Journal articles on the topic 'Nuclear activation analysis'

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1

Heydorn, K. "Recent Developments in Nuclear Activation Analysis." Isotopenpraxis Isotopes in Environmental and Health Studies 24, no. 2 (January 1988): 45–48. http://dx.doi.org/10.1080/10256018808623895.

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2

Bujdosó, E. "Analysis by nuclear reactions and activation." Journal of Radioanalytical and Nuclear Chemistry 223, no. 1-2 (September 1997): 251–61. http://dx.doi.org/10.1007/bf02223397.

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3

Bujdosó, B. "Analysis by nuclear reactions and activation." Journal of Radioanalytical and Nuclear Chemistry Articles 178, no. 1 (February 1994): 207–36. http://dx.doi.org/10.1007/bf02068672.

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4

Bujdosó, E. "Analysis by nuclear reactions and activation." Journal of Radioanalytical and Nuclear Chemistry Articles 89, no. 1 (March 1985): 289–304. http://dx.doi.org/10.1007/bf02070218.

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5

Bujdosó, E. "Analysis by nuclear reactions and activation." Journal of Radioanalytical and Nuclear Chemistry Articles 102, no. 2 (December 1986): 551–78. http://dx.doi.org/10.1007/bf02047929.

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6

Bujdosó, E. "Analysis by nuclear reactions and activation." Journal of Radioanalytical and Nuclear Chemistry Articles 131, no. 1 (May 1989): 235–52. http://dx.doi.org/10.1007/bf02046626.

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7

Bujdosó, E. "Analysis by nuclear reactions and activation." Journal of Radioanalytical and Nuclear Chemistry 231, no. 1-2 (May 1998): 207–15. http://dx.doi.org/10.1007/bf02388036.

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8

Bujdosó, E. "Analysis by nuclear reactions and activation." Journal of Radioanalytical and Nuclear Chemistry 220, no. 2 (June 1997): 275–85. http://dx.doi.org/10.1007/bf02034873.

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9

Bujdosó, E. "Analysis by nuclear reactions and activation." Journal of Radioanalytical and Nuclear Chemistry Articles 116, no. 2 (December 1987): 471–88. http://dx.doi.org/10.1007/bf02035790.

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10

Bujdosó, E. "Analysis by nuclear reactions and activation." Journal of Radioanalytical and Nuclear Chemistry Articles 141, no. 2 (August 1990): 443–53. http://dx.doi.org/10.1007/bf02035811.

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11

Bujdosó, E. "Analysis by nuclear reactions and activation." Journal of Radioanalytical and Nuclear Chemistry Articles 196, no. 1 (September 1995): 179–206. http://dx.doi.org/10.1007/bf02036303.

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12

Bujdosó, E. "Analysis by nuclear reactions and activation." Journal of Radioanalytical and Nuclear Chemistry Articles 120, no. 2 (February 1988): 423–36. http://dx.doi.org/10.1007/bf02037358.

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13

Bujdosó, E. "Analysis by nuclear reactions and activation." Journal of Radioanalytical and Nuclear Chemistry Articles 129, no. 1 (January 1989): 207–25. http://dx.doi.org/10.1007/bf02037584.

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14

Bujdoso, E. "Analysis by nuclear reactions and activation." Journal of Radioanalytical and Nuclear Chemistry Articles 122, no. 2 (June 1988): 373–402. http://dx.doi.org/10.1007/bf02037785.

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15

Bujdosó, E. "Analysis by nuclear reactions and activation." Journal of Radioanalytical and Nuclear Chemistry Articles 89, no. 2 (April 1985): 609–38. http://dx.doi.org/10.1007/bf02040622.

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16

Bujdosó, E. "Analysis by nuclear reactions and activation." Journal of Radioanalytical and Nuclear Chemistry Articles 152, no. 1 (November 1991): 299–320. http://dx.doi.org/10.1007/bf02042162.

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17

Bujdosó, E. "Analysis by nuclear reactions and activation." Journal of Radioanalytical and Nuclear Chemistry Articles 203, no. 1 (February 1996): 199–227. http://dx.doi.org/10.1007/bf02060395.

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18

Bujdosó, E. "Analysis by nuclear reactions and activation." Journal of Radioanalytical and Nuclear Chemistry Articles 139, no. 1 (March 1990): 177–202. http://dx.doi.org/10.1007/bf02060466.

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19

Bujdosó, E. "Analysis by nuclear reactions and activation." Journal of Radioanalytical and Nuclear Chemistry Articles 133, no. 2 (October 1989): 421–38. http://dx.doi.org/10.1007/bf02060514.

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20

Bujdosó, E. "Analysis by nuclear reactions and activation." Journal of Radioanalytical and Nuclear Chemistry Articles 99, no. 1 (May 1986): 231–56. http://dx.doi.org/10.1007/bf02060843.

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21

Bujdosó, E. "Analysis by nuclear reactions and activation." Journal of Radioanalytical and Nuclear Chemistry Articles 132, no. 1 (July 1989): 189–207. http://dx.doi.org/10.1007/bf02060991.

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22

Bujdosó, E. "Analysis by nuclear reactions and activation." Journal of Radioanalytical and Nuclear Chemistry Articles 209, no. 1 (September 1996): 249–67. http://dx.doi.org/10.1007/bf02063550.

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23

Guinn, Vincent P. "A short history of nuclear activation analysis." Biological Trace Element Research 26-27, no. 1 (July 1990): 1–7. http://dx.doi.org/10.1007/bf02992652.

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24

Chibani, H., J. P. Stoquert, M. Hage-Ali, J. M. Koebel, M. Abdesselam, and P. Siffert. "Carbon analysis in CdTe by nuclear activation." Applied Surface Science 50, no. 1-4 (June 1991): 177–80. http://dx.doi.org/10.1016/0169-4332(91)90160-l.

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25

Rakovič, M., and N. Pilecká. "Nuclear interactions used in in vivo activation analysis." Journal of Radioanalytical and Nuclear Chemistry Articles 129, no. 1 (January 1989): 201–6. http://dx.doi.org/10.1007/bf02037583.

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26

Ivanova, E. A., and G. Ch Vafina. "Analysis of cell nuclear supramolecular structures during chromatin activation." Doklady Biological Sciences 406, no. 1-6 (January 2006): 73–75. http://dx.doi.org/10.1134/s0012496606010200.

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27

Bujdosó, E. "Analysis by nuclear reactions and activation a current bibliography." Journal of Radioanalytical and Nuclear Chemistry 242, no. 2 (November 1999): 577–85. http://dx.doi.org/10.1007/bf02345597.

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28

Bujdosó, E. "Analysis by nuclear reactions and activation A current bibliography." Journal of Radioanalytical and Nuclear Chemistry 240, no. 2 (May 1999): 693–704. http://dx.doi.org/10.1007/bf02349439.

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29

Trkov, Andrej, and Vladimir Radulović. "Nuclear reactions and physical models for neutron activation analysis." Journal of Radioanalytical and Nuclear Chemistry 304, no. 2 (January 14, 2015): 763–78. http://dx.doi.org/10.1007/s10967-014-3892-5.

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30

Bujdosó, E. "Analysis by nuclear reactions and activation a current bibliography." Journal of Radioanalytical and Nuclear Chemistry Articles 189, no. 2 (January 1995): 349–65. http://dx.doi.org/10.1007/bf02042615.

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31

Bujdosó, E. "Analysis by nuclear reactions and activation a current bibliography." Journal of Radioanalytical and Nuclear Chemistry Articles 149, no. 1 (May 1991): 183–99. http://dx.doi.org/10.1007/bf02053727.

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32

Bujdosó, E. "Analysis by nuclear reactions and activation a current bibliography." Journal of Radioanalytical and Nuclear Chemistry Articles 97, no. 1 (January 1986): 211–36. http://dx.doi.org/10.1007/bf02060421.

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33

Shaw, Denis. "Prompt gamma neutron activation analysis." Journal of Neutron Research 7, no. 3 (July 1, 1999): 181–94. http://dx.doi.org/10.1080/10238169908200115.

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34

Ho, Manh Dung, and Lathdavong Phonesavanh. "A review of nuclear data for the k₀-based neutron activation analysis." Nuclear Science and Technology 9, no. 1 (March 15, 2019): 28–33. http://dx.doi.org/10.53747/jnst.v9i1.57.

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Nuclear data for the k0-based neutron activation analysis (k0-NAA) including: k0-factors – combination of nuclear constants (atomic mass, isotopic abundance, gamma-ray yield and thermal neutron capture cross section); Q0 – the ratio of the resonance integral to thermal neutron capture cross section; and Er – effective resonance energy, along with the related nuclear data are presented and evaluated in the presentation. Accuracy and capability of k0-NAA depends considerably on the reliability of the above mentioned nuclear data. In general, the evaluation of nuclear data is essential and necessary in the field of nuclear science and technology, and this work is conducted by the nuclear data centers on the world as well as the research institutions where the nuclear data are usedfor R&D. Therefore, the evaluation of the nuclear data used in k0-NAA should also be performed so that some of data may no longer be appropriate should be redetermined. The evaluation of nuclear data in k0-NAA would contribute to the improvement of accuracy and reliability of the method, moreover, it would also contribute to the establishment a nuclear database in Vietnam in the future.
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35

Westphal, G. P., F. Grass, H. Lemmel, J. Sterba, P. Schröder, and Ch Bloch. "Automatic activation analysis." Journal of Radioanalytical and Nuclear Chemistry 271, no. 1 (January 2007): 145–50. http://dx.doi.org/10.1007/s10967-007-0120-6.

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36

Filistovich, V. J., T. N. Nedveckaite, and B. J. Styra. "Activation analysis of129I." Journal of Radioanalytical and Nuclear Chemistry Articles 97, no. 1 (January 1986): 123–30. http://dx.doi.org/10.1007/bf02060418.

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37

Papadopoulos, N. N., and K. M. Ochsenkühn. "Advanced Nuclear Physical Analytical Techniques." HNPS Proceedings 7 (December 5, 2019): 88. http://dx.doi.org/10.12681/hnps.2401.

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Among the modern analytical methods, the nuclear analytical techniques, and especially neutron activation analysis, pay an important role in accurate and sensitive analysis. The capabilities of this technique and its application range have broadened lately with the development and employment of a combination of special more or less novel sub-techniques. These techniques are (a) bss-free counting gamma-ray spectrometry, (b) radioactive decay compensation and (c) repeated activation and measurement. The first technique permits short-time measurements at high count rates in multielement activation analysis with a wide nuclide concentration and half-life range, while by the other two techniques the counting statistics can be improved considerably especially in short-lived nuclide analysis. Thus, because of the high throughput rate, more customers can be served even far from the reactor site by mailing the samples and getting the analytical results back.
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38

HALDEN, NORMAN M., and FRANK C. HAWTHORNE. "PROTON ACTIVATION ANALYSIS (PAA): A COMPLEMENT TO PIXE AND PIGE ANALYSIS." International Journal of PIXE 03, no. 01 (January 1993): 73–79. http://dx.doi.org/10.1142/s0129083593000069.

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At E p =40 MeV , protons have sufficient energy to overcome the coulomb barrier of most elements. The resultant interaction between protons and nucleii of many can produce radioactive isotopes via nuclear reactions. The decay schemes of isotopes created in this manner may include the emission X-rays and gamma-rays that can provide useful analytical information.
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39

Ryan, Christopher M., Craig M. Marianno, William S. Charlton, and William D. James. "Neutron activation analysis of concrete for cross-border nuclear security." Journal of Radioanalytical and Nuclear Chemistry 291, no. 1 (June 19, 2011): 267–72. http://dx.doi.org/10.1007/s10967-011-1272-y.

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40

Nicolaou, G. E., N. M. Spyrou, and Y. S. Khrbish. "The importance of the geometrical factor in nuclear activation analysis." Journal of Radioanalytical and Nuclear Chemistry Articles 114, no. 1 (August 1987): 195–202. http://dx.doi.org/10.1007/bf02048891.

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41

Grdeń, M. "Non-classical applications of chemical analysis based on nuclear activation." Journal of Radioanalytical and Nuclear Chemistry 323, no. 2 (December 5, 2019): 677–714. http://dx.doi.org/10.1007/s10967-019-06977-w.

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42

Žohar, Andrej, Igor Lengar, and Luka Snoj. "Analysis of water activation in fusion and fission nuclear facilities." Fusion Engineering and Design 160 (November 2020): 111828. http://dx.doi.org/10.1016/j.fusengdes.2020.111828.

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43

Lyon, W. S. "Current status of neutron activation analysis and aplied nuclear chemistry." Journal of Radioanalytical and Nuclear Chemistry Articles 140, no. 1 (May 1990): 205–14. http://dx.doi.org/10.1007/bf02037378.

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44

Lubis, Ali Arman. "Instrumental Neutron Activation Analysis (INAA) of Cisadane Estuarine Sediments." Jurnal Natur Indonesia 10, no. 1 (May 4, 2018): 58. http://dx.doi.org/10.31258/jnat.10.1.58-65.

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Nuclear analytical technique instrumental neutron activation analysis was employed for the multielemental analysis of sediments collected from Cisadane estuary. This analytical technique provides concentration of 20 elementswhich consist of heavy metals and rare earth elements simultaneously. Two sediments cores were collected using core sampler for determining the distribution of all elements in the depth profiles of sediments. Sediment cores were subdivided into 2 cm increment, dried and sent to reactor for irradiation using thermal flux of ?1013 neutrons.cm-2.s-1 for 20 minutes in Research Reactor Siwabessy, National Nuclear Energy Agency (BATAN), Serpong. Irradiated samples were measured using a multichannel analyzer (MCA) gamma spectrometer coupled with high purity germanium detector. Analysis of particle size was done since uptake of heavy metals by sediments is particle-size dependent. The results are presented and discussed.
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45

Thompson, Diana, Susan J. Parry, and R. Benzing. "Evaluation of nuclear effects in the analysis of plastics by neutron activation analysis." Journal of Radioanalytical and Nuclear Chemistry Letters 187, no. 4 (June 1994): 255–63. http://dx.doi.org/10.1007/bf02166553.

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46

Prasad, Shikha, Natallia Pinchuk, Stephen E. Anderson, and Ronald F. Fleming. "Geometry independent indium activation analysis." Nuclear Instruments and Methods in Physics Research Section A: Accelerators, Spectrometers, Detectors and Associated Equipment 624, no. 1 (December 2010): 180–83. http://dx.doi.org/10.1016/j.nima.2010.08.001.

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47

Andrianopoulos, A., and M. J. Hynes. "Sequence and functional analysis of the positively acting regulatory gene amdR from Aspergillus nidulans." Molecular and Cellular Biology 10, no. 6 (June 1990): 3194–203. http://dx.doi.org/10.1128/mcb.10.6.3194-3203.1990.

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The positively acting regulatory gene amdR of Aspergillus nidulans coordinately regulates the expression of five structural genes involved in the catabolism of certain amides (amdS), omega amino acids (gatA and gabA), and lactams (lamA and lamB) in the presence of omega amino acid inducers. Analysis of the amdR gene showed that it contains three small introns, heterogeneous 5' and 3' transcription sites, and multiple AUG codons prior to the major AUG initiator. The predicted amdR protein sequence has a cysteine-rich "zinc finger" DNA-binding motif at the amino-terminal end, four putative acidic transcription activation motifs in the carboxyl-terminal half, and two sequences homologous to the simian virus 40 large T antigen nuclear localization motif. These nuclear localization sequences overlap the cysteine-rich DNA-binding motif. A series of 5', 3', and internal deletions were examined in vivo for transcription activator function and showed that the amdR product contains at least two activation regions in the carboxyl-terminal half. Each of these activator amdR product contains at least two activation regions in the carboxyl-terminal half. Each of these activator regions may function independently, but both are required for wild-type levels of transcription activation. A number of the amdR deletion products were found to compete with the wild-type amdR product in vivo. Development of a rapid method for the localization of amdR mutations is presented, and using this technique, we localized and sequenced the mutation in the semiconstitutive amdR6c allele. The amdR6c missense mutation occurs in the middle of the gene, and it is suggested that it results in an altered protein which activates gene expression efficiently in the absence of an inducer.
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48

Andrianopoulos, A., and M. J. Hynes. "Sequence and functional analysis of the positively acting regulatory gene amdR from Aspergillus nidulans." Molecular and Cellular Biology 10, no. 6 (June 1990): 3194–203. http://dx.doi.org/10.1128/mcb.10.6.3194.

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The positively acting regulatory gene amdR of Aspergillus nidulans coordinately regulates the expression of five structural genes involved in the catabolism of certain amides (amdS), omega amino acids (gatA and gabA), and lactams (lamA and lamB) in the presence of omega amino acid inducers. Analysis of the amdR gene showed that it contains three small introns, heterogeneous 5' and 3' transcription sites, and multiple AUG codons prior to the major AUG initiator. The predicted amdR protein sequence has a cysteine-rich "zinc finger" DNA-binding motif at the amino-terminal end, four putative acidic transcription activation motifs in the carboxyl-terminal half, and two sequences homologous to the simian virus 40 large T antigen nuclear localization motif. These nuclear localization sequences overlap the cysteine-rich DNA-binding motif. A series of 5', 3', and internal deletions were examined in vivo for transcription activator function and showed that the amdR product contains at least two activation regions in the carboxyl-terminal half. Each of these activator amdR product contains at least two activation regions in the carboxyl-terminal half. Each of these activator regions may function independently, but both are required for wild-type levels of transcription activation. A number of the amdR deletion products were found to compete with the wild-type amdR product in vivo. Development of a rapid method for the localization of amdR mutations is presented, and using this technique, we localized and sequenced the mutation in the semiconstitutive amdR6c allele. The amdR6c missense mutation occurs in the middle of the gene, and it is suggested that it results in an altered protein which activates gene expression efficiently in the absence of an inducer.
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49

Papadopoulos, N. N., G. E. Hatzakis, A. C. Salevris, and N. F. Tsagas. "Optimized automated activation analysis." Journal of Radioanalytical and Nuclear Chemistry 215, no. 1 (January 1997): 103–10. http://dx.doi.org/10.1007/bf02109885.

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50

Tölgyessy, J., and M. Harangozo. "Flow-injection activation analysis." Journal of Radioanalytical and Nuclear Chemistry Letters 176, no. 2 (August 1993): 113–15. http://dx.doi.org/10.1007/bf02163191.

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