Elements In Particulate Matter Research Articles

Study on the distribution, enrichment and migration characteristics of trace elements in particulate matter during solid waste combustion

Trace element emissions caused by the entrainment of particulate matter (PM) has led to serious environmental pollution. This research focuses on the distribution, enrichment and migration characteristics of trace elements in different sizes of PM during the typical solid waste combustion. The results indicate that the mass concentration of trace elements in different PM is closely related to their volatility. Volatile trace elements such as Cu, In, Ag, Pb, and Cd tend to distribute in PM1. Higher temperatures facilitate the volatilization of trace elements, promoting their migration and enrichment in finer PM. The removal effect of Si–Al-based additives on trace elements in PM1 decreases with the increase of Si/Al ratio. Among them, the removal efficiency of 5% kaolin is the best. After the addition of Si–Al-additives, Zn and In mainly migrate to PM1-10, while Cu, V, Mo, As, Se, Cr, Ba, Mn, Co, Sr, and Ti mainly migrate to PM10+. Ag, Pb, and Cd migrate to both PM1-10 and PM10+ simultaneously.

Seasonal Disparities of Human Health Risk and Particle-Bound Metal Characteristics Associated with Atmospheric Particles in a Fishery Harbor.

The effects of atmospheric pollution from ship emissions have been considered for several harbors worldwide. The health risk assessment and source apportionment of particle-bound metals in a fishery harbor were investigated in this study. The most abundant metal elements in particulate matter (PM) on all sampling days in three seasons were Fe (280.94 ± 136.93 ng/m3), Al (116.40 ± 71.25 ng/m3), and Zn (110.55 ± 26.70 ng/m3). The ratios of V/Ni were 1.44 ± 0.31, 1.48 ± 0.09 and 1.87 ± 0.06 in PM10, PM2.5, and PM1, respectively. Meanwhile, the ratios higher than 1 indicated that fuel oil combustion from ship emission in fishery harbor. The highest deposits of total particle-bound metals in the human respiratory tract were in the head airway (HA), accounting for 76.77 ± 2.29% of the total particle-bound metal concentration, followed by 5.32 ± 0.13% and 2.53 ± 0.15% in the alveolar region (AR) and tracheobronchial (TB) region, respectively. The total cancer risk (CR) of inhalation exposure to local residents exceeded 10-6. Mean total CR values followed the sequence: autumn (1.24 × 10-4) > winter (8.53 × 10-5) > spring (2.77 × 10-6). Source apportionment of related metal emissions was mobile pollution emissions (vehicle/boat) (37.10-48.92%), metal fumes of arc welding exhaust (19.68-34.42%), spray-painting process (12.34-16.24%), combustion emissions (6.32-13.12%), and metal machining processes (9.04-16.31%) in Singda fishing harbor. These results suggest that proper control of heavy metals from each potential source in fishing harbor areas should be carried out to reduce the carcinogenic risk of adverse health effects.

Deposition of heavy metals in biological tissues of workers in metal workshops.

Welding and cutting of metals produce large amounts of particulate matter (PM), which poses a significant health risk to exposed workers. Appropriate biological markers to estimate exposure are of great interest for occupational health and safety. Here, hair and nail samples from metal workers were analyzed, which appear to be more suitable than blood or urine samples for assessing long-term exposure. Four workshops working with steel components were included in the study. The hair and nail samples were analyzed by inductively coupled plasma mass spectrometry (ICP-MS) to measure the concentrations of 12 elements. At the workplaces, the concentrations of 15 elements in particulate matter were determined using X-ray fluorescence (XRF) and particle-induced X-ray emission (PIXE) techniques. The hair and nail samples of the workers contained significantly higher metal concentrations than the analytical results of a nonexposed control group. The most significant difference between the groups was found for Ti, Mn, Fe, and Co.

Composition of inorganic elements in fine particulate matter emitted during surface fire in relation to moisture content of forest floor combustibles

The moisture content of combustible material on the forest floor is constantly changing due to environmental factors, which have a direct impact on the composition and emission intensity of particulate matter released during fire. In this study, an indoor biomass combustion analysis device was used to analyze the emission characteristics of fine particulate matter (PM2.5) from combustion of herbaceous combustible materials with different moisture contents (0%, 15%, and 30%). The composition of inorganic elements in PM2.5 (Zn, K, Mg, Ca, and other 13 measurable elements) were determined by inductively coupled plasma-mass spectrometer (ICP-MS). The results showed that the PM2.5 emission factor increased significantly with the increase of moisture content of combustible materials in the range of 11.63 ± 0.55 for dry samples to 36.71 ± 1.21 g/kg for samples with 30% moisture content. The main elemental components of PM2.5 were K, Zn, Ca, Mg, and Na and K, Ca, Mg, and Na emission factors increased with the increase of moisture content of combustibles. The proportion of macronutrients in PM2.5 released by combustion of each herb increased as the moisture content increased, but the proportion of trace elements gradually decreased. There was a good correlation between elemental composition of PM2.5 and that of herbaceous combustibles. The results provide evidence that the moisture content of combustible materials has a significant effect on the emission of inorganic elements in particulate matter, and hence cautions should be exercised during fuel reduction treatments, such as early prescribed fire.

Concentration, Source, and Health Risk Assessment of PM1 Heavy Metals in Typical Pollution Processes in Zhengzhou

Heavy metal elements in particulate matter can cause adverse effects on human health, and the smaller the particle size, the greater the harm. A total of 16 heavy metal elements (Al, Si, K, Ca, V, Cr, Mn, Fe, Ni, Cu, Zn, As, Se, Ba, Pb, and Cd) in PM1 were continuously determined by an online heavy metal observation instrument in Zhengzhou city from January 7 to 25, 2021. The results showed that ρ(K) concentration was the highest during the observation period (0.62 μg·m-3). According to pollutant concentration and meteorological characteristics, the observation period was divided into clean days, dust days, and haze days. The contribution of heavy metal pollution characteristics and health risk assessment in atmospheric PM1 was different under different pollution processes. The US EPA health risk assessment method was used to assess the health risks of heavy metals, and the enrichment factor method and positive matrix factorization (PMF) were used to analyze the sources of heavy metals. The influence of the transmission was evaluated by using the concentration-weighted trajectory (CWT) method and the backward trajectory method. The results show that the enrichment factors of Zn, As, Se, Pb, and Cd were more than 100 under different pollution processes, which were greatly affected by human activities. During the sampling period, the main sources of heavy metals were industrial sources, coal/biomass sources, motor vehicle sources, and dust sources. The results of the health risk assessment were substituted into PMF analysis, and it was found that industrial sources were the main contributing sources of carcinogenic and non-carcinogenic health risks during cleaning days, dust days, and haze days, and the carcinogenic risk of heavy metal elements in PM1 in this region for adults exceeded that for children. CWT and backward trajectory methods revealed that regional transmission was one of the main factors affecting local health risks.

Human health risk assessment in opencast coal mines and coal-fired thermal power plants surrounding area due to inhalation

The study aimed to provide quantitative data on air pollution on people living in an industrial area of middle India. The twenty-four monitoring of nitrogen dioxide concentrations, sulfur dioxide, PM2.5 and PM10 was used to investigate people's exposure and health effects in the surrounding study area from January 2016 to December 2017. The particulate matter concentrations and associated elements in particulate matter were analyzed by gravimetric analysis and DBAAS, ICP-OES, Ion-Chromatography, Mercury analyzer, and CHNS analyzer.A risk level of metals in human health was occurring in the following decreasing order as Pb > Zn > Mn > Co > Cr > Ni > Hg > Cd > As, and risk level of metals in human health of carcinogenic and non-carcinogenic metals were observed to be lower than USEPA standard risk level of metals under acceptable level (10−6 year−1). The strongest association of metals areareare found for PM2.5 followed by PM10, with no indication of a threshold value for the health effects.

Quantification of Minor Chemical Elements in Particulate Matter Collected from In-Use Diesel Engine Passenger Vehicles by Laser-Induced Breakdown Spectroscopy

This research qualitatively and quantitatively characterises the minor chemical elements in diesel particulate matter (DPM). DPM was extracted from in-use diesel engine passenger vehicles of diverse types and models from major brand car producers in Europe. We analysed particulate matter extracted from the exhaust manifold part from passenger vehicles that are used in daily life environment. To qualitatively and quantitatively characterise the DPM, we employed the high-resolution Laser-Induced Breakdown Spectroscopy analytical technique (LIBS). Qualitative spectrochemical LIBS analyses confirmed the presence of minor chemical elements—silicon, nickel, titan, potassium, strontium, and molybdenum in DPM. For quantification of the LIBS signal, the calibration functions were constructed from internal calibration standards. Different concentrations of detected minor elements Si, Ni, Ti, K, Sr, and Mo were measured with respect to the type of complex particulate matter.

Geochemical insights into spatial and temporal evolution of sediment at catchment scale (Egoutier stream, France)

The transfer and storage of chemical elements in particulate matter are controlled by physical, chemical and biological processes. Their dynamics are well understood, especially in environments that show strong tectonic and/or geomorphic pressures, and are frequently reconstructed over centuries or decades to evaluate climate change effects for example. However, observations carried out at high spatial and temporal resolutions are less common, particularly in lowland areas. The present study aimed to better understand the links between earth surface processes, such as soil weathering and erosion, by combining pedology, geochemistry and hydrology at a small catchment scale. It focuses on the transfer of selected chemical elements (Ca, K, Ti, Fe, Mn, Rb and Sr) associated with particulate erosion and transport. The first (topsoil) and last (subsoil) soil horizons from different soil profiles and stream bed-load sediments of the Egoutier catchment (8 km2, Loiret, France) were studied. The objective was to investigate the relationship between the weathering and erosion processes. The soils are developed on ancient alluvium as evidenced by their physical and chemical properties, which clearly displayed a weathering profile from bedrock to topsoil layers. Ca, Fe and Rb showed migration dynamics from the topsoils to the subsoils, whereas Mn appeared immobilized within topsoils. Enrichments of all investigated elements increased in bed-load sediments. Topsoil erosion is the main source of sediment. However, Fe and Rb enrichments also highlight the remobilization of subsoils during periods of enhanced precipitation. Furthermore, Fe and Rb enrichments show a selective erosion of clay minerals. K and Sr contents evidence mineral break-up processes favoring mechanical erosion of all mineral phases. Moreover, their enrichments can be interpreted as the result of higher erosion rates and deposition during high rainfall events. The same conclusion can be drawn for Mn and Ca although their spatial variabilities depend on contributions from runoff in urban areas, as rainwaters from anthropized areas supply Ca mineral phases and diluted Mn depleted bearing phases from topsoil layers.

Qualitative and Quantitative Characterisation of Major Elements in Particulate Matter from In-use Diesel Engine Passenger Vehicles by LIBS

In this research we apply a high-resolution optical emission spectroscopy technique for spectrochemical analysis of collected diesel particulate matter. We use the laser-induced breakdown spectroscopy technique (LIBS) for qualitative and quantitative measurements of major chemical elements present in the particulate matter generated from different diesel engine passenger vehicles in use. The high-resolution LIBS technique can instantly measure major chemical elements within the diverse particulate matter matrices.

Exposure to ambient particulate matter elements and blood levels of gamma-glutamyl transferase (GGT) in a large Austrian cohort.

Exposure to ambient particulate matter elements and blood levels of gamma-glutamyl transferase (GGT) in a large Austrian cohort.

Pollution Characteristics and Potential Ecological Risks of Heavy Metals in Road Dust in Beijing

Based on the concentrations of 21 inorganic elements in particulate matter with diameters less than 10 μm (PM10) in 2004, and PM2.5 in 2004 and 2013 of representative road dust in Beijing, the pollution characteristics and potential ecological risks of heavy metals in this dust were analyzed and discussed. The results showed that the six main elements in road dust in Beijing were Si, Ca, Al, Fe, Mg, and K, and the proportions of the total content of the six elements in PM10 in 2004, PM2.5 in 2004, and PM2.5 in 2013 accounted for 96.51%, 96.42%, and 96.53% of the total content of all elements tested, respectively. The elemental enrichment level and the pollution degree and the potential ecological risk of heavy metal in road dust in Beijing in 2004 were PM2.5>PM10. Se, a characteristic element of coal dust, was highly enriched in PM2.5 in 2004, and Cd was high in PM10 and PM2.5 in 2004 with enrichment factors of 1024.03, 68.15, and 871.55, respectively. Co, Zn, Ca, and Cu were significantly enriched in PM10 and PM2.5 in 2004 with enrichment factors of 12.93, 12.33, 8.30, and 8.07 in PM10 and 17.41, 21.80, 12.83, and 19.73 in PM2.5, respectively; Na and Si were not enriched in the road dust. The pollution load index (PLI) of heavy metals was 3.95 in PM10 and 7.71 in PM2.5 in 2004. Owing to the implementation of dust, motor vehicles, and combustion source control measures in Beijing and the relocation of the Shougang corporation, the elemental enrichment level, pollution degree, and potential ecological risk of heavy metals in road dust PM2.5 in 2013 were significantly lower than those in 2004. The enrichment factors of Cd and Se in PM2.5 in 2013 decreased to 98.47 and 0.95, respectively; those of Cu, Ca, and Zn decreased to 11.90, 8.84, and 8.20, respectively; and PLI decreased to 2.56. The results showed that the total potential ecological risk of heavy metals in road dust in Beijing was extremely strong. Heavy metal Cd was the most significant pollution factor and the main potential ecological risk source; its potential ecological risk index (RI) contribution to the total RI of heavy metals was more than 85%. In 2004, the pollution degree of heavy metals in road dust of main roads was significantly higher than that for other road types. The pollution degree of heavy metals in PM10 was main road > expressway entrance to Beijing > secondary main road > ring road; that for PM2.5 was main road > ring road > expressway entrance to Beijing > secondary main road. For PM2.5 in 2013, however, the order was expressway entrance to Beijing > main road > ring road > secondary main road. The pollution degree of heavy metals in road dust of secondary main roads was significantly lower than that for other road types. In 2013, for road dust PM2.5 in Beijing, the correlation of heavy metals Ti, Zn, V, Cr, Cu, Pb, and Ni was significant owing mainly to traffic-related emissions.

A comparative chemical study of PM10 in three Latin American cities: Lima, Medellín, and São Paulo

The study was part of the South American Emissions, Megacities and Climate Project (SAEMC). The objective was to identify and quantify organic and elemental carbon (OC and EC), monosaccharides, polycyclic aromatic hydrocarbons (PAHs), oxy and nitro-PAHs, water-soluble ions (WSI), and elements in particulate matter collected in intensive campaigns during a period (June, 2010) in Sao Paulo (Brazil), Lima (Peru), and Medellin (Colombia). PM10 concentration was higher in Sao Paulo than in the other two sites and 75% of the samples had concentrations above the World Health Organization (WHO) guideline. High concentrations of levoglucosan, a biomass burning tracer, highlighted the importance of this source in the Brazilian megacity. Levoglucosan-to-mannosan ratios for Sao Paulo suggested sugarcane burning, which in 2010 occurred in 70% of the state municipalities during harvest. Vehicular-related elements (Fe and Cu) had higher concentrations in Sao Paulo. As and Pb in Medellin were attributed to industrial emissions. Ni in Lima was associated with emissions from metal smelting facilities and ship heavy oil combustion. Higher total PAH concentrations and benzo[a]pyrene equivalent (BaPE) index in Sao Paulo indicated a stronger influence of vehicular exhaust in this megacity. The results highlighted the importance of biomass burning and vehicular sources for Sao Paulo, vehicular exhaust, biomass burning, and industrial sources for Medellin, and marine aerosol, together with vehicular, industrial, and ship exhaust, for Lima.

High-resolution sampling and analysis of ambient particulate matter in the Pearl River Delta region of southern China: source apportionment and health risk implications

Abstract. Hazardous air pollutants, such as trace elements in particulate matter (PM), are known or highly suspected to cause detrimental effects on human health. To understand the sources and associated risks of PM to human health, hourly time-integrated major trace elements in size-segregated coarse (PM2.5–10) and fine (PM2.5) particulate matter were collected at the industrial city of Foshan in the Pearl River Delta region, China. Receptor modeling of the data set by positive matrix factorization (PMF) was used to identify six sources contributing to PM2.5 and PM10 concentrations at the site. Dominant sources included industrial coal combustion, secondary inorganic aerosol, motor vehicles and construction dust along with two intermittent sources (biomass combustion and marine aerosol). The biomass combustion source was found to be a significant contributor to peak PM2.5 episodes along with motor vehicles and industrial coal combustion. Conditional probability function (CPF) analysis was applied to estimate the source locations using the PMF-resolved source contribution coupled with the surface wind direction data. Health exposure risk of hazardous trace elements (Pb, As, Si, Cr, Mn and Ni) and source-specific values were estimated. The total hazard quotient (HQ) of PM2.5 was 2.09, higher than the acceptable limit (HQ = 1). The total carcinogenic risk (CR) was 3.37 × 10−3 for PM2.5, which was 3 times higher than the least stringent limit (1.0 × 10−4). Among the selected trace elements, As and Pb posed the highest non-carcinogenic and carcinogenic risks to human health, respectively. In addition, our results show that the industrial coal combustion source is the dominant non-carcinogenic and carcinogenic risk contributor, highlighting the need for stringent control of this source. This study provides new insight for policy makers to prioritize sources in air quality management and health risk reduction.

Assessment of trace elements characteristics and human health risk of exposure to ambient PM2.5 in Hangzhou, China

ABSTRACTA method for simultaneously determining the trace elements in particulate matter (PM) (PM2.5) by inductively coupled plasma mass spectrometry was established. The PM2.5-loaded filter samples were digested under the optimised conditions including a mixture of HNO3–HCl–HF with ultrasonication proceeding at 70°C for 2 h. Recoveries of 90.83–103.33% were achieved for 20 elements (Co, Sr, Ag, Cd, Sb, La, Ce, Sm, W etc.) in NIST standard reference material 1648a (urban PM). PM2.5 samples were collected at urban site in Hangzhou from August 2015 to November 2015. PM2.5 concentrations of 15% sampling days exceeded the daily limitation and the mean concentrations of PM2.5 from August to November reached the 66.4% of the limitation. PM2.5 concentrations in summer were higher than that in autumn. The concentration of Zn was highest, following with Al, Pb, Mn, Cu and As. Significant enrichment was observed in Mn, Zn, Pb, Ag, V, Ni, Cu, As, Se, Hg, Co, Cd and W, which was probably induced by vehicular exhaust, oil and residual fuel combustion and industrial emissions. The daily mass concentrations of PM2.5 and elements fluctuated significantly. Rainfall could significantly reduce the concentration of Ti, Mn, Cu, Zn, As, Se, Hg, Sr, Ag, Cd, Sb, La, Ce, Sm and Pb, and the risk levels of carcinogenic elements and non-carcinogenic elements in rain day were significantly lower (43.7–81.4%) than those in non-rain day. The risk levels of Co, Cd and As could lead to adverse health outcomes through the respiratory system, which should deserve more attention, while the risk levels of Ni and non-carcinogenic elements (Hg, Mn, Cu, Zn, Pb, V) were under average risk acceptance.

Determination of Platinum Group Elements in Particulate Matter by Inductively Coupled Plasma Mass Spectrometry

This study examined a method for determination of rhodium (Rh), palladium (Pd) and platinum (Pt) in particulate matter using standard solutions, model samples and certified reference materials (NIST 1648a and ERM CZ120). The method was based on microwave digestion followed by inductively coupled plasma mass spectrometry (ICP-MS). The results showed that the stability of the standard solution mixture of Rh, Pd and Pt was better when chlorides were present in the solution. A membrane filter and one type of quartz filter were the most adequate for analyzing platinum group elements (PGE). Respective limits of detection for Rh, Pd and Pt were 0.028, 0.503 and 0.0265pg/m3 with a membrane filter and 0.478, 4.530 and 0.070pg/m3 for one type of quartz filters. The sample matrix had no significant effects on the determination of three PGEs.

Effect of additives on particulate matter formation of solid biofuel blends from wood and straw

The combustion of solid biofuels is characterized by the formation of particulate matter emissions harmful to humans and the environment. Inorganic elements which are volatile under high temperatures (∼600–1200 °C) are emitted as vapor, then cooling down in the flue gas, and are re-sublimated and emitted as solid particulate matter emissions (fly ash). Thus, the objective of this paper is it to summarize the current knowledge of the forming mechanism of these particulate matter emissions taking place during the combustion of wood and straw, and bring the elements in particulate matter with the help of additive in a stable solid phase, so they stay in the bottom ash and are not emitted. Here, two different additives are tested, based on Al, Mg and Ca. Important in this respect is the knowledge of the chemical formations during the combustion process of the different ash-forming elements contained within solid biofuels. Therefore, the chemical binding forms of the ash-forming elements (Si, Al, Fe, Ca, Mg, Mn, Na, K, P, S, and Cl) within the solid biofuel are presented. Based on this, possible conversion products are discussed including theoretical calculated intermediates; this includes the chemical conversion pathway. On this basis, additives are identified based on the difference of the elemental composition of wood/straw blends to wood and the results of the formation of particulate matter during combustion are assessed in lab scale. The additives are composed of Al2O3, CaHPO4, and CaCO3 or Al2O3, MgHPO4, and MgCO3. The results from the characterization techniques TGA, AAS, IC, and XRD show that the formation of particulate matter during a complete thermo-chemical conversion can be suppressed to certain extend.

Trace elements in particulate matter from metropolitan regions of Northern China: Sources, concentrations and size distributions

Public concerns over airborne trace elements (TEs) in metropolitan areas are increasing, but long-term and multi-site observations of size-resolved aerosol TEs in China are still lacking. Here, we identify highly elevated levels of atmospheric TEs in megacities and industrial sites in a Beijing–Tianjin–Hebei urban agglomeration relative to background areas, with the annual mean values of As, Pb, Ni, Cd and Mn exceeding the acceptable limits of the World Health Organization. Despite the spatial variability in concentrations, the size distribution pattern of each trace element was quite similar across the region. Crustal elements of Al and Fe were mainly found in coarse particles (2.1–9μm), whereas the main fraction of toxic metals, such as Cu, Zn, As, Se, Cd and Pb, was found in submicron particles (<1.1μm). These toxic metals were enriched by over 100-fold relative to the Earth's crust. The size distributions of Na, Mg, K, Ca, V, Cr, Mn, Ni, Mo and Ba were bimodal, with two peaks at 0.43–0.65μm and 4.7–5.8μm. The combination of the size distribution information, principal component analysis and air mass back trajectory model offered a robust technique for distinguishing the main sources for airborne TEs, e.g., soil dust, fossil fuel combustion and industrial emissions, at different sites. In addition, higher elemental concentrations coincided with westerly flow, indicating that polluted soil and fugitive dust were major sources of TEs on the regional scale. However, the contribution of coal burning, iron industry/oil combustion and non–ferrous smelters to atmospheric metal pollution in Northern China should be given more attention. Considering that the concentrations of heavy metals associated with fine particles in the target region were significantly higher than those in other Asian sites, the implementations of strict environmental standards in China are required to reduce the amounts of these hazardous pollutants released into the atmosphere.

Trace elements in particulate matter of ambient air at petroleum filling stations

Size segregated suspended particulate matter (PM2.5 and PM10-2.5) in air at four major petroleum-filling stations in Ile-Ife, Nigeria, were monitored using double staged “Gent” stacked samplers to assess variations in mass loads and elemental concentrations of 25 elements. Na, Mg, Al, Si, P, S, Cl, K, Ca, Ti, V, Cr, Mn, Fe, Ni, Cu, Zn, Br, Rb, Sr, Zr, Cs, Ta, W, and Pb were determined in both fractions by external ion beam proton-induced X-ray emission technique. Enrichment factors and pollution indices were calculated and results revealed that most elements were anthropogenic in both fractions with concentrations exceeding the World Health Organization guideline standards.

Characterization and Cytotoxicity of PM

Background: The potential impact of municipal solid waste incineration (MSWI), which is an anthropogenic source of aerosol emissions, is of great public health concern. This study investigated the characterization and cytotoxic effects of ambient ultrafine particles (PM<0.2), fine particles (PM0.2–2.5) and coarse particles (PM2.5–10) collected around a municipal solid waste incineration (MSWI) plant in the Pudong district of Shanghai. Methods: Mass concentrations of trace elements in particulate matter (PM) samples were determined using ICP-MS (Inductively Coupled Plasma Mass Spectrometry). The cytotoxicity of sampled atmospheric PM was evaluated by cell viability and reactive oxygen species (ROS) levels in A549 cells. Result: The mass percentage of PM0.2–2.5 accounted for 72.91% of the total mass of PM. Crustal metals (Mg, Al, and Ti) were abundant in the coarse particles, while the anthropogenic elements (V, Ni, Cu, Zn, Cd, and Pb) were dominant in the fine particles. The enrichment factors of Zn, Cd and Pb in the fine and ultrafine particles were extremely high (>100). The cytotoxicity of the size-resolved particles was in the order of coarse particles < fine particles < ultrafine particles. Conclusions: Fine particles dominated the MSWI ambient particles. Emissions from the MSWI could bring contamination of anthropogenic elements (Zn, Cd and Pb) into ambient environment. The PM around the MSWI plant displayed an additive toxic effect, and the ultrafine and fine particles possessed higher biological toxicity than the coarse particles.

Trace elements pollution and toxicity of airborne PM10 in a coal industrial city

Trace elements in particulate matter associated with coal industries hold high risk to human health. Understanding the contents and occurrences of modes of these elements as well as their contribution to particulate toxicity is significant both environmentally and pathologically. A total of 24 PM10 samples were collected in Pingdingshan City, a coal industrial city in North China, in both winter and summer of 2008. An inductively coupled plasma mass spectrometry (ICP–MS) was used to determine the concentrations of 12 trace elements associated with coal industries (Cr, Ni, Cu, Zn, As, Mo, Cd, Sn, Sb, Tl, Pb, and Bi) in PM10 samples. The results indicated that the trace element concentrations were higher in winter than in summer; due mainly to more coal combustion during winter and to the different meteorological conditions of these two seasons. The soluble proportions of these trace elements compared with total values of intact whole samples were higher in winter than in summer, and this difference was attributed mainly to more SO2 reacting with pre–existing particles to form soluble particles in winter. Of all the analyzed elements, Ni, Tl, Sb, Mo, and Cd occurred mainly in the soluble state (>50% in the soluble fraction), Cr, Cu, Zn, and As occurred in both the soluble and insoluble state (20% to 50% in the soluble fraction), and Sn, Pb, and Bi occurred mainly in the insoluble state (<20% in the soluble fraction). A plasmid DNA assay indicated that winter samples had higher toxicity than summer samples. The correlation of PM10 toxicity (TD50 value) with the contribution of various trace elements to DNA damage (trace element concentration) was further analyzed, and the results indicated that PM10 toxicity was caused mainly by the soluble fractions of trace elements, including those of Ni, Pb, Cu, Cd, As, Zn, Cr, and Tl, which were the major toxic trace elements in Pingdingshan PM10.