Cette thèse porte sur l’étude théorique du transport d’un faisceau intense d’électrons relativistes dans une cible solide. Dans la première partie nous présentons les interprétations théoriques d’une partie des résultats d’une campagne d’expérience portant sur la production et le transport d’électrons relativistes dans une cible d’aluminium. Nous y démontrons la prédominance des e?ets collectifs sur les e?ets collisionels dans la première dizaine de microns de propagation grâce à des modèles de transports déjà existant au début de cette thèse. Ces modèles deviennent insu?sants dans le cas du transport de faisceau dans un isolant. Aussi, dans la deuxième partie, nous présentons un modèle de propagation du faisceau d’électrons relativistes dans un diélectrique incluant l’e?et de l’ionisation de la cible par le faisceau. Nous y quanti?ons les pertes d’énergies des électrons en fonction des paramètres du faisceau et du milieu environnant, et nous démontrons l’existence d’un régime de propagation pour lequel les électrons du plasma ne sont pas à l’équilibre thermodynamique local avec les ions. Ces résultats ont été comparés et con?rmés avec un code cinétique qui prend en compte l’ionisation par champ électrique et par collisions entre les électrons du plasma et les ions. Nous avons examiné la stabilité du faisceau et montré que ce dernier pouvait exciter deux types d’instabilités transverses sur des longueurs de propagation de l’ordre de 30 à 300 µm en fonction de la taille de la perturbation. / This PhD thesis is a theoretical study of high-current relativistic electron beam transport through solid targets. In the ?rst part, we present an interpretation of a part of experimental results of laser– produced electron beam transport in aluminium foil targets. We have estimated the fast electron beam characteristics and we demonstrated that the collective e?ects dominate the transport in the ?rst tens of µm of propagation. These quantitative estimates were done with the transport models already existing at the beginning of this thesis. These models are no longer su?cient in the case a fast electron beam propagation in insulator targets. Thus, in the second part, we have developed a propagation model of the beam that includes the e?ects of electric ?eld ionization and the collisional ionization by the plasma electrons. We present estimates of the electron energy loss induced by the target ionization, and we discuss its dependence on the beam and target parameters. In the case of a relatively low fast electron density, we demonstrated that the beam creates a plasma where the electons are not in a local thermodynamic equilibrium with ions. We have examined the beam stability and we demonstrated that transverse instabilities can be excited by the relativistic electron beam over the propagation distances of 30 - 300 µm depending on the perturbation wavelength.

No presente trabalho foram estudadas as propriedades mecâncias (resistência à tração e porcentagem de alongamento na ruptura e resistência à perfuração), propriedades ópticas, permeabilidade ao gás oxigênio e ao vapor d\'água, migração total em simulante aquoso (ácido acético 3%) e gorduroso (n- heptano), e a formação de produtos voláteis da radiólise, com vistas à avaliar o efeito da radiação ionizante (raios gama e feixe de elétrons) em filmes flexíveis mono e multicamadas comerciais, fabricados no Brasil para a indústria de produtos cárneos. Os filmes estudados foram: um monocamada de polietileno de baixa densidade (LDPE) e um multicamadas coextrusado composto de polietileno de baixa densidade (LDPE), copolímero de etileno e álcool vinílico (EVOH) e poliamida (PA), ou seja, a estrutura: LDPE/EVOH/PA. As irradiações foram realizadas em uma fonte de 60Co do tipo Gammacell e em um acelerador de elétrons do tipo eletrostático (l,5MeV), com doses de até 30 kGy, na temperatura ambiente e presença de ar. As alterações nas propriedades foram avaliadas de acordo com a dose de radiação aplicada, oito dias após a irradiação e novamente, dois a três meses após a irradiação. Os resultados mostraram que as reações de cisão predominaram sobre as reações de reticulação para ambos os filmes estudados, irradiados com raios gama ou com feixe de elétrons. As variações observadas em função da irradiação, nas propriedades avaliadas não limitam a aplicação final desses filmes, uma vez que não ultrapassaram o limite de segurança especificado pelo fabricante em nenhuma dose e período em que foram estudadas. Concluiu-se que os filmes estudados podem ser utilizados, sob o ponto de vista das propriedades avaliadas, como embalagens para produtos pasteurizáveis por radiação e radioesterilizáveis usando irradiadores gama ou aceleradores de elétrons, nas doses de radiação estudadas. / In this study the mechanical properties (tensile strength and percentage elongation at break and penetration resistance), optical properties, gas oxygen and water vapor permeability, the overall migration tests into aqueous food simulant (3% aqueous acetic acid) and fatty food simulant (n-heptane), as well as the formation of volatile radiation product tests were used to evaluate the effects of ionizing radiation (gamma irradiation or electron-beam irradiation) on commercial monolayer and multilayer flexible plastics packaging materials. These films are two typical materials produced in Brazil for industrial meat packaging, one of them is a monolayer low-density polyethylene (LDPE) and other is a multilayer co extruded low-density polyethylene (LDPE), ethylene vinyl alcohol (EVOH), polyamide (PA) based film (LDPE/EVOH/PA). Film samples were irradiated with doses up to 30 kGy, at room temperature and in the presence of air with gamma rays using a 60Co facility and electron beam from 1.5 MeV electrostatic accelerator. Alterations of these properties were detected according to the dose applied initially eight day after irradiation took place and new alterations of these values when the properties were evaluate two to three months after irradiation process. The results showed that scission reactions are higher than cross-linking process for both studied films, irradiated with gamma rays and electron beam. The evaluated properties of the irradiated films were not affected significantly with the dose range and period studied. The monolayer Unipac PE-60 and the multilayer Lovaflex CH 130 films can be used as food packaging materials for food pasteurization and in the sterilization process of by ionizing radiation using a gamma facilities and electron beam accelerators in commercial scale.

No presente trabalho foram estudadas as propriedades mecâncias (resistência à tração e porcentagem de alongamento na ruptura e resistência à perfuração), propriedades ópticas, permeabilidade ao gás oxigênio e ao vapor d\'água, migração total em simulante aquoso (ácido acético 3%) e gorduroso (n- heptano), e a formação de produtos voláteis da radiólise, com vistas à avaliar o efeito da radiação ionizante (raios gama e feixe de elétrons) em filmes flexíveis mono e multicamadas comerciais, fabricados no Brasil para a indústria de produtos cárneos. Os filmes estudados foram: um monocamada de polietileno de baixa densidade (LDPE) e um multicamadas coextrusado composto de polietileno de baixa densidade (LDPE), copolímero de etileno e álcool vinílico (EVOH) e poliamida (PA), ou seja, a estrutura: LDPE/EVOH/PA. As irradiações foram realizadas em uma fonte de 60Co do tipo Gammacell e em um acelerador de elétrons do tipo eletrostático (l,5MeV), com doses de até 30 kGy, na temperatura ambiente e presença de ar. As alterações nas propriedades foram avaliadas de acordo com a dose de radiação aplicada, oito dias após a irradiação e novamente, dois a três meses após a irradiação. Os resultados mostraram que as reações de cisão predominaram sobre as reações de reticulação para ambos os filmes estudados, irradiados com raios gama ou com feixe de elétrons. As variações observadas em função da irradiação, nas propriedades avaliadas não limitam a aplicação final desses filmes, uma vez que não ultrapassaram o limite de segurança especificado pelo fabricante em nenhuma dose e período em que foram estudadas. Concluiu-se que os filmes estudados podem ser utilizados, sob o ponto de vista das propriedades avaliadas, como embalagens para produtos pasteurizáveis por radiação e radioesterilizáveis usando irradiadores gama ou aceleradores de elétrons, nas doses de radiação estudadas. / In this study the mechanical properties (tensile strength and percentage elongation at break and penetration resistance), optical properties, gas oxygen and water vapor permeability, the overall migration tests into aqueous food simulant (3% aqueous acetic acid) and fatty food simulant (n-heptane), as well as the formation of volatile radiation product tests were used to evaluate the effects of ionizing radiation (gamma irradiation or electron-beam irradiation) on commercial monolayer and multilayer flexible plastics packaging materials. These films are two typical materials produced in Brazil for industrial meat packaging, one of them is a monolayer low-density polyethylene (LDPE) and other is a multilayer co extruded low-density polyethylene (LDPE), ethylene vinyl alcohol (EVOH), polyamide (PA) based film (LDPE/EVOH/PA). Film samples were irradiated with doses up to 30 kGy, at room temperature and in the presence of air with gamma rays using a 60Co facility and electron beam from 1.5 MeV electrostatic accelerator. Alterations of these properties were detected according to the dose applied initially eight day after irradiation took place and new alterations of these values when the properties were evaluate two to three months after irradiation process. The results showed that scission reactions are higher than cross-linking process for both studied films, irradiated with gamma rays and electron beam. The evaluated properties of the irradiated films were not affected significantly with the dose range and period studied. The monolayer Unipac PE-60 and the multilayer Lovaflex CH 130 films can be used as food packaging materials for food pasteurization and in the sterilization process of by ionizing radiation using a gamma facilities and electron beam accelerators in commercial scale.

Made available in DSpace on 2014-10-09T12:42:10Z (GMT). No. of bitstreams: 0 / Made available in DSpace on 2014-10-09T14:04:49Z (GMT). No. of bitstreams: 0 / Dissertação (Mestrado) / IPEN/D / Instituto de Pesquisas Energeticas e Nucleares - IPEN-CNEN/SP

Orientadores: Antonio J. Ramirez, Maria Clara F. Ierardi / Dissertação (mestrado) - Universidade Estadual de Campinas, Faculdade de Engenharia Mecanica / Made available in DSpace on 2018-08-09T21:56:05Z (GMT). No. of bitstreams: 1 Seraphim_RafaelMolena_M.pdf: 6485115 bytes, checksum: 380cfffee5fa982ec74a9cdc78c88e3a (MD5) Previous issue date: 2007 / Resumo: O avanço cientifico no estudo de átomos, moléculas e proteínas tem recebido uma contribuição significativa dos aceleradores de partículas, que em sua grande maioria são utilizados para a geração de radiação síncrotron. Por isso, o aprimoramento destas máquinas mostra-se de extrema importância para manter a ciência em seu contínuo avanço. O sistema de vácuo destas máquinas apresenta-se como um importante parâmetro para o seu bom funcionamento e melhorias neste promovem diretamente melhorias na qualidade da radiação síncrotron gerada. Logo, o desenvolvimento deste trabalho teve como principal objetivo o estudo das juntas soldadas das câmaras de vácuo que compõem o acelerador do Laboratório Nacional de Luz Síncrotron (LNLS). As juntas foram preparadas com o processo de soldagem GTAW (Gás Tungsten Arc Welding) mediante a utilização de diferentes gases de proteção, como Argônio, Hélio e Nitrogênio, e misturas entre estes. Os estudos concentraram-se na análise da influência dos gases de proteção na dessorção de gases das juntas soldadas. Para a caracterização destas utilizaram-se as técnicas de análise de superfícies Dessorção Estimulada por Elétrons (DEE) e Dessorção Estimulada por Fótons (DEF). Adicionalmente, realizou-se um estudo comparativo entre as duas técnicas buscando-se estabelecer relações entre os resultados fornecidos pelas mesmas. Os resultados mostraram que a dessorção de gases independe do gás de proteção de soldagem, mas depende sim do nível de oxidação das juntas soldadas, as quais podem apresentar altas taxas de dessorção caso estejam muito oxidadas e os óxidos não sejam camadas contínuas. Em conclusão pode-se dizer que as juntas soldadas para câmaras de vácuo de aceleradores de partículas devem apresentar baixos níveis de oxidação, e apesar das semelhanças encontradas entre a DEE e a DEF é aconselhável utilizar a DEF para a caracterização de superfícies para trabalharem com radiação síncrotron / Abstract: The scientific advance of atoms, molecules and proteins studies has received an important contribution from particle accelerators, which are mainly used to generate synchrotron radiation. Hence, the improvement of these machines is necessary to maintain the continuous advance of science. One of the key components for the adequate operation of these accelerators is the vacuum system. Thus, its improvement directly impacts on the quality of the generated synchrotron radiation. Therefore, the principal purpose of this work is to study the gas desorption from the welding joints on the particle accelerators vacuum chambers. The welds were prepared using the GTAW (Gas Tungsten Arc Welding) process with different shielding gases, as argon, helium and nitrogen, and some mixtures of them. The study concentrated on the analysis of the shielding gas influence on the gas desorption from the welded joints. The gas desorption of the joints was evaluated using Electron Stimulated Desorption (ESD) and Photon Stimulated Desorption (PSD). In addition, it was carried out a comparative study between both desorption techniques to establish relationships between the results provided by them. The results showed that the gas desorption from the welding joints does not depend on the welding shielding gas, but on the oxidation level of the joint, which can present high desorption yield if it is highly oxidized and these oxides are not a continuous film. Therefore, it is advisable to minimize the oxidation during welding of vacuum chambers for particle accelerators. Regarding the comparison between ESD and PSD they were found some similarities. However, PSD will have better performance characterizing surfaces that will be exposed to synchrotron radiation / Mestrado / Materiais e Processos de Fabricação / Mestre em Engenharia Mecânica

Made available in DSpace on 2014-10-09T12:42:10Z (GMT). No. of bitstreams: 0 / Made available in DSpace on 2014-10-09T14:04:49Z (GMT). No. of bitstreams: 0 / No campo da medicina, a radiação ionizante é utilizada tanto para fins terapêuticos como para fins diagnósticos, englobando assim um amplo intervalo de doses de diferentes tipos de radiações. Para assegurar que a finalidade da prática esteja sendo alcançada, são necessários estudos detalhados de detectores e dispositivos que respondam a diferentes tipos de radiações. Neste trabalho foi realizada a caracterização dosimétrica de amostras de BeO utilizando as técnicas de termoluminescência (TL) e luminescência opticamente estimulada (OSL) comparando-se as respostas para as radiações alfa, beta e X e propondose um sistema adequado para sua utilização em monitoração de feixes destas radiações. Dentre os principais resultados obtidos estão: alta sensibilidade à radiação beta para ambas as técnicas empregadas, boa reprodutibilidade das respostas TL e OSL (coeficientes de variação inferiores a 5%), uma dependência energética máxima da radiação X de 28% para técnica TL, e de apenas 7% para a técnica OSL, dentro dos intervalos de energia estudados. As características dosimétricas obtidas neste trabalho mostram a possibilidade de aplicação das amostras de BeO em dosimetria das radiações ionizantes X, alfa e beta, considerando os intervalos de dose empregados, pelas técnicas de TL e OSL. Pelos resultados obtidos, as amostras de BeO apresentaram sua utilização potencial para dosimetria de feixes de radiodiagnóstico e radioterapia. / Dissertação (Mestrado) / IPEN/D / Instituto de Pesquisas Energeticas e Nucleares - IPEN-CNEN/SP

Submitted by Maria Eneide de Souza Araujo (mearaujo@ipen.br) on 2017-03-10T16:49:56Z No. of bitstreams: 0 / Made available in DSpace on 2017-03-10T16:49:56Z (GMT). No. of bitstreams: 0 / A saúde do meio ambiente vem sendo comprometida devido ao descarte incorreto de produtos e seus subprodutos. Dentre os contaminantes emergentes encontram-se os fármacos, causadores de problemas ambientais por serem descartados no meio ambiente através dos efluentes. As técnicas convencionais de tratamento são insuficientes na remoção de diversos fármacos, por apresentarem resíduos resistentes e baixa biodegradabilidade. Sendo assim os processos oxidativos avançados vêm sendo estudados como alternativa para o tratamento de diferentes tipos de efluentes. O objetivo desse trabalho foi aplicar o processo de irradiação com feixe de elétrons para reduzir os efeitos tóxicos do propranolol, e de sua mistura com cloridrato de fluoxetina, em solução aquosa. Foram realizados ensaios ecotoxicológicos com o fármaco propranolol, e de sua mistura com o cloridrato de fluoxetina, utilizando como organismos-teste o microcrustáceo Daphnia similis, e a bactéria Vibrio fischeri. Observamos que o organismo D. similis mostrou-se mais sensível as amostras de fármacos quando comparado à bactéria V.fischeri. Após serem submetidas ao tratamento com radiação ionizante, todas as doses aplicadas para o propranolol e a mistura, mostraram significativa redução de toxicidade, tendo como organismo-teste D. similis. Para a bactéria V. fischeri apenas na dose de 5,0 kGy foi verificada a redução da toxicidade para o fármaco propranolol. Quanto à mistura dos fármacos, apenas as doses de 2,5 e 5,0 kGy apresentaram eficiência de remoção da toxicidade. A dose 5,0 kGy mostrou-se a melhor, apresentando redução de 79,94% para D. similis, e 15,64% para V. fischeri, quando expostas ao fármaco propranolol. Quanto à mistura, apresentou 81,59% e 26,93%, para D.similis e V.fischeri, respectivamente. / Dissertação (Mestrado em Tecnologia Nuclear) / IPEN/D / Instituto de Pesquisas Energeticas e Nucleares - IPEN-CNEN/SP

Les lasers de puissance permettent depuis une dizaine d'années de produire des faisceaux de particules accélérées dans lesquels quelques 1012 électrons, protons sont accélérés en quelques ps. Nous avons simulé et développé des diagnostiques, utilisant l'activation nucléaire, pour qualifier les distributions angulaire et en énergie des faisceaux de particules générés. Les techniques de caractérisation sont présentées et illustrées à l'aide des résultats obtenus dans différentes expériences réalisées auprès des lasers de puissance. Nous envisageons d'utiliser ces faisceaux pour exciter des états nucléaires dans des environnements plasma. Celui-ci peut en effet influencer des caractéristiques intrinsèques du noyau comme la durée de vie de certains états isomériques. Dans le cadre de la préparation de telles expériences, nous avons mesuré la section efficace de la réaction (g,n) permettant de produire l'état isomérique du 84Rb à 463 keV d'énergie d'excitation, à l'aide de l'accélérateur ELSA du CEA/DIF de Bruyères-le-Châtel.

Among various nanomaterials, metal nanoparticles are the widely studied ones because of their pronounced distinct properties arising in the nanometer size regime, which can be tailored easily by tuning predominantly their size and shape. During the past few decades, scientists are engaged in developing new synthetic methodologies for the synthesis of metal nanoparticles which can be divided into two broad categories: i) top-down approach, utilizing physical methods and ii) bottom-up approach, employing chemical methods. As the chemical methods offer better control over particle size, numerous chemical methods have been developed to obtain metal nanoparticles with narrow size distribution. However, these two approaches have their own merits and demerits; they are not complementary to each other and also not sustainable for real time applications. Recent focus on the synthesis of metal nanoparticles is towards the development of green and sustainable synthetic methodologies. A solid state route is an exciting prospect in this direction because it eliminates usage of organic solvents thus, makes the overall process green and at the same time leads to the realization of large quantity of the materials, which is required for many applications. However, the major obstacle associated with the development of a solid state synthetic route is the lack of fundamental understanding regarding the formation mechanism of the nanoparticles in the solid state. Additionally, due to the heterogeneity present in the solid mixture, it is very difficult to ensure the proximity between the capping agent and nuclei which plays the most decisive role in the growth process. Recently, employment of amine–borane compounds as reducing agents emerged as a better prospect towards the development of sustainable synthetic routes for metal nanoparticles because they offer a variety of advantages over the traditional borohydrides. Being soluble in organic medium, amine– borane allows the reaction to be carried out in a single phase and due to its mild reducing ability a much better control over the nucleation and growth processes is realized. However, the most exciting feature of these compounds is that their reducing ability is not only limited to the solution state, they can also bring out the reduction of metal ions in the solid state. With the availability of a variety of amine–boranes of varying reducing ability, it opens up a possibility to modulate the nanostructure in both solid and solution states by a judicious choice of reducing agent. Although our current understanding regarding the growth behavior of nanoparticles has advanced remarkably, however, most often it is some classical model which is invoked to understand these processes. With the recent developments in in situ transmission electron microscopy techniques, it is now possible to unravel more complex growth trajectories of nanoparticles. These studies not only expand the scope of the present knowledge but also opens up possibilities for many future developments. Objectives • To develop an atom economy solid state synthetic methodology for the synthesis of metal nanoparticles employing amine–boranes as reducing agents. • To gain a mechanistic insight into the formation mechanisms of nanoparticles in the solid state by using amine–boranes with differing reducing ability. • Synthesis of bimetallic nanoparticles as well as supported metal nanoparticles in the solid state using ammonia borane as the reducing agent. • To develop a new in situ seeding growth methodology for the synthesis of core@shell nanoparticles composed of noble metals by employing a very weak reducing agent, trimethylamine borane and their transformation to their thermodynamically stable alloy counterparts. • Synthesis of highly monodisperse ultra-small colloidal calcium nanoparticles with different capping agents such as hexadecylamine, octadecylamine, poly(vinylpyrrolidone) and a combination of hexadecylamine/poly(vinylpyrrolidone) using the solvated metal atom dispersion (SMAD) method. To study the coalescence behavior of a pair of calcium nanoparticles under an electron beam by employing in situ TEM technique. Significant results An atom economy solid state synthetic route has been developed for the synthesis of metal nanoparticles from simple metal salts using amine–boranes as reducing agents. Amine–borane plays a dual role here: acts as a reducing agent thus brings out the reduction of metal ions and decomposes simultaneously to generate B-N based compounds which acts as a capping agent to stabilize the particles in the nanosize regime. This essentially minimizes the number of reagents used and hence simplifying and eliminating the purification procedures and thus, brings out an atom economy to the overall process. Additionally, as the reactions were carried out in the solid state, it eliminates use of organic solvents which have many adverse effects on the environment, thus makes the synthetic route, green. The particle size and the size distribution were tuned by employing amine–boranes with differing reducing abilities. Three different amine–boranes have been employed: ammonia borane (AB), dimethylamine borane (DMAB), and trimethylamine borane (TMAB) whose reducing ability varies as AB > DMAB >> TMAB. It was found that in case of AB, it is the polyborazylene or BNHx polymer whereas, in case of DMAB and TMAB, the complexing amines act as the stabilizing agents. Several controlled studies also showed that the rate of addition of metal salt to AB is the crucial step and has a profound effect on the particle size as well as the size distribution. It was also found that an optimum ratio of amine–borane to metal salt is important to realize the smallest possible size with narrowest size distribution. Whereas, use of AB and TMAB resulted in the smallest sized particles with best size distribution, usage of DMAB provided larger particles that are also polydisperse in nature. Based on several experiments along with available data, the formation mechanism of metal nanoparticles in the solid state has been proposed. Highly monodisperse Cu, Ag, Au, Pd, and Ir nanoparticles were realized using the solid state route described herein. The solid state route was extended to the synthesis of bimetallic nanoparticles as well as supported metal nanoparticles. Employment of metal nitrate as the metal precursor and ammonia borane as the reducing agent resulted in highly exothermic reaction. The heat evolved in this reaction was exploited successfully towards mixing of the constituent elements thus allowing the alloy formation to occur at much lower temperature (60 oC) compared to the traditional solid state metallurgical methods (temperature used in these cases are > 1000 oC). Synthesis of highly monodisperse 2-3 nm Cu/Au and 5-8 nm Cu/Ag nanoparticles were demonstrated herein. Alumina and silica supported Pt and Pd nanoparticles have also been prepared. Use of ammonia borane as the reducing agent in the solid state brought out the reduction of metal ions to metal nanoparticles and the simultaneous generation of BNHx polymer which encapsulates the metal (Pt and Pd) nanoparticles supported on support materials. Treatment of these materials with methanol resulted in the solvolysis of BNHx polymer and its complete removal to finally provide metal nanoparticles on the support materials. An in situ seeding growth methodology for the synthesis of bimetallic nanoparticles with core@shell architecture composed of noble metals has been developed using trimethylamine borane (TMAB) as the reducing agent. The key idea of this synthetic procedure is that, TMAB being a weak reducing agent is able to differentiate the smallest possible window of reduction potential and hence reduces the metal ions sequentially. A dramatic solvent effect was noted in the preparation of Ag nanoparticles: Ag nanoparticles were obtained at room temperature when dry THF was used as the solvent whereas, reflux condition was required to realize the same using wet THF as the solvent. However, no such behavior was noted in the preparation of Au and Pd nanoparticles wherein Au and Pd nanoparticles were obtained at room temperature and reflux conditions, respectively. This difference in reduction behavior was successfully exploited to synthesize Au@Ag, Ag@Au, and Ag@Pd nanoparticles. All these core@shell nanoparticles were further transformed to their alloy counterparts under very mild conditions reported to date. Highly monodisperse, ultrasmall, colloidal Ca nanoparticles with a size regime of 2-4 nm were synthesized using solvated metal atom dispersion (SMAD) method and digestive ripening technique. Hexadecylamine (HDA) was used as the stabilizing agent in this case. Employment of capping agent with a longer chain length, octadecylamine afforded even smaller sized particles. However, when poly(vinylpyrrolidone) (PVP), a branched chain polymer was used as the capping agent, agglomerated particles were realized together with small particles of 3-6 nm. Use of a combination of PVP and HDA resulted in spherical particles of 2-3 nm size with narrow size distribution. Growth of Ca nanoparticles via colaesence mechanism was observed under an electron beam. Employing in situ transmission electron microscopy technique, real time coalescence between a pair of Ca nanoparticles were detected and details of coalescence steps were analyzed.

Les lasers de puissance permettent depuis une dizaine d'années de produire des faisceaux de particules accélérées dans lesquels quelques 1012 électrons, protons sont accélérés en quelques ps. Nous avons simulé et développé des diagnostiques, utilisant l'activation nucléaire, pour qualifier les distributions angulaire et en énergie des faisceaux de particules générés. Les techniques de caractérisation sont présentées et illustrées à l'aide des résultats obtenus dans différentes expériences réalisées auprès des lasers de puissance. Nous envisageons d'utiliser ces faisceaux pour exciter des états nucléaires dans des environnements plasma. Celui-ci peut en effet influencer des caractéristiques intrinsèques du noyau comme la durée de vie de certains états isomériques. Dans le cadre de la préparation de telles expériences, nous avons mesuré la section efficace de la réaction (g,n) permettant de produire l'état isomérique du 84Rb à 463 keV d'énergie d'excitation, à l'aide de l'accélérateur ELSA du CEA/DIF de Bruyères-le-Châtel. / Since the laser tens years, the Ultra High Intensity Laser offer the opportunities to produce accelerated particle beams with contain more than 1012 electrons, protons accelerated into few ps. We have simulated and developed some diagnostics based on the nuclear activation to characterize both the angular and the energy distribution of the particle beams produced with intense lasers. The characterization methods which are presented and illustrated by the means of results obtained in different experiments. We would use the particle beams produced to excite nuclear state in a plasma environment. It can modify intrinsic characteristics of the nuclei such as the half-life of some isomeric state. To prepare this kind of experiments, we have measured the nuclear reaction cross section (g,n) to produce the isomeric state of the 84Rb, which has an excitation energy around 463 keV, with the electron accelerator ELSA of CEA/DIF in Bruyères-le-Châtel.