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Articles

Real-time separation of aerosolized Staphylococcus epidermidis and polystyrene latex particles with similar size distributions

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Pages 1389-1397 | Received 15 Feb 2017, Accepted 27 Jun 2017, Published online: 14 Jul 2017

Figures & data

Figure 1. Concept of real time separation of similar sized Staphylococcus epidermidis and polystyrene latex (PSL).

Figure 1. Concept of real time separation of similar sized Staphylococcus epidermidis and polystyrene latex (PSL).

Figure 2. Experimental setup for measuring (a) concentration using an aerodynamic particle sizer (APS), and (b) ATP luminescence.

Figure 2. Experimental setup for measuring (a) concentration using an aerodynamic particle sizer (APS), and (b) ATP luminescence.

Figure 3. Size distributions of Staphylococcus epidermidis and polystyrene latex (PSL) aerosols. (Each measurement was repeated three times. Each data point presents the average and error bars present the standard deviation.)

Figure 3. Size distributions of Staphylococcus epidermidis and polystyrene latex (PSL) aerosols. (Each measurement was repeated three times. Each data point presents the average and error bars present the standard deviation.)

Figure 4. Current-voltage (I-V) characteristics of the aerosol charger. (Each measurement was repeated three times. Each data point presents the average and error bars present the standard deviation.)

Figure 4. Current-voltage (I-V) characteristics of the aerosol charger. (Each measurement was repeated three times. Each data point presents the average and error bars present the standard deviation.)

Figure 5. Bacterial standard curve for quantifying aerosol bacteria. (Each measurement was repeated three times. Each data point presents the average and error bars present the standard deviation.)

Figure 5. Bacterial standard curve for quantifying aerosol bacteria. (Each measurement was repeated three times. Each data point presents the average and error bars present the standard deviation.)

Table 1. Maximum recoveries for Staphylococcus epidermidis with different flow rates.

Figure 6. Ratio of particle (Staphylococcus epidermidis and polystyrene latex) concentrations at outlet 1 to aerosol inlet concentration with varying voltage. (Each measurement was repeated three times. Each data point presents the average and error bars present the standard deviation.)

Figure 6. Ratio of particle (Staphylococcus epidermidis and polystyrene latex) concentrations at outlet 1 to aerosol inlet concentration with varying voltage. (Each measurement was repeated three times. Each data point presents the average and error bars present the standard deviation.)

Figure 7. Fraction of particles carrying specific charge number. (Each measurement was repeated three times. Each data point presents the average and error bars present the standard deviation.)

Figure 7. Fraction of particles carrying specific charge number. (Each measurement was repeated three times. Each data point presents the average and error bars present the standard deviation.)

Figure 8. Fates of polystyrene latex (PSL) and Staphylococcus epidermidis through the analyzer. (Each measurement was repeated three times. Each data point presents the average and error bars present the standard deviation.)

Figure 8. Fates of polystyrene latex (PSL) and Staphylococcus epidermidis through the analyzer. (Each measurement was repeated three times. Each data point presents the average and error bars present the standard deviation.)

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