Nemzeti érdekek az EU-ban. Az olasz európa-politika tanulságai, különös tekintettel az európai gazdasági kormányzásban betöltött szerepre = National Interests in the EU. Experiences of Italy’s European policy with special regard to its role in the European economic governance

A disszertáció a hazai és a nemzetközi szakirodalom elemzésén keresztül vizsgálja a nemzeti és az európai (közösségi) érdek viszonyát, ezek alakulását az integrációs folyamatban. Választ próbál találni arra, hogy mi a fő oka annak az utóbbi évtizedben egyre inkább erősödő jelenségnek, amely az EU nemzetek feletti jellegének visszaszorulásában, és ezzel párhuzamosan a közösségi szakpolitikák alakításakor a kormányközi logika érvényesülésének erősödésében összegezhető. Az elemzés során nem lehet eltekinteni az európai integráció társadalmi aspektusaitól, így ezek között kiemelten a projekttel való lakossági azonosulás, más szóval az egyébként sokdimenziós, tagállamonként és időben változó identitás problematikájától. A dolgozat kiemelten foglalkozik az olasz Európa-politika fejlődésével és érvényesülésével. Róma EU-politikájának elemzése már csak azért is érdekes feladat, mert Itália európai középhatalmi státuszából adódóan az a klasszikus közösségi-államközi, látszólag ellentétes „módszer” metszéspontjában található. Megnyilvánulási formái ennek megfelelően – a külső szemlélő számára akár bizonytalankodásnak hatóan - váltakozó hangsúllyal ötvözik a nemzetek feletti és a kormányközi stratégiát. Az olasz integrációs politika hagyományainak, általános geopolitikai-külpolitikai keretrendszerének, változásainak részletes elemzése elengedhetetlen az egyes szakpolitikák terén tanúsított olasz törekvések megértéséhez. (...

Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study

Background Huntington's disease is caused by a CAG repeat expansion in the huntingtin gene, HTT. Age at onset has been used as a quantitative phenotype in genetic analysis looking for Huntington's disease modifiers, but is hard to define and not always available. Therefore, we aimed to generate a novel measure of disease progression and to identify genetic markers associated with this progression measure. Methods We generated a progression score on the basis of principal component analysis of prospectively acquired longitudinal changes in motor, cognitive, and imaging measures in the 218 indivduals in the TRACK-HD cohort of Huntington's disease gene mutation carriers (data collected 2008–11). We generated a parallel progression score using data from 1773 previously genotyped participants from the European Huntington's Disease Network REGISTRY study of Huntington's disease mutation carriers (data collected 2003–13). We did a genome-wide association analyses in terms of progression for 216 TRACK-HD participants and 1773 REGISTRY participants, then a meta-analysis of these results was undertaken. Findings Longitudinal motor, cognitive, and imaging scores were correlated with each other in TRACK-HD participants, justifying use of a single, cross-domain measure of disease progression in both studies. The TRACK-HD and REGISTRY progression measures were correlated with each other (r=0·674), and with age at onset (TRACK-HD, r=0·315; REGISTRY, r=0·234). The meta-analysis of progression in TRACK-HD and REGISTRY gave a genome-wide significant signal (p=1·12 × 10−10) on chromosome 5 spanning three genes: MSH3, DHFR, and MTRNR2L2. The genes in this locus were associated with progression in TRACK-HD (MSH3 p=2·94 × 10−8 DHFR p=8·37 × 10−7 MTRNR2L2 p=2·15 × 10−9) and to a lesser extent in REGISTRY (MSH3 p=9·36 × 10−4 DHFR p=8·45 × 10−4 MTRNR2L2 p=1·20 × 10−3). The lead single nucleotide polymorphism (SNP) in TRACK-HD (rs557874766) was genome-wide significant in the meta-analysis (p=1·58 × 10−8), and encodes an aminoacid change (Pro67Ala) in MSH3. In TRACK-HD, each copy of the minor allele at this SNP was associated with a 0·4 units per year (95% CI 0·16–0·66) reduction in the rate of change of the Unified Huntington's Disease Rating Scale (UHDRS) Total Motor Score, and a reduction of 0·12 units per year (95% CI 0·06–0·18) in the rate of change of UHDRS Total Functional Capacity score. These associations remained significant after adjusting for age of onset. Interpretation The multidomain progression measure in TRACK-HD was associated with a functional variant that was genome-wide significant in our meta-analysis. The association in only 216 participants implies that the progression measure is a sensitive reflection of disease burden, that the effect size at this locus is large, or both. Knockout of Msh3 reduces somatic expansion in Huntington's disease mouse models, suggesting this mechanism as an area for future therapeutic investigation

TiO2 and Fe2O3 Films for Photoelectrochemical Water Splitting

Titanium oxide (TiO2) and iron oxide (α-Fe2O3) hematite films have potential applications as photoanodes in electrochemical water splitting. In the present work TiO2 and α-Fe2O3 thin films were prepared by two methods, e.g., sol-gel and High Power Impulse Magnetron Sputtering (HiPIMS) and judged on the basis of physical properties such as crystalline structure and surface topography and functional properties such as simulated photoelectrochemical (PEC) water splitting conditions. It was revealed that the HiPIMS method already provides crystalline structures of anatase TiO2 and hematite Fe2O3 during the deposition, whereas to finalize the sol-gel route the as-deposited films must always be annealed to obtain the crystalline phase. Regarding the PEC activity, both TiO2 films show similar photocurrent density, but only when illuminated by UV light. A different situation was observed for hematite films where plasmatic films showed a tenfold enhancement of the stable photocurrent density over the sol-gel hematite films for both UV and visible irradiation. The superior properties of plasmatic films could be explained by ability to address some of the hematite drawbacks by the deposition of very thin films (25 nm) consisting of small densely packed particles and by doping with Sn

Immobilization of exfoliated g-C3N4 for photocatalytical removal of organic pollutants from water

Graphitic carbon nitride (g-C3N4) was synthesized from melamine and exfoliated by thermal treatment. Exfoliated g-C3N4 particles were immobilized by electrophoretic deposition from an ultrasonically treated ethanolic suspension aged up to 12 weeks. During the aging of the suspension, the separation of particles bigger than 10 mu m was observed. The separated stable part of the suspension contained particles with a relatively uniform size distribution, enabling the fabrication of g-C3N4 films that were stable in a stirred aqueous solution. Such stable immobilized particles of exfoliated g-C3N4 are reported for the first time. The photocatalytic activity of such layers was evaluated using aqueous solutions of Acid Orange 7 (AO7) and 4-chlorophenol (4-CP). The photocatalytic decomposition of AO7 was faster in comparison with the decomposition of 4-CP. Mineralization was observed in the case of AO7, but not in the case of 4-CP, where the decrease of 4-CP concentration is due to 4-CP polymerization and the formation of a dimer, C12H8Cl2O2. This indicates that the use of g-C3N4 as a photocatalyst for oxidative degradation of organic compounds in water is limited.Web of Science112art. no. 20

TiO2 and Fe2O3 Films for Photoelectrochemical Water Splitting

Titanium oxide (TiO2) and iron oxide (α-Fe2O3) hematite films have potential applications as photoanodes in electrochemical water splitting. In the present work TiO2 and α-Fe2O3 thin films were prepared by two methods, e.g., sol-gel and High Power Impulse Magnetron Sputtering (HiPIMS) and judged on the basis of physical properties such as crystalline structure and surface topography and functional properties such as simulated photoelectrochemical (PEC) water splitting conditions. It was revealed that the HiPIMS method already provides crystalline structures of anatase TiO2 and hematite Fe2O3 during the deposition, whereas to finalize the sol-gel route the as-deposited films must always be annealed to obtain the crystalline phase. Regarding the PEC activity, both TiO2 films show similar photocurrent density, but only when illuminated by UV light. A different situation was observed for hematite films where plasmatic films showed a tenfold enhancement of the stable photocurrent density over the sol-gel hematite films for both UV and visible irradiation. The superior properties of plasmatic films could be explained by ability to address some of the hematite drawbacks by the deposition of very thin films (25 nm) consisting of small densely packed particles and by doping with Sn

Photocatalytic behavior of nanosized TiO2 immobilized on layered double hydroxides by delamination/restacking process

International audienceIntroduction Efficient immobilization of TiO2 nanoparticles on the surface of Mg2Al-LDH nanosheets was performed by delamination/restacking process. Experimental part The structural and textural properties of as-prepared nanocomposite were deeply analyzed using different solid-state characterization techniques such as: X-ray powder diffraction, Fourier transform infrared spectroscopy, and Raman spectroscopies, chemical analysis, X-ray photoelecton spectroscopy, N2 adsorption-desorption, and electronic microscopy. Results and discussion The photocatalytic properties of immobilized TiO2 nanoparticles on Mg2Al were investigated using the photodegradation of two model pollutants: Orange II and 4-chlorophenol, and compared with pure colloidal TiO2 solution. Conclusion It appears that Orange II photodegradation was systematically faster and more efficient than 4-chlorophenol photodegradation regardless of the medium pH. Moreover under slightly basic conditions, even if the TiO2 photocatalytic efficiency decreases, photodegradation performed in presence of easily recovered TiO2/Mg2Al1.5 nanocomposite gives rise to comparable or better results than pure TiO2

Photocatalytic properties of aqueous systems containing TiO2 nanoparticles

International audienceThis work describes the aging of aqueous colloidal TiO2 nanoparticles at different temperatures and pH values. Emphasis was particularly given to the behaviour in the alkaline region, since this has not yet been properly reported. Aging of colloidal TiO2 suspensions has previously been investigated using spectroscopic methods (band gap energy determination) and a dynamic light scattering method (particle size determination). The photocatalytic activity, representing the most important property of TiO2 nanoparticles, was determined through the quantum yield of 4-chlorophenol degradation. It was found that the size of acidic colloidal TiO2 particles depends on the storing temperature; lower temperature leads to a small increase in particle size. The process of aging of TiO2 nanoparticles consists in slow re-crystallization that leads to slightly larger particles, and it seems that this process is faster at higher temperatures. In alkaline environments it was found that the change in particle size depends on the type of alkaline reagent used (KOH and NH4OH), on its concentration and also on the starting concentration of the TiO2 suspension. In contrast to the quantum yield of acidic TiO2, the quantum yield of alkaline suspensions decreased during aging