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In the last decade or so, an evolution in experimental relativistic laser-plasma physics has led to highly sophisticated lasers which are now capable of generating ultra-short pulses and can be focused to intensities in excess of 1021 W cm-2. The laser interaction with solid or gas targets can generate collimated beams of highly energetic electrons, protons and ions. These high-intensity laser systems, therefore, turn out to be versatile and powerful sources of radiation and high-energy particles, without recourse to large-scale facilities such as nuclear reactors or particle accelerators. The potential to induce various kinds of nuclear reactions with laser-induced radiation fields has been demonstrated at several laboratories in recent years. The present paper lays out a comprehensive overview of nuclear reactions induced by high-intensity laser matter interactions. Mechanisms for electron, proton and ion acceleration, in addition to secondary bremsstrahlung, positron and neutron production, are addressed, with a focus on the types of nuclear reactions that are possible and potential applications. Discussion of the extrapolation of these processes and applications to the next generation of table-top lasers under construction is also presented.

International audience; Hole-doped Ca 3 Co 4 O 9 (Co349) ceramics were prepared using solid-state reaction. Two processing strategies have been used to produce the thermoelectric oxide ceramics, Conventional and Spark Plasma (SPS) Sintering to control the grains consolidation, texturation and sample densification. Thermoelectric properties were measured and the influence of the processing conditions on the properties was evidenced. SPS favours shorter elaboration times and produces samples with larger thermoelectric properties due to better densification and alignment. The effect of the free deformation and texturation using the SPS technique is discussed. Seebeck coefficient values of 180 μV/K at 873 K are obtained.

The β--decay of 147Cs to 147Ba has been studied by means of γ- and X-ray spectroscopy. A new level scheme of 147Ba is significantly modified and extended in comparison to the one previously reported. The Advanced Time-Delayed βγγ(t) method has been applied to measure half-lives of the 46.2 and 85.4 keV levels in 147Ba yielding T 1/2 of 510(80) ps and 370(100) ps, respectively. The lifetime results combined with the deduced internal conversion coefficients allowed to assign M1 multipolarity to three γ transitions. The B(M1) values obtained for the 39.2, 46.2 and 85.4 keV transitions range from 0.017 to 0.043 W.u. and represent typical B(M1) strength in the Ba-Er region. Model calculations using a shell correction approach with the axially deformed Woods-Saxon potential predict for 147Ba an octupole deformed ground state with β3 = 0.11.

A relativistic electron beam, generated by relativistic self-focusing of an ultra-high-intensity laser pulse in a He gas jet, was targeted onto high-Z materials for conversion to high-energy bremsstrahlung. Nuclear reactions in the primary converter materials as well as in secondary and tertiary targets placed directly behind the converter were analyzed with time-resolved γ-spectroscopy. The electron-jet temperature of more than 35 MeV, matching the giant dipole resonances of heavy nuclei, enabled us to efficiently generate photo-induced nuclear reactions. The measured temperatures are significantly higher than suggested by ponderomotive scaling. We supplemented our earlier measurement of the (γ, n) reaction cross section of 129I with a method solely based on nuclear reactions. The photo-induced transmutation yields were increased by two orders of magnitude compared to earlier experiments. Simulations with the Monte Carlo code MCNPX confirm the experimental results .

We report the first successful laser-induced transmutation of 129I, one of the key radionuclides in the nuclear fuel cycle. 129I with a half-life of 15.7 million years is transmuted into 128I with a half-life of 25 min through a (γ, n) reaction using laser-generated Bremsstrahlung. The integral cross-section value for the (γ, n) reaction is determined. These experiments offer a new approach to studying transmutation reactions with neutral and charged particles without resource to nuclear reactors or particle accelerators.

A comprehensive study has been carried out of the yield pattern of fission products formed in fast neutron-induced fission of 233U. The isotope separator on-line facility at Studsvik to the R2-0 nuclear reactor was used for rapid separation of the fission products. At a target temperature of 2250°C fission products of the elements from zinc (Z = 30) to barium (Z = 56) are released, with the exception of yttrium, zirconium, niobium, molybdenum, technetium, ruthenium and rhodium. The individual isotopes are then available for study, implying that an almost complete mapping of the yield distribution can be made. In the analysis, the delay between production and measurement and the overall separator efficiency for three consecutive elements (the one under study and its parent and grand parent) are taken into account. Independent and/or cumulative yields have been obtained for 203 nuclear species, among them 59 isomeric states.

The structural change occurring in between the paraelectric and the ferroelectric phases is investigated by means of X-ray diffraction. Details of the structure in both phases are obtained and the role of the lone pair is discussed in the light of structural data. In agreement with the 2/ m to m symmetry lowering, polar displacements are found within the m plane away from a particular crystallographic direction but antiparallel displacements occur also. These results are discussed in the frame of the phenomenological theory which predicts a particular temperature dependence of the dielectric polarization in this crystal.

In this study the kinetics and phase changes which occurred during the convective drying of a model car paint based on the polyurethane chemistry is described. The competition between the kinetics of the solvent removal and the phase changes, such as the gelation and/or the vitrification of the polyurethane, needs to be taken into account to avoid the defects in the resulting dried coating. The kinetics of polycondensation of a two-component polyurethane based on polyester triol and triisocyanate in a mixture of various solvents was studied as a 100 µm thick layer on sheet molding compound (SMC) and zinc plated steel plates. Differential scanning calorimetry (DSC) and Fourier-Transform infrared spectrometry (FTIR) and thermogravimetric analysis (TGA) during isothermal curings allowed us to determine the rate constants and the activation energies by using second and third order autocatalytic models.

Molecular dynamics simulations have been carried out on fully atomistic models of amorphous polymers. Both bulk structures and thin films were simulated for a wide range of thermoplastics such as PS, PMMA, poly (phenylene-ether) (PPE), poly (etherimide) (PEI). The influence of molecular weight and functional end-groups was investigated. The comparison between “bulk” and “surface” models clearly shows the increase of molecular mobility and a strong decrease in density at the vicinity of free surfaces. Simulated surface tensions, computed by different methods, are generally overestimated as compared to the experimental ones.PVT (Pressure-Volume-Temperature) measurements have been conducted, as another method to compute physical properties of amorphous polymers. From such measurements, cohesive energy densities, interaction parameters, and then interfacial properties, were obtained for various thermoplastics and the corresponding incompatible melts. Such a tool could be used for designing polymer surfaces and interfaces in polymer blends.