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| Titel |
Development of a mobile and high-precision atmospheric CO2 monitoring station |
| VerfasserIn |
M. Molnár, L. Haszpra, I. Major, É. Svingor, M. Veres |
| Konferenz |
EGU General Assembly 2009
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| Medientyp |
Artikel
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| Sprache |
Englisch
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| Digitales Dokument |
PDF |
| Erschienen |
In: GRA - Volume 11 (2009) |
| Datensatznummer |
250028255
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| Zusammenfassung |
| Nowadays one of the most burning questions for the science is the rate and the reasons of the recent climate change. Greenhouse gases (GHG), mainly CO2 and CH4 in the atmosphere could affect the climate of our planet. However, the relation between the amount of atmospheric GHG and the climate is complex, full with interactions and feedbacks partly poorly known even by now. The only way to understand the processes, to trace the changes, to develop and validate mathematical models for forecasts is the extensive, high precision, continuous monitoring of the atmosphere.
Fossil fuel CO2 emissions are a major component of the European carbon budget. Separation of the fossil fuel signal from the natural biogenic one in the atmosphere is, therefore, a crucial task for quantifying exchange flux of the continental biosphere through atmospheric observations and inverse modelling. An independent method to estimate trace gas emissions is the top-down approach, using atmospheric CO2 concentration measurements combined with simultaneous radiocarbon (14C) observations. As adding fossil fuel CO2 to the atmosphere, therefore, leads not only to an increase in the CO2 content of the atmosphere but also to a decrease in the 14C/12C ratio in atmospheric CO2.
The ATOMKI has more than two decade long experience in atmospheric 14CO2 monitoring. As a part of an ongoing research project being carried out in Hungary to investigate the amount and temporal and spatial variations of fossil fuel CO2 in the near surface atmosphere we developed a mobile and high-precision atmospheric CO2 monitoring station. We describe the layout and the operation of the measuring system which is designed for the continuous, unattended monitoring of CO2 mixing ratio in the near surface atmosphere based on an Ultramat 6F (Siemens) infrared gas analyser. In the station one atmospheric 14CO2 sampling unit is also installed which is developed and widely used since more than one decade by ATOMKI.
Mixing ratio of CO2 is measured at 2 m above the ground by the monitoring station. Air is pumped through a 9.5-mm-diameter plastic tube (PFA, Swagelok) to a CO2 analyser located in a container box. Container box (Containex) is 1.5 m wide, 1.2 m deep and 2.2 m high, designed as a mobile measuring room which is field deployable, only electric power is required. A 15 micron pore size stainless steel Tee-Type (Swagelok) particle filter is located at the inlet of the sampler tube. Diaphragm pump (KNF) is used to draw air continuously through the sampling tube from monitoring level at flow rate of ~ 2 L/min. After leaving the pump, the air at 5 psig overpressure enters a glass trap for liquid water that is cooled in a regular household refrigerator, to dry the air to a dew point of 3°-4°C. Liquid water is forced out through an orifice at the bottom of the trap. The air sample inlet tube and the standard gases (Linde Hungary) are connected to miniature solenoid valves (S Series, ASCO Numatics) in a manifold which are normally closed and controlled by the CO2 analyser, which selects which gas is sampled. The air leaving the manifold through its common outlet is further dried to a dew point of about -25°C by passage through a 360-cm-long Nafion drier (Permapure), so that the water vapour interference and dilution effect are <0.1 ppm equivalent CO2. The Nafion drier is purged in a counter flow (300 cm3/min) arrangement using waste sample air that has been further dried by passage through anhydrous CaSO4 (Drierite).
Analysis is carried out using an infrared gas analyser Ultramat 6F which is a specialised model for field applications by Siemens. A constant sample flow rate of
300 cm3/min is maintained by a mass flow controller (Aalborg). The reference cell of the CO2 analyzer is continuously flushed with a compressed reference gas of 350 ppm CO2 in synthetic air (Messer Hungarogáz). The basic calibration cycle is 2 hours, consisting of a zero-point calibration and a span calibration. Each calibration is consisting of 2 min flushing and 20 sec signal integration. The usual change of the response function is below 0.2 ppm after 2 hours following a previous calibration. The analyser measures the CO2 mixing ratio in the sample gas in every 3 seconds. Output data are registered by a data logger developed for this application (Special Control Devices).
The overall uncertainty of our atmospheric CO2 mixing ratio measurements is < 0.5 ppm (< 0,2 %). This level of error is acceptable for fossil fuel CO2 calculations as the uncertainty of the other required parameter radiocarbon content of atmospheric CO2 is usually 0.3-0.5%. Using the developed mobile and high-precision atmospheric CO2 monitoring station we plan to determine the fossil fuel CO2 amount in the air of different cities and other average industrial regions in Hungary.
This research project was supported by Hungarian NSF (Ref No. F69029). |
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