Chia-Hsiang Lai*a,
Chia-Hua Linb,
Chang-Chun Liaoc,
Kuen-Yuan Chuangd and
Yen-Ping Penge
aDepartment of Safety Health and Environmental Engineering, Central Taiwan University of Science and Technology, Taichung, Taiwan. E-mail: chlai2@ctust.edu.tw; Tel: +8864-22391647
bDepartment of Biotechnology, National Formosa University, Yunlin, 63208, Taiwan
cInstitute of Safety Health and Environmental Engineering, Central Taiwan University of Science and Technology, Taichung, Taiwan
dDepartment of Safety Health and Environmental Engineering, Central Taiwan University of Science and Technology, Taichung, Taiwan
eDepartment of Environmental Science and Engineering, Tung Hai University, Taichung, Taiwan
First published on 15th January 2018
The health and environmental effects of metal-containing carbon black (CB) particles emitted from a CB feeding area near a tire manufacturing plant were investigated. The mass ratios of PM1 and PM0.1 (UFPs) relative to TSP were 13.84% ± 4.88% and 50.84% ± 4.29%, respectively. The most abundant elements in all fractions were Fe, Al, and Zn. The mean percentage contributions of Al, Fe, Zn, Cu, and Co to the coarse particles ranged from 49.1% to 69.1%, thus indicating that the Al, Fe, and Zn contents in the CB particles were affected by workplace emissions. The ratios of the total mean deposition fluxes of atmospheric particle-bound heavy metals in the human respiratory tracts of workers/adults, workers/children, and adults/children were approximately 5.5, 11.0, and 2.0, respectively. The integrated risks of five elements via two exposure pathways to adults and children were 1.1 × 10−4 and 1.7 × 10−5, respectively; these numbers reflect the high cumulative carcinogenic risk posed by these toxic metals to local residents (both adults and children; limit, 10−6). These results demonstrate the potential health risk presented by particle-bound heavy metals to humans residing near tire manufacturing plants via inhalation and dermal contact exposure.
CB is poorly soluble and nano-sized.4 The increased biological potency of ultrafine particles is related to the content of redox cycling organic chemicals and their ability to damage mitochondria.8 Besides increasing reactive oxygen species, nano-sized CB causes loss of cell viability in endothelial cells and promotes adhesion of monocytes, both of which accelerate the development of atherosclerosis.9 CB aggregates cause endothelial dysfunction by activating ROCK.10,11 Moreover, trace elements (Ca, Cu, Fe, Mn, K, Pb, As, Cr, Se, and Zn) have been found in samples of CB.12 Cd, Cr and Pb are known to cause deleterious effects on human health.13 Arsenic (As) can cause serious disturbances of cardiovascular and central nervous system.14 Long-term exposure to Pb may lead to memory deterioration, prolonged reaction times and reduced ability to understand. Dietary Cr intakes were assumed to be directly correlated with breast cancer mortalities.15 Although CB is known to typically contain large quantities of elemental carbon and PAHs, some toxic components of the material, e.g., metals, are not widely discussed. CB is emitted during industrial manufacturing, and the particles are deposited in the human respiratory tract by breathing and exposure to polluted environments. As the specific effects of the size distributions of metal-containing CB particles on workers and residents in tire manufacturing plants and the surrounding areas are not known, analyzing the hazards and risks of exposure to different sizes of metal-containing particles is an important and novel research topic.
The objective of this study is to collect and analyze size-segregated suspended particle samples for the presence of heavy metals. Respiration and dermal contact are regarded as significant intake pathways of human exposure to heavy metals. The CB feeding and surrounding areas of a tire manufacturing plant were selected as sampling sites, and the size distributions of heavy metals were characterized and used to estimate deposition fluxes in the human respiratory system via a model developed by the International Commission on Radiological Protection (ICRP). Finally, the carcinogenic effects of exposure to heavy metal-containing particles through inhalation and dermal contact were evaluated.
In this study, the sampled particles were collected from the feeding and surrounding area simultaneously during the feeding process. Atmospheric particles were collected at two sampling sites for 20 days in March and April 2016 using a 12-stage micro-orifice uniform deposit impactor (MOUDI II, model M110-R). Sampling was carried out at a flow rate of 30 L min−1 and air particulate samples of different size fractions were collected from each sampling site over 24 h. Four hundred and eighty air samples were collected. The Central Taiwan's weather station located at approximately 1.5 km toward north–northwest (NNW) of the sampling site provides meteorological parameters including pressure, temperature, wind speed, wind direction, and relative humidity (RH). The mean pressure was 1012.44 ± 2.57 (hPa), mean temperature was 22.34 ± 3.40 °C, mean RH was 83.62 ± 7.31%, and prevailing wind direction was northwest (NW) during the sampling periods. The sampling site was located downwind of CB-emitting source in surrounding area. The 50% cut off diameters (D50) of the MOUDI stages were 10.0, 5.6, 3.2, 1.8, 1.0, 0.56, 0.32, 0.18, 0.10, and 0.056 μm and included inlet (18 μm) and exit (<0.056 μm) stages. Size-segregated particles were classified as coarse (aerodynamic diameter > 1.8 μm) and ultrafine (aerodynamic diameter < 0.1 μm). The distance between the sampling site and the CB feeding area was approximately 2 m. Another sampling site representing the surrounding area was located near a fence about 15 m from the factory building. Several farmlands and irrigation rivers of agricultural land are affected by CB emissions near the tire manufacturing plant. The inlet of the MOUDI sampler place in the CB feeding area was set 1.5 m high from the ground. Ambient air samples of the surrounding area were also collected from the roof of a building located near the factory fence at a height of about 3 m above ground level. A total of 240 particle samples (20 samples containing 12 size fractions) were collected from every sampling site. Mixed cellulose ester (MCE) membrane filters (Advantec MFS Inc., 47 mm diameter, 0.45 μm pore size) were used as the substrate in all stages of collection the MOUDI sampler. Both blank and loaded MCE substrates were conditioned for 24 h by maintaining a humidity of 40% ± 5% and temperature of 25 ± 2 °C to equilibrate before and after each sampling. A laboratory standard weight of 10 mg was measured before, during, and after each weighing session to ensure accuracy of the weight measurements. Each filter was weighed on an electrical balance with a sensitivity of 10 μg, and the suspended particulate matter (PM) concentration was determined by dividing the particle mass by the volume of the sampled air. Fig. 1 shows a flowchart of the sampling and analysis procedures.
Step 1: Each filter was placed in a 100 mL Teflon microwave digestion vessel with 10 mL of a mixture of concentrated HNO3 (70%, trace metal grade) and de-ionized water at a volume ratio of 1:1 in preparation for microwave digestion.
Step 2: The microwave temperature was increased from room temperature to 200 °C over 6.5 min.
Step 3: The temperature was maintained at 200 °C for another 10 min.
Step 4: The samples were cooled for 20 min, and the digested solution was diluted to 20 mL using 20% HNO3 in de-ionized water. The resulting diluted solution was used for metal analysis.
Calibration was performed using multi-element (metal) standards (i.e., certified reference materials) in a 20% (v/v) HNO3 solution. The detection limit of the ICP-OES instrument for the 13 metals was 0.91–3.52 ng m−3. Field and laboratory blank samples were subjected to the same analytical procedure as the samples that were regularly analyzed, and sample data were corrected by subtraction of the filter blanks. This study measured recoveries with one medium blank and two spiked medium blanks per 20 samples. Recovery efficiencies were determined by performing the same experimental procedures using solutions containing known metal concentrations as samples. The recovery values of the metals ranged from 91.1% to 98.5%.
(1) |
(2) |
(3) |
(4) |
DFT = ∑(DFi × Ci) × V | (5) |
The health risk presented by metal inhalation to persons working in the CB feeding area was evaluated by quantifying the risk of developing cancer using a probabilistic approach. This study adopted the inhalation exposure model of the United States Environmental Protection Agency (US-EPA) baseline risk assessment approach.19 The EPA Integrated Risk Information Database and International Agency for Research on Cancer classify pollutants as carcinogens. This investigation found that Cr, Ni, Cd, and As are carcinogenic and could affect the human immune system through the respiratory system. The average daily exposure dose of metallic particles through inhalation (ADDinh) and dermal contact (ADDderm) were calculated using the following equations:16,20
(6) |
(7) |
Cancer risk (CR) estimates were compared with carcinogenic regulatory levels of concern, i.e., 10−6 to 10−4. Health risk can be quantified using the following equation:
CR = ADD × SF | (8) |
Aerodynamic diameter (μm) | Surrounding area | CB feeding workplace |
---|---|---|
>18 | 8.29 ± 4.92 | 250.33 ± 170.02 |
10–18 | 7.77 ± 4.49 | 72.18 ± 36.65 |
5.6–10 | 8.72 ± 4.61 | 184.27 ± 108.56 |
3.2–5.6 | 9.48 ± 4.96 | 166.85 ± 70.80 |
1.8–3.2 | 8.91 ± 4.18 | 83.53 ± 36.62 |
1.0–1.8 | 9.49 ± 4.86 | 49.49 ± 19.08 |
0.56–1.0 | 14.20 ± 9.11 | 44.26 ± 24.36 |
0.32–0.56 | 9.64 ± 5.23 | 24.43 ± 8.88 |
0.18–0.32 | 9.25 ± 4.06 | 27.08 ± 9.83 |
0.1–0.18 | 7.17 ± 3.93 | 23.34 ± 8.03 |
0.056–0.1 | 6.28 ± 3.46 | 9.70 ± 5.84 |
<0.056 | 8.47 ± 5.45 | 9.31 ± 3.59 |
Total | 107.66 ± 54.43 | 944.76 ± 456.36 |
PM10 (PM10/TSP) | 91.59 ± 45.66 (85.36 ± 2.48%) | 622.24 ± 268.49 (68.10 ± 7.60%) |
PM1 (PM1/TSP) | 54.99 ± 28.06 (50.84 ± 4.29%) | 138.11 ± 53.33 (16.91 ± 7.45%) |
UFPs (UFPs/TSP) | 14.74 ± 8.01 (13.84 ± 4.88%) | 19.01 ± 7.02 (2.67 ± 1.92%) |
MMD (μm) | 0.56 ± 0.11 | 2.28 ± 0.61 |
Differences in particle mass and size distributions between the surrounding and CB feeding areas were compared. Table 1 shows that the UFPs/TSP and PM1/TSP ratios in the CB feeding area were 2.67% ± 1.92% and 16.91% ± 7.45%, respectively. The mass ratio of particles sized below 1 μm in the CB feeding area was significantly less than that in the surrounding area. However, the PM1 mass was distributed over more than 50% of the surrounding area, which suggests that the total mass of airborne particles is still incorporated with the submicron particles in this study.
Metals | Surrounding area | CB feeding process | ||
---|---|---|---|---|
Concentration (ng m−3) | Weight percentage (%) | Concentration (ng m−3) | Weight percentage (%) | |
Al | 224.2 ± 186.4 | 19.9 ± 8.6 | 3113.3 ± 2017.1 | 23.3 ± 4.6 |
Cd | 4.8 ± 1.3 | 0.5 ± 0.3 | 30.5 ± 17.1 | 0.4 ± 0.3 |
Co | 2.6 ± 1.4 | 0.3 ± 0.1 | 58.8 ± 37.5 | 0.8 ± 0.6 |
Cr | 33.8 ± 5.3 | 3.6 ± 1.1 | 74.5 ± 27.1 | 1.0 ± 0.9 |
Cu | 10.7 ± 7.9 | 0.9 ± 0.5 | 53.2 ± 20.9 | 0.7 ± 0.6 |
Fe | 403.2 ± 137.9 | 39.2 ± 6.9 | 1519.1 ± 875.0 | 11.0 ± 1.2 |
Ga | 30.9 ± 6.6 | 3.2 ± 1.2 | 94.6 ± 23.7 | 1.2 ± 1.0 |
In | 7.1 ± 3.7 | 0.7 ± 0.3 | 12.6 ± 10.7 | 0.2 ± 0.1 |
Mn | 24.2 ± 10.2 | 2.6 ± 1.3 | 87.0 ± 37.2 | 0.8 ± 0.4 |
Ni | 18.5 ± 7.7 | 1.9 ± 0.9 | 31.5 ± 20.0 | 0.3 ± 0.2 |
Pb | 50.0 ± 21.9 | 4.9 ± 1.2 | 112.1 ± 38.8 | 1.0 ± 0.5 |
Sr | 20.9 ± 7.1 | 2.1 ± 0.9 | 190.3 ± 27.1 | 2.1 ± 1.9 |
Zn | 203.5 ± 75.9 | 20.2 ± 6.9 | 8622.0 ± 5679.0 | 57.3 ± 10.4 |
Total | 1034.3 ± 355.8 | 13999.6 ± 8362.4 |
The most abundant elements (Fe, Al, and Zn) in all fractions in the surrounding area were similar to those in the CB feeding area. The abundance of these three metal elements is believed to be influenced by CB feeding emissions. Fe, not Zn, was the most abundant metal relative to the total metal concentration in the surrounding area. Individual metal elements are affected to an appreciable extent by other pollution sources. Heavy-duty diesel vehicles and forklift trucks are operated near the tire factory fence, causing increases in Fe concentration in the surrounding area. Previous studies have indicated that Fe could be emitted by both exhaust (diesel emissions)25,26 and non-exhaust (brake wear and road dust)24,27 traffic sources. Diesel exhaust is the most important traffic-related nanoparticle source.28 Table 3(a) indicates that Al, Cu, Fe, and Pb are the most abundant metallic elements in UFPs in the surrounding area. These metals (Al, Cu, and Fe) are mainly associated with diesel sources.25,26 To obtain further information of the main Pb source in the surrounding area, we applied partial correlation to measure the degree of association between two random variables (Fe, Pb, and Cu) with the effect of a set of controlling random variables removed (Al); the results of this analysis are shown in Table 3(b). Analysis indicated that Fe and Cu were highly correlated with each other (0.81, p < 0.05) and that Pb was lowly negatively correlated with Fe and Cu (−0.43 and −0.24, respectively; p > 0.05). These results reveal that Pb in UFPs is not likely emitted by CB feeding or traffic sources. By contrast, other metals (e.g., Al, Fe, and Zn) in UFPs in the surrounding area could be associated with tire manufacturing plant emissions.
(a) Spearman correlation | |||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Al | Fe | Zn | Sr | Cu | Mn | Ni | Pb | Cd | Co | Cr | Ga | In | |
a *significant level (p < 0.05, two-tailed); **significant level (p < 0.01, two-tailed). | |||||||||||||
Al | 1 | ||||||||||||
Fe | 0.82** | 1 | |||||||||||
Zn | 1.00 | ||||||||||||
Sr | 1.00 | ||||||||||||
Cu | 0.87** | 0.94** | 1.00 | ||||||||||
Mn | 1.00 | ||||||||||||
Ni | 0.76** | 1.00 | |||||||||||
Pb | 0.91** | 0.65* | 0.74** | 1.00 | |||||||||
Cd | 0.63* | 0.68* | 1.00 | ||||||||||
Co | 0.71* | 0.79** | 1.00 | ||||||||||
Cr | 0.62* | 1.00 | |||||||||||
Ga | 0.61* | 0.65* | 0.64* | 1.00 | |||||||||
In | 0.85 | 0.70 | 1 |
(b) Particle correlation: control variable (Al) | |||
---|---|---|---|
Fe | Pb | Cu | |
Fe | 1 | ||
Pb | −0.43 | 1 | |
Cu | 0.81** | −0.24 | 11 |
Fig. 2 shows the mean normalized size distributions of total metal concentrations in the atmosphere of the CB feeding and surrounding areas; a unimodal distribution located at 5.6–10 μm was observed at the two sites. The mass median diameter (MMD) of the total metal concentrations in the surrounding and CB feeding areas were 1.21 ± 0.41 μm and 2.05 ± 0.79 μm, respectively, which suggests that the airborne total metals in these sites were incorporated in submicron and fine particles, respectively. Fig. 3 shows the mean normalized size distributions of individual metal concentrations in surrounding areas. Fig. 3(a) and (b) show that Al, Mn, and Cu have a unimodal distribution, exhibiting a major peak at 3.2, 0.18, and 5.6 μm, respectively. Fig. 3(a) shows that Al and Fe, exhibiting a major peak at 3.2 μm, are the most abundant metals in the surrounding area. On the contrary, Fig. 3(c) shows that the other metals do not have significant variances in particle-size distributions in the surrounding area. Although the exposure hazard of submicron-sized particles for residents was higher than that of fine particles for workers, long-term inhalation of high toxic metal levels in the CB feeding area may lead to adverse health effects among workers. Assessment of the CR presented by carcinogenic metals is discussed later in this study.
Fig. 2 Size distributions of total particle-bound heavy metals in the ambient air of the CB feeding and surrounding areas. (a) CB feeding workplace. (b) Surrounding area. |
Fig. 3 Size distributions of individual particle-bound heavy metals in the ambient air of surrounding areas. |
Fig. 4 Dendrogram results of the Ward method of hierarchical cluster analysis of 13 elements in the (a) CB feeding and (b) surrounding areas. |
Fig. 5(a) and (b) respectively illustrate the total relative contents of metals in particles sampled at the CB feeding and surrounding areas. Fig. 5(a) shows that the Al, Fe, and Zn metal contents in coarse particles (49.1–62.0%) contributed the most to the total PM content, followed by those in PM0.1–1.8 (23.2–36.8%) and UFPs (14.5–32.5%). Other metal contents were distributed mainly in UFPs (46.3–67.7%), thus demonstrating that UFPs pose greater adverse health effects than larger particles per unit mass in the CB feeding area. Since no other raw materials were fed in the workshop, the metal contents of the collected particles clearly represent the characteristics of raw CB nanoparticles.
Fig. 5 Triangular diagrams showing heavy metal speciation in different particle sizes: (a) carbon black feeding and (b) surrounding areas. |
Fig. 5(b) shows that the mean percentage contributions of Al, Fe, Zn, Cu, and Co in the coarse particles ranged from 49.1% to 69.1%, thus indicating that the content contributions of Al, Fe, and Zn to coarse particles were affected by CB feeding area emissions. Although Cu and Co may be emitted by crustal elements, the results of the present study suggest that most of the Cu in the coarse particles comes from the road dust of the surrounding area. Road dust contains dust from the brakes and tires of vehicles. The average mass median diameters of brake dust range from 0.62 μm to 2.49 μm.32 The Cu content of brake dust has been recognized to be a significant pollutant,24,33 contributing 47% of the total Cu load in urban runoff.24,34 Cu is used to control heat transport.35 A large amount of Mn, which probably comes from the fumes produced during manual metal arc welding in the tire plant, was observed in PM0.1–1.8 (67.8%). The diameters of most of the particles found in emitted welding fumes range from 0.56 μm to 0.1 μm.36 Besides Fe, Cr, and Ni, welding fumes contain high concentrations of Mn and Zn.37 Some combinations of multiple elements have been found to be specific to particular sources or process, thereby enabling these particle classes to be used as markers.38 However, most of the toxic metals found in PM0.1–1.8 were observed in the surrounding atmosphere of the tire manufacturing plant.
To assess the health risk posed by toxic metals in the ambient air of surrounding areas to residents (both adults and children), the carcinogenic effects of toxic metals via the major exposure pathways of inhalation and dermal contact were estimated. The CRs of toxic metals in the total PM presented by these two exposure pathways are shown in Fig. 7. The dermal contact CR of the ambient air of the surrounding area was highest for Co (3.3 × 10−5), followed by Cd (2.9 × 10−5) and Cr (2.3 × 10−5) for adults. The mean dermal contact CR of five elements for adults was approximately 10 times higher than that for children. Means inhalation of the CR presented by Cd, Co, Cr, Ni, and Pb as determined by the ICRP model. Among the CRs determined, the CR presented by Cd inhalation of the total PM for adults and children was the highest, followed by those of Co and Ni. Because the inhalation rates of the total PM in the respiratory tract were not 100%, the CR presented by dermal contact was higher than that presented by inhalation. These results are consistent with those of other studies.39–43 The CRs presented by inhalation for children were higher than those for adults. The CR of Cd inhalation for adults and children and that of Co inhalation for children exceeded the 10−6 benchmark level. The integrated risks presented by five elements via two exposure pathways to adults and children were 1.1 × 10−4 and 1.7 × 10−5, respectively, thus demonstrating the high cumulative CR posed by these metals to local residents (both adults and children).
Toxic metals have attracted growing attention in urban cities near industrial plants because of the effects of PM on public health. The daily intakes of toxic constituents via ingestion, dermal contact, and inhalation have been calculated, and, among the three pathways, the respiratory system was found to provide the easiest exposure route. The adverse effects of inhaled toxic metals can be widely found in previous publications that used 75% penetration levels to assess fractions containing high concentrations of total particle-bound contaminants penetrating the lungs.16,44–46 In this study, the majority (59.02% ± 35.58%) of the deposition amounts among residents was observed in the HA; only 2.68% ± 0.32% and 7.02% ± 0.49% of the total particles were deposited in the TB and AR, respectively (Table 4). The mean total portions deposited in the respiratory tract of residents and workers were 88.24% and 82.56%, respectively. A similar trend was observed in the e-waste recycling zone. The results of the present study suggest that the inhalable fraction deposited into the AR was much lower than the empirical value of 75%. Therefore, assessments based on total contaminants could show overestimated exposure risks.
Site | HA | TB | AR |
---|---|---|---|
Surrounding area | 59.02 ± 35.58 | 2.68 ± 0.32 | 7.02 ± 0.49 |
Workplace | 73.22 ± 2.59 | 2.49 ± 0.29 | 5.19 ± 1.13 |
The ICRP model used in the current study presents a number of limitations, such as underestimation of the deposition of ultrafine particles in the lower human respiratory tract47 and ignorance of the presence and commensurate effects of naturally occurring structural elements of the lungs (e.g., cartilaginous rings, carinal ridges), which have been demonstrated to affect the motion of inhaled air.48 While these limitations could affect the assessment of CRs, the results still provide important insights into novel protection strategies associated with exposure to particle-bound metals.
This journal is © The Royal Society of Chemistry 2018 |