of the Metal-Foam Gasoline Particulate Filter (GPF) on the Vehicle Performance in a Turbocharged Gasoline Direct Injection Vehicle over FTP-75

Worldwide regulations on particulate matter for passenger vehicles have become stricter in recent years, which makes it difficult to satisfy for gasoline direct injection (GDI) vehicles. In this study, the level of reduction efficiency of particle emissions with a metal-foam gasoline particulate filter (GPF) for the turbocharged GDI vehicle was evaluated in the federal test procedure (FTP)-75 mode operation. The particle number (PN) emissions were analyzed using the AVL particle counter (APC) and fast response differential mobility spectrometer (DMS500) for particle size distribution. The PN concentration from the base GDI vehicle with only TWC is 1.64 E+12 number/km (#/km), while the value of the GPF-equipped case is 5.02 E+11 #/km with 69 % filtration efficiency in the vehicle test mode. In particular, the reduction rate of small particles under 23 nm in size was strongly improved with the additional installation of the metal-foam GPF. The maximum pressure drop through the GPF reached approximately 39 mbar at the highest acceleration point of phase 1 of the FTP-75 mode. The upstream temperature of the GPF was distributed at approximately 380 ∼ 510 oC in the vehicle test. The results show that the GPF-equipped GDI vehicle can satisfy the stringent particle regulation by Euro 6 in a straightforward manner.

The influence of different types of reactant ions on the ionization behavior of polycyclic aromatic hydrocarbons in corona discharge ion mobility spectrometry

Some polycyclic aromatic hydrocarbons (PAHs) are considered to be cancer-causing chemicals, and ion mobility spectrometry (IMS) is used for on-site detection of such hazardous chemicals. In IMS, the ionization behavior of analytes is affected by the types of reactant ions (RIs). In the present work, the influence of different types of RIs on the ionization behaviors of PAHs in an ion mobility spectrometer equipped with a corona discharge ionization source was investigated using various RIs. Selected PAHs were dissolved in anisole, fluorobenzene, chlorobenzene, or bromobenzene. The IMS analysis procedure was performed as follows: (a) the PAH solution was dropped onto the smear matrix; (b) the smear matrix was immediately inserted into the sample inlet to minimize evaporation of the solvent; and (c) the IMS analysis was performed. The lowest amount studied was 10 ng. Variations in the IMS spectra with time were investigated. PAHs were not ionized by RIs of protonated molecules ([M + H]+ ) such as air/moisture and acetone, but they were ionized by charge transfer reactions with RIs of molecular ions (M•+ ) of solvents such as anisole, fluorobenzene, chlorobenzene, and bromobenzene. The PAH ions were detected following a time delay of ~1-5 s after the sample introduction, and the times at which the maximum intensities for the PAHs were observed were different. The detection limits of PAHs in chlorobenzene were on the whole better than those in other solvents, whereas those in fluorobenzene were worse. The detection limits of pyrene and benzo[a]anthracene were better than those of the other PAHs irrespective of the solvent used. PAH molecules were ionized by charge transfer reactions with RIs of the solvents, and their ions were detected ~1-5 s after sample introduction. The order of the ionization efficiency was chlorobenzene > anisole > bromobenzene > fluorobenzene.

Enhancement of Characteristics of Field Asymmetric Ion Mobility Spectrometer with Laser Ionization for Detection of Explosives in Vapor Phase

Ion mobility spectrometry instrumentation today is widespread in the area of transport security and counterterrorism. This method of detection of explosive substances is highly appreciated for the existence of portable detectors capable of detecting concentrations of 10−13–10−14 g/cm3 at atmospheric pressure using traditional ionization methods including corona discharge and beta radiation. However, low vapor pressure of some explosives imposes requirements on limit of detection (LOD) down to 10–15‒10−16 g/cm3. In this paper we compare a radioactive 63Ni ionization source with a laser ionization source and reveal the parameters of laser ionization of a group of explosives, namely trinitrotoluene (TNT), cyclotrimethylene-trinitramine (RDX), cyclotetramethylene-tetranitramine (HMX) and pentaerythritol tetranitrate (PETN), which can reduce the limit of detection of portable devices. A laser ionization source can provide a higher signal to noise ratio than radioactive 63Ni at optimal intensity of laser radiation for PETN and HMX of 3 × 107 W/cm2 and 2.5 × 107 W/cm2, respectively. Limits of detection were estimated: 3 × 10−15 g/cm3 for RDX, 8 × 10−15 g/cm3 for PETN and less than 3 × 10−15 g/cm3 for HMX. These results are promising to further improve the capabilities of detectors of low volatility explosives without sacrificing portability, light weight and reasonable cost of the laser source.

In situ monitoring of photocatalyzed isomerization reactions on a microchip flow reactor by IR-MALDI ion mobility spectrometry

The visible-light photocatalytic E/Z isomerization of olefins can be mediated by a wide spectrum of triplet sensitizers (photocatalysts). However, the search for the most efficient photocatalysts through screenings in photo batch reactors is material and time consuming. Capillary and microchip flow reactors can accelerate this screening process. Combined with a fast analytical technique for isomer differentiation, these reactors can enable high-throughput analyses. Ion mobility (IM) spectrometry is a cost-effective technique that allows simple isomer separation and detection on the millisecond timescale. This work introduces a hyphenation method consisting of a microchip reactor and an infrared matrix-assisted laser desorption ionization (IR-MALDI) ion mobility spectrometer that has the potential for high-throughput analysis. The photocatalyzed E/Z isomerization of ethyl-3-(pyridine-3-yl)but-2-enoate (E-1) as a model substrate was chosen to demonstrate the capability of this device. Classic organic triplet sensitizers as well as Ru-, Ir-, and Cu-based complexes were tested as catalysts. The ionization efficiency of the Z-isomer is much higher at atmospheric pressure which is due to a higher proton affinity. In order to suppress proton transfer reactions by limiting the number of collisions, an IM spectrometer working at reduced pressure (max. 100 mbar) was employed. This design reduced charge transfer reactions and allowed the quantitative determination of the reaction yield in real time. Among 14 catalysts tested, four catalysts could be determined as efficient sensitizers for the E/Z isomerization of ethyl cinnamate derivative E-1. Conversion rates of up to 80% were achieved in irradiation time sequences of 10 up to 180 s. With respect to current studies found in the literature, this reduces the acquisition times from several hours to only a few minutes per scan.

Influence of fuel injection pressure and injection timing on nanoparticle emission in light-duty gasoline/diesel RCCI engine

This work investigates the influence of fuel injection events on the nanoparticle emission characteristics of light-duty gasoline-diesel RCCI engine. The formation of nanoparticle emissions strongly depends on fuel injection events. The present study experimentally investigates the influence of diesel injection pressure, injection timing, and port-injected gasoline mass on the nanoparticles emitted from the gasoline-diesel RCCI engine. For this purpose, the engine is tested at different engine speeds and a fixed load of 1.5 bar BMEP without exhaust gas recirculation. The particle-size and number distribution (PSD) and total particle number (total PN) concentration are measured using a differential mobility spectrometer. The results depict that at higher diesel injection pressure (IP) operation, the peak of the NMP increases while the AMP peak decreases for neat diesel operation as well as RCCI engine. Nucleation, as well as accumulation mode particles, increases with advanced diesel injection timing in RCCI combustion. An increase in port fuel injected mass also leads to an increase in the total particle concentration and total unburned hydrocarbon (THC) emissions.

Continuous Dissolved Gas Tracing of Fracture‐Matrix Exchanges

AbstractTransport in fractured media plays an important role in a range of processes, from rock weathering and microbial processes to contaminant transport, and energy extraction and storage. Diffusive transfer between the fracture fluid and the rock matrix is often a key element in these applications. But the multiscale heterogeneity of fractures renders the field assessment of these processes extremely challenging. This study explores the use of dissolved gases as tracers of fracture‐matrix interactions, which can be measured continuously and highly accurately using mobile mass spectrometers. Since their diffusion coefficients vary significantly, multiple gases are used to probe different scales of fracture‐matrix exchanges. Tracer tests with helium, xenon, and argon were performed in a fractured chalk aquifer, and resulting tracer breakthrough curves are modeled. Results show that continuous dissolved gas tracing with multiple tracers provides key constrains on fracture‐matrix interactions and reveal unexpected scale effects in fracture‐matrix exchange rates.

Spatial distribution of the dropless ESI charged particles at IMS entrance

An experimental study and comparison of spatial distributions of charged particles for conventional electrospray (ESI) and for dropless electrospray with a dynamic flow splitter of analyzed solution at atmospheric pressure and room temperature was carried out. Comparison of distributions shows that the characteristic regions of ion formation differ significantly. The obtained dropless electrospay spatial distributions are matched with inlet parameters of optimized transfer system of an ion mobility spectrometer (IMS) based on electrostatic focusing of the charged particles.

Enhanced Resolving Power by Moving Field Ion Mobility Spectrometry.

Ion mobility spectrometry is a powerful detection method widely used in various applications. Particularly in field applications, ion mobility spectrometers (IMSs) are useful because of their extremely low detection limits at short measuring periods and their compact and robust design. However, especially small IMSs suffer from the consequences of low resolving power when compared to laboratory systems. Therefore, in this paper, we present a new approach to increase the resolving power of a drift time IMS without employing higher drift voltages and bulky power supplies. The so-called moving field IMS (MOF-IMS) presented here allows a more effective use of the available voltage because of a segmented drift region where only a small part is supplied with voltage. Even with the basic version of an MOF-IMS presented here, it was possible to increase the resolving power by 60% from 60 to 95 without increasing the required drift voltage.

Ion Mobility Shift of Isotopologues in a High Kinetic Energy Ion Mobility Spectrometer (HiKE-IMS) at Elevated Effective Temperatures.

Ion mobility spectrometers (IMS) separate ions mainly by ion-neutral collision cross section and to a lesser extent by ion mass and effective temperature. When investigating isotopologues, the difference in collision cross section can be assumed negligible. Since the mobility shift of isotopologues is thus mainly caused by their difference in mass and effective temperature, the investigation of isotopologues can provide important insights into the theory of ion mobility. However, in classical IMS operated at ambient pressure, cluster formation with neutral molecules occurs, which significantly influences the mobility shift of isotopologues and thus makes a sound investigation of the effect of ion mass and effective temperature on the ion mobility difficult. In this work, the relative ion mobility of several organic compounds and their 13C-labeled isotopologues is studied in a High Kinetic Energy Ion Mobility Spectrometer (HiKE-IMS) at high reduced electric fields up to 120 Td, which allows the investigation of nonclustered ion species and thus enables a sound investigation of the mobility shift of isotopologues. The results show that the measured relative ion mobilities of isotopologues having the same effective temperature and, thus, their ion mass dominating the relative ion mobility agree well with theoretical relative ion mobilities predicted by the theory of ion mobility.

Field-Dependent Reduced Ion Mobilities of Positive and Negative Ions in Air and Nitrogen in High Kinetic Energy Ion Mobility Spectrometry (HiKE-IMS).

In High Kinetic Energy Ion Mobility Spectrometry (HiKE-IMS), ions are formed in a reaction region and separated in a drift region, which is similar to classical drift tube ion mobility spectrometers (IMS) operated at ambient pressure. However, in contrast to the latter, the HiKE-IMS is operated at a decreased background pressure of 10-40 mbar and achieves high reduced electric field strengths of up to 120 Td in both the reaction and the drift region. Thus, the HiKE-IMS allows insights into the chemical kinetics of ion-bound water cluster systems at effective ion temperatures exceeding 1000 K, although it is operated at the low absolute temperature of 45 °C. In this work, a HiKE-IMS with a high resolving power of RP = 140 is used to study the dependence of reduced ion mobilities on the drift gas humidity and the effective ion temperature for the positive reactant ions H3O+(H2O)n, O2+(H2O)n, NO+(H2O)n, NO2+(H2O)n, and NH4+(H2O)n, as well as the negative reactant ions O2-(H2O)n, O3-(H2O)n, CO3-(H2O)n, HCO3-(H2O)n, and NO2-(H2O)n. By varying the reduced electric field strength in the drift region, cluster transitions are observed in the ion mobility spectra. This is demonstrated for the cluster systems H3O+(H2O)n and NO+(H2O)n.

Influence of unsaturation of hydrocarbons on the characteristics and carcinogenicity of soot particles

This paper concerns the effect of unsaturation of hydrocarbons (single, double, and triple bonds) on soot particle characteristics (mass, number, and size) and on the carcinogenicity of soot particles. The soot particles were produced from oxygen-free pyrolysis of five hydrocarbons, namely: propane, propylene, ethane, ethylene, and acetylene. The characteristics of soot particles were measured with the aid of a differential mobility spectrometer (Cambustion-DMS-500) and measurement of soot mass concentration was confirmed using gravimetric filter measurements. The soot particle carcinogenicity was estimated from the emission quantities of total polyaromatic hydrocarbons (PAHs) and the toxicity equivalent factor (TEF) of each PAH. Oxygen-free pyrolysis of the hydrocarbon fuels was conducted in a laminar tube reactor within the temperature range of 1050 –1350oC at a constant nitrogen flow rate of 20 L/min and constant fuel flow rate of 1% (vol) on carbon-1 basis. The experimental results showed that increasing unsaturation of fuels from single to double and to triple bonds increased the mass concentration, particle size, number concentration, and carcinogenicity of soot particle notably at the initial temperature of 1050 oC. Increase in the pyrolysis temperature of the tube reactor from 1050 – 1350oC, increased the mass concentration and sizes of the soot particle while the number concentration and carcinogenicity of the soot particle decreased. There was a positive correlation between the soot particle number and the corresponding soot particle carcinogenicity, while a negative correlation was observed between the soot particle mass and size with soot particle carcinogenicity regardless of the pyrolysis temperature examined. The potential implication of these observations is that, low-temperature combustion (LTC) applications, aimed at reducing emissions of soot and NOx, could produce higher soot particle number concentration of higher carcinogenicity.

Evaluation of handheld and portable Raman spectrometers with different laser excitation wavelengths for the detection and characterization of organic minerals.

Organic minerals occur rather rarely in some types of peat bogs, sedimentary geological environments, and hydrothermal veins. Commonly, calcium oxalates are produced by several plants, terpenoids are often associated with conifers. Because of the organic precursor, these minerals, from the smallest group of the mineralogical system, are sometimes considered as biomarkers. Potential detection of these compounds has high relevance in the fields of exobiology or geobiology. Here we show the potential of four portable Raman spectrometers, using different excitation wavelengths and technologies (operating at 532, 785, and 1064nm together with an advanced spectrometer using the sequentially shifted excitation (SSE) technology), for the rapid and non-destructive identification of these phases. For the organic minerals investigated here, the most intense Raman bands are generally detected at the expected wavenumber positions ±1-4cm-1 in the region 100-2000cm-1 in the spectra obtained from all spectrometers. Additionally, two spectrometers (the 532nm instrument and the SSE) are capable of detecting Raman bands in the higher wavenumber shift region of 2000-3500cm-1, allowing the more detailed characterization and differentiation of the related phases. From this work, and on the basis of the experimental data obtained, it is clear that the longer laser excitation wavelengths are more preferable for organic minerals identification due to the better mitigation of fluorescence emission. In contrast, the Raman spectrometer equipped with the shortest excitation wavelength (532nm) gives a significantly higher spectral resolution and a more detailed discrimination of the Raman bands, provided that the conditions of general lower level of fluorescence emission are met. The results presented in the current study complement the knowledge on minerals and biomarkers of relevance for Martian environments which have been measured with mobile Raman spectrometers. The outcome creates a solid base towards the use of lightweight mobile Raman systems that can be used outdoors and on terrestrial outcrops. Moreover, these results and conclusions are of use for the further development of dedicated spectrometers destined for the instrumental suites on planetary rovers, in the frame of the forthcoming exobiology focused missions to Mars to be launched by NASA and ESA.

Compact and Sensitive Dual Drift Tube Ion Mobility Spectrometer with a New Dual Field Switching Ion Shutter for Simultaneous Detection of Both Ion Polarities.

Ion mobility spectrometers (IMS) with field switching ion shutters are an excellent choice for trace gas detection, being extremely sensitive while having fast response times. However, as different target molecules may form positive, negative, or even ions of both polarities, it is beneficial to simultaneously detect both ion polarities. Here, we present a dual drift tube IMS with a new dual field switching ion shutter for gating both ion polarities and an X-ray ionization source in orthogonal configuration. The dual field switching ion shutter allows significantly improved ion gating and ion accumulation due to improved shielding of the ionization region from the drift field. Equipped with two 75 mm long high-performance drift tubes, the dual IMS reaches high resolving power of R = 90 with detection limits in the lower pptv range for different ketones, chlorinated hydrocarbons and methyl salicylate that forms ions in both polarities.