Organophosphate Esters in Building Materials from China: Levels, Sources, Emissions, and Preliminary Assessment of Human Exposure.

Source characteristics and health risks of indoor organophosphate esters (OPEs) are limited by the lack of knowledge on emission processes. This study attempted to integrate the contents and emissions of OPEs from indoor building materials to assess human health effects. Thirteen OPEs were investigated in 80 pieces of six categories of building materials. OPEs are ubiquitous in the building materials and ∑13OPE contents varied significantly (p < 0.05) from 72.8 ng/g (seam agent) to 109,900 ng/g (wallpaper). Emission characteristics of OPEs from the building materials were examined based on a microchamber method. Depending on the sample category, the observed initial area-specific emission rates of ∑13OPEs varied from 154 ng/m2/h (carpet) to 2760 ng/m2/h (wooden floorboard). Moreover, the emission rate model was developed to predict the release levels of individual OPEs, quantify source contributions, and assess associated exposure risks. Source apportionments of indoor OPEs exhibited heterogeneities in multiple environmental media. The joint OPE contribution of wallpaper and wooden floorboard to indoor dust was up to 94.8%, while latex paint and wooden floorboard were the main OPE contributors to indoor air (54.2%) and surface (76.1%), respectively. Risk assessment showed that the carcinogenic risks of tris(2-chloroethyl) phosphate (3.35 × 10-7) were close to the acceptable level (1 × 10-6) and deserved special attention.

Partitioning of Neutral PFAS in Homes and Release to the Outdoor Environment: Results from the IPA Campaign.

The distribution and fate of per- and polyfluoroalkyl substances (PFAS) in homes are not well understood. To address this, we measured nine neutral PFAS in dust, airborne particles, dryer lint, and on heating and air conditioning (HAC) filters in 11 homes in North Carolina as part of the Indoor PFAS Assessment (IPA) Campaign and compared them with concurrently collected gas and cloth measurements. Fluorotelomer alcohols (FTOHs) contributed most (≥75%) to total (∑) measured neutral PFAS concentrations in dust, HAC filter, and dryer lint samples, with mean ∑(FTOH) concentrations of 207 ng/g, 549 ng/g, and 84 ng/g, respectively. In particles, perfluorooctane sulfonamidoethanols (FOSEs) dominated, with a mean ∑(FOSE) concentration of 0.28 ng/m3 or 75,467 ng/g. For FTOHs and FOSEs, resulting mean dust-air, HAC filter-air, dryer lint-air and particle-air partition coefficients in units of log(m3/µg) ranged (across species) from -5.1 to -3.6, -4.9 to -3.5, -5.4 to -4.1, and -3.2 to -0.78, respectively. We estimate that cloth, gas phase, and HAC filters are the largest reservoirs for FTOHs, while cloth, HAC filters, and dust are the largest reservoirs for FOSEs. Release rates of neutral PFAS from homes to the outdoor environment are reported.

Large Particle Emissions from Human Vocalization and Playing of Wind Instruments.

Humans emit large salivary particles when talking, singing, and playing musical instruments, which have implications for respiratory disease transmission. Yet little work has been done to characterize the emission rates and size distributions of such particles. This work characterized large particle (dp > 35 µm in aerodynamic diameter) emissions from 70 volunteers of varying age and sex while vocalizing and playing wind instruments. Mitigation efficacies for face masks (while singing) and bell covers (while playing instruments) were also examined. Geometric mean particle count emission rates varied from 3.8 min-1 (geometric standard deviation [GSD] = 3.1) for brass instruments playing to 95.1 min-1 (GSD = 3.8) for talking. On average, talking produced the highest emission rates for large particles, in terms of both number and mass, followed by singing and then instrument playing. Neither age, sex, CO2 emissions, nor loudness (average dBA) were significant predictors of large particle emissions, contrary to previous findings for smaller particle sizes (i.e., for dp < 35 µm). Size distributions were similar between talking and singing (count median diameter = 53.0 µm, GSD = 1.69). Bell covers did not affect large particle emissions from most wind instruments, but face masks reduced large particle count emissions for singing by 92.5% (95% CI: 97.9%, 73.7%).

Quantifying Concentrations and Emissions of Hexachlorobutadiene - A New Atmospheric Persistent Organic Pollutant in northern China.

Hexachlorobutadiene (HCBD) was listed as a new persistent organic pollutant for global regulation under Stockholm Convention in 2015, and there has been scarce information on its atmospheric concentrations, distributions, and emission sources. HCBD air samples were collected and analyzed to characterize concentrations and distributions at high elevation and urban sites as well as emission source locations in Northern China. We found ambient concentrations of HCBD in Northern China averaged at 34 ± 16 and 36 ± 28 pptv at urban sites in Jinan and Tai'an, respectively, and 31 ± 21 pptv at a high-elevation site Mount Tai. HCBD concentrations at the high elevation and urban sites were found to be affected by long-range transport under the influence of the East Asian monsoon climate. Over potential sources areas, we found concentrations of 76 ± 33 pptv in a mixed factory park, 59 ± 21 pptv in a rubber plant and 74 ± 8 pptv in a municipal solid waste (MSW) landfill area, which were all several times higher than in urban sites. The large concentration gradient across the various environments revealed strong emission sources of HCBD, especially over MSW landfill and Cl-compound production and application areas. An emission rate of 9.2 × 104 kg/yr and an oxidation rate of 32.9 kg/yr for HCBD were estimated for the mixed factory park. OH and Cl are much more active in reaction with HCBD than other oxidants in the atmosphere. Dry deposition and oxidation removed about 5.3% and 0.04%, respectively, of the emitted, suggesting that ∼95% of the emitted HCBD remaining in the atmosphere and could be transported for redistribution. Our findings revealed significant emission sources of HCBD in northern China, which was in turn affected by major sources in East-central China. The regional influence of HCBD pollution warrants serious concerns and points to the need to develop mitigation strategies.

The Effect of Human Occupancy on Indoor Air Quality through Real-Time Measurements of Key Pollutants.

The primarily emitted compounds by human presence, e.g., skin and volatile organic compounds (VOCs) in breath, can react with typical indoor air oxidants, ozone (O3), and hydroxyl radicals (OH), leading to secondary organic compounds. Nevertheless, our understanding about the formation processes of the compounds through reactions of indoor air oxidants with primary emitted pollutants is still incomplete. In this study we performed real-time measurements of nitrous acid (HONO), nitrogen oxides (NOx = NO + NO2), O3, and VOCs to investigate the contribution of human presence and human activity, e.g., mopping the floor, to secondary organic compounds. During human occupancy a significant increase was observed of 1-butene, isoprene, and d-limonene exhaled by the four adults in the room and an increase of methyl vinyl ketone/methacrolein, methylglyoxal, and 3-methylfuran, formed as secondary compounds through reactions of OH radicals with isoprene. Intriguingly, the level of some compounds (e.g., m/z 126, 6-methyl-5-hepten-2-one, m/z 152, dihydrocarvone, and m/z 194, geranyl acetone) formed through reactions of O3 with the primary compounds was higher in the presence of four adults than during the period of mopping the floor with commercial detergent. These results indicate that human presence can additionally degrade the indoor air quality.

A holistic modeling framework for estimating the influence of climate change on indoor air quality.

The IPCC 2021 report predicts rising global temperatures and more frequent extreme weather events in the future, which will have different effects on the regional climate and concentrations of ambient air pollutants. Consequently, changes in heat and mass transfer between the inside and outside of buildings will also have an increasing impact on indoor air quality. It is therefore surprising that indoor spaces and occupant well-being still play a subordinate role in the studies of climate change. To increase awareness for this topic, the Indoor Air Quality Climate Change (IAQCC) model system was developed, which allows short and long-term predictions of the indoor climate with respect to outdoor conditions. The IAQCC is a holistic model that combines different scenarios in the form of submodels: building physics, indoor emissions, chemical-physical reaction and transformation, mold growth, and indoor exposure. IAQCC allows simulation of indoor gas and particle concentrations with outdoor influences, indoor materials and activity emissions, particle deposition and coagulation, gas reactions, and SVOC partitioning. These key processes are fundamentally linked to temperature and relative humidity. With the aid of the building physics model, the indoor temperature and humidity, and pollutant transport in building zones can be simulated. The exposure model refers to the calculated concentrations and provides evaluations of indoor thermal comfort and exposure to gaseous, particulate, and microbial pollutants.

Fugitive Emissions of Volatile Organic Compounds from a Tailings Pond in the Oil Sands Region of Alberta.

Tailings ponds in the oil sands (OS) region in Alberta, Canada, have been associated with fugitive emissions of volatile organic compounds (VOCs) and other pollutants to the atmosphere. However, the contribution of tailings ponds to the total fugitive emissions of VOCs from OS operations remains uncertain. To address this knowledge gap, a field study was conducted in the summer of 2017 at Suncor's Pond 2/3 to estimate emissions of a suite of pollutants including 68 VOCs using a combination of micrometeorological methods and measurements from a flux tower. The results indicate that in 2017, Pond 2/3 was an emission source of 3322 ± 727 tons of VOCs including alkanes, aromatics, and oxygenated and sulfur-containing organics. While the total VOC emissions were approximately a factor of 2 higher than those reported by Suncor, the individual VOC species emissions varied by up to a factor of 12. A chemical mass balance (CMB) receptor model was used to estimate the contribution of the tailings pond to VOC pollution events in a nearby First Nations and Metis community in Fort McKay. CMB results indicate that Suncor Pond 2/3 contributed up to 57% to the total mass of VOCs measured at Fort McKay, reinforcing the importance of accurate VOC emission estimation methods for tailings ponds.

Evaluating Indoor Air Chemical Diversity, Indoor-to-Outdoor Emissions, and Surface Reservoirs Using High-Resolution Mass Spectrometry.

Detailed offline speciation of gas- and particle-phase organic compounds was conducted using gas/liquid chromatography with traditional and high-resolution mass spectrometers in a hybrid targeted/nontargeted analysis. Observations were focused on an unoccupied home and were compared to two other indoor sites. Observed gas-phase organic compounds span the volatile to semivolatile range, while functionalized organic aerosols extend from intermediate volatility to ultra-low volatility, including a mix of oxygen, nitrogen, and sulfur-containing species. Total gas-phase abundances of hydrocarbon and oxygenated gas-phase complex mixtures were elevated indoors and strongly correlated in the unoccupied home. While gas-phase concentrations of individual compounds generally decreased slightly with greater ventilation, their elevated ratios relative to controlled emissions of tracer species suggest that the dilution of gas-phase concentrations increases off-gassing from surfaces and other indoor reservoirs, with volatility-dependent responses to dynamically changing environmental factors. Indoor-outdoor emissions of gas-phase intermediate-volatility/semivolatile organic hydrocarbons from the unoccupied home averaged 6-11 mg h-1, doubling with ventilation. While the largest single-compound emissions observed were furfural (61-275 mg h-1) and acetic acid, observations spanned a wide range of individual volatile chemical products (e.g., terpenoids, glycol ethers, phthalates, other oxygenates), highlighting the abundance of long-lived reservoirs resulting from prior indoor use or materials, and their gradual transport outdoors.

Potentially toxic elements leachates from cigarette butts into different types of water: A threat for aquatic environments and ecosystems?

Trillions of cigarette butts (CBs) are released into the environment and the leached potentially toxic elements (PTEs) from CBs may contaminate the environments. In this study, the leaching of PTEs including both heavy metals and metalloids (metal(loid)s) from CBs into deionized water (DW), tap water (TW), and seawater (SW) was checked during the different contact times (from 60 min to 60 days). According to the results, PTEs were leached from CBs into different water samples. However, there were no significant differences between leachates in DW and TW samples (p > 0.05). The results of the distribution coefficient indicated the high tendency of most PTEs to enter the liquid phase. The levels of leached PTEs into DW and TW exceeded the standards of surface freshwater to maintain aquatic life. Although the maximum level of leached metal(loid)s into DW, TW, and SW occurred at different times, for each type of water sample no significant differences were found among the levels of most PTEs at various contact times. Based on the results, the levels of leached metal(loid)s from CBs in seawater peak soon after being released into the water, while for the freshwater, they occur after some days. This phenomenon could possibly have short-term and long-term effects on marine and freshwater organisms, respectively. Due to the ability of the dissolved PTEs to integrate into the aquatic/terrestrial food web and threaten human health, some control measures regarding the disposal of CBs are necessary.

Emission rate of carbon dioxide while sleeping.

Humans emit carbon dioxide (CO2 ) as a product of their metabolism. Its concentration in buildings is used as a marker of ventilation rate (VR) and degree of mixing of supply air, and indoor air quality (IAQ). The CO2 emission rate (CER) may be used to estimate the ventilation rate. Many studies have measured CERs from subjects who were awake but little data are available from sleeping subjects and the present publication was intended to reduce this gap in knowledge. Seven females (29 ± 5 years old; BMI: 22.2 ± 0.8 kg/m2 ) and four males (27 ± 1 years old; BMI: 20.5 ± 1.5 kg/m2 ) slept for four consecutive nights in a specially constructed capsule at two temperatures (24 and 28°C) and two VRs that maintained CO2  levels at ca. 800 ppm and 1700 ppm simulating sleeping conditions reported in the literature. The order of exposure was balanced, and the first night was for adaptation. Their physiological responses, including heart rate, pNN50, core body temperature, and skin temperature, were measured as well as sleep quality, and subjective responses were collected each evening and morning. Measured steady-state CO2 concentrations during sleep were used to estimate CERs with a mass-balance equation. The average CER was 11.0 ± 1.4 L/h per person and was 8% higher for males than for females (P < 0.05). Increasing the temperature or decreasing IAQ by decreasing VR had no effects on measured CERs and caused no observable differences in physiological responses. We also calculated CERs for sleeping subjects using the published data on sleep energy expenditure (SEE) and Respiratory Quotient (RQ), and our measured CERs confirmed both these calculations and the CERs predicted using the equations provided by ASHRAE Standard 62.1, ASHRAE Handbook, and ASTM D6245-18. The present results provide a valuable and helpful reference for the design and control of bedroom ventilation but require confirmation and extension to other age groups and populations.

Particle number emission rates of aerosol sources in 40 German households and their contributions to ultrafine and fine particle exposure.

More representative data on source-specific particle number emission rates and associated exposure in European households are needed. In this study, indoor and outdoor particle number size distributions (10-800 nm) were measured in 40 German households under real-use conditions in over 500 days. Particle number emission rates were derived for around 800 reported indoor source events. The highest emission rate was caused by burning candles (5.3 × 1013  h-1 ). Data were analyzed by the single-parameter approach (SPA) and the indoor aerosol dynamics model approach (IAM). Due to the consideration of particle deposition, coagulation, and time-dependent ventilation rates, the emission rates of the IAM approach were about twice as high as those of the SPA. Correction factors are proposed to convert the emission rates obtained from the SPA approach into more realistic values. Overall, indoor sources contributed ~ 56% of the daily-integrated particle number exposure in households under study. Burning candles and opening the window leads to seasonal differences in the contributions of indoor sources to residential exposure (70% and 40% in the cold and warm season, respectively). Application of the IAM approach allowed to attribute the contributions of outdoor particles to the penetration through building shell and entry through open windows (26% and 15%, respectively).

Particulate emission rates for open surfaces in Australian open cut black coal mines.

Accurate estimation of particulate emissions is fundamental to assessing the air quality risks posed by existing and proposed open cut black coal mines. The currently available emission estimation techniques are based on a limited range of empirical studies, and the need for additional research and development of activity and region specific particulate emission estimation methods has been recognised. This paper presents the results of empirical testing of particulate emission rates for open area surfaces in open cut black coal mines in three Australian regions. The emission rates are provided for specific wind speeds, thus allowing adjustment of emission rates for prevailing meteorology in these regions. The influence of surface watering as a control technique is also considered. Particulate emission rates are presented for a range of coal mining sources, and for specific wind speeds. Comparison of the emission rates with the existing published research confirms the emission rates are consistent with current approaches. This research significantly expands our current understanding by presenting emission rates for a range of open area sources, for specific wind speeds and surface watering controls. This more detailed emission estimation dataset provides for adjustments to default particulate emission rates to allow site specific data to be integrated into emissions estimation. This will result in more accurate emissions estimates for existing and future projects and reduce the potential for significant over- or under-estimation of particulate emissions from surface sources in open cut coal mines.

Contributions of burner, pan, meat and salt to PM emission during grilling.

Grilling ground beef meat was conducted in two locations at Nazarbayev University, Kazakhstan. The experiments were designed such that only particles from beef meat were isolated. A similar experimental protocol was applied at both locations. The average particle number and mass emission rates for grilling pure meat itself (excluding particles from pan and burner) were found to be 9.4 × 1012(SD = 7.2 × 1012 particle min-1 and 7.6 × 10 (SD = 6.3 × 10) mg.min-1, respectively. The PM emissions (number and mass) from the burner were found to be negligible compared to the pan and meat emissions. Ultrafine particle (UFP) concentrations from the heated pan itself were comparable to those of grilled meat. However, the particle mass concentrations from the pan itself were negligible. Approximately an hour of continuous heating resulted in zero emissions from the pan.

Impact of material emissions and sorption of volatile organic compounds on indoor air quality in a low energy building: Field measurements and modeling.

The assessment of VOC emission rates and sorption coefficients was performed for ten surfaces present within a classroom, using field and laboratory emission cells (FLEC) coupled to online and off-line VOC quantification techniques. A total of 21 identified VOCs were emitted by the different surfaces. VOC emission rates measured using PTR-ToF-MS were compared to gas chromatographic measurements. The results showed that the two methods are complementary to one another. Sorption parameters were also successfully measured for a mixture of 14 VOCs within a few hours (<17 hours per surface). A study of the spatial and temporal variability of the measured parameters was also carried out on the two surfaces that presented the most potential for interaction with VOCs, accounting for the largest surface areas within the room. The dataset of emission rates and sorption parameters was used in the INCA-Indoor model to predict indoor air concentrations of VOCs that are compared to experimental values measured in the room. Modeling results showed that sorption processes had a limited effect on indoor concentrations of VOCs for these field campaigns. Modeled daily profiles show good agreement with the experimental observations for VOCs such as toluene (indoor source) and xylenes (outdoor source) but underestimate concentrations of methanol (both indoor and outdoor sources).

Surgical Space Suits Increase Particle and Microbiological Emission Rates in a Simulated Surgical Environment.

BACKGROUND: The role of space suits in the prevention of orthopedic prosthetic joint infection remains unclear. Recent evidence suggests that space suits may in fact contribute to increased infection rates, with bioaerosol emissions from space suits identified as a potential cause. This study aimed to compare the particle and microbiological emission rates (PER and MER) of space suits and standard surgical clothing. METHODS: A comparison of emission rates between space suits and standard surgical clothing was performed in a simulated surgical environment during 5 separate experiments. Particle counts were analyzed with 2 separate particle counters capable of detecting particles between 0.1 and 20 µm. An Andersen impactor was used to sample bacteria, with culture counts performed at 24 and 48 hours. RESULTS: Four experiments consistently showed statistically significant increases in both PER and MER when space suits are used compared with standard surgical clothing. One experiment showed inconsistent results, with a trend toward increases in both PER and MER when space suits are used compared with standard surgical clothing. CONCLUSION: Space suits cause increased PER and MER compared with standard surgical clothing. This finding provides mechanistic evidence to support the increased prosthetic joint infection rates observed in clinical studies.

Optimizing the Point-Source Emission Rates and Geometries of Pheromone Mating Disruption Mega-Dispensers.

High-emission-rate "mega-dispensers" have come into increasing use for sex pheromone mating disruption of moth pests over the past two decades. These commercially available dispensers successfully suppress mating and reduce crop damage when they are deployed at very low to moderate densities, ranging from 1 to 5/ha to 100-1000/ha, depending on the dispenser types and their corresponding pheromone emission rates. Whereas traditionally the emission rates for successful commercial mating disruption formulations have been measured in terms of amounts (usually milligram) emitted by the disruptant application per acre or hectare per day, we suggest that emission rates should be measured on a per-dispenser per-minute basis. In addition we suggest, because of our knowledge concerning upwind flight of male moths being dependent on contact with pheromone plume strands, that more attention needs to be paid to optimizing the flux within plume strands that shear off of any mating disruption dispenser's surface. By measuring the emission rates on a per-minute basis and measuring the plume strand concentrations emanating from the dispensers, it may help improve the ability of the dispensers to initiate upwind flight from males and initiate their habituation to the pheromone farther downwind than can otherwise be achieved. In addition, by optimizing plume strand flux by paying attention to the geometries and compactness of mating disruption mega-dispensers may help reduce the cost of mega-dispenser disruption formulations by improving their behavioral efficacy while maintaining field longevity and using lower loading rates per dispenser.

Determining source strength of semivolatile organic compounds using measured concentrations in indoor dust.

UNLABELLED: Consumer products and building materials emit a number of semivolatile organic compounds (SVOCs) in the indoor environment. Because indoor SVOCs accumulate in dust, we explore the use of dust to determine source strength and report here on analysis of dust samples collected in 30 US homes for six phthalates, four personal care product ingredients, and five flame retardants. We then use a fugacity-based indoor mass balance model to estimate the whole-house emission rates of SVOCs that would account for the measured dust concentrations. Di-2-ethylhexyl phthalate (DEHP) and di-iso-nonyl phthalate (DiNP) were the most abundant compounds in these dust samples. On the other hand, the estimated emission rate of diethyl phthalate is the largest among phthalates, although its dust concentration is over two orders of magnitude smaller than DEHP and DiNP. The magnitude of the estimated emission rate that corresponds to the measured dust concentration is found to be inversely correlated with the vapor pressure of the compound, indicating that dust concentrations alone cannot be used to determine which compounds have the greatest emission rates. The combined dust-assay modeling approach shows promise for estimating indoor emission rates for SVOCs. PRACTICAL IMPLICATIONS: The combined dust-assay modeling approach in this study can be used to predict the source strength of indoor released compounds, integrating emissions from consumer products, building materials, and other home furnishings. Our findings show that estimated emission rates are closely related to not only the level of compounds on dust, but also the vapor pressure of the compound. Thus, a fugacity-based indoor mass balance model and measured dust concentrations can be used to estimate the whole-house emission rates from all sources in actual indoor settings, when individual sources of emissions are unknown.

Modeled occupational exposures to gas-phase medical laser-generated air contaminants.

Exposure monitoring data indicate the potential for substantive exposure to laser-generated air contaminants (LGAC); however the diversity of medical lasers and their applications limit generalization from direct workplace monitoring. Emission rates of seven previously reported gas-phase constituents of medical laser-generated air contaminants (LGAC) were determined experimentally and used in a semi-empirical two-zone model to estimate a range of plausible occupational exposures to health care staff. Single-source emission rates were generated in an emission chamber as a one-compartment mass balance model at steady-state. Clinical facility parameters such as room size and ventilation rate were based on standard ventilation and environmental conditions required for a laser surgical facility in compliance with regulatory agencies. All input variables in the model including point source emission rates were varied over an appropriate distribution in a Monte Carlo simulation to generate a range of time-weighted average (TWA) concentrations in the near and far field zones of the room in a conservative approach inclusive of all contributing factors to inform future predictive models. The concentrations were assessed for risk and the highest values were shown to be at least three orders of magnitude lower than the relevant occupational exposure limits (OELs). Estimated values do not appear to present a significant exposure hazard within the conditions of our emission rate estimates.

Fractions of smoke leakage into indoor space from residential solid fuel combustion in chimney stoves.

Severe indoor air pollution from solid-fuel combustion is a global health concern. Although stove chimneys can expel most of the smoke to outside, unignorable amounts can remain indoors, known as indoor fugitive emissions. Quantitative analyses of indoor emission rates (IER) and indoor fugitive fractions (IFF) are limited, particularly in field settings. This study quantified the IERs and IFFs of particulate matters (PMs) from residential solid fuel combustion, covering different fuel-stove combinations in rural China. The study showed that both IERs and IFFs were not normally distributed. The median IER for PM2.5, which peaked at 860 mg/min, was 32 mg/min. IERs very significantly among different fuel and stove types, with biomass pellets and improved stoves demonstrating lower IERs than traditional biomass and coal. Approximately 27% of PM2.5 was leaked into indoor air, but this fraction ranged largely from a low percentage to 80%. Higher IFFs were observed for coals burned in traditional stoves. The median IFFs of organic carbon and elemental carbon were 26% (12%-43% as the interquartile range) and 19% (9%-40%), respectively. The chimney lifting effect significantly affected the degree of indoor leakage, with relatively low IFFs under high gas velocity conditions. Chimney exhaust and fugitive smoke had distinct size distributions, and small particles exhibited fewer leakages than coarse particles. The study provides valuable datasets for quantifying internal combustion impacts on indoor air quality and consequently human health.

Multi-sensor monitoring and analysis of indoor pollutant emissions in response to laser cutter operating conditions.

This study analyzed pollutant emissions from laser cutters used in modeling in a laboratory, which can have harmful effects on indoor air quality and health. Four conditions were tested: material thickness, laser cutter strength, minimum strength per thickness, and air purifier level. Four pollutants were analyzed: PM2.5, HCHO, VOCs, and CO2. The study found that the emissions of PM2.5, HCHO, and VOCs increased with paperboard thickness, while CO2 emissions were not significant. PM2.5 was more affected by laser cutting strength, while HCHO and VOCs were more affected by paperboard thickness. Additionally, we analyzed the PM2.5 emission rates based on the thickness of the paperboard and the laser cutting strength. Therefore, emission rates based on thickness and laser cutting strength ranged from 7275 to 18,783 µg/min. The air purifier significantly reduced PM2.5 but not HCHO and VOCs. To reduce these gaseous pollutants, combining mechanical ventilation or using an air purifier with a filter that adsorbs HCHO and VOCs is effective. This study highlights the importance of considering laser cutters as a potential source of indoor air pollutants and implementing measures to mitigate their harmful effects.