Office of Aerospace Medicine Technical Reports
FAA Office of Aerospace Medicine
Civil Aerospace Medical Institute
Report No: DOT/FAA/AM-89/13
Title and Subtitle: Airliner cabin ozone: an updated review.
Report Date: December 1989
Authors: Melton CE.
Abstract: The recent literature pertaining to ozone contamination of airliner cabins is reviewed. Measurements in airliner cabins without filters showed that ozone levels were about 50 percent of atmospheric ozone. Filters were about 90 percent effective in destroying ozone.
Ozone (0.12 to 0.14 ppmv) caused mild subjective respiratory irritation in exercising men, but 0.20 to 0.30 ppmv did not have adverse effects on patients with chronic heart or lung disease. Ozone (1.0 to 2.0 ppmv) decreased survival time of influenza-infected rats and mice and suppressed the capacity of lung macrophages to destroy Listeria. Airway responses to ozone are divided into an early parasympathetically mediated bronchoconstrictive phase and a later histamine-mediated congestive phase.
Key Words: capacity (quantity), diseases, survival (general), time, adverse conditions, lung, respiratory system, patients, mice, contamination, ozone, heart, irritation, listeria, destruction.
No. of Pages: 19
Civil Aerospace Medical Institute
Report No: DOT/FAA/AM-89/13
Title and Subtitle: Airliner cabin ozone: an updated review.
Report Date: December 1989
Authors: Melton CE.
Abstract: The recent literature pertaining to ozone contamination of airliner cabins is reviewed. Measurements in airliner cabins without filters showed that ozone levels were about 50 percent of atmospheric ozone. Filters were about 90 percent effective in destroying ozone.
Ozone (0.12 to 0.14 ppmv) caused mild subjective respiratory irritation in exercising men, but 0.20 to 0.30 ppmv did not have adverse effects on patients with chronic heart or lung disease. Ozone (1.0 to 2.0 ppmv) decreased survival time of influenza-infected rats and mice and suppressed the capacity of lung macrophages to destroy Listeria. Airway responses to ozone are divided into an early parasympathetically mediated bronchoconstrictive phase and a later histamine-mediated congestive phase.
Key Words: capacity (quantity), diseases, survival (general), time, adverse conditions, lung, respiratory system, patients, mice, contamination, ozone, heart, irritation, listeria, destruction.
No. of Pages: 19
Last updated: Friday, June 1, 2012