2004
DOI: 10.1504/ijep.2004.005548
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Time-resolved ammonia measurement in vehicle exhaust

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Cited by 31 publications
(15 citation statements)
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“…The temperature of the tube was increased by 1.5 K min −1 to a final temperature of 543 K. Downstream of the heated glass tube the reaction gas was diluted with 250 mL min −1 high‐purity synthetic air (99.999%, 20.5% O 2 in N 2 ) and transferred through a heated PTFE line (453 K, Winkler GmbH, Heidelberg, Germany) to a Fourier transform infrared (FTIR) spectrometer (CX‐4000, Gasmet Technologies Oy, Helsinki, Finland). The N 2 O mixing ratios and reaction by‐products (H 2 O, NH 3 , NO, NO 2 , HNO 3 ) were quantified in real‐time by FTIR spectroscopy . Downstream of the FTIR spectrometer the process gas was dynamically diluted to a constant N 2 O mole fraction of 90 ppm.…”
Section: Methodsmentioning
confidence: 99%
“…The temperature of the tube was increased by 1.5 K min −1 to a final temperature of 543 K. Downstream of the heated glass tube the reaction gas was diluted with 250 mL min −1 high‐purity synthetic air (99.999%, 20.5% O 2 in N 2 ) and transferred through a heated PTFE line (453 K, Winkler GmbH, Heidelberg, Germany) to a Fourier transform infrared (FTIR) spectrometer (CX‐4000, Gasmet Technologies Oy, Helsinki, Finland). The N 2 O mixing ratios and reaction by‐products (H 2 O, NH 3 , NO, NO 2 , HNO 3 ) were quantified in real‐time by FTIR spectroscopy . Downstream of the FTIR spectrometer the process gas was dynamically diluted to a constant N 2 O mole fraction of 90 ppm.…”
Section: Methodsmentioning
confidence: 99%
“…Ammonia can be absorbed in condensed water or react with acidic compounds present in the exhaust or along the system. Previous studies have reported that ammonia sticks, and it is also adsorbed on the surfaces of sampling and analysis equipment, as well as on the dilute exhaust systems’ walls (Durbin et al 2002 ; Heeb et al 2006 , 2012 , 2008 ; Mohn et al 2004 ). Ammonia is delayed in the constant volume sampler (CVS) making time-resolved ammonia analysis from the CVS tunnel extremely difficult (Mohn et al 2004 ).…”
Section: Introductionmentioning
confidence: 99%
“…Previous studies have reported that ammonia sticks, and it is also adsorbed on the surfaces of sampling and analysis equipment, as well as on the dilute exhaust systems’ walls (Durbin et al 2002 ; Heeb et al 2006 , 2012 , 2008 ; Mohn et al 2004 ). Ammonia is delayed in the constant volume sampler (CVS) making time-resolved ammonia analysis from the CVS tunnel extremely difficult (Mohn et al 2004 ). As a result, exhaust tailpipe measurements have been considered to be the most appropriate approach for measuring vehicular ammonia emission on chassis dynamometer tests (Durbin et al 2002 ; Heeb et al 2006 , 2012 , 2008; Mohn et al 2004 ).…”
Section: Introductionmentioning
confidence: 99%
“…An infrared spectrum with 0.5 cm −1 optical resolution was recorded every three seconds, and trace gas (N 2 O, CO, CH 4 , CO 2 and H 2 O) mixing ratios were retrieved by classical least square fitting in selected wavelength regions (Mohn et al, 2004. Calibration spectra were recorded under identical instrumental and spectroscopic conditions from certified and diluted calibration gases or by continuous injection of liquids into nitrogen.…”
Section: On-line Ftir Analysis Of Mixing Ratiosmentioning
confidence: 99%