Filter evaluation and selection for heating, ventilation, and air conditioning systems during and beyond the COVID-19 pandemic.

Particle size removal efficiencies for 0.1-1.0 µm ( PSE 0.1 - 1.0 $$ {PSE}_{0.1-1.0} $$ ) and 0.3-1.0 µm ( PSE 0.3 - 1.0 $$ {PSE}_{0.3-1.0} $$ ) diameter of Minimum Efficiency Reporting Value (MERV) filters, an electrostatic enhanced air filter (EEAF), and their two-stage filtration systems were evaluated. Considering the most penetrating particle size was 0.1-0.4 µm particulate matter (PM), the PSE 0.1 - 1.0 $$ {PSE}_{0.1-1.0} $$ as an evaluation parameter deserves more attention during the COVID-19 pandemic, compared to the PSE 0.3 - 1.0 $$ {PSE}_{0.3-1.0} $$ . The MERV 13 filters were recommended for a single-stage filtration system because of their superior quality factor (QF) compared to MERV 6, MERV 8, MERV 11 filters, and the EEAF. Combined MERV 8 + MERV 11 filters have the highest QF compared to MERV 6 + MERV 11 filters and EEAF + MERV 11 filters; regarding 50% of PSE 0.1 - 1.0 $$ {PSE}_{0.1-1.0} $$ as the filtration requirements of two-stage filtration systems, the MERV 8 + MERV 11 filtration system can achieve this value at 1.0 m/s air velocity, while PSE 0.1 - 1.0 $$ {PSE}_{0.1-1.0} $$ values were lower than 50% at 1.5 m/s and 2.0 m/s. EEAF obtained a better PSE 0.3 - 1.0 $$ {PSE}_{0.3-1.0} $$ in the full-recirculated test rig than in the single-pass mode owing to active ionization effects when EEAF was charged by alternating current.

Relationship between Coating-Induced Soot Aggregate Restructuring and Primary Particle Number.

The restructuring of monodisperse soot aggregates due to coatings of secondary organic aerosol (SOA) was investigated in a series of photo-oxidation chamber experiments. Soot aggregates were generated by one of three sources (an ethylene premixed burner, a methane inverted diffusion burner, or a diesel generator), treated by denuding, size-selected by a differential mobility analyzer, and injected into a smog chamber, where they were exposed to the photo-oxidation products of p-xylene, which partitioned to form SOA coatings. The evolution of aggregates from their initial to final morphologies was investigated in situ by mobility and mass measurements and ex situ by transmission electron microscopy. At a given initial aggregate mobility diameter, diesel aggregates are less dense and composed of smaller primary particles than those generated by the two burners, and they restructure to a smaller final mobility diameter. Remarkably, the final degrees of restructuring of aggregates from all three sources exhibit the same linear dependence on the number of primary particles per aggregate. The observed linear relationship, valid for the atmospherically relevant SOA coating investigated here, could allow modelers to predict the evolution of aggregate morphology based on a single property of the aggregates.

Soot aggregate restructuring due to coatings of secondary organic aerosol derived from aromatic precursors.

Restructuring of monodisperse soot aggregates due to coatings of secondary organic aerosol (SOA) derived from hydroxyl radical-initiated oxidation of toluene, p-xylene, ethylbenzene, and benzene was investigated in a series of photo-oxidation (smog) chamber experiments. Soot aggregates were generated by combustion of ethylene using a McKenna burner, treated by denuding, size-selected by a differential mobility analyzer, and injected into a smog chamber, where they were exposed to low vapor pressure products of aromatic hydrocarbon oxidation, which formed SOA coatings. Aggregate restructuring began once a threshold coating mass was reached, and the degree of the subsequent restructuring increased with mass growth factor. Although significantly compacted, fully processed aggregates were not spherical, with a mass-mobility exponent of 2.78, so additional SOA was required to fill indentations between collapsed branches of the restructured aggregates before the dynamic shape factor of coated particles approached 1. Trends in diameter growth factor, effective density, and dynamic shape factor with increasing mass growth factor indicate distinct stages in soot aggregate processing by SOA coatings. The final degree and coating mass dependence of soot restructuring were found to be the same for SOA coatings from all four aromatic precursors, indicating that the surface tensions of the SOA coatings are similar.

Viral load of SARS-CoV-2 in droplets and bioaerosols directly captured during breathing, speaking and coughing.

Determining the viral load and infectivity of SARS-CoV-2 in macroscopic respiratory droplets, bioaerosols, and other bodily fluids and secretions is important for identifying transmission modes, assessing risks and informing public health guidelines. Here we show that viral load of SARS-CoV-2 Ribonucleic Acid (RNA) in participants' naso-pharyngeal (NP) swabs positively correlated with RNA viral load they emitted in both droplets >10 [Formula: see text] and bioaerosols <10 [Formula: see text] directly captured during the combined expiratory activities of breathing, speaking and coughing using a standardized protocol, although the NP swabs had [Formula: see text] 10[Formula: see text] more RNA on average. By identifying highly-infectious individuals (maximum of 18,000 PFU/mL in NP), we retrieved higher numbers of SARS-CoV-2 RNA gene copies in bioaerosol samples (maximum of 4.8[Formula: see text] gene copies/mL and minimum cycle threshold of 26.2) relative to other studies. However, all attempts to identify infectious virus in size-segregated droplets and bioaerosols were negative by plaque assay (0 of 58). This outcome is partly attributed to the insufficient amount of viral material in each sample (as indicated by SARS-CoV-2 gene copies) or may indicate no infectious virus was present in such samples, although other possible factors are identified.

Comprehensive characterization of mainstream marijuana and tobacco smoke.

Recent increases in marijuana use and legalization without adequate knowledge of the risks necessitate the characterization of the billions of nanoparticles contained in each puff of smoke. Tobacco smoke offers a benchmark given that it has been extensively studied. Tobacco and marijuana smoke particles are quantitatively similar in volatility, shape, density and number concentration, albeit with differences in size, total mass and chemical composition. Particles from marijuana smoke are on average 29% larger in mobility diameter than particles from tobacco smoke and contain 3.4× more total mass. New measurements of semi-volatile fractions determine over 97% of the mass and volume of the particles from either smoke source are comprised of semi-volatile compounds. For tobacco and marijuana smoke, respectively, 4350 and 2575 different compounds are detected, of which, 670 and 536 (231 in common) are tentatively identified, and of these, 173 and 110 different compounds (69 in common) are known to cause negative health effects through carcinogenic, mutagenic, teratogenic, or other toxic mechanisms. This study demonstrates striking similarities between marijuana and tobacco smoke in terms of their physical and chemical properties.

Effect of electrostatic charge on deposition of uniformly charged monodisperse particles in the nasal extrathoracic airways of an infant.

BACKGROUND: The fraction of inhaled particles depositing in the nasal extrathoracic airways determines the amount of particles delivered to the lungs of infants. Electrostatic charge on particles can affect this deposition, and for this reason, deposition of charged aerosol particles in the Alberta Idealized Infant nasal geometry is examined. METHODS: Charged aerosol particles were generated via Plateau-Rayleigh jet breakup atomization with induction charging. Nasal deposition was measured by collecting particles on a filter membrane at the inlet and outlet of the airway and measuring their mass with an ultramicrobalance. The experiments were carried out using monodisperse, uniformly charged particles with aerodynamic diameters of 3-6 µm at two flow rates of 7.5 and 15 L/min, for a charge range of 0-10,000 e per particle. RESULTS: Electrostatic charge effects are largest for the lowest flow rate, smallest particle size, and highest charge level, with deposition in this case being approximately three times that for neutral particles. Higher flow rates and larger particle size result in much weaker electrostatic effects, with even the highest charge levels giving only a few percent higher deposition for the largest particle size and flow rate considered in this study. A dimensionless empirical relation based on the experimental data was developed for predicting deposition of charged particles in the idealized infant airway. CONCLUSION: Electrostatic charge on inhaled aerosol particles has only a minor effect on deposition for large particles at higher flow rates, because in this case inertial impaction dominates deposition. However, for particles with low inertia, for example, small particles or low flow rates, large values of electrostatic charge strongly increase nasal deposition in the present infant extrathoracic airway.

Performance of pressurized metered-dose inhalers at extreme temperature conditions.

The performance of pressurized metered-dose inhalers (pMDIs) under a variety of temperature conditions was investigated. The effects of both inhaler temperature and ambient temperature were considered. The inhaler temperature ranged from -13.0°C to 41.7°C and the ambient temperature ranged from -12.0°C to 41.7°C. The in vitro lung dose was measured for four widely available pMDIs: Airomir(TM) , QVAR(TM) , Symbicort(®) , and Ventolin(®) . The in vitro lung dose through an Alberta Idealized Throat was measured by gravimetric assay, which was verified by UV spectroscopic assay. A decrease in the in vitro lung dose was observed for all evaluated pMDIs when ambient temperature and device temperature were simultaneously reduced, decreasing on average by 70% at the coldest temperatures, whereas increasing on average by 25% at the elevated temperature condition. In vitro lung dose is strongly dependent on both inhaler temperature and ambient temperature with the tested pMDIs.

The effect of altitude on inhaler performance.

The purpose of the study is to understand the effect of altitude on the performance of selected pressurized metered dose inhalers (pMDIs) and dry powder inhalers (DPIs). A testing apparatus that created consistent breath profiles through the Alberta Idealized Throat was designed to test five pMDIs and two DPIs at altitudes of 670, 2450, 3260, and 4300 m. Both gravimetric and chemical assays were conducted to determine the in vitro lung dose. Additionally, spray duration and shot weight for pMDIs and device resistance for DPI were measured. There was no significant change in in vitro lung dose for any of the pMDIs tested. Shot weight and spray duration were unaffected. The device resistance of the DPIs decreased with increasing altitude and was successfully modeled as a function of ambient pressure. The in vitro lung dose of both DPIs showed no significant change when operated with an inhaler pressure drop of 4 kPa, but for the Bricanyl(®) Turbuhaler(®), a significant decrease occurred when matching the volumetric inspiratory flow rate to that of the baseline altitude.

Response to comment on "Radiative absorption enhancements due to the mixing state of atmospheric black carbon".

Jacobson argues that our statement that "many climate models may overestimate warming by BC" has not been demonstrated. Jacobson challenges our results on the basis that we have misinterpreted some model results, omitted optical focusing under high relative humidity conditions and by involatile components, and because our measurements consist of only two locations over short atmospheric time periods. We address each of these arguments, acknowledging important issues and clarifying some misconceptions, and stand by our observations. We acknowledge that Jacobson identified one detail in our experimental technique that places an additional constraint on the interpretation of our observations and reduces somewhat the potential consequences of the stated implications.

Radiative absorption enhancements due to the mixing state of atmospheric black carbon.

Atmospheric black carbon (BC) warms Earth's climate, and its reduction has been targeted for near-term climate change mitigation. Models that include forcing by BC assume internal mixing with non-BC aerosol components that enhance BC absorption, often by a factor of ~2; such model estimates have yet to be clearly validated through atmospheric observations. Here, direct in situ measurements of BC absorption enhancements (E(abs)) and mixing state are reported for two California regions. The observed E(abs) is small-6% on average at 532 nm-and increases weakly with photochemical aging. The E(abs) is less than predicted from observationally constrained theoretical calculations, suggesting that many climate models may overestimate warming by BC. These ambient observations stand in contrast to laboratory measurements that show substantial E(abs) for BC are possible.