Sputtering of hydrocarbons by ion-induced breaking of chemical bonds

While the physical sputtering of atoms caused by keV and MeV ions has been studied extensively both by molecular dynamics (MD) simulation and experiments, the mechanisms leading to atom and molecule erosion at energies 1–100 eV are not very well understood. We now describe how low-energy hydrogen ions can cause erosion of carbon atoms and hydrocarbon molecules by entering the region of a carbon–carbon chemical bond and hence breaking it, a process we call ‘swift chemical sputtering'. In the particular case of hydrogen bombardment of carbon-based materials, we further show that this can lead to erosion yields far exceeding those expected for a physical sputtering process.     

Comparative exergy analysis of direct alcohol fuel cells using fuel mixtures

Within the last years there has been increasing interest in direct liquid fuel cells as power sources for portable devices and, in the future, power plants for electric vehicles and other transport media as ships will join those applications. Methanol is considerably more convenient and easy to use than gaseous hydrogen and a considerable work is devoted to the development of direct methanol fuel cells. But ethanol has much lower toxicity and from an ecological viewpoint ethanol is exceptional among all other types of fuel as is the only chemical fuel in renewable supply. The aim of this study is to investigate the possibility of using direct alcohol fuel cells fed with alcohol mixtures. For this purpose, a comparative exergy analysis of a direct alcohol fuel cell fed with alcohol mixtures against the same fuel cell fed with single alcohols is performed. The exergetic efficiency and the exergy loss and destruction are calculated and compared in each case. When alcohol mixtures are fed to the fuel cell, the contribution of each fuel to the fuel cell performance is weighted attending to their relative proportion in the aqueous solution. The optimum alcohol composition for methanol/ethanol mixtures has been determined.     

Measurement of lipid peroxidation in vivo: A comparison of different procedures

A study was undertaken to investigate whether some of the methods commonly used to detect lipid peroxidation of cellular membranes in vivo correlate with each other. The study was performed with the livers of bromobenzene-intoxicated mice, in which lipid peroxidation develops when the depletion of glutathione (GSH) reaches a threshold value. The methods tested and compared were the following: i) measurement of the malondialdehyde (MDA) content of the liver; ii) detection of diene conjugation absorption in liver phospholipids; iii) measurement of the loss of polyunsaturated fatty acids in liver phospholipids; and iv) determination of carbonyl functions formed in acyl residues of membrane phospholipids as a result of the peroxidative breakdown of phospholipid fatty acids. Correlations among the values obtained with these methods showed high statistical significances, indicating that the procedures measure lipid peroxidation in vivo with comparable reliability. Analogously, the four methods appeared also to correlate when applied to in vitro microsomal lipid peroxidation.     

Responses of braconid parasitoidsMicroplitis croceipes (Cresson) andM. demolitor Wilkinson to stereoisomers of kairomone 13-methylhentriacontane

The responses ofMicroplitis croceipes (Cresson) andMicroplitis demolitor Wilkinson to theR andS stereoisomers of the kairomone 13-meth-ylhentriacontane were evaluated. Singly and in combination at 5, 50-, and 500-ng dosage levels each were tested. There was a linear dosage response by both species to the three dosages. Furthermore, there was no difference between responses to the two stereoisomers or their combination by either species at any dosage level. The effects of the two stereoisomers were fully interchangeable and additive. This is the first report of parasitoid responses to stereoisomers of a kairomone.     

A DMA study of the interfacial changes on injection‐molded iPP/mica composites modified by a p‐phenylen‐bis‐maleamic acid grafted atactic polypropylene

Present work concerns to the study of the dynamic mechanical and thermal responses of selected polypropylene (iPP)/mica composites with a modified interface from the matrix side by using a p‐phenylen‐bis‐maleamic acid grafted atactic polypropylene, coming from a byproduct of industrial polymerization reactors. Thus, the study is mainly focused on the 75/25 iPP/mica ratio since it was identified in previous works as providing the maximum inter mica particle distance to assure they should participate in the overall process of dissipation of the mechanical energy supplied to the composites. Hence, the present dynamic mechanical analysis discussion tries to correlate the damping responses of the injection‐molded composites with those previously obtained but over compression molded composites as the basis of further studies all along the compositional iPP/mica map. Therefore, the latter let us, on the one hand, to follow how the main values of the different dynamic mechanical analysis parameters vary because of the interfacial modifier presence, and on the other, to develop a robust correlation between them and the corresponding macroscopic mechanical parameters. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 45366.     

Gas Phase Synthesis of Multifunctional Fe‐Based Nanocubes

Magnetron‐sputtering inert‐gas condensation is an emerging technique offering single‐step, chemical‐free synthesis of nanoparticles with well‐defined morphologies optimized for specific applications. In this study, the authors report a flexible approach to produce Fe nanocubes as building blocks for high‐performance NO₂ gas sensor devices, and hybrid FeAu nanocubes with magneto‐plasmonic properties. Considering that nucleation happens within a short distance from the sputtering target, the authors utilize the high‐permeability and resultant screening effect induced by magnetic Fe targets of various thicknesses to manipulate the magnetic field configuration and plasma confinement. The authors thus readily switch from bimodal to single‐Gaussian size distributions of Fe nanocubes by modifying their primordial thermal environments, as explained by a combination of modeling methods. Simultaneously, the authors obtain a material yield increase of more than one order of magnitude compared to experiments using postgrowth mass filtration. The effectiveness of the method is demonstrated by the deposition of Fe nanocubes on microhotplate devices, leading to unprecedented NO₂ detection performance for Fe‐based chemoresistive gas sensors. The exceedingly low detection limit down to 3 ppb is attributed to a morphological change in operando from Fe/Fe‐oxide core/shell to specific hollow‐nanocube structures, as revealed by in situ environmental transmission electron microscopy.     

Prediction of wrinkle tendencies in explicit sheet metal-forming simulations

In large-scale numerical simulations of sheet metal-forming processes there is a need for assessing wrinkle formation tendencies at early stages of the computations. An algorithmic procedure for early prediction of wrinkles is presented, that makes use of the continuum mechanical behaviour of elastoplastic structures near buckling. The procedure has been implemented into an explicit finite element code and the performance is demonstrated on some example problems. © 1997 John Wiley & Sons, Ltd.     

Pooled versus separate measurements of tree-ring stable isotopes

δ¹³C and δ¹⁸O of tree rings contain time integrated information about the environmental conditions weighted by seasonal growth dynamics and are well established as sources of palaeoclimatic and ecophysiological data. Annually resolved isotope chronologies are frequently produced by pooling dated growth rings from several trees prior to the isotopic analyses. This procedure has the advantage of saving time and resources, but precludes from defining the isotopic error or statistical uncertainty related to the inter-tree variability. Up to now only a few studies have compared isotope series from pooled tree rings with isotopic measurements from individual trees. We tested whether or not the δ¹³C and the δ¹⁸O chronologies derived from pooled and from individual tree rings display significant differences at two locations from the Iberian Peninsula to assess advantages and constraints of both methodologies. The comparisons along the period 1900-2003 reveal a good agreement between pooled chronologies and the two mean master series which were created by averaging raw individual values (Mean) or by generating a mass calibrated mean (MassC). In most of the cases, pooled chronologies show high synchronicity with averaged individual samples at interannual scale but some differences also show up especially when comparing δ¹⁸O decadal to multi-decadal variations. Moreover, differences in the first order autocorrelation among individuals may be obscured by pooling strategies. The lack of replication of pooled chronologies prevents detection of a bias due to a higher mass contribution of one sample but uncertainties associated with the analytical process itself, as sample inhomogeneity, seems to account for the observed differences.     

An investigation of particle deposition mechanisms during impregnation of dual‐scale fabrics with micro particle image velocimetry

Injection moulding processing of composite materials most often includes infiltration of a thermoset resin into a multi‐scale porous fabric. Controlling the fluid flow within the multi‐scale fabric is essential for the quality of the final composite material, since the transport of fluid between regions with different scales is of importance for phenomena such as void formation and filtration of particle doped resins. Hence, the transient flow behaviour in dual scale porous media is investigated in detail with Micro Particle Image Velocimetry. These experiments show that the fluid transport between the two scales can be controlled by the injection velocity. Validation of the measured velocity fields furthermore shows excellent agreement with theory and that transport between the two scales can be substantial at the flow front but negligible up‐stream it. POLYM. COMPOS., 31:1232–1240, 2010. © 2009 Society of Plastics Engineers     

Connecting dopant bond type with electronic structure in N-doped graphene

Robust methods to tune the unique electronic properties of graphene by chemical modification are in great demand due to the potential of the two dimensional material to impact a range of device applications. Here we show that carbon and nitrogen core-level resonant X-ray spectroscopy is a sensitive probe of chemical bonding and electronic structure of chemical dopants introduced in single-sheet graphene films. In conjunction with density functional theory based calculations, we are able to obtain a detailed picture of bond types and electronic structure in graphene doped with nitrogen at the sub-percent level. We show that different N-bond types, including graphitic, pyridinic, and nitrilic, can exist in a single, dilutely N-doped graphene sheet. We show that these various bond types have profoundly different effects on the carrier concentration, indicating that control over the dopant bond type is a crucial requirement in advancing graphene electronics.