21 research outputs found
Doping Dependence of the Redistribution of Optical Spectral Weight in BiSrCaCuO
We present the ab-plane optical conductivity of four single crystals of
BiSrCaCuO (Bi2212) with different carrier doping
levels from the strongly underdoped to the strongly overdoped range with
=66, 88, 77, and 67 K respectively. We focus on the redistribution of the
low frequency optical spectral weight (SW) in the superconducting and normal
states. The temperature dependence of the low-frequency spectral weight in the
normal state is significantly stronger in the overdoped regime. In agreement
with other studies, the superconducting order is marked by an increase of the
low frequency SW for low doping, while the SW decreases for the highly
overdoped sample. The effect crosses through zero at a doping concentration
=0.19 which is slightly to the right of the maximum of the
superconducting dome. This sign change is not reproduced by the BCS model
calculations, assuming the electron-momentum dispersion known from published
ARPES data. Recent Cluster Dynamical Mean Field Theory (CDMFT) calculations
based on the Hubbard and t-J models, agree in several relevant respects with
the experimental data
EBSD, SEM and FIB characterisation of subsurface deformation during tribocorrosion of stainless steel in sulphuric acid
The tribocorrosion behaviour of a 304L stainless steel/alumina contact was investigated in sulphuric acid at two imposed potentials (cathodic and passive) The metal deformation below the surface was investigated by analyzing cross sections using secondary electron microscopy (SEM) and electron back scatter diffraction (EBSD) Cross sections were also prepared using focussed ion beam (FIB) and analyzed by in situ SEM. AES depth profiling was used to analyze surface composition Metal subsurface deformation resulted in the build up of a deformed layer of approximately 20 mu m thickness in the near surface zone within the wear track This layer exhibited a deformation gradient with high deformation close to the surface resulting in grain refinement down to 10 nm The applied potential influenced the deformation at passive applied potential more strain was accumulated below the surface resulting in more pronounced grain refinement and higher density of defects. Using AES analysis no alumina transfer from the counter body or any significant burying of oxide below the surface could be detected (C) 2010 Elsevier B.V All rights reserved
Der Verbleib kupferbasierter Fungizide in Weinbergböden: Eine Fallstudie der stabilen Kupfer-Isotopenverhältnisse und Elektronenspinresonanz von Calco- und Vertisolen in Soave (Italien)
Kupferbasierte Fungizide sind im Weinbau weit verbreitet und im biologischen Weinbau die einzig erlaubten Pestizide zur Bekämpfung von falschem Mehltau. Durch den intensiven, dauerhaften Gebrauch von Kupfer reichert sich dieser, mit wachsenden ökotoxikologischen Konsequenzen, in Weinbergböden an. In dieser Studie untersuchen wir den Verbleib von Kupfer in einem Calcosol und einem Vertisol aus Soave (Italien). Beide Böden werden seit über 50 Jahren mit Kupfer behandelt. Wir stellen Massenbilanzen auf und nutzen die innovative Kombination aus Messung stabiler Cu-Isotopenverhältnisse und Elektronenspinresonanzspektroskopie (ESR), um Einblicke in die biogeochemischen Mechanismen der Kupferbindung zu erlangen. Die untersuchten Böden weisen hohe exogene Kupfergehalte auf, welche eine Akkumulation der heutigen maximalen Behandlungsmenge über 50 Jahre überschreiten. Dies belegt, dass einmal sehr viel größere Mengen Cu im Weinbau verwendet wurden und dass ein Großteil dieses Kupfers in den jeweiligen Böden verbleibt. In Vertisolen fallen die Cu-Konzentrationen unter dem vertischen Horizont schnell auf die geogene Hintergrundkonzentration, wobei in Calcosolen dieser Abfall progressiver erfolgt. Isotopenverhältnisse unterscheiden sich zwischen den verschieden Bodentypen (δCu-65 zwischen 0.12 und 0.37 ‰), obwohl sie die gleiche Behandlung erfahren haben. Kupferisotope in Oberböden sind schwerer als in Unterböden und Citratextraktionen zeigen, dass mobiles Kupfer isotopisch schwerer ist als der Gesamtgehalt. Die Horizonte des Calcosols sind systematisch leichter als die des Vertisols, was auf unterschiedliche biogeochemische Bindungsmechanismen von Kupfer hinweist. Dies wird durch die ESR-Spektren bestätigt. In Oberböden zeigen sie eine Kupferbindung an organisches Material, wobei es im gesamten Bodenprofil Unterschiede in der Cu-Bindung zwischen den beiden Bodentypen gibt. Wenn jedoch Horizonte des Calcosols mit Säure entkalkt werden, nähren sich deren ESR-Spektren denen der Vertisole an, wohingegen letztere nicht auf eine Säurebehandlung reagieren. Somit wird gezeigt, dass in Calcosolen Karbonate an der Bindung von Kupfer beteiligt sind wobei in Vertisolen der vertische Horizont eine wichtige Rolle spielt. Darüber hinaus wird durch die analoge Variation von ESR-Spektren und Isotopenverhältnissen wird die Anwendbarkeit von Cu-Isotopenanalysen und ESR-Spektroskopie zur Aufklärung von biogeochemischen Prozessen in Böden demonstriert
Geochemical and mineralogical evolution of the Zn-Cd-Pb bearing tailings from the Saint-Salvy mine, France
4 million tonnes of waste generated by the treatment plant of the Saint-Salvy Zn mine have been dumped in
a storage dam. Sulphides (3.5%) and Mn-siderite (20%) oxydize and dissolve. Drainage water exports most of SO
and Mn released. According to geochemical modelling taking into account slightly acidic pH and slightly reducing
conditions within the tailings, ferrihydrite precipitates in situ inducing partial immobilization of Fe, and partial
retention of Zn, Pb and Cd. Time required for site inertization is estimated around a century
Precision-cut dog renal cortical slices in dynamic organ culture for the study of cisplatin nephrotoxicity
L-ascorbic acid regulates growth and metabolism of renal cells: improvements in cell culture
Relation between microstructure and Charpy impact properties of an elemental and pre-alloyed 14Cr ODS ferritic steel powder after hot isostatic pressing
Activation of surrogate death receptor signaling triggers peroxynitrite-dependent execution of cisplatin-resistant cancer cells
Platinum-based drugs remain as the cornerstone of cancer chemotherapy; however, development of multidrug resistance presents a therapeutic challenge. This study aims at understanding the molecular mechanisms underlying resistance to cisplatin and unraveling surrogate signaling networks that could revert sensitivity to apoptosis stimuli. We made use of three different sets of cell lines, A549 and H2030 non-small-cell lung cancer (NSCLC) and A2780 ovarian cancer cells and their cisplatin-resistant variants. Here we report that cisplatin-resistant cell lines displayed a multidrug-resistant phenotype. Changes in mitochondrial metabolism and defective mitochondrial signaling were unraveled in the resistant cells. More interestingly, a marked increase in sensitivity of the resistant cells to death receptor-induced apoptosis, in particular TRAIL (TNF-related apoptosis-inducing ligand)-mediated execution, was observed. Although this was not associated with an increase in gene transcription, a significant increase in the localization of TRAIL death receptor, DR4, to the lipid raft subdomains of plasma membrane was detected in the resistant variants. Furthermore, exposure of cisplatin-resistant cells to TRAIL resulted in upregulation of inducible nitric oxide synthase (iNOS) and increase in nitric oxide (NO) production that triggered the generation of peroxynitrite (ONOO(-)). Scavenging ONOO(-) rescued cells from TRAIL-induced apoptosis, thereby suggesting a critical role of ONOO(-) in TRAIL-induced execution of cisplatin-resistant cells. Notably, preincubation of cells with TRAIL restored sensitivity of resistant cells to cisplatin. These data provide compelling evidence for employing strategies to trigger death receptor signaling as a second-line treatment for cisplatin-resistant cancers