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Journal articles on the topic 'Ion mass spectrometry'

Author: Grafiati

Published: 4 June 2021

Last updated: 12 February 2022

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1

Pollard, Matthew J., Christopher K. Hilton, Hongli Li, Kimberly Kaplan, Richard A. Yost, and Herbert H. Hill. "Ion mobility spectrometer—field asymmetric ion mobility spectrometer-mass spectrometry." International Journal for Ion Mobility Spectrometry 14, no. 1 (2011): 15–22. http://dx.doi.org/10.1007/s12127-011-0058-9.

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2

Lawrence, A. H., and A. A. Nanji. "Ion mobility spectrometry and ion mobility spectrometry/mass spectrometric characterization of dimenhydrinate." Biological Mass Spectrometry 16, no. 1-12 (1988): 345–47. http://dx.doi.org/10.1002/bms.1200160167.

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3

Tose, Lilian V., Paolo Benigni, Dennys Leyva, et al. "Coupling trapped ion mobility spectrometry to mass spectrometry: trapped ion mobility spectrometry-time-of-flight mass spectrometry versus trapped ion mobility spectrometry-Fourier transform ion cyclotron resonance mass spectrometry." Rapid Communications in Mass Spectrometry 32, no. 15 (2018): 1287–95. http://dx.doi.org/10.1002/rcm.8165.

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4

ISHIKAWA, Shuji, and Yuko TAKEGUCHI. "Secondary Ion Mass Spectrometry." Journal of the Japan Society of Colour Material 86, no. 10 (2013): 386–91. http://dx.doi.org/10.4011/shikizai.86.386.

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5

Hayashi, Akio, Nobutake Sato, Haruo Hosoda, and Ushio Takeda. "Ion Mobility Mass Spectrometry." Japanese Journal of Pesticide Science 42, no. 1 (2017): 187–96. http://dx.doi.org/10.1584/jpestics.w17-55.

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6

FUJITA, Koichi. "Secondary Ion Mass Spectrometry." Journal of the Japan Society of Colour Material 79, no. 2 (2006): 81–85. http://dx.doi.org/10.4011/shikizai1937.79.81.

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7

COOKS, R. GRAHAM, GARY L. GLISH, SCOTT A. MCLUCKEY, and RAYMOND E. KAISER. "Ion Trap Mass Spectrometry." Chemical & Engineering News 69, no. 12 (1991): 26–41. http://dx.doi.org/10.1021/cen-v069n012.p026.

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8

Griffiths, Jennifer. "Secondary Ion Mass Spectrometry." Analytical Chemistry 80, no. 19 (2008): 7194–97. http://dx.doi.org/10.1021/ac801528u.

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9

Williams, Peter. "Secondary Ion Mass Spectrometry." Annual Review of Materials Science 15, no. 1 (1985): 517–48. http://dx.doi.org/10.1146/annurev.ms.15.080185.002505.

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10

Turecek, Frantisek, and Ming Gu. "Survivor ion mass spectrometry." Organic Mass Spectrometry 27, no. 11 (1992): 1335–36. http://dx.doi.org/10.1002/oms.1210271132.

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11

Kanu, Abu B., Prabha Dwivedi, Maggie Tam, Laura Matz, and Herbert H. Hill. "Ion mobility-mass spectrometry." Journal of Mass Spectrometry 43, no. 1 (2008): 1–22. http://dx.doi.org/10.1002/jms.1383.

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12

Zalm, PC. "Secondary ion mass spectrometry." Vacuum 45, no. 6-7 (1994): 753–72. http://dx.doi.org/10.1016/0042-207x(94)90113-9.

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13

March, Raymond E. "Ion trap mass spectrometry." International Journal of Mass Spectrometry and Ion Processes 118-119 (September 1992): 71–135. http://dx.doi.org/10.1016/0168-1176(92)85059-9.

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14

Cooks, R. G., K. A. Cox, and J. D. Williams. "High-performance mass spectrometry with the ion trap mass spectrometer." Journal of Protein Chemistry 11, no. 4 (1992): 376–77. http://dx.doi.org/10.1007/bf01673733.

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15

Braselton, W. Emmett, Regg D. Neiger, and Robert H. Poppenga. "Confirmation of Indandione Rodenticide Toxicoses by Mass Spectrometry/Mass Spectrometry." Journal of Veterinary Diagnostic Investigation 4, no. 4 (1992): 441–46. http://dx.doi.org/10.1177/104063879200400413.

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Mass spectrometry/mass spectrometry (MS/MS) with collision-activated dissociation (CAD) was utilized to unequivocally distinguish 1,3-indandione rodenticides in 2 cases of anticoagulant toxicosis. Anecdotal evidence provided by the veterinarian in a case involving feedlot cows and physical evidence at the site of occurrence in a similar case involving lambs strongly implicated diphenadione (diphacinone; DP) in both instances. However, high performance liquid chromatography indicated chlorophacinone (CP), not DP, was present in the blood samples obtained from both cows and lambs. Intact 1,3-ind

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16

Annesley, Thomas M. "Ion Suppression in Mass Spectrometry." Clinical Chemistry 49, no. 7 (2003): 1041–44. http://dx.doi.org/10.1373/49.7.1041.

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Abstract Background: Mass spectrometry (MS) is being introduced into a large number of clinical laboratories. It provides specificity because of its ability to monitor selected mass ions, sensitivity because of the enhanced signal-to-noise ratio, and speed because it can help avoid the need for intensive sample cleanup and long analysis times. However, MS is not without problems related to interference, especially through ion suppression effects. Ion suppression results from the presence of less volatile compounds that can change the efficiency of droplet formation or droplet evaporation, whic

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17

Collins, D., and M. Lee. "Developments in ion mobility spectrometry–mass spectrometry." Analytical and Bioanalytical Chemistry 372, no. 1 (2001): 66–73. http://dx.doi.org/10.1007/s00216-001-1195-5.

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18

Abdelhameed, Ali S., Adnan A. Kadi, Hatem A. Abdel-Aziz, Rihab F. Angawi, Mohamed W. Attwa, and Khalid A. Al-Rashood. "Multistage Fragmentation of Ion Trap Mass Spectrometry System and Pseudo-MS3of Triple Quadrupole Mass Spectrometry Characterize Certain (E)-3-(Dimethylamino)-1-arylprop-2-en-1-ones: A Comparative Study." Scientific World Journal 2014 (2014): 1–9. http://dx.doi.org/10.1155/2014/702819.

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A new approach was recently introduced to improve the structure elucidation power of tandem mass spectrometry simulating the MS3of ion trap mass spectrometry system overcoming the different drawbacks of the latter. The fact that collision induced dissociation in the triple quadrupole mass spectrometer system provides richer fragment ions compared to those achieved in the ion trap mass spectrometer system utilizing resonance excitation. Moreover, extracting comprehensive spectra in the ion trap needs multistage fragmentation, whereas similar fragment ions may be acquired from one stage product

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19

Kim, S. H., and G. E. Spangler. "Ion Mobility Spectrometry/Mass Spectromentry of Two Structurally Different Ions Having Identical Ion Mass." Analytical Chemistry 57, no. 2 (1985): 567–69. http://dx.doi.org/10.1021/ac50001a056.

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20

Kiss, András, Donald F. Smith, Julia H. Jungmann, and Ron M. A. Heeren. "Cluster secondary ion mass spectrometry microscope mode mass spectrometry imaging." Rapid Communications in Mass Spectrometry 27, no. 24 (2013): 2745–50. http://dx.doi.org/10.1002/rcm.6719.

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21

Sauvage, François-Ludovic, Franck Saint-marcoux, Bénédicte Duretz, Didier Deporte, Gérard Lachatre, and Pierre Marquet. "Screening of Drugs and Toxic Compounds with Liquid Chromatography-Linear Ion Trap Tandem Mass Spectrometry." Clinical Chemistry 52, no. 9 (2006): 1735–42. http://dx.doi.org/10.1373/clinchem.2006.067116.

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Abstract Background: In clinical and forensic toxicology, general unknown screening is used to detect and identify exogenous compounds. In this study, we aimed to develop a comprehensive general unknown screening method based on liquid chromatography coupled with a hybrid triple-quadrupole linear ion trap mass spectrometer. Methods: After solid-phase extraction, separation was performed using gradient reversed-phase chromatography. The mass spectrometer was operated in the information-dependent acquisition mode, switching between a survey scan acquired in the Enhanced Mass Spectrometry mode wi

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22

Grasserbauer, M. "Quantitative secondary ion mass spectrometry." Journal of Research of the National Bureau of Standards 93, no. 3 (1988): 510. http://dx.doi.org/10.6028/jres.093.140.

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23

Cooks, R. Graham, and Raymond E. Kaiser. "Quadrupole ion trap mass spectrometry." Accounts of Chemical Research 23, no. 7 (1990): 213–19. http://dx.doi.org/10.1021/ar00175a002.

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24

Morrison, G. H. "Editorial. Secondary Ion Mass Spectrometry." Analytical Chemistry 58, no. 1 (1986): 1. http://dx.doi.org/10.1021/ac00292a600.

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25

Freeman, Stewart P. H. T., Richard P. Shanks, Xavier Donzel, and Gabriel Gaubert. "Radiocarbon positive-ion mass spectrometry." Nuclear Instruments and Methods in Physics Research Section B: Beam Interactions with Materials and Atoms 361 (October 2015): 229–32. http://dx.doi.org/10.1016/j.nimb.2015.04.034.

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26

Odom, Robert W. "Secondary Ion Mass Spectrometry Imaging." Applied Spectroscopy Reviews 29, no. 1 (1994): 67–116. http://dx.doi.org/10.1080/05704929408000898.

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27

Kudo, Masahiro, and Susumu Nagayama. "Secondary Ion Mass Spectrometry (SIMS)." Zairyo-to-Kankyo 42, no. 5 (1993): 312–21. http://dx.doi.org/10.3323/jcorr1991.42.312.

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28

Kornienko, Oleg, Peter T. A. Reilly, William B. Whitten, and J. Michael Ramsey. "Micro ion trap mass spectrometry." Rapid Communications in Mass Spectrometry 18, no. 6 (2004): 742. http://dx.doi.org/10.1002/rcm.1387.

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29

Kornienko, Oleg, Peter T. A. Reilly, William B. Whitten, and J. Michael Ramsey. "Micro ion trap mass spectrometry." Rapid Communications in Mass Spectrometry 13, no. 1 (1999): 50–53. http://dx.doi.org/10.1002/(sici)1097-0231(19990115)13:1<50::aid-rcm449>3.0.co;2-k.

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30

TSUNOYAMA, Kouzou. "Quantitative Secondary Ion Mass Spectrometry." Hyomen Kagaku 7, no. 3 (1986): 237–42. http://dx.doi.org/10.1380/jsssj.7.237.

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31

Olthoff, James K., and Robert J. Cotter. "Liquid secondary ion mass spectrometry." Nuclear Instruments and Methods in Physics Research Section B: Beam Interactions with Materials and Atoms 26, no. 4 (1987): 566–70. http://dx.doi.org/10.1016/0168-583x(87)90544-1.

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32

Parker, J. E. "Ion Chemistry and Mass Spectrometry." International Journal of Mass Spectrometry and Ion Processes 76, no. 1 (1987): R7—R8. http://dx.doi.org/10.1016/0168-1176(87)85016-4.

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33

Catinella, Silvia, Pietro Traldi, Xuewu Jiang, et al. "Negative-ion mass spectrometry in a commercial gas chromatography/ion-trap mass spectrometer system." Rapid Communications in Mass Spectrometry 9, no. 13 (1995): 1302–9. http://dx.doi.org/10.1002/rcm.1290091316.

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34

Budzikiewicz, H. "Selected reviews on mass spectrometric topics. XLII. Ion trap mass spectrometry." Mass Spectrometry Reviews 11, no. 1 (1992): 69. http://dx.doi.org/10.1002/mas.1280110105.

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35

Cole, Richard B., Stephen Boue, and A. Kamel Harrata. "Implementation of liquid secondary ion mass spectrometry on quadrupole mass spectrometers." Analytica Chimica Acta 267, no. 1 (1992): 121–29. http://dx.doi.org/10.1016/0003-2670(92)85013-v.

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36

Böhme, Diethard K. "Gaseous ions and chemical mass spectrometry." Canadian Journal of Chemistry 86, no. 3 (2008): 177–98. http://dx.doi.org/10.1139/v07-146.

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The intrinsic chemical reactivities of ions can be monitored in the gas phase using mass spectrometers that are coupled to appropriate ion sources and reaction cells. Here the author surveys his own experiences over the past 40 years as an ion chemist. He used flow-tube techniques for room temperature measurements of the intrinsic chemical reactivities of a large variety of positive and negative ions, including bare atomic ions, ions found in solution, biological ions, carbonaceous ions, and interstellar, cometary, and ionospheric ions. Progress in the measurement of chemical reactions of thes

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37

Donnelly, J. R., G. W. Sovocool, and R. K. Mitchum. "Ion Abundance Criteria for Gas Chromatographic/Mass Spectrometric Environmental Analysis." Journal of AOAC INTERNATIONAL 71, no. 2 (1988): 434–39. http://dx.doi.org/10.1093/jaoac/71.2.434.

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Abstract Mass and intensity calibration of gas chromatograph/mass spectrometer (GC/MS) responses is an important quality assurance issue for chemical analysis. Ion abundance calibration with decafluorotriphenylphosphine (DFTPP) was applied in 1975 to standardize quadrupole spectra to resemble the ion abundances that were obtainable from magnetic sector mass spectrometers. Modern &lt;j uadrupole mass spectrometers provide significantly greater high-mass sensitivity than allowed under the 1975 study. Thus, those recommendations were reevaluated with 2 approaches. First, an interlaboratory st

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38

Hirata, K., K. Yamada, A. Chiba, Y. Hirano, and Y. Saitoh. "Secondary ion mass spectrometry using energetic cluster ion beams: Toward highly sensitive imaging mass spectrometry." Nuclear Instruments and Methods in Physics Research Section B: Beam Interactions with Materials and Atoms 479 (September 2020): 240–45. http://dx.doi.org/10.1016/j.nimb.2020.06.027.

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39

Louris, John N., Jennifer S. Brodbelt-Lustig, R. Graham Cooks, Gary L. Glish, Gary J. van Berkel, and Scott A. McLuckey. "Ion isolation and sequential stages of mass spectrometry in a quadrupole ion trap mass spectrometer." International Journal of Mass Spectrometry and Ion Processes 96, no. 2 (1990): 117–37. http://dx.doi.org/10.1016/0168-1176(90)87025-c.

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40

Kissel, Jochen, and Franz R. Krueger. "Time-of-flight mass spectrometric analysis of ion formation in hypervelocity impact of organic polymer microspheres: comparison with secondary ion mass spectrometry,252Cf mass spectrometry and laser mass spectrometry." Rapid Communications in Mass Spectrometry 15, no. 18 (2001): 1713–18. http://dx.doi.org/10.1002/rcm.431.

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41

Botamanenko, Daniel Y., and Martin F. Jarrold. "Ion-Ion Interactions in Charge Detection Mass Spectrometry." Journal of The American Society for Mass Spectrometry 30, no. 12 (2019): 2741–49. http://dx.doi.org/10.1007/s13361-019-02343-y.

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42

Thalassinos, K., S. E. Slade, K. R. Jennings, et al. "Ion mobility mass spectrometry of proteins in a modified commercial mass spectrometer." International Journal of Mass Spectrometry 236, no. 1-3 (2004): 55–63. http://dx.doi.org/10.1016/j.ijms.2004.05.008.

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43

Kaiser, Raymond E., Jon D. Williams, Stephen A. Lammert, R. Graham Cooks, and Don Zakett. "Thermospray liquid chromatography—mass spectrometry with a quadrupole ion trap mass spectrometer." Journal of Chromatography B: Biomedical Sciences and Applications 562, no. 1-2 (1991): 3–11. http://dx.doi.org/10.1016/0378-4347(91)80559-u.

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44

Yurimoto, Hisayoshi, and Shigeho Sueno. "Secondary ion mass spectrometry for insulators." Nihon Kessho Gakkaishi 29, no. 4 (1987): 259–69. http://dx.doi.org/10.5940/jcrsj.29.259.

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45

Katz, W., and J. G. Newman. "Fundamentals of Secondary Ion Mass Spectrometry." MRS Bulletin 12, no. 6 (1987): 40–47. http://dx.doi.org/10.1557/s088376940006721x.

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AbstractThis article presents an overview of our current understanding of the fundamental factors underlying Secondary Ion Mass Spectrometry (SIMS). Included is a discussion of the sputtering process and possible mechanisms which produce ejected ions. Presently available instrumentation for SIMS analysis is discussed and some examples of SIMS analysis are also given.

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46

Futrell, J. H., and M. E. Rose. "Gaseous ion chemistry and mass spectrometry." Analytica Chimica Acta 194 (1987): 334. http://dx.doi.org/10.1016/s0003-2670(00)84797-2.

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47

Benninghoven, A., A. M. Huber, and H. W. Werner. "Secondary ion mass spectrometry (SIMS VI)." Analytica Chimica Acta 215 (1988): 366. http://dx.doi.org/10.1016/s0003-2670(00)85312-x.

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48

Mesa Sanchez, Daniela, Steve Creger, Veerupaksh Singla, Ruwan T. Kurulugama, John Fjeldsted, and Julia Laskin. "Ion Mobility-Mass Spectrometry Imaging Workflow." Journal of the American Society for Mass Spectrometry 31, no. 12 (2020): 2437–42. http://dx.doi.org/10.1021/jasms.0c00142.

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49

Handley, Judith. "Product Review: Secondary Ion Mass Spectrometry." Analytical Chemistry 74, no. 11 (2002): 335 A—341 A. http://dx.doi.org/10.1021/ac022041e.

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50

Yakovlev, B. S., V. L. Talrose, and Catherine Fenselau. "Membrane Ion Source for Mass Spectrometry." Analytical Chemistry 66, no. 10 (1994): 1704–7. http://dx.doi.org/10.1021/ac00082a017.

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