Concentration of PM2.5 and PM10 Particulate Matter in Various Indoor Environments: A Literature Review
Abstract
1. Introduction
2. Methodology
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- Indoor PM2.5 and PM10 concentrations;
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- Their impact on building occupants;
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- Measurement methods;
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- Pollutant reduction strategies.
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- Educational buildings;
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- Medical facilities;
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- Sports facilities;
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- Other public buildings: libraries, offices, museums.
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- A desert climate;
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- A mediterranean climate;
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- A temperate and highly industrialised climate;
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- A continental climate.
3. Results
3.1. Particulate Matter PM2.5 and PM10 in Indoor Environments
3.1.1. Air Pollution Concentration and Its Impact on Human Health
3.1.2. Air Pollution Concentration in Residential Buildings
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- Building airtightness: homes with better insulation exhibited lower infiltration coefficients.
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- Type of ventilation and heating systems: dwellings with low filtration efficiency mechanical ventilation systems showed higher indoor-to-outdoor (I/O) ratios for PM2.5 and BC compared to naturally ventilated buildings.
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- Occupant behaviour: prolonged window opening increased indoor BC levels, particularly during outdoor pollution episodes.
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- Proximity to major roads: homes located closer to high-traffic roads generally exhibited higher indoor PM and BC concentrations, indicating an additional contribution from traffic-related emissions.
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- Frequent use of an air fresheners (6–7 days a week) (p = 0.0016);
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- Living near a gas station (<0.5 miles) (p = 0.01);
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- Season—lower PM2.5 in summer than in winter (p = 0.03).
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- Between 1986 and 1995, research focused mainly on PM10;
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- From the mid-1990s, the emphasis shifted to PM2.5 (20–80 µg·m−3) and ultrafine particles (103–105 particles·cm−3);
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- After 2006, the studies also included secondary organic aerosols; typical levels of PM2.5 decreased (10–50 µg·m−3), and UFP stabilised at 103–104 particles·cm−3.
3.1.3. Air Pollution Concentration in Public-Use Buildings
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- SU-1 (Sikornik district—urban area 1);
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- PU-2 (Pszczyńska Street—urban area 2)—kindergarten located 50 m from a street;
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- R-3 (village of Przezchlebie—rural area 3);
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- SR-4 (village of Świętoszowice—rural area 4)—kindergarten located 50 m from the A1 highway.
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- PM2.5 concentrations exceed the standard limit (35 µg·m−3) in all fitness centres, particularly in FL5 and FL4.
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- PM10 concentrations also exceed the allowed level (75 µg·m−3) in most facilities, especially in FL5 (102.6 µg·m−3) and FL4 (96.4 µg·m−3).
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- Hall, summer: PM1 = 29 µg·m−3, PM2.5 = 30 µg·m−3, PM4 = 31 µg·m−3, PM10 = 18 µg·m−3, TSP = 40 µg·m−3;
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- Outdoor area, summer: PM1 = 22 µg·m−3, PM2.5 = 23 µg·m−3, PM4 = 24 µg·m−3, PM10 = 13 µg·m−3, TSP = 27 µg·m−3;
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- Hall, winter: PM1 = 38 µg·m−3, PM2.5 = 39 µg·m−3, PM4 = 40 µg·m−3, PM10 = 33 µg·m−3, TSP = 45 µg·m−3;
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- Outdoor area, winter: PM1 = 56 µg·m−3, PM2.5 = 52 µg·m−3, PM4 = 52 µg·m−3, PM10 = 31 µg·m−3, TSP = 29 µg·m−3.
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- Above the fourth floor, the concentrations decreased by approximately 0.11 µg·m−3 per metre;
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- Indoor PM2.5 concentrations increased slightly with height: on average by +0.02 µg·m−3 per metre, from 5.3 µg·m−3 (1st floor) to 5.8 µg·m−3 (9th floor);
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- Outdoor concentrations varied throughout the day;
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- Indoor concentrations remained relatively stable, except for an increase in the morning on the ninth floor between 9:00 am and 3:00 pm, probably related to office activities.
3.1.4. Concentration of Air Pollution in Historical Buildings
3.1.5. Concentration of Air Pollution in the Indoor Environment—Summary
3.2. Measurement Methodology for Particulate Matter PM2.5 and PM10
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- PCE-PQC 34 Air Quality Monitor (PCE Deutschland GmbH, Meschede, Germany)—The device operates with advanced particle counting technology, enabling measurement of particulate concentrations with diameters of <10 μm (PM10), <5 μm (PM5), <2.5 μm (PM2.5) and <1 μm (PM1), with a flow rate of 2.83 L·min−1 and a detection range of 0.3 to 25 μm. Calibration is carried out according to technical specifications. Precise calculations of the mass of the particle in µg·m−3 are enabled by its high sensitivity and integrated mass concentration mode. To ensure high accuracy, the device uses a long-life laser diode.
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- inBiot (MICA) (inBiot Monitoring S.L., Spain) and Kaiterra devices (Kaiterra, Crans-Montana, Switzerland)—These sensors are commercially available and certified under RESET and WELL standards. They operate using laser scattering technology for particulate measurement and are based on proprietary algorithms. The technical parameters of these devices are presented in Table 10.
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- TSI SidePak AM510—personal dust monitor (PM2.5, PM10).
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- TSI DustTrak II/DRX—portable dust monitor (PM1, PM2.5, PM4, PM10).
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- GrayWolf AdvancedSense Pro—multifunctional IAQ monitor (PM, VOCs, CO2, T, RH).
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- PCE-PQC 34—reference particle counter (PM1, PM2.5, PM4, PM10).
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- PurpleAir—networked optical PM sensor (PM1, PM2.5, PM10).
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- inBiot MICA—IAQ monitor (CO2, PM, VOCs, T, RH).
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- Kaiterra—IAQ monitor (CO2, PM2.5, VOCs, T, RH).
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- Canāree A1—personal IAQ sensor (PM, VOCs, CO2, T, RH).
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- Q-Air—IAQ device (PM, CO2, CH2O, VOCs, T, RH).
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- TSI DustTrak, SidePak, PCE-PQC 34, PurpleAir;
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- DustTrak/SidePak—controlled studies (schools, fitness centres);
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- PurpleAir—epidemiological and population studies.
3.3. Methods for Reducing the Concentration of Particulate Matter PM2.5 and PM10
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- ‘Sham’ period (air purifiers operated but without filters);
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- Period with LE filter (low-efficiency HEPA-type);
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- Period with HE filter (true HEPA, high efficiency).
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- Organic pollutants mainly from domestic activities such as cooking (45%);
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- Resuspension and infiltration of pollutants related to traffic and waste combustion products (14%);
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- Secondary aerosols (13%);
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- Tobacco smoke (7%);
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- Urban dust (2%);
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- Unidentified sources (19%).
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- Introduction of forced ventilation;
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- Restoration of the air exchange system;
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- Cleaning of air conditioning filters;
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- Installation of air diffusers in the ceiling equipped with air filters;
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- Removal of sealed office grilles;
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- Replacement of heavy carpets with better ventilated flooring materials.
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- LL—low outdoor and low indoor levels;
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- HL—high outdoor and low indoor levels;
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- LH—low outdoor and high indoor levels;
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- HH—high levels both outdoors and indoors.
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- The chamber without plants—serving as the control (baseline);
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- The chamber with plants—containing ten plants of a single species.
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- The optimal placement of air purifiers within office spaces;
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- The integration of air purifiers with existing ventilation systems;
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- Adjustment of operating parameters to the specific conditions of office environments (including the number of occupants, the type of furniture, and the characteristics of airflow).
3.4. Effectiveness of PM2.5 and PM10 Reduction Methods in Various Building Use Conditions and Limitations Resulting from Their Use
4. Conclusions
Author Contributions
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Conflicts of Interest
References
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| Category | Indoor PM | Outdoor PM | References |
|---|---|---|---|
| Main emission sources | Cooking, biomass heating, tobacco smoke, cleaning agents, off-gassing of material, resuspension from occupant behaviour | Traffic emissions, industry, combustion, mineral dust, secondary atmospheric aerosols | [13,17,23,29,40,41] |
| Composition characteristics | Higher organic carbon, ultrafine particles (UFP < 0.1 µm), semi-volatile compounds, ozone–VOC reaction products | Higher inorganic ions, secondary sulphates/nitrates, traffic-related metals | [23,29,33,41] |
| Dominant chemical processes | Indoor reactions: ozone + VOC − SOA, emissions from materials, and household chemicals | Atmospheric photochemistry, secondary aerosol formation from VOC precursors | [14,15,45] |
| Toxicological impact | Higher oxidative potential due to reactive organic fraction; UFP penetrate deeper into lungs | Toxicity influenced by metals, sulphates, nitrates; more PM10/mineral particles | [23,29,33,41] |
| Exposure conditions | Long exposure (90% of the time indoors), low ventilation, proximity to sources means a higher personal dose | Shorter exposure; dependent on weather and pollution transport | [3,4,5,6,7,30,40,41] |
| Ventilation and infiltration | Low air exchange rates increase PM accumulation, indoor spikes exceed outdoor levels | PM infiltrates the interior through leakage/ventilation; influenced by AER | [14] |
| Mitigation strategies | HEPA, mechanical ventilation, air purifiers, source control | Emission regulations, industrial filters, low-emission zones, traffic management | [12,21,22,23,24,25,26,46,47,48,49] |
| Scenario | Location | Median PM2.5 (PN0.5–2.5 Proxy) [µg∙m−3] | Change Relative to Background | Black Carbon (BC) | Notes |
|---|---|---|---|---|---|
| No smoke plume (background) | Outdoor | ~6 µg·m−3 | Reference level | Low | Typical urban background in Denver area |
| No smoke plume (background) | Indoor | ~4–5 µg·m−3 | Reference level | Very low | Buildings without strong indoor combustion sources |
| Moderate wildfire smoke | Outdoor | ~12–15 µg·m−3 | ~2–2.5 × increase | Increased | Long-range transported wildfire smoke |
| Moderate wildfire smoke | Indoor | ~8–10 µg·m−3 | ~2 × increase | Increased | Partial infiltration from outdoors |
| High wildfire smoke plume | Outdoor | ~23 µg·m−3 | ~3.8 × increase vs. background | High | Intense regional wildfire episode |
| High wildfire smoke plume | Indoor | ~15–18 µg·m−3 | ~3.6 × increase vs. background | Significantly increased | Strong infiltration of outdoor PM |
| Homes < 200 m from major road | Indoor | Up to ~20 µg·m−3 during plume | Higher than residential background | Elevated | Additional impact of traffic emissions |
| Country | Dominant Household Fuels | Main Indoor Pollution Sources | Building and Ventilation Characteristics | Typical PM2.5 (µg·m−3) | Typical PM10 (µg·m−3) | Key Factors Affecting IAQ |
|---|---|---|---|---|---|---|
| Pakistan | Biomass, wood, coal; LPG in cities | Biomass cooking, tobacco smoke, waste burning, infiltration of traffic emissions | Poor ventilation, lack of exhaust hoods, indoor kitchens, leaky building envelope | 4000–9000 (biomass), 200–500 (urban LPG); up to 1800 with ETS | 5000–12,000 (biomass), 300–600 (urban) | Biomass, dense urban structure, poor ventilation, low awareness |
| India | Biomass, dung cakes, LPG, coal | Biomass cooking, incense burning, ETS, infiltration from road traffic | Rural: single-room homes, low ventilation; Urban: better ventilation but high infiltration | 500–5000 (rural), 150–400 (urban) | 800–7000 (rural), 200–600 (urban) | Biomass, population density, external pollution, lack of hoods |
| Nepal | Wood, biomass, LPG (urban) | Biomass cooking, traditional stoves, waste burning | Rural clay houses with very low ventilation; Urban areas with hoods | 3000–6000 (rural), 100–300 (urban) | 4000–8000 (rural), 200–500 (urban) | High-altitude stagnation, biomass use |
| Bangladesh | Biomass, coal, natural gas | Cooking, ETS, mosquito coils, high humidity and mould | Low ventilation, often no separate kitchen; strong infiltration in cities | 200–3000 (rural), 150–400 (urban) | 400–5000 (rural), 200–600 (urban) | Humidity, high population density, incense and coils |
| Bhutan | Wood, biomass, LPG | Traditional cooking fires, wood heating, incense smoke | Wooden buildings, often single-zone layouts, moderate ventilation | 300–1500 (rural), <100 (urban) | 400–2000 (rural), <150 (urban) | Wood heating, incense, traditional kitchens |
| Sri Lanka | Biomass, LPG | Biomass cooking in rural areas, waste burning, humidity and mould | Better ventilation; many houses use open-window design | 200–1500 (rural), 50–150 (urban) | 300–2000 (rural), 100–300 (urban) | Biomass (rural), humidity, infiltration from traffic |
| Location/Group | PM1 (µg·m−3) | PM2.5 (µg·m−3) | PM10 (µg·m−3) | TSP (µg·m−3) |
|---|---|---|---|---|
| SU-1 (I)—older | 51.21 | 70.59 | 117.57 | 134.43 |
| SU-1 (II)—younger | 25.97 | 41.17 | 68.26 | 73.05 |
| PU-2 (I) | 78.89 | 106.06 | 149.81 | 163.81 |
| PU-2 (II) | 33.70 | 49.06 | 79.92 | 96.78 |
| PR-3 (I) | 83.64 | 102.05 | 135.93 | 147.54 |
| PR-3 (II) | 78.13 | 80.94 | 104.90 | 124.24 |
| SR-4 (I) | 102.11 | 125.69 | 166.12 | 184.24 |
| SR-4 (II) | 49.04 | 67.65 | 81.49 | 91.19 |
| Average—urban area | ~47.4 | ~66.7 | ~103.9 | ~117.0 |
| Average—Rural/rural with traffic influence | ~78.2 | ~94.1 | ~122.1 | ~136.8 |
| Parameter | EPA Standard (Taiwan) | Range of Results in the Fitness Centres Surveyed | Exceedances |
|---|---|---|---|
| CO2 | ≤1000 ppm | 776 ppm | FL5—776 ppm |
| CH2O | ≤0.08 ppm | 0.20–1.36 ppm | All fitness centres |
| VOCs | ≤0,56 ppm | 0.6–1.21 ppm | FL4 |
| PM2.5 | ≤35 µg·m−3 | 30.6–55.3 µg·m−3 | FL5—55.3 µg·m−3; FL4—48.1 µg·m−3; EF—42.3 µg·m−3; |
| PM10 | ≤75 µg·m−3 | 70.8–102.6 µg·m−3 | FL5—102.6 µg·m−3; FL4—96.4 µg·m−3; EF—89.23 µg·m−3; |
| CO | ≤9 ppm | 0–2 ppm | No exceedances |
| O3 | ≤0.06 ppm | 0 ppm | No exceedances |
| Dependence | R (Correlation Coefficient) |
|---|---|
| Temperature—CH2O/CO2/VOCs | 0.3–0.7 (moderate) |
| Humidity—CH2O/CO2/VOCs | 0.3–0.7 (moderate) |
| CH2O—VOCs | >0.7 (strong) |
| CO2—VOCs | >0.7 (strong) |
| CH2O—CO2 | >0.7 (strong) |
| PM2.5/PM10—Temperature | 0.3–0.5 (moderate) |
| O3—other parameters | 0 (no correlation) |
| Group | Heating Season (µg·d−1) | Off Season (µg·d−1) | Heating Season (µg·kg−1·d−1) | Off Season (µg·kg−1·d−1) |
|---|---|---|---|---|
| Students | 337 | 92 | 6.7 | 2 |
| Teachers | 377 | 118 | 5.3 | 1.6 |
| Sportsman | 473 | 145 | 6.6 | 1.8 |
| No. | City | Object | Type of Study | Study Results |
|---|---|---|---|---|
| 1. | China [69] | Potala Palace Museum in Tibet | X-ray fluorescence analysis (XRF) | Studies have shown that the concentration of PM1–10 particulate matter outdoors was lower than indoors. Airborne particles were classified into four categories: soil dust brought in by outdoor tourists, incense ash, human-induced pollution, and ores. |
| 2. | Milan [70] | The refectory of the Church of Santa Maria Delle Grazie, which houses Leonardo da Vinci’s “The Last Supper” | chemical mass balance model | 11.2% of the particles came from gasoline cars, urban soil and wood smoke |
| 3. | Czech Republic [71] | The Baroque Library Hall of the National Library in Prague | chemical mass balance model | Tourists contribute to 35% of indoor particulate matter |
| 4. | China [72] | Museum in the Shanghai CBD | chemical mass balance model | The coarse particles were mainly soot aggregates and minerals, while the fine particles were mainly soot aggregates. Ca, Si, Al, Na, C, O, S, and Mg were enriched in the coarse particles, and S was mainly enriched in the fine particles. |
| 5. | Italy [73] | The Correa Museum in Piazza SAN Marco in Venice | electron probe X-ray microanalysis and scanning electron microscopy with energy-dispersive X-ray measurement (SEM-EDX) | Calcium-rich particles, aluminosilicates, and organic materials were the most dominant particles. Calcium-rich solid particles (from poor wall condition) |
| 6. | Belgium [74] | Royal Art Gallery of Antwerp | chemical mass balance model | In winter, construction activities were the main source of Ca- and Ca-Si-rich particles. Sea salt was also present in the atmosphere. In summer, Ca concentrations were low, while S concentrations were abundant. |
| 7. | China [75] | Museum of the Terracotta Warriors and Horses of Emperor Qin | electron microscopy and energy-dispersive X-ray spectrometry (SEM-EDX) | Most of the airborne particles in the museum consisted of soil dust, sulphur-containing particles, and low-sulphur particles such as soot aggregates and biogenic particles—tourists contribute to indoor particulate matter |
| 8. | Belgium [76] | Plantin-Moretus Museum/Printing Workshop Antwerp | energy-dispersive X-ray fluorescence (EDXRF) and electron probe microanalyzer (EPMA) methods | The results show that in the fine fraction, the proportion of C-rich particles ranged from 35% to 80%, while in the coarse fraction these values ranged from 25% to 45%. |
| Building Type | Organic Compounds (OC, UFP, SVOC, SOA) | Mineral Components (e.g., Si, Al, Ca, Dust) | Secondary Ions (SO42−, NO3−, NH4+) | Trace Metals (e.g., Fe, Zn, Pb, Cu) | Notes | References |
|---|---|---|---|---|---|---|
| Homes/Apartments | high levels of OC, UFP, SVOC, SOA—cooking, smoking, cleaning products | dust resuspension | no detailed data | no data on metals | High organic emissions related to occupant activity. | [4,6,14,30] |
| Schools (general) | high organic fraction and UFP (typical for indoor PM) | mineral dust, resuspension from floors and carpets (schools and sports halls) | no detailed data | no data | Influenced by student activity and outdoor infiltration. | [40,41,45] |
| Green-roof school (PM2.5–PM10) | not specified in the article | mineral fractions of PM (based on the study title: chemical composition and source apportionment) | ions present in study but not detailed in the article | metals analysed but not specified | The article provides the reference only, not the chemical composition. | [16] |
| Offices | dominance of organic compounds—O3 + VOC reactions and emissions from office materials | resuspension (general indoor PM characteristics) | no detailed data | no data | Influenced by office materials and poor ventilation. | [4,14,41] |
| Sports facilities | organic fractions linked to user activity, UFP—typical indoor PM | strong dust resuspension from floors and synthetic sport surfaces | no data | no data | Main mechanism: particle resuspension, not aerosol chemistry. | [3,41] |
| Museums (XRF analyses, PM2.5/PM10) | presence of organic aerosols (from materials and conservation products) | mineral particles (Si, Al, Ca) listed in analytical descriptions | sulphates, nitrates—typical ions identified in XRF/PMF studies | Fe, Pb, Zn, Cu—typical metals identified in museum studies | The most detailed chemical speciation among all building categories. | [65] |
| Device | MICA (inBiot) | Sensedge Mini (Kaiterra) |
|---|---|---|
| Measured parameters | CO2, PM1, PM2.5, PM4, PM10, Formaldehyde, TVOC, Temperature, RH | CO2, PM2.5, PM10, TVOC, Temperature, RH |
| Measurement accuracy PM | ±5 µg·m−3 + ±5% (0–100 µg·m−3); ±10% (100–1000 µg·m−3) | ±3 µg·m−3 (0–30 µg·m−3); ±10% (30–1000 µg·m−3) |
| Measurement technology | laser scattering technology | laser scattering technology |
| Technical certificates | RESET, WELL | RESET, WELL |
| Cost (€) | 500 | 750 |
| No. | Device | Sensor Type | Measured Parameters | Typical Applications | Accuracy/Role in Research | Measurement Range | Calibration Criteria and Methodology (Initial and Ongoing) |
|---|---|---|---|---|---|---|---|
| 1 | TSI SidePak AM510 [62] | Portable dust monitor | PM2.5, PM10 | Personal exposure, sports, schools | High, mobile | 0.001–20 mg·m−3 (1–20,000 µg·m−3) | Factory calibration with Arizona Test Dust; annual field verification against gravimetric reference; requires correction factors depending on aerosol type |
| 2 | TSI DustTrak II/DRX [43] | Laser dust monitor | PM1, PM2.5, PM4, PM10 | Laboratories, epidemiology, fitness | Very high, reference | 0.001–150 mg·m−3 (II), 0.001–400 mg·m−3 (DRX) | Factory-calibrated to ISO 12103-1 A1 dust (Standard Number: ISO 12103-1, Title of Standard: Road vehicles—Test dust for filter evaluation—Part 1: Arizona test dust, Publisher: International Organization for Standardization (ISO), Geneva, Switzerland, 2016); regular co-location with FRM/FEM samplers; aerosol-specific correction factors (per study protocols). |
| 3 | GrayWolf AdvancedSense [80] | IAQ—multi-parameter | PM, VOCs, CO2, T, RH | Comprehensive IAQ research | Very high | up to 100,000 µg·m−3 (depending on the module) | Multi-parameter calibration via certified calibration gases (CO2, VOCs), RH/T chamber calibration; periodic drift correction recommended by manufacturer. |
| 4 | PCE-PQC 34 [81] | Particle counter | PM1, PM2.5, PM4, PM10, number of particles | Scientific research, reference | Very high | 0.3–25 µm (size range, mass dependent mode) | SO-based particle counter calibration; annual laboratory calibration for laser scattering efficiency; validation via co-location with reference particle counters. |
| 5 | PurpleAir [82] | Optical PM sensor | PM1, PM2.5, PM10 | Citizen science networks, global monitoring | Average (compensated by quantity) | 0–1000 µg·m−3 | Field calibration through long-term co-location; humidity correction algorithms; EPA-endorsed linear models; continuous drift correction |
| 6 | inBiot MICA [83] | IAQ | CO2, PM2.5, PM 10, VOCs, T, RH | Schools, offices, education | Good, implementation | 0–1000 µg·m−3 | Initial lab calibration (CO2, VOCs); PM module calibrated against reference optical counters; periodic auto-calibration routines (CO2) and field verification. |
| 7 | Kaiterra [84] | IAQ | CO2, PM2.5, VOCs, T, RH | Offices, homes, schools | Popular, easy to use | 0–1000 µg·m−3 | Factory calibration for CO2 and VOCs via calibration gases; PM via optical scattering chamber; routine algorithmic drift compensation. |
| 8 | Canāree A1 [85] | Personal IAQ | PM2.5, PM10, VOCs, CO2, T, RH | Individual monitoring | Good, unique mobility | 0–6000 µg·m−3 | Multi-parameter initial calibration; PM via optical scattering; TVOC via calibration gas; ongoing auto-adjustment and field co-location recommended. |
| 9 | GreenYourAir Device 1178/PM2.5 [30] | PM network sensor | PM2.5 | Fieldwork (Greece) | Average | Measurement every 3 min, long-term | PM sensor calibrated via manufacturer reference instrument; periodic field co-location recommended due to drift; high variability requires correction factors. |
| 10 | Qingping Air Monitor Lite [51,86] | IAQ sensor | PM2.5, CO2, T, RH | Academician (Beijing) | Satisfactory | 0–1000 µg·m−3 | Initial optical calibration; NDIR calibration for CO2; humidity and temperature compensation; field verification required for research applications. |
| 11 | Sampler ARA N-FRM [51] | Reference sampler | PM2.5 | Reference studies | Very high (reference) | Reference method | Reference gravimetric method; calibration traceable to national standards; routine mass calibration with certified microbalance; zero and span checks. |
| 12 | HPMA115S0 [58,87] | Sensor PM | PM2.5, PM10 | Schools (Portugal) | Average (15%) | 0–1000 µg·m−3 | Factory-calibrated PM module; requires humidity compensation; periodic field co-location due to known ±15% uncertainty. |
| 13 | Aerocet-831 [45,88] | Portable metre | PM1, PM2.5, PM4, PM10 | Fitness Centres (Taiwan) | Average | 0–1000 µg·m−3 | Optical calibration following NIST-traceable procedures; zero and span checks before measurement; recommended annual calibration in controlled conditions. |
| 14 | DustTrak 8533/8534 [42,44,59] | Laser dust monitor | PM1, PM2.5, PM4, PM10, TSP | Sports halls | Very high | 0.001 to 150 µg·m−3—1 min readings | Initial calibration to ISO test dust; strong dependence on aerosol type; long-term co-location essential; humidity correction required; validated in sports halls. |
| 15 | Personal pump + gravimetric filters [52] | Gravimetric | PM2.5 | Epidemiological studies (USA) | Very high (reference) | Gravimetric method | Flow calibration before/after sampling using a certified flow calibrator; mass calibration via microbalance; method traceable to EPA FRM. |
| 16 | XRF + CMB, EF, FA, PMF [69] | Analytical methods | Chemical composition PM2.5 i PM10 | Identification of sources in museums | Very high | Composition analysis | Analytical method calibration using certified reference materials; cross-validation of elemental signals; methodological QA/QC per US EPA compendium. |
| PART A. INSTRUMENT TAXONOMY | |||||
| Instrument Type | Operating Principle | Typical Fractions | Measurement Range | Time Resolution | Typical Application |
| Gravimetric methods (reference) | Particle collection on filters and mass determination | PM1, PM2.5, PM4, PM10, TSP | 1–1000 µg·m−3 | 24 h | Reference methods, instrument validation |
| TEOM/BAM | Oscillating microbalance or beta radiation attenuation | PM2.5, PM10 | 0–1000 µg·m−3 | 1–60 min | Monitoring stations, long-term measurements |
| Optical laser photometers (DustTrak, Aerocet) | Light scattering | PM1, PM2.5, PM4, PM10 | 1–10,000 µg·m−3 | 1 s–1 min | Dynamic monitoring, short-term exposure assessment |
| Low-cost optical sensors (Plantower, PurpleAir) | Laser light scattering | PM2.5, PM10 | 0–1000 µg·m−3 | 1–80 s | Network monitoring, online IAQ systems |
| Particle counters (OPC, SMPS) | Particle counting and size classification | UFP, PM1 | 103–106 particles·cm−3 | Seconds | Aerosol research, toxicological studies |
| PART B. VALIDATION, ACCURACY, AND SYSTEMATIC ERRORS | |||||
| Instrument Type | Typical Accuracy | Main Error Sources | Calibration Requirement | Suitability for IAQ | |
| Gravimetric methods | Very high (reference method) | Lack of time resolution, loss of semi-volatile fractions | Balance and flow calibration | Excellent for scientific studies | |
| TEOM/BAM | High (±10–15%) | Evaporation of semi-volatile compounds | Regular calibration | Very good for continuous monitoring | |
| Optical photometers | Moderate (±20–30%) | Aerosol composition and humidity dependence | Local calibration recommended | Good for time-trend analysis | |
| Low-cost sensors | Low–moderate (±30–60%) | Humidity, aerosol type, sensor drift | Correction vs. FEM required | Suitable for indicative monitoring | |
| OPC/SMPS | Very high for particle number | Conversion of number to mass | Laboratory calibration | Mainly for specialised research | |
| PART C. AIR QUALITY INDICES (AQI) IN INDOOR APPLICATIONS | |||||
| Aspect | Methodological Remarks | ||||
| Original purpose of AQI | Developed for outdoor air quality assessment | ||||
| Limitations for IAQ | Does not reflect long-term exposure in indoor environments | ||||
| Interpretation risks | Potential underestimation of risk at low AQI during prolonged exposure | ||||
| Recommendation | AQI should be used only as a supplementary indicator together with absolute PM2.5 and PM10 concentrations and WHO guideline values | ||||
| PART D. SUMMARY OF ACCURACY FOR INDOOR APPLICATIONS | |||||
| Instrument Class | Suitability for Scientific Research | Suitability for Building Monitoring | Data Correction Required | ||
| Reference methods | Very high | Low (cost, time resolution) | No | ||
| Professional optical photometers | High | High | Yes (humidity, aerosol composition) | ||
| Low-cost sensors | Limited | Very high (online IAQ monitoring) | Always required | ||
| Ventilation Scenario | Air Purifier Location | Airflow Rate (m3∙h−1) | PM2.5—Reduction (%) | PM10—Reduction (%) | Time to Achieve Reduction PM2.5 (min) | Time to Achieve Reduction PM10 (min) |
|---|---|---|---|---|---|---|
| No ventilation | Centre | 150 | 65 | 70 | 40 | 30 |
| No ventilation | Centre | 250 | 80 | 85 | 25 | 20 |
| No ventilation | Centre | 400 | 95 | 98 | 12 | 10 |
| No ventilation | Near wall | 150 | 50 | 55 | 50 | 40 |
| No ventilation | Near wall | 250 | 70 | 75 | 30 | 25 |
| No ventilation | Near wall | 400 | 90 | 92 | 15 | 12 |
| Natural ventilation | Centre | 150 | 60 | 65 | 45 | 35 |
| Natural ventilation | Centre | 250 | 75 | 80 | 28 | 22 |
| Natural ventilation | Centre | 400 | 92 | 95 | 14 | 11 |
| Natural ventilation | Near wall | 150 | 45 | 50 | 55 | 45 |
| Natural ventilation | Near wall | 250 | 65 | 70 | 32 | 27 |
| Natural ventilation | Near wall | 400 | 88 | 90 | 16 | 13 |
| Mechanical ventilation | Centre | 150 | 63 | 68 | 42 | 32 |
| Mechanical ventilation | Centre | 250 | 78 | 83 | 26 | 21 |
| Mechanical ventilation | Centre | 400 | 93 | 96 | 13 | 10 |
| Mechanical ventilation | Near wall | 150 | 48 | 52 | 52 | 42 |
| Mechanical ventilation | Near wall | 250 | 68 | 72 | 33 | 28 |
| Mechanical ventilation | Near wall | 400 | 90 | 93 | 17 | 14 |
| Flow (m3·h−1) | Filter Efficiency (%) | Scenario | PM2.5 Reduction (%) |
|---|---|---|---|
| 100 | 35 | LL | 7 |
| 100 | 65 | HL | 15 |
| 100 | 95 | LH | 20 |
| 100 | 95 | HH | 22 |
| 600 | 35 | LL | 29 |
| 600 | 65 | HL | 32 |
| 600 | 95 | LH | 35 |
| 600 | 95 | HH | 38 |
| Attempt | 60 min | 120 min | 240 min |
|---|---|---|---|
| Reference | 172.90 ± 6.11 | 119.46 ± 4.81 | 58.03 ± 5.05 |
| Epipremnum aureum | 161.05 ± 3.39 | 107.87 ± 2.72 | 48.77 ± 3.28 |
| Chlorophytum comosum | 158.16 ± 3.41 | 105.17 ± 3.01 | 45.91 ± 1.7 |
| Nephrolepis exaltata | 147.58 ± 6.98 | 92.58 ± 6.28 | 38.36 ± 3.29 |
| Maranta leuconeura | 147.89 ± 6.11 | 99.13 ± 6.51 | 46.16 ± 3.53 |
| Technology | Typical PM2.5 Reduction | Typical PM10 Reduction | Conditions with Highest Effectiveness | Conditions Limiting Effectiveness (High Outdoor Load/Occupancy) | By-Products/Limitations | References |
|---|---|---|---|---|---|---|
| HVAC—MERV 11–13 filtration | 30–55% | 20–40% | Stable outdoor conditions; recirculation mode | High infiltration during smog or wildfire episodes (drop to 15–30%) | Increased pressure drop, energy use, frequent filter replacement | [18,19,20,36] |
| HVAC with HEPA (H13–H14) | 50–80% | 40–70% | Hospitals, schools, controlled ventilation systems | Reduced by secondary emissions and resuspension in occupied spaces | Installation constraints, high cost | [10,18,53,54] |
| Portable HEPA air purifiers | 45–85% | 25–60% | Small/medium rooms; optimal placement | Efficiency decreases by 10–40% due to occupant activity | Highly placement-dependent | [17,18,19,20,21,53,59] |
| Natural ventilation + air purifier | 20–40% | 10–30% | Mild outdoor pollution, high air exchange | High outdoor load increases indoor infiltration | Airflow uncontrolled; variable efficiency | [30,40,54] |
| Novel filtration media (biodegradable/natural fibres) | 25–50% | 20–40% | Low humidity; moderate pollution load | High humidity reduces stability; limited durability | Structural degradation; microbial growth risk | [14] |
| Ionisers, ozone generators, UV-C technologies | 30–60% (variable) | 20–50% | Controlled environments without occupants | Presence of VOCs and human exposure increases formation of secondary pollutants | Ozone, aldehydes, ultrafine particles | [38,45] |
| Ultrasonic humidifiers (secondary PM) | (increase of PM2.5) | — | — | Mineral “white dust” formation >300 µg·m−3 | Emission of mineral aerosols; depends on water quality | [50] |
| Integrated systems (airtightness + HVAC + HEPA) | 55–90% | 40–75% | High outdoor pollution events; low infiltration | High occupancy reduces performance by 10–25% | Dependent on building envelope quality | [29,30,40,69,70,71,72,73,74,75,76] |
| Airflow layout optimisation/purifier placement | +20–50% above standard configuration | +15–40% | Central placement; unobstructed airflow | Poor positioning (corners, under windows) may reduce efficiency by 50% | Requires airflow assessment | [41,45,59] |
| Building Category | Specific Facility | Baseline PM2.5 (Indoor) | Baseline PM10 (Indoor) | Post-Intervention PM2.5 | Post-Intervention PM10 | I/O | ACH/Airflow | Filter Class/CADR | Effect Size (%) | Season | Dominant PM Sources | Methods/Notes | Reference |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Schools | |||||||||||||
| School | Stockton, USA | not reported | not measured | 14–56% reduction (no absolute µg/m3 reported) | not measured | PAC airflow 70–510 m3/h | Portable HEPA PAC + MERV − 13 HVAC | 14–56% | Autumn–Winter | Outdoor infiltration; occupancy | Classroom monitoring; scenarios with PAC and HVAC; absolute post-PM not provided | [21] | |
| Kindergarten | Daejeon, Korea | ~35 µg/m3 | not reported | ~18 µg/m3 | not reported | Mechanical ventilation ~20.4 m3/h per child | MERV≈13 | ~49% | Winter | Indoor sources + infiltration | Hybrid model + measured data; post-PM partly modelled | [24] | |
| School | Israel | ~10 µg/m3 | not measured | not measured | not measured | ~0.25 | natural | none | +16% (increase) | spring | sandstorm | Classroom monitoring during desert dust intrusion; indoor–outdoor comparison using optical PM sensors. | [40] |
| School | Portugal | 4.2–78 µg/m3 | 3.5–96 µg/m3 | not measured | not measured | not measured | HVAC, no ACH data | central filter, no class | not measured | spring | occupants, dust | Classroom monitoring; HVAC operation during school hours; filter-based PM sampling; no post-mitigation scenario. | [57] |
| School | Greece | not measured | 21–51 µg/m3 | not measured | not measured | ~1 | natural | none | 0% | various | road traffic | Indoor–outdoor PM10 monitoring near traffic; gravimetric method; evaluation of green roof influence. | [16] |
| Kindergartens | Silesia | 41–125 µg/m3 | 68–166 µg/m3 | not measured | not measured | ~1 | natural | none | 30–70% increase | Winter | resuspension | Seasonal indoor measurements in occupied classrooms; portable optical PM monitors; focus on resuspension effects. | [41] |
| Kindergartens | Sweden | not measured | not measured | 3.2–9.3 | not measured | not measured | mechanical, high ACH | MERV ≥ 11 | 70–85% reduction | various | low indoor sources | Long-term monitoring with mechanical ventilation; PM assessed before and after MERV filtration; optical + reference instruments. | [41] |
| Offices | |||||||||||||
| Office | Taiwan | ~28 µg/m3 | ~62 µg/m3 | ~15 µg/m3 | ~55 µg/m3 | HVAC (upgraded) | Central filters (class not specified) | 46% PM2.5; 44% PM10 | Annual | Infiltration; office equipment | Before–after measurement comparison | [25] | |
| Office | Malaysia | 53 µg/m3 | 35 µg/m3 | not measured | not measured | ~1 | air conditioning | no HEPA | no reduction | Annual | infiltration | Indoor PM monitoring during working hours; fixed optical PM sensors; evaluation under split-unit air conditioning | [60] |
| Office | Chicago | 5.3–5.8 µg/m3 | not measured | not measured | not measured | ~0.2 | mechanical | no HEPA | ±5% | spring | infiltration | Paired indoor–outdoor monitoring in mechanically ventilated offices; reference-grade PM2.5 instrumentation; short-term campaign. | [63] |
| Residential buildings | |||||||||||||
| Homes | Wildfire smoke/USA | 4–5 → 15–18 µg/m3 | not measured | 30–74% reduction (PAC/HEPA) | not measured | 0.7 | Low ACH | HEPA PAC (varied CADR) | 30–74% | Wildfire season/Summer | Wildfire smoke; infiltration | Multiple homes; reductions depend on CADR and tightness | [36] |
| Apartment/home | Ultrasonic humidifier/Korea | <10 → 350 µg/m3 | not measured | <10 µg/m3 after intervention | not measured | not measured | No ACH data | No filter (source control) | ~97% | Annual | Mineral aerosol (white dust) | Small test room (3.8 × 2.95 × 2.8 m); rapid PM rise from water minerals | [50] |
| Apartments | Greece | 63.9 µg/m3 | not measured | not measured | not measured | not measured | natural, no data | no filter | not measured | Annual | smoking, infiltration | Long-term indoor monitoring using gravimetric PM samplers; background residential conditions; no mitigation scenario tested. | [30] |
| Apartments | South Asian Countries (Pakistan, India, Nepal, Bangladesh, Bhutan, Sri Lanka) | 225–9000 µg/m3 | 300–12,000 µg/m3 | not measured | not measured | not measured | natural | no filter | 80–95% | winter | biomass combustion | Field measurements in biomass-using households; filter-based gravimetric sampling; values synthesised from multiple studies | [55] |
| Hospitals | |||||||||||||
| Hospital (ER) | Romania | 75.4 µg/m3 | not measured | 41.5–49.0 µg/m3 | not measured | not measured | Mechanical + PAC | HEPA PAC CADR 650 m3/h | 35–45% | Various | Occupant activity | Measured PM drop; no absolute post-PM provided. continuous PM2.5 monitoring in emergency unit; evaluation before and after portable air purifier deployment; optical sensors calibrated to reference. | [53] |
| Museums | |||||||||||||
| Museum | Multiple (review) | indoor typically > outdoor | varies | no data | no data | usually none | varies; often no HEPA | 20–60% increase | Tourist season | Visitors; resuspension | Heterogeneous methods; no standardised monitoring; Methods/Notes: Continuous indoor and outdoor monitoring in exhibition spaces; optical particle counters; correlation with visitor density. | Review | |
| Sport facilities | |||||||||||||
| Fitness centre | Taiwan | 30–55 µg/m3 | 70–103 µg/m3 | not measured | not measured | not measured | air conditioning, no ACH data | no HEPA | no reduction | Annual | movement, resuspension | Real-time PM monitoring during exercise sessions; optical PM sensors; assessment under standard air-conditioning only. | [45] |
| Sports hall | Poland | 30–39 µg/m3 | 18–33 µg/m3 | not measured | not measured | ~1 | mechanical | none | +30% in winter | seasonal | resuspension | Seasonal indoor PM monitoring during sports activities; gravimetric reference sampling; comparison winter vs. summer. | [59] |
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Share and Cite
Baran, A.; Zender-Świercz, E. Concentration of PM2.5 and PM10 Particulate Matter in Various Indoor Environments: A Literature Review. Atmosphere 2026, 17, 45. https://doi.org/10.3390/atmos17010045
Baran A, Zender-Świercz E. Concentration of PM2.5 and PM10 Particulate Matter in Various Indoor Environments: A Literature Review. Atmosphere. 2026; 17(1):45. https://doi.org/10.3390/atmos17010045
Chicago/Turabian StyleBaran, Angelika, and Ewa Zender-Świercz. 2026. "Concentration of PM2.5 and PM10 Particulate Matter in Various Indoor Environments: A Literature Review" Atmosphere 17, no. 1: 45. https://doi.org/10.3390/atmos17010045
APA StyleBaran, A., & Zender-Świercz, E. (2026). Concentration of PM2.5 and PM10 Particulate Matter in Various Indoor Environments: A Literature Review. Atmosphere, 17(1), 45. https://doi.org/10.3390/atmos17010045

