Academic literature on the topic 'Nuclear products'
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Journal articles on the topic "Nuclear products"
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.
Full textVaca, 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.
Full textAzechi, Hiroshi. "Fuel Diagnostics, Using Nuclear Reaction Products." Kakuyūgō kenkyū 59, no. 2 (1988): 111–22. http://dx.doi.org/10.1585/jspf1958.59.111.
Full textAOKI, 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.
Full textDumitru, 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.
Full textYang, 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.
Full textAjlouni, 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.
Full textde 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.
Full textPimshin, 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.
Full textPavlath, 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.
Full textDissertations / Theses on the topic "Nuclear products"
Todd, Jamie R. D. (James Robert Drysdale). "Angular distributions and kinetic energies of fission products from the 238U(12C,f) reaction." Thesis, McGill University, 1991. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=59911.
Full textBlaylock, Dwayne Patrick. "Activation products in the biological shield of the Georgia Tech Research Reactor." Thesis, Georgia Institute of Technology, 1997. http://hdl.handle.net/1853/19431.
Full textNogueira, Cláudio Rodrigo [UNESP]. "Constituintes micromoleculares de Aristolochia melastoma Manso: compostos nitrados." Universidade Estadual Paulista (UNESP), 2010. http://hdl.handle.net/11449/97013.
Full textConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
O presente trabalho descreve o isolamento e identificação dos constituintes químicos de Aristolochia melastoma Manso. O extrato acetônico de caules e raízes foi fracionado por cromatografia em coluna de sílica gel, e as frações obtidas foram submetidas a outros fracionamentos cromatográficos (CCDP, Sephadex LH-20, CC de C-18 e CLAE) e/ou lavagens com solventes orgânicos, resultando no isolamento de vinte compostos conhecidos: aristolactama AII, 9,9'-diacetato-secoisolariciresinol dimetil éter, tirosol, ácido p-hidroxibenzóico, ácido vanilínico, ácidos aristolóquicos I e II, aristolocatos de sódio IIIa e IVa, 4,5-dioxodeidroasimilobíneo, aristolocato de sódio I, sitosterol 3-O-β-D-glucopiranosídeo, glicerol, talictosídeo, uridina, talictricosídeo, icarisídeo D2, adenosina, kaempferol 3-O-β-robinobiosídeo e isorhamnetina 3-O-β-robinobiosídeo. A lignana 9,9'-diacetato-secoisolariciresinol dimetil éter e talictricosídeo são relatados pela primeira vez na família Aristolochiaceae. As identificações desses compostos foram baseadas nas análises dos seus dados espectrométricos (RMN 1D e 2D, UV e EM). Além disso, a análise dos dados obtidos a partir de literatura especializada acerca da ocorrência e biogênese de derivados nitrofeniletílicos sugere que a família Aristolochiaceae pode ter evoluído no sentido de formação de compostos nitrados
This work describes the isolation and identification of the chemical constituents of A. melastoma Manso. The acetone extract from stems and roots was fractionated by CC over silica gel and the resultant fractions were subjected to other chromatographic methods (PTLC, Sephadex LH-20, CC RP-18, and HPLC) and/or washed with organic solvents to give twenty known compounds: aristolactam AII, secoisolariciresinol dimethyl ether diacetate, tyrosol, p-hydroxybenzoic acid, vanillic acid, sodium aristolochates I, IIIa, and IVa, 4,5-dioxodehydroasimilobine, aristolochic acids I and II, sitosterol-3-O-β-D-glucopyranoside, glycerol, uridine, thalictoside, icariside D2, adenosine, thalictricoside, kaempferol 3-O-β-robinobioside, and isorhamnetin 3-O-β-robinobioside. Among these, secoisolariciresinol dimethyl ether diacetate and thalictricoside have being reported for the first time in the Aristolochiaceae family. The identifications of these compounds were based on analyses of their spectroscopic data (1D- and 2D-NMR, UV, and MS). Furthermore, an analysis of data obtained from specialized literature on the occurrence and biogenesis of nitrophenylethyl derivatives suggests that the Aristolochiaceae family may have evolved towards nitro compounds
Solares, Hernández Guido Renato. "An automated computer controlled counting system for radionuclide analysis of corrosion products in LWR coolant systems." Thesis, Massachusetts Institute of Technology, 1988. http://hdl.handle.net/1721.1/14384.
Full textEL-HAJJE, REFAAT Safety Science Faculty of Science UNSW. "A SIMULTANEOUS MEASUREMENT OF THE ANGULAR DISTRIBUTION, MASS AND KINETIC ENERGY OF 235U AND 232Th FISSION FRAGMENTS." Awarded by:University of New South Wales. School of Safety Science, 2000. http://handle.unsw.edu.au/1959.4/17612.
Full textNair, Margie May. "The application of nuclear magnetic resonance in the structural elucidation of natural products." Master's thesis, University of Cape Town, 1994. http://hdl.handle.net/11427/16004.
Full textMultipulse Nuclear Magnetic Resonance (NMR) techniques were investigated via structural assignment of various natural products. The natural products chosen for investigation of 2D NMR spectroscopy as a structural tool were the opium alkaloids codeine and papaverine, the diterpenoid alkaloids delphinine and aconitine and the triterpenoid derivatives of cucurbitaceae. One dimensional NMR spectroscopy viz 1H, 13C and Distortionless Enhancement by Polarisation Transfer (DEPT) spectroscopy was initially applied to obtain a level of indication of the complexity of the structural problem solving. Various multipulse techniques were chosen depending on the sample quantity available, the sensitivity of the technique, the information provided and its applicabilty in the field of natural products. Both homonuclear scalar and dipolar correlation as well as short and long range heteronuclear correlation was investigated. The homonuclear Correlation Spectroscopy (COSY) experiment which revealed scalar 1H-1H scalar correlations was adequate for the structural assignment. The Heteronuclear Multiple Quantum Coherence (HMQC) experiment offered greater sensitivity on small sample quantities whilst the long range Heteronuclear Correlation (HETCOR) and Heteronuclear Multiple Bond Coherence (HMBC) experiments were essential for complete assignment of the quaternary groups. The stereochemical designation of some of the compounds was confirmed using the Rotating Frame Overhauser Enhancement Spectroscopy (ROESY) experiment which proved to be a more applicable pulse sequence for the natural products under investigation. The 1H and 13C assignments of these derivatives and the experimental approach used to obtain this data was compared to that present in the literature. The results indicate that apart from offering tremendous versatility depending on the special attributes of the compound, two dimensional NMR techniques are imperative for the unambiguous structural assignment of natural products.
Mazzeu, Bruna Fonseca [UNESP]. "Estudo de aspectos químicos, biológicos e biossintéticos em Piper fuligineum Kunth(Piperaceae)." Universidade Estadual Paulista (UNESP), 2014. http://hdl.handle.net/11449/110696.
Full textO perfil químico de folhas e frutos de Piper fuligineum foi analisado por cromatografia líquida de alta eficiência. A composição química de média polaridade dos dois órgãos vegetais apresentou semelhança. As análises demonstraram também que os frutos apresentavam composição química complexa, principalmente devido a presença de substâncias de maior polaridade. Essas análises permitiram selecionar as folhas de P. fuligineum para dar continuidade aos estudos químicos. Estes estudos resultaram no isolamento de cinco substâncias, sendo duas kavalactonas: (E)-6-(8-feniletil)-4-metoxi-2H-piran-2-ona e 6-(2-fenil-7,8-diidroxetil)-4-metoxi-2H-piran-2-ona; uma cromanona: (2,2-dimetil-4-oxocromano-6-carboxilato de metila) e dois derivados prenilados do acido benzoico: 4-hidroxi-3-(3-metilbutil-2-en-1-il)benzoato de metila e 4-metoxi-3-(3-metil-1-oxobut-2-en-1-il) benzoato de metila. As estruturas químicas das substâncias foram determinadas utilizando técnicas espectrométricas, incluindo RMN 1D e 2D. Todas as substâncias estão sendo descritas pela primeira vez em Piper fuligineum. A substância 4 é inédita como produto natural. O extrato etanolico das folhas e as frações obtidas de P. fuligineum foram avaliadas quanto ao potencial tripanocida frente à forma epimastigota da cepa Y de Trypanosoma cruzi, mostrando promissora atividade do extrato etanólico com IC50 de 26,67 g.mL-1 quando comparado com o controle positivo, benznidazol, com IC50 de 11,11 g.mL-1. O extrato acetato de etila, a fração clorofórmica e a substância 1 foram submetidos a testes antifúngicos frente aos fungos Candida albicans, C.krusei, C. tropicalis, C. parapsilosis e a levedura Cryptococcus neoformans. O extrato apresentou forte atividade frente ao fungo Candida tropicalis e moderada atividade frente aos fungos C. krusei, C. parapsilosis e a levedura Cryptococcus neoformans, enquanto a fração clorofórmica apresentou forte atividade frente ao...
The chemical profile of leaves and fruits of Piper fuligineum was analyzed by high performance liquid chromatography. The chemical composition of medium polarity related to leaves and fruits showed great similarity. The analysis also showed that the chemical composition of the fruits was more complex, mainly due to the presence of more polar substances. These analyzes allowed the selection of the leaves of P. fuligineum to continue the chemical studies. The chemical studies of the leaves of Piper fuligienum resulted in the isolation of six compunds, including two kavalactones (4- methoxy-6- [(E)-2-phenyl -vinyl] -2H-pyran-2-one and 6-(1,2-dihydroxy-2-phenyl- ethyl)-4-methoxy-2H- pyran-2-one), one chromanone (methyl-2,2-dimethyl-4-oxo-6- cromanacarboxylate) and two prenylated derivatives of benzoic acid (methyl-4-hydroxy-3-(3-methyl-2- buten-1-yl) benzoate and methyl-4-methoxy-3-(3-methyl -2-butenoyl) benzoate. The chemical structures of the isolated compounds were determined using spectrometric techniques, including 1D and 2D NMR. All compounds were described for the first time in Piper fuligineum, and the compound 4 is a new natural product. The ethanolic leaf extract and fractions obtained from P. fuligineum were evaluated for trypanocidal potential against epimastigote form of Trypanosoma cruzi Y strain, showing promising activity of the ethanol extract with IC50 of 26.67 g.mL-1 compared with the positive control benznidazole, with IC50 of 11.11 g.mL-1. The ethyl acetate extract, the chloroform fraction and substance 1 underwent antifungal drugs against fungi Candida albicans, C.krusei, C. tropicalis, C. parapsilosis and Cryptococcus neoformans yeast. The extract showed strong activity against the fungus Candida tropicalis and moderate activity against fungi C. krusei, C. parapsilosis and Cryptococcus neoformans yeast while the chloroform fraction showed strong activity against the fungus C. krusei, and moderate activity against...
Mazzeu, Bruna Fonseca. "Estudo de aspectos químicos, biológicos e biossintéticos em Piper fuligineum Kunth(Piperaceae) /." Araraquara, 2014. http://hdl.handle.net/11449/110696.
Full textBanca: Nivaldo Boralle
Banca: Marcos Pivatto
Resumo: O perfil químico de folhas e frutos de Piper fuligineum foi analisado por cromatografia líquida de alta eficiência. A composição química de média polaridade dos dois órgãos vegetais apresentou semelhança. As análises demonstraram também que os frutos apresentavam composição química complexa, principalmente devido a presença de substâncias de maior polaridade. Essas análises permitiram selecionar as folhas de P. fuligineum para dar continuidade aos estudos químicos. Estes estudos resultaram no isolamento de cinco substâncias, sendo duas kavalactonas: (E)-6-(8-feniletil)-4-metoxi-2H-piran-2-ona e 6-(2-fenil-7,8-diidroxetil)-4-metoxi-2H-piran-2-ona; uma cromanona: (2,2-dimetil-4-oxocromano-6-carboxilato de metila) e dois derivados prenilados do acido benzoico: 4-hidroxi-3-(3-metilbutil-2-en-1-il)benzoato de metila e 4-metoxi-3-(3-metil-1-oxobut-2-en-1-il) benzoato de metila. As estruturas químicas das substâncias foram determinadas utilizando técnicas espectrométricas, incluindo RMN 1D e 2D. Todas as substâncias estão sendo descritas pela primeira vez em Piper fuligineum. A substância 4 é inédita como produto natural. O extrato etanolico das folhas e as frações obtidas de P. fuligineum foram avaliadas quanto ao potencial tripanocida frente à forma epimastigota da cepa Y de Trypanosoma cruzi, mostrando promissora atividade do extrato etanólico com IC50 de 26,67 g.mL-1 quando comparado com o controle positivo, benznidazol, com IC50 de 11,11 g.mL-1. O extrato acetato de etila, a fração clorofórmica e a substância 1 foram submetidos a testes antifúngicos frente aos fungos Candida albicans, C.krusei, C. tropicalis, C. parapsilosis e a levedura Cryptococcus neoformans. O extrato apresentou forte atividade frente ao fungo Candida tropicalis e moderada atividade frente aos fungos C. krusei, C. parapsilosis e a levedura Cryptococcus neoformans, enquanto a fração clorofórmica apresentou forte atividade frente ao...
Abstract: The chemical profile of leaves and fruits of Piper fuligineum was analyzed by high performance liquid chromatography. The chemical composition of medium polarity related to leaves and fruits showed great similarity. The analysis also showed that the chemical composition of the fruits was more complex, mainly due to the presence of more polar substances. These analyzes allowed the selection of the leaves of P. fuligineum to continue the chemical studies. The chemical studies of the leaves of Piper fuligienum resulted in the isolation of six compunds, including two kavalactones (4- methoxy-6- [(E)-2-phenyl -vinyl] -2H-pyran-2-one and 6-(1,2-dihydroxy-2-phenyl- ethyl)-4-methoxy-2H- pyran-2-one), one chromanone (methyl-2,2-dimethyl-4-oxo-6- cromanacarboxylate) and two prenylated derivatives of benzoic acid (methyl-4-hydroxy-3-(3-methyl-2- buten-1-yl) benzoate and methyl-4-methoxy-3-(3-methyl -2-butenoyl) benzoate. The chemical structures of the isolated compounds were determined using spectrometric techniques, including 1D and 2D NMR. All compounds were described for the first time in Piper fuligineum, and the compound 4 is a new natural product. The ethanolic leaf extract and fractions obtained from P. fuligineum were evaluated for trypanocidal potential against epimastigote form of Trypanosoma cruzi Y strain, showing promising activity of the ethanol extract with IC50 of 26.67 g.mL-1 compared with the positive control benznidazole, with IC50 of 11.11 g.mL-1. The ethyl acetate extract, the chloroform fraction and substance 1 underwent antifungal drugs against fungi Candida albicans, C.krusei, C. tropicalis, C. parapsilosis and Cryptococcus neoformans yeast. The extract showed strong activity against the fungus Candida tropicalis and moderate activity against fungi C. krusei, C. parapsilosis and Cryptococcus neoformans yeast while the chloroform fraction showed strong activity against the fungus C. krusei, and moderate activity against...
Mestre
Wooten, Hasani Omar. "Calculation of internal dose conversion factors for selected spallation products." Thesis, Georgia Institute of Technology, 2002. http://hdl.handle.net/1853/17247.
Full textXue, Sha. "Modeling and experiment of fission products release and interaction with coolant for defective fuel in Light Water Reactor(LWR)." The Ohio State University, 2017. http://rave.ohiolink.edu/etdc/view?acc_num=osu1492734885411167.
Full textBooks on the topic "Nuclear products"
Vasilenko, I. I︠A︡. Biologicheskoe deĭstvie produktov i︠a︡dernogo delenii︠a︡: Biological action of nuclear fission products. Moskva: Izdatelʹstvo "BINOM", 2011.
Find full textInternational Workshop on Nuclear Fission and Fission-Product Spectroscopy. Nuclear fission and fission-product spectroscopy: 3rd International Workshop on Nuclear Fission and Fission-Product Spectroscopy, Cadarache, France, 11-14 May 2005. Melville, NY: American Institute of Physics, 2006.
Find full textHassmann, Klaus. Spaltproduktfreisetzung bei Kernschmelzen: Methodische Bestimmung und experimentelle Absicherung. Köln: TÜV Rheinland, 1987.
Find full textGauld, I. C. Validation of SCALE 5 decay heat predictions for LWR spent nuclear fuel. Washington, DC: U.S. Nuclear Regulatory Commission, Office of Nuclear Reactor Regulation, 2010.
Find full textSlugeň, Vladimír. Safety of VVER-440 reactors: Barriers against fission products release. London: Springer, 2011.
Find full textLian, Z. W. Convective-diffusive transport of fission products in the gap of a failed fuel element. Chalk River, Ont: Chalk River Laboratories, 1995.
Find full textBook chapters on the topic "Nuclear products"
Way, K., and E. P. Wigner. "The Rate of Decay of Fission Products." In Nuclear Energy, 428–40. Berlin, Heidelberg: Springer Berlin Heidelberg, 1992. http://dx.doi.org/10.1007/978-3-642-77425-6_27.
Full textRateb, Mostafa E., Jioji Tabudravu, and Rainer Ebel. "NMR characterisation of natural products derived from under-explored microorganisms." In Nuclear Magnetic Resonance, 240–68. Cambridge: Royal Society of Chemistry, 2016. http://dx.doi.org/10.1039/9781782624103-00240.
Full textSzabo, Les J., and Anthony R. Cashmore. "Targeting Nuclear Gene Products into Chloroplasts." In Plant DNA Infectious Agents, 321–39. Vienna: Springer Vienna, 1987. http://dx.doi.org/10.1007/978-3-7091-6977-3_15.
Full textMasterson, Robert E. "Fission Products, Xenon Transients, and Reactor Accidents." In Introduction to Nuclear Reactor Physics, 877–910. Boca Raton : Taylor & Francis, a CRC title, part of the Taylor & Francis imprint, a member of the Taylor & Francis Group, the academic division of T&F Informa, plc, [2017]: CRC Press, 2017. http://dx.doi.org/10.1201/9781315118055-21.
Full textBharadwaj, S. R., R. Mishra, M. Basu, and D. Das. "Thermochemistry of Thoria-based Fuel and Fission Products Interactions." In Thoria-based Nuclear Fuels, 107–56. London: Springer London, 2013. http://dx.doi.org/10.1007/978-1-4471-5589-8_4.
Full textNihei, Naoto. "Radioactivity in Agricultural Products in Fukushima." In Agricultural Implications of the Fukushima Nuclear Accident, 73–85. Tokyo: Springer Japan, 2013. http://dx.doi.org/10.1007/978-4-431-54328-2_8.
Full textDas, D., M. Basu, S. Kolay, and A. N. Shirsat. "Transport Properties of Gaseous and Volatile Fission Products in Thoria-based Fuels." In Thoria-based Nuclear Fuels, 157–203. London: Springer London, 2013. http://dx.doi.org/10.1007/978-1-4471-5589-8_5.
Full textBarkhudarov, Rudolf M. "Radiological Consequences of Global Fallouts of Nuclear Explosion Products over the USSR Territory in 1966–1986." In Atmospheric Nuclear Tests, 261–70. Berlin, Heidelberg: Springer Berlin Heidelberg, 1998. http://dx.doi.org/10.1007/978-3-662-03610-5_18.
Full textSchmidt, G. W., L. E. Sieburth, K. H. Jensen, K. L. Greer, F. G. Plumley, and D. L. Herrin. "Photosystem II Biogenesis: Roles of Nuclear Gene Products." In Progress in Photosynthesis Research, 637–44. Dordrecht: Springer Netherlands, 1987. http://dx.doi.org/10.1007/978-94-017-0519-6_131.
Full textSchneider, Bernd. "Nuclear Magnetic Resonance Spectroscopic Analysis of Enzyme Products." In Progress in Botany 72, 183–206. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-13145-5_7.
Full textConference papers on the topic "Nuclear products"
Hou, Fei. "The Investigation on Interactive Products for Propaganda of Nuclear Safety in Public." In 2013 21st International Conference on Nuclear Engineering. American Society of Mechanical Engineers, 2013. http://dx.doi.org/10.1115/icone21-16099.
Full textMaitra, Debajyoti, and Phani P. Gudipati. "Stainless Steel Extrusions and Product Properties for High Pressure-High Temperature (HPHT) Applications." In ASME 2018 Symposium on Elevated Temperature Application of Materials for Fossil, Nuclear, and Petrochemical Industries. American Society of Mechanical Engineers, 2018. http://dx.doi.org/10.1115/etam2018-6704.
Full textIgnatyuk, A. V. "Testing of Nuclear Data Libraries for Fission Products." In INTERNATIONAL CONFERENCE ON NUCLEAR DATA FOR SCIENCE AND TECHNOLOGY. AIP, 2005. http://dx.doi.org/10.1063/1.1944976.
Full textTuli, Jagdish K. "Evaluated Nuclear Structure Data File and Related Products." In INTERNATIONAL CONFERENCE ON NUCLEAR DATA FOR SCIENCE AND TECHNOLOGY. AIP, 2005. http://dx.doi.org/10.1063/1.1945002.
Full textGranja, Carlos, Jan Jakubek, Pedro N. de Faria, Rubens Lichtenthaler, Alinka Lepine-Szily, and Stanislav Pospisil. "Resolving nuclear reaction products at solenoid focal spot." In 2011 IEEE Nuclear Science Symposium and Medical Imaging Conference (2011 NSS/MIC). IEEE, 2011. http://dx.doi.org/10.1109/nssmic.2011.6154385.
Full textCoffey, K., Y. Sohn, and K. Graydon. "Diffusion of Fission Products in Nuclear Grade Graphite." In 2020 ANS Virtual Winter Meeting. AMNS, 2020. http://dx.doi.org/10.13182/t123-33102.
Full textAli, Seik Mansoor, Vishnu Verma, S. G. Markandeya, A. K. Ghosh, and H. S. Kushwaha. "Thermal Analysis of a Marine Products Irradiator and Its Transportation Cask." In 12th International Conference on Nuclear Engineering. ASMEDC, 2004. http://dx.doi.org/10.1115/icone12-49237.
Full textYee, Frank, Sermet Kuran, Mike Soulard, and Zhenhua Zhang. "AFCR and EC6: The Two Sister Products." In 2013 21st International Conference on Nuclear Engineering. American Society of Mechanical Engineers, 2013. http://dx.doi.org/10.1115/icone21-16646.
Full textOLEA, NICOLAS. "PLASTIC, PLASTICIZERS AND CONSUMER PRODUCTS." In International Seminar on Nuclear War and Planetary Emergencies 42nd Session. WORLD SCIENTIFIC, 2010. http://dx.doi.org/10.1142/9789814327503_0076.
Full textBresee, James C., Patricia D. Paviet, and Terry A. Todd. "US Department of Energy’s CoDCon Project: An Aqueous Safeguards R&D Program." In 2017 25th International Conference on Nuclear Engineering. American Society of Mechanical Engineers, 2017. http://dx.doi.org/10.1115/icone25-67965.
Full textReports on the topic "Nuclear products"
Shook, H. E. Jr. Solvent degradation products in nuclear fuel processing solvents. Office of Scientific and Technical Information (OSTI), June 1988. http://dx.doi.org/10.2172/7057142.
Full textWalker, H., F. Aluzzi, K. Foster, B. Pobanz, and B. Sher. GIS Symbology for FRMAC/CMHT Radiological/Nuclear Products. Office of Scientific and Technical Information (OSTI), October 2008. http://dx.doi.org/10.2172/945537.
Full textMarleau, Peter, and Matthew Shinner. Special Nuclear Material Detection and Monitoring by Environmental Activation Products Detection. Office of Scientific and Technical Information (OSTI), October 2018. http://dx.doi.org/10.2172/1481527.
Full textKuchka, M. R. Post transcriptional regulation of chloroplast gene expression by nuclear encoded gene products. Office of Scientific and Technical Information (OSTI), January 1992. http://dx.doi.org/10.2172/7309627.
Full textKuchka, M. R. Post transcriptional regulation of chloroplast gene expression by nuclear encoded gene products. Office of Scientific and Technical Information (OSTI), January 1992. http://dx.doi.org/10.2172/5268747.
Full textKuchka, M. R. Post-transcriptional regulation of chloroplast gene expression by nuclear encoded gene products. Office of Scientific and Technical Information (OSTI), August 1999. http://dx.doi.org/10.2172/764181.
Full textCooper, T. D. Spent Nuclear Fuel project estimate of volatile fission products release from multi-canister overpacks. Office of Scientific and Technical Information (OSTI), August 1996. http://dx.doi.org/10.2172/658110.
Full textTotemeier, T. C. Oxidation of ZPPR fuel corrosion products : National Spent Nuclear Fuel program FY 1999 final report. Office of Scientific and Technical Information (OSTI), November 1999. http://dx.doi.org/10.2172/816758.
Full textPeter C. Burns, Robert J. Finch, and David J. Wronkiewicz. Direct Investigations of the Immobilization of Radionuclides in the Alteration Products of Spent Nuclear Fuel. Office of Scientific and Technical Information (OSTI), December 2004. http://dx.doi.org/10.2172/835725.
Full textGALLEGOS, DAVID P., DORTHE B. CARR, PRESTON B. HERRINGTON, JAMES M. HARRIS, C. L. EDWARDS, STEVEN R. TAYLOR, JOHN J. ZUCCA, DAVID B. HARRIS, DALE N. ANDERSON, and LESLIE A. CASEY. The Integration Process Design for Incorporating Information Products into the National Nuclear Security Administration Knowledge Base. Office of Scientific and Technical Information (OSTI), November 2001. http://dx.doi.org/10.2172/789512.
Full text