Consistency of Ozone and Nitrogen Oxides Standards at Tropospherically Relevant Mixing Ratios |
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| Authors: | Timothy H Bertram Ronald C Cohen William J Thorn III |
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| Institution: | 1. Department of Chemistry , University of California , Berkeley , CA , USA;2. Departments of Chemistry, and Earth , University of California , Berkeley , CA , USA;3. Planetary Science , University of California , Berkeley , CA , USA;4. National Institute of Standards and Technology , Gaithersburg , MD , USA |
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| Abstract: | Abstract The absolute accuracy and long‐term precision of atmospheric measurements hinge on the quality of the instrumentation and calibration standards. To assess the consistency of the ozone (O3) and nitrogen oxides (NOx) standards maintained at the National Institute of Standards and Technology (NIST), these standards were compared through the gas‐phase titration of O3 with nitric oxide (NO). NO and O3 were monitored using chemiluminescence and UV absorption, respectively. Nitrogen dioxide (NO2) was monitored directly by laser‐induced fluorescence and indirectly by catalytic conversion to NO, followed by chemiluminescence. The observed equivalent loss of both NO and O3 and the formation of NO2 in these experiments was within 1% on average over the range of 40–200 nmol mol?1 of NO in excess O3, indicating that these instruments, when calibrated with the NIST O3 and NO standards and the NO2 permeation calibration system, are consistent to within 1% at tropospherically relevant mixing ratios of O3. Experiments conducted at higher initial NO mixing ratios or in excess NO are not in as good agreement. The largest discrepancies are associated with the chemiluminescence measurements. These results indicate the presence of systematic biases under these specific conditions. Prospects for improving these experiments are discussed. |
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