We demonstrate that the critical size cluster concept, commonly used in a nucleation theory, should be given some further attention. It has been implied that the supercritical cluster (size larger than critical) can grow via condensation. However, as we show, there is a size range, where the arrival of a vapor molecule onto a cluster surface leads to such a heating of the supercritical cluster that, due to possible evaporation, makes it unstable and, therefore, disables its condensation growth. The described phenomenon leads to substantial accumulation of certain size clusters in the system, which is clearly evident from our experimental investigation. The found suppression of the nucleus growth within the certain size range (exceeding critical) has fundamental implications for many systems where the generation of nanoparticles occur at high temperatures.

A B S T R A C TAn inactivation of airborne pathogenic Middle East Respiratory Syndrome (MERS-CoV) virus was investigated under controlled laboratory conditions. Two sets of climatic conditions were used in the experiments; (1) representing common office environment (25°C and 79% RH) and (2) climatic conditions of the Middle Eastern region where the virus was originated from (38°C and 24% RH). At the lower temperature, the virus demonstrated high robustness and strong capability to survive with about 63.5% of microorganisms remaining infectious 60 min after aerosolisation. Fortunately, virus decay was much stronger for hot and dry air scenario with only 4.7% survival over 60 min procedure. Fig. 4. Microbial relative survival in airborne form (error bars represent standard deviation of at least 3 measurements). O.V. Pyankov et al.

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A new personal bioaerosol sampler has recently been developed and evaluated for sampling of viable airborne bacteria and fungi under controlled laboratory conditions and in the field. The operational principle of the device is based on the passage of air through porous medium immersed in liquid. This process leads to the formation of bubbles within the filter as the carrier gas passes through and thus provides effective mechanisms for aerosol removal. As demonstrated in previous studies, the culturability of sampled bacterium and fungi remained high for the entire 8-h sampling period. The present study is the first step of the evaluation of the new sampler for monitoring of viable airborne viruses. It focuses on the investigation of the inactivation rate of viruses in the bubbling process during 4 h of continuous operation. Four microbes were used in this study, influenza, measles, mumps, and vaccinia viruses. It was found that the use of distilled water as the collection fluid was associated with a relatively high decay rate. A significant improvement was achieved by utilizing virus maintenance fluid prepared by using Hank's solution with appropriate additives. The survival rates of the influenza, measles, and mumps viruses were increased by 1.4 log, 0.83 log, and 0.82 log, respectively, after the first hour of operation compared to bubbling through the sterile water. The same trend was observed throughout the entire 4-h experiment. There was no significant difference observed only for the robust vaccinia virus.

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The influence of particle shape on filtration processes was investigated. Two types of particles, including spherical polystyrene latex (PSL) and iron oxide, and perfect cubes of magnesium oxide, were examined. It was found that the removal efficiency of spherical particles on fibrous filters is very similar for corresponding sizes within the range of 50-300 nm, regardless of the fact that the densities of PSL and iron oxide differ by a factor of five. On the other hand, the removal efficiency of magnesium oxide cubic particles was measured, and found to be much lower than the removal efficiency for the aerodynamically similar spheres. Such disparity was ascribed to the different nature of the motion of the spherical and cubic particles along the fiber surface, following the initial collision. After touching the fiber surface and before coming to rest, the spherical particles could either slide or roll compared to the cubic ones, which could either slide or tumble. During tumbling, the area of contact between the particle and the fiber changes significantly, thus affecting the bounce probability, whilst for the spheres, the area of contact remains the same for any point of the particle trajectory. The extra probability of particle bounce by the cubes was derived from the experimental data. The particle kinetic energy was proposed to be responsible for the difference in removal efficiency of particles with alternative shapes, if all other process parameters remain the same. The increase in kinetic energy is shown to favor the increase of the bounce probability.

We have recently developed a new personal sampler and demonstrated its feasibility for detection of viable airborne microorganisms including bacteria, fungi and viruses. To accelerate the time-consuming analytical procedure involving 2-5 days of biological testing, we employed a real-time PCR protocol in conjunction with the personal sampler for collection of airborne viruses. The advantage of this approach is that if the presence of a particular pathogen in the air is detected by the PCR, the remaining collecting liquid can be further analysed by more time-consuming biological methods to estimate the number of airborne infectious/live microorganisms. As sampling of bioaerosols in natural environments is likely to be associated with substantial contamination by a range of microorganisms commonly existing in an ambient air, an investigation of the specificity of detection by targeted PCR analysis is required. Here we present the results of the study on the detection of Influenza virus in the ambient air contaminated with high concentrations of bacteria and fungi using real-time PCR protocol. The combined sampling PCR detection method was found to be fully feasible for the rapid ( approximately 2.5 h) and highly specific (no cross-reactivity) identification of the labile airborne virus in the air containing elevated concentrations of other microorganisms.