A theory and method of calculation is presented for determining changes in instrument response and hence apparent gas concentration which arise in non-dispersive infrared gas analyzers when gas mixtures with varying carrier gases are analyzed. The theory is based on variations in pressure-broadening in the sample cell of the analyzer and initial comparisons with experimental values for CO 2 -in-air and CO 2 -in-N 2 indicate good agreement between theory and experiment. DOI: 10.1111/j.2153-3490.1982.tb01827.x
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David Griffith (1982) studied this question.
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