Thesis (Ph. D.)--University of Wisconsin--Madison, 1970. / Typescript. Vita. Description based on print version record. Includes bibliographical references (leaves 98-106).

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A number of leaks of radioactive liquors to ground are known to have occurred from several plant buildings, vaults and disposal trenches within and around the Separation area at the Sellafield nuclear site over the past 50 years1. The most significant of these leaks have occurred from the Magnox Silo, the Caesium Extraction Plant, the Magnox Reprocessing Pump House, the Sludge Storage Tanks, the Burial Pits and the Medium Active Evaporation and Thermal Denitration Plant. The radioactive contamination will be accompanied by other components of spent fuel reprocessing, including inorganic salts from neutralised acids, solvents and other organic compounds along with the typical contaminants commonly associated with large industrial activity such as heavy metals, fuel, oils, degreasing agents etc. The research in this thesis describes the effects of common industrial contaminants on the behaviour of Cs and Sr sorption to bentonite and montmorillonite clay minerals. Batch sorption experiments of Cs and Sr uptake onto bentonite and montmorillonite in a number of complex systems were investigated as follows: 1. Initial batch sorption experiments investigating the normal behaviour of the clay minerals. 2. Introduction of anthropogenic organic ligands EDTA, NTA and picolinic acid into the system and their influence on Sr and Cs uptake. 3. Time dependent studies investigating the effect that residence time of the anthropogenic organic ligands has on the sorption properties of montmorillonite and bentonite. 4. Quaternary systems where simulant Magnox sludge equilibrated water, at a number of concentrations, was introduced to ternary systems containing anthropogenic organic ligands. 5. Time dependent studies investigating the effect of hydrocarbons TCE, toluene and naphthalene on the uptake of Cs and Sr to bentonite and montmorillonite. The batch sorption experiments show that the presence of anthropogenic organic ligands reduces the uptake of Cs and Sr by both montmorillonite and bentonite. It is also shown that the presence of simulant Magnox sludge in quaternary systems can also reduce the uptake of Cs and Sr, with significant reductions in sorption observed for Sr sorption in EDTA quaternary systems. Further, the uptake of Cs and Sr to bentonite and montmorillonite appears to decrease with increasing anthropogenic organic ligand residence time. This suggests that the ligands are altering the surface of the clay minerals reducing the number of available binding sites. The influence of hydrocarbons shows a significant decrease in sorption after 3 months for Cs and Sr sorption to montmorillonite. There were no further significant changes for all other hydrocarbon systems investigated.

Cette thèse s’inscrit dans le cadre du projet « NanoFret », financé par L’Agence Nationale de Recherche (ANR). Elle visait à développer de nouveaux complexes luminescents de lanthanides dans le but de les utiliser dans le diagnostic du choc septique. Le complexe idéal devait posséder une longueur d’onde d’excitation élevée, un temps de vie de luminescence long et une brillance élevée. Nos complexes devaient présenter un nombre important de groupements chromophoriques. Nous avons travaillé sur plusieurs types de ligands afin d’améliorer ces propriétés. La recherche sur les ligands dérivés du cyanophénol a permis d’obtenir un ligand qui est utilisé comme sensibilisateur des nanoparticules « ultra-brillantes ». Les ligands poly-picolinates sont des ligands très intéressants mais nécessite encore d’être perfectionnés afin d’obtenir la géométrie de complexation souhaitée. Les complexes des ligands benzyle-cyclène et pyridine-bispyrazole sont de bonnes plateformes pour la synthèse de complexes luminescents de lanthanides. Les perspectives de ces travaux concernent l’optimisation des chromophores afin d’atteindre des longueurs d’ondes d’excitation supérieures. / This work is part of the "NanoFret" project, funded by the “Agence National de Recherche” (ANR). It aimed to develop new luminescent lanthanide complexes for their use in the diagnosis of septic shock. The ideal complex should have a high excitation wavelength, a long luminescence lifetime and high brightness. The complexes should then present a significant number of chromophoric groups. We worked on several types of ligands to improve these properties. Research on derivatives of cyanophenol ligands allowed to get a ligand used as a sensitizer for "ultra-bright" Ln(III) nanoparticles. Poly-picolinates ligands are very interesting ligands but still needs to be improved in order to obtain the desired complexing geometry. Complexes of benzyl-cyclen ligands and pyridine-bispyrazole ligands are good platforms for the synthesis of luminescent lanthanide complexes. The perspectives of these works concern the optimization of chromophores to achieve higher excitation wavelengths.

Characterising the geochemistry and speciation of major contaminant radionuclides is crucial in order to understand their behaviour and migration in complex environmental systems. Organic complexing agents used in nuclear decontamination have been found to enhance migration of radionuclides at contaminated sites; however, the mechanisms of the interactions in complex environments are poorly understood. In this work, radionuclide speciation and sorption behaviour were investigated in order to identify interactions between four key radionuclides with different oxidation states (Cs(I) and Sr(II) as important fission products; Th(IV) and U(VI) as representative actinides), three anthropogenic organic complexing agents with different denticities (EDTA, NTA and picolinic acid as common co-contaminants), and natural sand (as simple environmental solid phase). A UV spectrophotometric and an IC method were developed to monitor the behaviour of EDTA, NTA and picolinic acid in the later experiments. The optimised methods were simple, applied widely-available instrumentation and achieved the necessary analytical figures of merit to allow a compound specific determination over variable background levels of DOC and in the presence of natural cations, anions and radionuclides. The effect of the ligands on the solubility of the radionuclides was studied using a natural sand matrix and pure silica for comparison of anions, cations and organic carbon. In the silica system, the presence of EDTA, NTA and, to a lesser extent, picolinic acid, showed a clear net effect of increasing Th and U solubility. Conversely, in the sand system, the sorption of Th and U was kinetically controlled and radionuclide complexation by the ligands enhanced the rate of sorption, by a mechanism identified as metal exchange with matrix metals. Experiments in which excess EDTA, NTA and picolinic acid (40 – 100 fold excess) were pre-equilibrated with Th and U prior to contact with the sand, to allow a greater degree of radionuclide complex formation, resulted in enhanced rates of sorption. This confirmed that the radionuclide complexes interacted with the sand surface more readily than uncomplexed Th or U. Overall this shows that Th and U mobility would be lowered in this natural sand by the presence of organic co-contaminants. In contrast, the complexation of Sr with the complexing agents was rapid and the effect of the ligands was observed as a net increase on Sr solubility (EDTA, picolinic acid) or sorption (NTA). As expected, Cs did not interact with the ligands, and showed rapid sorption kinetics. Finally, ESI-MS was used to study competitive interactions in the aqueous Th-Mn-ligand ternary system. Quantification presented a challenge, however, the careful approach taken to determine the signal correction allowed the competitive interactions between Mn and Th for EDTA to be studied semi-quantitatively. In an EDTA limited system, Th displaced Mn from the EDTA complex, even in the presence of a higher Mn concentration, which was consistent with the higher stability constant of the Th-EDTA complex.

<p>Diabetes mellitus is one of the most threatening epidemics of modern times with rapidly increasing incidence. Vanadium and peroxovanadium compounds have been shown to exert insulin–like actions and, in contrast to insulin, are orally applicable. However, problems with side–effects and toxicity remain. The exact mechanism(s) by which these compounds act are not yet fully known. Thus, a better understanding of the aqueous chemistry of vanadates and peroxovanadates in the presence of various (bio)ligands is needed.</p><p>The present thesis summarises six papers dealing mainly with aqueous speciation in different vanadate – and peroxovanadate – ligand systems of biological and medical relevance. Altogether, five ligands have been studied, including important blood constituents (lactate, citrate and phosphate), a potential drug candidate (picolinic acid), and a dipeptide (alanyl serine) to model the interaction of (peroxo)vanadate in the active site of enzymes. Since all five ligands have been studied both with vanadates and peroxovanadates, the number of systems described in the present work is eleven, including the vanadate – citrate – lactate mixed ligand system. The pH–independent formation constants have been determined for 33 ternary vanadate – ligand, 41 quaternary peroxovanadate – ligand and two vanadate – mixed ligand species in addition to the p<i>K</i>_a values of all five ligands. These constants have been used to model physiological conditions, and the biomedical relevance of the different species is discussed.</p><p>The studies have been performed at 25 ºC in the physiological medium of 0.150 M Na(Cl), i.e. the ionic strength of human blood. No buffers have been used, and wide pH–ranges have usually been covered. The applied experimental techniques comprise mostly ⁵¹V NMR and potentiometry, but ³¹P, ¹³C, ¹H and ¹⁴N NMR as well as EPR and ESI–MS have also been used to gain additional information. Multimethod data have been treated by the least–squares program LAKE and modelling has been carried out by the software package WinSGW.</p><p>Whenever possible, solution structures of the species have been proposed. In addition, simple biological tests have been carried out to determine the stability of the formed peroxovanadate complexes in the presence of human catalase. A brief comparison is given of the different vanadate – ligand and peroxovanadate – ligand systems with emphasis on observed trends and general features.</p>

Diabetes mellitus is one of the most threatening epidemics of modern times with rapidly increasing incidence. Vanadium and peroxovanadium compounds have been shown to exert insulin–like actions and, in contrast to insulin, are orally applicable. However, problems with side–effects and toxicity remain. The exact mechanism(s) by which these compounds act are not yet fully known. Thus, a better understanding of the aqueous chemistry of vanadates and peroxovanadates in the presence of various (bio)ligands is needed. The present thesis summarises six papers dealing mainly with aqueous speciation in different vanadate – and peroxovanadate – ligand systems of biological and medical relevance. Altogether, five ligands have been studied, including important blood constituents (lactate, citrate and phosphate), a potential drug candidate (picolinic acid), and a dipeptide (alanyl serine) to model the interaction of (peroxo)vanadate in the active site of enzymes. Since all five ligands have been studied both with vanadates and peroxovanadates, the number of systems described in the present work is eleven, including the vanadate – citrate – lactate mixed ligand system. The pH–independent formation constants have been determined for 33 ternary vanadate – ligand, 41 quaternary peroxovanadate – ligand and two vanadate – mixed ligand species in addition to the pKa values of all five ligands. These constants have been used to model physiological conditions, and the biomedical relevance of the different species is discussed. The studies have been performed at 25 ºC in the physiological medium of 0.150 M Na(Cl), i.e. the ionic strength of human blood. No buffers have been used, and wide pH–ranges have usually been covered. The applied experimental techniques comprise mostly 51V NMR and potentiometry, but 31P, 13C, 1H and 14N NMR as well as EPR and ESI–MS have also been used to gain additional information. Multimethod data have been treated by the least–squares program LAKE and modelling has been carried out by the software package WinSGW. Whenever possible, solution structures of the species have been proposed. In addition, simple biological tests have been carried out to determine the stability of the formed peroxovanadate complexes in the presence of human catalase. A brief comparison is given of the different vanadate – ligand and peroxovanadate – ligand systems with emphasis on observed trends and general features.