1,629 research outputs found
Remark on Remnant and Residue Entropy with GUP
In this article, close to the Planck scale, we discuss on the remnant and
residue entropy from a Rutz-Schwarzschild black hole in the frame of Finsler
geometry. Employing the corrected Hamilton-Jacobi equation, the tunneling
radiation of a scalar particle is presented, and the revised tunneling
temperature and revised entropy are also found. Taking into account generalized
uncertainty principle (GUP), we analyze the remnant stability and residue
entropy based on thermodynamic phase transition. In addition, the effects of
the Finsler perturbation parameter, GUP parameter and angular momentum
parameter on remnant and residual entropy are also discussed.Comment: 18 pages, 5 figures, 2 table
(E)-N′-(2,5-Dimethoxybenzylidene)-3,4-dihydroxybenzohydrazide monohydrate
In the title compound, C16H16N2O5·H2O, the dihedral angle between the two benzene rings is 25.9 (1)°. Intramolecular O—H⋯O and N—H⋯O hydrogen bonds are observed. In the crystal, the components are linked into a three-dimensional network by O—H⋯O and O—H⋯(O,O) hydrogen bonds
Poly[[aqua(μ2-oxalato)(μ2-2-oxidopyridinium-3-carboxylato)holmium(III)] monohydrate]
In the title complex, {[Ho(C2O4)(C6H4NO3)(H2O)]·(H2O)}n, the HoIII ion is coordinated by three O atoms from two 2-oxidopyridinium-3-carboxylate ligands, four O atoms from two oxalate ligands and one water molecule in a distorted bicapped trigonal-prismatic geometry. The 2-oxidopyridinium-3-carboxylate and oxalate ligands link the HoIII ions into a layer in (100). These layers are further connected by intermolecular O—H⋯O hydrogen bonds involving the coordinated water molecules to assemble a three-dimensional supramolecular network. The uncoordinated water molecule is involved in N—H⋯O and O—H⋯O hydrogen bonds within the layer
Poly[bis(4,4′-bipyridine)(μ3-4,4′-dicarboxybiphenyl-3,3′-dicarboxylato)iron(II)]
In the polymeric title complex, [Fe(C16H8O8)(C10H8N2)2]n, the iron(II) cation is coordinated by four O atoms from three different 4,4′-dicarboxybiphenyl-3,3′-dicarboxylate ligands and two N atoms from two 4,4′-bipyridine ligands in a distorted octahedral geometry. The 4,4′-dicarboxybiphenyl-3,3′-dicarboxylate ligands bridge adjacent cations, forming chains parallel to the c axis. The chains are further connected by intermolecular O—H⋯N hydrogen bonds, forming two-dimensional supramolecular layers parallel to (010)
Coronavirus Spike Protein Inhibits Host Cell Translation by Interaction with eIF3f
In response to viral infection, the expression of numerous host genes, including predominantly a number of proinflammatory cytokines and chemokines, is usually up-regulated at both transcriptional and translational levels. It was noted that in cells infected with coronavirus, transcription and translation of some of these genes were differentially induced. Drastic induction of their expression at the transcriptional level was observed in cells infected with coronavirus. However, induction of the same genes at the translational level was usually found to be minimal to moderate. To investigate the underlying mechanisms, yeast two-hybrid screen was carried out using SARS-CoV proteins as baits, revealing that a subunit of the eukaryotic initiation factor 3 (eIF3), eIF3f, may interact with the N-terminal region of the SARS-CoV spike (S) protein. This interaction was subsequently confirmed by co-immunoprecipitation and immunofluorescent staining. Meanwhile, parallel experiments confirmed that eIF3f could also interact with the S protein of another coronavirus, the avian coronavirus infectious bronchitis virus (IBV). These interactions led to the inhibition of translation of a reporter gene in both in vitro expression system and intact cells. Interestingly, IBV-infected cells stably expressing a Flag-tagged eIF3f showed much higher translation of IL-6 and IL-8, suggesting that the interaction between coronavirus S protein and eIF3f plays a functional role in controlling the expression of host genes, especially genes that are induced during coronavirus infection cycles. This study reveals a novel mechanism exploited by coronavirus to regulate viral pathogenesis
Numerical simulation of dental resurfacing of a feldspar porcelain with coarse diamond burs
Dental bioceramics are more and more attractive to both dentists and patients due to their unique biocompatibility and esthetics; they can be fabricated efficiently using chair-side CAD/CAM dental systems. However, the failure rate of ceramic prostheses is noticeable high. The major clinical failure mode lies in surface and subsurface damage in the ceramic prostheses due to their inherent brittleness. In clinical practice, ceramic prostheses are intraorally adjusted and resurfaced using dental handpieces/burs for marginal and occlusal fit. The clinical adjustments using abrasive burs produce surface and subsurface damage in prostheses. This paper will address this issue via numerical simulation. Finite element analysis was utilised to model the dental resurfacing of a feldspar porcelain with coarse diamond burs and to predict the degrees of subsurface damage of the porcelain prostheses
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Unsaturated Ligands Seed an Order to Disorder Transition in Mixed Ligand Shells of CdSe/CdS Quantum Dots.
A phase transition within the ligand shell of core/shell quantum dots is studied in the prototypical system of colloidal CdSe/CdS quantum dots with a ligand shell composed of bound oleate (OA) and octadecylphosphonate (ODPA). The ligand shell composition is tuned using a ligand exchange procedure and quantified through proton NMR spectroscopy. Temperature-dependent photoluminescence spectroscopy reveals a signature of a phase transition within the organic ligand shell. Surprisingly, the ligand order to disorder phase transition triggers an abrupt increase in the photoluminescence quantum yield (PLQY) and full-width at half-maximum (FWHM) with increasing temperature. The temperature and width of the phase transition show a clear dependence on ligand shell composition, such that QDs with higher ODPA fractions have sharper phase transitions that occur at higher temperatures. In order to gain a molecular understanding of the changes in ligand ordering, Fourier transform infrared and vibrational sum frequency generation spectroscopies are performed. These measurements confirm that an order/disorder transition in the ligand shell tracks with the photoluminescence changes that accompany the ligand phase transition. The phase transition is simulated through a lattice model that suggests that the ligand shell is well-mixed and does not have completely segregated domains of OA and ODPA. Furthermore, we show that the unsaturated chains of OA seed disorder within the ligand shell
Sensing performance of Nanocrystalline Graphite Based Humidity Sensors
Environmental sensors play a crucial role in a wide range of applications. Amongst them, humidity sensors that are stable and operational in harsh environments are incredibly important for process control and monitoring. Nanocrystalline graphite (NCG) is a type of carbon-based thin film material. Previous work has shown that NCG has excellent mechanical properties and is able to withstand high radiation doses. The granular structure of the NCG film makes it a good candidate for humidity sensing as the film consists of conductive graphitic grains with a high density of sp2 bonds and amorphous grain boundaries with high resistivity, adsorption of water molecule onto the film forms conductive pathways between grains through the Grotthuss mechanism which lowers the resistance of the film by a measurable amount. Here we report for the first time, a working humidity sensor with linear response, fabricated using NCG as the sensing material for harsh, real-world environments, which include exposure to weak acids via rainfall, UV radiation, mechanical wear, and high humidity environments. The calculated sensitivity of the best-fabricated sensor is S = 0.0334%, with a maximum resistance change of -4.4 kOhms, over the range of 15% RH to 85% RH. The response time of the sensor is 20ms with the current measurement setup. The baseline resistance value of the sensor at 15% RH is 210 kOhms. The sensor has the potential to be used as a humidity sensor for harsh environments due to the chemical, thermal and mechanical stability of the NCG film
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