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Journal articles on the topic 'Nuclear products'

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Published: 4 June 2021
Last updated: 4 February 2022

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1

Reinov, O. I. "On products of nuclear operators." Functional Analysis and Its Applications 51, no. 4 (October 2017): 316–17. http://dx.doi.org/10.1007/s10688-017-0199-7.

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2

Vaca, Carlos E., and Mats Harms-Ringdahl. "Nuclear membrane lipid peroxidation products bind to nuclear macromolecules." Archives of Biochemistry and Biophysics 269, no. 2 (March 1989): 548–54. http://dx.doi.org/10.1016/0003-9861(89)90139-2.

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3

Azechi, Hiroshi. "Fuel Diagnostics, Using Nuclear Reaction Products." Kakuyūgō kenkyū 59, no. 2 (1988): 111–22. http://dx.doi.org/10.1585/jspf1958.59.111.

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4

AOKI, T., Y. KURATA, H. EBIHARA, and N. YOSHIKAWA. "Search for Nuclear Products of The D+D Nuclear Fusion." International Journal of the Society of Materials Engineering for Resources 6, no. 1 (1998): 22–25. http://dx.doi.org/10.5188/ijsmer.6.22.

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5

Dumitru, Raluca, and Costel Peligrad. "Nuclear and type I $C^*$-crossed products." Journal of Operator Theory 69, no. 1 (January 8, 2013): 287–96. http://dx.doi.org/10.7900/jot.2010dec08.1907.

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6

Yang, Chunyan, Qianrong Li, and Yong Li. "Targeting Nuclear Receptors with Marine Natural Products." Marine Drugs 12, no. 2 (January 27, 2014): 601–35. http://dx.doi.org/10.3390/md12020601.

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7

Ajlouni, A. W., Y. S. Almasa`efa, and M. Abdelsalam. "Nuclear Fission Products: From Source to Environment." Journal of Environmental Science and Technology 3, no. 4 (September 15, 2010): 182–94. http://dx.doi.org/10.3923/jest.2010.182.194.

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8

de Jesus, A. S. M. "Authentication of gold products by nuclear methods." Gold Bulletin 18, no. 4 (December 1985): 132–39. http://dx.doi.org/10.1007/bf03214695.

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9

Pimshin, Yu I., G. A. Naumenko, L. V. Postoy, and S. M. Burdakov. "Monitoring of the Nuclear Engineering Large Size Products." Global Nuclear Safety 11, no. 2 (June 2017): 47–55. http://dx.doi.org/10.26583/gns-2017-02-04.

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10

Pavlath, Grace K., Kevin Rich, Steven G. Webster, and Helen M. Blau. "Localization of muscle gene products in nuclear domains." Nature 337, no. 6207 (February 1989): 570–73. http://dx.doi.org/10.1038/337570a0.

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11

ITO, Yoshiaki. "Regulation of DNA Replication by Nuclear Protooncogene Products." Kagaku To Seibutsu 30, no. 4 (1992): 217–23. http://dx.doi.org/10.1271/kagakutoseibutsu1962.30.217.

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12

Paul, M., D. Fink, and G. Hollos. "Recoil accelerator mass spectrometry of nuclear reaction products." Nuclear Instruments and Methods in Physics Research Section B: Beam Interactions with Materials and Atoms 29, no. 1-2 (November 1987): 393–97. http://dx.doi.org/10.1016/0168-583x(87)90272-2.

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13

Vaca, Carlos E., and Mats Harms-Ringdahl. "Interaction of lipid peroxidation products with nuclear macromolecules." Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism 1001, no. 1 (January 1989): 35–43. http://dx.doi.org/10.1016/0005-2760(89)90304-4.

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14

Ruby, Lawrence, J. Warren Stearns, and Robert V. Pyle. "Neutral-beam species determination from nuclear reaction products." Nuclear Instruments and Methods in Physics Research Section A: Accelerators, Spectrometers, Detectors and Associated Equipment 248, no. 2-3 (August 1986): 501–5. http://dx.doi.org/10.1016/0168-9002(86)91040-5.

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15

Wise, C. "Recoil release of fission products from nuclear fuel." Journal of Nuclear Materials 136, no. 1 (October 1985): 30–47. http://dx.doi.org/10.1016/0022-3115(85)90028-5.

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16

Albertone, Luca, Massimo Altavilla, Manuela Marga, Laura Porzio, Giuseppe Tozzi, and Pierangelo Tura. "Control Experiences Regarding Clearable Materials from Nuclear Power Plants and Nuclear Installations: Scaling Factors Determination and Measurements’ Acceptance Criteria Definition." Environments 6, no. 11 (November 17, 2019): 120. http://dx.doi.org/10.3390/environments6110120.

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Arpa Piemonte has been carrying out, for a long time, controls on clearable materials from nuclear power plants to verify compliance with clearance levels set by ISIN (Ispettorato Nazionale per la Sicurezza Nucleare e la Radioprotezione - National Inspectorate for Nuclear Safety and Radiation Protection) in the technical prescriptions attached to the Ministerial Decree decommissioning authorization or into category A source authorization (higher level of associated risk, according to the categorization defined in the Italian Legislative Decree No. 230/95). After the experience undertaken at the “FN” (Fabbricazioni Nucleari) Bosco Marengo nuclear installation, some controls have been conducted at the Trino nuclear power plant “E. Fermi,” “LivaNova” nuclear installation based in Saluggia, and “EUREX” (Enriched Uranium Extraction) nuclear installation, also based in Saluggia, according to modalities that envisage, as a final control, the determination of γ-emitting radionuclides through in situ gamma spectrometry measurements. Clearance levels’ compliance verification should be performed for all radionuclides potentially present, including those that are not easily measurable (DTM, Difficult To Measure). It is therefore necessary to carry out upstream, based on a representative number of samples, those radionuclides’ determination in order to estimate scaling factors (SF), defined through the logarithmic average of the ratios between the i-th DTM radionuclide concentration and the related key nuclide. Specific radiochemistry is used for defining DTMs’ concentrations, such as Fe-55, Ni-59, Ni-63, Sr-90, Pu-238, and Pu-239/Pu-240. As a key nuclide, Co-60 was chosen for the activation products (Fe-55, Ni-59, Ni-63) and Cs-137 for fission products (Sr-90) and plutonium (Pu- 238, Pu-239/Pu-240, and Pu-241). The presence of very low radioactivity concentrations, often below the detection limits, can make it difficult to determine the related scaling factors. In this work, the results obtained and measurements’ acceptability criteria are presented, defined with ISIN, that can be used for confirming or excluding a radionuclide presence in the process of verifying clearance levels’ compliance. They are also exposed to evaluations regarding samples’ representativeness chosen for scaling factors’ assessment.
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17

Doizi, D., S. Reymond la Ruinaz, I. Haykal, L. Manceron, A. Perrin, V. Boudon, J. Vander Auwera, F. Kwabia tchana, and M. Faye. "Analytical measurements of fission products during a severe nuclear accident." EPJ Web of Conferences 170 (2018): 08005. http://dx.doi.org/10.1051/epjconf/201817008005.

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The Fukushima accident emphasized the fact that ways to monitor in real time the evolution of a nuclear reactor during a severe accident remain to be developed. No fission products were monitored during twelve days; only dose rates were measured, which is not sufficient to carry out an online diagnosis of the event. The first measurements were announced with little reliability for low volatile fission products. In order to improve the safety of nuclear plants and minimize the industrial, ecological and health consequences of a severe accident, it is necessary to develop new reliable measurement systems, operating at the earliest and closest to the emission source of fission products. Through the French program ANR « Projet d’Investissement d’Avenir », the aim of the DECA-PF project (diagnosis of core degradation from fission products measurements) is to monitor in real time the release of the major fission products (krypton, xenon, gaseous forms of iodine and ruthenium) outside the nuclear reactor containment. These products are released at different times during a nuclear accident and at different states of the nuclear core degradation. Thus, monitoring these fission products gives information on the situation inside the containment and helps to apply the Severe Accident Management procedures. Analytical techniques have been proposed and evaluated. The results are discussed here.
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18

Lykova, Zinaida A. "Hochschild cohomology of tensor products of topological algebras." Proceedings of the Edinburgh Mathematical Society 53, no. 2 (April 30, 2010): 447–70. http://dx.doi.org/10.1017/s0013091508001065.

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AbstractWe describe explicitly the continuous Hochschild and cyclic cohomology groups of certain tensor products of $\widehat{\otimes}$-algebras which are Fréchet spaces or nuclear DF-spaces. To this end we establish the existence of topological isomorphisms in the Künneth formula for the cohomology of complete nuclear DF-complexes and in the Künneth formula for continuous Hochschild cohomology of nuclear $\widehat{\otimes}$-algebras which are Fréchet spaces or DF-spaces for which all boundary maps of the standard homology complexes have closed ranges.
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19

Ngwenya, N., and E. M. N. Chirwa. "Biological removal of cationic fission products from nuclear wastewater." Water Science and Technology 63, no. 1 (January 1, 2011): 124–28. http://dx.doi.org/10.2166/wst.2011.021.

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Nuclear energy is becoming a preferred energy source amidst rising concerns over the impacts of fossil fuel based energy on global warming and climate change. However, the radioactive waste generated during nuclear power generation contains harmful long-lived fission products such as strontium (Sr). In this study, cationic strontium uptake from solution by microbial cultures obtained from mine wastewater is evaluated. A high strontium removal capacity (qmax) with maximum loading of 444 mg/g biomass was achieved by a mixed sulphate reducing bacteria (SRB) culture. Sr removal in SRB was facilitated by cell surface based electrostatic interactions with the formation of weak ionic bonds, as 68% of the adsorbed Sr2+ was easily desorbed from the biomass in an ion exchange reaction with MgCl2. To a lesser extent, precipitation reactions were also found to account for the removal of Sr from aqueous solution as about 3% of the sorbed Sr was precipitated due to the presence of chemical ligands while the remainder occurred as an immobile fraction. Further analysis of the Sr-loaded SRB biomass by scanning electron microscopy (SEM) coupled to energy dispersive X-ray (EDX) confirmed extracellular Sr2+ precipitation as a result of chemical interaction. In summary, the obtained results demonstrate the prospects of using biological technologies for the remediation of industrial wastewaters contaminated by fission products.
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20

Rozlosnik, N., C. S. Glavák, J. Pálfalvi, L. Sajó-Bohus, and C. Birattari. "Investigation of nuclear reaction products by atomic force microscopy." Radiation Measurements 28, no. 1-6 (January 1997): 277–80. http://dx.doi.org/10.1016/s1350-4487(97)00081-4.

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21

Tkac, Peter, Sergey Chemerisov, Roman Gromov, Jeongseog Song, Jerry Nolen, Vakhtang Makarashvili, and George Vandegrift. "Side-reaction products identified for photo-nuclear production of99Mo." Journal of Radioanalytical and Nuclear Chemistry 326, no. 1 (August 13, 2020): 543–53. http://dx.doi.org/10.1007/s10967-020-07307-1.

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22

Chatterjee, Tapan K., and Rory A. Fisher. "Novel Alternative Splicing and Nuclear Localization of HumanRGS12Gene Products." Journal of Biological Chemistry 275, no. 38 (June 26, 2000): 29660–71. http://dx.doi.org/10.1074/jbc.m000330200.

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23

Coker, David T., Alexander G. King, Dirk L. Mumford, and Craig S. Nessel. "Carcinogenic Assessment of Petroleum Products by Nuclear Magnetic Resonance." Analytical Communications 34, no. 5 (1997): 137–40. http://dx.doi.org/10.1039/a701248i.

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24

Silberberg, R., and C. H. Tsao. "Spallation processes and nuclear interaction products of cosmic rays." Physics Reports 191, no. 6 (August 1990): 351–408. http://dx.doi.org/10.1016/0370-1573(90)90109-f.

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25

Rainone, Timothy, and Christopher Schafhauser. "Crossed products of nuclear C⁎-algebras and their traces." Advances in Mathematics 347 (April 2019): 105–49. http://dx.doi.org/10.1016/j.aim.2019.01.045.

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26

Adeleye, S. A., R. Rãutiu, D. A. White, and P. G. Clay. "Clay minerals as sorbents for nuclear reactor activation products." Journal of Materials Science 30, no. 3 (February 1995): 583–86. http://dx.doi.org/10.1007/bf00356314.

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27

Grambow, Bernd. "Mobile fission and activation products in nuclear waste disposal." Journal of Contaminant Hydrology 102, no. 3-4 (December 2008): 180–86. http://dx.doi.org/10.1016/j.jconhyd.2008.10.006.

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28

Cubicciotti, Daniel. "Vapor transport of fission products under nuclear accident conditions." Journal of Nuclear Materials 154, no. 1 (June 1988): 53–61. http://dx.doi.org/10.1016/0022-3115(88)90118-3.

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29

Jamjoom, Fatmah B. "NuclearJC-algebras and tensor products of types." International Journal of Mathematics and Mathematical Sciences 16, no. 4 (1993): 717–23. http://dx.doi.org/10.1155/s0161171293000894.

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This article is a continuation of [1], to which the reader is referred for the definition and properties of theJC-tensor product of twoJC-algebras. Our standard references for nuclear and postliminalC*-algebras are[2,3,4,5,6,7]. We extend the notion of nuclearity toJC-algebras and prove that postliminalJC-algebras are nuclear. In contrast with the situation which occurs forC*-algebras, theJC-tensor product of two postliminalJC-algebras turns out, in general, to be non-postliminal and can even be anitliminal.
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30

Cautain, Bastien, Nuria de Pedro, Virginia Murillo Garzón, María Muñoz de Escalona, Victor González Menéndez, José R. Tormo, Jesús Martin, et al. "High-Content Screening of Natural Products Reveals Novel Nuclear Export Inhibitors." Journal of Biomolecular Screening 19, no. 1 (September 17, 2013): 57–65. http://dx.doi.org/10.1177/1087057113501389.

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Natural products are considered an extremely valuable source for the discovery of new drugs against diverse pathologies. As yet, we have only explored a fraction of the diversity of bioactive compounds, and opportunities for discovering new natural products leading to new drugs are huge. In the present study, U2nesRELOC, a previously established cell-based imaging assay, was employed to screen a collection of extracts of microbial origin for nuclear export inhibition activity. The fluorescent signal of untreated U2nesRELOC cells localizes predominantly to the cytoplasm. Upon treatment with the nuclear export inhibitor leptomycin B, the fluorescent-tagged reporter proteins appear as speckles in the nucleus. A proprietary collection of extracts from fungi, actinomycetes, and unicellular bacteria that covers an uncommonly broad chemical space was used to interrogate this nuclear export assay system. A two-step image-based analysis allowed us to identify 12 extracts with biological activities that are not associated with previously known active metabolites. The fractionation and structural elucidation of active compounds revealed several chemical structures with nuclear export inhibition activity. Here we show that substrates of the nuclear export receptor CRM1, such as Rev, FOXO3a and NF-κB, accumulate in the nucleus in the presence of the fungal metabolite MDN-0105 with an IC50 value of 3.4 µM. Many important processes in tumor formation and progression, as well as in many viral infections, critically depend on the nucleocytoplasmic trafficking of proteins and RNA molecules. Therefore, the disruption of nuclear export is emerging as a novel therapeutic approach with enormous clinical potential. Our work highlights the potential of applying high-throughput phenotypic imaging on natural product extracts to identify novel nuclear export inhibitors.
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31

Tran, Duc Thiep, Thi An Truong, Minh Hue Bui, Viet Cuong Phan, Belov A. G., and Mitrofanov S. "The nuclear channel effect in the isomeric ratio of the reaction products." Nuclear Science and Technology 9, no. 1 (March 15, 2019): 9–20. http://dx.doi.org/10.53747/jnst.v9i1.55.

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This work presents the experimental study of the isomeric ratio of 115mCd to 115gCd produced in 116Cd(γ, n)115m,gCd photonuclear reaction and 116Cd(n, γ)115m,gCd neutron capture reaction by thermal, epithermal and mixed thermal and epithermal neutrons. The investigated samples were natural cadmium irradiated at the bremsstrahlung photon flux, in the neutron source constructed at the electron accelerator Microtron MT-25 of the Flerov Laboratory of Nuclear Reaction, Joint Institute for Nuclear Research, Dubna, Russia. The results were analyzed, discussed, compared and combined with those of other authors in the existing literature to examine the role of the nuclear channel effect in the isomeric ratio and provide the nuclear data for theoretical model interpretation of nuclear reactions and applied research.
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32

Prelas, M. A., F. P. Boody, G. H. Miley, and J. F. Kunze. "Nuclear driven flashlamps." Laser and Particle Beams 6, no. 1 (February 1988): 25–62. http://dx.doi.org/10.1017/s0263034600003803.

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Due to the low power density of pumping schemes for nuclear-pumped lasers prior to 1978, a method of utilizing the efficient production of narrow band fluorescence from excimers was developed. This method has since been referred to as a nuclear driven flashlamp. It is possible to achieve sufficient power densities, when combining the flashlamp with novel techniques of reactor/laser interfaces, to drive efficient, high power lasers directly with products from nuclear reactions.
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33

Mayer, K., M. Wallenius, Zsolt Varga, T. Wiss, and T. Fanghänel. "Investigative radiochemistry – a key element in nuclear forensics." Proceedings in Radiochemistry 1, no. 1 (September 1, 2011): 145–49. http://dx.doi.org/10.1524/rcpr.2011.0027.

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AbstractSince the fall of the Iron Curtain illicit trafficking of nuclear and radioactive material has become an issue of concern both on the political and the scientific level. Seized material may be analysed in order to obtain clues on its origin and intended use and to prevent diversion of material from the same source in the future. Nuclear materials (uranium or plutonium) are of particular worry due to the nuclear proliferation risk associated with the material. Nuclear forensic investigations are aimed at the fact that nuclear material carries (inherent) information on its history, including on its origin and the processes applied for its production. Important conclusions can be drawn from decay products, activation products and fission products. Chemical impurities and the isotopic composition of certain major and minor constituents may provide additional information. Comparison of the measured results with nuclear material databases may yield evidence on the production site. The paper will describe the methodologies developed for addressing the above issues, focussing on radiochemical methods. Examples of nuclear forensic casework will illustrate the experience gathered in these areas.
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34

&NA;. "New Products." Investigative Radiology 30, no. 2 (February 1995): 131–32. http://dx.doi.org/10.1097/00004424-199502000-00013.

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35

&NA;. "New Products." Investigative Radiology 30, no. 3 (March 1995): 197–98. http://dx.doi.org/10.1097/00004424-199503000-00012.

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36

&NA;. "New Products." Investigative Radiology 30, no. 4 (April 1995): 266. http://dx.doi.org/10.1097/00004424-199504000-00011.

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37

&NA;. "New Products." Investigative Radiology 30, no. 5 (May 1995): 326–27. http://dx.doi.org/10.1097/00004424-199505000-00012.

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38

&NA;. "New Products." Investigative Radiology 30, no. 6 (June 1995): 386–87. http://dx.doi.org/10.1097/00004424-199506000-00012.

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39

&NA;. "New Products." Investigative Radiology 30, no. 7 (July 1995): 449. http://dx.doi.org/10.1097/00004424-199507000-00010.

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40

&NA;. "New Products." Investigative Radiology 30, no. 8 (August 1995): 508–9. http://dx.doi.org/10.1097/00004424-199508000-00010.

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41

&NA;. "New Products." Investigative Radiology 30, no. 9 (September 1995): 564–65. http://dx.doi.org/10.1097/00004424-199509000-00010.

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42

&NA;. "New Products." Investigative Radiology 30, no. 10 (October 1995): 622–23. http://dx.doi.org/10.1097/00004424-199510000-00009.

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43

&NA;. "New Products." Investigative Radiology 30, no. 11 (November 1995): 691. http://dx.doi.org/10.1097/00004424-199511000-00010.

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44

&NA;. "New Products." Investigative Radiology 30, no. 12 (December 1995): 766–67. http://dx.doi.org/10.1097/00004424-199512000-00012.

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45

&NA;. "New Products." INVESTIGATIVE RADIOLOGY 32, no. 9 (September 1997): 579. http://dx.doi.org/10.1097/00004424-199709000-00012.

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&NA;. "New Products." INVESTIGATIVE RADIOLOGY 32, no. 9 (September 1997): 579. http://dx.doi.org/10.1097/00004424-199709000-00013.

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47

&NA;. "New Products." Clinical Nuclear Medicine 19, no. 3 (March 1994): 276. http://dx.doi.org/10.1097/00003072-199403000-00070.

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48

&NA;. "New Products." Clinical Nuclear Medicine 19, no. 4 (April 1994): 382–83. http://dx.doi.org/10.1097/00003072-199404000-00027.

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49

Ananchenko, G. S., E. G. Bagryanskaya, and R. Z. Sagdeev. "Low magnetic field electron–nuclear resonance transitions detected by nuclear polarization of radical reaction products." Chemical Physics Letters 282, no. 5-6 (January 1998): 450–55. http://dx.doi.org/10.1016/s0009-2614(97)01237-2.

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50

Ruhman, N., V. Grantham, and C. Martin. "The Effectiveness of Decontamination Products in the Nuclear Medicine Department." Journal of Nuclear Medicine Technology 38, no. 4 (November 15, 2010): 191–94. http://dx.doi.org/10.2967/jnmt.110.076919.

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