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Journal articles on the topic '242Pu'

Author: Grafiati
Published: 4 June 2021
Last updated: 18 February 2022

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1

Gul, K., M. Ahmad, M. Anwar, and S. M. Saleem. "Measurements of Neutron Fission Cross Sections of237Np,240Pu,241Pu,242Pu,244Pu, and241Am at 14.7 MeV." Nuclear Science and Engineering 94, no. 1 (1986): 42–45. http://dx.doi.org/10.13182/nse86-a17115.

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2

Al Qaaod, Amer, Volodymyr Pavlovych, Danas Ridikas, Volodymyr Gulik, and Esmat Amin. "Computational study on distribution feasibility of radioactive waste transmutation in accelerator driven system." Nuclear Technology and Radiation Protection 35, no. 4 (2020): 294–303. http://dx.doi.org/10.2298/ntrp2004294q.

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In this paper, the feasibility of high-level radioactive waste transmutation in accelerator driven system sub-critical reactor assembly, has been studied for two zone's model and with three different core configurations. The inner zone has a fast neutron spectrum and the outer one has a thermal neutron spectrum. The subcritical core is coupled with external neutron source of energy 14 MeV (D-T source). The effects of high level waste isotopes sample (238Pu, 239Pu, 240Pu, 241Pu, 242Pu, 241Am, 243Am, 244Cm, and 245Cm) distribution on the neutron spectrum and burnup performance in the inner zone
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3

Demattè, L., C. Wagemans, R. Barthélémy, P. D'hondt, and A. Deruytter. "Fragments' mass and energy characteristics in the spontaneous fission of 236Pu, 238Pu, 240Pu, 242Pu, and 244Pu." Nuclear Physics A 617, no. 3 (1997): 331–46. http://dx.doi.org/10.1016/s0375-9474(97)00032-8.

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4

Ramebäck, H., A. Tovedal, P. Lagerkvist, S. Jonsson, and A. Vesterlund. "Alpha spectrometry and liquid scintillation counting for the measurement of 238Pu, 239Pu, 240Pu, 241Pu, 242Pu and age." Applied Radiation and Isotopes 164 (October 2020): 109293. http://dx.doi.org/10.1016/j.apradiso.2020.109293.

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5

Bélier, G., J. Aupiais, G. Sibbens, A. Moens, and D. Vanleeuw. "Use of active scintillating targets in nuclear physics experiments - Measurement of spontaneous fission." EPJ Web of Conferences 193 (2018): 04001. http://dx.doi.org/10.1051/epjconf/201819304001.

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A novel detector has been used, in order to perform measurements of spontaneous fission to α-decay ratios for 240Pu, 242Pu and 252Cf isotopes. The detectors are based on the well-known technique of liquid scintillating counting. The principle and advantages of the use of such detectors in nuclear physics is discussed. The application to the characterization of spontaneous fission is described and it is demonstrated that highly precise measurements are possible, and that the main limit is due to the isotopic content knowledge of the measured samples.
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6

Rizzo, Axel, Claire Vaglio-Gaudard, Gilles Noguere, Romain Eschbach, Gabriele Grassi, and Julie-Fiona Martin. "Feedback from experimental isotopic compositions of used nuclear fuels on neutron cross sections and cumulative fission yields of the JEFF-3.1.1 library by using integral data assimilation." EPJ Nuclear Sciences & Technologies 5 (2019): 24. http://dx.doi.org/10.1051/epjn/2019056.

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Comparisons of calculated and experimental isotopic compositions of used nuclear fuels can provide valuable information on the quality of nuclear data involved in neutronic calculations. The experimental database used in the present study − containing more than a thousand isotopic ratio measurements for UOX and MOX fuels with burnup ranging from 10 GWd/t up to 85 GWd/t − allowed to investigate 45 isotopic ratios covering a large number of actinides (U, Np, Pu, Am and Cm) and fission products (Nd, Cs, Sm, Eu, Gd, Ru, Ce, Tc, Mo, Ag and Rh). The Integral Data Assimilation procedure implemented i
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7

Noyau, S., Philippe Garcia, B. Pasquet, I. Roure, Fabienne Audubert, and Alexandre Maître. "Towards Measuring the Pu Self-Diffusion Coefficient in Polycrystalline U0.55Pu0.45O2±x." Defect and Diffusion Forum 323-325 (April 2012): 203–8. http://dx.doi.org/10.4028/www.scientific.net/ddf.323-325.203.

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This paper describes an original method to measure the plutonium self-diffusion coefficient in the mixed oxide U0.55Pu0.45O2±x. This method is based on using 242Pu as a tracer atom. A thin film of the tracer was deposited on the well-polished surface of the samples and then diffusion annealings were performed from 1500°C to 1700°C, in an Ar-H2 5% atmosphere. The oxygen potential was fixed at-395 kJ.mol-1. After annealing, the 242Pu self-diffusion profiles were established by means of secondary ion mass spectrometry (SIMS). The 242Pu concentration profiles were determined by assessing the relat
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8

Lerendegui-Marco, J., C. Guerrero, E. Mendoza та ін. "Measurement of the 242Pu(n, γ) cross section from thermal to 500 keV at the Budapest research reactor and CERN n_TOF-EAR1 facilities". EPJ Web of Conferences 239 (2020): 01019. http://dx.doi.org/10.1051/epjconf/202023901019.

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The design and operation of innovative nuclear systems requires a better knowledge of the capture and fission cross sections of the Pu isotopes. For the case of capture on 242Pu, a reduction of the uncertainty in the fast region down to 8-12% is required. Moreover, aiming at improving the evaluation of the fast energy range in terms of average parameters, the OECD NEA High Priority Request List (HPRL) requests high-resolution capture measurements with improved accuracy below 2 keV. The current uncertainties also affect the thermal point, where previous experiments deviate from each other by 20
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9

Donard, O. F. X., F. Bruneau, M. Moldovan, H. Garraud, V. N. Epov, and D. Boust. "Multi-isotopic determination of plutonium (239Pu, 240Pu, 241Pu and 242Pu) in marine sediments using sector-field inductively coupled plasma mass spectrometry." Analytica Chimica Acta 587, no. 2 (2007): 170–79. http://dx.doi.org/10.1016/j.aca.2007.01.047.

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10

Soldatov, A. S., A. I. Blokhin, A. V. Ignatyuk, and A. N. Storozhenko. "Photofission of 238Pu, 240Pu, and 242Pu in the energy range 5–10 MeV." Physics of Atomic Nuclei 63, no. 1 (2000): 31–39. http://dx.doi.org/10.1134/1.855603.

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11

Kögler, Toni, Roland Beyer, Arnd R. Junghans, Ronald Schwengner, and Andreas Wagner. "Determination of the fast-neutron-induced fission cross-section of 242Pu at nELBE." EPJ Web of Conferences 169 (2018): 00009. http://dx.doi.org/10.1051/epjconf/201816900009.

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The fast-neutron-induced fission cross section of 242Pu was determined in the energy range of 0.5 MeV to 10MeV at the neutron time-of-flight facility nELBE. Using a parallel-plate fission ionization chamber this quantity was measured relative to 235U(n,f). The number of target nuclei was thereby calculated by means of measuring the spontaneous fission rate of 242Pu. An MCNP 6 neutron transport simulation was used to correct the relative cross section for neutron scattering. The determined results are in good agreement with current experimental and evaluated data sets.
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12

Buckner, M. Q., C. Y. Wu, R. A. Henderson, et al. "242Pu absolute neutron-capture cross section measurement." EPJ Web of Conferences 146 (2017): 11011. http://dx.doi.org/10.1051/epjconf/201714611011.

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13

Weigmann, H., J. A. Wartena, and C. Bürkholz. "Neutron-induced fission cross section of 242Pu." Nuclear Physics A 438, no. 2 (1985): 333–53. http://dx.doi.org/10.1016/0375-9474(85)90379-3.

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14

Günay, M. "The production of238–242Pu(n,γ)239–243Pu fissionable fluids in a fusion-fission hybrid reactor". Kerntechnik 79, № 1 (2014): 58–62. http://dx.doi.org/10.3139/124.110364.

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15

Quinto, Francesca, Erich Hrnecek, Michael Krachler, William Shotyk, Peter Steier, and Stephan R. Winkler. "Determination of 239Pu, 240Pu, 241Pu and 242Pu at femtogram and attogram levels – evidence for the migration of fallout plutonium in an ombrotrophic peat bog profile." Environmental Science: Processes & Impacts 15, no. 4 (2013): 839. http://dx.doi.org/10.1039/c3em30910j.

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16

Staples, Parrish, and Kevin Morley. "Neutron-Induced Fission Cross-Section Ratios for239Pu,240Pu,242Pu, and244Pu Relative to235U from 0.5 to 400 MeV." Nuclear Science and Engineering 129, no. 2 (1998): 149–63. http://dx.doi.org/10.13182/nse98-a1969.

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17

Sibbens, G., A. Moens, R. Eykens, et al. "Preparation of 240Pu and 242Pu targets to improve cross-section measurements for advanced reactors and fuel cycles." Journal of Radioanalytical and Nuclear Chemistry 299, no. 2 (2013): 1093–98. http://dx.doi.org/10.1007/s10967-013-2668-7.

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18

Engle, J. W., E. R. Birnbaum, F. M. Nortier, J. A. Rau, K. D. John, and H. R. Trellue. "Purification of 242Pu by irradiation with thermal neutrons." Nuclear Instruments and Methods in Physics Research Section B: Beam Interactions with Materials and Atoms 298 (March 2013): 70–75. http://dx.doi.org/10.1016/j.nimb.2012.12.044.

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19

Swinhoe, M. T., T. Iwamoto, and T. Tamura. "Determination of 242Pu by correlation with 239Pu only." Nuclear Instruments and Methods in Physics Research Section A: Accelerators, Spectrometers, Detectors and Associated Equipment 615, no. 1 (2010): 136–37. http://dx.doi.org/10.1016/j.nima.2010.01.003.

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20

Zadehrafi, M., M. R. Pahlavani, and M. R. Ioan. "Tin-accompanied and true ternary fission of 242Pu." Chinese Physics C 43, no. 9 (2019): 094101. http://dx.doi.org/10.1088/1674-1137/43/9/094101.

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21

Urlass, Sebastian, Roland Beyer, Arnd Rudolf Junghans, Toni Kögler, Ronald Schwengner та Andreas Wagner. "Measurement of the prompt fissionγ-ray spectrum of 242Pu". EPJ Web of Conferences 169 (2018): 00026. http://dx.doi.org/10.1051/epjconf/201816900026.

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The prompt γ-ray spectrum of fission fragments is important in understanding the dynamics of the fission process, as well as for nuclear engineering in terms of predicting the γ-ray heating in nuclear reactors. The γ-ray spectrum measured from the fission fragments of the spontaneous fission of 242Pu will be presented here. A fission chamber containing in total 37mg of 242Pu was used as active sample. The γ-quanta were detected with high time- and energy-resolution using LaBr3 and HPGe detectors, respectively, in coincidence with spontaneous fission events detected by the fission chamber. The
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22

Toribio, M., A. Padró, J. F. Garcı́a, and G. Rauret. "Determination of mixtures of alpha emitting isotopes (242Pu, 239+240Pu, 238Pu) by using liquid scintillation–moving curve fitting." Analytica Chimica Acta 380, no. 1 (1999): 83–92. http://dx.doi.org/10.1016/s0003-2670(98)00645-x.

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23

Jakopič, Rožle, Stephan Richter, Heinz Kühn, and Yetunde Aregbe. "Determination of 240Pu/239Pu, 241Pu/239Pu and 242Pu/239Pu isotope ratios in environmental reference materials and samples from Chernobyl by thermal ionization mass spectrometry (TIMS) and filament carburization." Journal of Analytical Atomic Spectrometry 25, no. 6 (2010): 815. http://dx.doi.org/10.1039/b925918j.

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24

Rich, E., A. Tudora, G. Noguere, J. Tommasi, and J. F. Lebrat. "Modeling of then+242Pu Reactions for Fast Reactor Applications." Nuclear Science and Engineering 162, no. 2 (2009): 178–91. http://dx.doi.org/10.13182/nse162-178.

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25

Sarkar, Arnab, Raju Shah, K. Sasibhusan, et al. "Isotopic correlation for 242Pu composition prediction: Multivariate regresssion approach." Applied Radiation and Isotopes 95 (January 2015): 169–73. http://dx.doi.org/10.1016/j.apradiso.2014.11.001.

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26

Croft, Stephen, and Andrea Favalli. "Review and Evaluation of the Spontaneous Fission Half-lives of 238Pu, 240Pu, and 242Pu and the Corresponding Specific Fission Rates." Nuclear Data Sheets 175 (July 2021): 269–87. http://dx.doi.org/10.1016/j.nds.2021.06.003.

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27

Salminen-Paatero, Susanna, Julius Vira, and Jussi Paatero. "Measurements and modeling of airborne plutonium in Subarctic Finland between 1965 and 2011." Atmospheric Chemistry and Physics 20, no. 9 (2020): 5759–69. http://dx.doi.org/10.5194/acp-20-5759-2020.

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Abstract. The activity concentrations of 238,239,240Pu and 241Am (for determining its mother nuclide, 241Pu) as well as activity ratios of 238Pu/239+240Pu, 241Pu/239+240Pu and 239+240Pu/137Cs and the mass ratio of 240Pu∕239Pu were determined from air filter samples collected in Rovaniemi (Finnish Lapland) in 1965 to 2011. The origin of plutonium in surface air was assessed based on these data from long time series. The most important Pu sources in the surface air of Rovaniemi were atmospheric nuclear-weapon testing in the 1950s and 1960s, later nuclear tests in 1973–1980 and the SNAP-9A satell
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28

Guan, Yongjing, Shaohan Sun, Huijuan Wang, et al. "Accelerator Mass Spectrometry Analysis of 237NP in Environmental Samples." Radiocarbon 61, no. 5 (2019): 1423–30. http://dx.doi.org/10.1017/rdc.2019.67.

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ABSTRACTTo determine the 237Np concentration originating from global fallout in the environment, samples were collected from Guangxi, south of China, and measured by accelerator mass spectrometry (AMS) at CIRCE. Serials standard samples and environment samples were prepared and measured using 242Pu as a tracer. The result indicates that the detection limit of 237Np as low as 10–15 g can be obtained. The concentration of 237Np in the environmental samples is less than 49.09 pg/kg (i.e. 1.280 mBq/kg), and the most probable value of 237Np is approximately 20 pg/kg (i.e. 0.53 mBq/kg).
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29

Tudora, Anabella. "Neutron cross-sections of 242Pu in the energy range 5–20 MeV." Annals of Nuclear Energy 27, no. 18 (2000): 1669–81. http://dx.doi.org/10.1016/s0306-4549(00)00018-9.

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30

Vladuca, G., M. Sin, and A. Tudora. "Neutron cross sections of 242Pu in the energy range 0.01–6 MeV." Annals of Nuclear Energy 24, no. 14 (1997): 1141–49. http://dx.doi.org/10.1016/s0306-4549(96)00105-3.

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31

Alamelu, D., Sumana Chakraborty, and Suresh K. Aggarwal. "A critical evaluation of different isotope correlations for the determination of 242Pu." Applied Radiation and Isotopes 68, no. 12 (2010): 2416–20. http://dx.doi.org/10.1016/j.apradiso.2010.06.025.

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32

Vascon, A., J. Runke, N. Trautmann, B. Cremer, K. Eberhardt, and Ch E. Düllmann. "Quantitative molecular plating of large-area 242Pu targets with improved layer properties." Applied Radiation and Isotopes 95 (January 2015): 36–43. http://dx.doi.org/10.1016/j.apradiso.2014.10.002.

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33

Vaninbroukx, R., G. Bortels, and B. Denecke. "Alpha-particle and gamma-ray emission probabilities in the decay of 242Pu." International Journal of Radiation Applications and Instrumentation. Part A. Applied Radiation and Isotopes 37, no. 12 (1986): 1167–72. http://dx.doi.org/10.1016/0883-2889(86)90001-8.

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34

Berndt, Reinhard, and Patricia Mortreau. "Determination of 242Pu abundance in plutonium samples using self-fluorescent X-ray emission." Nuclear Instruments and Methods in Physics Research Section A: Accelerators, Spectrometers, Detectors and Associated Equipment 940 (October 2019): 66–71. http://dx.doi.org/10.1016/j.nima.2019.04.075.

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35

Tsinganis, A., E. Berthoumieux, C. Guerrero, et al. "Measurement of the 242Pu(n,f) Cross Section at the CERN n_TOF Facility." Nuclear Data Sheets 119 (May 2014): 58–60. http://dx.doi.org/10.1016/j.nds.2014.08.018.

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36

Tsinganis, A., E. Berthoumieux, C. Guerrero, et al. "Measurement of the 242Pu(n,f) cross-section at the CERN n_TOF facility." HNPS Proceedings 22 (March 8, 2019): 28. http://dx.doi.org/10.12681/hnps.1926.

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Knowledge of neutron cross-sections of various plutonium isotopes and other minor actinides is crucial for the design of advanced nuclear systems. The 240,242Pu(n,f) cross-sections were measured at the CERN n_TOF facility, taking advantage of the wide energy range (from thermal to GeV) and the high instantaneous flux of the neutron beam. In this work, preliminary results are presented along with a theoretical cross-section calculation performed with the EMPIRE code.
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37

Jovančević, N., P. Salvador-Castineira, L. Daraban, et al. "Neutron-induced fission cross section of 242Pu from 15 MeV to 20 MeV." EPJ Web of Conferences 146 (2017): 04044. http://dx.doi.org/10.1051/epjconf/201714604044.

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38

Qiao, Jixin, Xiaolin Hou, Per Roos, and Manuel Miró. "Reliable determination of 237Np in environmental solid samples using 242Pu as a potential tracer." Talanta 84, no. 2 (2011): 494–500. http://dx.doi.org/10.1016/j.talanta.2011.01.040.

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39

Kniajeva, G. N., L. Krupa, A. A. Bogachev, et al. "Neutron and gamma-ray emission in the proton induced fission of 238U and 242Pu." Nuclear Physics A 734 (April 2004): E25—E28. http://dx.doi.org/10.1016/j.nuclphysa.2004.03.011.

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40

Sadiq, S., D. Ram, R. Devi, and S. K. Khosa. "A study of positive parity yrast bands of 230–240U and 236–242Pu nuclei." Indian Journal of Physics 89, no. 7 (2014): 713–22. http://dx.doi.org/10.1007/s12648-014-0639-7.

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41

Tolmachev, S. Y., M. E. Ketterer, D. Hare, P. Doble, and A. C. James. "The US Transuranium and Uranium Registries: forty years' experience and new directions in the analysis of actinides in human tissues." Proceedings in Radiochemistry 1, no. 1 (2011): 173–81. http://dx.doi.org/10.1524/rcpr.2011.0032.

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Abstract The US Transuranium and Uranium Registries (USTUR) studies the distribution, biokinetics and tissue dosimetry of actinide elements through radiochemical analysis of autopsy tissues voluntarily donated by occupationally exposed persons. The paper provides an overview of the analytical methods for plutonium (Pu), americium (Am) and uranium (U) isotopic determination in human tissues currently applied at USTUR. The results of inter-comparing 239+240Pu, 241Am and 234,235,238U determinations by sector field inductively coupled mass spectrometry (SF-ICP-MS), α-spectrometry (AS) and kinetic
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42

Gallardo, Athena Marie, Chit Than, Carolyn Wong, and Ralf Sudowe. "A Rapid Method for Quantification OF 242Pu in Urine Using Extraction Chromatography and ICP-MS." Health Physics 112, no. 3 (2017): 246–51. http://dx.doi.org/10.1097/hp.0000000000000607.

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43

Bolsunovsky, A., L. Bondareva, F. Sukhorukov, and M. Melgunov. "Accumulation of 242Pu by a macrophyte of the Yenisei River (Elodea canadensis) in laboratory experiments." Chemosphere 75, no. 3 (2009): 284–88. http://dx.doi.org/10.1016/j.chemosphere.2008.12.036.

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44

Schillebeeckx, P., C. Wagemans, A. J. Deruytter, and R. Barthélémy. "Comparative study of the fragments' mass and energy characteristics in the spontaneous fussion of 238Pu, 240Pu and 242Pu and in the thermal-neutron-induced fission of 239Pu." Nuclear Physics A 545, no. 3 (1992): 623–45. http://dx.doi.org/10.1016/0375-9474(92)90296-v.

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45

Kaiba, Tanja, Vladimir Radulović, Gašper Žerovnik, et al. "Calculations to Support On-line Neutron Spectrum Adjustment by Measurements with Miniature Fission Chambers in the JSI TRIGA Reactor." EPJ Web of Conferences 170 (2018): 04012. http://dx.doi.org/10.1051/epjconf/201817004012.

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Preliminary calculations were performed with the aim to establish optimal experimental conditions for the measurement campaign within the collaboration between the Jožef Stefan Institute (JSI) and Commissariat à l’Énergie Atomique et aux Énergies Alternatives (CEA Cadarache). The goal of the project is to additionally characterize the neutron spectruminside the JSI TRIGA reactor core with focus on the measurement epi-thermal and fast part of the spectrum. Measurements will be performed with fission chambers containing different fissile materials (235U, 237Np and 242Pu) covered with thermal neu
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46

Aleeva, T. B., A. V. Bushuev, A. F. Kozhin, V. N. Zubarev, and A. F. Myrzin. "Development of the method of isotopic correlations for determining the relative 242Pu content in plutonium samples." Atomic Energy 106, no. 6 (2009): 423–26. http://dx.doi.org/10.1007/s10512-009-9181-7.

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47

Genreith, Christoph, Matthias Rossbach, Eric Mauerhofer, Tamás Belgya, and Guido Caspary. "Measurement of thermal neutron capture cross sections of 237Np and 242Pu using prompt gamma neutron activation." Journal of Radioanalytical and Nuclear Chemistry 296, no. 2 (2012): 699–703. http://dx.doi.org/10.1007/s10967-012-2080-8.

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48

Gupta, Dharmendra K., Frank Tawussi, Alex Hölzer, Linda Hamann, and Clemens Walther. "Investigation of low-level 242Pu contamination on nutrition disturbance and oxidative stress in Solanum tuberosum L." Environmental Science and Pollution Research 24, no. 19 (2017): 16050–61. http://dx.doi.org/10.1007/s11356-017-9071-9.

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49

Bu, W. T., J. Zheng, T. Aono, et al. "Vertical distributions of plutonium isotopes in marine sediment cores off the Fukushima coast after the Fukushima Dai-ichi Nuclear Power Plant accident." Biogeosciences 10, no. 4 (2013): 2497–511. http://dx.doi.org/10.5194/bg-10-2497-2013.

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Abstract. The Fukushima Dai-ichi Nuclear Power Plant (FDNPP) accident led to the release of large amounts of radionuclides into the atmosphere as well as direct discharges into the sea. In contrast to the intensive studies on the distribution of the released high volatility fission products, such as 131I, 134Cs and 137Cs, similar studies of the actinides, especially the Pu isotopes, are limited. To obtain the vertical distribution of Pu isotopes in marine sediments and to better assess the possible contamination of Pu from the FDNPP accident in the marine environment, we determined the activit
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50

Bu, W. T., J. Zheng, T. Aono, et al. "Determination of plutonium isotopes in marine sediments off the Fukushima coast following the Fukushima Dai-ichi Nuclear Power Plant accident." Biogeosciences Discussions 10, no. 1 (2013): 643–80. http://dx.doi.org/10.5194/bgd-10-643-2013.

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Abstract. The Fukushima Dai-ichi Nuclear Power Plant (FDNPP) accident led to the release of large amounts of radionuclides into the atmosphere as well as direct discharges into the sea. In contrast to the intensive studies on the distribution of the released high volatility fission products, such as 131I, 134Cs and 137Cs, similar studies of the actinides, especially the Pu isotopes, are limited. To obtain the vertical distribution of Pu isotopes in marine sediments and to better assess the possible contamination of Pu from the FDNPP accident in the marine environment, we determined the activit
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