| 1. |
- Galle, Bo, 1952, et al.
(författare)
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Network for Observation of Volcanic and Atmospheric Change (NOVAC)-A global network for volcanic gas monitoring: Network layout and instrument description
- 2010
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Ingår i: Journal of Geophysical Research. - 0148-0227 .- 2156-2202. ; 115:D5, s. Art. no. D05304-
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Tidskriftsartikel (refereegranskat)abstract
- This paper presents the global project Network for Observation of Volcanic and Atmospheric Change (NOVAC), the aim of which is automatic gas emission monitoring at active volcanoes worldwide. Data from the network will be used primarily for volcanic risk assessment but also for geophysical research, studies of atmospheric change, and ground validation of satellite instruments. A novel type of instrument, the scanning miniaturized differential optical absorption spectroscopy (Mini-DOAS) instrument, is applied in the network to measure volcanic gas emissions by UV absorption spectroscopy. The instrument is set up 5-10 km downwind of the volcano under study, and typically two to four instruments are deployed at each volcano in order to cover different wind directions and to facilitate measurements of plume height and plume direction. Two different versions of the instrument have been developed. Version I was designed to be a robust and simple instrument for measurement of volcanic SO2 emissions at high time resolution with minimal power consumption. Version II was designed to allow the best possible spectroscopy and enhanced flexibility in regard to measurement geometry at the cost of larger complexity, power consumption, and price. In this paper the project is described, as well as the developed software, the hardware of the two instrument versions, measurement strategies, data communication, and archiving routines. As of April 2009 a total of 46 instruments have been installed at 18 volcanoes worldwide. As a typical example, the installation at Tungurahua volcano in Ecuador is described, together with some results from the first 21 months of operation at this volcano.
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| 2. |
- Kim, S. W., et al.
(författare)
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Evaluations of NOx and highly reactive VOC emission inventories in Texas and their implications for ozone plume simulations during the Texas Air Quality Study 2006
- 2011
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Ingår i: Atmospheric Chemistry and Physics. - : Copernicus GmbH. - 1680-7316 .- 1680-7324. ; 11:22, s. 11361-11386
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Tidskriftsartikel (refereegranskat)abstract
- Satellite and aircraft observations made during the 2006 Texas Air Quality Study (TexAQS) detected strong urban, industrial and power plant plumes in Texas. We simulated these plumes using the Weather Research and Forecasting-Chemistry (WRF-Chem) model with input from the US EPA's 2005 National Emission Inventory (NEI-2005), in order to evaluate emissions of nitrogen oxides (NOx = NO + NO2) and volatile organic compounds (VOCs) in the cities of Houston and Dallas-FortWorth. We compared the model results with satellite retrievals of tropospheric nitrogen dioxide (NO2) columns and airborne in-situ observations of several trace gases including NOx and a number of VOCs. The model and satellite NO2 columns agree well for regions with large power plants and for urban areas that are dominated by mobile sources, such as Dallas. How-ever, in Houston, where significant mobile, industrial, and inport marine vessel sources contribute to NOx emissions, the model NO2 columns are approximately 50 %-70 % higher than the satellite columns. Similar conclusions are drawn from comparisons of the model results with the TexAQS 2006 aircraft observations in Dallas and Houston. For Dallas plumes, the model-simulated NO2 showed good agreement with the aircraft observations. In contrast, the model-simulated NO2 is similar to 60 % higher than the aircraft observations in the Houston plumes. Further analysis indicates that the NEI-2005 NOx emissions over the Houston Ship Channel area are overestimated while the urban Houston NOx emissions are reasonably represented. The comparisons of model and aircraft observations confirm that highly reactive VOC emissions originating from industrial sources in Houston are underestimated in NEI-2005. The update of VOC emissions based on Solar Occultation Flux measurements during the field campaign leads to improved model simulations of ethylene, propylene, and formaldehyde. Reducing NOx emissions in the Houston Ship Channel and increasing highly reactive VOC emissions from the point sources in Houston improve the model's capability of simulating ozone (O-3) plumes observed by the NOAA WP-3D aircraft, although the deficiencies in the model O-3 simulations indicate that many challenges remain for a full understanding of the O-3 formation mechanisms in Houston.
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| 3. |
- Mellqvist, Johan, 1965, et al.
(författare)
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Measurements of industrial emissions of alkenes in Texas using the solar occultation flux method
- 2010
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Ingår i: Journal of Geophysical Research. - 0148-0227 .- 2156-2202. ; 115
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Tidskriftsartikel (refereegranskat)abstract
- Solar occultation flux (SOF) measurements of alkenes have been conducted to identify and quantify the largest emission sources in the vicinity of Houston and in SE Texas during September 2006 as part of the TexAQS 2006 campaign. The measurements have been compared to emission inventories and have been conducted in parallel with airborne plume studies. The SOF measurements show that the hourly gas emissions from the large petrochemical and refining complexes in the Houston Ship Channel area and Mount Belvieu during September 2006 corresponded to 1250 +/- 180 kg/h of ethene and 2140 +/- 520 kg/h of propene, with an estimated uncertainty of about 35%. This can be compared to the 2006 emission inventory value for ethene and propene of 145 +/- 4 and 181 +/- 42 kg/h, respectively. On average, for all measurements during the campaign, the discrepancy factor is 10.2(+ 8,-5) for ethene and 11.7(+ 7,-4) for propene. The largest emission source was Mount Belvieu, NE of the Houston Ship Channel, with ethene and propene emissions corresponding to 440 +/- 130 kg/h and 490 +/- 190 kg/h, respectively. Large variability of propene was observed from several petrochemical industries, for which the largest reported emission sources are flares. The SOF alkene emissions agree within 50% with emissions derived from airborne measurements at three different sites. The airborne measurements also provide support to the SOF error budget.
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| 4. |
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| 5. |
- Rivera, Claudia, 1976, et al.
(författare)
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NO2 fluxes from Tijuana using a mobile mini-DOAS during Cal-Mex 2010
- 2013
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Ingår i: Atmospheric Environment. - : Elsevier BV. - 1873-2844 .- 1352-2310. ; 70, s. 532-539
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Tidskriftsartikel (refereegranskat)abstract
- NO2 fluxes were measured using a mobile mini-DOAS during Cal-Mex 2010 field study, between May 15 and June 30, 2010, from the urban area of Tijuana, Baja California as well as the Rosarito power plant The average calculated NO2 fluxes were 328 +/- 184 (269 +/- 201) g s(-1), and 23.4 +/- 4.9 (12.9 +/- 11.9) g s(-1) for Tijuana urban area and Rosarito power plant, respectively, using model based wind fields and onsite measurements (in parenthesis). Wind speed and wind direction data needed to estimate the fluxes were both modeled and obtained from radiosondes launched regularly during the field campaign, whereas the mixing layer height throughout the entire field campaign was measured using a ceilometer. Large variations in the NO2 fluxes from both the Tijuana urban area and Rosarito power plant were observed during Cal-Mex 2010; however, the variability was less when model based wind fields were used. Qualitative comparisons of modeled and measured plumes from the Tijuana urban area and Rosarito power plant showed good agreement.
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| 6. |
- Rivera, Claudia, 1976, et al.
(författare)
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Quantification of NO2 and SO2 emissions from the Houston Ship Channel and Texas City industrial areas during the 2006 Texas Air Quality Study
- 2010
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Ingår i: Journal of Geophysical Research. - 0148-0227 .- 2156-2202. ; 115
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Tidskriftsartikel (refereegranskat)abstract
- In August-September 2006, as part of the Second Texas Air Quality Study, NO2 and SO2 emissions from the Houston Ship Channel and Texas City industrial areas were quantified using mobile mini-differential optical absorption spectroscopy instruments. The measured NO2 emissions from the Houston Ship Channel and Texas City industrial areas were 2542 and 452 kg h(-1), respectively, yielding NOx emissions 70% and 43%, respectively, above the reported inventory values. Quantified SO2 emissions from the Houston Ship Channel area were 1749 kg h(-1) and were found to be 34% above the values reported in the inventory. Short-term variability of NO2 and SO2 emissions was found at the Houston Ship Channel. On 31 August 2006, a plume was detected at the HSC during three consecutive measurements, yielding a HCHO flux of 481 kg h(-1). This event has been mainly attributed to photochemical production.
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