Rl. Pastel et Rc. Sausa, DETECTION OF NO AND NO2 BY (2-RESONANCE-ENHANCED MULTIPHOTON IONIZATION AND PHOTOACOUSTIC-SPECTROSCOPY NEAR 454 NM(2)), Applied optics, 35(21), 1996, pp. 4046-4052
Trace concentrations of NO and NO2 are detected with a dye laser opera
ting near 454 nm. NO is detected by a (2 + 2) resonance-enhanced multi
photon ionization process by means of NO A (2) Sigma(+)-X (II)-I-2(0,
0) transitions with miniature electrodes, and NO2 is detected by a one
-photon absorption photoacoustic process by means of NO2 (A) over tild
e' B-2(1)(0, 8, 0)- (X) over tilde (2)A(1)(0, 0, 0) transitions with a
miniature microphone. Rotationally resolved excitation spectra show t
hat the spectral resolution is sufficiently high to identify these spe
cies at 1 atm. The technique's analytical merits are evaluated as func
tions of concentration, pressure, and laser intensities. Low laser int
ensities favor NO2 photoacoustic detection whereas high laser intensit
ies favor NO ionization. Limits of detection (signal-to-noise ratio 3)
of 160 parts in 10(9) for NO and 400 parts in 10(9) for NO2 are deter
mined at 1 atm for a 10-s integration time. Signal response and noise
analyses show that three decades of NO/NO2 mixtures can be measured wi
th a computational relative error in concentration that is three times
the relative error in measuring the NO and NO2 signals. (C) 1996 Opti
cal Society of America