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.     

Relationship of indoor and outdoor air pollutants in a naturally ventilated historical building envelope

Concentrations of NO₂, O₃, SO₂, acetic and formic acids, HNO₃ and NH₃ were measured inside and outside a historical building, the Baroque Library Hall (BLH) in the National Library in Prague (Czech Republic). The naturally ventilated system of the building, the restriction of personnel access, reduced groups of visitors and absence of activities which could influence indoor pollutant concentrations are characteristics that make the Baroque Library Hall a suitable location to study the influence of outdoor environment on the indoor air quality. The relationship between indoor and outdoor (I/O) concentration was investigated to assess the infiltration of outdoor generated pollutants. Outdoor and indoor pollution sources were determined and, infiltration of ammonium nitrate and a shift of the equilibrium to the gas phase were the reason for the high concentration of ammonia measured inside the BLH. A significant seasonal variation was observed and interpreted as a consequence of different infiltration regime associated with indoor–outdoor temperature differences, which in addition drives dilution processes of indoor generated pollutants. Based on the indoor air quality assessment performed in the BLH with regard to human and material exposure, there is reason for concern about material preservation and in particular paper at the BLH.     

Real-time measurements of PM2.5 and ozone to assess the effectiveness of residential indoor air filtration in Shanghai homes

Portable air cleaners are increasingly used in polluted areas in an attempt to reduce human exposure; however, there has been limited work characterizing their effectiveness at reducing exposure. With this in mind, we recruited forty-three children with asthma from suburban Shanghai and deployed air cleaners (with HEPA and activated carbon filters) in their bedrooms. During both 2-week filtration and non-filtration periods, low-cost PM_2.5 and O₃ air monitors were used to measure pollutants indoors, outdoors, and for personal exposure. Indoor PM_2.5 concentrations were reduced substantially with the use of air cleaners, from 34 ± 17 to 10 ± 8 µg/m³, with roughly 80% of indoor PM_2.5 estimated to come from outdoor sources. Personal exposure to PM_2.5 was reduced from 40 ± 17 to 25 ± 14 µg/m³. The more modest reductions in personal exposure and high contribution of outdoor PM_2.5 to indoor concentrations highlight the need to reduce outdoor PM_2.5 and/or to clean indoor air in multiple locations. Indoor O₃ concentrations were generally low (mean = 8±4 ppb), and no significant difference was seen by filtration status. The concentrations of pollutants and the air cleaner effectiveness were highly variable over time and across homes, highlighting the usefulness of real-time air monitors for understanding individual exposure reduction strategies.     

Particulate reactive oxygen species on total suspended particles – measurements in residences in Austin,Texas

The biologically relevant characteristics of particulate matter (PM) in homes are important to assessing human health. The concentration of particulate reactive oxygen species (ROS) was assessed in eight homes and was found to be lower inside (mean ± s.e. = 1.59 ± 0.33 nmol/m³) than outside (2.35 ± 0.57 nmol/m³). Indoor particulate ROS concentrations were substantial and a major fraction of indoor particulate ROS existed on PM_2.5 (58 ± 10%), which is important from a health perspective as PM_2.5 can carry ROS deep into the lungs. No obvious relationships were evident between selected building characteristics and indoor particulate ROS concentrations, but this observation would need to be verified by larger, controlled studies. Controlled experiments conducted at a test house suggest that indoor ozone and terpene concentrations substantially influence indoor particulate ROS concentrations when outdoor ozone concentrations are low, but have a weaker influence on indoor particulate ROS concentrations when outdoor ozone concentrations are high. The combination of substantial indoor concentrations and the time spent indoors suggest that further work is warranted to assess the key parameters that drive indoor particulate ROS concentrations.     

Particulate matter and gaseous pollutants in residences in Antwerp, Belgium

This comprehensive study, a first in Flanders, Belgium, aimed at characterizing the residential indoor air quality of subgroups that took part in the European Community Respiratory Health Survey (ECRHS I—1991 and ECHRS II—1996) questionnaire-based asthma and related illnesses studies. This pilot study aimed at the evaluation of particulate matter and various inorganic gaseous compounds in residences in Antwerp. In addition personal exposure to the gaseous compounds of one individual per residence was assessed. The main objective was to obtain some base-line pollutant levels and compare these with studies performed in other cities, to estimate the indoor air quality in residences in Antwerp. Correlations between the various pollutant levels, indoor:outdoor ratios and the micro-environments of each residence were investigated. This paper presents results on indoor and ambient PM₁, PM_2.5 and PM₁₀ mass concentrations, its elemental composition in terms of K, Ca, Ti, V, Cr, Mn, Fe, Ni, Cu, Zn, Br, Pb, Al, Si, S and Cl and the water-soluble ionic concentrations in terms of SO₄²⁻, NO₃²⁻, Cl⁻, NH₄⁺ K⁺, Ca²⁺. In addition, indoor, ambient and personal exposure levels of the gases NO₂, SO₂, and O₃ were determined. Elevated indoor:outdoor ratios were found for NO₂ in residences containing gas stoves. In smoker's houses increased PM concentrations of 58 and 43% were found for the fine and coarse fractions respectively. Contrary to the fact that all I/O ratios of the registered elements in each individual house were significantly correlated to each other, no correlation could be established between the I/O ratios of the different houses, thus indicating a unique micro-environment for each residence. Linear relationships between the particulate matter elemental composition, SO₂ and O₃ levels indoors and outdoors could be established. No linear relationships between indoor and outdoor NO₂ and particulate mass concentrations were found.     

Household and behavioral determinants of indoor PM2.5 in a rural solid fuel burning Native American community

Indoor and outdoor concentrations of PM_2.5 were measured for 24 h during heating and non-heating seasons in a rural solid fuel burning Native American community. Household building characteristics were collected during the initial home sampling visit using technician walkthrough questionnaires, and behavioral factors were collected through questionnaires by interviewers. To identify seasonal behavioral factors and household characteristics associated with indoor PM_2.5, data were analyzed separately by heating and non-heating seasons using multivariable regression. Concentrations of PM_2.5 were significantly higher during the heating season (indoor: 36.2 μg/m³; outdoor: 22.1 μg/m³) compared with the non-heating season (indoor: 14.6 μg/m³; outdoor: 9.3 μg/m³). Heating season indoor PM_2.5 was strongly associated with heating fuel type, housing type, indoor pests, use of a climate control unit, number of interior doors, and indoor relative humidity. During the non-heating season, different behavioral and household characteristics were associated with indoor PM_2.5 concentrations (indoor smoking and/or burning incense, opening doors and windows, area of surrounding environment, building size and height, and outdoor PM_2.5). Homes heated with coal and/or wood, or a combination of coal and/or wood with electricity and/or natural gas had elevated indoor PM_2.5 concentrations that exceeded both the EPA ambient standard (35 μg/m³) and the WHO guideline (25 μg/m³).     

Airborne endotoxin concentrations in indoor and outdoor particulate matter and their predictors in an urban city

Endotoxins are an important biological component of particulate matter and have been associated with adverse effects on human health. There have been some recent studies on airborne endotoxin concentrations. We collected fine (PM_2.5) and coarse (PM_10‐2.5) particulate matter twice on weekdays and weekends each for 48 hour, inside and outside 55 homes in an urban city in Japan. Endotoxin concentrations in both fractions were measured using the kinetic Limulus Amebocyte Lysate assay. The relationships between endotoxin concentrations and household characteristics were evaluated for each fraction. Both indoor and outdoor endotoxin concentrations were higher in PM_2.5 than in PM_10‐2.5. In both PM_2.5 and PM_10‐2.5, indoor endotoxin concentrations were higher than outdoor concentrations, and the indoor endotoxin concentrations significantly correlated with outdoor concentrations in each fraction (R²=0.458 and 0.198, respectively). Indoor endotoxin concentrations in PM_2.5 were significantly higher in homes with tatami or carpet flooring and in homes with pets, and lower in homes that used air purifiers. Indoor endotoxin concentrations in PM_10‐2.5 were significantly higher in homes with two or more children and homes with tatami or carpet flooring. These results showed that the indoor endotoxin concentrations were associated with the household characteristics in addition to outdoor endotoxin concentrations.     

HVAC air-quality model and its use to test a PM2.5 control strategy

This paper presents a MATLAB^® Simulink air-quality model of a commercial building with a heating, ventilation, and air conditioning (HVAC) system in Fairbanks, Alaska. Outdoor and indoor real-time fine particulate matter (PM_2.5) levels were measured at this building during a summer wild-fire smoke episode and then during a winter period. The correlation coefficient between the model-predicted and the measured indoor concentrations was 0.99 for the summer and 0.98 for the winter, justifying the usability of the model for further studies. An HVAC control algorithm was developed that reduces the indoor PM_2.5 levels. The algorithm was tested using the HVAC Simulink model and the outdoor PM_2.5 data from the summer smoke episode. The average indoor PM_2.5 level with this control algorithm was 65% lower than with the regular control. Thanks to the PM_2.5 control strategy being automatically engaged only during episodes, it was shown to have the potential of significantly reducing the indoor PM_2.5 levels without significantly compromising the purpose of the original control strategy.     

Indoor and outdoor PM2.5 and PM10 concentrations in the air during a dust storm

Asian dust storms (ADS) originating from the arid deserts of Mongolia and China are a well-known springtime meteorological phenomenon throughout East Asia. The ventilation systems in office utilize air from outside and therefore it is necessary to understand how these dust storms affect the concentrations of PM_2.5 and PM₁₀ in both the indoor and outdoor air. We measured dust storm pollution particles in an office building using a direct-reading instrument (PC-2 Quartz Crystal Microbalance, QCM) that measured particle size and concentration every 10 min for 1 h, three times a day. A three-fold increase in the concentrations of PM_2.5 and PM₁₀ in the indoor and outdoor air was recorded during the dust storms. After adjusting for other covariates, autoregression models indicated that PM_2.5 and PM₁₀ in the indoor air increased significantly (21.7 μg/m³ and 23.0 μg/m³ respectively) during dust storms. The ventilation systems in high-rise buildings utilize air from outside and therefore the indoor concentrations of fine and coarse particles in the air inside the buildings are significantly affected by outside air pollutants, especially during dust storms.     

Variation in indoor particle number and PM2.5 concentrations in a radio station surrounded by busy roads before and after an upgrade of the HVAC system

Indoor particle number and PM_2.5 concentrations were investigated in a radio station surrounded by busy roads. Two extensive field measurement campaigns were conducted to determine the critical parameters affecting indoor air quality. The results indicated that indoor particle number and PM_2.5 concentrations were governed by outdoor air, and were significantly affected by the location of air intake and design of HVAC system. Prior to the upgrade of the HVAC system and relocation of the air intake, the indoor median particle number concentration was 7.4×10³ particles/cm³ and the median PM_2.5 concentration was 7 μg/m³. After the relocation of air intake and the redesign of the HVAC system, the indoor particle number concentration was between 2.3×10³ and 3.4×10³ particles/cm³, with a median value of 2.7×10³ particles/cm³, and the indoor PM_2.5 concentration was in the range of 3–5 μg/m³, with a median value of 4 μg/m³. By relocating the air intake of the HVAC, the outdoor particle number and PM_2.5 concentrations near the air intake were reduced by 35% and 55%, respectively. In addition, with the relocation of air intake and the redesign of the HVAC system, the particle number penetration rate was reduced from 42% to 14%, and the overall filtration efficiency of the HVAC system (relocation of air intake, pre-filter, AHU and particle losses in the air duct) increased from 58% to 86%. For PM_2.5, the penetration rate after the upgrade was approximately 18% and the overall filtration efficiency was 82%. This study demonstrates that by using a comprehensive approach, including the assessment of outdoor conditions and characterisation of ventilation and filtration parameters, satisfactory indoor air quality can be achieved, even for those indoor environments facing challenging outdoor air conditions.     

Indoor Air Quality Investigations at Five Classrooms

Abstract Five classrooms, air-conditioned or naturally ventilated, at five different schools were chosen for comparison of indoor and outdoor air quality. Temperature, relative humidity (RH), carbon dioxide (CO₂), sulphur dioxide (SO₂), nitric oxide (NO), nitrogen dioxide (NO₂), particulate matter with diameter less than 10 mm (PM₁₀), formaldehyde (HCHO), and total bacteria counts were monitored at indoor and outdoor locations simultaneously. Respirable particulate matter was found to be the worst among parameters measured in this study. The indoor and outdoor average PM₁₀ concentrations exceeded the Hong Kong standards, and the maximum indoor PM₁₀ level was even at 472 μ;g/m³. Air cleaners could be used in classrooms to reduce the high PM₁₀ concentration. Indoor CO₂ concentrations often exceeded 1,000 μl/l indicating inadequate ventilation. Lowering the occupancy and increasing breaks between classes could alleviate the high CO₂ concentrations. Though the maximum indoor CO₂ level reached 5,900 μl/l during class at one of the sites, CO₂ concentrations were still at levels that pose no health threats.     

Real‐time transformation of outdoor aerosol components upon transport indoors measured with aerosol mass spectrometry

Outdoor aerosols are transported indoors, where their component concentrations depend on aerosol size, physiochemical properties, indoor sources and losses, and cross‐environment gradients of temperature and relative humidity. We explored these dependencies by measuring real‐time outdoor and indoor non‐refractory, submicron (PM₁) aerosol component mass concentrations in a mixed‐use laboratory space with an Aerodyne mini‐aerosol mass spectrometer (AMS) and black carbon (BC) with an aethalometer. The median indoor/outdoor (I/O) ratios were 0.60 for sulfate, 0.25 for nitrate, 0.52 for ammonium, 0.73 for organics, and 0.61 for BC. Positive matrix factorization (PMF) on organic aerosol data identified hydrocarbon‐like (HOA), cooking (COA), and oxygenated (OOA) factors. By assuming sulfate was nonvolatile, lost only by mechanical processes, and without indoor sources, the transformations of other components i due to partitioning changes or indoor sources were parameterized by normalizing their I/O ratios by sulfate's I/O ratio, that is, (I/O)_i/SO4. Component‐specific behavior was quantified by regressions of (I/O)_i/SO4 to outdoor‐to‐indoor temperature differences. Nitrate and HOA strongly and OOA weakly showed losses with increasing temperatures indoors vs. outdoors, and HOA likely had an indoor source. To our knowledge, this is the first reported deployment of an AMS to analyze real‐time indoor aerosol composition and outdoor‐to‐indoor transformation.     

Chemical characterization of indoor and outdoor fine particulate matter in an occupied apartment in Rome,Italy

The daily concentration and chemical composition of PM_2.5 was determined in indoor and outdoor 24‐h samples simultaneously collected for a total of 5 weeks during a winter and a summer period in an apartment sited in Rome, Italy. The use of a specifically developed very quiet sampler (<35 dB) allowed the execution of the study while the family living in the apartment led its normal life. The indoor concentration of PM_2.5 showed a small seasonal variation, while outdoor values were much higher during the winter study. Outdoor sources were found to contribute significantly to indoor PM concentration especially during the summer, when the apartment was naturally ventilated by opening the windows. During the winter the infiltration of outdoor PM components was lower and mostly regulated by the particle dimensions. Organics displayed In/Out ratios higher than unity during both periods; their indoor production increased significantly during the weekends, where the family stayed mostly at home. PM components were grouped into macrosources (soil, sea, secondary inorganics, traffic, organics). During the summer the main contributions to outdoor PM_2.5 came from soil (30%), secondary inorganics (29%) and organics (22%). Organics dominated both indoor PM_2.5 during the summer (60%) and outdoor and indoor PM_2.5 during the winter (51% and 66%, respectively).     

Particle‐associated polycyclic aromatic hydrocarbons in a representative urban location (indoor‐outdoor) from South Europe: Assessment of potential sources and cancer risk to humans

PM₁₀‐bound polycyclic aromatic hydrocarbons (PAHs) levels were monitored at urban locations (outdoor/indoor) within the city of Madrid between May 2017 and April 2018. Fourteen PAH congeners were measured, potential emission sources were identified as were potential carcinogenic risks. The ΣPAHs averaged 0.577 and 0.186 ng/m³ in outdoor and indoor air, with a high linear correlation per individual mean PAH and month. The largest contributors to the ΣPAHs were the high‐molecular‐weight PAHs. Principal component analysis‐multiple linear regression results showed that emissions from diesel and vehicular processes explained 27% and 23% of the total variance of outdoor and indoor air, while combustion processes accounted for 30% and 25% in ambient and indoor air, respectively. During the cold season, biomass burning plus coal and wood combustion were additional sources of outdoor emissions. The heavy‐, medium‐ and light‐molecular‐weight PAH originating from outdoor sources accounted for 72%, 80%, and ~60% of the indoor levels of the three respective PAH groups. Average BaP concentration was 0.029 and 0.016 ng/m³ in outdoor and indoor air, respectively. Estimated BaPeq concentration averaged 0.072, 0.035, and 0.027 ng/m³ for outdoor, indoor, and indoor‐generated individual PAH concentrations, respectively. The estimated carcinogenic risk falls within the range of acceptable risk targeted by the US‐EPA.     

A chamber study of secondary organic aerosol formation by limonene ozonolysis

Abstract Limonene ozonolysis was examined under conditions relevant to indoor environments in terms of temperatures, air exchange rates, and reagent concentrations. Secondary organic aerosols (SOA) produced and particle‐bound reactive oxygen species (ROS) were studied under situations when the product of the two reagent concentrations was constant, the specific concentration combinations play an important role in determining the total SOA formed. A combination of concentration ratios of ozone/limonene between 1 and 2 produce the maximum SOA concentration. The two enantiomers, R‐(+)‐limonene and S‐(?)‐limonene, were found to have similar SOA yields. The measured ROS concentrations for limonene and ozone concentrations relevant to prevailing indoor concentrations ranged from 5.2 to 14.5 nmol/m³ equivalent of H₂O₂. It was found that particle samples aged for 24 h in freezer lost a discernible fraction of the ROS compared to fresh samples. The residual ROS concentrations were around 83–97% of the values obtained from the analysis of samples immediately after collection. The ROS formed from limonene ozonolysis could be separated into three categories as short‐lived, high reactive, and volatile; semi‐volatile and relatively stable; non‐volatile and low‐reactive species based on ROS measurements under various conditions. Such chemical and physical characterization of the ROS in terms of reactivity and volatility provides useful insights into nature of ROS.

Practical Implications

A better understanding of the formation mechanism of secondary organic aerosol generated from indoor chemistry allows us to evaluate and predict the exposure under such environments. Measurements of particle‐bound ROS shed light on potential adverse health effect associated with exposure to particles.

     

Indoor/outdoor relationships of size-resolved particle concentrations in naturally ventilated school environments

Assessment of indoor air quality in typical classrooms is vital to students’ health and their performance. The present study was designed to monitor indoor and outdoor size-resolved particle concentrations in a naturally ventilated classroom and investigate factors influencing their levels and relationships. The experiments were performed, at normal ventilation condition with doors and windows opened, on the top floor of a public school building near a busy commercial area of Chiang Mai, Thailand. The particle number concentrations were measured using an optical counter with four size intervals between 0.3 and 5.0 μm. The dataset was collected during weekdays and weekends with a 24 h sampling period over November and December 2005. It was observed that the median indoor particle number concentrations during daytime for 0.3–0.5, 0.5–1.0, 1.0–2.5, and 2.5–5.0 μm size intervals were about 1.6×10⁸, 1.7×10⁷, 1.2×10⁶, and 4.1×10⁵ particles/m³, respectively. It was also found that concentrations at weekends were slightly higher those measured on weekdays, and at night, appeared to be higher than daytime. Indoor particles were observed to exhibit similar temporal variation pattern with outdoor particles. Results suggested that a significant contribution to indoor particles was from penetration of outdoor particles, whereas indoor sources generated from occupant activity did not show strong evidence. High outdoor particle loading and high air exchange rate were thought to be predominant causes. Ratios of indoor-to-outdoor (I/O) particle concentrations varied in a relatively narrow range from 0.69 to 0.88 with average values well below 1. The I/O ratios were in the range from 0.74 to 0.88 for submicrometer particles and from 0.69 to 0.80 for supermicrometer particles.     

Assessment of chemical and microbiological parameters of indoor swimming pool atmosphere using multiple comparisons

The aim of this study was to evaluate the air quality of an indoor swimming pool, analyzing diurnal and seasonal variations in microbiological counts and chemical parameters. The results indicated that yeast and bacteria counts, as well as carbon dioxide (CO₂), nitrogen oxides (NO_x) and O₃ concentrations, showed significant diurnal difference. On the other hand, temperature, relative humidity (R.H.), yeast counts and concentrations of CO₂, particles, O₃, toluene, and benzene showed seasonal differences. In addition, the relationship between indoor and outdoor air and the degree of correlation between the different parameters have been calculated, suggesting that CO₂, fine particles and NO_x would have indoor origin due to the human activity and secondary reactions favored by the chemical and environmental conditions of the swimming pool; while O₃, benzene and toluene, would come from outside, mainly. The overall results indicated that indoor air quality (IAQ) in the swimming pool building was deficient by the high levels of CO₂ and microorganisms, low temperatures, and high R.H., because frequently the limits established by the legislation were exceeded. This fact could be due to the poor ventilation and the inadequate operation of heating, ventilation, and air‐conditioning systems.     

Secondary organic aerosol from α‐pinene ozonolysis in dynamic chamber system

Abstract Abstract The formation of secondary organic aerosol (SOA) produced from α‐pinene ozonolysis was examined using a dynamic chamber system that allowed the simulation of ventilated indoor environments. Particle‐bound reactive species (ROS) including peroxides, peroxy radicals and ions that could penetrate into the lungs and deliver oxidative stress to the tissue causing damage were quantitatively determined from filters collected from the chamber. ROS was determined using dichlorofluorescin such that resulting fluorescent intensities were converted to equivalent H₂O₂ concentrations. Measured ROS concentrations at α‐pinene and ozone concentrations relevant to prevailing indoor concentrations ranged from 1.1 to 7.2 nmol/m³ of H₂O₂. Particle density was also determined from scanning mobility particle sizer measurements and mass collected onto filters to obtain volume and mass concentration, respectively. Partitioning theory reveals the fact that with increased SOA mass loading, even for more volatile species, partitioning onto particle phase is favored relative to low SOA mass loadings. Other recent studies have found changes in composition of the SOA depending on the precursor VOC concentrations. This behavior was reflected in these experiments in terms of a change of density. Measured densities ranged from 1.07 to 1.69 g/cm³.     

Wood stove use and other determinants of personal and indoor exposures to particulate air pollution and ozone among elderly persons in a Northern Suburb

A six‐month winter‐spring study was conducted in a suburb of the northern European city of Kuopio, Finland, to identify and quantify factors determining daily personal exposure and home indoor levels of fine particulate matter (PM_2.5, diameter <2.5 µm) and its light absorption coefficient (PM_2.5abs), a proxy for combustion‐derived black carbon. Moreover, determinants of home indoor ozone (O₃) concentration were examined. Local central site outdoor, home indoor, and personal daily levels of pollutants were monitored in this suburb among 37 elderly residents. Outdoor concentrations of the pollutants were significant determinants of their levels in home indoor air and personal exposures. Natural ventilation in the detached and row houses increased personal exposure to PM_2.5, but not to PM_2.5abs, when compared with mechanical ventilation. Only cooking out of the recorded household activities increased indoor PM_2.5. The use of a wood stove room heater or wood‐fired sauna stove was associated with elevated concentrations of personal PM_2.5 and PM_2.5abs, and indoor PM_2.5abs. Candle burning increased daily indoor and personal PM_2.5abs, and it was also a determinant of indoor ozone level. In conclusion, relatively short‐lasting wood and candle burning of a few hours increased residents’ daily exposure to potentially hazardous, combustion‐derived carbonaceous particulate matter.     

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.