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Artículos de revistas sobre el tema "Field spectrometry"

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Autor: Grafiati

Publicado: 11 de marzo de 2023

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1

Dorozhkin, I. P., Yu V. Baklanova y Ye V. Mustafina. "DEVELOPMENT OF FIELD SPECTROMETRY DATABASE". NNC RK Bulletin, n.º 2 (17 de octubre de 2021): 19–24. http://dx.doi.org/10.52676/1729-7885-2021-2-19-24.

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The paper considers the issues in design and development of databases for storage and processing gamma-spectrometric information. A model is presented that allows one to describe the conceptual schemes for storing and processing data obtained during field gamma-spectrometric surveys in principle and, in particular, on the territory of the Semipalatinsk test site. The possibilities of the database of field spectrometry are described. The interface for interaction between the user and the database management system has been implemented.

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2

Pollard, Matthew J., Christopher K. Hilton, Hongli Li, Kimberly Kaplan, Richard A. Yost y Herbert H. Hill. "Ion mobility spectrometer—field asymmetric ion mobility spectrometer-mass spectrometry". International Journal for Ion Mobility Spectrometry 14, n.º 1 (9 de marzo de 2011): 15–22. http://dx.doi.org/10.1007/s12127-011-0058-9.

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3

DEUTSCH, JOSEPH, CHAIM GILON y MICHAEL CHOREV. "FIELD DESORPTION MASS SPECTROMETRY". International Journal of Peptide and Protein Research 18, n.º 2 (12 de enero de 2009): 203–7. http://dx.doi.org/10.1111/j.1399-3011.1981.tb02058.x.

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4

Renault, Mikael, Yassine Hadjar, Sylvain Blaize, Aurélien Bruyant, Laurent Arnaud, Gilles Lerondel y Pascal Royer. "Bidimensional near-field sampling spectrometry". Optics Letters 35, n.º 19 (30 de septiembre de 2010): 3303. http://dx.doi.org/10.1364/ol.35.003303.

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5

Grimm, Ronald L. y J. L. Beauchamp. "Field-Induced Droplet Ionization Mass Spectrometry". Journal of Physical Chemistry B 107, n.º 51 (diciembre de 2003): 14161–63. http://dx.doi.org/10.1021/jp037099r.

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6

Hawkes, N. P., K. A. A. Gamage y G. C. Taylor. "Digital approaches to field neutron spectrometry". Radiation Measurements 45, n.º 10 (diciembre de 2010): 1305–8. http://dx.doi.org/10.1016/j.radmeas.2010.06.043.

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7

Leisch, M. "Three-dimensional field ion mass spectrometry". Fresenius' Journal of Analytical Chemistry 349, n.º 1-3 (1994): 102–6. http://dx.doi.org/10.1007/bf00323231.

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8

van der Greef, J. "Field desorption mass spectrometry in bioanalysis". TrAC Trends in Analytical Chemistry 5, n.º 9 (enero de 1986): 241–46. http://dx.doi.org/10.1016/0165-9936(86)85062-2.

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9

Behrens, Rolf, Hayo Zutz y Julian Busse. "Spectrometry of pulsed photon radiation". Journal of Radiological Protection 42, n.º 1 (17 de enero de 2022): 011507. http://dx.doi.org/10.1088/1361-6498/ac3dd0.

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Abstract The energy distribution (spectrum) of pulsed photon radiation can hardly be measured using active devices, therefore, a thermoluminescence detector (TLD)-based few-channel spectrometer is used in combination with a Bayesian data analysis to help resolve this problem. The spectrometer consists of 30 TLD layers interspaced by absorbers made of plastics and metals with increasing atomic numbers and thickness. Thus, the main idea behind the device is the deeper the radiation penetrates—the higher the radiation’s energy when the radiation impinges perpendicular to the front of the spectrometer. From the doses measured in the TLD layers and from further prior available information, the photon spectrum is deduced using a Bayesian data analysis leading to absolute spectra and doses including their uncertainties and coverage intervals. This spectrometer was successfully used in two different scenarios, i.e. for the spectrometry of the radiation field two different industrial type open beam pulsed x-ray generators and secondly in three different radiation fields of a medical accelerator.

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10

Purves, Randy W. y Roger Guevremont. "Electrospray Ionization High-Field Asymmetric Waveform Ion Mobility Spectrometry−Mass Spectrometry". Analytical Chemistry 71, n.º 13 (julio de 1999): 2346–57. http://dx.doi.org/10.1021/ac981380y.

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11

Davis, Stephen C., Gregory M. Neumann y Peter J. Derrick. "Field desorption mass spectrometry with suppression of the high field". Analytical Chemistry 59, n.º 9 (mayo de 1987): 1360–62. http://dx.doi.org/10.1021/ac00136a021.

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12

Heleg-Shabtai, Vered, Amalia Zaltsman, Mali Sharon, Hagai Sharabi, Ido Nir, Dana Marder, Guy Cohen, Izhar Ron y Alexander Pevzner. "Explosive vapour/particles detection using SERS substrates and a hand-held Raman detector". RSC Advances 11, n.º 42 (2021): 26029–36. http://dx.doi.org/10.1039/d1ra04637c.

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13

Swearingen, Kristian E. y Robert L. Moritz. "High-field asymmetric waveform ion mobility spectrometry for mass spectrometry-based proteomics". Expert Review of Proteomics 9, n.º 5 (octubre de 2012): 505–17. http://dx.doi.org/10.1586/epr.12.50.

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14

Blazso, Marianne, Emma Jakab, Tamas Szekely, Bernd Plage y Hans-rolf Schulten. "Pyrolysis–gas chromatography mass spectrometry and field ionization mass spectrometry of polyquinones". Journal of Polymer Science Part A: Polymer Chemistry 27, n.º 3 (febrero de 1989): 1027–43. http://dx.doi.org/10.1002/pola.1989.080270325.

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15

Kudo, K., N. Takeda, S. Koshikawa, H. Toyokawa, H. Ohgaki y M. Matzke. "Photon spectrometry in thermal neutron standard field". Nuclear Instruments and Methods in Physics Research Section A: Accelerators, Spectrometers, Detectors and Associated Equipment 476, n.º 1-2 (enero de 2002): 213–17. http://dx.doi.org/10.1016/s0168-9002(01)01434-6.

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16

Hayashi, H., H. Iwai y F. Okuyama. "FIELD IONIZATION MASS SPECTROMETRY OF ORGANIC PLASMAS". Le Journal de Physique Colloques 48, n.º C6 (noviembre de 1987): C6–247—C6–251. http://dx.doi.org/10.1051/jphyscol:1987640.

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17

Chen, Xingshuo y R. Graham Cooks. "Accelerated reactions in field desorption mass spectrometry". Journal of Mass Spectrometry 53, n.º 10 (16 de agosto de 2018): 942–46. http://dx.doi.org/10.1002/jms.4254.

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18

Lattimer, Robert P. "Pyrolysis field ionization mass spectrometry of polyolefins". Journal of Analytical and Applied Pyrolysis 31 (febrero de 1995): 203–25. http://dx.doi.org/10.1016/0165-2370(94)00824-k.

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19

Lattimer, Robert P. y Harts-Rolf Schulten. "FIELD IONIZATION AND FIELD DESORPTION MASS SPECTROMETRY: PAST, PRESENT, AND FUTURE". Analytical Chemistry 61, n.º 21 (noviembre de 1989): 1201A—1215A. http://dx.doi.org/10.1021/ac00196a721.

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20

Sparkman, O. David. "The 12th Sanibel Conference on Mass Spectrometry: Field-Portable and Miniature Mass Spectrometry". Journal of the American Society for Mass Spectrometry 11, n.º 5 (mayo de 2000): 468–71. http://dx.doi.org/10.1016/s1044-0305(00)00118-5.

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21

GUEVREMONT, R. "High-field asymmetric waveform ion mobility spectrometry: A new tool for mass spectrometry". Journal of Chromatography A 1058, n.º 1-2 (26 de noviembre de 2004): 3–19. http://dx.doi.org/10.1016/s0021-9673(04)01478-5.

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22

Kolakowski, Beata M., Margaret A. McCooeye y Zoltan Mester. "Compensation voltage shifting in high-field asymmetric waveform ion mobility spectrometry-mass spectrometry". Rapid Communications in Mass Spectrometry 20, n.º 22 (2006): 3319–29. http://dx.doi.org/10.1002/rcm.2739.

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23

Manard, Manuel J., Rusty Trainham, Stephan Weeks, Stephen L. Coy, Evgeny V. Krylov y Erkinjon G. Nazarov. "Differential mobility spectrometry/mass spectrometry: The design of a new mass spectrometer for real-time chemical analysis in the field". International Journal of Mass Spectrometry 295, n.º 3 (agosto de 2010): 138–44. http://dx.doi.org/10.1016/j.ijms.2010.03.011.

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24

Povinec, P., M. Betti, A. Jull y P. Vojtyla. "New isotope technologies in environmental physics". Acta Physica Slovaca. Reviews and Tutorials 58, n.º 1 (1 de febrero de 2008): 1–154. http://dx.doi.org/10.2478/v10155-010-0088-6.

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New isotope technologies in environmental physicsAs the levels of radionuclides observed at present in the environment are very low, high sensitive analytical systems are required for carrying out environmental investigations. We review recent progress which has been done in low-level counting techniques in both radiometrics and mass spectrometry sectors, with emphasis on underground laboratories, Monte Carlo (GEANT) simulation of background of HPGe detectors operating in various configurations, secondary ionisation mass spectrometry, and accelerator mass spectrometry. Applications of radiometrics and mass spectrometry techniques in radioecology and climate change studies are presented and discussed as well. The review should help readers in better orientation on recent developments in the field of low-level counting and spectrometry, and to advice on construction principles of underground laboratories, as well as on criteria how to choose low or high energy mass spectrometers for environmental investigations.

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25

Titarenko, Olga. "Hydrocarbon deposit mapping validation by the means of ground-based spectrometry, remote sensing and geophysical data". Ukrainian journal of remote sensing, n.º 21 (15 de julio de 2019): 23–28. http://dx.doi.org/10.36023/ujrs.2019.21.151.

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The probability estimation of oil and gas inside certain area is essential for decision making on the industrial exploitation of oil and gas bearing features. A quantitative assessment of the hydrocarbon contour mapping accuracy using ground-based spectrometric measurements, remote, geological and geophysical data requires a special validation procedure. Its purpose is to evaluate achieved accuracy and reliability as well as the conformance to specified requirements. The input data for validation of the hydrocarbon deposit contour by field spectrometry are the one points’ locations relative to the other contours detected by independent methods, such as remote, geological and geophysical. As the field spectrometry performed along spatial trace, the geometric drifts of other methods’ cross-points are estimated. The algorithm for the validation of hydrocarbon deposit contour mapping by field spectrometry, remote, geological and geophysical data is proposed in this paper. The algorithm was tested on over the Novotroitsky and East Rogintsy hydrocarbon deposits (Ukraine). Measurements along 14 spatial traces over the Novotroitsky’s deposit and 28 traces over the East Rogintsy’s one was carried out to perform validation. The average error probability was 0.28, which demonstrates an admissible reliability of hydrocarbon deposits contours’ mapping by field spectrometry data. The preliminary validation estimates engagement during the hydrocarbon deposits mapping provides the fact-based statistical consistency of the quantitative measurements received. In addition, it is possible to filter the outliers reasonable before final information product release, which will enhance the overall reliability.

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26

Gunzer, Frank. "Evaluation of calculated negative mode ion mobilities of small molecules in air". European Journal of Mass Spectrometry 23, n.º 6 (31 de agosto de 2017): 369–75. http://dx.doi.org/10.1177/1469066717729299.

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Ion mobility spectrometry is a well-known technique employed for the detection and analysis of gaseous substances. In pharmaceutical applications, it is furthermore used for structural analysis of compounds, especially in combination with mass spectrometry. In this field, the comparison of calculated collision cross sections and ion mobilities of theoretic model compounds with experimental values measured with ion mobility spectrometers helps to determine the compound’s structure. For positive mode ion mobility spectrometry, the calculated mobilities using the Trajectory Method show in general a deviation of 10% or less from experimental values. In this article, it was analyzed how well the calculated values reproduce the experimental values obtained with negative mode ion mobility spectrometry including symmetric and asymmetric analyte clusters. Furthermore, the influence of four different partial charge models on the results was investigated.

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27

Schulten, Hans-Rolf, Bernd Plage y Robert P. Lattimer. "Pyrolysis-Field Ionization Mass Spectrometry of Rubber Vulcanizates". Rubber Chemistry and Technology 62, n.º 4 (1 de septiembre de 1989): 698–708. http://dx.doi.org/10.5254/1.3536269.

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Abstract Time-/temperature-resolved Py-FIMS allows for the identification of rubber components in compounds containing normal organic additives. Signals due to polymer pyrolyzates, which may be masked by processing oil in nontemperature resolved spectra, are easily obtained. Py-FI spectra from cured BR and NR differ from the corresponding uncured samples in that signals from sulfur-containing oligomers are observed. For SBR, the signals from sulfur-containing pyrolyzates were not distinguishable in the complex mixture of hydrocarbon fragments that was produced. Therefore, unambiguous distinction between cured and uncured SBR was difficult. Since Py-FI mass spectra for rubber blends appear similar to the sum of the corresponding single component spectra, secondary reactions of chain fragments from the two blend components are minimal. These results are consistent with Curie-point Py-MS studies which also showed little interaction between components in blends. Since the Py-FI mass spectrum of the styrene-butadiene block copolymer is similar to the sum of single component spectra, it is obvious that styrene-butadiene sequences are not very abundant. In contrast, mixed oligomers containing both styrene and butadiene units are found for SBR copolymers. The absence of styrene dimer and trimer, as well as high-mass oligomers of butadiene, indicates that the amount of block styrene is very low. Furthermore, the large numbers of mixed oligomers indicates a random sequence distribution. In summary, Py-FIMS is a very effective technique for direct rubber compound analysis. The sample can be examined directly, without pretreatment, and both organic additives and the rubber components can be identified in the same experiment. With programmed heating of the rubber, one can obtain separate (time-/temperature-resolved) FI mass spectra for the organic additives and the rubber pyrolyzates. The results are interesting in that much higher mass oligomers can be observed by Py-FIMS than are detected by other methods of Py-MS. For example, while the low voltage Py-EIMS typically shows no higher oligomers than trimer or tetramer for diene rubbers, Py-FIMS shows sequences containing perhaps 15–20 monomer units. This improved performance is due mainly to (a) the close proximity of the pyrolysis chamber to the field emitter (which minimizes secondary reactions) and (b) the very soft ionization provided by the FI technique. In favorable cases, Py-FIMS can be used to study long sequences in homopolymers, copolymers, and blends. As we have noted, pendent groups (e.g., mercaptobenzothiazyl) and crosslinks may be detected among the pyrolysis products. While some rubbers (e.g., polyisoprene) thermally degrade to give high abundances of oligomers, others degrade in a more random fashion (e.g., SBR) to give very complex mixtures of pyrolyzates. Polystyrene is an interesting case in which thermal degradation by retropolymerization (unzipping) is so prevalent that the monomer is by far the dominant pyrolyzate, and long oligomeric sequences are precluded. Thus, while Py-FIMS can easily be used for qualitative identification of rubber components, more detailed information may or may not be discernible in analysis of a particular rubber sample.

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28

Jia, Kun, Bingfang Wu, Yichen Tian, Qiangzi Li y Xin Du. "Spectral Discrimination of Opium Poppy Using Field Spectrometry". IEEE Transactions on Geoscience and Remote Sensing 49, n.º 9 (septiembre de 2011): 3414–22. http://dx.doi.org/10.1109/tgrs.2011.2126582.

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29

Yang, Zhang, van der Meer y Kroonenberg. "Geochemistry and field spectrometry for detecting hydrocarbon microseepage". Terra Nova 10, n.º 5 (septiembre de 1998): 231–35. http://dx.doi.org/10.1046/j.1365-3121.1998.00196.x.

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30

Jardine, Daniel R., Susan Nekula, N. Than-Trong, Paul R. Haddad, Peter J. Derrick, Eva Grespos y James H. O'Donnell. "Field desorption mass spectrometry of poly(olefin sulfones)". Macromolecules 19, n.º 6 (noviembre de 1986): 1770–72. http://dx.doi.org/10.1021/ma00160a050.

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31

Plage, Bernd y Hans Rolf Schulten. "Pyrolysis-field ionization mass spectrometry of epoxy resins". Macromolecules 21, n.º 7 (julio de 1988): 2018–27. http://dx.doi.org/10.1021/ma00185a023.

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32

Alevra, A. V., H. Klein, K. Knauf y J. Wittstock. "Neutron Field Spectrometry for Radiation Protection Dosimetry Purposes". Radiation Protection Dosimetry 44, n.º 1-4 (1 de noviembre de 1992): 223–26. http://dx.doi.org/10.1093/oxfordjournals.rpd.a081436.

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33

Alevra, A. V., H. Klein, K. Knauf y J. Wittstock. "Neutron Field Spectrometry for Radiation Protection Dosimetry Purposes". Radiation Protection Dosimetry 44, n.º 1-4 (1 de noviembre de 1992): 223–26. http://dx.doi.org/10.1093/rpd/44.1-4.223.

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34

Lattimer, Robert P. "Pyrolysis field ionization mass spectrometry of hydrocarbon polymers". Journal of Analytical and Applied Pyrolysis 39, n.º 2 (febrero de 1997): 115–27. http://dx.doi.org/10.1016/s0165-2370(96)00966-7.

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35

Aznar, J. C., H. Paucar-Munoz, M. Richer-Laflèche y Y. Bégin. "Field litter thickness assessed by gamma-ray spectrometry". Forest Ecology and Management 260, n.º 10 (octubre de 2010): 1640–45. http://dx.doi.org/10.1016/j.foreco.2010.07.022.

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36

Zaia, Joseph. "Mass Spectrometry and the Emerging Field of Glycomics". Chemistry & Biology 15, n.º 9 (septiembre de 2008): 881–92. http://dx.doi.org/10.1016/j.chembiol.2008.07.016.

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37

Baykut, Gökhan y Jochen Franzen. "Mobile mass spectrometry; a decade of field applications". TrAC Trends in Analytical Chemistry 13, n.º 7 (agosto de 1994): 267–75. http://dx.doi.org/10.1016/0165-9936(94)87063-2.

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38

Makas, Alexei L. y Mikhail L. Troshkov. "Field gas chromatography–mass spectrometry for fast analysis". Journal of Chromatography B 800, n.º 1-2 (febrero de 2004): 55–61. http://dx.doi.org/10.1016/j.jchromb.2003.08.054.

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39

Nyadong, Leonard, Jinfeng Lai, Carol Thompsen, Chris J. LaFrancois, Xinheng Cai, Chunxia Song, Jieming Wang y Wei Wang. "High-Field Orbitrap Mass Spectrometry and Tandem Mass Spectrometry for Molecular Characterization of Asphaltenes". Energy & Fuels 32, n.º 1 (22 de diciembre de 2017): 294–305. http://dx.doi.org/10.1021/acs.energyfuels.7b03177.

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40

Ivanov, Yu D., T. O. Pleshakova, K. A. Malsagova, A. L. Kaysheva, A. T. Kopylov, A. A. Izotov, V. Yu Tatur et al. "AFM fishing of proteins under impulse electric field". Biomeditsinskaya Khimiya 62, n.º 4 (2016): 439–46. http://dx.doi.org/10.18097/pbmc20166204439.

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A combination of (atomic force microscopy)-based fishing (AFM-fishing) and mass spectrometry allows to capture protein molecules from solutions, concentrate and visualize them on an atomically flat surface of the AFM chip and identify by subsequent mass spectrometric analysis. In order to increase the AFM-fishing efficiency we have applied pulsed voltage with the rise time of the front of about 1 ns to the AFM chip. The AFM-chip was made using a conductive material, highly oriented pyrolytic graphite (HOPG). The increased efficiency of AFM-fishing has been demonstrated using detection of cytochrome b5 protein. Selection of the stimulating pulse with a rise time of 1 ns, corresponding to the GHz frequency range, by the effect of intrinsic emission from water observed in this frequency range during water injection into the cell.

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41

Karabagias, Ioannis K. "Advances of Spectrometric Techniques in Food Analysis and Food Authentication Implemented with Chemometrics". Foods 9, n.º 11 (27 de octubre de 2020): 1550. http://dx.doi.org/10.3390/foods9111550.

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Given the continuous consumer demand for products of high quality and specific origin, there is a great tendency for the application of multiple instrumental techniques for the complete characterization of foodstuffs or related natural products. Spectrometric techniques usually offer a full and rapid screenshot of products’ composition and properties by the determination of specific bio-molecules such as sugars, minerals, polyphenols, volatile compounds, amino acids, organic acids, etc. The present special issue aimed firstly to enhance the advances of the application of spectrometric techniques such as gas chromatography coupled to mass spectrometry (GC-MS), inductively coupled plasma optical emission spectrometry (ICP-OES), isotope ratio mass spectrometry (IRMS), nuclear magnetic resonance (NMR), Raman spectroscopy, or any other spectrometric technique, in the analysis of foodstuffs such as meat, milk, cheese, potatoes, vegetables, fruits/fruit juices, honey, olive oil, chocolate, and other natural products. An additional goal was to fill the gap between food composition/food properties/natural products properties and food/natural products authenticity, using supervised and non-supervised chemometrics. Of the 18 submitted articles, nine were eventually published, providing new information to the field.

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42

Chen, Chiing Chang, Yu Rou Jiang y Ken Hao Chang. "The Hydrothermal Synthesis of β-ZnMoO₄ for UV or Visible-Light-Responsive Photocatalytic Dedradation of Victoria Blue R". Advanced Materials Research 557-559 (julio de 2012): 761–66. http://dx.doi.org/10.4028/www.scientific.net/amr.557-559.761.

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In this study, hydrothermal reaction with Na2MoO4 and Zn(NO3)2as a precursor were investigated for the synthesis of β-ZnMoO4. The β-ZnMoO4were characterized by the X-ray diffractometer (XRD), electron microscopy with the field emission scanning electron microscopy with energy dispersive X-ray spectrometer (FE-SEM-EDS), high resolution X-ray photoelectron spectrometry (HR-XPS), UV-vis diffuse reflectance spectrometry (UV-DRS), and Fourier transform infrared spectrometry (FT-IR). Diffuse UV-vis spectra show the β-ZnMoO4materials to be indirect semiconductors with an optical bandgap of 2.48-2.64 eV. The photocatalytic efficiencies of powder suspensions were evaluated by measuring the Victoria Blue R (VBR) concentration. This is the first reveal that excellent activities of β-ZnMoO4are a promising visible-light-responsive photocatalyst.

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43

Kosevich, Marina V. y Vadim S. Shelkovsky. "A new type of graphite emitter for field ionization/field desorption mass spectrometry". Rapid Communications in Mass Spectrometry 7, n.º 9 (septiembre de 1993): 805–11. http://dx.doi.org/10.1002/rcm.1290070905.

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44

Lapolla, Annunziata, Simona Porcu y Pietro Traldi. "Mass Spectrometry for Diabetic Nephropathy Monitoring: New Effective Tools for Physicians". ISRN Endocrinology 2012 (20 de mayo de 2012): 1–13. http://dx.doi.org/10.5402/2012/768159.

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The main aim of diabetic nephropathy monitoring is to identify molecular markers, that is, to find changes occurring at metabolome and proteome levels indicative of the disease’s development. The mass spectrometry methods available today have been successfully applied to this field. This paper provides a short description of the basic aspects of the mass spectrometric methods used for diabetic nephropathy monitoring, reporting and discussing the results obtained using different approaches.

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45

Geladi, Paul y Eigil Dåbakk. "An Overview of Chemometrics Applications in near Infrared Spectrometry". Journal of Near Infrared Spectroscopy 3, n.º 3 (junio de 1995): 119–32. http://dx.doi.org/10.1255/jnirs.63.

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Near infrared (NIR) spectrometry has found wide use in academic applications, forensic research and in industry. While the use of NIR has been extended to new fields, there have also been enormous developments in the field of multivariate calibration. Some of these developments were due to demands in NIR applications while others came from related spectral techniques. In this paper some trends and developments in multivariate calibration and the use of NIR spectrometry are presented and commented upon. A complete overview would be quite impossible, but an attempt is made to present a good selection of what is going on in the field, with appropriate comments.

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46

Shvartsburg, Alexandre A., Tadeusz Bryskiewicz, Randy W. Purves, Keqi Tang, Roger Guevremont y Richard D. Smith. "Field Asymmetric Waveform Ion Mobility Spectrometry Studies of Proteins: Dipole Alignment in Ion Mobility Spectrometry?" Journal of Physical Chemistry B 110, n.º 43 (noviembre de 2006): 21966–80. http://dx.doi.org/10.1021/jp062573p.

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47

Purves, Randy W., David A. Barnett y Roger Guevremont. "Separation of protein conformers using electrospray-high field asymmetric waveform ion mobility spectrometry-mass spectrometry". International Journal of Mass Spectrometry 197, n.º 1-3 (febrero de 2000): 163–77. http://dx.doi.org/10.1016/s1387-3806(99)00240-7.

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48

Meng, Fan, Zefang Liu, Pengfei Wu, Weiwei Feng y Jiangong Cui. "Design Study of Broadband and Ultrahigh-Resolution Imaging Spectrometer Using Snapshot Multimode Interference in Fiber Bundles". Photonics 9, n.º 5 (11 de mayo de 2022): 334. http://dx.doi.org/10.3390/photonics9050334.

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Imaging spectrometry plays a significant role in various scientific realms. Although imaging spectrometers based on different schemes have been proposed, the pursuit of compact and high-performance devices is still ongoing. A compact broadband and ultrahigh-resolution imaging spectrometer (CBURIS) is presented, which comprises a microlens array, multiple fiber bundles, a microscope, and a two-dimensional detector array. The principle of the device is to spatially sample and integrate the field information via the front microlens array and then further process with the fiber bundles and imaging system based on the multimode interference theory. From both the theoretical and numerical analysis, this CBURIS design is a superior concept that not only achieves a 0.17° spatial resolution and ultrahigh spectral resolution (resolving power exceeds 2.58 × 106 at 1.55 µm) from the visible to mid-infrared region but also has the advantages of snapshot measurement, thermal stability, and a compact footprint compared with most existing imaging spectrometers.

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KUMOOKA, Yoshio. "Analysis of Tackifier Resin by Field Desorption Mass Spectrometry". BUNSEKI KAGAKU 60, n.º 3 (2011): 293–300. http://dx.doi.org/10.2116/bunsekikagaku.60.293.

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Cui, Qi, Jongchan Park, R. Theodore Smith y Liang Gao. "Snapshot hyperspectral light field imaging using image mapping spectrometry". Optics Letters 45, n.º 3 (31 de enero de 2020): 772. http://dx.doi.org/10.1364/ol.382088.

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