Measurement uncertainty of coulometric trace humidity sensors

2018 ◽  
Vol 85 (12) ◽  
pp. 746-753
Author(s):  
Carlo Tiebe ◽  
Marc Detjens ◽  
Ulrich Banach ◽  
Thomas Hübert

Abstract Especially trace amounts of water vapour in gases can be reliably determined by coulometric trace humidity sensors. The principle of these sensors is based on water vapour absorption in a hygroscopic layer and its subsequent electrolytic decomposition. The calibration of sensors was performed in the humidity range, expressed as frost point temperature, from -30\hspace{0.1667em}^\circ \mathrm{C} to -80\hspace{0.1667em}^\circ \mathrm{C}. This range is equivalent to volume fractions smaller than 376 µL·L−1. Generated humidity was measured with coulometric sensors and a chilled dew point hygrometer that was used as reference. An empirical non-linear function was found between sensor signal and measured reference humidity. This function consists of two parameters with a measurement uncertainty. Both calibration parameters were checked by means of one-way analysis of variance. It showed that gas specific function can be used for humidity measurement in nitrogen, hydrogen, dinitrogen monoxide, compressed and synthetic air. It is possible to determine trace humidity in all tested gases with an expanded uncertainty less than 2.1 K (coverage factor k=2) regarding frost point temperature.

Energies ◽  
2019 ◽  
Vol 12 (9) ◽  
pp. 1585 ◽  
Author(s):  
Nataliia Fedorova ◽  
Pegah Aziziyanesfahani ◽  
Vojislav Jovicic ◽  
Ana Zbogar-Rasic ◽  
Muhammad Jehanzaib Khan ◽  
...  

Thermal energy of flue gases (FG) dissipating from industrial facilities into the environment, constitute around 20% of the total dissipated thermal energy. Being part of the FG, water vapour carries thermal energy out of the system in the form of the latent heat, which can be recovered by condensation, thus increasing the overall efficiency of an industrial process. The limiting factor in this case is the low dew point temperature (usually 40–60 °C) of the water vapour in the FG. The increase of the dew point temperature can be achieved by increasing the water content or pressure. Taking these measures as a basis, the presented work investigated the following concepts for increasing the dew point temperature: humidification of the flue gas using water, humidification using steam, compression of the FG and usage of the steam ejector. Modelling of these concepts was performed using the commercial software Aspen®. The humidification of the FG using water resulted in the negligible increase in the dew point (3 °C). Using steam humidification the temperatures of up to 92 °C were reached, while the use of steam ejector led to few degrees higher dew point temperatures. However, both concepts proved to be energy demanding, due to the energy requirements for the steam generation. The FG compression enabled the achievement of a 97 °C dew point temperature, being both energy-efficient and exhibiting the lowest energy cost.


2011 ◽  
Vol 33 (8-9) ◽  
pp. 1568-1582 ◽  
Author(s):  
L. Lages Martins ◽  
A. Silva Ribeiro ◽  
J. Alves e Sousa ◽  
Alistair B. Forbes

2019 ◽  
Vol 8 (3) ◽  
pp. 28
Author(s):  
Davidson Odafe Akpootu ◽  
Mukhtar Isah Iliyasu ◽  
Wahidat Mustapha ◽  
Simeon Imaben Salifu ◽  
Hassan Taiwo Sulu ◽  
...  

2019 ◽  
Author(s):  
Dipayan Paul ◽  
Hubertus A. Scheeren ◽  
Henk G. Jansen ◽  
Bert A. M. Kers ◽  
John B. Miller ◽  
...  

Abstract. Atmospheric flask samples are either collected at atmospheric pressure by simply opening a valve of a pre-evacuated flask, or pressurized with the help of a pump to a few bar above ambient providing large air samples for analysis. Under humid conditions, there is a risk that water vapour in the sample leads to condensation on the walls of the flask, notably at higher than ambient sampling pressures. Liquid water in sample flasks is known to affect the CO2 mixing ratios and also alters the isotopic composition of oxygen (17O and 18O) in CO2 via isotopic equilibration. Hence, for accurate determination of CO2 mole fractions and its stable isotopic composition, it is vital to dry the air samples to a sufficiently low dew point before they are pressurized in flasks to avoid condensation. Moreover, the drying system itself should not influence the mixing ratio and the isotopic composition of CO2, nor of the other constituents under study. For the "Airborne Stable Isotopes of Carbon from the Amazon" (ASICA) project focusing on accurate measurements of CO2 and its singly-substituted stable isotopologues over the Amazon, an air drying system was needed capable of removing water vapour from air sampled at a dew point better than −2 °C, high flow rates up to 12 L/min, and without the need for electrical power. Since to date, no commercial air drying device is available that meets these requirements, we designed and built our own consumable-free, power-free, and portable drying system based on multi-tube Nafion™ gas sample driers (Perma Pure, Lakewood, USA). The required dry purge air is provided by feeding the exhaust flow of the flasks sampling system through a dry molecular sieve (type 3A) cartridge. In this study we describe the systematic evaluation of our Nafion-based air sample dryer with emphasis on its performance concerning the measurements of atmospheric CO2 mole fractions and the three singly-substituted isotopologues of CO2 (16O13C16O, 16O12C17O and 16O12C18O), as well as the trace gas species CH4, CO, N2O, and SF6. Experimental results simulating extreme tropical conditions (saturated air at 33 °C) indicated that the response of the air dryer is almost instantaneous and that approximately 85 L of air, containing up to 4 % water vapour, can be processed staying below a −2 °C dew point temperature (at 275 kPa). We estimated that least 8 flasks can be sampled (at an overpressure of 275 kPa) with a water vapour content below −2 °C dew point temperature during a typical flight sampling up to 5 km altitude over the Amazon, whereas the remaining samples would stay well below 5 °C dew point temperature (at 275 kPa). The performance of the air dryer on measurements of CO2, CH4, CO, N2O, and SF6, and the CO2 isotopologues 16O13C16O and 16O12C18O was tested in the laboratory simulating real sampling conditions by compressing humidified air from a calibrated cylinder, after being dried by the air dryer, into sample flasks. We found that the mole fraction and the isotopic composition difference between the different test conditions (including the dryer) and the base condition (dry air, without dryer) remained well within or very close to, in the case of N2O, the WMO recommended compatibility goals for independent measurement programs, proving that the test condition induced no significant bias on the sample measurements.


2006 ◽  
Vol 51 ◽  
pp. 197-200
Author(s):  
S. Krutovertsev ◽  
A. Tarasova ◽  
L. Krutovertseva ◽  
A. Zorin ◽  
O. Ivanova

Constraction and characteristics of sorption polymeric relative humidity sensors, sorption SiOx microhumidity sensors, and condensation type (dew point) sensors are compared. The characteristics of the sensors are examined in dew point range from -80 to +20oC. An integrated multifunctional humidity sensor, for measurements in wide humidity range at different conditions is developed. The sensors are intended for use in various branches of industry, and in scientific researches.


2011 ◽  
Vol 4 (2) ◽  
pp. 289-296 ◽  
Author(s):  
T. Thornberry ◽  
T. Gierczak ◽  
R. S. Gao ◽  
H. Vömel ◽  
L. A. Watts ◽  
...  

Abstract. Chilled mirror hygrometers (CMH) are widely used to measure water vapour in the troposphere and lower stratosphere from balloon-borne sondes. Systematic discrepancies among in situ water vapour instruments have been observed at low water vapour mixing ratios (<5 ppm) in the upper troposphere and lower stratosphere (UT/LS). Understanding the source of the measurement discrepancies is important for a more accurate and reliable determination of water vapour abundance in this region. We have conducted a laboratory study to investigate the potential interference of gas-phase nitric acid (HNO3) with the measurement of frost point temperature, and consequently the water vapour mixing ratio, determined by CMH under conditions representative of operation in the UT/LS. No detectable interference in the measured frost point temperature was found for HNO3 mixing ratios of up to 4 ppb for exposure times up to 150 min. HNO3 was observed to co-condense on the mirror frost, with the adsorbed mass increasing linearly with time at constant exposure levels. Over the duration of a typical balloon sonde ascent (90–120 min), the maximum accumulated HNO3 amounts were comparable to monolayer coverage of the geometric mirror surface area, which corresponds to only a small fraction of the actual frost layer surface area. This small amount of co-condensed HNO3 is consistent with the observed lack of HNO3 interference in the frost point measurement because the CMH utilizes significant reductions (>10%) in surface reflectivity by the condensate to determine H2O.


2010 ◽  
Vol 3 (4) ◽  
pp. 3725-3745
Author(s):  
T. Thornberry ◽  
T. Gierczak ◽  
R. S. Gao ◽  
H. Vömel ◽  
L. A. Watts ◽  
...  

Abstract. Chilled mirror hygrometers (CMH) are widely used to measure water vapour in the troposphere and lower stratosphere from balloon-borne sondes. Systematic discrepancies among in situ water vapour instruments have been observed at low water vapour mixing ratios (<5 ppm) in the upper troposphere and lower stratosphere (UT/LS). Understanding the source of the measurement discrepancies is important for a more accurate and reliable determination of water vapour abundance in this region. We have conducted a laboratory study to investigate the potential interference of gas-phase nitric acid (HNO3) with the measurement of frost point temperature, and consequently the water vapour mixing ratio, determined by CMH under conditions representative of operation in the UT/LS. No detectable interference in the measured frost point temperature was found for HNO3 mixing ratios of up to 4 ppb for exposure times up to 150 min. HNO3 was observed to co-condense on the mirror frost, with the adsorbed mass increasing linearly with time at constant exposure levels. Over the duration of a typical balloon sonde ascent (90–120 min), the maximum accumulated HNO3 amounts were comparable to monolayer coverage of the geometric mirror surface area, which corresponds to only a small fraction of the actual frost layer surface area. This small amount of co-condensed HNO3 is consistent with the observed lack of HNO3 interference in the frost point measurement because the CMH utilizes significant reductions (>10%) in surface reflectivity by the condensate to determine H2O.


2017 ◽  
Vol 730 ◽  
pp. 587-594
Author(s):  
Yun Kyung Bae ◽  
Dong Eun Lee ◽  
Dong Hoon Hyun

The purpose of this paper is to propose appropriate evaluation method of measurement uncertainty with respect to the measurement results of polymer thin film capacitive humidity sensor according to dew point temperature variation. All of the evaluation process concerning the measurement uncertainty of polymer thin film capacitive humidity sensor is based on experiment and numerical analysis. To estimate uncertainty contribution properly for polymer thin film capacitive sensor strongly influenced by measurement environment, the experiments are performed in the reference relative humidity range from 5 % to 30 % at a setting dry bulb temperature of 23°C. Also, the reference standards are chilled mirror hygrometer (CMH) and platinum resistance thermometer (PRT). In particular, the uncertainty sources are considered differently according to the range of below or above 0°C, reference dew point. From the budgets, uncertainty contributions to the standard uncertainty are clearly dominated by the effect of the uncertainty due to super-cooling in case of condition below 0°C, dew point temperature. Also, the contributions for stability and distribution of humidity generator have a mainly effect on the expanded uncertainty of polymeric humidity sensor. It is desired that measurement uncertainties of polymeric humidity sensor are comprised separately on the basis of reference dew point, 0°C. The evaluation procedure of measurement uncertainty is developed in accordance with the principles established in the documents EA-4/02, Expression of the Uncertainty of Measurement in Calibration [1].


2015 ◽  
Vol 789-790 ◽  
pp. 519-525
Author(s):  
Yun Kyung Bae ◽  
Dong Hoon Hyun

The purpose of this paper is to analyze the effect of tube length in calibration instrumentation on dew point measurement of dew point sensors (DPS) and evaluation of measurement uncertainty. When measuring dew point temperature, various tube lengths between dew point generator and dew point sensor (DPS) cause a significant error due to moisture absorption of inner tube. The measurement is carried out to analyze the variation on measured dew point temperature for four cases of tube lengths with 300 mm, 1200 mm, 2500 mm and 5000 mm. The dew point temperature measurements were performed in the range from-60 °C to 10 °C by using calibrated standard chilled mirror hygrometer as reference standard. In order to investigate contribution to the standard uncertainty for the tube length variation as an uncertainty source, expanded uncertainties were evaluated for the cases including the effect of tube length variation as an uncertainty source and excluding it at each measurement point. The measurement was conducted according to standard calibration procedure of Korea Testing Laboratory which assures suitability and traceable results. It is also based on international standards.


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