An indoor air purification technique, which combines unipolar ion emission and photocatalytic oxidation (promoted by a specially designed RCI cell), was investigated in two test chambers, 2.75 m3 and 24.3 m3, using nonbiological and biological challenge aerosols. The reduction in particle concentration was measured size selectively in real-time, and the Air Cleaning Factor and the Clean Air Delivery Rate (CADR) were determined. While testing with virions and bacteria, bioaerosol samples were collected and analyzed, and the microorganism survival rate was determined as a function of exposure time. We observed that the aerosol concentration decreased approximately 10 to approximately 100 times more rapidly when the purifier operated as compared to the natural decay. The data suggest that the tested portable unit operating in approximately 25 m3 non-ventilated room is capable to provide CADR-values more than twice as great than the conventional closed-loop HVAC system with a rating 8 filter. The particle removal occurred due to unipolar ion emission, while the inactivation of viable airborne microorganisms was associated with photocatalytic oxidation. Approximately 90% of initially viable MS2 viruses were inactivated resulting from 10 to 60 min exposure to the photocatalytic oxidation. Approximately 75% of viable B. subtilis spores were inactivated in 10 min, and about 90% or greater after 30 min. The biological and chemical mechanisms that led to the inactivation of stress-resistant airborne viruses and bacterial spores were reviewed.

The performance of three filtering facepiece respirators (two models of N99 and one N95) challenged with an inert aerosol (NaCl) and three virus aerosols (enterobacteriophages MS2 and T4 and Bacillus subtilis phage)-all with significant ultrafine components-was examined using a manikin-based protocol with respirators sealed on manikins. Three inhalation flow rates, 30, 85, and 150 l min(-1), were tested. The filter penetration and the quality factor were determined. Between-respirator and within-respirator comparisons of penetration values were performed. At the most penetrating particle size (MPPS), >3% of MS2 virions penetrated through filters of both N99 models at an inhalation flow rate of 85 l min(-1). Inhalation airflow had a significant effect upon particle penetration through the tested respirator filters. The filter quality factor was found suitable for making relative performance comparisons. The MPPS for challenge aerosols was <0.1 mum in electrical mobility diameter for all tested respirators. Mean particle penetration (by count) was significantly increased when the size fraction of <0.1 mum was included as compared to particles >0.1 mum. The filtration performance of the N95 respirator approached that of the two models of N99 over the range of particle sizes tested ( approximately 0.02 to 0.5 mum). Filter penetration of the tested biological aerosols did not exceed that of inert NaCl aerosol. The results suggest that inert NaCl aerosols may generally be appropriate for modeling filter penetration of similarly sized virions.

Recent interest in exposures to ultrafine particles (less than 100 nm) in both environmental and occupational settings led the authors to question whether the protocols used to certify respirator filters provide adequate attention to ultrafine aerosols. The authors reviewed the particle size distribution of challenge aerosols and evaluated the aerosol measurement method currently employed in the National Institute for Occupational Safety and Health (NIOSH) particulate respirator certification protocol for its ability to measure the contribution of ultrafine particles to filter penetration. Also considered were the differences between mechanical and electrically charged (electret) filters in light of the most penetrating particle size. It was found that the sodium chloride (NaCl) and dioctylphthalate (DOP) aerosols currently used in respirator certification tests contain a significant fraction of particles in the ultrafine region. However, the photometric method deployed in the certification test is not capable of adequately measuring light scatter of particles below approximately 100 nm in diameter. Specifically, 68% (by count) and 8% (by mass) of the challenge NaCl aerosol particles and 10% (by count) and 0.3% (by mass) of the DOP particles below 100 nm do not significantly contribute to the filter penetration measurement. In addition, the most penetrating particle size for electret filters likely occurs at 100 nm or less under test conditions similar to those used in filter certification. The authors conclude, therefore, that the existing NIOSH certification protocol may not represent a worst-case assessment for electret filters because it has limited ability to determine the contribution of ultrafine aerosols, which include the most penetrating particle size for electret filters. Possible strategies to assess ultrafine particle penetration in the certification protocol are discussed.

Immunohistochemistry using the anti-mitochondria antibody proved to be a highly sensitive and specific method for light microscopic identification of mitochondria and superior to routine H & E or PTAH stain especially in the detection of isolated oncocytic cells.

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