A new method for layer 2 loop prevention in software defined networks

Telecommunication Systems - Broadcast storm refers to the bandwidth saturation caused by broadcast traffic flows when a loop exists and it can quickly lead to the network failure. In legacy...     

Passivity-based control of nonlinear teleoperation systems with non-passive interaction forces

Intelligent Service Robotics - This paper addresses the problem of asymptotic stability and position tracking in nonlinear teleoperation systems interacting with non-passive operator and...     

Silane-functionalized Al2O3-modified polyurethane powder coatings: Nonisothermal degradation kinetics and mechanistic insights

This work reports on nonisothermal degradation kinetics of polyurethane (PU)-based powder coatings containing 1, 3, and 5%wt% vinyltrimethoxysilane functionalized Al₂O₃ (V-Al₂O₃) nanoparticles. Thermogravimetric analysis of PU/V-Al₂O₃ powder coatings with different V-Al₂O₃ contents has been performed at different heating rates. Variation of activation energy (E_a) of PU/V-Al₂O₃ powder coatings was modeled as a function of partial mass loss by using Kissinger–Akahira–Sunose, Ozawa–Wall–Flynn and modified Coats–Redfern isoconversional approaches. The results revealed hindered decomposition process of PU/V-Al₂O₃ nanocomposite powder coatings, featured by an increase in activation energy of degradation from ∼158 for blank PU to 225, 183, and 229 kJ/mol for nanocomposites filled with 1, 3, and 5 wt% of V-Al₂O₃, respectively. Likewise, pre-exponential factor values increased for samples containing V-Al₂O₃ nanoparticles compared to that of blank sample. Sestak–Berggren kinetic model appropriately captured thermal degradation behavior of PU/V-Al₂O₃ nanocomposites than that of nth order decomposition kinetic reaction models.     

Scouting around 1,2,3,4-Tetrahydrochromeno[3,2-c]pyridin-10-ones for Single- and Multitarget Ligands Directed towards Relevant Alzheimer's Targets

A number of 1,2,3,4-tetrahydrochromeno[3,2-c]pyridin-10-one derivatives have been synthesized and screened against different targets involved in the onset and progression of Alzheimer's disease (AD), such as acetyl- and butyrylcholinesterase (AChE and BChE), monoamine oxidases A and B (MAO A and B), aggregation of β-amyloid (Aβ) and reactive oxygen species (ROS) production. Derivatives 1 c , 3 b , 4 and 5 a showed multifaceted profiles of promising anti-AD features and returned well-balanced multitargeting inhibitory activities. Moreover, compound 1 f , a potent and selective human MAO B inhibitor (IC₅₀=0.89 μM), proved to be a safe neuroprotectant in a human neuroblastoma cell line (SH-SY5Y) by improving viability impaired by Aβ_1–42 and pro-oxidant insult. Furthermore, structure–activity relationships (SARs) and docking models were derived in order to assist further hit-to-lead optimization stage.     

Hierarchical 3D starfish-like Ni3S4–NiS on reduced graphene oxide for high-performance supercapacitors

In this research, Ni₃S₄–NiS with starfish morphology was synthesized with a simple hydrothermal method and then hybridized with reduced graphene oxide (rGO) as a material for high-performance supercapacitors. The crystal structure and morphology of the as-prepared materials were studied by X-ray diffraction spectroscopy and electron microscopy. Uniform distribution of Ni₃S₄–NiS on rGO was observed from electron microscopy images. The results showed that Ni₃S₄–NiS/rGO with a specific capacitance of 1578 Fg^-1 and discharge time of 603 s at the current density of 0.5 Ag^-1 has more capacity and stability relative to Ni₃S₄–NiS. The cyclic stability after 5000 cycles showed that the Ni₃S₄–NiS/rGO electrode is stable, and 91% of its corresponding initial capacitance retained at the end of 5000 cycles. The good results in capacitance and stability of this electrode can be regarded as an improvement for the development of highly efficient and economic supercapacitors for portable electronic devices.     

Ablation behavior of organoclay‐NBR insulator: Modeling and experimental

Nitrile‐based nanocomposite heat insulators are very attractive materials compared with their similar nonelastomeric counterparts, due to their higher deformation bearing capacity in special applications. Modeling of these ablative nanocomposites enables us to determine the exact required thickness of the insulator and temperature distribution across it at predetermined thermal conditions. The complete form of the ablation equation is a transient nonlinear second‐order differential equation with variable temperature‐dependent thermo‐physical properties, which must be determined during thermal degradation. In this work, in addition to experimental investigation of ablative elastomeric nanocomposites based on NBR, the ablation process is modeled analytically with perturbation theory in the Lagrangian coordinate system because of surface recession and moving boundaries. Kirchhoff transformation was used to get rid of the temperature dependence of k in each zonal of virgin and char. The theoretical results were confirmed by experimental data obtained from the oxyacetylene flame test. The results proposed a competitive nitrile‐based nanocomposite heat insulator with superior ablation properties: mass ablation rate 0.014 g s^?1, linear ablation rate 0.012 mm s^?1, and insulating index number 6800 s m^?1, under a standard test with a heat flux of 2500 kW m^?2 for 15 seconds.