Attraction of common Australian blowflies to algal affected remains, and the specific effect of algae present in the food substrate on growth and survival of <i>Calliphora stygia</i>

Attraction of common Australian blowflies to algal affected remains, and the specific effect of algae present in the food substrate on growth and survival of Calliphora stygia</i

Improving quantification using curtain flow chromatography columns in the analysis of labile compounds: a study on amino acids.

The performance of curtain flow chromatography column technology with MS detection was evaluated for the analysis of labile compounds. The curtain flow column design allows for separations that are faster and/or more sensitive than conventional columns, depending on how exactly the curtain flow column is configured. For example, when mass spectral detection is employed, the curtain flow column can yield separations that are 5-times faster than conventional columns when the curtain flow and the conventional columns have the same internal diameter. Or when the internal diameter of the conventional column is reduced in order to yield the same analytical through-put as the curtain flow column, the sensitivity on the curtain flow column can be as much as 66-fold higher than the conventional column. As a consequence of the higher analytical through-put less standardization is required in the analysis of labile compounds because less sample degradation is apparent. Consequently the sample integrity is preserved yielding data of a higher quality

The effect of the anti-coagulant EDTA on the deposition and adhesion of whole blood deposits on non-porous substrates

An investigation into whether the addition of a commonly used anti-coagulant agent like ethylenediaminetetraacetic acid (EDTA) has an impact on the adhesion potential of blood to non-porous substrates was conducted. Two non-porous substrates (aluminum and polypropylene) exhibiting six different surface roughness categories (R1–R6) were used as test substrates upon which either whole blood or blood treated with EDTA was deposited. Samples were exposed to different drying periods (24 hours, 48 hours, and 1 week) before undergoing a tapping agitation experiment in order to evaluate the adhesion to the surface. Clear differences in adhesion potential were observed between whole blood and blood treated with EDTA. Blood treated with EDTA displayed a stronger adhesion strength to aluminum after a drying time of 24 h pre-agitation, while whole blood presented with a stronger adhesion strength at the drying time of 48 h and 1 week. Both EDTA-treated and EDTA-untreated blood was shown to dislodge less easily on polypropylene with the only difference observed on smooth surfaces (0.51–1.50 μm surface roughness). Thus, when conducting transfer studies using smooth hydrophobic substrates like polypropylene or considering the likelihood of transfer given specific case scenarios, differences in adhesion strength of blood due to hydrophobic substrate characteristics and a decreased surface area need to be considered. Overall, whole blood displayed a better adhesion strength to aluminum, emphasizing that indirect transfer probability experiments using EDTA blood on substrates like aluminum should take an increased dislodgment tendency into account in their transfer estimations.</p

Stimuli-responsive heterojunctions based photo-electrocatalytic membrane reactors for reactive filtration of persistent organic pollutants

The design of semiconducting metal oxide heterojunctions is promising to overcome conventional limitations associated to photocatalysis or electrocatalysis, such as fast recombination of electron-hole pairs and poor long-term stability leading to low catalytic performance. A route to tackle this issue is to design catalysts at the atomic levels by arranging order and controlling nanoscale interfaces to yield catalytic materials with greater response rates and stability to dissolution or corrosion. The present study focuses on the formation of such nanoscale heterojunctions between TiO2 and ZnO via atomic layer deposition across conductive and porous stainless-steel substrates to develop enhanced photo-electro-responsive catalytic membrane reactors. The heterojunction nano-sheet based structures produced higher density of electron and hole pairs and offered efficient separation of charges, longer lifetime of photo-generated electrons compared to single metal oxides, resulting in enhanced photocurrent efficiency. The tailoring of both the nanoscale dimensions of the metal oxide layers and the stacking of these inorganic nano-sheets led to the development of multi-heterojunctions, of a few tens of nanometres, deposited across conductive porous substrates. The high electron mobility across the heterojunction nano-sheets increased the oxygen evolution potential from 1.4 to 1.7 eV, leading to enhanced electrochemical reactions, as well as offered photocurrent densities 2–3 times higher than pristine single metal oxide membranes. The formation of type II heterojunction structures between TiO2 and ZnO leads to band alignment at the interface, yielding an efficient charge separation mechanism and high catalytic performance. A prototype of novel cross-flow filtration module was designed in this study to support the coupling of photo-electrocatalysis on the membrane surface and simultaneous pressure driven membrane processes. The designed 3D printed modules demonstrated highly enhanced degradation of several persistent organic pollutants, leading to reactivity up to 75 × 10−3 min−1 up to 500 % greater compared to single metal oxides generated with the same conditions. The intimate and synergistic interactions across the stacked metal oxide nano-sheets enabled high catalytic efficiency and stability, opening new avenues stimuli-responsive membranes scale up and implementation in wastewater remediation and compact reactors design, where sieving and reactivity are of prime importance

Dynamic Reactive Ionization with Cluster Secondary Ion Mass Spectrometry

[Image: see text] Gas cluster ion beams (GCIB) have been tuned to enhance secondary ion yields by doping small gas molecules such as CH(4), CO(2), and O(2) into an Ar cluster projectile, Ar(n)(+) (n = 1000–10,000) to form a mixed cluster. The ‘tailored beam’ has the potential to expand the application of secondary ion mass spectrometry for two- and three-dimensional molecular specific imaging. Here, we examine the possibility of further enhancing the ionization by doping HCl into the Ar cluster. Water deposited on the target surface facilitates the dissociation of HCl. This concerted effect, occurring only at the impact site of the cluster, arises since the HCl is chemically induced to ionize to H(+) and Cl(−), allowing improved protonation of neutral molecular species. This hypothesis is confirmed by depth profiling through a trehalose thin film exposed to D(2)O vapor, resulting in ~20-fold increase in protonated molecules. The results show that it is possible to dynamically maintain optimum ionization conditions during depth profiling by proper adjustment of the water vapor pressure. Protonation and H–D exchange in the trehalose molecule M was monitored upon deposition of D(2)O on the target surface, leading to the observation of [M(n)* + H](+) or [M(n)* + D](+) ions, where n = 1–8 hydrogen atoms in the trehalose molecule M have been replaced by deuterium. In general, we discuss the role of surface chemistry and dynamic reactive ionization of organic molecules in increasing the secondary ion yield