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Technical Paper

Influence of photolysis on multispectral photoacoustic measurement of nitrogen dioxide concentration

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Pages 1091-1097 | Published online: 20 Aug 2013

Figures & data

Figure 1. Experimental setup used by Harshbarger et al. (1973).

Figure 1. Experimental setup used by Harshbarger et al. (1973).

Figure 2. Comparison of the optical extinction and spectrophone (i.e., photoacoustic) spectra of NO2 at 1333 Pa pressure (Harshbarger et al., 1973).

Figure 2. Comparison of the optical extinction and spectrophone (i.e., photoacoustic) spectra of NO2 at 1333 Pa pressure (Harshbarger et al., 1973).

Figure 3. NO2 gas calibration results at 405 nm from CitationLewis (2007).

Figure 3. NO2 gas calibration results at 405 nm from CitationLewis (2007).

Figure 4. Absorption cross-section spectrum of NO2 at 294 K (CitationVandaele, 1998).

Figure 4. Absorption cross-section spectrum of NO2 at 294 K (CitationVandaele, 1998).

Figure 5. Schematic diagram of the photoacoustic instrument, including two lasers, chopper, photoacoustic resonator with microphone and piezoelectric transducer, two lock-in amplifiers, and personal computer (PC) (color figure available online).

Figure 5. Schematic diagram of the photoacoustic instrument, including two lasers, chopper, photoacoustic resonator with microphone and piezoelectric transducer, two lock-in amplifiers, and personal computer (PC) (color figure available online).

Figure 6. NO2 calibration of the photoacoustic instrument at 532 nm. For NO2, the absorption coefficient is equal to the extinction coefficient. The measurement with the uncalibrated instrument (shown as gray solid line) is adjusted by multiplying with a constant, yielding the calibrated absorption coefficient, shown as gray dashed line.

Figure 6. NO2 calibration of the photoacoustic instrument at 532 nm. For NO2, the absorption coefficient is equal to the extinction coefficient. The measurement with the uncalibrated instrument (shown as gray solid line) is adjusted by multiplying with a constant, yielding the calibrated absorption coefficient, shown as gray dashed line.

Figure 7. Short-term measurement of the sample absorption coefficient at 532 nm with 405-nm laser on and off.

Figure 7. Short-term measurement of the sample absorption coefficient at 532 nm with 405-nm laser on and off.

Figure 8. Photolysis of NO2 caused by the 405-nm laser. The line shows the change of the sample absorption coefficient at 532 nm due to the photolysis of NO2 caused by the 405-nm laser with 123 mW laser power. The difference between absorption coefficients and NO2 concentrations with the 405-nm laser turned on and off is ∼11%.

Figure 8. Photolysis of NO2 caused by the 405-nm laser. The line shows the change of the sample absorption coefficient at 532 nm due to the photolysis of NO2 caused by the 405-nm laser with 123 mW laser power. The difference between absorption coefficients and NO2 concentrations with the 405-nm laser turned on and off is ∼11%.

Figure 9. Sample absorption coefficient at 532 nm with the 405-nm laser turned on and off followed by high-frequency modulation of the 405-nm laser power simulating operation conditions for multispectral photoacoustic instruments.

Figure 9. Sample absorption coefficient at 532 nm with the 405-nm laser turned on and off followed by high-frequency modulation of the 405-nm laser power simulating operation conditions for multispectral photoacoustic instruments.

Figure 10. Change of sample light absorption coefficient measured at 405 nm. The difference between 405-nm absorption coefficients with the 532-nm laser turned on and off is ∼2%.

Figure 10. Change of sample light absorption coefficient measured at 405 nm. The difference between 405-nm absorption coefficients with the 532-nm laser turned on and off is ∼2%.

Figure 11. NO concentration change measured by the NO analyzer. Photolysis of NO2 at 405 nm was sufficiently strong that the NO analyzer was saturated at its upper limit of 20,000 ppb by the NO produced.

Figure 11. NO concentration change measured by the NO analyzer. Photolysis of NO2 at 405 nm was sufficiently strong that the NO analyzer was saturated at its upper limit of 20,000 ppb by the NO produced.

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