An exponential matrix method for the buckling analysis of underground pipelines subjected to landslide loads

Abstract Due to their dimensions, long pipelines often cross areas that are highly susceptible to landslides. In Italy, this problem requires special attention, as many slow-moving landslides interact with buried pipelines. The paper analyzes such interaction problem with particular reference to buckling analysis, tackling the solution of the governing equations by an exponential matrix method. In the paper the basic equation, its computational aspects and numerical analysis options are outlined. Representative results of the proposed methodology and potential applications on buckling analysis of buried pipes are presented

Bioalcohol Reforming: An Overview of the Recent Advances for the Enhancement of Catalyst Stability

The growing demand for energy production highlights the shortage of traditional resources and the related environmental issues. The adoption of bioalcohols (i.e., alcohols produced from biomass or biological routes) is progressively becoming an interesting approach that is used to restrict the consumption of fossil fuels. Bioethanol, biomethanol, bioglycerol, and other bioalcohols (propanol and butanol) represent attractive feedstocks for catalytic reforming and production of hydrogen, which is considered the fuel of the future. Different processes are already available, including steam reforming, oxidative reforming, dry reforming, and aqueous-phase reforming. Achieving the desired hydrogen selectivity is one of the main challenges, due to the occurrence of side reactions that cause coke formation and catalyst deactivation. The aims of this review are related to the critical identification of the formation of carbon roots and the deactivation of catalysts in bioalcohol reforming reactions. Furthermore, attention is focused on the strategies used to improve the durability and stability of the catalysts, with particular attention paid to the innovative formulations developed over the last 5 years

Quinine sulfate and bacterial invasion

BACKGROUND: As many patients who receive antimalarial drugs for treatment of noninfectious, inflammatory diseases are also immunosuppressed and might have a concomitant bacterial infection, we studied the effectiveness of these drugs against bacterial infections, to find out whether they could protect against (and even treat) such conditions and obviate the need for an additional antibiotic drug. METHODS: Effect of QS on bacterial growth: Escherichia coli (E. coli) HB101 pRI203 were cultured overnight at 37°C in TSB and inoculated (approx 1 × 10(7) cells /ml) in MEM in the presence of QS at various concentrations (0, 50 and 100 μM). The effect of QS at concentration of 50 and 100 μM on the entry process of E. coli HB101 pRI203 into HeLa cells was studied under different experimental conditions: 1. QS was incubated with 3 × 10(5) HeLa cells for 60 min at 37°C prior to infection. 2. QS was added to HeLa cell monolayers during the infection period. RESULTS: QS showed no antibacterial activity after 24 h of incubation. The invasive efficiency of the bacteria was significantly inhibited at a dose-dependent manner, when QS was added to HeLa cells for 60 min at 37°C prior to infection (condition 1), and to a lesser extent when added during the period of infection (condition 2). CONCLUSIONS: Although the antimalarials are generally regarded as being inactive against most extracellular bacterial species, our results indicate that QS significantly inhibited the internalization/invasion efficacy of E. coli in the host cells

Multi-disciplinary analysis and optimization Java tool for aircraft design

The first stages of the aircraft design process require to carry out multi-disciplinary analyses as fast as possible, and with a certain grade of accuracy. During the conceptual and the preliminary phases, the goal is to search for the design that best fulfils the requirements. This work presents a Java framework, named JPAD, developed at the University of Naples Federico II by the Design of Aircraft and Flight technologies research group (DAF) to perform multi-disciplinary analysis and optimization of transport aircraft. This paper describes all the JPAD capabilities, focusing on the sensitivity analyses and optimization modules. At the end, a case study concerning the optimization of a regional turboprop aircraft model similar to the well-known ATR72 will be presented

Java framework for parametric aircraft design - Ground performance

This paper aims to introduce the take-off and landing performance analysis modules of the software library named Java toolchain of Programs for Aircraft Design (JPAD), dedicated to the aircraft preliminary design. An overview of JPAD is also presented. Design/methodology/approach: The calculation of the take-off and landing distances has been implemented using a simulation-based approach. This expects to solve an appropriate set of ordinary differential equations, which describes the aircraft equations of motion during all the take-off and landing phases. Tests upon two aircraft models (ATR72 and B747-100B) have been performed to compare the obtained output with the performance data retrieved from the related flight manuals. Findings: The tool developed has proven to be very reliable and versatile, as it performs the calculation of the required performance with almost no computational effort and with a good accuracy, providing a less than the 5 per cent difference with respect to the statistical trend and a difference from the flight manual or public brochure data around 10 per cent. Originality/value: The use of a simulation-based approach to have a more accurate estimation of the ground performance with respect to classic semi-empirical equations. Although performing the simulation of the aircraft motion, the approach shown is very time-saving and can be easily implemented in an optimization cycle

Electronic structure of copper phthalocyanine:An experimental and theoretical study of occupied and unoccupied levels

An experimental and theoretical study of the electronic structure of copper phthalocyanine (CuPc) molecule is presented. We performed x-ray photoemission spectroscopy (XPS) and photoabsorption [x-ray absorption near-edge structure (XANES)] gas phase experiments and we compared the results with self-consistent field, density functional theory (DFT), and static-exchange theoretical calculations. In addition, ultraviolet photoelectron spectra (UPS) allowed disentangling several outer molecular orbitals. A detailed study of the two highest occupied orbitals (having a(1u) and b(1g) symmetries) is presented: the high energy resolution available for UPS measurements allowed resolving an extra feature assigned to vibrational stretching in the pyrrole rings. This observation, together with the computed DFT electron density distributions of the outer valence orbitals, suggests that the a(1u) orbital (the highest occupied molecular orbital) is mainly localized on the carbon atoms of pyrrole rings and it is doubly occupied, while the b(1g) orbital, singly occupied, is mainly localized on the Cu atom. Ab initio calculations of XPS and XANES spectra at carbon K-edge of CuPc are also presented. The comparison between experiment and theory revealed that, in spite of being formally not equivalent, carbon atoms of the benzene rings experience a similar electronic environment. Carbon K-edge absorption spectra were interpreted in terms of different contributions coming from chemically shifted C 1s orbitals of the nonequivalent carbon atoms on the inner ring of the molecule formed by the sequence of CN bonds and on the benzene rings, respectively, and also in terms of different electronic distributions of the excited lowest unoccupied molecular orbital (LUMO) and LUMO+1. In particular, the degenerate LUMO appears to be mostly localized on the inner pyrrole ring

Noble Metals-Based Catalysts for Hydrogen Production via Bioethanol Reforming in A Fluidized Bed Reactor

In this work, Pt-Ni/CeO2-SiO2, as well as Ru-Ni/CeO2-SiO2 catalysts, were obtained at different loadings of the noble metal (in the interval 0–3 wt%) and tested for oxidative steam reforming of ethanol. Stability performance was evaluated at 500 °C for 25 h under a steam to ethanol ratio of 4 and an oxygen to ethanol ratio of 0.5. The weight hourly space velocity was fixed to 60 h−1, which is considerably higher than the typical values selected for such processes. All the catalysts deactivated with time-on-stream, due to the severe operative conditions selected. However, the highest ethanol conversion (above 95%) and hydrogen yield (30%) at the end of the test were recorded over the 2 wt%Pt-10 wt%Ni/CeO2-SiO2 catalyst, which also displayed a limited carbon formation rate (1.5 × 10−6 gcoke·gcatalyst−1·gcarbon,fed−1·h−1, reduced almost 5 times compared to the samples that had a Pt or Ru content of 0.5 wt%). Thus, the latter catalyst was identified as a promising candidate for future tests under real bioethanol mixture

Stacking sequences in composite laminates through design optimization

AbstractComposites are experiencing a new era. The spatial resolution at which is to date possible to build up complex architectured microstructures through additive manufacturing-based and sintering of powder metals 3D printing techniques, as well as the recent improvements in both filament winding and automated fiber deposition processes, are opening new unforeseeable scenarios for applying optimization strategies to the design of high-performance structures and metamaterials that could previously be only theoretically conceived. Motivated by these new possibilities, the present work, by combining computational methods, analytical approaches and experimental analysis, shows how finite element Design Optimization algorithms can be ad hoc rewritten by identifying as design variables the orientation of the reinforcing fibers in each ply of a layered structure for redesigning fiber-reinforced composites exhibiting at the same time high stiffness and toughening, two features generally in competition each other. To highlight the flexibility and the effectiveness of the proposed strategy, after a brief recalling of the essential theoretical remarks and the implemented procedure, selected example applications are finally illustrated on laminated plates under different boundary conditions, cylindrical layered shells with varying curvature subjected to point loads and composite tubes made of carbon fiber-reinforced polymers, recently employed as structural components in advanced aerospace engineering applications

Electronic structure of copper phthalocyanine:An experimental and theoretical study of occupied and unoccupied levels

An experimental and theoretical study of the electronic structure of copper phthalocyanine (CuPc) molecule is presented. We performed x-ray photoemission spectroscopy (XPS) and photoabsorption [x-ray absorption near-edge structure (XANES)] gas phase experiments and we compared the results with self-consistent field, density functional theory (DFT), and static-exchange theoretical calculations. In addition, ultraviolet photoelectron spectra (UPS) allowed disentangling several outer molecular orbitals. A detailed study of the two highest occupied orbitals (having a(1u) and b(1g) symmetries) is presented: the high energy resolution available for UPS measurements allowed resolving an extra feature assigned to vibrational stretching in the pyrrole rings. This observation, together with the computed DFT electron density distributions of the outer valence orbitals, suggests that the a(1u) orbital (the highest occupied molecular orbital) is mainly localized on the carbon atoms of pyrrole rings and it is doubly occupied, while the b(1g) orbital, singly occupied, is mainly localized on the Cu atom. Ab initio calculations of XPS and XANES spectra at carbon K-edge of CuPc are also presented. The comparison between experiment and theory revealed that, in spite of being formally not equivalent, carbon atoms of the benzene rings experience a similar electronic environment. Carbon K-edge absorption spectra were interpreted in terms of different contributions coming from chemically shifted C 1s orbitals of the nonequivalent carbon atoms on the inner ring of the molecule formed by the sequence of CN bonds and on the benzene rings, respectively, and also in terms of different electronic distributions of the excited lowest unoccupied molecular orbital (LUMO) and LUMO+1. In particular, the degenerate LUMO appears to be mostly localized on the inner pyrrole ring