768 research outputs found
Surface Properties of SiCp/Al Composite by Powder-Mixed EDM
AbstractThis paper uses a kind of moderate volume fraction (40%) of SiC particle reinforced Al matrix composites (SiCp/Al) to research how the surface properties are affected in conventional EDM (EDM) and powder-mixed EDM (PMEDM). By means of environment scanning electron microscope (ESEM) and HIT friction and wear tester, surface micro-topography, elements and wear resistance were analyzed. Experiments and researches indicate that compared with EDM, the surface properties machined by using PMEDM are improved greatly. The PMEDM surface roughness decreases about 31.5%; corrosion resistance is better too; and wear resistance is twice of EDM. Powder-mixed EDM has promising applications in metal matrix composites machining field
High-temperature oxidation of nickel-based alloys and estimation of the adhesion strength of resulting oxide layers
The kinetics of isothermal oxidation (1100°C) of commercial nickel-based alloys with different content of sulfur (0.22â3.2 wt ppm) is studied. The adhesion strength in a metal/oxide system is estimated as a function of sulfur content and duration of high-temperature exposure. The scratch-test technique is proposed to quantitatively estimate the work of adhesion of resulting oxide films. It is found that the film microstructure is composed of an inner α-Al2O3 layer and an outer NiAl2O4 spinel layer, which are separated by discrete inclusions of TiO2. Residual stresses in the oxide film are experimentally determined by X-ray diffraction. spinel layer, which are separated by discrete inclusions of TiO2. Residual stresses in the oxide film are experimentally determined by X-ray diffractio
Lepton Polarization and Forward-Backward Asymmetries in b -> s tau+ tau-
We study the spin polarizations of both tau leptons in the decay b -> s tau+
tau-. In addition to the polarization asymmetries involving a single tau, we
construct asymmetries for the case where both polarizations are simultaneously
measured. We also study forward-backward asymmetries with polarized tau's. We
find that a large number of asymmetries are predicted to be large, >~ 10%. This
permits the measurement of all Wilson coefficients and the b-quark mass, thus
allowing the standard model (SM) to be exhaustively tested. Furthermore, there
are many unique signals for the presence of new physics. For example,
asymmetries involving triple-product correlations are predicted to be tiny
within the SM, O(10^{-2}). Their observation would be a clear signal of new
physics.Comment: 21 pages, LaTeX, 4 figures (included). Paper somewhat reorganized,
references greatly expanded, conclusions unchange
Unique intrahepatic transcriptomics profiles discriminate the clinical phases of a chronic HBV infection
Chronic hepatitis B is a highly heterogeneous liver disease characterized by phases with fluctuations in viral replication and progressive liver damage in some, but not all infected individuals. Despite four decades of research, insight into host determinants underlying these distinct clinical phases-immunotolerant, immune active, inactive carrier, and HBeAg-negative hepatitis±remains elusive. We performed an in-depth transcriptome analysis of archived FFPE liver biopsies of each clinical phase to address host determinants associated with the natural history. Therefore, we determined, for the first time, intrahepatic global expression profiles of well-characterized chronic HBV patients at different clinical phases. Our data, obtained by microarray, demonstrate that B cells and NK/cytotoxicrelated genes in the liver, including CD19, TNFRSF13C, GZMH, and KIR2DS3, were differentially expressed across the clinical HBV phases, which was confirmed by modular analysis and also Nanostring arrays in an independent cohort. Compared to the immunotolerant phase, 92 genes were differentially expressed in the liver during the immune active phase, 46 in the inactive carrier phase, and 71 in the HBeAg-negative phase. Furthermore, our study also revealed distinctive transcription of genes associated with cell cycle activity, NF-ÎșB signaling, cytotoxic function and mitochondrial respiration between clinical phases. Our data define for the first time using microarray unique transcriptomes in the HBV-infected liver during consecutive clinical phases. We demonstrate that fluctuations of viral loads and liver damage coincide with fluctuations in the liver transcriptome and point to functionalimmune and non-immune-components contributing to the clinical phenotype in patients
Electrical resistivity at large temperatures: Saturation and lack thereof
Many transition metal compounds show saturation of the resistivity at high
temperatures, T, while the alkali-doped fullerenes and the high-Tc cuprates are
usually considered to show no saturation. We present a model of transition
metal compounds, showing saturation, and a model of alkali-doped fullerenes,
showing no saturation. To analyze the results we use the f-sum rule, which
leads to an approximate upper limit for the resistivity at large T. For some
systems and at low T, the resistivity increases so rapidly that this upper
limit is approached for experimental T. The resistivity then saturates. For a
model of transition metal compounds with weakly interacting electrons, the
upper limit corresponds to a mean free path consistent with the Ioffe-Regel
condition. For a model of the high Tc cuprates with strongly interacting
electrons, however, the upper limit is much larger than the Ioffe-Regel
condition suggests. Since this limit is not exceeded by experimental data, the
data are consistent with saturation also for the cuprates. After "saturation"
the resistivity usually grows slowly. For the alkali-doped fullerenes,
"saturation" can be considered to have happened already for T=0, due to
orientational disorder. For these systems, however, the resistivity grows so
rapidly after "saturation" that this concept is meaningless. This is due to the
small band width and to the coupling to the level energies of the important
phonons.Comment: 22 pages, RevTeX, 19 eps figures, additional material available at
http://www.mpi-stuttgart.mpg.de/andersen/fullerene
A first-principles approach to electrical transport in atomic-scale nanostructures
We present a first-principles numerical implementation of Landauer formalism
for electrical transport in nanostructures characterized down to the atomic
level. The novelty and interest of our method lies essentially on two facts.
First of all, it makes use of the versatile Gaussian98 code, which is widely
used within the quantum chemistry community. Secondly, it incorporates the
semi-infinite electrodes in a very generic and efficient way by means of Bethe
lattices. We name this method the Gaussian Embedded Cluster Method (GECM). In
order to make contact with other proposed implementations, we illustrate our
technique by calculating the conductance in some well-studied systems such as
metallic (Al and Au) nanocontacts and C-atom chains connected to metallic (Al
and Au) electrodes. In the case of Al nanocontacts the conductance turns out to
be quite dependent on the detailed atomic arrangement. On the contrary, the
conductance in Au nanocontacts presents quite universal features. In the case
of C chains, where the self-consistency guarantees the local charge transfer
and the correct alignment of the molecular and electrode levels, we find that
the conductance oscillates with the number of atoms in the chain regardless of
the type of electrode. However, for short chains and Al electrodes the even-odd
periodicity is reversed at equilibrium bond distances.Comment: 14 pages, two-column format, submitted to PR
Gene expression-based classification of non-small cell lung carcinomas and survival prediction
Background: Current clinical therapy of non-small cell lung cancer depends on histo-pathological classification. This approach poorly predicts clinical outcome for individual patients. Gene expression profiling holds promise to improve clinical stratification, thus paving the way for individualized therapy. Methodology and Principal Findings:A genome-wide gene expression analysis was performed on a cohort of 91 patients. We used 91 tumor- and 65 adjacent normal lung tissue samples. We defined sets of predictor genes (probe sets) with the expression profiles. The power of predictor genes was evaluated using an independent cohort of 96 non-small cell lung cancer- and 6 normal lung samples. We identified a tumor signature of 5 genes that aggregates the 156 tumor and normal samples into the expected groups. We also identified a histology signature of 75 genes, which classifies the samples in the major histological subtypes of non-small cell lung cancer. Correlation analysis identified 17 genes which showed the best association with post-surgery survival time. This signature was used for stratification of all patients in two risk groups. Kaplan-Meier survival curves show that the two groups display a significant difference in post-surgery survival time (p = 5.6E-6). The performance of the signatures was validated using a patient cohort of similar size (Duke University, n = 96). Compared to previously published prognostic signatures for NSCLC, the 17 gene signature performed well on these two cohorts. Conclusions:The gene signatures identified are promising tools for histo-pathological classification of non-small cell lung cancer, and may improve the prediction of clinical outcome
A Model Independent Analysis of the Rare B Decay B -> X_s l^+ l^-
The most general model-independent analysis of the rare decay, \Bsll,
is presented. There are ten independent local four-Fermi interactions which may
contribute to this process. The branching ratio, the forward-backward
asymmetry, and the double differential rate are written as functions of the
Wilson coefficients of the ten operators. We also study the correlation between
the branching ratio and the forward-backward asymmetry by changing each
coefficient. This procedure tells us which types of operator contribute to the
process, and it will be very useful to pin down new physics systematically,
once we have the experimental data with high statistics and the deviation from
the Standard Model is found.Comment: 32 pages, 21 figures, LaTe
Multivalent S2-based vaccines provide broad protection against SARS-CoV-2 variants of concern and pangolin coronaviruses
Background: The COVID-19 pandemic continues to cause morbidity and mortality worldwide. Most approved COVID-19 vaccines generate a neutralizing antibody response that primarily targets the highly variable receptor-binding domain (RBD) of the SARS-CoV-2 spike (S) protein. SARS-CoV-2 âvariants of concernâ have acquired mutations in this domain allowing them to evade vaccine-induced humoral immunity. Recent approaches to improve the breadth of protection beyond SARS-CoV-2 have required the use of mixtures of RBD antigens from different sarbecoviruses. It may therefore be beneficial to develop a vaccine in which the protective immune response targets a more conserved region of the S protein. Methods: Here we have developed a vaccine based on the conserved S2 subunit of the S protein and optimized the adjuvant and immunization regimen in Syrian hamsters and BALB/c mice. We have characterized the efficacy of the vaccine against SARS-CoV-2 variants and other coronaviruses. Findings: Immunization with S2-based constructs elicited a broadly cross-reactive IgG antibody response that recognized the spike proteins of not only SARS-CoV-2 variants, but also SARS-CoV-1, and the four endemic human coronaviruses. Importantly, immunization reduced virus titers in respiratory tissues in vaccinated animals challenged with SARS-CoV-2 variants B.1.351 (beta), B.1.617.2 (delta), and BA.1 (omicron) as well as a pangolin coronavirus. Interpretation: These results suggest that S2-based constructs can elicit a broadly cross-reactive antibody response resulting in limited virus replication, thus providing a framework for designing vaccines that elicit broad protection against coronaviruses. Funding: NIH, Japan Agency for Medical Research and Development, Garry Betty/ V Foundation Chair Fund, and NSF
- âŠ