The Global Biogeochemical Silicon Cycle

Silicon is one of the most important elements in the current age of the anthropocene. It has numerous industrial applications, and supports a high-tech multi-billion Euro industry. Silicon has a fascinating biological and geological cycle, interacting with other globally important biogeochemical cycles. In this review, we bring together both biological and geological aspects of the silicon cycle to provide a general, comprehensive review of the cycling of silicon in the environment. We hope this review will provide inspiration for researchers to study this fascinating element, as well as providing a background environmental context to those interested in silicon.     

Antennal sensilla of two parasitoid wasps: a comparative scanning electron microscopy study

Two closely related parasitoid wasp species, Cotesia glomerata (L.) and Cotesia rubecula (Marshall) (Hymenoptera:Braconidae), are different in their associative learning of plant odors. To provide a solid basis for our research on the mechanisms that underlie this difference, we described the morphology of the antennal sensilla of these two species using scanning electron microscopy complemented with transmission electron microscopy. Female and male antennae of both species have the same six types of sensilla. We classified these sensilla as sensilla trichodea without pores, sensilla trichodea with a tip pore, sensilla trichodea with wall pores, sensilla coeloconica type I, sensilla coeloconica type II, and sensilla placodea. We conclude that the morphology, numbers, and distribution of the sensory receptors are highly similar in these two closely related wasp species. Differences between species and sexes occurred only in sensilla placodea numbers. C. rubecula has more sensilla placodea than C. glomerata and males of both species have a larger number and a higher density of sensilla placodea compared to females of the same species.     

Investigations on vinylene carbonate. IV. Radiation induced graft copolymerization of vinylene carbonate and N-vinyl-N-methylacetamide onto polyethylene films

Graft copolymerization of binary mixtures of vinylene carbonate (VCA) and N-vinyl–N–methylacetamide (VIMA) onto low density polyethylene (LDPE) films was studied by the mutual γ-irradiation technique. Sufficient amounts of functionally active VCA groups could be grafted onto the surface and the hydrophilicity of the surface was also improved. The grafting of VCA onto polyethylene films in the binary solutions was found to be promoted by the presence of VIMA, thus showing a positive synergism. The VCA content in the graft copolymers was always higher than in the copolymers obtained by homogeneous copolymerization using the same monomer feed composition. The monomer reactivity ratios, as well as a preferential partitioning of the monomers surrounding the polymeric substrate, were considered to explain the grafting reactions in the binary systems.     

Morphology and property changes in PLA/PHBV blends as function of blend composition

PLA/PHBV blends were prepared by melt mixing. The morphology and physical properties of the blends and neat polymers were investigated. Scanning electron microscopy (SEM) studies provided evidence of interfacial cavities and weak interfacial interaction between the two polymers, and no obvious co-continuous morphology was observed in any of the investigated blends. Positron annihilation lifetime spectroscopy (PALS) indicated the presence of open-volume cavities with sub-nanometre diameters; far smaller than observed from the SEM images. The mean size and relative concentration of these cavities increased with increasing PHBV content. A weak negative deviation in the mean size for low PHBV content possibly indicates some degree of partial miscibility. The glass transition temperature of PLA in the blends decreased with increasing PHBV content, and offers support to some PHBV being miscible with the PLA. The degree of crystallinity in the blends show interesting behaviour that may be explained in terms of the complex morphology observed for these blends. The thermal conductivity of the samples varied with composition, but increased with increasing PHBV content, which was probably related to the increasing crystallinity. Both the tensile strength and Young’s modulus decreased with increasing PHBV content for the sequence of blends, and both parameters exhibited maximum values for 10 wt.% PHBV. For samples between 50/50 and 10/90 PLA/PHBV the tensile strength and Young’s modulus were comparable to or lower than those for both the neat polymers.     

Thermal and thermomechanical properties of poly(butylene succinate) nanocomposites

This article describes the thermal and thermomechanical properties of poly(butylene succinate) (PBS) and its nanocomposites. PBS nanocomposites with three different weight ratios of organically modified synthetic fluorine mica (OMSFM) have been prepared by melt-mixing in a batch mixer at 140 degrees C. The structure and morphology of the nanocomposites were characterized by X-ray diffraction (XRD) analyses and transmission electron microscopy (TEM) observations that reveal the homogeneous dispersion of the intercalated silicate layers into the PBS matrix. The thermal properties of pure PBS and the nanocomposite samples were studied by both conventional and temperature modulated differential scanning calorimetry (DSC) analyses, which show multiple melting behavior of the PBS matrix. The investigation of the thermomechanical properties was performed by dynamic mechanical analysis. Results reveal significant improvement in the storage modulus of neat PBS upon addition of OMSFM. The tensile modulus of neat PBS is also increased substantially with the addition of OMSFM, however, the strength at yield and elongation at break of neat PBS systematically decreases with the loading of OMSFM. The thermal stability of the nanocomposites compared to that of the pure polymer sample was examined under both pyrolytic and thermo-oxidative environments. It is shown that the thermal stability of PBS is increased moderately in the presence of 3 wt% of OMSFM, but there is no significant effect on further silicate loading in the oxidative environment. In the nitrogen environment, however, the thermal stability systematically decreases with increasing clay loading.     

Optimization of Sandwich Composites Fuselages Under Flight Loads

The sandwich composites fuselages appear to be a promising choice for the future aircrafts because of their structural efficiency and functional integration advantages. However, the design of sandwich composites is more complex than other structures because of many involved variables. In this paper, the fuselage is designed as a sandwich composites cylinder, and its structural optimization using the finite element method (FEM) is outlined to obtain the minimum weight. The constraints include structural stability and the composites failure criteria. In order to get a verification baseline for the FEM analysis, the stability of sandwich structures is studied and the optimal design is performed based on the analytical formulae. Then, the predicted buckling loads and the optimization results obtained from a FEM model are compared with that from the analytical formulas, and a good agreement is achieved. A detailed parametric optimal design for the sandwich composites cylinder is conducted. The optimization method used here includes two steps: the minimization of the layer thickness followed by tailoring of the fiber orientation. The factors comprise layer number, fiber orientation, core thickness, frame dimension and spacing. Results show that the two-step optimization is an effective method for the sandwich composites and the foam sandwich cylinder with core thickness of 5 mm and frame pitch of 0.5 m exhibits the minimum weight.     

Toward implantable devices for angle-sensitive,lens-less,multifluorescent, single-photon lifetime imaging in the brain using Fabry–Perot and absorptive color filters

Implantable image sensors have the potential to revolutionize neuroscience. Due to their small form factor requirements;however, conventional filters and optics...     

Inverse gas chromatography for the determination of the dispersive surface free energy and acid–base interactions of a sheet molding compound. I. Matrix material and glass

Sheet molding compound is a material composed of a polyester thermosetting matrix with a thermoplastic, an inorganic filler, a metal oxide, reinforcement fibers, and material performance enhancers embedded in the crosslinked matrix. To achieve the optimum mechanical properties required for the composite material, the surface free energy of the polyester composite needs to be understood. In this study, the composite matrix and glass reinforcement fibers are compared with respect to their surface free energy and acid–base characteristics on the basis of inverse gas chromatography measurements. The inverse gas chromatography results for the matrix and glass are compared to previous results found for sized and unsized cellulosic fibers. The inverse gas chromatography data are used to assess chemical modifications performed on the biobased fibers to predict improvements in the fiber/matrix interaction, and this provides inferences on the overall composite cohesion. Our results show first that any fiber reinforcement system for the polyester composite material has to be acidic to promote good adhesion as the matrix system is very basic and second that the individual dispersive surface energies of the components of the matrix interact in a weighted average to determine the overall surface energy of the composite. Also, a commercial glass reinforcement sized for polyester has been found to have a lower interaction parameter than literature values for cellulosic fibers. This finding suggests that cellulosic fibers might have an advantage in competing with a conventional glass‐fiber reinforcement system in fiber/matrix bonding for sheet molding compound composites. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

On the (un)conditionality of automatic attitude activation: The valence proportion effect.

Affective priming studies have shown that participants are faster to pronounce affectively polarized target words that are preceded by affectively congruent prime words than affectively polarized target words that are preceded by affectively incongruent prime words. We examined whether affective priming of naming responses depends on the valence proportion (i.e., the proportion of stimuli that are affectively polarized). In one group of participants, experimental trials were embedded in a context of filler trials that consisted of affectively polarized stimulus materials (i.e., high valence proportion condition). In a second group, the same set of experimental trials was embedded in a context of filler trials consisting of neutral stimuli (i.e., low valence proportion condition). Results showed that affective priming of naming responses was significantly stronger in the high valence proportion condition than in the low valence proportion condition. We conclude that (a) subtle aspects of the procedure can influence affective priming of naming responses, (b) finding affective priming of naming responses does not allow for the conclusion that affective stimulus processing is unconditional, and (c) affective stimulus processing depends on selective attention for affective stimulus information. (PsycINFO Database Record (c) 2011 APA, all rights reserved)