Evaluation of a coupled dispersion and aerosol process model against measurements near a major road

International audienceA field measurement campaign was conducted near a major road "Itäväylä" in an urban area in Helsinki in 17?20 February 2003. Aerosol measurements were conducted using a mobile laboratory "Sniffer" at various distances from the road, and at an urban background location. Measurements included particle size distribution in the size range of 7 nm?10 ?m (aerodynamic diameter) by the Electrical Low Pressure Impactor (ELPI) and in the size range of 3?50 nm (mobility diameter) by Scanning Mobility Particle Sizer (SMPS), total number concentration of particles larger than 3 nm detected by an ultrafine condensation particle counter (UCPC), temperature, relative humidity, wind speed and direction, driving route of the mobile laboratory, and traffic density on the studied road. In this study, we have compared measured concentration data with the predictions of the road network dispersion model CAR-FMI used in combination with an aerosol process model MONO32. The vehicular exhaust emissions, and atmospheric dispersion and transformation of fine and ultrafine particles was evaluated within the distance scale of 200 m (corresponding to a time scale of a couple of minutes). We computed the temporal evolution of the number concentrations, size distributions and chemical compositions of various particle size classes. The atmospheric dilution rate of particles is obtained from the roadside dispersion model CAR-FMI. Considering the evolution of total number concentration, dilution was shown to be the most important process. The influence of coagulation and condensation on the number concentrations of particle size modes was found to be negligible at this distance scale. Condensation was found to affect the evolution of particle diameter in the two smallest particle modes. The assumed value of the concentration of condensable organic vapour of 1012 molecules cm?3 was shown to be in a disagreement with the measured particle size evolution, while the modelling runs with the concentration of condensable organic vapour of 109?1010 molecules cm?3 resulted in particle sizes that were closest to the measured values

Long-Term Exposure to Traffic-Related Air Pollution Associated with Blood Pressure and Self-Reported Hypertension in a Danish Cohort

Background: Short-term exposure to air pollution has been associated with changes in blood pressure (BP) and emergency department visits for hypertension, but little is known about the effects of long-term exposure to traffic-related air pollution on BP and hypertension

Evaluation and modelling of the size fractionated aerosol particle number concentration measurements nearby a major road in Helsinki ? Part I: Modelling results within the LIPIKA project

International audienceA field measurement campaign was conducted near a major road "Itäväylä" in an urban area in Helsinki in 17?20 February 2003. Aerosol measurements were conducted using a mobile laboratory "Sniffer" at various distances from the road, and at an urban background location. Measurements included particle size distribution in the size range of 7 nm?10 ?m (aerodynamic diameter) by the Electrical Low Pressure Impactor (ELPI) and in the size range of 3?50 nm (mobility diameter) by Scanning Mobility Particle Sizer (SMPS), total number concentration of particles larger than 3 nm detected by an ultrafine condensation particle counter (UCPC), temperature, relative humidity, wind speed and direction, driving route of the mobile laboratory, and traffic density on the studied road. In this study, we have compared measured concentration data with the predictions of the road network dispersion model CAR-FMI used in combination with an aerosol process model MONO32. For model comparison purposes, one of the cases was additionally computed using the aerosol process model UHMA, combined with the CAR-FMI model. The vehicular exhaust emissions, and atmospheric dispersion and transformation of fine and ultrafine particles was evaluated within the distance scale of 200 m (corresponding to a time scale of a couple of minutes). We computed the temporal evolution of the number concentrations, size distributions and chemical compositions of various particle size classes. The atmospheric dilution rate of particles is obtained from the roadside dispersion model CAR-FMI. Considering the evolution of total number concentration, dilution was shown to be the most important process. The influence of coagulation and condensation on the number concentrations of particle size modes was found to be negligible on this distance scale. Condensation was found to affect the evolution of particle diameter in the two smallest particle modes. The assumed value of the concentration of condensable organic vapour of 1012 molecules cm?3 was shown to be in a disagreement with the measured particle size evolution, while the modelling runs with the concentration of condensable organic vapour of 109?1010 molecules cm?3 resulted in particle sizes that were closest to the measured values

Atmospheric number size distributions of soot particles and estimation of emission factors

International audienceNumber fractions of externally mixed particles of four different sizes (30, 50, 80, and 150 nm in diameter) were measured using a Volatility Tandem DMA. The system was operated in a street canyon (Eisenbahnstrasse, EI) and at an urban background site (Institute for Tropospheric Research, IfT), both in the city of Leipzig, Germany as well as at a rural site (Melpitz (ME), a village near Leipzig). Intensive campaigns of 3?5 weeks each took place in summer 2003 as well as in winter 2003/2004. The data set thus obtained provides mean number fractions of externally mixed soot particles of atmospheric aerosols in differently polluted areas and different seasons (e.g. at 80 nm on working days, 60% (EI), 22% (IfT), and 6% (ME) in summer and 26% (IfT), and 13% (ME) in winter). Furthermore, a new method is used to calculate the size distribution of these externally mixed soot particles from parallel number size distribution measurements. A decrease of the externally mixed soot fraction with decreasing urbanity and a diurnal variation linked to the daily traffic changes demonstrate, that the traffic emissions have a significant impact on the soot fraction in urban areas. This influence becomes less in rural areas, due to atmospheric mixing and transformation processes. For estimating the source strength of soot particles emitted by vehicles (veh), soot particle emission factors were calculated using the Operational Street Pollution Model (OSPM). The emission factor for an average vehicle was found to be (1.5±0.4)·1014 #/(km·veh). The separation of the emission factor into passenger cars ((5.8±2)·1013 #/(km·veh)) and trucks ((2.5±0.9)·1015 #/(km·veh)) yielded in a 40-times higher emission factor for trucks compared to passenger cars

Kortlægning af trafikal luftforurening og virkemiddelkatalog for Frederiksberg Kommune: Artikel

DCE – Nationalt Center for Miljø og Energi, Aarhus Universitet har for Frederiksberg Kommune udarbejdet en kortlægning af luftforurening (Jensen et al., 2020a) og et virkemiddelkatalog for forbedring af luftkvaliteten (Jensen et al., 2020b). De to rapporter indgår som fagligt baggrundsmateriale for Frederiksberg Kommunes egen formulering af en luftforureningsstrategi - STRATEGI FOR REN LUFT – 2030, som blev udgivet i august 2021 (Frederiksberg Kommune, 2021). Artiklen beskriver kortlægningen af luftforureningen i Frederiksberg Kommune og dens helbredsmæssige konsekvenser. Kortlægningen indeholder en luftkvalitetsvurdering med geografisk beskrivelse af luftkvaliteten; en kildeopgørelse, som beskriver emissionen fordelt på kilder, og kildernes bidrag til luftkvaliteten; samt luftforureningens helbredseffekter og tilhørende samfundsmæssige omkostninger (eksterne omkostninger). Endvidere præsenteres et virkemiddelkatalog for reduktion af luftforurening i Frederiksberg Kommune med fokus på kommunale virkemidler inden for trafik, og en konsekvensvurdering af virkemidlerne. Virkemidler beskrives inden for indsatsområderne: By- og trafikplanlægning, elektrificering af transport, økonomiske virkemidler og regulering af transport, samt ikke-kildebaserede virkemidlers rensning af miljøet. Væsentlige lokale kilder til luftforurening er trafik og brændeovne, hvor denne artiklen alene omhandler trafik

Road salt emissions: A comparison of measurements and modelling using the NORTRIP road dust emission model

AbstractDe-icing of road surfaces is necessary in many countries during winter to improve vehicle traction. Large amounts of salt, most often sodium chloride, are applied every year. Most of this salt is removed through drainage or traffic spray processes but a certain amount may be suspended, after drying of the road surface, into the air and will contribute to the concentration of particulate matter. Though some measurements of salt concentrations are available near roads, the link between road maintenance salting activities and observed concentrations of salt in ambient air is yet to be quantified. In this study the NORTRIP road dust emission model, which estimates the emissions of both dust and salt from the road surface, is applied at five sites in four Nordic countries for ten separate winter periods where daily mean ambient air measurements of salt concentrations are available. The model is capable of reproducing many of the salt emission episodes, both in time and intensity, but also fails on other occasions. The observed mean concentration of salt in PM10, over all ten datasets, is 4.2 μg/m3 and the modelled mean is 2.8 μg/m3, giving a fractional bias of −0.38. The RMSE of the mean concentrations, over all 10 datasets, is 2.9 μg/m3 with an average R2 of 0.28. The mean concentration of salt is similar to the mean exhaust contribution during the winter periods of 2.6 μg/m3. The contribution of salt to the kerbside winter mean PM10 concentration is estimated to increase by 4.1 ± 3.4 μg/m3 for every kg/m2 of salt applied on the road surface during the winter season. Additional sensitivity studies showed that the accurate logging of salt applications is a prerequisite for predicting salt emissions, as well as good quality data on precipitation. It also highlights the need for more simultaneous measurements of salt loading together with ambient air concentrations to help improve model parameterisations of salt and moisture removal processes

Micro-scale Modelling of the Urban Wind Speed for Air Pollution Applications

Modelling wind speeds in urban areas have many applications e.g. in relation to assessment of wind energy, modelling air pollution, and building design and engineering. Models for extrapolating the urban wind speed exist, but little attention has been paid to the influence of the upwind terrain and the foundations for the extrapolation schemes. To analyse the influence of the upwind terrain and the foundations for the extrapolation of the urban wind speed, measurements from six urban and non-urban stations were explored, and a model for the urban wind speed with and without upwind influence was developed and validated. The agreement between the wind directions at the stations is found to be good, and the influence of atmospheric stability, horizontal temperature gradients, land-sea breeze, temperature, global radiation and Monin-Obukhov Length is found to be small, although future work should explore if this is valid for other urban areas. Moreover, the model is found to perform reasonably well, but the upwind influence is overestimated. Areas of model improvement are thus identified. The upwind terrain thus influences the modelling of the urban wind speed to a large extent, and the fundamental assumptions for the extrapolation scheme are fulfilled for this specific case

Residential exposure to PM_2.5 components and risk of childhood non-hodgkin lymphoma in Denmark:A nationwide register-based case-control study

In a recent study, we observed an increased risk of childhood non-Hodgkin lymphoma (NHL) associated with exposure to fine atmospheric particulate matter (PM2.5) and black carbon (BC). In this nationwide register-based case-control study, we focus on specific components of PM2.5 in relation to childhood NHL in Denmark (1981–2013) by identifying all incidents of childhood NHL cases in the Danish Cancer Registry (n = 170) and four (cancer-free) randomly selected controls matched by date of birth and sex. We applied PM2.5 concentrations and the following sub-components: secondary organic aerosols (SOA), secondary inorganic aerosols (SIA; i.e., NO3−, NH4+ and SO42−), BC, organic carbon (OC) and sea salt. We calculated a time-weighted exposure average from birth to index-date at all addresses. Odds ratios (ORs) were adjusted for register-based socio-demographic variables. We observed adjusted ORs and 95% confidence intervals (95% CI) of 2.05 (1.10, 3.83) per interquartile range (IQR, 4.83 µg/m3) PM2.5 and 1.73 (0.68, 4.41) per IQR (3.71 µg/m3) SIA, 0.95 (0.71, 1.29) per IQR (0.05 µg/m3) SOA, 1.22 (1.02, 1.46) per IQR (0.39 µg/m3) BC, 1.02 (0.83, 1.26) per IQR (0.56 µg/m3) OC and 1.01 (0.79, 1.30) per IQR (0.87 µg/m3) sea salt, respectively. The estimates were attenuated after adjustment for PM2.5, whereas the OR for PM2.5 remained increased regardless of adjustment for specific components. The findings indicate that the previously observed relation between PM2.5 and childhood NHL may be related to BC (as reported in our previous study) but also partly to SIA, but the role of specific chemical components of PM2.5 remains ambiguous