Relevant bibliographies by topics / Mass spectroscopy

Academic literature on the topic 'Mass spectroscopy'

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Published: 4 June 2021
Last updated: 27 July 2024

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Journal articles on the topic "Mass spectroscopy"

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Kemper, P. "Mass Spectroscopy." International Journal of Mass Spectrometry and Ion Processes 107, no. 2 (July 1991): 377. http://dx.doi.org/10.1016/0168-1176(91)80072-u.

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Ravn, Helge L. "Mass spectroscopy." Nuclear Instruments and Methods in Physics Research Section B: Beam Interactions with Materials and Atoms 35, no. 2 (December 1988): 196–97. http://dx.doi.org/10.1016/0168-583x(88)90493-4.

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P, D. "Mass spectroscopy." Journal of Molecular Structure 161 (October 1987): 347. http://dx.doi.org/10.1016/0022-2860(87)85086-x.

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Derrick, Peter J. "Mass spectroscopy at high mass." Fresenius' Zeitschrift für analytische Chemie 324, no. 5 (January 1986): 486–91. http://dx.doi.org/10.1007/bf00474121.

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Andersen, Hans Henrik. "Mass spectroscopy 2." Nuclear Instruments and Methods in Physics Research Section B: Beam Interactions with Materials and Atoms 53, no. 2 (February 1991): 233. http://dx.doi.org/10.1016/0168-583x(91)95667-3.

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Ostrowski, A. N., H. G. Bohlen, A. S. Demyanova, B. Gebauer, R. Kalpakchieva, Ch Langner, H. Lenske, et al. "Mass spectroscopy of13Be." Zeitschrift für Physik A Hadrons and Nuclei 343, no. 4 (December 1992): 489–90. http://dx.doi.org/10.1007/bf01289828.

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Baxter, A. M., A. P. Byrne, G. D. Dracoulis, R. V. F. Janssens, I. G. Bearden, R. G. Henry, D. Nisius, et al. "Spectroscopy ofPb186with mass identification." Physical Review C 48, no. 5 (November 1, 1993): R2140—R2143. http://dx.doi.org/10.1103/physrevc.48.r2140.

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OHKUBO, M. "Superconductivity for Mass Spectroscopy." IEICE Transactions on Electronics E90-C, no. 3 (March 1, 2007): 550–55. http://dx.doi.org/10.1093/ietele/e90-c.3.550.

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Recnagel, E. "Mass spectroscopy of clusters." Vacuum 39, no. 7-8 (January 1989): 861. http://dx.doi.org/10.1016/0042-207x(89)90062-6.

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Gordon, John. "Resolving Mass Spectroscopy Problems." Physics Bulletin 39, no. 7 (July 1988): 277–79. http://dx.doi.org/10.1088/0031-9112/39/7/019.

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Dissertations / Theses on the topic "Mass spectroscopy"

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Massa, D. L. "Discussion: Spectroscopy and Mass-Loss Diagnostics." Universität Potsdam, 2007. http://opus.kobv.de/ubp/volltexte/2008/1782/.

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Rogers, Kevin Shaun. "Laser desorption/laser ionization mass spectroscopy." Thesis, University of Salford, 1993. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.357037.

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Lorenz, Martin. "Matrix-isolation spectroscopy of mass-selected ions." [S.l. : s.n.], 2000. http://deposit.ddb.de/cgi-bin/dokserv?idn=962027340.

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Boyce, Kevin Robert. "Improved single ion cyclotron resonance mass spectroscopy." Thesis, Massachusetts Institute of Technology, 1993. http://hdl.handle.net/1721.1/42551.

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Natarajan, Vasant. "Penning trap mass spectroscopy at 0.1 ppb." Thesis, Massachusetts Institute of Technology, 1993. http://hdl.handle.net/1721.1/28017.

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Cornell, Eric Allin. "Mass spectroscopy using single ion cyclotron resonance." Thesis, Massachusetts Institute of Technology, 1990. http://hdl.handle.net/1721.1/13562.

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Bagga, Amit. "Femtosecond Laser Mass Spectroscopy of Cyclic Aromatic Hydrocarbons." Thesis, Université d'Ottawa / University of Ottawa, 2018. http://hdl.handle.net/10393/37098.

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Cyclic Aromatic molecules are the subject of continued research due to their highly advantageous characteristics which can be exploited in the areas of pharmaceuticals, material science and nano-electronics. While the defining properties and criteria for a molecule to be considered aromatic are very specific and well established, the degree of aromaticity of these molecules and their corresponding ordering remains a source of continued debate. Given that the macroscopic aromatic properties are fundamentally rooted in the underlying electronic structure and molecular dynamics, these properties can be probed in numerous ways. One such method is to exploit the strong laser field as it pertains to non-linear light-matter interaction. More specifically, the study of photoionization, as a direct resultant effect of strong field light-matter interaction, gives us direct insight into electronic and spatial properties as captured via mass spectroscopy. As a strong-field process, photoionization is effective because the variables that influence its results are also the ones that define aromaticity thus a correlation can be postulated. Other strong field advanced techniques to probe aromacity such as High Harmonic Generation (HHG) have already been successful shown by our group to be effective spectroscopic tools. In this way, photoionization provides supporting evidence to enhance the understanding of these novel spectroscopic tools. This thesis demonstrates that photoionization mass spectroscopy can be used as a probe into the aromaticity order of 5-membered cyclic aromatic molecules. Furthermore, the thesis will show that photoionization results correlate with the previously conducted HHG studies in this area thus further supporting these techniques as sensitive spectroscopic tools into aromaticity. The first part of this thesis describes the characterization of aromatic molecules and the corresponding process to obtain photoionization results that can be correlated to aromaticity. In the second part, these results are compared to the theoretical model and HHG demonstrating consistent results. The third and final component of this thesis describes future work, namely two-colour control of photoionization which is intended to provide greater resolution and variation of photoionization spectra thereby providing a more comprehensive and conclusive understanding of the proposed correlation with aromaticity.
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Parry, Christopher Mark. "Spectroscopy of neutron deficient mass A=130 nuclei." Thesis, University of York, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.313864.

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Cartwright, Peter C. "Mass selective laser photoionisation spectroscopy of copper dimer." Thesis, University of Edinburgh, 1989. http://hdl.handle.net/1842/13333.

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HUTH, THOMAS CARL. "ANALYTICAL MASS SPECTROMETRY WITH A SELECTIVE VACUUM ULTRAVIOLET PHOTOIONIZATION SOURCE." Diss., The University of Arizona, 1986. http://hdl.handle.net/10150/183916.

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The vacuum ultraviolet molecular hydrogen laser is evaluated as a selective ion source for analytical mass spectrometry of easily-ionized compounds. The types of compounds ionized below the photon energy of 7.8 eV include polynuclear aromatic hydrocarbons, and many amines and nitrogen-containing heterocycles. The latter two categories encompass a large number of pharmaceuticals and drugs of abuse. H₂ laser photoionization produces parent molecular ions only, for all compounds studied thus far. Selectivity of the threshold photoionization process is very high, as compounds within as little as 0.2 eV above the threshold are completely rejected. The ability of the technique to discriminate against interfering matrix components is demonstrated for both simple synthetic and complex "real world" mixtures. Easily interpreted spectra are obtained from simple extracts of spiked coffee, beer, soy sauce, urine and blood serum. The most important interference is shown to be electron impact ionization arising from acceleration of stray electrons in the ion source. Most of this ionization is caused by low-energy secondaries generated when stray primaries are collected by the ion source electrodes. The primaries are produced mainly by interaction of scattered laser radiation with metal surfaces. This interference can be controlled through proper instrumental design.
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Books on the topic "Mass spectroscopy"

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1936-, Barber R. C., and Venkatasubramanian V. S. 1930-, eds. Mass spectroscopy. 2nd ed. Cambridge [Cambridgeshire]: Cambridge University Press, 1986.

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F, Linskens H., and Jackson J. F, eds. Gas chromatography/mass spectroscopy. Berlin: Springer-Verlag, 1986.

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A, Bykovskiĭ I͡U. Lazernai͡a mass-spektrometrii͡a. Moskva: Ėnergoatomizdat, 1985.

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Bykovskiĭ, I︠U︡ A. Lazernai︠a︡ mass-spektrometrii︠a︡. Moskva: Ėnergoatomizdat, 1985.

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L, Busch Kenneth, ed. Understanding mass spectra: A basic approach. New York: Wiley, 1999.

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1952-, Vertes Akos, Gijbels R, and Adams Fred 1938-, eds. Laser ionization mass analysis. New York: Wiley & Sons, 1993.

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Gopi, Sreeraj, Augustine Amalraj, and Shintu Jude. High-Resolution Mass Spectroscopy for Phytochemical Analysis. New York: Apple Academic Press, 2021. http://dx.doi.org/10.1201/9781003153146.

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M, Lubman David, ed. Lasers and mass spectrometry. New York: Oxford University Press, 1990.

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1951-, Buchanan Michelle V., American Chemical Society. Division of Analytical Chemistry., and American Chemical Society Meeting, eds. Fourier transform mass spectrometry: Evolution, innovation, and applications. Washington, DC: American Chemical Society, 1987.

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A Handbook of spectroscopic data chemistry (UV, IR, PMR, 13CNMR and mass spectroscopy). Jaipur: Oxford Book Co., 2009.

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Book chapters on the topic "Mass spectroscopy"

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Morgan, Michael M., MacDonald J. Christie, Thomas Steckler, Ben J. Harrison, Christos Pantelis, Christof Baltes, Thomas Mueggler, et al. "Mass Spectroscopy." In Encyclopedia of Psychopharmacology, 750. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-540-68706-1_4343.

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Pomeranz, Yeshajahu, and Clifton E. Meloan. "Mass Spectroscopy." In Food Analysis, 243–61. Boston, MA: Springer US, 1994. http://dx.doi.org/10.1007/978-1-4615-6998-5_17.

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Zhu, Zifu, and Alina M. Alb. "Mass Spectroscopy." In Monitoring Polymerization Reactions, 201–27. Hoboken, NJ: John Wiley & Sons, 2014. http://dx.doi.org/10.1002/9781118733813.ch10.

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Bruno, Thomas J., and Paris D. N. Svoronos. "Mass Spectroscopy." In CRC Handbook of Basic Tables for Chemical Analysis, 565–86. Fourth edition. | Boca Raton, FL : CRC Press, 2020.: CRC Press, 2020. http://dx.doi.org/10.1201/b22281-11.

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Gandhi, Kamal, Neelima Sharma, Priyae Brath Gautam, Rajan Sharma, Bimlesh Mann, and Vanita Pandey. "Mass Spectroscopy." In Springer Protocols Handbooks, 199–217. New York, NY: Springer US, 2022. http://dx.doi.org/10.1007/978-1-0716-1940-7_10.

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Kemp, William. "Mass Spectrometry." In Organic Spectroscopy, 285–341. London: Macmillan Education UK, 1991. http://dx.doi.org/10.1007/978-1-349-15203-2_5.

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Yadav, L. D. S. "Mass Spectroscopy (MS)." In Organic Spectroscopy, 250–94. Dordrecht: Springer Netherlands, 2005. http://dx.doi.org/10.1007/978-1-4020-2575-4_8.

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Przybylski, Michael, Wolfgang Weinmann, and Thilo A. Fligge. "Mass Spectrometry." In Handbook of Spectroscopy, 327–62. Weinheim, FRG: Wiley-VCH Verlag GmbH & Co. KGaA, 2005. http://dx.doi.org/10.1002/3527602305.ch10.

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Davies, Antony N. "Mass Spectrometry." In Handbook of Spectroscopy, 488–504. Weinheim, FRG: Wiley-VCH Verlag GmbH & Co. KGaA, 2005. http://dx.doi.org/10.1002/3527602305.ch24.

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Przybylski, Michael. "Mass Spectrometry." In Handbook of Spectroscopy, 355–406. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527654703.ch11.

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Conference papers on the topic "Mass spectroscopy"

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Goldman, T. "PentaQuark Mass and Structure." In HADRON SPECTROSCOPY: Eleventh International Conference on Hadron Spectroscopy. AIP, 2006. http://dx.doi.org/10.1063/1.2176500.

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Noya, Hiroshi. "The Mass Spectra of the Peculiar Hadrons." In HADRON SPECTROSCOPY: Eleventh International Conference on Hadron Spectroscopy. AIP, 2006. http://dx.doi.org/10.1063/1.2176507.

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Lee, Su Houng. "The mass of charmonium in nuclear matter." In HADRON SPECTROSCOPY: Tenth International Conference on Hadron Spectroscopy. AIP, 2004. http://dx.doi.org/10.1063/1.1799795.

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Ligabue, Franco. "W mass and width determination at LEP II." In HADRON SPECTROSCOPY: Ninth International Conference on Hadron Spectroscopy. AIP, 2002. http://dx.doi.org/10.1063/1.1482466.

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Van Bramer, S. E., and M. V. Johnston. "10.5 eV Photoionization Mass Spectroscopy." In Laser Applications to Chemical Analysis. Washington, D.C.: Optica Publishing Group, 1990. http://dx.doi.org/10.1364/laca.1990.pd1.

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Laser ionization is becoming an increasingly powerful tool in mass spectroscopy. By frequency tripling the third harmonic of a Nd:YAG laser (355 nm) in a mixture of xenon and argon, it is possible to produce coherent vacuum ultraviolet (VUV) radiation at 118 nm (10.5 eV) for laser ionization mass spectroscopy. 10.5 eV photoionization is a potentially powerful tool for soft ionization. Since 10.5 eV is close to the ionization energy of most molecules, little fragmentation should be induced. Since no resonant intermediate state is required in a one photon process the ionization efficiency should be relatively high and consistent for most compounds when compared to multiphoton ionization. The 10.5 eV mass spectra of aliphatic C8 compounds with functional groups which induce extensive fragmentation will be discussed in this presentation.
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Ebert, D. "Heavy Quark Potential and Mass Spectra of Heavy Mesons." In HADRON SPECTROSCOPY: Ninth International Conference on Hadron Spectroscopy. AIP, 2002. http://dx.doi.org/10.1063/1.1482462.

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Helvajian, Henry. "Small Satellites: The Desire for a Mass Producible, Mass Customizable Nanosatellite." In Applied Industrial Optics: Spectroscopy, Imaging and Metrology. Washington, D.C.: OSA, 2012. http://dx.doi.org/10.1364/aio.2012.jm1a.4.

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Syage, Jack A., and John E. Wessel. "Ion Dip Spectroscopy and Multiresonant Processes in Aromatic Molecules by Supersonic Molecular Beam Mass Spectroscopy." In Laser Applications to Chemical Analysis. Washington, D.C.: Optica Publishing Group, 1987. http://dx.doi.org/10.1364/laca.1987.pdp12.

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Kuzmenko, D. S. "Mass spectrum of heavy hybrid mesons in the QCD string model." In HADRON SPECTROSCOPY: Tenth International Conference on Hadron Spectroscopy. AIP, 2004. http://dx.doi.org/10.1063/1.1799743.

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Larciprete, R., M. Stuke, and V. Magni. "Laser mass spectroscopy for laser CVD." In Conference on Lasers and Electro-Optics. Washington, D.C.: OSA, 1986. http://dx.doi.org/10.1364/cleo.1986.tue3.

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Reports on the topic "Mass spectroscopy"

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Cabrielse, Gerald. Antiprotons, Antihydrogen and Mass Spectroscopy. Fort Belvoir, VA: Defense Technical Information Center, March 2001. http://dx.doi.org/10.21236/ada388318.

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Hansen, Nils. FLAME-SAMPLING PHOTOIONIZATION MASS SPECTROSCOPY - FINAL TECHNICAL REPORT. Office of Scientific and Technical Information (OSTI), February 2013. http://dx.doi.org/10.2172/1072170.

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Baturin, Pavlo. Spectroscopy of electroproduced light to medium mass lambda hypernuclei. Office of Scientific and Technical Information (OSTI), January 2010. http://dx.doi.org/10.2172/989488.

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Bernstein, E. R., and H. S. Im. Mass Resolved Excitation Spectroscopy of Benzyl and Phenylnitrene Radicals. Fort Belvoir, VA: Defense Technical Information Center, July 1991. http://dx.doi.org/10.21236/ada239394.

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Broome, Scott, and Matthew Paul. Diffusive Properties of UNESE Core Samples via Continuously Monitored Mass Spectroscopy. Office of Scientific and Technical Information (OSTI), July 2019. http://dx.doi.org/10.2172/1762962.

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Schlack, Trevor, Samuel Beal, Elizabeth Corriveau, and Jay Clausen. Detection limits of trinitrotoluene and ammonium nitrate in soil by Raman spectroscopy. Engineer Research and Development Center (U.S.), February 2022. http://dx.doi.org/10.21079/11681/43302.

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The detection limit of 2,4,6-trinitrotoluene (TNT) and ammonium nitrate (AN) in mixtures of Ottawa sand (OS) was studied using a Raman microscope applying conventional calibration curves, Pearson correlation coefficients, and two-sample t-tests. By constructing calibration curves, the conventionally defined detection limits were estimated to be 1.9 ± 0.4% by mass in OS and 1.9 ± 0.3% by mass in OS for TNT and AN. Both TNT and AN were detectable in concentrations as low as 1% by mass when Pearson correlation coefficients were used to compare averaged spectra to a library containing spectra from a range of soil types. AN was detectable in concentrations as low as 1% by mass when a test sample of spectra was compared to the same library using two-sample t-tests. TNT was not detectable at a concentration of 1% by mass when using two-sample t-tests.
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Anderson, Timothy J. Mass Spectrometry and Fourier Transform Infrared Spectroscopy for Analysis of Biological Materials. Office of Scientific and Technical Information (OSTI), December 2014. http://dx.doi.org/10.2172/1226565.

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Hutchinson, J. M. R., and K. G. W. Inn. [Atom-counting standards and Doppler-free resonance ionization mass spectroscopy]. [Progress report]. Office of Scientific and Technical Information (OSTI), December 1988. http://dx.doi.org/10.2172/10180897.

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Venhaus, Thomas J. Campaign 1.7 Pu Aging. Development of Time of Flight Secondary Ion Mass Spectroscopy. Office of Scientific and Technical Information (OSTI), September 2015. http://dx.doi.org/10.2172/1214635.

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Thornberg, S. M., C. D. Mowry, M. R. Keenan, S. F. A. Bender, and T. Owen. Real-time monitoring of volatile organic compounds using chemical ionization mass spectroscopy: Final report. Office of Scientific and Technical Information (OSTI), April 1997. http://dx.doi.org/10.2172/481566.

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