Relevant bibliographies by topics / Miniature mass spectrometers

Academic literature on the topic 'Miniature mass spectrometers'

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Published: 10 December 2022
Last updated: 28 January 2023

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Journal articles on the topic "Miniature mass spectrometers"

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Ouyang, Zheng, and R. Graham Cooks. "Miniature Mass Spectrometers." Annual Review of Analytical Chemistry 2, no. 1 (July 19, 2009): 187–214. http://dx.doi.org/10.1146/annurev-anchem-060908-155229.

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Ouyang, Zheng, Robert J. Noll, and R. Graham Cooks. "Handheld Miniature Ion Trap Mass Spectrometers." Analytical Chemistry 81, no. 7 (April 2009): 2421–25. http://dx.doi.org/10.1021/ac900292w.

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Ioanoviciu, Damaschin, and Cornel Cuna. "Miniature time-of-flight mass spectrometers." Journal of Mass Spectrometry 38, no. 12 (2003): 1270–71. http://dx.doi.org/10.1002/jms.536.

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Snyder, Dalton T., Christopher J. Pulliam, Zheng Ouyang, and R. Graham Cooks. "Miniature and Fieldable Mass Spectrometers: Recent Advances." Analytical Chemistry 88, no. 1 (October 21, 2015): 2–29. http://dx.doi.org/10.1021/acs.analchem.5b03070.

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Yu, Quan, Kai Ni, Fei Tang, and Xiao Hao Wang. "Progress in the Development of a Miniature Mass Spectrometry." Applied Mechanics and Materials 241-244 (December 2012): 529–32. http://dx.doi.org/10.4028/www.scientific.net/amm.241-244.529.

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Mass spectrometer is one of the most versatile tools in current analytical science, which can perform both qualitative and quantitative chemical identification with high sensitivity, high accuracy and low consumption. Currently, the development of miniature mass spectrometer has received growing interest, since it provides a rapid way for online detection and real-time analysis. Quadrupole analyzer has been widely used in quantitative analysis, and it can be easily miniaturized for the purpose of developing portable mass spectrometers. A portable quadrupole mass spectrometer was developed for in-situ analysis, which can perform both qualitative and quantitative analysis for solid or liquid samples in atmospheric conditions.
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Babapour Ghadikolaee, Mohammad Reza. "Millimeter-Scale PIG Source for Miniature Mass Spectrometers." Journal of Fusion Energy 31, no. 6 (January 22, 2012): 566–68. http://dx.doi.org/10.1007/s10894-012-9508-6.

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Guo, Qi, Lijuan Gao, Yanbing Zhai, and Wei Xu. "Recent developments of miniature ion trap mass spectrometers." Chinese Chemical Letters 29, no. 11 (November 2018): 1578–84. http://dx.doi.org/10.1016/j.cclet.2017.12.009.

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Gao, Liang, Qingyu Song, Robert J. Noll, Jason Duncan, R. Graham Cooks, and Zheng Ouyang. "Glow discharge electron impact ionization source for miniature mass spectrometers." Journal of Mass Spectrometry 42, no. 5 (2007): 675–80. http://dx.doi.org/10.1002/jms.1201.

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Sparkman, O. David. "Focus on field-portable and miniature mass spectrometers. Presentations from the 12th Sanibel Conference on Mass Spectrometry." Journal of the American Society for Mass Spectrometry 12, no. 6 (June 2001): 617–18. http://dx.doi.org/10.1016/s1044-0305(01)00244-6.

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Brinckerhoff, W. B., T. J. Cornish, R. W. McEntire, A. F. Cheng, and R. C. Benson. "Miniature time-of-flight mass spectrometers for in situ composition studies." Acta Astronautica 52, no. 2-6 (January 2003): 397–404. http://dx.doi.org/10.1016/s0094-5765(02)00180-7.

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Dissertations / Theses on the topic "Miniature mass spectrometers"

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Fox, James D. "Miniature Mass Spectrometry: Theory, Development and Applications." Thesis, University of North Texas, 2013. https://digital.library.unt.edu/ark:/67531/metadc407824/.

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As mass analyzer technology has continued to improve over the last fifty years, the prospect of field-portable mass spectrometers has garnered interest from many research groups and organizations. Designing a field portable instrument entails more than the scaling down of current commercial systems. Additional considerations such as power consumption, vacuum requirements and ruggedization also play key roles. In this research, two avenues were pursued in the initial development of a portable system. First, micrometer-scale mass analyzers and other electrostatic components were fabricated using silicon on insulator-deep reactive ion etching, and tested. Second, the dimensions of an ion trap were scaled to the millimeter level and fabricated from common metals and commercially available vacuum plastics. This instrument was tested for use in ion isolation and collision induced dissociation for secondary mass spectrometry and confirmatory analyses of unknowns. In addition to portable instrumentation, miniature mass spectrometers show potential for usage in process and reaction monitoring. To this end, a commercial residual gas analyzer was used to monitor plasma deposition and cleaning inside of a chamber designed for laser ablation and soft landing-ion mobility to generate metal-main group clusters. This chamber was also equipped for multiple types of spectral analysis in order to identify and characterize the clusters. Finally, a portion of this research was dedicated to method development in sample collection and analysis for forensic study. A new method for the analysis of illicit chemistries collected via electrostatic lifting is presented. This method incorporates surface-enhanced Raman microscopy as a prescreening tool for nanoextraction and nanospray ionization mass spectrometry.
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Chaudhary, Ashish. "Miniature Ion Optics Towards a Micro Mass Spectrometer." Scholar Commons, 2014. https://scholarcommons.usf.edu/etd/5410.

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This PhD dissertation reports the development of miniature ion optics components of a mass spectrometer (MS) with the ultimate goal to lay the foundation for a compact low-power micromachined MS (µMS) for broad-range chemical analysis. Miniaturization of two specific components a) RF ion traps and b) an ion funnel have been investigated and miniature low-power versions of these components have been developed and demonstrated successfully in lab experiments. Power savings, simpler electronics and packaging schemes required to operate the micro-scale RF cylindrical ion traps have been the key motivation driving this research. Microfabricated cylindrical ion traps (µCITs) and arrays in silicon, silicon-on-insulator and stainless steel substrates have been demonstrated and average power of as low as 55 mW for a low mass range (28 to 136 amu) and mass spectra with better than a unit-mass-resolution have been recorded. For the ion funnel miniaturization effort, simple assembly, small form factor and ease of integration have been emphasized. A simplification of the conventional 3D ion funnel design, called the planar ion funnel, has been developed in a single plate and has been tested to demonstrate ion funneling at medium vacuum levels (1E-5 Torr) using DC voltages and power less than 0.5 W. Miniaturization of these components also enables use of other novel ion optics components, packaging and integration, which will allow a new class of µMS architectures amenable for radical miniaturization.
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Hemond, Brian D. (Brian David Thomson). "Development and performance of a miniature, low cost mass spectrometer." Thesis, Massachusetts Institute of Technology, 2011. http://hdl.handle.net/1721.1/67584.

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Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Mechanical Engineering, 2011.
Cataloged from PDF version of thesis.
Includes bibliographical references (p. 111-112).
A miniature, low cost mass spectrometer has been developed that is capable of unit resolution over a mass range of 10 to 50 AMU. The design of the mass spectrometer incorporates several new features that enhance the performance of the design over comparable instruments. An efficient ion source allows a relatively low power consumption without sacrificing resolution. Variable geometry mechanical filters allow for variable resolution. An onboard ion pump removes the need for an external pumping source. An onboard digital controller allows a large degree of flexibility over the operation of the mass spectrometer while eliminating the need for high voltage electrical feedthroughs. The miniature mass spectrometer is sensitive to fractions of a percentage of inlet gas, and formatted mass spectra are returned digitally to a laptop.
by Brian D. Hemond.
Ph.D.
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Hood, Derrell L. "Development of a Novel Loeb-Eiber Mass Filter." Ohio University / OhioLINK, 2009. http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1248981763.

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Royer, Clément. "Etude des performances des spectromètres miniatures infrarouge à base d'AOTF Pre-launch radiometric calibration of the infrared spectrometer onboard SuperCam for the Mars2020 rover." Thesis, université Paris-Saclay, 2020. http://www.theses.fr/2020UPASP085.

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Depuis une vingtaine d'années, la spectroscopie de réflectance proche-infrarouge appliquée à la planétologie a révolutionné notre vision des surfaces planétaires, grâce notamment à la découverte de phyllosilicates à la surface de Mars par les instruments OMEGA (Observatoire pour la Minéralogie, l'Eau, les Glaces et l'Activité) à bord de la sonde européenne Mars Express, et CRISM (Compact Reconnaissance Infrared Spectrometer for Mars) embarqué sur la sonde Mars Reconnaissance Orbiter, en 2005 et 2007. Ces deux missions spatiales ont ouvert la voie à l'étude approfondie de toutes les surfaces planétaires dans le proche-infrarouge (entre 1 et 5 µm), à la recherche de leur composition minéralogique et des processus d'altération passés et présents.Dans l'optique d'équiper toute sonde interplanétaire, voire même in-situ, avec des spectromètres proche-infrarouge, il est nécessaire de développer une nouvelle génération d'instruments à la fois compacts et performants. L'AOTF (Acousto-Optic Tunable Filter) utilisé en tant que monochromateur est une technologie-clé sur laquelle pourront s'appuyer ces instruments. Les deux spectromètres au coeur de ma thèse, IRS (Infrared Spectrometer) équipant l'instrument combiné SuperCam à bord du rover Perseverance, et ExoCam, au stade de R&T à l'Institut d'Astrophysique Spatiale, exploitent le potentiel de ce composant pour produire des données scientifiques de haute qualité avec un volume réduit.Ma thèse a ainsi contenu deux volets principaux : la préparation et la réalisation de l'étalonnage radiométrique des modèles de vol et de qualification de IRS/SuperCam, et le développement d'un simulateur d'observations infrarouge pour les futures opérations du rover Perseverance d'une part ; et l'étude des performances de l'imagerie hyperspectrale proche-infrarouge utilisant l'AOTF en transmission avec le programme de R&T ExoCam, accompagnée du développement d'un modèle radiométrique du banc de R&T permettant de projeter les résultats obtenus sur table à de futures opérations dans l'espace
During the past 20 years, reflectance near-infrared spectroscopy applied to planetary exploration has brought a new sight on planetary surfaces, mainly thanks to the discovery of Martian phyllosilicates by OMEGA (Observatoire pour la Minéralogie, l'Eau, les Glaces et l'Activité) on-board the European probe Mars Express, and CRISM (Compact Reconnaissance Infrared Spectrometer for Mars) equipping the probe Mars Reconnaissance Orbiter, in 2005 and 2007. These two space missions have paved the way to the thorough study of the surface of planetary bodies in the near-infrared (between 1 and 5 µm), searching for their mineral composition and past/present alteration processes.In order to board a infrared spectrometer in every interplanetary, and even in-situ probes, it is necessary to design a new generation of instruments both compact and efficient. The AOTF-based (Acousto-Optic Tunable Filter) monochromator is a key technology to fulfill this objective. The two spectrometers studied in the frame of my PhD thesis, IRS (Infrared Spectrometer) on-board the SuperCam instrument on Perseverance rover, and ExoCam, in R&T at the IAS (Institut d'Astrophysique Spatiale), benefit from this subsystem to produce high quality science data with a small volume occupation.My PhD thesis has been thus divided in two main parts: the preparation and performance of the radiometric calibration of the IRS/SuperCam qualification and flight models, and the design of an infrared observation simulator for the future Perseverance operations; the study of the performance of hyperspectral near-infrared imagery using an AOTF in transmission, throught the ExoCam R&T program, along with the development of a radiometric model of the R&T breadboard allowing to extrapolate lab results to future space operations
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Graichen, Adam. "Enhanced detection strategies accomplished through metal binding and miniature mass spectrometry." 2013. https://scholarworks.umass.edu/dissertations/AAI3556252.

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A multiplexed method for performing MS/MS on multiple ions simultaneously in a miniature rectilinear ion trap (RIT) mass spectrometer has been developed. This method uses an ion encoding procedure that relies on the mass bias that exists when ions are externally injected into an RIT operated with only a single phase RF applied to one pair of electrodes. The ion injection profile under such conditions ions is Gaussian-like over a wide range of RF amplitudes, or low mass cutoff (LMCO) values, during ion accumulation. We show that this distribution is related to ion m/z, and is likely caused by ions having an optimal range of pseudo-potential well depths for efficient trapping. Based on this observation, precursor ion intensity changes between two different injection LMCO values can be predicted, and these ion intensity changes are found to be carried through to their corresponding product ions, enabling multiplexed MS/MS spectra to be deconvoluted. The gas-phase reactions of a series of coordinatively unsaturated [Ni(L) n]y+ complexes, where L is a nitrogen-containing ligand, with chemical warfare agent (CWA) simulants in a miniature rectilinear ion trap mass spectrometer were investigated as part of a new approach to detect CWA. Results show that the metal complex ions can react with low concentrations of several CWA simulants, including dipropyl sulfide (simulant for mustard gas), acetonitrile (simulant for the nerve agent tabun), and diethyl phosphite (simulant for nerve agents sarin, soman, tabun, and VX), thereby providing a sensitive means of detecting these compounds. The [Ni(L)n] 2+ complexes are found to be particularly reactive with the simulants of mustard gas and tabun, allowing their detection at low parts-per-billion (ppb) levels. These detection limits are well below the median lethal doses for these CWAs, which indicates the applicability of this new approach, and are about two orders of magnitude lower than electron ionization detection limits on the same mass spectrometer. The use of coordinatively unsaturated metal complexes as reagent ions offers the possibility of further tuning the ion-molecule chemistry so that desired compounds can be detected selectively or at even lower concentrations. Mass spectrometry has become a tool for studying noncovalently bound complexes. Specifically, electrospray ionization mass spectrometry (ESI-MS) has found increasing use for the determination of affinity (Ka) or dissociation (Kd) constants. Direct measurement of the equilibrium components by ESI-MS is the most straightforward approach for determining binding equilibrium constants, but this approach is prone to error and has some inherent limitations. Transferring complexes from solution to the gas phase may perturb the equilibrium concentrations and/or different ionization efficiencies may cause the resulting ion signals not to reflect actual solution concentrations. Furthermore, ESI only works under a limited range of solvent conditions (i.e. low ionic strengths), which limits the broad applicability of this approach. We propose an approach based on covalent labeling in the context of metal-catalyzed oxidation (MCO) reactions that, when combined with MS, overcomes such limitations when determining metal-ligand binding constants. The MCO-MS approach will provide concurrent information regarding metal binding site and metal-protein binding affinity. Optimization of the MCO reaction through isotopic mass tags will permit enhanced identification of modified residues. Application of this method to study the affinity and binding interactions of other divalent metals with β2m are likely to provide insight into the specificity of copper for causing β2m amyloid formation.
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(7874093), Fan Pu. "MASS SPECTROMETRY AT POINT-OF-CARE: SIMPLE YET POWERFUL SOLUTIONS FOR BETTER HEALTH." Thesis, 2019.

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The superior sensitivity and selectivity obtained with mass spectrometry (MS) is hardly matched by other analytical technologies, therefore it is an indispensable tool for modern society. Traditionally, MS is coupled with chromatography separation and performed in centralized analytical laboratories, which often requires extensive sample preparation and expensive instrumentation. With the advancements in the field of ambient MS and miniature MS, MS analysis at point-of-care (POC) has become a reality. Ambient MS includes a variety of methods for sampling and ionization, but they all share a common feature: they require little to no sample preparation. This has made rapid analysis of untreated sample possible and speed of MS analysis is significantly improved. Miniature MS, on the other hand, shrinks down the sizes of conventional benchtop instruments so they become portable or fieldable. In this dissertation, I documented the developments of ambient MS methods and applications of miniature MS for a variety of health-related topics, which include preclinical pharmacokinetics, intraoperative diagnosis, drug adherence monitoring and food safety.

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(5930282), Dalton T. Snyder. "One- and Two-dimensional Mass Spectrometry in a Linear Quadrupole Ion Trap." Thesis, 2019.

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Amongst the various classes of mass analyzers, the quadrupole ion trap (QIT) is by far the most versatile. Although it can achieve only modest resolution (unit) and mass accuracy (101-102 ppm), it has high sensitivity and selectivity, can operate at pressures exceeding 10-3 torr, is tolerant to various electrode imperfections, and has single analyzer tandem mass spectrometry (MS/MS) capabilities in the form of product ion scans. These characteristics make the QIT ideal for mass spectrometer miniaturization, as most of the fundamental performance metrics of the QIT do not depend on device size. As such, the current drive in miniature systems is to adopt miniature ion traps in various forms – 3D, linear, toroidal, rectilinear, cylindrical, arrays, etc.

Despite being one of the two common mass analyzers with inherent MS/MS capabilities (the other being the Fourier transform ion cyclotron resonance mass spectrometer), it is commonly accepted that the QIT cannot perform one-dimensional precursor ion scans and neutral loss scans - the other two main MS/MS scan modes - or two-dimensional MS/MS scans. The former two are usually conducted in triple quadrupole instruments in which a first and third quadrupole are used to mass select precursor and product ions while fragmentation occurs in an intermediate collision cell. The third scan can be accomplished by acquiring a product ion scan of every precursor ion, thus revealing the entire 2D MS/MS data domain (precursor ion m/z vs. product ion m/z). This, however, is not one scan but a set of scans. Because the ion trap is a tandem-in-time instrument rather than a tandem-in-space analyzer, precursor ion scans, neutral loss scans, and 2D MS/MS are, at best, difficult.

Yet miniature mass spectrometers utilizing quadrupole ion traps for mass analysis would perhaps benefit the most from precursor scans, neutral loss scans, and 2D MS/MS because they generally have acquisition rates (# scans/s) an order of magnitude lower than their benchtop counterparts. This is because they usually use a discontinuous atmospheric pressure interface (DAPI) to reduce the gas load on the backing pumps, resulting in a ~1 scan/s acquisition rate and making the commonly-used data-dependent acquisition method (i.e. obtaining a product ion scan for every abundant precursor ion) inefficient in terms of sample consumption, time, and instrument power. Precursor and neutral loss scans targeting specific molecular functionality of interest - as well as 2D MS/MS – are more efficient ways of moving through the MS/MS data domain and thus pair quite readily with miniature ion traps.

Herein we demonstrate that precursor ion scans, neutral loss scans, and 2D MS/MS are all possible in a linear quadrupole ion trap operated in the orthogonal double resonance mode on both benchtop and portable mass spectrometers. Through application of multiple resonance frequencies matching the secular frequencies of precursor and/or product ions of interest, we show that precursor ions can be fragmented mass-selectively and product ions ejected simultaneously, preserving their relationship, precursor ion -> product ion + neutral, in the time domain and hence allowing the correlation between precursor and product ions without prior isolation. By fixing or scanning the resonance frequencies corresponding to the targeted precursor and product ions, a precursor ion scan or neutral loss scan can be conducted in a single mass analyzer. We further show that 2D MS/MS - acquisition of all precursor ion m/z values and a product ion mass spectrum for every precursor ion, all in a single scan - is possible using similar methodology. These scan modes are particularly valuable for origin-of-life and forensic applications for which the value of miniature mass spectrometers is readily evident.
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(8054564), Katherine Elisabeth Wehde. "THE DEVELOPMENT OF MASS SPECTROMETRIC METHODS FOR THE DETERMINATION OF THE CHEMICAL COMPOSITION OF COMPLEX MIXTURES RELEVANT TO THE ENERGY SECTOR AND THE DEVELOPMENT OF A NEW DEVICE FOR CHEMICALLY ENHANCED OIL RECOVERY FORMULATION EVALUATION." Thesis, 2019.

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This dissertation focused on the development of mass spectrometric methodologies, separation techniques, and engineered devices for the optimal analysis of complex mixtures relevant to the energy sector, such as alternative fuels, petroleum-based fuels, crude oils, and processed base oils. Mass spectrometry (MS) has been widely recognized as a powerful tool for the analysis of complex mixtures. In complex energy samples, such as petroleum-based fuels, alternative fuels, and oils, high-resolution MS alone may not be sufficient to elucidate chemical composition information. Separation before MS analysis is often necessary for such highly complex energy samples. For volatile samples, in-line two-dimensional gas chromatography (GC×GC) can be used to separate complex mixtures prior to ionization. This technique allows for a more accurate determination of the compounds in a mixture, by simplifying the mixture into its components prior to ionization, separation based on mass-to-charge ratio (m/z), and detection. A GC×GC coupled to a high-resolution time-of-flight MS was utilized in this research to determine the chemical composition of alternative aviation fuels, a petroleum-based aviation fuel, and alternative aviation fuel candidates and blending components as well as processed base oils.

Additionally, as the cutting edge of science and technology evolve, methods and equipment must be updated and adapted for new samples or new sector demands. One such case, explored in this dissertation, was the validation of an updated standardized method, ASTM D2425 2019. This updated standardized method was investigated for a new instrument and new sample type for a quadrupole MS to analyze a renewable aviation fuel. Lastly, the development and evaluation of a miniaturized coreflood device for analyzing candidate chemically enhanced oil recovery (cEOR) formulations of brine, surfactant(s), and polymer(s) was conducted. The miniaturized device was used in the evaluation of two different cEOR formulations to determine if the components of the recovered oil changed.
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Books on the topic "Miniature mass spectrometers"

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Séverine, Le Gac, and Berg A. van den, eds. Miniaturization and mass spectrometry. Cambridge, UK: RSC Publishing, 2009.

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Knapp, Daniel, Daniel Figeys, Albert van den Berg, Severine le Gac, and Gary A. Schultz. Miniaturization and Mass Spectrometry. Royal Society of Chemistry, The, 2008.

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National Aeronautics and Space Administration (NASA) Staff. Design of an Improved Miniature Ion Neutral Mass Spectrometer for NASA Applications. Independently Published, 2018.

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Development of a miniature mass analyzer and associated instrumentation for improved capabilities in the analysis of low energy plasmas from a rocket or satellite platform: Final technical report. [Washington, D.C]: National Aeronautics and Space Administration, 1992.

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United States. National Aeronautics and Space Administration., ed. Development of a miniature mass analyzer and associated instrumentation for improved capabilities in the analysis of low energy plasmas from a rocket or satellite platform: Final technical report. [Washington, D.C]: National Aeronautics and Space Administration, 1992.

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Book chapters on the topic "Miniature mass spectrometers"

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"Ion Traps for Miniature,Multiplexed, and Soft-Landing Technologies." In Practical Aspects of Trapped Ion Mass Spectrometry, Volume IV, 197–276. CRC Press, 2010. http://dx.doi.org/10.1201/9781420083729-8.

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Smith, Scott, Christopher Mulligan, Qingyu Song, Robert Noll, R. Cooks, and Zheng Ouyang. "Ion Traps for Miniature, Multiplexed, and Soft-Landing Technologies." In Practical Aspects of Trapped Ion Mass Spectrometry, Volume IV, 169–247. CRC Press, 2010. http://dx.doi.org/10.1201/9781420083729-c2.

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Taylor, S., and N. France. "Miniature and Micro Mass Spectrometry for Nanoscale Sensing Applications: An Overview." In Newest Updates in Physical Science Research Vol. 14, 147–53. Book Publisher International (a part of SCIENCEDOMAIN International), 2021. http://dx.doi.org/10.9734/bpi/nupsr/v14/10189d.

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Ruff, Steven W., Joshua L. Bandfield, Philip R. Christensen, Timothy D. Glotch, Victoria E. Hamilton, and A. Deanne Rogers. "Thermal Infrared Remote Sensing of Mars from Rovers Using the Miniature Thermal Emission Spectrometer." In Remote Compositional Analysis, 499–512. Cambridge University Press, 2019. http://dx.doi.org/10.1017/9781316888872.027.

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Conference papers on the topic "Miniature mass spectrometers"

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Holland, Paul M., Ara Chutjian, Murray R. Darrach, and Otto J. Orient. "Miniaturized GC/MS instrumentation for in situ measurements: micro gas chromatography coupled with miniature quadrupole array and Paul ion trap mass spectrometers." In SPIE Proceedings, edited by Gregory H. Bearman and Patricia M. Beauchamp. SPIE, 2003. http://dx.doi.org/10.1117/12.520539.

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McLoughlin, Michael P., Charles W. Anderson, Wayne A. Bryden, Micah A. Carlson, Scott A. Ecelberger, and Harvey W. Ko. "Miniature time-of-flight mass spectrometer." In BiOS '98 International Biomedical Optics Symposium, edited by Robert A. Lieberman and Tuan Vo-Dinh. SPIE, 1998. http://dx.doi.org/10.1117/12.308045.

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Babij, Michał, Teodor Gotszalk, Zbigniew W. Kowalski, Karol Nitsch, Jerzy Silberring, and Marek Smoluch. "Miniature plasma jet for mass spectrometry." In Electron Technology Conference 2013, edited by Pawel Szczepanski, Ryszard Kisiel, and Ryszard S. Romaniuk. SPIE, 2013. http://dx.doi.org/10.1117/12.2029792.

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Finlay, A. "Miniature mass spectrometry: status and prospects." In IEE Seminar and Exhibition on MEMS Sensor Technologies. IEE, 2005. http://dx.doi.org/10.1049/ic:20050123.

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Szyszka, Piotr, Tomasz Grzebyk, Michal Krysztof, Anna Gorecka-Drzazga, and Jan A. Dziuban. "Miniature mass spectrometer integrated on a chip." In 2017 30th International Vacuum Nanoelectronics Conference (IVNC). IEEE, 2017. http://dx.doi.org/10.1109/ivnc.2017.8051602.

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Maas, J. D., W. Xu, P. I. Hendricks, and W. J. Chappell. "Miniature radio frequency ion trap mass spectrometry." In 2010 IEEE/MTT-S International Microwave Symposium - MTT 2010. IEEE, 2010. http://dx.doi.org/10.1109/mwsym.2010.5515697.

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Maas, Jeffrey D., Wei Xu, Paul Hendricks, and William J. Chappell. "Miniature radio frequency ion trap mass spectrometry." In 2010 IEEE/MTT-S International Microwave Symposium - MTT 2010. IEEE, 2010. http://dx.doi.org/10.1109/mwsym.2010.5516819.

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Sinha, Mahadeva P. "Miniature Mass Spectrometer (MMS) For Contaminant Gas Monitoring." In International Conference On Environmental Systems. 400 Commonwealth Drive, Warrendale, PA, United States: SAE International, 1997. http://dx.doi.org/10.4271/972492.

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Taylor, Steve, Balasingam Srigengan, J. R. Gibson, Dick Tindall, Richard R. A. Syms, Tom Tate, and Munir M. Ahmad. "Miniature mass spectrometer for chemical and biological sensing." In AeroSense 2000, edited by Patrick J. Gardner. SPIE, 2000. http://dx.doi.org/10.1117/12.394074.

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Jordan, J., G. Irwin, and J. Hoffman. "A miniature laser mass spectrometer system for planetary studies." In 40th AIAA Aerospace Sciences Meeting & Exhibit. Reston, Virigina: American Institute of Aeronautics and Astronautics, 2002. http://dx.doi.org/10.2514/6.2002-464.

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Reports on the topic "Miniature mass spectrometers"

1

Spencer, W. A. Miniature Mass Spectrometers for Hydrogen Isotopic Analyses. Office of Scientific and Technical Information (OSTI), May 2003. http://dx.doi.org/10.2172/811368.

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2

Hiller, j. m. Solid Phase Microextraction and Miniature Time-of-Flight Mass Spectrometer. Office of Scientific and Technical Information (OSTI), January 1999. http://dx.doi.org/10.2172/4086.

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You might also be interested in the extended bibliographies on the topic 'Miniature mass spectrometers' for particular source types:
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