期刊
SUSTAINABILITY
卷 13, 期 21, 页码 -出版社
MDPI
DOI: 10.3390/su132112203
关键词
respiratory aerosols; carbon dioxide; airborne transmission; indoor air quality; COVID-19
资金
- BERTHA-The Danish Big Data Centre for Environment and Health, - Novo Nordisk Foundation Challenge Programme [NNF17OC0027864]
The study found a strong correlation between respiratory aerosols and CO2 concentrations, suggesting that CO2 measurements could be used to estimate viral exposure. While it is difficult to measure source-specific aerosols with low-cost sensors, the increase in respiratory aerosols and CO2 was linear over time.
Respiratory aerosols from breathing and talking are an important transmission route for viruses, including severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Previous studies have found that particles with diameters ranging from 10 nm to 145 mu m are produced from different regions in the respiratory system and especially smaller particles can remain airborne for long periods while carrying viral RNA. We present the first study in which respiratory aerosols have been simultaneously measured with carbon dioxide (CO2) to establish the correlation between the two concentrations. CO2 concentrations are easily available through low-cost sensors and could be used to estimate viral exposure through this correlation, whereas source-specific aerosol measurements are complicated and not possible with low-cost sensors. The increase in both respiratory aerosols and CO2 was linear over ten minutes in a 2 m3 chamber for all participants, suggesting a strong correlation. On average, talking released more particles than breathing, with 14,600 & PLUSMN; 16,800 min(-1) (one-sigma standard deviation) and 6210 & PLUSMN; 5630 min(-1) on average, respectively, while CO2 increased with 139 & PLUSMN; 33 ppm min(-1) during talking and 143 & PLUSMN; 29 ppm min(-1) during breathing. Assuming a typical viral load of 7x106 RNA copies per mL of oral fluid, ten minutes of talking and breathing are estimated to produce 1 and 16 suspended RNA copies, respectively, correlating to a CO2 concentration of around 1800 ppm in a 2 m3 chamber. However, viral loads can vary by several orders of magnitude depending on the stage of the disease and the individual. It was therefore concluded that, by measuring CO2 concentrations, only the number and volume concentrations of released particles can be estimated with reasonable certainty, while the number of suspended RNA copies cannot.
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