Considering the worldwide growing discharge of minor actinides and the current need for geological disposal facilities for radioactive waste, this work provides a contribution to the safety case concerning Np transport if it would be released from deep repository sites and moving from alkaline cement conditions (near-field) to more neutral environmental conditions (far-field). The reducing conditions in a nuclear waste repository render neptunium tetravalent, which is assumed to be immobile in aqueous environment due to the low solubility solution of Np(IV). For tetravalent actinide nuclides, the most significant transport should occur via colloidal particles. This work demonstrates the formation of intrinsic neptunium dioxide nanocrystals and amorphous Np(IV) silica colloids under environmentally relevant conditions. The dissociation of the initial soluble Np(IV) complex (i.e. [Np(IV)(CO3)5]6-) induces the intrinsic formation of nanocrystalline NpO2 in the solution phase. The resulting irregularly shaped nanocrystals with an average size of 4 nm exhibit a face-centered cubic (fcc), fluorite-type structure (space group ). The NCs tend to agglomerate under ambient conditions due to the weakly charged hydrodynamic surface at neutral pH (zetapotential ~0 mV). The formation of micron-sized agglomerates, composed of nanocrystals of 2-5 nm in size, and the subsequent precipitation cause immobilization of the major amount of Np(IV) in the Np carbonate system. Agglomeration of NpO2 nanocrystals in dependence on time was indicated by PCS and UV-vis absorption spectroscopy with the changes of baseline characteristics and absorption maximum at 742 nm. Hitherto, unknown polynuclear species as intermediate species of NpO2 nanocrystal formation were isolated from solution and observed by HR-TEM. These polynuclear Np species appear as dimers, trimers and hexanuclear compounds in analogy with those reported for other actinides. Intrinsic formation of NpO2 (fcc) nanocrystals under ambient environmental conditions is prevented by admixing silicic acid: amorphous Np(IV) silica colloids are formed when silicate is present in carbonate solution. Herein, the initial molar ratio of Si to Np in solution lead to the formation of Np(IV) silica particles of different composition and size where Si content determines the structure and stability of resulting colloids. Implications for different electronic structures of Np(IV) in dependence on Si content in the solid phase are given by the shift of the absorption maximum at 742 nm characteristic for Np(IV) colloids, silica excess of 5 times the magnitude of Si to Np reveal a redshift up to 6 nm in the colloidal UV-vis spectrum. Precipitation of Np(IV) particles in the ternary system results in a different coordination sphere of Np(IV) compared to the binary system, and the incorporation of Si into internal structure of Np(IV) silica colloids in coffinite-like structure is confirmed by EXAFS. TEM confirms different kinds of particle morphologies in dependence on the silica content. Silica-poor systems reveal porous particles in the micron-range which consist of irregular cross-linked hydrolyzed Np(IV) silica compartments with pores <15 nm. In contrast, long-term stabilized and silica-enriched systems are characterized by isolated particles with an average particle size of 45 nm. Agglomerates of such isolated Np(IV) silica particles appear as consolidated amorphous solids with a densely closed surface and exhibit no internal fractures. The latter mentioned morphology of Np(IV) silica particles might facilitate the migration behavior of Np(IV) in a stabilized colloidal form under environmental conditions. The silica-enriched particles with densely closed surface are long-term stabilized as colloidal dispersion (>1 year) due to repulsion effects caused by significant surface charge. Particles synthesized from Si/Np = 9/1 carry exclusively negative surface charge in nearly the whole pH range from pH 3 to pH 10 with zetapotential = (-) 5 to (-) 30 mV. The zeta potentials of all particle systems containing silica are significantly shifted to more negative values below pH 7 where the isoelectrical point shifts from pH = 8.0 to 2.6 effecting negative charge under ambient conditions which supports electrostatic stabilization of Np(IV) particles. Particle surface charge at the slipping plane, particle size and shape necessarily depend on the initial magnitude of Si content in solution during particle formation. Particular changes of the morphology and internal structure of different Np(IV) silica colloids by aging are indicated by TEM and XPS. The composition and the crystallinity state of the initially formed amorphous phases partially changed into well-ordered nanocrystalline units characterized with fcc structure. The presence of silicate under conditions expected in a nuclear waste repository significantly influences the solubility of Np(IV) and provoke the stabilization of waterborne Np(IV) up to concentrations of 10-3 M, exceeding Np´s solubility limit by a factor of up 10.000. Neptunium and silicate significantly interact with each other, and thereby changing their individual hydrolysis and polymerization behavior. Silicate prevents the intrinsic formation of NpO2 NCs in fcc-structure, and at the same time, Np(IV) prevents the polymerization of silicate. Both processes result in the formation of Np(IV) silica colloids which possibly influence the migration behavior and fate of Np in the waste repositories and surrounding environments. For tetravalent actinides in general, the most significant transport in the environment would occur by colloidal particles. Therefore, Np(IV) silica colloids could have a significant implication in the migration of Np, the important minor actinide in the waste repositories, via colloidal transport.

Les nanocristaux semi-conducteurs colloïdaux possèdent des propriétés photo-physiques qui en font des objets de choix pour des applications variées, comme le marquage biologique, le photovoltaïque ou encore l'optique quantique. Dans cette thèse, nous étudions les modifications, introduites par des réseaux d'or, de la fluorescence de nanocristaux CdSe/CdS à coquille épaisse. Nous présentons tout d'abord les propriétés fondamentales de ces nanocristaux de CdSe/CdS puis la manière dont leurs propriétés d'émission peuvent être contrôlées par l'environnement électromagnétique, en détaillant en particulier le cas d'un couplage avec des plasmons de surface. Des simulations réalisées par nos collaborateurs du LICB dans le cadre d'un projet ANR sont ensuite comparées à nos mesures expérimentales. Nous observons que le couplage des nano-émetteurs individuels au réseau d'or permet à la fois d'accélérer l'émission spontanée et de mieux la collecter. Les structures métalliques sont optimisées pour que les améliorations détectées soient peu sensibles à la position de l'émetteur. Un effet supplémentaire est le contrôle de la polarisation de l'émission qui se révèle être fixée pa r le réseau. Nous rapportons également des changements dans la statistique temporelle d'émission des photons et notamment la suppression totale du scintillement. Les métaux étant connus pour leurs pertes ohmiques, des expériences ont été réalisées pour montrer que les pertes non radiatives qu'elles entraînent peuvent être réduites à basse température. Nous avons examiné le cas d'une surface d'or plane ainsi que des réseaux linéaires et circulaires. Enfin, une nouvelle méthode de post-traitement a été développée en parallèle. Elle permet par exemple d'étudier les variations de l'efficacité quantique bi-excitonique dans des nanocristaux enrobés d'or suivant l'état de charge de l'émetteur. / Colloidal semiconductor nanocrystals are fluorescent nano-objects exhibiting discrete energy levels which justify their second appellation: quantum dots (QDs). Due to their high efficiency and ease of use, they find potential applications in a wide range of fields. Their usefulness for biological labeling, optoelectronic components in flat screens, light harvesting or quantum optics has been demonstrated by many studies. In this thesis, we use gold gratings in order to modify the emission properties of CdSe/CdS core-shell nanocrystals. After a brief presentation of their electronic and fluorescence properties, we explain how those properties can be modified by the control of the electromagnetic environment with particular care to the case of surface plasmons. We then show through experiment and simulations that those plasmons enable better collection efficiency, faster photo-luminescence decay rates, and polarized emission without being particularly restricting towards QD positioning. Changes in the emission statistics are also observed, notably total suppression of the blinking in the fluorescence intensity. Further experiments at low temperature have been realized in order to assess the importance of the gold ohmic losses. We investigated the case of a flat gold film as well as linear and circular gratings. A new post-selection method is also introduced and used to study the variations of the bi-excitonic quantum yield for nanocrystals embedded in a gold nano-resonator as a function of the ionization state of the emitter.

京都大学 / 0048 / 新制・課程博士 / 博士(理学) / 甲第21333号 / 理博第4429号 / 新制||理||1636(附属図書館) / 京都大学大学院理学研究科化学専攻 / (主査)教授 寺西 利治, 教授 倉田 博基, 教授 時任 宣博 / 学位規則第4条第1項該当 / Doctor of Science / Kyoto University / DGAM

No description available.

No description available.

No description available.

<p>Please email me at kdunn@celccocontrols.com to confirm receipt of my thesis.</p> <p>Thanks,</p> <p>Kayne</p> / <p>In current microelectronic interconnect technology, significant delay is incurred due to capacitances in the intermediate and global interconnect layers. To avoid capacitive effects optical interconnects can be used; however conventional technologies are expensive to manufacture. One method to address these issues is to make use of quantum confinement effects and states lying within the bandgap of the material to enhance luminescence in a CMOS compatible silicon based system. Thin SiCxNy films appear to be suitable to work as luminescent silicon based films due to their lower direct bandgap and chemical stability but have not yet been studied in great detail.</p> <p>This thesis is an exploratory work aiming to assess the suitability of SiCxNy films for the above applications and to identify future research areas. The films analyzed in this thesis were manufactured on the inductively coupled plasma-chemical vapour deposition reactor (ICP-CVD) at McMaster University. The ICP-CVD produces films of high uniformity by using a remote RF plasma and an arrangement of high vacuum pumps to attain a vacuum on the order of 10-7Torr.</p> <p>Several experimental techniques have been used to analyse the films. The complex index of refraction has been determined through the use of ellipsometry giving results typical of that of a-SiNx:H. The photoluminescence spectroscopy results show a large broad emission peak with at least one shoulder at higher energies. The precise luminescence mechanism(s) could not be identified though a strong relationship with the bonding state of nitrogen has been found. The composition and structure of the films, as determined through ion beam measurements, infrared absorption measurements, and transmission electron microscopy measurements demonstrate the formation of a two phase structure consisting of carbon rich clusters surrounded by a mostly silicon nitride matrix. These carbon rich regions have some graphitic character and act to dampen the luminescence.</p> / Master of Applied Science (MASc)

The goal of this work was to quantify the mechanical properties of cellulose nanocrystal (CNC)-based thin films using a polystyrene (PS) structuring approach. This structuring approach was used to biaxially wrinkle CNC-polymer and all-CNC films, in order to assess how changes in the film fabrication process affected the elastic modulus of these films. All films were prepared on pre-stressed PS substrates and structured by heating them above the glass transition temperature of PS, which caused the substrates to shrink and the films to wrinkle biaxially. CNC-polymer films were prepared using the layer-by-layer approach, where three parameters were modified to obtain films of varying compositions: 1) type of polymer (xyloglucan, XG, or polyethyleneimine, PEI), 2) polymer concentration (0.1 wt% or 1 wt%), and 3) film thickness (i.e., number of deposited bilayers). After these films were structured, their elastic moduli were calculated to be 70 ± 2 GPa for CNC-XG0.1, 72 ± 2 GPa for CNC-PEI0.1, and 32.2 ± 0.8 GPa for CNC-PEI1.0 films, indicating that the mechanical properties of CNC-polymer films changed with film composition. This structuring method was also found to provide a humidity-independent measurement of the modulus due to the irreversible nature of the wrinkling. Next, to prepare all-CNC films, CNC suspensions were evaporated under conditions designed to control the film thickness (using 0.005 wt% – 8 wt% CNC suspensions) and CNC nanoparticle orientation (chiral nematic, isotropic, or uniaxial). Suspensions were dried slowly under vacuum, quickly by heating, or by spin-coating to form films with chiral nematic, isotropic, or uniaxial (radial) CNC orientations, respectively. Following structuring, these wrinkled films showed unique morphologies that changed with nanoparticle orientation, suggesting that their mechanical properties are dependent on the CNC orientation within the films. The work presented in this thesis implies that the mechanical properties of films fabricated from hygroscopic bio-based nanomaterials can be assessed in a humidity-independent way by using the structuring method presented. Quantifying the mechanical properties of these films is critical to assess the potential applications of CNCs, where CNC-based materials may be used in developing paper-based electronics, extracellular matrix mimics, and plant cell wall mimics. / Thesis / Master of Science (MSc)

Tesis por compendio / [EN] The current PhD thesis deals with the development and characterization of novel nanocomposites based on biodegradable poly(mannitol sebacate) (PMS) matrices with tailored properties and shape-memory capabilities for biomedical applications. Two types of fillers -cellulose nanocrystals (CNC) and electrospun poly(lactic acid) nanofibers (NF-PLA)- were used as reinforcement in order to induce and/or enhance the shape-memory properties of PMS matrices. Also, different crosslinking profiles and stoichiometric ratios between mannitol and sebacic acid (1:1 and 1:2) were studied and evaluated to obtain samples with low and high degrees of crosslinking. An appropriate combination of the crosslinking profile and the monomer ratio for PMS matrix, as well as the addition of low content of CNC, allowed the development of PMS/CNC nanocomposites with a wide range of mechanical properties and degradation profiles. On the other hand, highly oriented poly(lactic acid) (PLA) nanofiber mats obtained by electrospinning were embedded in the PMS matrices. An enhancement of up to 53-fold in the Young's modulus was observed for PMS/NF-PLA nanocomposites filled with 15 wt% of PLA nanofibers. The incorporation of fillers (CNC and NF-PLA) allowed the development of thermally active shape-memory nanocomposites with an enhancement of parameters such as recovery stress and shape fixity. The electrospun PLA-reinforced nanocomposites, offered the best balance of mechanical and thermal properties, as well as a greater control of the transition temperature for switching the change of shape, within a useful range of temperatures. Owing to that, these materials may be of interest as smart responsive systems in long-term biomedical applications. / [ES] La presente tesis doctoral, se centra en el desarrollo y caracterización de nuevos nanocompuestos biodegradables, a partir de matrices de poli(mannitol sebacato) (PMS) con propiedades a medida y capacidades de memoria de forma para aplicaciones biomédicas. Dos tipos de cargas -nanocristales de celulosa (CNC) y nanofibras de ácido poliláctico (NF-PLA) obtenidas mediante electrospinning- se han utilizado como refuerzo, con la finalidad de inducir y/o mejorar las propiedades de memoria de forma en matrices de PMS. Se han estudiado y evaluado diferentes tratamientos de curado y ratios de reacción entre el mannitol y ácido sebácico (1:1 y 1:2), con la finalidad de obtener muestras con bajo y alto grado de reticulación. Una combinación adecuada del tratamiento de curado y el ratio entre monómeros del PMS, así como la adición de bajos contenidos de CNC, permitió desarrollar nanocompuestos de PMS/CNC con un amplio rango de propiedades mecánicas y perfiles de degradación. Por otro lado, se han producido mats de nanofibras de ácido poliláctico (PLA) con alta orientación mediante la técnica de electrospinning, para embeberse en matrices de PMS, observándose una mejora de hasta 53 veces en el módulo de Young para nanocompuestos de PMS/NF-PLA con un 15% en peso de nanofibras. La incorporación de cargas (CNC y NF-PLA) permitió el desarrollo de nanocompuestos con memoria de forma activada térmicamente, con una mejora de parámetros tales como la fuerza de recuperación y la capacidad de fijación. Los nanocompuestos reforzados con NF-PLA obtenidas por electrospinning, ofrecieron el mejor balance de propiedades mecánicas y térmicas, así como un mayor control de la temperatura de transición para la activación del cambio de forma en un intervalo útil de temperaturas. Por todo ello, estos materiales pueden resultar de interés como sistemas activos en aplicaciones biomédicas de larga duración. / [CA] La present tesi doctoral se centra en el desenvolupament i caracterització de nous nanocompostos biodegradables a partir de matrius de poli(mannitol sebacato) (PMS) amb propietats a mesura i capacitats de memòria de forma per a aplicacions biomèdiques. Dos tipus de càrregues -nanocristals de cel·lulosa (CNC) i nanofibres d'àcid polilàctic (NF-PLA) obtingudes mitjançant electrospinning- s'han utilitzat com a reforç amb la finalitat d'induir i/o millorar les propietats de memòria de forma en matrius de PMS. S'han estudiat i avaluat diferents tractaments de curat i ràtios de reacció entre el mannitol i àcid sebàcic (1:1 i 1:2) amb la finalitat d'obtenir mostres amb baix i alt grau de reticulació. Una combinació adequada del tractament de curat i el ràtio entre monòmers del PMS, així com l'addició de baixos continguts de CNC, va permetre desenvolupar nanocompostos de PMS/CNC amb un ampli rang de propietats mecàniques i perfils de degradació. D'altra banda, s'han produït mats de nanofibres d'àcid polilàctic (PLA) amb alta orientació mitjançant la tècnica de electrospinning, per embeure's en matrius de PMS, observant-se una millora de fins a 53 vegades en el mòdul de Young per nanocompostos de PMS/NF-PLA amb un 15% en pes de nanofibres. La incorporació de càrregues (CNC i NF-PLA) va permetre el desenvolupament de nanocompostos amb memòria de forma activada tèrmicament, amb una millora de paràmetres tals com la força de recuperació i la capacitat de fixació. Els nanocompostos reforçats amb NF-PLA obtingudes per electrospinning, van oferir el millor balanç de propietats mecàniques i tèrmiques, així com un major control de la temperatura de transició per a l'activació del canvi de forma en un interval útil de temperatures. Per tot això, aquests materials poden resultar d'interés com a sistemes actius en aplicacions biomèdiques de llarga durada. / Sonseca Olalla, A. (2015). DEVELOPMENT OF SHAPE-MEMORY COMPOSITES BASED ON A BIODEGRADABLE POLYESTER ELASTOMER [Tesis doctoral]. Universitat Politècnica de València. https://doi.org/10.4995/Thesis/10251/54129 / Compendio

<p dir="ltr">Nucleic acids are promising drug candidates as they can address diseases with few “druggable” targets. Nevertheless, nucleic acids are challenging to deliver because of their large molecular weights, dense negative charges, proinflammatory activities, and short half-lives in biological fluids. Synthetic gene carriers based on cationic polymers or lipids have been used to overcome these challenges; however, their cationic nature results in dose-limiting toxicities and accelerated removal by the filtering MPS organs after systemic administration. In the past six years, several nucleic acid-based therapeutics have been approved by the FDA, formulated as lipid nanoparticles (LNPs). Nonetheless, LNPs show extensive liver accumulation after intravenous administration and, hence, are only indicated for hepatic or local vaccine delivery applications. Therefore, there is a critical unmet need for a nanocarrier that delivers nucleic acids to the extrahepatic organs without significant toxicities. To address this need, we developed Nanosac, a deformable and non-cationic nanocarrier, to deliver siRNA to solid tumors. Deformability can improve multiple aspects of the nanoparticle biotransport, ranging from circulation time and protein corona composition to biodistribution and interactions with the target cells. Meanwhile, a non-cationic carrier avoids proinflammatory complications and rapid clearance of cationic nanoparticles. For this application, we used siRNAs targeting CD47/SIRPa and PD-l/PD-L1 immune checkpoints due to their critical roles as “don't-eat-me” and “don't-find-me” signals to immune cells, respectively, which interfere with the development of innate and adaptive antitumor immune responses.</p><p dir="ltr">In the same context of enhancing the tumor delivery of nanomedicine, we developed two formulations for the small-molecule chemo drug, carfilzomib (CFZ). A nanocrystal formulation with optimized particle size had high CFZ loading, adequate colloidal stability in circulation and better antitumor activity in mice than the FDA-approved CFZ formulation. Despite its improved efficacy, the stiff nanocrystals aggravated CFZ immunotoxicity due to its excessive accumulation in mice spleens. To address this issue, we employed Nanosac technology for CFZ delivery, exploiting its deformability to reduce the non-specific spleen distribution and enhance CFZ tolerability.</p><p dir="ltr">Our results showed that Nanosac delivered siRNA to tumor cells and silenced the target protein expression better than LNPs. <i>In vivo</i>, Nanosac reduced siRNA accumulation in the MPS organs and achieved greater siRNA-mediated tumor suppression than LNPs in two murine tumor models. Moreover, Nanosac achieved greater checkpoint protein silencing in tumors, but less silencing in the MPS organs than LNPs, highlighting their differential biodistribution. The superior Nanosac performance relative to LNPs after systemic delivery is likely due to the difference in their protein coronas and cellular delivery capabilities. In addition, CFZ loading in Nanosac ameliorated CFZ immune cell toxicity <i>in vitro</i> and improved its tolerability in mice while maintaining similar therapeutic efficacy compared to the stiff nanocrystal formulation. Collectively, these findings highlight nanocarrier deformability and corona composition as viable strategies to improve the extrahepatic delivery of nucleic acids as well as to minimize toxicities related to extensive NP distribution to the off-target MPS organs.</p>