Characterization of fine particle emissions from incense burning

Incense burning is an important indoor source of airborne particles. In this study, the emission factors of PM_2.5 and its chemical constituents emitted from six different brands of incense sticks were determined. Controlled experiments were conducted to measure the mass concentration of PM_2.5 and to determine its chemical composition (elemental carbon (EC), organic carbon (OC), metals, and ions). Measurements showed that the emissions vary for different brands of incense sticks, with smokeless incense sticks emitting the least amount. PM_2.5 emission factors range from 0.4 (smokeless incense stick) to 44.5 mg/g. Results also show that the amount of metals emitted is highly dependent on the quantity of metals present in the incense sticks. In addition, the information obtained from the controlled experiments is used to predict the concentration of PM_2.5 at incense smoke-influenced microenvironments, such as temples and homes, in order to assess the potential indoor exposure during the course of incense burning. Comparison with indoor air quality guidelines suggests that inhalation of incense smoke can pose adverse health impacts.     

Heavy incense burning in temples promotes exposure risk from airborne PMs and carcinogenic PAHs

We present the mechanistic-based exposure and risk models, appraised with reported empirical data, to assess how the human exposure to airborne particulate matters (PMs) and carcinogenic polycyclic aromatic hydrocarbons (PAHs) during heavy incense burning episodes in temples. The models integrate size-dependent PM levels inside a temple from a published exploratory study associated with a human expiratory tract (HRT) model taking into account the personal exposure levels and size distributions in the HRT. The probabilistic exposure profiles of total-PAH levels inside a temple and internal PAHs doses are characterized by a physiologically based pharmacokinetic (PBPK) model with the reconstructed dose-response relationships based on an empirical three-parameter Hill equation model, describing PAHs toxicity for DNA adducts formation and lung tumor incidence responses in human white blood cells and lung. Results show that the alveolar-interstitial (AI) region has a lower mass median diameter (0.29 microm) than that in extrathoracic (ET(1), 0.37 microm), brochial (BB, 0.36 microm) and bronchiolar (bb, 0.32 microm) regions. The 50% probability (risk=0.5) of exceeding the DNA adducts frequency (DA(f)) ratio of 1.28 (95% CI: 0.55-2.40) and 1.78 (95% CI: 0.84-2.95) for external exposure of B[a]P and B[a]P(eq), respectively. The 10% (risk=0.1) probability or more of human affected by lung tumor is approximately 7.62x10(-5)% (95% CI: 3.39x10(-5)-1.71x10(-4)%) and 3.87x10(-4)% (95% CI: 1.72x10(-4)-8.69x10(-4)%) for internal exposure of B[a]P and B[a]P(eq), respectively. Our results implicate that exposure to smoke emitted from heavy incense burning may promote lung cancer risk. Our study provides a quantitative basis for objective risk prediction of heavy incense burning exposure in temples and for evaluating the effectiveness of management.     

Characteritization of, and health risks from, polychlorinated dibenzo-p-dioxins/dibenzofurans from incense burned in a temple

Polychlorinated dibenzo-p-dioxins/dibenzofurans (PCDD/Fs) may cause adverse health effects. However, PCDD/F emissions from burning incense in temples have rarely been addressed. This study investigates PCDD/F emissions from burning incense in a temple. The mean total PCDD/F concentrations were 72.4-82.2 pg Nm^− 3 at two indoor sites; their corresponding mean total PCDD/Fs I-TEQ concentrations (0.24-0.27 pg I-TEQ Nm^− 3) were ~ 11 times that at a background location. In air samples collected from burning incense, OCDFs accounted for approximately 90% of total PCDD/Fs at the two indoor sites and an outdoor site near the temple, while the major PCDD/Fs in incense ash were PCDDs. The total PCDD/F content and toxic equivalent value of incense ash were 617 pg g^− 1 and 1.55 pg I-TEQ g^− 1, respectively. At the three sites inside/outside the temple, the air and ash samples contained the same four primary PCDD/Fs-OCDD, 1,2,3,4,6,7,8-HpCDD, OCDF and 1,2,3,4,6,7,8-HpCDF. The Cl⁻ emission factor, which is related to the PCDD/F formation, from burning incense was 0.454 mg g^− 1. The resultant lifetime average daily dose and cancer risk for temple workers were 0.00964 pg I-TEQ day^− 1 kg^− 1 and 9.64 × 10^− 6, respectively, approximately 2 times that for residents near the temple (0.00489 pg I-TEQ day^− 1 kg^− 1 and 4.89 × 10^− 6, respectively). We suggest that the chlorine content in incense must be regulated, and the high risk of PCDD/F exposure from burning incense for temple workers and visitors should be of concern.     

Indoor air pollution from particulate matter emissions in different households in rural areas of Bangladesh

Indoor air pollution from the combustion of traditional biomass fuels (wood, cow dung, and crop wastes) is a significant public health problem predominantly for poor populations in many developing countries. It is particularly problematic for the women who are normally responsible for food preparation and cooking, and for infants/young children who spend time around their mothers near the cooking area. Airborne particulate matter (PM) samples were collected from cooking and living areas in homes in a rural area of Bangladesh to investigate the impact of fuel use, kitchen configurations, and ventilation on indoor air quality and to apportion the source contributions of the measured trace metals and BC concentrations. Lower PM concentrations were observed when liquefied petroleum gas (LPG) was used for cooking. PM concentrations varied significantly depending on the position of kitchen, fuel use and ventilation rates. From reconstructed mass (RCM) calculations, it was found that the major constituent of the PM was carbonaceous matter. Soil and smoke were identified as components from elemental composition data. It was also found that some kitchen configurations have lower PM concentrations than others even with the use of low-grade biomass fuels. Adoption of these kitchen configurations would be a cost-effective approach in reducing exposures from cooking in these rural areas.     

Interaction patterns of major air pollutants in Hong Kong territory

Air pollution in a metropolitan city like Hong Kong is a major obstacle to improve air quality and living environment due to the high population density and the vehicle emission increases. The high air pollutant levels impose harm to the human health and impair the city image. The characteristic analysis of air pollutants is very important and necessary to pollutant monitoring, forecasting and controlling. In this study, the interaction patterns of principle air pollutants, e.g. nitrogen dioxide (NO(2)), nitric oxide (NO), nitric oxides (NO(x)) and ozone (O(3)), a secondary pollutant, are investigated based on the measured database in four selected areas, which covers two urban types (i.e. residential area, mixed residential/commercial/industrial area) in Hong Kong, during the period of 1999-2001. The study involves analyzing the chemical and physical properties, the characteristics of air pollutants and the factors affecting such interactions using statistical method. The results reveal several routines in urban air pollutants' variations, interaction and trends from macro aspect.     

Carbonaceous characteristics of atmospheric particulate matter in Hong Kong

To determine the characteristic of carbonaceous species in atmospheric particles in Hong Kong, PM₁₀ and PM_2.5 samples were collected using high volume (hi-vol.) air samplers from November 2000 to February 2001. The organic carbon (OC) and elemental carbon (EC) were analyzed by the selective thermal manganese dioxide oxidation (TMO) method. The ratios of PM_2.5/PM₁₀ mass ratios were 0.61, 0.78 and 0.53 for particulate matter collected at PolyU station (PolyU, near a major traffic corridor), Kwun Tong station (KT, mixed residential/commercial/industrial) and the Hok Tsui background station (HT), respectively. These results indicate that the PM_2.5 concentrations constitute the majority of the PM₁₀ concentrations, especially in urban and industrial areas of Hong Kong. The average concentrations at the three sites ranged from 73.11 to 83.52 μg/m³ for PM₁₀ and from 42.37 to 57.38 μg/m³ for PM_2.5. The highest daily mass concentrations of PM₁₀ and PM_2.5 were 125.89 μg/m³ and 116.89 μg/m³ at KT, respectively. The correlation between PM₁₀ and PM_2.5 was high at KT and HT (r>0.9, P<0.01). This means that the sources of PM₁₀ and PM_2.5 may be the same at both sites. The highest mean concentration of OC (12.02 μg/m³) and EC (6.86 μg/m³) in PM₁₀ was found at the PolyU among the three sites. For PM_2.5, the highest mean concentration of OC (10.16 μg/m³) was at KT while the highest mean concentration of EC (7.95 μg/m³) was at PolyU. However, the background concentrations at HT were higher than another background area, Kosan, Korea. Transportation of pollutants from the Asian continent may be responsible for the elevations of EC+OC at the remote site. More than 74% of the EC and more than 79% of the OC were found in the PM_2.5 fraction at the three sampling locations. At PolyU station, PM_2.5 consisted of 18.18% OC and 11.16% EC while 17.70% OC and 8.81% EC were found in KT station. Thus OC and EC are major constituents of aerosols in Hong Kong. OC/EC ratios for PM₁₀ and PM_2.5 were less than 2 at PolyU and KT stations while the ratio exceeded 3 at HT background station. This indicates that OC measured in the urban area may be emitted directly as a primary aerosol.     

Real-time molecular characterization of air pollutants in a Hong Kong residence: Implication of indoor source emissions and heterogeneous chemistry

Due to the high health risks associated with indoor air pollutants and long-term exposure, indoor air quality has received increasing attention. In this study, we put emphasis on the molecular composition, source emissions, and chemical aging of air pollutants in a residence with designed activities mimicking ordinary Hong Kong homes. More than 150 air pollutants were detected at molecular level, 87 of which were quantified at a time resolution of not less than 1 hour. The indoor-to-outdoor ratios were higher than 1 for most of the primary air pollutants, due to emissions of indoor activities and indoor backgrounds (especially for aldehydes). In contrast, many secondary air pollutants exhibited higher concentrations in outdoor air. Painting ranked first in aldehyde emissions, which also caused great enhancement of aromatics. Incense burning had the highest emissions of particle-phase organics, with vanillic acid and syringic acid as markers. The other noteworthy fingerprints enabled by online measurements included linoleic acid, cholesterol, and oleic acid for cooking, 2,5-dimethylfuran, stigmasterol, iso-/anteiso-alkanes, and fructose isomers for smoking, C₂₈-C₃₄ even n-alkanes for candle burning, and monoterpenes for the use of air freshener, cleaning agents, and camphor oil. We showed clear evidence of chemical aging of cooking emissions, giving a hint of indoor heterogeneous chemistry. This study highlights the value of organic molecules measured at high time resolutions in enhancing our knowledge on indoor air quality.     

Indoor air quality in Portuguese schools: levels and sources of pollutants

Indoor air quality (IAQ) parameters in 73 primary classrooms in Porto were examined for the purpose of assessing levels of volatile organic compounds (VOCs), aldehydes, particulate matter, ventilation rates and bioaerosols within and between schools, and potential sources. Levels of VOCs, aldehydes, PM_2.5, PM₁₀, bacteria and fungi, carbon dioxide (CO₂), carbon monoxide, temperature and relative humidity were measured indoors and outdoors and a walkthrough survey was performed concurrently. Ventilation rates were derived from CO₂ and occupancy data. Concentrations of CO₂ exceeding 1000 ppm were often encountered, indicating poor ventilation. Most VOCs had low concentrations (median of individual species <5 μg/m³) and were below the respective WHO guidelines. Concentrations of particulate matter and culturable bacteria were frequently higher than guidelines/reference values. The variability of VOCs, aldehydes, bioaerosol concentrations, and CO₂ levels between schools exceeded the variability within schools. These findings indicate that IAQ problems may persist in classrooms where pollutant sources exist and classrooms are poorly ventilated; source control strategies (related to building location, occupant behavior, maintenance/cleaning activities) are deemed to be the most reliable for the prevention of adverse health consequences in children in schools.     

The effects of an energy efficiency retrofit on indoor air quality

To investigate the impacts of an energy efficiency retrofit, indoor air quality and resident health were evaluated at a low‐income senior housing apartment complex in Phoenix, Arizona, before and after a green energy building renovation. Indoor and outdoor air quality sampling was carried out simultaneously with a questionnaire to characterize personal habits and general health of residents. Measured indoor formaldehyde levels before the building retrofit routinely exceeded reference exposure limits, but in the long‐term follow‐up sampling, indoor formaldehyde decreased for the entire study population by a statistically significant margin. Indoor PM levels were dominated by fine particles and showed a statistically significant decrease in the long‐term follow‐up sampling within certain resident subpopulations (i.e. residents who report smoking and residents who had lived longer at the apartment complex).     

Assessment of ventilation and indoor air pollutants in nursery and elementary schools in France

The aim of this study was to characterize the relationship between Indoor Air Quality (IAQ) and ventilation in French classrooms. Various parameters were measured over one school week, including volatile organic compounds, aldehydes, particulate matter (PM_2.5 mass concentration and number concentration), carbon dioxide (CO₂), air temperature, and relative humidity in 51 classrooms at 17 schools. The ventilation was characterized by several indicators, such as the air exchange rate, ventilation rate (VR), and air stuffiness index (ICONE), that are linked to indoor CO₂ concentration. The influences of the season (heating or non‐heating), type of school (nursery or elementary), and ventilation on the IAQ were studied. Based on the minimum value of 4.2 l/s per person required by the French legislation for mechanically ventilated classrooms, 91% of the classrooms had insufficient ventilation. The VR was significantly higher in mechanically ventilated classrooms compared with naturally ventilated rooms. The correlations between IAQ and ventilation vary according to the location of the primary source of each pollutant (outdoor vs. indoor), and for an indoor source, whether it is associated with occupant activity or continuous emission.     

Impact of cement factory operations on air quality and human health in Ewekoro Local Government Area,South-Western Nigeria

The concentrations of pollutants associated with cement production and the effects on ambient air and community health were assessed in this study. Suspended particulates were monitored using a Negretti 1000^TM air sampler. Additionally, an Ogawa^TM sampler was employed to assess levels of selected gaseous pollutants at selected sites. To collect data on health status, a questionnaire survey was used for selected neighbouring communities and clinic records for industry workers. The data were analysed with the aid of percentage, variation test, correlation and regression statistics. Mean concentrations of particulate matter of 10?μ (74–338?μg/m³) and 2.5?μ (28–116?μg/m³) were significantly higher than permissible limits (50?μg/m³ and 10?μg/m³) within and around the production plant. At all sites, levels of sulphur dioxide (0.1–12?ppb), nitrogen dioxide (0.1–13?ppb) and carbon monoxide (0.1–1.7?ppm) were below the allowable limits for human exposure. Analysis of variance showed significant spatial variations (p?相似文献   

Transport of particulate and gaseous pollutants in the vicinity of a human body

A uniform pollutant concentration in indoor environments can be an inappropriate representation of breathing concentration. This is especially true when local airflow in the vicinity of an occupant is dominant in transporting pollutants. The present study investigates the airflow in the vicinity of a human body, effects of respiration on breathing concentration of particulate and gaseous pollutants, and inhalation exposure in relation to source position and overall airflow patterns. It is based on experiments with a human simulator in a full-scale environmental chamber. Airflow and pollutant concentrations in the vicinity of a thermal manikin are monitored, while varying parameters including breathing, arm/hand movements, and ventilation system. Results show that breathing of a sedentary manikin has a measurable influence on the airflow in breathing zone, whereas it has very small impacts on occupant thermal plume. Also, localized hand motions have insignificant effects on the thermal plume. The results indicate that overall airflow pattern affect the inhaled particle concentrations. With highly mixed airflow in the space, relatively uniform concentration patterns occur in the occupant vicinity. However, with stratified airflow patterns, non-uniform concentration patterns are observed due to the occupant thermal plume. With a particle source at floor level and in near proximity to an occupant, inhaled particle concentrations are up to four times higher than the ambient concentrations. This finding implies that occupant thermal plume may play a significant role in transporting pollutants from floor level to the breathing zone. The non-uniform concentration observed with stratified flow also suggests caution in estimating inhalation exposure using a “well-mixed” mass balance model.     

Factors affecting variability in gaseous and particle microenvironmental air pollutant concentrations in Hong Kong primary and secondary schools

School-age children are particularly susceptible to exposure to air pollutants. To quantify factors affecting children's exposure at school, indoor and outdoor microenvironmental air pollutant concentrations were measured at 32 selected primary and secondary schools in Hong Kong. Real-time PM₁₀, PM_2.5, NO_2, and O₃ concentrations were measured in 76 classrooms and 23 non-classrooms. Potential explanatory factors related to building characteristics, ventilation practice, and occupant activities were measured or recorded. Their relationship with indoor measured concentrations was examined using mixed linear regression models. Ten factors were significantly associated with indoor microenvironmental concentrations, together accounting for 74%, 61%, 46%, and 38% of variations observed for PM_2.5, PM₁₀, O_3, and NO₂ microenvironmental concentrations, respectively. Outdoor concentration is the single largest predictor for indoor concentrations. Infiltrated outdoor air pollution contributes to 90%, 70%, 75%, and 50% of PM_2.5, PM₁₀, O_3, and NO₂ microenvironmental concentrations, respectively, in classrooms during school hours. Interventions to reduce indoor microenvironmental concentrations can be prioritized in reducing ambient air pollution and infiltration of outdoor pollution. Infiltration factors derived from linear regression models provide useful information on outdoor infiltration and help address the gap in generalizable parameter values that can be used to predict school microenvironmental concentrations.     

Comparative characterization of particle emissions from asbestos and non-asbestos cement roof slates

The first aim of this study was to characterise total and size-fractionated particulate matter (PM) aerosol, including fibres, released from the processing operations of cement roofing slates. The second aim was to compare particle emissions from asbestos-cement and non-asbestos cement sheets, with respect to total and size-fractionated particulate matter as well as fibres emissions. Asbestos and cellulose-based cement sheets were compared during slate treatment processes, namely crushing, rubbing, rasping and scrubbing. Generated PM and fibres were classified by a variety of methods (PM_2.5 and PM₁₀ cyclones, aerodynamic particle spectrometer and optical particle counter). A substantial variation in the mass of generated particles has been noticed, both within each PM fraction and between different treatment processes. The PM₁₀/PM_total concentration ratio ranged from 70 to 98% and PM_2.5/PM_total ratio equalled to ∼20%. The new generation non-asbestos sheets produced three times higher PM emissions than asbestos-cement sheets during crushing operation. Particle size distribution of number concentrations was mostly bimodal (two modes at 0.5 and 2.5 μm). With respect to fibres, the release of cellulose fibres from non-asbestos slates was from 1.8 to 13 times lower in comparison with asbestos fibres. At the same time, cellulose fibre length was 1.4–1.6 times lower. Hence, new generation non-asbestos roofing slates were proved to be less hazardous from the point of view of fibre release, but more hazardous with respect to total particle release.     

Characteristics of carbonaceous aerosols in ambient PM10 and PM2.5 particles in Dar es Salaam, Tanzania

Ambient daytime and nighttime PM₁₀ and PM_2.5 samples were collected in parallel at a kerbside in Dar es Salaam in August and September 2005 (dry season) and in April and May 2006 (wet season). All samples were analyzed for the particulate matter mass, for organic, elemental, and total carbon (OC, EC, and TC), and for water-soluble OC (WSOC). The average PM₁₀ and PM_2.5 mass concentrations and associated standard deviations were 76 ± 32 µg/m³ and 26 ± 7 µg/m³ for the 2005 dry season and 52 ± 27 µg/m³ and 19 ± 10 µg/m³ for the 2006 wet season campaign. On average, TC accounted for 29% of the PM₁₀ mass and 49% of the PM_2.5 mass for the 2005 dry season campaign and the corresponding values for the 2006 wet season campaign were 35% and 59%. There was little difference between the two campaigns for the WSOC/OC ratios with the PM_2.5 fraction having higher ratios than the PM₁₀ fraction during each campaign. Also for EC/TC higher ratios were noted in PM_2.5 than in PM₁₀, but the ratios were substantially larger in the 2006 wet season than in the 2005 dry season. The large EC/TC ratios (means 0.22-0.38) reflect the substantial impact from traffic at Dar es Salaam, as was also apparent from the clear diurnal variation in OC levels, with higher values during the day. A simple source apportionment approach was used to apportion the OC to traffic and charcoal burning. On average, 70% of the PM₁₀ OC was attributed to traffic and 30% to charcoal burning in both campaigns. A definite explanation for the substantially larger EC/TC ratios in the 2006 campaign as compared to the 2005 campaign is not available.     

Dependence of urban air pollutants on meteorology

Dependence of air pollutants on meteorology is presented with the aim of understanding the governing processes pollutants phase interaction. Intensive measurements of particulate matter (PM10) and gaseous materials (e.g., CO, NO2, SO2, and O3) are carried out regularly in 2002 at 14 measurement sites distributed over the whole territory of Great Cairo by the Egyptian Environmental Affairs Agency to assess the characteristics of air pollutants. The discussions in this work are based upon measurements performed at Abbassiya site as a case study. The nature of the contributing sources has been investigated and some attempts have been made to indicate the role played by neighboring regions in determining the air quality at the site mentioned. The results hint that, wind direction was found to have an influence not only on pollutant concentrations but also on the correlation between pollutants. As expected, the pollutants associated with traffic were at highest ambient concentration levels when wind speed was low. At higher wind speeds, dust and sand from the surrounding desert was entrained by the wind, thus contributing to ambient particulate matter levels. We also found that, the highest average concentration for NO2 and O3 occurred at humidity相似文献   

Assessing air quality in Hong Kong: A proposed,revised air pollution index (API)

The Environment Protection Department of Hong Kong has been using an air pollution index (API) to report the status of ambient air quality since 1995. Such an index system was first developed by the USA Environmental Protection Authority. The API compares five main air pollutants, i.e. sulfur dioxide (SO₂), respirable suspended particulates (RSP), nitrogen dioxide (NO₂), carbon monoxide (CO) and Ozone (O₃) as sub-indexes, which are calculated separately from a segmented linear function that transforms ambient pollutants concentrations into a normalized scale extending from 0 to 500. The resultant pollution level is described by the maximal value of these five sub-indexes. The limitation of this API system is that it considers only one pollutant with the maximum value at a time but reflects other pollutants concurrently. In this study, a revised air quality index (RAPI) is proposed based on the entropy function, which combines the effect of all pollutants on public health. The design of the revised index is based on database of air pollutants collected at two air quality monitoring stations in Hong Kong, i.e. a roadside station in Mong Kok and a general station in Sha Tin. Compared with the existing API, values of RAPI (calculated from data collected for API) at both stations are at higher levels and provide more information of levels of all pollutants. Therefore, RAPI should be representatively and widely used to provide the public with a better indicator of air quality. In addition, variations and oscillations of pollutants concentrations were also examined and the results show that RSP and NO₂ contribute more to the overall pollution level than other components. It is suggested that more abatement strategies be focused on these pollutants to improve air quality in the future.     

Evaluation of methods for quantifying agricultural emissions of air, water and soil pollutants

Integrated assessments that analyze global warming, acidification, eutrophication and ozone related problems simultaneously, need complete, detailed and consistent emission estimates that consider possible interrelations between different pollutants. We discuss three types of emission estimation methods: emission factor, regression analyses and process-based methods. Selected examples of these are reviewed to illustrate the large variety in methods available. We present an approach for the evaluation of emission estimation methods which follows three steps: (1) Comparison, (2) Scoring and (3) Multi-Criteria Analysis (MCA). We demonstrate the usefulness of this approach by applying it to a case study for the Czech Republic. Firstly we compare selected methods with respect to characteristics which we consider as requirements to quantify emissions of air, water and soil pollutants in an integrated way. We observe that none of the selected methods fully meet our defined characteristics. Secondly, we score the methods with respect to three types of criteria. This evaluation reveals large differences between the methods. We conclude that the following methods best meet our criteria: the IPCC Guidelines, methods from INITIATOR, and the detailed method of the EMEP/CORINAIR Guidebook. Finally, we perform a Multi-Criteria Analysis to analyze how our conclusions change if one considers certain criteria as more important than others. Based on this analysis we suggest that combining parts of each of the three methods forms a sound basis for a new emission estimation method for quantifying agricultural emissions of air, water and soil pollution simultaneously.     

Non-exhaust emissions of PM and the efficiency of emission reduction by road sweeping and washing in the Netherlands

From research on PM_2.5 and PM₁₀ in 2007/2008 in the Netherlands, it was concluded that the coarse fraction (PM_2.5-10) attributed 60% and 50% respectively, to the urban-regional and street-urban increments of PM₁₀. Contrary to Scandinavian and Mediterranean countries which exhibit significant seasonal variation in the coarse fraction of particulate matter (PM), in the Netherlands the coarse fraction in PM at a street location is rather constant during the year. Non-exhaust emissions by road traffic are identified as the main source for coarse PM in urban areas. Non-exhaust emissions mainly originate from re-suspension of accumulated deposited PM and road wear related particles, while primary tire and brake wear hardly contribute to the mass of non-exhaust emissions. However, tire and brake wear can clearly be identified in the total mass through the presence of the heavy metals: zinc, a tracer for tire wear and copper, a tracer for brake wear.The efficiency of road sweeping and washing to reduce non-exhaust emissions in a street-canyon in Amsterdam was investigated. The increments of the coarse fraction at a kerbside location and a housing façade location versus the urban background were measured at days with and without sweeping and washing. It was concluded that this measure did not significantly reduce non-exhaust emissions.