Techniques for Dispersion of Microorganisms into Air

ABSTRACT

Many commercially available devices initially developed for dispersion of biologically inert particles have been adopted for aerosolization of microoganisms in laboratory settings. However, these dispersion devices are not always adequate for microbial particles, as they do not simulate natural release into air. Wet dispersion methods are appropriate for viruses and most bacteria, whereas dry methods are more suitable for most fungal and actinomycete spores. Characteristics of the resulting aerosol are dependent on the dispersing shear forces and the sensitivity and agglomeration of the tested microorganisms. Consequently, each microbial group may need a specific dispersion technique. The following devices have been developed and tested in this study: the bubbling aerosol disperser, the agar-tube disperser, and the swirling-flow disperser. Testing included the evaluation of both physical and microbiological characteristics of aerosolized microorganisms. Each of the dispersers has shown several advantages over commercially available ones. When used for the dispersion of bacteria from the liquid suspension, the bubbling aerosol disperser was found to produce considerably fewer amounts of microbial fragments and much lower levels of microbial metabolic injury than the commercially available Collison nebulizer. Fungal spores dispersed from their colonies by the agar-tube disperser were found to have a more stable aerosol concentration and a lower fraction of agglomerates than achievable by conventional powder dispersion. The swirling-flow dispersion technique was used for aerosolization of actinomycetes because the agar-tube disperser could not provide a stable concentration of these spores due to their smaller size. The tests have shown that new methods minimize the changes of properties of the microorganisms during their aerosolization in the laboratory.     

Retarding Thermal Degradation in Hybrid Perovskites by Ionic Liquid Additives

Recent years have witnessed considerable progress in the development of solar cells based on lead halide perovskite materials. However, their intrinsic instability remains a limitation. In this context, the interplay between the thermal degradation and the hydrophobicity of perovskite materials is investigated. To this end, the salt 1‐(4‐ethenylbenzyl)‐3‐(3,3,4,4,5,5,6,6,7,7,8,8,8‐tridecafluorooctylimidazolium iodide (ETI), is employed as an additive in hybrid perovskites, endowing the photoactive materials with high thermal stability and hydrophobicity. The ETI additive inhibits methylammonium (MA) permeation in methylammonium lead triiodide (MAPbI₃) occurring due to intrinsic thermal degradation, by inhibiting out‐diffusion of the MA⁺ cation, preserving the pristine material and preventing decomposition. With this simple approach, high efficiency solar cells based on the unstable MAPbI₃ perovskite are markedly stabilized under maximum power point tracking, leading to greater than twice the preserved efficiency after 700 h of continuous light illumination and heating (60 °C). These results suggest a strategy to tackle the intrinsic thermal decomposition of MAI, an essential component in all state‐of‐the‐art perovskite compositions.     

Characteristics of Zinc Corrosion and Formation of Conversion Films on the Zinc Surface in Acidic Solutions of Cr(III) Compounds

The influence of the components of an acidic solution: Cr(III) nitrate-malonic acid-Co(II) salt and treatment conditions on zinc dissolution and formation of Chromate films as well as on their decorative and protective properties have been studied using the analytical, XPS, structural and accelerated corrosion test methods. An organic acid is the main component, which has an essential influence on zinc dissolution and formation of Chromate films as well as their decorative and protective properties. The influence of organic acid is directly related with the state of the Cr³⁺ ions in chromating solution. When the Cr³⁺ ions are in the form of hexaaquaions, the organic acid increases the quantities of the zinc dissolved and the Cr(III) deposited on the zinc surface (especially at 60°C). It also predetermines the formation of a thick, porous Chromate film with large cracks at 60°C. Its decorative and protective properties are rather poor. When Cr³⁺ ions are in the form of a complex with organic acid, the quantities of the zinc dissolved and the Cr(III) deposited on the zinc surface significantly decrease and thinner Chromate films with an even surface, good decorative appearance and high corrosion resistance are formed Decorative blue-bright Cr(VI)-free films with a slight iridescent tint, obtained in solution, containing Cr(III) nitrate (0.2), malonic acid (0.3) and Co(II) nitrate (0.02) mol dm^?3, at p H 1.6-2.0 at room temperature over 30–60 s, possess corrosion resistance (192–240 h in a salt spray chamber) similar to that of iridescent Chromate films, obtained in acidic Cr(VI) solution.     

Reduced Efficiency Roll‐Off and Improved Stability of Mixed 2D/3D Perovskite Light Emitting Diodes by Balancing Charge Injection

Perovskite light emitting diodes (PeLEDs) have reached external quantum efficiencies (EQEs) over 21%. Their EQE, however, drops at increasing current densities (J) and their lifetime is still limited to just a few hours. The mechanisms leading to EQE roll‐off and device instability require thorough investigation. Here, improvement in EQE, EQE roll‐off, and lifetime of PeLEDs is demonstrated by tuning the balance of electron/hole transport into a mixed 2D/3D perovskite emissive layer. The mixed 2D/3D perovskite layer induces exciton confinement and beneficially influences the electron/hole distribution inside the perovskite layer. By tuning the electron injection to match the hole injection in such active layer, a nearly flat EQE for J = 0.1–200 mA cm^?2, a reduced EQE roll‐off until J = 250 mA cm^?2, and a half‐lifetime of ≈47 h at J = 10 mA cm^?2 is reached. A model is also proposed to explain these improvements that account for the spatial electron/hole distributions.     

Double Charge Transfer Dominates in Carrier Localization in Low Bandgap Sites of Heterogeneous Lead Halide Perovskites

Heterogeneous organic-inorganic halide perovskites possess inherent non-uniformities in bandgap that are sometimes engineered and exploited on purpose, like in quasi-2D perovskites. In these systems, charge carrier and excitation energy migration to lower-bandgap sites are key processes governing luminescence. The question, which of them dominates in particular materials and under specific experimental conditions, still remains unanswered, especially when charge carriers comprise excitons. In this study transient absorption (TA) and transient photoluminescence (PL) techniques are combined to address the excited state dynamics in quasi-2D and other heterogeneous perovskite structures in broad temperature range, from room temperature down to 15 K. The data provide clear evidence that charge carrier transfer rather than energy migration dominates in heterogeneous quasi-2D perovskite films.     

Dispersion‐Dominated Photocurrent in Polymer:Fullerene Solar Cells

Organic bulk heterojunction solar cells are often regarded as near‐equilibrium devices, whose kinetics are set by well‐defined charge carrier mobilities, and relaxation in the density of states is commonly ignored or included purely phenomenologically. Here, the motion of photocreated charges is studied experimentally with picosecond time resolution by a combination of time‐resolved optical probing of electric field and photocurrent measurements, and the data are used to define parameters for kinetic Monte Carlo modelling. The results show that charge carrier motion in a prototypical polymer:fullerene solar cell under operational conditions is orders of magnitude faster than would be expected on the basis of corresponding near‐equilibrium mobilities, and is extremely dispersive. There is no unique mobility. The distribution of extraction times of photocreated charges in operating organic solar cells can be experimentally determined from the charge collection transients measured under pulsed excitation. Finally, a remarkable distribution of the photocurrent over energy is found, in which the most relaxed charge carriers in fact counteract the net photocurrent.     

Preparation and functional characterization of magnetoelectric Ba(Ti1-xFex)O3-x/2 ceramics. Application for a miniaturized resonator antenna

Diluted magnetic oxides attracted a great interest in the last years as materials for spintronics and magnetoelectric devices. We propose in the present paper such a magnetoelectric ceramic system for an application as miniaturized resonator antenna in GHz range. BaTi_1-xFe_xO_3-x/2 (0?≤?x?≤?0.02) polycrystalline ceramics have been produced by solid state reaction. X-ray diffraction analysis and Rietveld refinement have shown that Fe doping of BaTiO₃ lattice produces a transition from tetragonal crystalline symmetry (for x?≤?0.01) to a superposition of tetragonal and hexagonal phases for the compositions x?=?0.015 and 0.02. As result of Fe addition, the Curie temperature of BaTi_1-xFe_xO_3-x/2 ceramics exhibit a shift from 127?°C towards lower values and reaches 85?°C for x?=?0.02. A competition between weak ferromagnetic and antiferromagnetic character as a function of composition and temperature is determined both by the presence of transition metal ion and of the oxygen vacancies. Due to its electromagnetic properties, an optimized composition x?=?0.01 was used for producing a miniaturized antenna which was found to show a frequency dependent S₁₁ response similar to the simulated one.     

Influence of Corrosion on Microstructure of Chromated Zinc Surfaces. Part 1. Microstructure changes of electrodeposited zinc in the process of chromating

The microstructure of zinc surfaces has been investigated using x-ray photoeiectron spectroscopy and scanning electron microscopy. The inclusion of a 0.5% HNO₃ bright dip stage into the technological process of zinc chromating stimulates equal-rate generation of anode-active spots on zinc surfaces and at the same time influences the formation of more uniform conversion coating. Intensive zinc surface etching is observed under the forming conversion coating.     

Ursolic and Oleanolic Acids: Plant Metabolites with Neuroprotective Potential

Ursolic and oleanolic acids are secondary plant metabolites that are known to be involved in the plant defence system against water loss and pathogens. Nowadays these triterpenoids are also regarded as potential pharmaceutical compounds and there is mounting experimental data that either purified compounds or triterpenoid-enriched plant extracts exert various beneficial effects, including anti-oxidative, anti-inflammatory and anticancer, on model systems of both human or animal origin. Some of those effects have been linked to the ability of ursolic and oleanolic acids to modulate intracellular antioxidant systems and also inflammation and cell death-related pathways. Therefore, our aim was to review current studies on the distribution of ursolic and oleanolic acids in plants, bioavailability and pharmacokinetic properties of these triterpenoids and their derivatives, and to discuss their neuroprotective effects in vitro and in vivo.     

Oil spill fluorosensing lidar for inclined onshore or shipboard operation

An oil spill detection fluorosensing lidar for onshore or shipboard operation is described. Some difficulties for its operation arise from the inclined path of rays. This is due to the increased reflection of the laser beam at the air-water interface, the decreased fluorescence signal, and the increased background light when compared with other instruments having a close-to-nadir measuring geometry. The analysis of these problems shows that they significantly reduce the detection distance in the presence of a flat water surface. However, waves on the water surface weaken the influence of the laser beam reflections but at the same time cause a variable fluorescence signal, which makes specific signal processing necessary for increased detection ranges. A fluorescence data processing method is proposed that efficiently eliminates the background water column fluorescence from signals such as yellow substance. This enables oil fluorescence to be distinguished from variable natural water fluorescence.