Relief distribution networks: a systematic review

In the last 20 years, Emergency Management has received increasing attention from the scientific community. Meanwhile, the study of relief distribution networks has become one of the most popular topics within the Emergency Management field. In fact, the number and variety of contributions devoted to the design or the management of relief distribution networks has exploded in the recent years, motivating the need for a structured and systematic analysis of the works on this specific topic. To this end, this paper presents a systematic review of contributions on relief distribution networks in response to disasters. Through a systematic and scientific methodology, it gathers and consolidates the published research works in a transparent and objective way. It pursues three goals. First, to conduct an up-to-date survey of the research in relief distribution networks focusing on the logistics aspects of the problem, which despite the number of previous reviews has been overlooked in the past. Second, to highlight the trends and the most promising challenges in the modeling and resolution approaches and, finally, to identify future research perspectives that need to be explored.     

Radical chain reduction of alkylboron compounds with catechols

The conversion of alkylboranes to the corresponding alkanes is classically per-formed via protonolysis of alkylboranes. This simple reaction requires the use of severe reaction conditions, that is, treatment with a carboxylic acid at high temperature (>150 °C). We report here a mild radical procedure for the transformation of organoboranes to alkanes. 4-tert-Butylcatechol, a well-established radical inhibitor and antioxidant, is acting as a source of hydrogen atoms. An efficient chain reaction is observed due to the exceptional reactivity of phenoxyl radicals toward alkylboranes. The reaction has been applied to a wide range of organoboron derivatives such as B-alkylcatecholboranes, trialkylboranes, pinacolboronates, and alkylboronic acids. Furthermore, the so far elusive rate constants for the hydrogen transfer between secondary alkyl radical and catechol derivatives have been experimentally determined. Interestingly, they are less than 1 order of magnitude slower than that of tin hydride at 80 °C, making catechols particularly attractive for a wide range of transformations involving C-C bond formation.     

From micro to nano reentrant structures: hysteresis on superomniphobic surfaces

The paper reports on the wetting characterization of two surfaces presenting reentrant shapes at micro- and nanoscale using low surface tension liquids (down to 28 mN/m). On the one hand, mushroom-like microstructures are fabricated by molding poly(dimethylsiloxane) (PDMS) onto a patterned sacrificial photoresist bilayer. On the other hand, zinc oxide nanostructures (ZnO NS) are synthesized by easy and fast chemical bath deposition technique. The PDMS and ZnO NS surfaces are then chemically modified with 1H,1H,2H,2H-perfluorodecyltrichlorosilane in vapor phase. Both PDMS and ZnO NS surfaces exhibit a large apparent contact angle (>150°) and contact angle hysteresis varying from 50° to a quasi-null value. This large discrepancy can be ascribed to the length scale and topography of the structures, promoting either a vertical imbibition or a lateral spreading within the roughness.     

Unsymmetrical Binding Modes of the HOPNO Inhibitor of Tyrosinase: From Model Complexes to the Enzyme

The deciphering of the binding mode of tyrosinase (Ty) inhibitors is essential to understand how to regulate the tyrosinase activity. In this paper, by combining experimental and theoretical methods, we studied an unsymmetrical tyrosinase functional model and its interaction with 2‐hydroxypyridine‐N‐oxide (HOPNO), a new and efficient competitive inhibitor for bacterial Ty. The tyrosinase model was a dinuclear copper complex bridged by a chelated ring with two different complexing arms (namely (bis(2‐ethylpyridyl)amino)methyl and (bis(2‐methylpyridyl)amino)methyl). The geometrical asymmetry of the complex induces an unsymmetrical binding of HOPNO. Comparisons have been made with the binding modes obtained on similar symmetrical complexes. Finally, by using quantum mechanics/molecular mechanics (QM/MM) calculations, we studied the binding mode in tyrosinase from a bacterial source. A new unsymmetrical binding mode was obtained, which was linked to the second coordination sphere of the enzyme.     

Synthesis and glycosidase inhibition properties of triazole-linked calixarene–iminosugar clusters

Calixarene–iminosugar derivatives bearing four 1-deoxynojirimycin units at the upper or lower rim of calix[4]arenes in a fixed cone conformation were synthesized by copper-catalyzed azide-alkyne cycloaddition (CuAAC) and their inhibitory activity was evaluated against five glycosidases. Modest but significant affinity enhancements of up to seven per 1-deoxynojirimycin unit over the monovalent iminosugar derivative were observed for the inhibition of Jack bean (Canavalia ensiformis) α-mannosidase. It was also demonstrated that the residual copper ions did not contribute to the inhibitory properties of the newly prepared calixarene-based multivalent iminosugars.     

Nonlinear elastodynamics in micro-inhomogeneous solids observed by head-wave based dynamic acoustoelastic testing

Dynamic acoustoelastic testing provides a more complete insight into the acoustic nonlinearity exhibited by micro-inhomogeneous media like granular and cracked materials. This method consists of measuring time of flight and energy modulations of pulsed ultrasonic waves induced by a low-frequency standing wave. Here pulsed ultrasonic head waves were employed to assess elastic and dissipative nonlinearities in a region near the surface of a solid. Synchronization of the ultrasound pulse sequence with the low-frequency excitation provided instantaneous variations in the elastic modulus and the attenuation as functions of the instantaneous low-frequency strain. Weak quadratic elastic nonlinearity and no dissipative nonlinearity were detected in duralumin. In limestone, distinction between tensile and compressive behaviors revealed an asymmetry in the acoustic nonlinearity and hysteresis in both the elastic modulus and the attenuation variations. Measured nonlinear acoustical parameters are in good agreement with values obtained by different techniques. Reversible acoustically induced conditioning modified the acoustic nonlinearity both quantitatively and qualitatively. It reduced tension-compression asymmetry, suggesting a nonequilibrium modification of the sources of acoustic nonlinearity. Additionally to the metrology of the acoustic nonlinearity, head wave based dynamic acoustoelastic testing may be a useful tool to monitor changes in the microstructure or the accumulation of damage in solids.     

High-accuracy acoustic detection of nonclassical component of material nonlinearity

The aim is to assess the nonclassical component of material nonlinearity in several classes of materials with weak, intermediate, and high nonlinear properties. In this contribution, an optimized nonlinear resonant ultrasound spectroscopy (NRUS) measuring and data processing protocol applied to small samples is described. The protocol is used to overcome the effects of environmental condition changes that take place during an experiment, and that may mask the intrinsic nonlinearity. External temperature fluctuation is identified as a primary source of measurement contamination. For instance, a variation of 0.1?°C produced a frequency variation of 0.01%, which is similar to the expected nonlinear frequency shift for weakly nonlinear materials. In order to overcome environmental effects, the reference frequency measurements are repeated before each excitation level and then used to compute nonlinear parameters. Using this approach, relative resonant frequency shifts of 10(-5) can be measured, which is below the limit of 10(-4) often considered as the limit of NRUS sensitivity under common experimental conditions. Due to enhanced sensitivity resulting from the correction procedure applied in this work, nonclassical nonlinearity in materials that before have been assumed to only be classically nonlinear in past work (steel, brass, and aluminum) is reported.     

Temperature and Inoculum Origin Influence the Performance of Ex-Situ Biological Hydrogen Methanation

The conversion of H₂ into methane can be carried out by microorganisms in a process so-called biomethanation. In ex-situ biomethanation H₂ and CO₂ gas are exogenous to the system. One of the main limitations of the biomethanation process is the low gas-liquid transfer rate and solubility of H₂ which are strongly influenced by the temperature. Hydrogenotrophic methanogens that are responsible for the biomethanation reaction are also very sensitive to temperature variations. The aim of this work was to evaluate the impact of temperature on batch biomethanation process in mixed culture. The performances of mesophilic and thermophilic inocula were assessed at 4 temperatures (24, 35, 55 and 65 °C). A negative impact of the low temperature (24 °C) was observed on microbial kinetics. Although methane production rate was higher at 55 and 65 °C (respectively 290 ± 55 and 309 ± 109 mL CH₄/L.day for the mesophilic inoculum) than at 24 and 35 °C (respectively 156 ± 41 and 253 ± 51 mL CH₄/L.day), the instability of the system substantially increased, likely because of a strong dominance of only Methanothermobacter species. Considering the maximal methane production rates and their stability all along the experiments, an optimal temperature range of 35 °C or 55 °C is recommended to operate ex-situ biomethanation process.     

Radical Reductive Alkylation of Enamines: Conversion of the Products into Alkenes and Primary Amines

Procedures for the conversion of tertiary amines, obtained by radical reductive alkylation of enamines, into alkenes (Cope reaction) and primary amines (double β-elimination reaction) are presented.     

A fully anisotropic hierarchical hybrid cellular automaton algorithm to simulate bone remodeling

Computational models of the bone remodeling process have been utilized to further our understanding of the adaptation of bone architecture to changes in its mechanical environment. The hierarchical hybrid cellular automata (HHCA) algorithm is a multi-scale approach for the simulation of the adaptation of bone. Currently, this remodeling algorithm utilizes the apparent material properties of the trabecular architecture. The objective of this work is to increase the fidelity of the HHCA algorithm by incorporating the local anisotropic properties of these structures. Preliminary analyses display improved efficiency and a more consistent material distribution when incorporating anisotropic properties into the HHCA methodology.