Academic literature on the topic 'Nuclear size (Physics)'
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Journal articles on the topic "Nuclear size (Physics)"
Bonatsos, D., and C. Dascaloyannis. "Quantum algebraic symmetries in nuclear physics." HNPS Proceedings 3 (December 5, 2019): 175. http://dx.doi.org/10.12681/hnps.2384.
Full textAlmoukhalalati, Adel, Avijit Shee, and Trond Saue. "Nuclear size effects in vibrational spectra." Physical Chemistry Chemical Physics 18, no. 22 (2016): 15406–17. http://dx.doi.org/10.1039/c6cp01913g.
Full textCampi, Xavler. "Finite size scaling in nuclear fragmentation." Nuclear Physics A 495, no. 1-2 (April 1989): 259–66. http://dx.doi.org/10.1016/0375-9474(89)90324-2.
Full textWolynec, E., V. A. Serrao, and M. N. Martins. "Nuclear size effects in virtual photon spectra." Journal of Physics G: Nuclear Physics 13, no. 4 (April 1987): 515–26. http://dx.doi.org/10.1088/0305-4616/13/4/015.
Full textChen, Jianming, Liyuan Zhang, and Ren-yuan Zhu. "Large size LSO and LYSO crystal scintillators for future high-energy physics and nuclear physics experiments." Nuclear Instruments and Methods in Physics Research Section A: Accelerators, Spectrometers, Detectors and Associated Equipment 572, no. 1 (March 2007): 218–24. http://dx.doi.org/10.1016/j.nima.2006.10.213.
Full textBespalov, V. I. "Large-Size Monosectorial Crystal Elements for Powerful Laser Systems." Journal of Nonlinear Optical Physics & Materials 06, no. 04 (December 1997): 467–72. http://dx.doi.org/10.1142/s0218863597000344.
Full textRajasekaran, M., and N. Meenakumari. "Finite size nucleonic effects in the nuclear medium." Pramana 39, no. 5 (November 1992): 559–63. http://dx.doi.org/10.1007/bf02847344.
Full textOgloblin, A. A., A. S. Demyanova, A. N. Danilov, T. L. Belyaeva, S. A. Goncharov, and W. Trzaska. "Nuclear states with anomalously large radius (size isomers)." Physics of Atomic Nuclei 79, no. 4 (July 2016): 514–24. http://dx.doi.org/10.1134/s1063778816040177.
Full textWei, Ye. "γ probe of nuclear dissipation." International Journal of Modern Physics E 23, no. 06 (June 2014): 1460003. http://dx.doi.org/10.1142/s0218301314600039.
Full textRenner, O., L. Juha, J. Krasa, E. Krousky, M. Pfeifer, A. Velyhan, C. Granja, et al. "Low-energy nuclear transitions in subrelativistic laser-generated plasmas." Laser and Particle Beams 26, no. 2 (June 2008): 249–57. http://dx.doi.org/10.1017/s0263034608000293.
Full textDissertations / Theses on the topic "Nuclear size (Physics)"
Li, Yu-Chu Maxwell. "Theory of cluster size distribution /." free to MU campus, to others for purchase, 1997. http://wwwlib.umi.com/cr/mo/fullcit?p9842595.
Full textWang, Qi. "The effect of nano size fillers on electrical performance of epoxy resin." Thesis, University of Southampton, 2012. https://eprints.soton.ac.uk/340660/.
Full textLindle, Molly Eileen. "Contact electrification and charge separation in volcanic plumes." Thesis, Georgia Institute of Technology, 2011. http://hdl.handle.net/1853/43726.
Full textMatsson, Ingvar. "Studies of Nuclear Fuel Performance Using On-site Gamma-ray Spectroscopy and In-pile Measurements." Doctoral thesis, Uppsala : Acta Universitatis Upsaliensis : Univ.-bibl. [distributör], 2006. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-6912.
Full textDhani, Anwar. "Gamma ray emission tomography and angular correlation measurements to study the distribution and binding site of selenium." Thesis, University of Surrey, 1989. http://epubs.surrey.ac.uk/844497/.
Full textRoth, Olivia. "Physical and Chemical Aspects of Radiation Induced Oxidative Dissolution of UO2." Licentiate thesis, KTH, Kemi, 2006. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-622.
Full textThe general subject of this thesis is oxidative dissolution of UO2. The dissolution of UO2 is mainly investigated because of the importance of the UO2 matrix of spent nuclear fuel as a barrier against radionuclide release in a future deep repository. U(IV) is extremely insoluble under the reducing conditions prevalent in a deep repository, whereas U(VI) is more soluble. Hence, oxidation of the UO2-matrix will affect its solubility and thereby its function as a barrier. In this thesis the relative efficiency of one- and two electron oxidants in dissolving UO2 is studied. The oxidative dissolution yield of UO2 was found to differ between one- and two-electron oxidants. At low oxidant concentrations the dissolution yields for one-electron oxidants are significantly lower than for two-electron oxidants. However, the dissolution yield for one-electron oxidants increases with increasing oxidant concentration, which could be rationalized by the increased probability for two consecutive one-electron oxidations at the same site and the increased possibility for disproportionation. Furthermore, the relative impact of radical and molecular radiolysis products on oxidative dissolution of UO2 is investigated. Experiments were performed where the amount of dissolved U(VI) was measured in γ-irradiated systems dominated by different oxidants. We have found that the UO2 dissolution rate in systems exposed to γ-irradiation can be estimated from oxidant concentrations derived from simulations of radiolysis in the corresponding homogeneous systems and rate constants for the surface reactions. These simulations show that for all systems studied in this work, the molecular oxidants will be the most important oxidants for long irradiation times (>10 hours). Similar simulations of α-irradiated systems show that in systems relevant for a deep repository for spent nuclear fuel, only the molecular oxidants (mainly H2O2) are of importance for the dissolution of the fuel matrix. The effect on UO2 reactivity by irradiation of the material is of importance when predicting the spent fuel dissolution rate since the fuel, due to its content of radionuclides, is exposed to continuous self-irradiation. The effect of irradiation on the reaction between solid UO2 and MnO4- in aqueous solutions was studied. It was found that irradiation of UO2 at doses >40 kGy increases the reactivity of the material up to ~1.3 times the reactivity of unirradiated UO2. The increased reactivity remains after the irradiation and can possibly be attributed to permanent changes in the material. This issue must be taken into account when predicting the reactivity of spent nuclear fuel since the fuel is exposed to doses >40 kGy after only a few days in the reactor. It has earlier been suggested that the rate of a heterogeneous liquid-solid reaction depends on the size of the solid particles. This was investigated for UO2 particles in this thesis. Experimental kinetic parameters are compared to the previously proposed equations for UO2 powder of four size fractions and a UO2 pellet. We have found that the particle size dependence of the second order rate constant and activation energy for oxidation of UO2 by MnO4- is described quite well by the proposed equations.
QC 20101123
Hammond, Richard. "The structural and electrical characterisation of SiGe heterostructures deposited on strain relaxed virtual substrates." Thesis, University of Warwick, 1998. http://wrap.warwick.ac.uk/50784/.
Full textGreen, Christopher Henry. "The design of an n-side silicon detector for ATLAS at the LHC and a search for supersymmetric electrons with the DELPHI detector at LEP." Thesis, University of Liverpool, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.243216.
Full textDurov, Sergiy. "Characterisation and noise analysis of high Ge content p-channel SiGe MOSFETs fabricated using virtual substrates." Thesis, University of Warwick, 2004. http://wrap.warwick.ac.uk/2567/.
Full textRoth, Olivia. "Physical and Chemical Aspects of Radiation Induced Oxidative Dissolution of UO2." Licentiate thesis, KTH, Chemistry, 2006. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-622.
Full textDenna licensiatavhandling behandlar oxidativ upplösning av UO2. Upplösning av UO2 studeras huvudsakligen då UO2-matrisen hos använt kärnbränsle förväntas fungera som en barriär mot frigörande av radionuklider i ett framtida djupförvar. Lösligheten av U(IV) är mycket låg under i djupförvaret rådande förhållanden emedan U(VI) har betydligt högre löslighet. Oxidation av UO2-matrisen kommer därför att påverka dess löslighet och därmed dess funktion som barriär. I denna avhandling studeras den relativa effektiviteten av en- och två-elektronoxidanter för upplösning av UO2. Vid låga oxidantkoncentrationer är utbytet för upplösningen för en-elektronoxidanter signifikant lägre än för två-elektronoxidanter. För en-elektronoxidanter ökar dock utbytet med ökande oxidanthalt, vilket kan förklaras av den ökade sannolikheten för två konsekutiva en-elektronoxidationer av samma reaktionssite och den ökade möjligheten till disproportionering.
Radikaler och molekylära radiolysprodukters relativa inverkan på oxidativ upplösning av UO2 studeras också i denna avhandling genom mätning av mängden upplöst U(VI) i γ-bestrålade system som dominerades av olika oxidanter. Dessa studier visade att upplösningshastigheten av UO2 kan uppskattas från oxidantkoncentrationer framtagna genom simuleringar av radiolys i motsvarande homogena system och hastighetskonstanterna för ytreaktionerna. Simuleringarna visar att de molekylära oxidanterna kommer vara de viktigaste oxidanterna i alla system i denna studie vid långa bestrålningstider (>10 timmar). Vid liknande simuleringar av α-bestrålade system fanns att vid förhållanden relevanta för ett djupförvar för använt kärnbränsle, är det endast de molekylära oxidanterna (i huvudsak H2O2) som är av betydelse för upplösningen av bränslematrisen.
Då använt kärnbränsle innehåller en mängd radionuklider som utsätter UO2-matrisen för kontinuerlig bestrålning, är det av vikt att undersöka hur bestrålning påverkar reaktiviteten av UO2. Bestrålningseffekten på reaktionen mellan UO2 och MnO4- studerades. Dessa försök visade att bestrålning av UO2 vid doser >40 kGy leder till att reaktiviteten ökar upp till 1.3 gånger reaktiviteten av obestrålad UO2. Den ökade reaktiviteten kvarstår efter bestrålningen och effekten kan därför möjligen tillskrivas permanenta förändringar i materialet. Vid uppskattning av reaktiviteten hos använt kärnbränsle måste hänsyn tas till denna effekt då bränslet redan efter ett par dagar i reaktor blivit utsatt för doser >40 kGy.
Det har tidigare föreslagits att hastigheten för en heterogen västka/fast-fas reaktion är beroende av partikelstorleken hos det fasta materialet, vilket har studerats för UO2-partiklar i denna avhandling. Experimentellt bestämda kinetiska parametrar jämförs med de föreslagna ekvationerna för fyra storleksfraktioner av UO2-pulver och en UO2-pellet. Studien visade partikelstorleksberoendet av andra ordningens hastighetskonstant och aktiveringsenergin för oxidation av UO2 med MnO4- beskrivs relativt väl av de föreslagna ekvationerna.
The general subject of this thesis is oxidative dissolution of UO2. The dissolution of UO2 is mainly investigated because of the importance of the UO2 matrix of spent nuclear fuel as a barrier against radionuclide release in a future deep repository. U(IV) is extremely insoluble under the reducing conditions prevalent in a deep repository, whereas U(VI) is more soluble. Hence, oxidation of the UO2-matrix will affect its solubility and thereby its function as a barrier. In this thesis the relative efficiency of one- and two electron oxidants in dissolving UO2 is studied. The oxidative dissolution yield of UO2 was found to differ between one- and two-electron oxidants. At low oxidant concentrations the dissolution yields for one-electron oxidants are significantly lower than for two-electron oxidants. However, the dissolution yield for one-electron oxidants increases with increasing oxidant concentration, which could be rationalized by the increased probability for two consecutive one-electron oxidations at the same site and the increased possibility for disproportionation.
Furthermore, the relative impact of radical and molecular radiolysis products on oxidative dissolution of UO2 is investigated. Experiments were performed where the amount of dissolved U(VI) was measured in γ-irradiated systems dominated by different oxidants. We have found that the UO2 dissolution rate in systems exposed to γ-irradiation can be estimated from oxidant concentrations derived from simulations of radiolysis in the corresponding homogeneous systems and rate constants for the surface reactions. These simulations show that for all systems studied in this work, the molecular oxidants will be the most important oxidants for long irradiation times (>10 hours). Similar simulations of α-irradiated systems show that in systems relevant for a deep repository for spent nuclear fuel, only the molecular oxidants (mainly H2O2) are of importance for the dissolution of the fuel matrix.
The effect on UO2 reactivity by irradiation of the material is of importance when predicting the spent fuel dissolution rate since the fuel, due to its content of radionuclides, is exposed to continuous self-irradiation. The effect of irradiation on the reaction between solid UO2 and MnO4- in aqueous solutions was studied. It was found that irradiation of UO2 at doses >40 kGy increases the reactivity of the material up to ~1.3 times the reactivity of unirradiated UO2. The increased reactivity remains after the irradiation and can possibly be attributed to permanent changes in the material. This issue must be taken into account when predicting the reactivity of spent nuclear fuel since the fuel is exposed to doses >40 kGy after only a few days in the reactor.
It has earlier been suggested that the rate of a heterogeneous liquid-solid reaction depends on the size of the solid particles. This was investigated for UO2 particles in this thesis. Experimental kinetic parameters are compared to the previously proposed equations for UO2 powder of four size fractions and a UO2 pellet. We have found that the particle size dependence of the second order rate constant and activation energy for oxidation of UO2 by MnO4- is described quite well by the proposed equations.
Books on the topic "Nuclear size (Physics)"
"Tōjisei Chikuseki Ringu ni yoru Fuantei Kaku no Shitsuryō Sokutei to Uchū Genso Gōsei" Wākushoppu (2005 Tsukuba Daigaku). "Tōjisei Chikuseki Ringu ni yoru Fuantei Kaku no Shitsuryō Sokutei to Uchū Genso Gōsei" Wākushoppu. Ibaraki-ken Tsukuba-shi: Tsukuba Daigaku Kenkyū Kiban Sōgō Sentā Ōyō Kasokuki Bumon, 2006.
Find full textIshkhanov, B. S. Razmer i forma atomnykh i͡a︡der. Moskva: Izd-vo Moskovskogo universiteta, 1990.
Find full textJ, Lloyd P., Royal Society of Chemistry (Great Britain). Analytical Division., German Institute of Chemical Engineers., and Groupement pour l'avancement des méthodes spectroscopiques et physico-chimiques d'analyse (France), eds. Particle size analysis 1985: Proceedings of the Fifth Partical Size Analysis Conference, University of Bradford, Yorkshire, UK, 16-19th September 1985. Chichester [West Sussex]: Wiley, 1987.
Find full textThe shape of powder-particle outlines. Taunton, Somerset, England: Research Studies Press Ltd., 1993.
Find full textUnited States. Dept. of Energy. Assistant Secretary for Environment, Safety, and Health. Tiger team assessment of the Argonne Illinois site. [Washington, D.C.]: U.S. Dept. of Energy, [Office of] Environment, Safety, and Health, 1990.
Find full textSerra, Pablo, and Sabre Kais. Finite Size Scaling and Critical Phenomena in Atomic and Molecular Physics. CRC, 2009.
Find full textBook chapters on the topic "Nuclear size (Physics)"
Belyaev, Alexander, and Douglas Ross. "Nuclear Size and Shape." In The Basics of Nuclear and Particle Physics, 17–36. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-80116-8_2.
Full textSinyavsky, Nikolay, Georgy V. Mozzhukhin, and Philip Dolinenkov. "Size Effect in 14N Nuclear Quadrupole Resonance Spectroscopy." In NATO Science for Peace and Security Series B: Physics and Biophysics, 69–76. Dordrecht: Springer Netherlands, 2013. http://dx.doi.org/10.1007/978-94-007-7265-6_6.
Full textSchnabel, Allard. "Pressure Ensemble and Dense Nuclear Matter with Finite Size Nucleons at Zero Temperature." In Physics of Strong Fields, 853–69. Boston, MA: Springer US, 1987. http://dx.doi.org/10.1007/978-1-4613-1889-7_47.
Full textStock, Reinhard. "Relativistic Nucleus-Nucleus Collisions and the QCD Matter Phase Diagram." In Particle Physics Reference Library, 311–453. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-38207-0_7.
Full textHenderson, R. W., and R. F. Smale. "External Exposure Estimates for Individuals Near the Nevada Test Site." In Nuclear Physical Methods in Radioecological Investigations of Nuclear Test Sites, 191–202. Dordrecht: Springer Netherlands, 2000. http://dx.doi.org/10.1007/978-94-011-4116-1_17.
Full textSimon, S. L. "Evaluation of Possible Radiation Exposures Near the Semipalatinsk Nuclear Test Site." In Nuclear Physical Methods in Radioecological Investigations of Nuclear Test Sites, 153–59. Dordrecht: Springer Netherlands, 2000. http://dx.doi.org/10.1007/978-94-011-4116-1_13.
Full textKadyrzhanov, K. K., S. B. Kislitsin, K. M. Kikkarin, A. T. Kuketaev, A. D. Lopuga, T. E. Turkebaev, and Kh Sirajet. "Database of the Radioecological Situation at the Semipalatinsk Nuclear Test Site." In Nuclear Physical Methods in Radioecological Investigations of Nuclear Test Sites, 223–30. Dordrecht: Springer Netherlands, 2000. http://dx.doi.org/10.1007/978-94-011-4116-1_20.
Full textKadyrzhanov, K. K., S. Khazhekber, I. V. Kazachevsky, S. N. Lukashenko, and V. P. Solodukhin. "Characterisation of Radionuclide Contamination at the Semipalatinsk Nuclear Test Site Territory." In Nuclear Physical Methods in Radioecological Investigations of Nuclear Test Sites, 75–87. Dordrecht: Springer Netherlands, 2000. http://dx.doi.org/10.1007/978-94-011-4116-1_6.
Full textPivovarov, S. P., A. B. Rukhin, and T. A. Seredavina. "ESR Investigation of Environmental Objects from the Semipalatinsk Nuclear Test Site Region." In Nuclear Physical Methods in Radioecological Investigations of Nuclear Test Sites, 173–79. Dordrecht: Springer Netherlands, 2000. http://dx.doi.org/10.1007/978-94-011-4116-1_15.
Full textHawkins, W. L., J. L. Thompson, and D. L. Finnegan. "Hydrogeological Investigations and Radionuclide Migration in Groundwater at the Nevada Test Site." In Nuclear Physical Methods in Radioecological Investigations of Nuclear Test Sites, 61–74. Dordrecht: Springer Netherlands, 2000. http://dx.doi.org/10.1007/978-94-011-4116-1_5.
Full textConference papers on the topic "Nuclear size (Physics)"
Yamagata, T., H. Akimune, S. Nakayama, T. Shima, and S. Miyamoto. "Medium Modification of α Cluster Size in 6Li." In Nuclear Physics and Gamma-Ray Sources for Nuclear Security and Nonproliferation. WORLD SCIENTIFIC, 2014. http://dx.doi.org/10.1142/9789814635455_0020.
Full textPereira, L. A., J. C. Hadler, A. L. Lixandrão F., S. Guedes, and R. H. Takizawa. "Study on the influence of CR-39 detector size on radon progeny detection in indoor environments." In XXXVI BRAZILIAN WORKSHOP ON NUCLEAR PHYSICS. AIP Publishing LLC, 2014. http://dx.doi.org/10.1063/1.4901779.
Full textWATANABE, Y. "DAQ SYSTEM FOR SMALL-MIDDLE SIZE NUCLEAR PHYSICS EXPERIMENTS: PRESENT AND FUTURE." In Proceedings of the 5th Italy-Japan Symposium. WORLD SCIENTIFIC, 2005. http://dx.doi.org/10.1142/9789812701565_0049.
Full textFernandes, Jaquiel S., Rodrigo Nagata, Anderson C. Moreira, Celso P. Fernandes, and Carlos R. Appoloni. "Multi-scale analysis in carbonates by X-ray microtomography: Characterization of the porosity and pore size distribution." In XXXV BRAZILIAN WORKSHOP ON NUCLEAR PHYSICS. AIP, 2013. http://dx.doi.org/10.1063/1.4804091.
Full textGlushkov, Alexander V. "Advanced Quantum Mechanical Calculation of Superheavy Ions: Energy Levels, Radiation and Finite Nuclear Size Effects." In LOW ENERGY ANTIPROTON PHYSICS: Eighth International Conference on Low Energy Antiproton Physics (LEAP '05). AIP, 2005. http://dx.doi.org/10.1063/1.2130168.
Full textDe Paoli, A. L., and R. M. Aguirre. "Nuclear matter low lying collective modes in a finite size model of nucleons." In VI LATIN AMERICAN SYMPOSIUM ON NUCLEAR PHYSICS AND APPLICATIONS. AIP, 2007. http://dx.doi.org/10.1063/1.2710650.
Full textNoronha-Hostler, Jacquelyn, Roland Katz, Caio A. G. Prado, Jorge Noronha, Alexandre A. P. Suaide, and Marcelo G. Munhoz. "Sensitivity of D meson azimuthal anisotropies to system size and nuclear structure." In 13th International Workshop in High pT Physics in the RHIC and LHC Era. Trieste, Italy: Sissa Medialab, 2019. http://dx.doi.org/10.22323/1.355.0010.
Full textPetrovici, M., A. Lindner, and A. Pop. "On similarities as a function of system size in heavy ion collisions." In EXOTIC NUCLEI AND NUCLEAR/PARTICLE ASTROPHYSICS (VII). PHYSICS WITH SMALL ACCELERATORS: Proceedings of the Carpathian Summer School of Physics 2018 (CSSP18). Author(s), 2019. http://dx.doi.org/10.1063/1.5091636.
Full textVoloshin, Sergei A. "Energy and system size dependence of elliptic ow: using rapidity gaps to suppress non- ow contribution." In INTERSECTIONS OF PARTICLE AND NUCLEAR PHYSICS: 9th Conference CIPAN2006. AIP, 2006. http://dx.doi.org/10.1063/1.2402731.
Full textArrington, J. "New measurements of the proton's size and structure using polarized photons." In 11TH CONFERENCE ON THE INTERSECTIONS OF PARTICLE AND NUCLEAR PHYSICS: (CIPANP 2012). AIP, 2013. http://dx.doi.org/10.1063/1.4826834.
Full textReports on the topic "Nuclear size (Physics)"
Corscadden, Louise, and Anjali Singh. Metabolism And Measurable Metabolic Parameters. ConductScience, December 2022. http://dx.doi.org/10.55157/me20221213.
Full text