1,007 research outputs found
Structure-function relationship of Strong Metal-Support Interaction studied on supported Pd reference catalysts
Transition metal oxide supported, nano-scaled noble metal catalysts are known to show a variety of surface modifications when they are being reduced at increasing temperatures. Such processes involve for example (surface) alloying and the formation of partially reduced oxidic support overlayers that are both induced by the so-called strong metal-support interaction (SMSI). The present work investigated a series of oxide supported Palladium powder catalysts with a loading variation between 1-5 wt.-% on their structure-function relationship after reduction in different media and at different temperatures to create a reference system and explore the nature of SMSI. Hereby surface and bulk sensitive techniques like XPS, chemisorption, TEM, DRIFTS or XRD were applied to study the influence of electronic and structural modifications on the activity in catalytic oxidation of carbon monoxide which served as the main test reaction and was conducted at ambient pressure. The catalysts were synthesized reproducibly by a controlled co-precipitation approach and by impregnation. The investigated Pd/iron oxide system shows palladium surface decoration at comparably low reduction temperatures. The surface cover was found to be volatile in oxygen containing atmosphere and formed reversibly. Dependent on the Pd particle size it increases the CO oxidation activity. Alloy formation occurs at higher reduction temperatures. In case of the Pd/zinc oxide system reversible surface alloying takes place during reduction that is also beneficial for CO oxidation, but again deactivates fast. When being reduced at even higher temperatures the additional formation of an oxidic overlayer could be observed that does not further activate the system but leads to an overall reduction of active sites. Due to alloy formation, the zinc oxide system at higher conversions shows a different selectivity behavior in acetylene hydrogenation, compared to the iron oxide system. Also in case of the Pd/titania system, reversible surface decoration by partially reduced support happens during reduction. Different to the other investigated systems the surface-cover reversibly decreases CO oxidation activity however. The Pd/alumina system was studied as a less reducible reference. As expected, it does not show SMSI-induced modifications. In the end the work clearly shows that CO oxidation is a convenient method to study activity and stability of SMSI and decouple it from other involved processes. The effects of surface modification on the catalytic activity in this test reaction however strongly depend on the specific system and pre-conditioning and can either be of activating or deactivating nature. The basic principles involved in case of SMSI seem to apply both in UHV model systems and at powder systems at ambient pressure as found by the catalytic measurements.Ăbergangsmetalloxid getrĂ€gerte, nano-skalige Edelmetall-Katalysatoren sind bekannt dafĂŒr, eine Reihe von OberflĂ€chen-VerĂ€nderungen zu erfahren, wenn sie bei erhöhter Temperatur reduziert werden. Diese Prozesse beinhalten beispielsweise (OberflĂ€chen-) Legierungsbildung und die Ausblidung von teilweise reduzierten, oxidischen TrĂ€ger- Schichten, in beiden FĂ€llen hervorgerufen durch Starke Metall-TrĂ€ger Wechselwirkung (Strong Metal-Support Interaction, SMSI). Die vorliegende Arbeit untersuchte eine Reihe von oxid-getrĂ€gerten Palladium Pulverkatalysatoren mit einer Variation der Beladung von 1- 5 Gewichts-% auf ihre Struktur-Eigenschafts Beziehungen nach Reduktion in verschiedenen Medien und bei veschiedenen Temperaturen, um ein Referenzsystem zu entwickeln und der Natur von SMSI auf den Grund zu gehen. Dabei kamen oberflĂ€chen- und volumensensitive Methoden wie XPS, Chemisorption, TEM, DRIFTS oder XRD zum Einsatz, um den Einfluss von elektronischen und strukturellen VerĂ€nderungen auf die AktivitĂ€t bei katalytischer Oxidation von Kohlenmonoxid zu untersuchen, welche als wichtigste Testreaktion bei Normaldruck durchgefĂŒhrt wurde. Die Katalysatoren wurden auf reproduzierbare Weise durch kontrollierte Ko-FĂ€llung und durch ImprĂ€gnierung hergestellt. Das untersuchte Pd/Eisenoxid System zeigt Bedeckung der Pd OberflĂ€che nach Reduktion bei vergleichsweise niedrigen Temperaturen. Diese Bedeckung war instabil in sauerstoffhaltiger Umgebung und bildete sich reversibel aus. AbhĂ€ngig von der Pd PartikelgröĂe erhöht sie die AktivitĂ€t bei der CO-Oxidation. Legierungsbildung findet bei höheren Reduktionstemperaturen statt. Im Falle von Pd/Zinkoxid findet reversible Legierungsbildung an der OberflĂ€che statt, die ebenfalls die CO-Oxidation begĂŒnstigt, aber ebenfalls schnell deaktiviert. Nach Reduktion bei noch höheren Temperaturen konnte die zusĂ€tzliche Ausbildung einer oxidischen Ăberschicht beobachtet werden, die das System nicht weiter aktivierte, sondern insgesamt die Zahl der aktiven PlĂ€tze reduzierte. Wegen Legierungsbildung zeigt das Zinkoxid-System bei höheren UmsĂ€tzen in der Acetylenhydrierung ein anderes SelektivitĂ€tsverhalten als das Eisenoxid-System. Im Fall von Pd/Titanoxid kommt es wĂ€hrend der Reduktion ebenfalls zu reversibler OberflĂ€chen- Bedeckung durch teilweise reduzierten TrĂ€ger. Anders als in den beiden anderen FĂ€llen verringert diese Schicht hier jedoch die AktivitĂ€t in der CO-Oxidation. Pd/Aluminiumoxid wurde als schwer reduzierbares Referenz-System untersucht. Wie erwartet zeigt es keine durch SMSI hervorgerufenen VerĂ€nderungen. Schlussendlich konnte in dieser Arbeit gezeigt werden, dass CO-Oxidation eine einfache und geeignete Methode ist, SMSI zu untersuchen und ihren Einfluss auf AktivitĂ€t und StabilitĂ€t von dem anderer Prozesse zu trennen. Die Effekte von OberflĂ€chenverĂ€nderungen auf die katalytische AktivitĂ€t dieser Test-Reaktion hĂ€ngen jedoch stark vom entsprechenden System und der Vorbehandlung ab und können sowohl aktivierender als auch deaktivierender Natur sein. Die Grundlegenden Prinzipien, die bei SMSI eine Rolle spielen, scheinen sowohl im Fall von Modell-Systemen unter UHV-Bedingungen als auch bei Pulver-Systemen bei Normaldruck zu gelten, wie durch die katalytischen Messungen gezeigt wurde
The RootScope: A Simple High-Throughput Screening System For Quantitating Gene Expression Dynamics In Plant Roots
Background: High temperature stress responses are vital for plant survival. The mechanisms that plants use to sense high temperatures are only partially understood and involve multiple sensing and signaling pathways. Here we describe the development of the RootScope, an automated microscopy system for quantitating heat shock responses in plant roots.Results: The promoter of Hsp17.6 was used to build a Hsp17.6(p):GFP transcriptional reporter that is induced by heat shock in Arabidopsis. An automated fluorescence microscopy system which enables multiple roots to be imaged in rapid succession was used to quantitate Hsp17.6p: GFP response dynamics. Hsp17.6(p):GFP signal increased with temperature increases from 28 degrees C to 37 degrees C. At 40 degrees C the kinetics and localization of the response are markedly different from those at 37 degrees C. This suggests that different mechanisms mediate heat shock responses above and below 37 degrees C. Finally, we demonstrate that Hsp17.6(p):GFP expression exhibits wave like dynamics in growing roots.Conclusions: The RootScope system is a simple and powerful platform for investigating the heat shock response in plants
Computer processing support, volume 4
There are no author-identified significant results in this report
Immunological consequences of using three different clinical/laboratory techniques of emulsifying peptide-based vaccines in incomplete Freund's adjuvant
Incomplete Freund's adjuvant (IFA) serves as a carrier for water-in-oil emulsion (W/O) vaccines. The stability of such emulsions greatly affects vaccine safety and efficacy since continued presence of antigen depots at lymphoid organs releasing low-level antigens is known to stimulate a potent immune response and high-level systemic release of antigens can lead to tolerance. W/O emulsions for the purpose of clinical and laboratory peptide-based vaccinations have been prepared using the techniques of syringe extrusion, vortex or high-speed homogenization. There is no consensus in the field over which technique would be best to use and no immunological data are available that compare the three techniques. In this study, we compared the immune responses induced by a peptide-based vaccine prepared using vortex, syringe-extrusion and homogenization. The vaccination led to tumor rejection by mice vaccinated with the peptide-based vaccine prepared using all three techniques. The immunological data from the in vivo cytotoxicity assay showed a trend for lower responses and a higher variability and greater range in the immune responses induced by a vaccine that was emulsified by the vortex or homogenizer techniques as compared to the syringe-extrusion technique. There were statistically significant lower numbers of IFNÎł-secreting cells induced when the mice were vaccinated with a peptide-based vaccine emulsion prepared using the vortex compared to the syringe-extrusion technique. At a suboptimal vaccine dose, the mice vaccinated with a peptide-based vaccine emulsion prepared using the vortex technique had the largest tumors compared to the syringe-extrusion or the homogenizer technique. In the setting of a busy pharmacy that prepares peptide-based vaccine emulsions for clinical studies, the vortex technique can still be used but we urge investigators to take special care in their choice of mixing vessels for the vortex technique as that can influence the stability of the emulsion. However, in instances where the optimal dose is unknown, we caution investigators against using the vortex technique to prepare the peptide-based vaccine emulsions. Overall, we report that all three techniques can be used to prepare peptide-based vaccine emulsions under optimal dose conditions and we discuss important details regarding the proper preparation of the emulsions
Effect of Preexisting Neutralizing Antibodies on the Anti-tumor Immune Response Induced by Chimeric Human Papillomavirus Virus-like Particle Vaccines
AbstractChimeric human papillomavirus virus-like particles (HPV cVLPs) carrying HPV16 E7 protein are potent vaccines for inducing cell-mediated immunity (CMI) against HPV-induced tumors in animal models. We tested the hypothesis that virion-neutralizing antibodies generated during an initial vaccination might prevent effective boosting of CMI to the cVLPs. Mice with circulating HPV16-neutralizing antibodies, generated by direct immunization with wild-type VLPs or by passive transfer of hyperimmune anti-HPV16 VLP mouse sera, were subsequently vaccinated with HPV16 E7-containing cVLPs. Mice with preexisting neutralizing antibodies were not protected from HPV16 E7-positive TC-1 tumor challenge, compared to the protection seen in mice lacking these antibodies. Antibody-coated VLPs bound very inefficiently to receptor-positive cell lines, suggesting that one of the mechanisms of antibody interference is blocking of VLP binding to its receptor and thereby uptake of VLPs by antigen-presenting cells. Our results suggest that repetitive vaccination with a cVLP for induction of cellular immune responses to an incorporated antigen may be of limited effectiveness due to the presence of neutralizing antibodies against the capsid proteins induced after the first application. This limitation could potentially be overcome by boosting with cVLPs containing the same target antigen incorporated into other papillomavirus-type VLPs
A Joint Venture of Ab Initio Molecular Dynamics, Coupled Cluster Electronic Structure Methods, and Liquid-State Theory to Compute Accurate Isotropic Hyperfine Constants of Nitroxide Probes in Water
The isotropic hyperfine coupling constant (HFCC, Aiso) of a pH-sensitive spin probe in a solution, HMI (2,2,3,4,5,5-hexamethylimidazolidin-1-oxyl, C9H19N2O) in water, is computed using an ensemble of state-of-the-art computational techniques and is gauged against X-band continuous wave electron paramagnetic resonance (EPR) measurement spectra at room temperature. Fundamentally, the investigation aims to delineate the cutting edge of current first-principles-based calculations of EPR parameters in aqueous solutions based on using rigorous statistical mechanics combined with correlated electronic structure techniques. In particular, the impact of solvation is described by exploiting fully atomistic, RISM integral equation, and implicit solvation approaches as offered by ab initio molecular dynamics (AIMD) of the periodic bulk solution (using the spin-polarized revPBE0-D3 hybrid functional), embedded cluster reference interaction site model integral equation theory (EC-RISM), and polarizable continuum embedding (using CPCM) of microsolvated complexes, respectively. HFCCs are obtained from efficient coupled cluster calculations (using open-shell DLPNO-CCSD theory) as well as from hybrid density functional theory (using revPBE0-D3). Re-solvation of âvertically desolvatedâ spin probe configuration snapshots by EC-RISM embedding is shown to provide significantly improved results compared to CPCM since only the former captures the inherent structural heterogeneity of the solvent close to the spin probe. The average values of the Aiso parameter obtained based on configurational statistics using explicit water within AIMD and from EC-RISM solvation are found to be satisfactorily close. Using either such explicit or RISM solvation in conjunction with DLPNO-CCSD calculations of the HFCCs provides an average Aiso parameter for HMI in aqueous solution at 300 K and 1 bar that is in good agreement with the experimentally determined one. The developed computational strategy is general in the sense that it can be readily applied to other spin probes of similar molecular complexity, to aqueous solutions beyond ambient conditions, as well as to other solvents in the longer run
L1-Specific Protection from Tumor Challenge Elicited by HPV16 Virus-like Particles
AbstractA single injection of HPV16 L1 virus-like particles induced potent CD8-mediated protection from tumor challenge by C3 cells, a line derived from embryonic mouse cells transfected with the HPV16 genome. L1 RNA, but not protein, was detected biochemically in C3 cells. These results indicate that low-level expression of HPV16 L1 can occur in proliferating cells and serve as a tumor vaccine target. Although L1 expression is generally thought to be restricted to terminally differentiated epithelial cells, these results suggest that additional analysis for low-level L1 expression in proliferating cells of HPV-induced lesions is warranted and might help in predicting the clinical potential of HPV L1 virus-like particle-based vaccines
Nitrogen isotope evidence for expanded ocean suboxia in the early Cenozoic
The million-year variability of the marine nitrogen cycle is poorly understood. Before 57 million years (Ma) ago, the ^(15)N/^(14)N ratio (ÎŽ^(15)N) of foraminifera shell-bound organic matter from three sediment cores was high, indicating expanded water column suboxia and denitrification. Between 57 and 50 Ma ago, ÎŽ^(15)N declined by 13 to 16 per mil in the North Pacific and by 3 to 8 per mil in the Atlantic. The decline preceded global cooling and appears to have coincided with the early stages of the Asia-India collision. Warm, salty intermediate-depth water forming along the Tethys Sea margins may have caused the expanded suboxia, ending with the collision. From 50 to 35 Ma ago, ÎŽ^(15)N was lower than modern values, suggesting widespread sedimentary denitrification on broad continental shelves. Î^(15)N rose at 35 Ma ago, as ice sheets grew, sea level fell, and continental shelves narrowed
Estimating the Predictive Value of Negative SARS-CoV-2 Results: A Prospective Study
© 2020 by The Society for Healthcare Epidemiology of America. All rights reserved. We performed a prospective study of 501 patients, regardless of symptoms, admitted to the hospital, to estimate the predictive value of a negative Nasopharyngeal swab for SARS-CoV-2. At a positivity rate of 10.2%, the estimated Negative Predictive Value (NPV) was 97.2% and NPV rose as prevalence decreased during the study
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