Determining the ventilation and aerosol deposition rates from routine indoor-air measurements

Measurement of air exchange rate provides critical information in energy and indoor-air quality studies. Continuous measurement of ventilation rates is a rather costly exercise and requires specific instrumentation. In this work, an alternative methodology is proposed and tested, where the air exchange rate is calculated by utilizing indoor and outdoor routine measurements of a common pollutant such as SO₂, whereas the uncertainties induced in the calculations are analytically determined. The application of this methodology is demonstrated, for three residential microenvironments in Athens, Greece, and the results are also compared against ventilation rates calculated from differential pressure measurements. The calculated time resolved ventilation rates were applied to the mass balance equation to estimate the particle loss rate which was found to agree with literature values at an average of 0.50 h^?1. The proposed method was further evaluated by applying a mass balance numerical model for the calculation of the indoor aerosol number concentrations, using the previously calculated ventilation rate, the outdoor measured number concentrations and the particle loss rates as input values. The model results for the indoors’ concentrations were found to be compared well with the experimentally measured values.     

Personal exposure measurement of students to various microenvironments inside and outside the college campus

This study characterizes the exposure of a typical Indian Institute of Technology Kanpur student to particulate matter and gaseous co-pollutants like carbon monoxide, volatile organic compounds, and nitrogen dioxide in various microenvironments, within and outside the college campus. Chemical analysis of filter, used for the particulate matter measurement, was also carried out to determine the concentration of various elements such as Ca, Cd, Cr, Cu, Fe, Mg, Pb, Zn, and anions like F^?, Cl^?, NO₃ ^?, and SO₄ ^2?. Furthermore, time activity diary along with temperature data was maintained for the precise evaluation and analysis of results for various microenvironments. The results showed PM₁₀ and PM_2.5 concentrations to be higher at some outdoor microenvironments, particularly near the Ganga riverbank. From the chemical analysis, concentrations of chloride and fluoride were found higher in indoor microenvironments as compared to outdoors. Also, nitrate concentrations were quite higher within the laboratory premises. Concentrations of Ca, Fe, and Mg were significant outdoors, whereas Na, Ca, Fe, and K were prominent indoors. The study highlights the real-time personal exposure of a student cohort to various toxic pollutants typically found within their breathing levels and their potential sources both indoors and outdoors.     

Systematic Biases in Measurement of Urban Nitrogen Dioxide using Passive Diffusion Samplers

Measurement of nitrogen dioxide using passivediffusion tube over 22 months in Cambridge, U.K. areanalysed as a function of sampler exposure time, andcompared with NO₂ concentrations obtained from aco-located chemiluminescence analyser. The averageratios of passive sampler to analyser NO₂ at acity centre site (mean NO₂ concentration 22 ppb)are 1.27 (n = 22), 1.16 (n = 34) and 1.11 (n = 7) forexposures of 1, 2 and 4-weeks, respectively. Modellingthe generation of extra NO₂ arising from chemicalreaction between co-diffusing NO and O₃ in thetube gave a ratio (modelled/measured) of 1.31 for1-week exposures. Such overestimation is greatest whenNO₂ constitutes, on average, about half of totalNO_x (= NO + NO₂) at the monitoring locality.Although 4-week exposures gave concentrations whichwere not significantly different from analyserNO₂, there was no correlation between thedatasets. At both the city-centre site and anothersemi-rural site (mean NO₂ concentration 11 ppb)the average of the aggregate of four consecutive1-week sampler exposures or of two consecutive 2-weeksampler exposures was systematically greater than fora single 4-week exposure.The results indicate two independent and opposingsystematic biases in measurement of NO₂ bypassive diffusion sampler: an exposure-timeindependent chemical overestimation with magnitudedetermined by local relative concentrations of NO andO₃ to NO₂, and an exposure-time dependentreduction in sampling efficiency. The impact of theseand other potential sources of systematic bias on theapplication of passive diffusion tubes for assessingambient concentrations of NO₂ in short (1-week)or long (4-week) exposures are discussed in detail.     

An Analysis of Secondary Pollutants in Buenos Aires City

Air pollutant concentrations from a monitoring campaign in Buenos Aires City, Argentina, are used to investigate the relationships between ambient levels of ozone (O₃), nitric oxide (NO) and nitrogen dioxide (NO₂) as a function of NO _x (=NO + NO₂). This campaign undertaken by the electricity sector was aimed at elucidating the apportionment of thermal power plants to air quality deterioration. Concentrations of carbon monoxide (CO) and sulphur dioxide (SO₂) were also registered. Photo stationary state (PSS) of the NO, NO₂, O₃ and peroxy radicals species has been analysed. The ‘oxidant’ level concept has been introduced, OX (=O₃ + NO₂), which varies with the level of NO _x . It is shown that this level is made up of NO _x -independent and NO _x -dependent contributions. The former is a regional contribution that equates the background O₃ level, whereas the latter is a local contribution that correlates with the level of primary pollution. Furthermore, the anticorrelation between NO₂ and O₃ levels, which is a characteristic of the atmospheric photo stationary cycle has been verified.The analysis of the concentration of the primary pollutants CO and NO strongly suggests that the vehicle traffic is the principal source of them. Levels of continuous measurements of SO₂ for Buenos Aires City are reported in this work as a complement of previously published results.     

Indoor NO2 pollution and personal exposure to NO2 in two areas with different outdoor NO2 pollution

Indoor NO₂ concentrations were measured in the kitchen, the living room and bedroom of 612 houses in two different areas in the Netherlands. In a group of housewives living in these homes, personal exposure to NO₂ was measured. NO₂ concentrations indoors were dependent on the presence or absence of (un)vented gas appliances. Personal NO₂ exposure was only different between the two areas in the group with the lowest indoor concentrations. In this study, it was determined that gas appliances inside the house are the most important factor with respect to NO₂ exposure and that outside NO₂ concentration played a secondary role, except in situations where gas appliances were absent.     

环境空气质量新标准对珠三角区域站空气质量评价的影响

利用粤港珠三角区域空气质量监控网中天湖、金果湾与万顷沙3个区域站2010年全年SO₂、NO₂、PM₁₀、O₃、PM_2.5与CO自动监测的数据,分析了实施环境空气质量新标准(GB 3095—2012)对这3个子站空气质量评价的影响。研究发现,若采用新标准,万顷沙的NO₂、PM₁₀和PM_2.5年均浓度将不同程度超标。这3个子站空气质量达标率下降7~28个百分点,空气污染指数从91%~99%下降至63%~91%;O₃的引入是导致空气质量达标率下降的最主要的原因;O₃将取代PM₁₀成为最主要的首要污染物,出现频率大于50%,且O₃(8 h)平均浓度的影响大于O₃ (1 h)浓度的影响。PM_2.5的纳入也是导致空气质量达标率下降的重要因素,其超标率为3%(金果湾)~16%(万顷沙)。NO₂标准的收严未对天湖与金果湾空气质量评价造成影响,但导致万顷沙NO₂的超标率从2%上升至10%,且NO₂作为首要污染物的比例达24%。     

A Multivariate Time Series Approach to Study the Interdependence among O3, NO x , and VOCs in Ambient Urban Atmosphere

A multivariate time series approach vector autoregression (VAR) along with impulse response function and variance decomposition technique has been employed to look into the interrelationship among O₃, NO, NO₂, and volatile organic compounds (VOCs, namely, benzene, ethylbenzene, toluene, and xylene in the present study) using 3 months long continuous time series data of 1 h average concentration of these pollutants at one of the traffic sites in Delhi, India. It is found that the VAR of order 2 (i.e., past two lagged values of 1 h interval) is sufficient to represent the observed time series at the station studied. The impulse response function and variance decomposition analysis indicate that O₃ concentration shows an immediate rise and persists for a longer duration (typically 8–10 h) once the impulse of NO₂, benzene, ethylbenzene, or xylene is given in the ambient environment. However, in case of toluene, the reverse effect has been observed. Since O₃ forms in the troposphere due to photolysis of NO₂, it is not surprising that its impulse triggers O₃ formation in the ambient environment. However, in case of VOCs, this has been attributed to their tendency to show higher inclination toward intermediary reactions leading to the formation of O₃ rather than their (VOCs) reaction with O₃. Among VOCs, only toluene has been observed to show higher inclination toward its reaction with O₃. Apart from this, variance decomposition technique also reveals that the relation of NO with NO₂ is more important than the relation of NO with O₃ creating a conducive atmosphere for O₃ formation in the present scenario. Thus, the multivariate time series approach provides significant insight about the role played by the dominant individual VOCs and NO _x in influencing the O₃ concentration in ambient urban atmosphere whereas a photochemical modeling approach gives an overall view of NO _x and VOCs behavior with respect to O₃ by using the O₃ isopleth technique.     

Extreme Nitrogen Oxide and Ozone Concentrations in Athens Atmosphere in Relation to Meteorological Conditions

In the present study, we investigate the variation of NO _x (NO + NO₂) and O₃ concentrations and the relation between the extreme events (episodes) of NO _x and O₃ concentrations and the relevant meteorological conditions in the urban atmosphere of the Athens basin. Hourly data of NO, NO₂ and O₃ concentrations from 10 representative monitoring sites located in the Athens basin were used, covering the 10-year time period from 1994 to 2003. The results of our analysis show that the concentrations of air pollutants differ significantly from one monitoring site to another, due to the location and proximity of each station to the emission sources. For each site, there are also significant differences in NO _x and O₃ concentrations from day to day, as well as from month to month and/or from season to season. The annual and seasonal variations show higher NO values in winter and lower in summer. On the contrary, NO₂ and O₃ values are higher in summer (photochemical production of O₃) and lower in winter. These differences are attributed, to a large extent, to the prevailing synoptic and meteorological conditions, the most important between them being the wind direction and speed as well as the atmospheric pressure. Our analysis of the identified 179 extreme NO _x air pollution events shows that most of them took place under anticyclonic conditions, associated with calm or weak winds (speed <2.5 ms⁻¹) of mostly southern to southwestern directions, as well as with low air temperatures and intense stable surface atmospheric conditions. There exists a significant decreasing tendency in NO _x air pollution episodic events over the 10-year study period, resulting in very few to none events in the period from 2000 to 2003. As far as it concerns the extreme O₃ concentrations, 34 air pollution events were identified, occurring under high air temperatures, variable weak winds and intense solar irradiation. The trends of O₃ concentrations are stronger in suburban sites than in urban ones.     

Growth impact of O3, NO2 and/or SO2 on pinus taeda

Seedlings of two full-sib families of loblolly pine expressing different degrees of sensitivity to O₃ were exposed to 0.05 ppm O₃, 0.10 ppm NO₂, and/or 0.14 ppm SO₂ for 6 hr/day for 28 consecutive days. The treatments were O₃, NO₂, SO₂ (each used alone), O₃+SO₂, O₃+NO₂, and O₃+NO₂+SO₂. Significant growth suppressions were noted with the relatively sensitive family in all but the the NO₂ alone treatments. The O₃+SO₂ treatment had a more significant effect than O₃ alone, but adding NO₂ had an inconsistent effect. Significant growth suppressions were noted for the relatively non-sensitive family only in the O₃+SO₂ and O₃+SO₂+NO₂ combination treatments. Adding NO₂ to O₃+SO₂ had a slightly stimulatory effect. The relatively sensitive pine family suffered a 30% height growth suppression versus a 14% height growth suppression for the relatively insensitive family when exposed to the 3 pollutant combination. Symptoms were noted on less than 4% of the foliage in the most severe treatments. The pollutant concentrations used in this study were below the National Ambient Air Quality Standards (NAAQS) for each pollutant.     

Assessment of indoor and outdoor particulate air pollution at an urban background site in Iran

The relationship between indoor and outdoor particulate air pollution was investigated at an urban background site on the Payambar Azam Campus of Mazandaran University of Medical Sciences in Sari, Northern Iran. The concentration of particulate matter sized with a diameter less than 1 μm (PM_1.0), 2.5 μm (PM_2.5), and 10 μm (PM₁₀) was evaluated at 5 outdoor and 12 indoor locations. Indoor sites included classrooms, corridors, and office sites in four university buildings. Outdoor PM concentrations were characterized at five locations around the university campus. Indoor and outdoor PM measurements (1-min resolution) were conducted in parallel during weekday mornings and afternoons. No difference found between indoor PM₁₀ (50.1 ± 32.1 μg/m³) and outdoor PM₁₀ concentrations (46.5 ± 26.0 μg/m³), indoor PM_2.5 (22.6 ± 17.4 μg/m³) and outdoor PM_2.5 concentration (22.2 ± 15.4 μg/m³), or indoor PM_1.0 (14.5 ± 13.4 μg/m³) and outdoor mean PM_1.0 concentrations (14.2 ± 12.3 μg/m³). Despite these similar concentrations, no correlations were found between outdoor and indoor PM levels. The present findings are not only of importance for the potential health effects of particulate air pollution on people who spend their daytime over a period of several hours in closed and confined spaces located at a university campus but also can inform regulatory about the improvement of indoor air quality, especially in developing countries.     

Monitoring of Criteria Air Pollutants in Bursa, Turkey

The concentrations of criteria air pollutants such as CO, NO_x (NO + NO₂), SO₂ and PM were measured in the period of May 2001 and April 2003 in the city of Bursa, Turkey. The average concentrations for this period were 1115±1600 μg/m³, 29±50 μg/m³, 51±24 μg/m³, 79±65 μg/m³, 40±35 μg/m³, 98±220 μg/m³, for CO, NO, NO₂, NO_x, SO₂ and PM, respectively. Temporal changes in concentrations were analyzed using meteorological factors. Correlations among pollutant concentrations and meteorological parameters showed weak relations nearly in all data. Lower concentrations were observed in the summer months while higher concentrations were measured in the winter months. The increase in winter concentrations was probably due to residential heating. Pollutants were associated with each other in order to have information about their origin. NO_x/SO₂ ratio was also examined to bring out the source origin contributing on air pollution (i.e., traffic or stationary).     

Indoor and outdoor PM mass and number concentrations at schools in the Athens area

Simultaneous indoor and outdoor PM₁₀ and PM_2.5 concentration measurements were conducted in seven primary schools in the Athens area. Both gravimetric samplers and continuous monitors were used. Filters were subsequently analyzed for anion species. Moreover ultrafine particles number concentration was monitored continuously indoors and outdoors. Mean 8-hr PM₁₀ concentration was measured equal to 229 ± 182 μg/m³ indoors and 166 ± 133 μg/m³ outdoors. The respective PM_2.5 concentrations were 82 ± 56 μg/m³ indoors and 56 ± 26 μg/m³ outdoors. Ultrafine particles 8-h mean number concentration was measured equal to 24,000 ± 17,900 particles/cm³ indoors and 32,000 ± 14,200 particles/cm³ outdoors. PM₁₀ outdoor concentrations exhibited a greater spatial variability than the corresponding PM_2.5 ones. I/O ratios were close or above 1.00 for PM₁₀ and PM_2.5 and smaller than 1.00 for ultrafine particles. Very high I/O ratios were observed when intense activities took place. The initial results of the chemical analysis showed that accounts for the 6.6 ± 3.5% of the PM₁₀ and for the 3.1 ± 1.4%.The corresponding results for PM_2.5 are 12.0 ± 7.7% for and 3.1 ± 1.9% for . PM_2.5 indoor concentrations were highly correlated with outdoor ones and the regression line had the largest slope and a very low intercept, indicative of no indoor sources of fine particulate . The results of the statistical analysis of indoor and outdoor concentration data support the use of as a proper surrogate for indoor PM of outdoor origin.     

Study on concentration of ambient NH 3 and interactions with some other ambient trace gases

We present diurnal variation of ambient ammonia (NH₃) in relation with other trace gases (O₃, CO, NO, NO₂, and SO₂) and meteorological parameters at an urban site of Delhi during winter period. For the first time, ambient ammonia (NH₃) was monitored very precisely and continuously using ammonia analyzer, which operates on chemiluminescence method. NH₃ estimation efficiency of the chemiluminescence method (>90%) is much higher than the conventional chemical trapping method (reproducibility 4.5%). Ambient NH₃ concentration reaches its maxima (46.17 ppb) at night and minimum during midday. Result reveals that the ambient ammonia (NH₃) concentration is positively correlated with ambient NO (r ²?=?0.79) and NO₂ (r ²?=?0.91) mixing ratio and negatively correlated with ambient temperature (r ²?=???0.32). Wind direction and wind speed indicates that the nearby (~500 m NW) agricultural fields may be major source of ambient NH₃ at the observational site.     

A Wavelet-based Neural Network Model to Predict Ambient Air Pollutants’ Concentration

The present paper proposes a wavelet based recurrent neural network model to forecast one step ahead hourly, daily mean and daily maximum concentrations of ambient CO, NO₂, NO, O₃, SO₂ and PM_2.5 — the most prevalent air pollutants in urban atmosphere. The time series of each air pollutant has been decomposed into different time-scale components using maximum overlap wavelet transform (MODWT). These time-scale components were made to pass through Elman network. The number of nodes in the network was decided on the basis of the strength (power) of the corresponding input signals. The wavelet network model was then used to obtain one-step ahead forecasts for a period extending from January 2009 to June 2010. The model results for out of sample forecast are reasonably good in terms of model performance parameters such as mean absolute error (MAE), mean absolute percentage error (MAPE), root mean square error (RMSE), normalized mean absolute error (NMSE), index of agreement (IOA) and standard average error (SAE). The MAPE values for daily maximum concentrations of CO, NO₂, NO, O₃, SO₂ and PM2.5 were found to be 9.5%, 17.37%, 21.20%, 13.79%, 17.77% and 11.94%, respectively, at ITO, Delhi, India. Bearing in mind that the forecasts are for daily maximum concentrations tested over a long validation period, the forecast performance of the model may be considered as reasonably good. The model results demonstrate that a judicious selection of wavelet network design may be employed successfully for air quality forecasting.     

珠三角典型城市COVID-19疫情封闭期间臭氧污染的放大效应研究

珠三角地区臭氧(O₃)已经逐步取代颗粒物成为主要大气污染物。对新型冠状病毒肺炎(COVID-19)疫情封闭期间珠三角城市背景污染效应(特别是对O₃的放大效应)进行了量化研究,发现PM_2.5和NO₂质量浓度均为工作日高于节假日,非疫情期高于疫情期。O₃质量浓度节假日高于工作日,其中疫情期节假日浓度最高。减排会增加低温高湿背景下O₃质量浓度,但会降低其极大值,并导致 O₃随温度和相对湿度的变化梯度减弱。疫情封闭期间异地输送对于局地O₃质量浓度的变化贡献突出。叠加疫情封闭影响的春节假期O₃质量浓度比节前工作日增加20.4%~41.7%,与一般年份特征相反,而NO₂降低65.3%~75.6%,降低程度强于一般年份。疫情封闭期春节期间O₃质量浓度比一般年份上升14.0%~25.9%,而NO₂质量浓度降低37.0%~54.5%。低湿晴好的天气为光化学反应提供有利条件,并且疫情封闭扩大了假期人为源减排规模,导致NO_x质量浓度进一步下降,使其对O₃的滴定效应减弱,同时静稳天气有利于O₃浓度的累积,导致局地O₃污染被逐步放大。     

Effect of particulate matter, atmospheric gases, temperature, and humidity on respiratory and circulatory diseases’ trends in Lisbon, Portugal

This study addresses the significant effects of both well-known contaminants (particles, gases) and less-studied variables (temperature, humidity) on serious, if relatively common, respiratory and circulatory diseases. The area of study is Lisbon, Portugal, and time series of health outcome (daily admissions in 12 hospitals) and environmental data (daily averages of air temperature, relative humidity, PM₁₀, SO₂, NO, NO₂, CO, and O₃) have been gathered for 1999–2004 to ascertain (1) whether concentrations of air pollutants and levels of temperature and humidity do interfere on human health, as gauged by hospital admissions due to respiratory and circulatory ailments; and (2) whether there is an effect of population age in such admissions. In general terms, statistically significant (p?<?0.001) correlations were found between hospital admissions and temperature, humidity, PM₁₀, and all gaseous pollutants except CO and NO. Age appears to influence respiratory conditions in association with temperature, whereas, for circulatory conditions, such an influence likely involves temperature as well as the gaseous pollutants NO₂ and SO₂.     

Nitrogen Dioxide in the Workplace Environment

Concentrations of nitrogen dioxide were measured in shops and car parks over a 19 week period during the winter. For the shops indoor:outdoor ratios varied from 0.34 to 0.54 with an average value of 0.44. NO2 levels ranged from 13 to 38 µg m-3. With little or no contribution from indoor sources, ambient concentrations are the primary factor in determining indoor levels. Concentrations of NO2 in car parks were similar to those measured at the kerb side. Concentrations in the payment booths were higher than those in shops and ranged from 42 to 60 µg m-3. Despite ventilation systems in the payment booths ratios of booth:car park NO2 varied from 0.65 to 0.86.     

Case studies on summertime measurements of O3, NO2, and SO2 with a DOAS system in an urban semi-industrial region in Athens, Greece

The objective of this study is to analyze the concentrations of SO₂, NO₂, and O₃ measured by a Differential Optical Absorption Spectroscopy (DOAS) system that was operating at the campus of Technological Education Institute of Piraeus during 2008 and 2009 warm periods (July to September) in relation to the prevailing meteorological conditions. The DOAS system was operating in a particularly polluted area of the West part of Attica basin on a continuous basis, measuring the concentration levels of the main pollutants (O₃, NO₂, and SO₂) as well as aromatic hydrocarbon substances (benzene, toluene, and xylene). According to the analysis, the SO₂ concentration levels at this measuring site are rather high and this may be attributed to the characteristics of this measuring site. Proximity of roadways and local circulation are just some of the factors that can affect the concentration levels of monitoring of pollutant concentrations such as NO₂ and surface ozone. The results provide evidence for the occurrence of an atmospheric phenomenon that produces higher ozone concentrations during weekends despite lower concentrations of ozone precursors. This phenomenon is known as the weekend effect.     

Application of the UAM-V and Use of Indicator Species to Assess Control Strategies for Ozone Reduction in the Lower Fraser Valley of British Columbia

Modelled and measured indicator species ratios of O₃/NOz, O₃/NOy, H₂O₂/HNO₃, HCNO/NOy for the Lower Fraser Valley were compared with VOC-NO_x-O₃ sensitivity threshold values reported in previous studies. Modelled region - specific indicator ratio thresholds derived from 50% NOx and 50% VOC reduction scenarios are provided. They show strongest agreement with the H₂O₂/HNO₃ ratio values found elsewhere. A clear transition region for the LFV from VOC to NOx sensitivity could not be identified, but there is evidence that O₃ concentrations in the western valley, dominated by metropolitan Vancouver, are VOC sensitive, and the more rural eastern valley O₃ concentrations exhibit greater NO_x sensitivity. The UAM-V Process Analysis utility was used to identify physical and chemical mechanisms which contributed to O₃ formation and destruction and indicate the key importance of entrainment from elevated layers generated by the highly complex meteorological conditions in determining near surface O₃ concentrations.