Search results for "Reaction"

showing 10 items of 6134 documents

Comparison of electromagnetic and nuclear dissociation of Ne-17

2018

8 pags., 10 figs., 3 tabs.

PhysicsCOLLISIONSInternal energy010308 nuclear & particles physics01 natural sciences7. Clean energySTATEDissociation (chemistry)CoincidenceCAPTUREReaction ratemedicine.anatomical_structureFragmentation (mass spectrometry)0103 physical sciencesmedicineHaloAtomic physics010306 general physicsGround stateDECAYNucleus
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Synthesis ofN=127isotones through (p,n) charge-exchange reactions induced by relativistic208Pb projectiles

2011

The production cross sections of four N=127 isotones ({sup 207}Hg, {sup 206}Au, {sup 205}Pt, and {sup 204}Ir) have been measured using (p,n) charge-exchange reactions, induced in collisions of a {sup 208}Pb primary beam at 1 A GeV with a Be target. These data allow one to investigate the use of a reaction mechanism to extend the limits of the chart of nuclides toward the important r-process nuclei in the region of the third peak of elemental abundance distribution.

PhysicsChemical kineticsNuclear reactionNuclear and High Energy PhysicsIsotopeNeutron emissionr-processProduction (computer science)Isotopes of goldNuclideAtomic physicsPhysical Review C
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Molecular dynamics simulations of elementary chemical processes in liquid water using combined density functional and molecular mechanics potentials.…

1997

A new approach to carry out molecular dynamics simulations of chemical reactions in solution using combined density functional theory/molecular mechanics potentials is presented. We focus our attention on the analysis of reactive trajectories, dynamic solvent effects and transmission coefficient rather than on the evaluation of free energy which is another important topic that will be examined elsewhere. In a previous paper we have described the generalities of this hybrid molecular dynamics method and it has been employed to investigate low energy barrier proton transfer process in water. The study of processes with activation energies larger than a few kT requires the use of specific tech…

PhysicsChemical processReaction stepMolecular dynamics method ; Chemical reactions ; Solvent effects ; Density functional theory ; WaterWaterGeneral Physics and AstronomyMolecular dynamics methodContext (language use)UNESCO::FÍSICA::Química físicaMolecular dynamicsChemical physicsChemical reactionsQuantum mechanicsSolvent effectsDensity functional theoryDensity functional theoryTransmission coefficientPhysical and Theoretical ChemistrySolvent effects:FÍSICA::Química física [UNESCO]QuantumThe Journal of Chemical Physics
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On time-resolved approach for phonon assisted interband transitions

2015

Photoexcited dynamics of electrons and holes in two-band dielectric, with special emphasis on back reaction of phonons are developed by combining the quantum electrodynamics and Baker-Campbell-Hausdorff (BCH) canonical transformation. These methods create an explicit time-domain representation of photoinduced processes and contribute in unifying phonon-assisted description of distribution functions of electron and hole quasiparticles for the description of observable effects of photoinduced processes in dielectrics.

PhysicsCondensed matter physicsPhononObservableCanonical transformationDielectricElectronCondensed Matter::Materials ScienceDistribution functionCondensed Matter::SuperconductivityQuantum mechanicsQuasiparticleCondensed Matter::Strongly Correlated ElectronsBack-reactionIOP Conference Series: Materials Science and Engineering
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Quantum mechanical study of the proton exchange in the ortho-para H2 conversion reaction at low temperature

2011

Ortho-para H2 conversion reactions mediated by the exchange of a H+ proton have been investigated at very low energy for the first time by means of a time independent quantum mechanical (TIQM) approach. State-to-state probabilities and cross sections for H+ + H 2 (v = 0, j = 0,1) processes have been calculated for a collision energy, Ec, ranging between 10-6 eV and 0.1 eV. Differential cross sections (DCSs) for H+ + H2 (v = 0, j = 1) → H+ + H2 (v′ = 0, j′ = 0) for very low energies only start to develop a proper global minimum around the sideways scattering direction ( ≈ 90°) at Ec = 10-3 eV. Rate coefficients, a crucial information required for astrophysical models, are provided between 10…

PhysicsConversion reaction010304 chemical physicsProtonScatteringMolecular cloudRelaxation (NMR)Hydrogen moleculeGeneral Physics and Astronomy010402 general chemistry7. Clean energy01 natural sciences[PHYS] Physics [physics]0104 chemical sciences[ PHYS.PHYS.PHYS-CHEM-PH ] Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]13. Climate action0103 physical sciences[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]Physical and Theoretical ChemistryAtomic physicsQuantumComputingMilieux_MISCELLANEOUSLine (formation)
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The influence of the solvent's mass on the location of the dividing surface for a model Hamiltonian

2019

The Transition State dividing surface is a key concept, not only for the precise calculation of the rate constant of a reaction, but also for the proper prediction of product ratios. The correct location of this surface is defined by the requirement that reactive trajectories do not recross it. In the case of reactions in solution the solvent plays an important role in the location of the dividing surface. In this paper we show with the aid of a model Hamiltonian that the effective mass of the solvent can dramatically change the location of the dividing surface. Keywords: Dynamical systems, Dividing surface, Reactions in solution, 2019 MSC: 00-01, 99-00

PhysicsDynamical systems theoryMathematical analysisSolvationlcsh:QD450-801General Physics and Astronomylcsh:Physical and theoretical chemistryDividing surfaceSurface reactionSistemes dinàmics diferenciablesChemical reactionlcsh:QC1-999Reactions in solutionSolventsymbols.namesakeReaction rate constantEffective mass (solid-state physics)Dynamical systemssymbolsPhysical and Theoretical ChemistryHamiltonian (quantum mechanics)lcsh:PhysicsFisicoquímica
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Recent advances in the description of reactions involving exotic nuclei

2019

In this contribution to the proceedings of the International Nuclear Physics Conference 2019, I review recent developments made in reaction models used to analyse data measured at radioactive-ion beam facilities to study exotic nuclear structures. I focus in particular on reactions like elastic scattering and breakup, which are used to study halo nuclei. Although these peculiar nuclei challenge usual nuclear-structure models, some can now be computed ab initio. This brief review illustrates the progresses made in nuclear-reaction theory in the last few years to improve the description of the projectile within reaction models. I dedicate this contribution to the memory of Mahir Hussein, who …

PhysicsElastic scatteringHistoryNuclear Theory010308 nuclear & particles physicsNuclear TheoryFOS: Physical sciences01 natural sciencesPhysique atomique et nucléaireComputer Science ApplicationsEducationNuclear physicsNuclear Theory (nucl-th)Reaction model0103 physical sciencesNuclear Experiment (nucl-ex)010306 general physicsNuclear ExperimentNuclear theoryNuclear Experiment
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The elastic scattering of 25MeV α-particles and neutron shell effects in the A = 50 TO A = 93 mass region

1982

Abstract Experimental elastic scattering angular distributions of 25 MeV α-particles scattered from 28 nuclei ranging from 50Cr to 93Nb have been measured and then analysed in terms of a regular optical model with standard Woods-Saxon geometries for both the real and imaginary potentials. The experimental distributions are well fitted over the whole angular range from 5° to 175° c.m. by the predictions, provided that a smaller than normal diffuseness is used for the imaginary potentials. The usual families of potentials with volume integrals differing by approximately 100 MeV · fm3 are found. The family with volume integral ranging from 540 to 420 MeV· fm3 over the nuclei studied has been c…

PhysicsElastic scatteringNuclear reactionNuclear and High Energy PhysicsPairingNuclear TheoryShell (structure)NeutronRadiusAtomic physicsNuclear ExperimentAbsorption (electromagnetic radiation)Volume integralNuclear Physics A
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Direct measurement of the radiative tail in electron scattering from atomic nuclei

1985

We have made a direct measurement of the radiative tail of the eleastic peak from several tungsten targets. The measured data have been compared to the results expected for both internal and external bremsstrahlung contributions. Even for targets as thick as 4% of a radiation length of tungsten, agreement between the results of the experiment and the predictions of the theory has been found to be unexpectedly good.

PhysicsElastic scatteringNuclear reactionNuclear and High Energy PhysicsScatteringBremsstrahlungchemistry.chemical_elementTungstenequipment and suppliesRadiation lengthchemistryRadiative transferAtomic physicsElectron scatteringPhysical Review C
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Transfer reactions on light exotic nuclei studied with CHIMERA detector at LNS

2014

The kinematical coincidence method is used to extract angular distribution of elastic scattering and transfer reactions. The detected light particle energy spectra are used to extract the angular distribution with around 1° resolution in the Center of Mass (CM) system. Examples with 10Be beam are presented. In the case of proton scattering, γ-ray coincidences are used to discriminate excited levels population from elastic scattering. © Owned by the authors, published by EDP Sciences, 2014.

PhysicsElastic scatteringeducation.field_of_studyPhysicsQC1-999PopulationResolution (electron density)Nuclear reactionCoincidenceSpectral linePhysics and Astronomy (all)Transfer reactionsExcited stateCenter of massAtomic physicseducationBeam (structure)EPJ Web of Conferences
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