Airborne measurements of peroxy radicals using the PERCA technique
被引:25
作者:
Green, TJ
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机构:Univ E Anglia, Sch Environm Sci, Norwich NR4 7DT, Norfolk, England
Green, TJ
Reeves, CE
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机构:Univ E Anglia, Sch Environm Sci, Norwich NR4 7DT, Norfolk, England
Reeves, CE
Brough, N
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机构:Univ E Anglia, Sch Environm Sci, Norwich NR4 7DT, Norfolk, England
Brough, N
Edwards, GD
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机构:Univ E Anglia, Sch Environm Sci, Norwich NR4 7DT, Norfolk, England
Edwards, GD
Monks, PS
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机构:Univ E Anglia, Sch Environm Sci, Norwich NR4 7DT, Norfolk, England
Monks, PS
Penkett, SA
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机构:Univ E Anglia, Sch Environm Sci, Norwich NR4 7DT, Norfolk, England
Penkett, SA
机构:
[1] Univ E Anglia, Sch Environm Sci, Norwich NR4 7DT, Norfolk, England
[2] Univ Leicester, Dept Chem, Leicester LE1 7RH, Leics, England
来源:
JOURNAL OF ENVIRONMENTAL MONITORING
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2003年
/
5卷
/
01期
关键词:
D O I:
10.1039/b204493e
中图分类号:
O65 [分析化学];
学科分类号:
070302 ;
081704 ;
摘要:
The Peroxy Radical Chemical Amplifier (PERCA) technique is a proven method for measurement of ambient levels of perox radicals at ground level. but there are no published instances of the technique being used oil an aerial platform. Here c describe deployment of a PERCA on the former UK Meteorological Office C-130 Hercules research aircraft. The instrument uses the established method of chemical amplification and conversion of peroxy radicals to nitrogen dioxide (NO2) by doping the sample air-flow matrix with CO and NO, subsequently measuring the NO2 yield with an improved 'Luminox' LMA-3 NO2 detector. NO2 from the amplification chemistry is distinguished from other sources of NO2 reaching the detector by periodically injecting CO similar to 1 s downstream of the NO injection point (termination mode). Chain lengths (CL's) for the amplification chemistry were topically similar to260 (ground level) to similar to200 (7,000 m). This variation with altitude is less than the variation associated with the 'age' of the PFA inlet material where the amplification chemistry occurs; CL's of similar to 200 with old tubing to similar to 300 with new clean tubing were typical (ground level values). The CL determinations were made in-flight using an onboard calibration unit based on the 254 nm photolysis of 7.5 to 10 parts per billion (by volume. ppb) of CH3I in air, producing CH3O2 in a quantitative manner. The noise-equivalent detection limit for peroxy radicals (HO2 + RO2) is 2 parts per trillion (by volume, pptv) at 3,650 m when the background ambient ozone levels are stable. based on a 5 min average of five 30 s amplification cycles and five 30 s termination cycles. This detection limit is a function of several factors but is most seriously degraded when there is large variability in the ambient ozone concentration. This paper describes the instrument design. considers its performance and proposes design improvements. It Concludes that the performance of an airborne PERCA in the free troposphere can be superior to that of ground-based instruments when similar sampling frequencies are compared.