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A mathematical model is proposed for studying the processes in a stationary plasma thruster (SPT), taking into account the ionization of the working substance, xenon, based on the hybrid equations of electromagnetic hydrodynamics (EMHD) of the plasma, which fully take into account the inertia of electrons. The choice of an EMHD model for studying plasma processes is predetermined by their small scale and low concentration of plasma particles in an SPT. The 1D2V case of plane symmetry is considered in detail, for which a numerical algorithm for studying solutions of hybrid equations of EMHD equations based on the method of macroparticles is constructed. A number of fundamental questions are solved: calculation of average values, interpolation, construction of the initial distribution of macroparticles, the choice of boundary conditions for the electric field, etc. The results of calculations with and without allowance for induction fields in a plasma thruster are presented. The effect of induction fields generated by plasma currents on processes in an SPT and the role of electron inertia have not been studied before, and the results obtained are original. In particular, a new nontraditional scheme for calculating the electric field based on the generalized Ohm's law is proposed, which in EMHD is reduced to a boundary value problem for an elliptic system of equations for the components of the electric field and, among other things, requires setting boundary conditions. The need for the spatial and temporal averaging of electromagnetic fields when calculating the acceleration of the thruster plasma, taking into account the induction field, is an important result. [ABSTRACT FROM AUTHOR]

Real-time breath analysis by high-resolution mass spectrometry (HRMS) is a promising method to noninvasively retrieve relevant biochemical information. In this work, we conducted a head-to-head comparison of two ionization techniques: Secondary electrospray ionization (SESI) and plasma ionization (PI), for the analysis of exhaled breath. Two commercially available SESI and PI sources were coupled to the same HRMS device to analyze breath of two healthy individuals in a longitudinal study. We analyzed 58 breath specimens in both platforms, leading to 2,209 and 2,296 features detected by SESI-HRMS and by PI-HRMS, respectively. 60% of all the mass spectral features were detected in both platforms. However, remarkable differences were noted in terms of the signal-to-noise ratio (S/N), whereby the median (interquartile range, IQR) S/N ratio for SESI-HRMS was 115 (IQR = 408), whereas for PI-HRMS it was 5 (IQR = 5). Differences in the mass spectral profiles for the same samples make the inter-comparability of both techniques problematic. Overall, we conclude that both techniques are excellent for real-time breath analysis because of the very rich mass spectral fingerprints. However, further work is needed to fully understand the exact metabolic insights one can gather using each of these platforms.

The sparking of cut grape hemispheres in a household microwave oven has been a poorly explained Internet parlor trick for over two decades. By expanding this phenomenon to whole spherical dimers of various grape-sized fruit and hydrogel water beads, we demonstrate that the formation of plasma is due to electromagnetic hotspots arising from the cooperative interaction of Mie resonances in the individual spheres. The large dielectric constant of water at the relevant gigahertz frequencies can be used to form systems that mimic surface plasmon resonances that are typically reserved for nanoscale metallic objects. The absorptive properties of water furthermore act to homogenize higher-mode profiles and to preferentially select evanescent field concentrations such as the axial hotspot. Thus, beyond providing an explanation for a popular-science phenomenon, we outline a method to experimentally model subwavelength field patterns using thermal imaging in macroscopic dielectric systems. [ABSTRACT FROM AUTHOR]

In this communication, we report on the real-time analysis of organic aerosol particles by Vacuum-assisted Plasma Ionization-Mass Spectrometry (Aero-VaPI-MS) using a home-built VaPI ion source coupled to a Synapt G2-S HDMS ion mobility-mass spectrometry (IM-MS) system. Standards of organic molecules of interest in prebiotic chemistry were used to generate aerosols. Monocaprin and decanoic acid aerosol particles were successfully detected in both the positive and negative ion modes, respectively. A complex aerosol mixture of different sizes of polymers of L-malic acid was also examined through ion mobility (IM) separations, resulting in the detection of polymers of up to eight monomeric units. This noncommercial plasma ion source is proposed as a low cost alternative to other plasma ionization platforms used for aerosol analysis, and a higher-performance alternative to more traditional aerosol mass spectrometers. VaPI provides robust online ionization of organics in aerosols without extensive ion activation, with the coupling to IM-MS providing higher peak capacity and excellent mass accuracy.ᅟ [ABSTRACT FROM AUTHOR]

Previously, we have reported the development of a miniature mass spectrometer with a continuous atmospheric pressure interface, whose sensitivity was sacrificed due to the limited gas flow rate. In this study, a circular lens was designed and integrated on the ion transfer pathway between the two pumping stages, and a ten-fold sensitivity improvement could be achieved when coupling with external ionization sources. Besides the capability of working with ionization sources in the atmosphere, there is also an in-vacuum plasma ionization source, so that both volatile and non-volatile samples could be analyzed. A 10 ppbv detection sensitivity was achieved for dimethyl methyl phosphonate (DMMP) in air using the plasma ionization source. Furthermore, the miniature mass spectrometer was also demonstrated for the direct analyses of progesterone in drinking water and atrazine in soil samples using paper spray and syringe spray, respectively. [ABSTRACT FROM AUTHOR]

The use of atmospheric pressure ionization (API) sources has become very popular for gas chromatography-mass spectrometry (GC-MS) determinations. GC-API-MS shows important advantages over traditional vacuum ionization sources such as a lower fragmentation preserving the molecular or quasi-molecular ion, the combination of GC separations with advanced mass spectrometers typically developed for liquid chromatography (LC) systems, a significantly higher sensitivity, or the reduction of costs due to the capability to use the same MS for both LC- and GC- couplings. For these reasons, the development of new API sources and GC-API-MS platforms has exponentially increased during the last years. Thus, this review is mainly focused on the last advances in GC-API-MS instrumentation. New setups and couplings on extensively reported API techniques as well as the development of new API sources for GC-MS coupling are thoroughly discussed. Moreover, novel ionization strategies have been reviewed to overcome some of the drawbacks of GC-API-MS methodologies. [Display omitted] • New API set-ups for GC-MS improve detectability, selectivity and precision. • New API sources based on plasma, laser or chemical ionization has been developed. • Controlled addition of modifiers may enable more selective and sensitive methods. • GC-MS data combining API and EI enhance the confidence level in non-target analysis. [ABSTRACT FROM AUTHOR]

Low molecular weight polar organics are commonly observed in spacecraft environments. Increasing concentrations of one or more of these contaminants can negatively impact Environmental Control and Life Support (ECLS) systems and/or the health of crew members, posing potential risks to the success of manned space missions. Ambient plasma ionization mass spectrometry (MS) is finding effective use as part of the analytical methodologies being tested for next-generation space module environmental analysis. However, ambient ionization methods employing atmospheric plasmas typically require relatively high operation voltages and power, thus limiting their applicability in combination with fieldable mass spectrometers. In this work, we investigate the use of a low power microplasma device in the microhollow cathode discharge (MHCD) configuration for the analysis of polar organics encountered in space missions. A metal-insulator-metal (MIM) structure with molybdenum foil disc electrodes and a mica insulator was used to form a 300 μm diameter plasma discharge cavity. We demonstrate the application of these MIM microplasmas as part of a versatile miniature ion source for the analysis of typical volatile contaminants found in the International Space Station (ISS) environment, highlighting their advantages as low cost and simple analytical devices. [ABSTRACT FROM AUTHOR]

A new ion generation method, named plasma-spray ionization (PLASI) for direct analysis of liquid streams, such as in continuous infusion experiments or liquid chromatography (LC), is reported. PLASI addresses many of the analytical limitations of electrospray ionization (ESI) and has potential for real time process stream analysis and reaction monitoring under atmospheric conditions in non-ESI friendly scenarios. In PLASI-mass spectrometry (MS), the liquid stream is pneumatically nebulized and partially charged at low voltages; the resultant aerosol is thus entrained with a gaseous plasma plume from a distal glow discharge prior to MS detection. PLASI-MS not only overcomes ESI-MS limitations but also generates simpler mass spectra with minimal adduct and cluster formation. PLASI utilizes the atomization capabilities of an ESI sprayer operated below the ESI threshold to generate gas-phase aerosols that are then ionized by the plasma stream. When operated at or above the ESI threshold, ionization by traditional ESI mechanisms is achieved. The multimodal nature of the technique enables readily switching between plasma and ESI operation. It is expected that PLASI will enable analyzing a wide range of analytes in complex matrices and less-restricted solvent systems, providing more flexibility than that achievable by ESI alone. [Figure not available: see fulltext.] [ABSTRACT FROM AUTHOR]

pulse Nd: YAG laser with pulse duration 5-10 ns, beam radius at focal point 0.2-0.4 mm, wavelengths 1064 nm, 532 nm and 238 nm with linearly polarized radiation and Gaussian beam profile, was impacted on a thin foil of titanium metal for generating plasma plume. Numerically, the above parameters were linked with average kinetic energy of the electrons and ions in the laser-induced plasma. In the present model, electrons having higher velocities are assumed to escape from plasma, that forms a negatively charged sheath around the plasma. It is seen from present computations that the forward directed nature of the laser evaporation process results from the anisotropic expansion velocities associated with different species. These velocities are mainly controlled by the initial dimension of the expanding plasma. An attempt was undertaken to estimate the length of the plume at different ambient gas pressures using an adiabatic expansion model. The rate of the plasma expansion for various Ar ion energies was derived from numerical calculations. A numerical definition of this plasma includes events like collisional/radiative, excitation/de-excitation and ionization/recombination processes involving multiples of energy levels with several ionization stages. Finally, based on a kinetic model, the plasma expansion rate across the laser beam axis was investigated. [ABSTRACT FROM AUTHOR]

Abstract: Several analytical techniques are currently used to determine mass-dependent molybdenum isotopic variations in natural materials using multiple-collector inductively coupled plasma mass spectrometry (MC-ICP-MS), including different methods for the separation of Mo from the sample and the correction for instrumental mass-dependent isotopic fractionation (instrumental mass bias). Both internal (“double-spiking” using two enriched Mo isotopes) and external (“zirconium doping” with standard-sample bracketing) techniques have been used in previous studies to deal with the effects of instrumental mass bias. The results of these studies have indicated that the precision for Mo isotopic analyses of natural (matrix-bearing) samples is a factor of ∼4–7× better using a double spike. Here we present a detailed study of the ability of MC-ICP-MS to determine, both precisely and accurately, the isotopic composition of Mo extracted from molybdenite using a low blank, high yield two-column procedure for Mo separation and a simple standard-sample bracketing approach to correct for instrumental mass bias. Based on analyses of molybdenites, the precision of this technique is shown to be similar to published double-spike data (within a factor of ∼2). All three of the known types of potential matrix effects in the MC-ICP-MS are also evaluated: automatrix effects, matrix effects due to Zr doping and matrix effects due to elements in the sample other than Mo and Zr. Each of these matrix effects is found to be either insignificant or controllable. Analyses of five molybdenites of hydrothermal origin reveal a range in their Mo isotopic composition that is a factor of ∼4 greater than the previous range reported for such samples. More detailed work is required to elucidate the origin of these mass-dependent Mo isotopic variations in molybdenites. [Copyright &y& Elsevier]

We describe analytical techniques for the measurement of 226Ra–230Th–238U disequilibria in volcanic rocks using plasma ionization multicollector mass spectrometry (MC-ICP-MS). Our methods build upon previous MC-ICP-MS techniques for 232Th/230Th and 238U/234U measurements with the addition of new chemical and/or mass spectrometric procedures for the determination of Th, U and 226Ra abundances. Using sample sizes that are similar to the requirements of state-of-the-art thermal ionization mass spectrometry (TIMS), we are able to measure Th isotope ratios and 226Ra–230Th–238U disequilibria with a precision that is at least ∼2–3× better than TIMS and U isotope ratios with a precision that is comparable to TIMS. Replicate analyses of a 226Ra–230Th–234U–238U radioactive equilibrium rock standard (Table Mountain Latite) demonstrate that our MC-ICP-MS techniques are also highly accurate. An additional bonus is that analyses of Ra, Th and U isotope ratios by MC-ICP-MS are much less time-consuming than by TIMS. These analytical improvements will increase the usefulness of U-series isotopes as high-resolution tracers of the nature and timing of magmatic processes at active volcanoes. [Copyright &y& Elsevier]

Real-time breath analysis by high-resolution mass spectrometry (HRMS) is a promising method to noninvasively retrieve relevant biochemical information. In this work, we conducted a head-to-head comparison of two ionization techniques: Secondary electrospray ionization (SESI) and plasma ionization (PI), for the analysis of exhaled breath. Two commercially available SESI and PI sources were coupled to the same HRMS device to analyze breath of two healthy individuals in a longitudinal study. We analyzed 58 breath specimens in both platforms, leading to 2,209 and 2,296 features detected by SESI-HRMS and by PI-HRMS, respectively. 60% of all the mass spectral features were detected in both platforms. However, remarkable differences were noted in terms of the signal-to-noise ratio (S/N), whereby the median (interquartile range, IQR) S/N ratio for SESI-HRMS was 115 (IQR = 408), whereas for PI-HRMS it was 5 (IQR = 5). Differences in the mass spectral profiles for the same samples make the inter-comparability of both techniques problematic. Overall, we conclude that both techniques are excellent for real-time breath analysis because of the very rich mass spectral fingerprints. However, further work is needed to fully understand the exact metabolic insights one can gather using each of these platforms., (Copyright 2022 Jiafa Zeng, Alexandra Christen, Kapil Dev Singh, Urs Frey, Pablo Sinues. License: This work is licensed under a Creative Commons Attribution 4.0 International License.)

Petroleomics, which is the characterization, separation, and quantification of the components of petroleum and crude oil, is an emerging area of study. However, the repertoire of analytical methods available to understand commercial automotive lubricant oils (ALOs) is very limited. Ambient mass spectrometry is one of the most sensitive analytical methods for real-time and in situ chemical analysis. With this technique, the chemical fingerprinting of ALOs can be performed quickly and simply using dielectric barrier discharge ionization time-of-flight mass spectrometry. In this study, the mass spectra of 35 samples were obtained without any sample preparation in positive-ion mode, and no carryover was observed. To elucidate the similarities and differences between the ALO samples, the data generated from these spectra were analyzed using four chemometric techniques: principal component analysis, multivariate curve resolution, hierarchical cluster analysis, and pattern recognition entropy. The ALO samples were readily differentiated according to their American Petroleum Institute classification and base oil types: mineral, semisynthetic, and synthetic. The development of this new methodology will aid in the semiquantitative control analysis of ALOs and offers an improved ability to identify the components therein.

The electron dynamics in the low-pressure operation regime (< 5 Pa) of a neon capacitively coupled plasma is investigated using phase-resolved optical emission spectroscopy. Plasma ionization and sustainment mechanisms are governed by the expanding and contracting sheath and complex wave-particle interactions. Electrons are energized through the advancing and retreating electric field of the RF sheath. The associated interaction of energetic sheath electrons with thermal bulk plasma electrons drives a two-stream instability also dissipating power in the plasma. [ABSTRACT FROM AUTHOR]