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AbstractAbstract
[en] Radioactive waste management is a rather difficult issue. In order to reduce the volume of waste storage, particularly the Cs 135 (radioactive half-life 2.3 106 years), liquid-liquid extraction experiments have shown that crown calixarenes were able to selectively extract cesium cation in wastes. However, the stability under radiolysis of this type of macrocycle is unknown and is the theme of this thesis. Through the coupling of electro-spray and mass spectrometry, the selectivity of crown calixarenes for cesium has been confirmed. The necessity to optimize operating conditions during the utilization of this ionization mode was acknowledged for a correct interpretation of mass spectrum. The solvent nature, source temperature, applied voltage on the cone, gaseous phase stability and species ionization desorption rate are indeed parameters that should be taken into account. Experiments show that the solution species stability is inverse to the one in gaseous phase. In a solution, species stability is linked to the nature of the solvent (solvating power) whereas in gaseous phase, it is linked to the cationic affinity. In the current radiolysis conditions it has been demonstrated that calixarenes have a stable structure. Degradation products are very largely substitution products and do not hinder the caesium cation complexing. Concerning the quantitative aspect, an estimation was produced, however results are not satisfying: reference product synthesis is in fact necessary in order to establish calibration curves that will allow to precisely dose the various components derived from radiolysis
[fr]
La gestion des dechets radioactifs est un lourd et difficile probleme dans le milieu nucleaire. Afin de reduire le volume des dechets a stocker, en particulier du Cs 135 (periode radioactive 2.3 106 ans), des experiences en extraction liquide-liquide ont montre que les calixarenes couronnes etaient capables d'extraire selectivement le cation cesium des dechets. Par contre, la stabilite sous radiolyse de ce type de macrocycle n'est pas connu et fait l'objet de cette these. Par l'utilisation du couplage electrospray/spectrometrie de masse, la selectivite des calixarenes couronnes vis a vis du cesium a pu etre confirmee. La necessite d'optimiser les conditions operatoires lors de l'utilisation de ce mode d'ionisation a ete mis en evidence en vue d'une interpretation correcte du spectre de masse. En effet, la nature du solvant, la temperature de la source, la tension appliquee sur le cone, la stabilite en phase gazeuse et le rendement d'ionisation desorption des especes sont des parametres a prendre en compte. Les experiences montrent que la stabilite des especes en solution est inverse a celle en phase gazeuse. En solution, la stabilite des especes est liee a la nature du solvant (pouvoir solvatant) tandis qu'en phase gazeuse, elle est liee a l'affinite cationique. Dans les conditions de radiolyse utilisees, il a ete demontre que les calixarenes possedent une structure stable. Les produits de degradation sont tres majoritairement des produits de substitution et ne genent pas la complexation du cation cesium. Pour ce qui est de l'aspect quantitatif, une estimation a ete realisee mais les resultats ne sont pas satisfaisants. En effet, la synthese de produits de reference est necessaire afin d'etablir des droites de calibration qui permettront de doser avec precision les differents composes issus de la radiolyse. (auteur)Original Title
Complexation des cations alcalins par les calixarenes en electrospray/spectrometrie de masse, specificite pour le cesium, influence de la solvatation sur les especes ioniques et stabilite radiolytique du milieu complexant
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31 May 2000; 274 p; 160 refs.; Available from the INIS Liaison Officer for France, see the 'INIS contacts' section of the INIS website for current contact and E-mail addresses: http://www.iaea.org/INIS/contacts/; These Docteur de l'Universite de Paris 6, Specialite: chimie analytique
Record Type
Report
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Thesis/Dissertation
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AROMATICS, BETA DECAY RADIOISOTOPES, BETA-MINUS DECAY RADIOISOTOPES, CEA, CESIUM ISOTOPES, CHARGED PARTICLES, CHEMICAL RADIATION EFFECTS, CHEMICAL REACTIONS, CONDENSED AROMATICS, DECOMPOSITION, ETHERS, EXTRACTION, FRENCH ORGANIZATIONS, INTERMEDIATE MASS NUCLEI, IONS, ISOMERIC TRANSITION ISOTOPES, ISOTOPES, MANAGEMENT, MINUTES LIVING RADIOISOTOPES, NATIONAL ORGANIZATIONS, NUCLEI, ODD-EVEN NUCLEI, ORGANIC COMPOUNDS, ORGANIC OXYGEN COMPOUNDS, PROCESSING, RADIATION EFFECTS, RADIOACTIVE WASTE MANAGEMENT, RADIOISOTOPES, SEPARATION PROCESSES, SORPTION, SPECTROSCOPY, WASTE MANAGEMENT, WASTE PROCESSING, YEARS LIVING RADIOISOTOPES
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