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Journal of Environmental Health Science and Engineering logoLink to Journal of Environmental Health Science and Engineering
. 2021 Sep 29;19(2):1817–1826. doi: 10.1007/s40201-021-00737-3

Identification of microplastics in conventional drinking water treatment plants in Tehran, Iran

Danial Adib 1, Roya Mafigholami 1,, Hossein Tabeshkia 1
PMCID: PMC8617154  PMID: 34900309

Abstract

The presence of microplastics (MPs), as an emerging pollutant is a growing concern in drinking water, yet most of the studies have been carried out in surface waters and wastewater treatment plants and there are few studies on MPs in drinking water treatment plants (DWTPs). This study investigates these particles in three different conventional DWTPs in the city of Tehran, Iran, and aims to analyze these particles down to the size of 1 µm. A scanning electron microscope was utilized in this study to quantitatively analyze MPs. Accordingly, the average abundance of MPs in raw and treated water samples varied from 1996 ± 268 to 2808 ± 80 MPs L−1 and 971 ± 103 to 1401 ± 86 MPs L−1, respectively. While particles smaller than 10 µm comprised 65–87% of MPs. Moreover, µ-Raman spectroscopy was used to characterize MPs. As the results, polypropylene, polyethylene terephthalate, and polyethylene were the most abundant identified polymers among MPs, comprising more than 53% of particles. Additionally, MPs were categorized as fibers, fragments, and spheres. This study fills the knowledge gap of MPs presence in Tehran conventional DWTPs which is of high importance since they supply drinking water for more than 8 million people and investigates the performance of conventional DWTPs in removing MPs.

Supplementary Information

The online version contains supplementary material available at 10.1007/s40201-021-00737-3.

Keywords: Microplastics (MPs), Drinking water treatment plants (DWTPs), Plastic pollution, Water treatment, Scanning electron microscope (SEM)

Introduction

Today, plastic products are found in almost all areas of our modern life such as clothing, cosmetics, and health care, transportation, communication, and food packaging to name a few [1]. Hence, the amount of plastic manufactured on a global scale reached 370 million metric tons in 2019 [2]. Accordingly, trends of global plastic production, consumer-use patterns, inappropriate disposal of plastic wastes, and demographics suggest an increase in plastic use in the future [3]. Since plastics hardly decompose due to their material properties, they remain in the environment for a long time [4] and are a potential hazard for the environment due to their ubiquitous presence [5]. This suggests an urgent need to investigate the risks which plastic particles might pose to living organisms and human beings. Identified as less than 5 mm in diameter, these small plastic particles or fibers are generally termed microplastics (MPs) [6]. MPs are divided into two categories: primary and secondary. Primary MPs are specifically realized for various applications and can be in the form of exfoliating products, air-blasting technology, and so forth [7]. Secondary MPs, meanwhile, derive from the fragmentation of the larger items by weathering [8] and photodegradation [9]. Many studies have conducted research on MPs in marine environments [1012], freshwater bodies [1317] and urban watersheds [18]. Mao et al. [19], for instance, investigated MPs in Wuliangsuhai Lake in northern China and detected these particles in all of the 32 samples with polystyrene as the most abundant polymer type and fibers as the most frequent shape of MPs. The primary environmental risk associated with MPs is their bioavailability to marine organisms [20] and ingestion by a large variety of farm and wild species [21] in the shape of bioaccumulation. When body ingests MPs, they absorb and distribute through the circulatory system and enter into different tissues, potentially resulting in several types of adverse effects [2225]. Most importantly, oxidative stress [26], cytotoxicity [27], and translocation to other tissues [28]. Likewise, the negative impact of distinct polymers on human health has been investigated. For instance, Polystyrene (PS) and Polyvinyl chloride (PVC), trigger reproductive abnormalities [29], inflammatory gene expression, and cell morphology of human gastric adenocarcinoma epithelial cells [30]. The number of studies evaluating MPs in water bodies is numerous throughout the world, however, limited studies have investigated the presence of MPs in WWTPs, DWTPs, and groundwater resources [3135]. Thus, further research on these facilities is of great need. For example, Pivokonsky et al. [36] investigated two DWTPs of the same river and they detected MPs ranging from 20 to 1200 particles in each L of their samples, with fragments as the most abundant shape of MPs larger than 1 µm. Moreover, Sarkar et al. [37] in 2021 analyzed microplastic removal rate of a DWTP in India that sourced from the Ganga River. They observed that raw water contained 17.88 items/L which is reduced by 63% and 85% in pulse clarification and sand filtration, respectively. Since DWTPs are home to the purification of water resources to millions of people in cities, the purpose of this study is to evaluate the presence and polymer types of MPs in Tehran DWTPs and compare the removal rate of MPs in raw and treated water of these conventional DWTPs. To the knowledge of the author, this is the first study that aims to evaluate MPs and the reduction efficiency of DWTPs in Iran.

Materials and methods

Sampling site and sample collection

In total, there are five conventional DWTPs in Tehran with the same system of water purification, including screening (except for DWTP 3), coagulation and flocculation, sand filtration and disinfection that three of them are fed by different rivers, so these three DWTPs were chosen to be investigated. In this study, the names of DWTPs were not mentioned for confidentiality reasons, so they are named DWTP 1 to 3. The DWTP number 1 is fed from Karaj and Kan River in the northwest of Tehran with the capacity of 7.2 m3 s−1, with screening mesh dimension of 2.9 × 0.9 m with pore size 4.5 × 4.5 cm. This DWTP contains 40 sand filtration systems with the surface area of 48 m2, 1.5 m deep, nominal capacity of 240 m3 h−1 and 0.9–1.3 mm particle size. The source of the DWTP number 2 is Jajrud River in the northeast of Tehran with the capacity of 4 m3 s−1, mesh dimension 3.1 × 2.1 m with pore size 3 × 6 cm. This DWTP contains 32 sand filtration systems with the surface area of 158 m2, nominal capacity of 15 m3 h−1, 1.2 m deep and 1–1.3 mm particle size. The DWTP number 3 receives water from Lar Dam in the northeast of Tehran with the capacity of 5.7 m3 s−1 and contains 48 sand filtration systems with surface area of 150 m2, 1.2 m deep, nominal capacity of 18.75 m3 h−1 and 0.9–1.3 mm particle size. However, this DWTP does not have screening process. All three DWTPs use ferric chloride as coagulant and chlorine as disinfectant in coagulation/flocculation and disinfection unit, respectively. For the sampling, dark glass bottles with a capacity of 2.5 L were used to collect water samples from the raw and treated water from the DWTPs. Sampling was conducted in three different time intervals in 2019, over four months from April to August to include both dry and wet season (first time in late April, second time in mid-June and the third time in early August), from 12 am to 1 pm. Each time, one sample from raw water and one sample from treated water were taken (18 samples comprising 45 L in total). Subsequently, collected samples were kept in the dark at 4 C before sample treatment.

Sample preparation

To prepare the samples, the Wet Peroxide Oxidation method [38] was applied on both raw and treated water samples to digest organic matter. To explain briefly, a 0.05 M Fe (II) solution was prepared by 15 g FeSO4·H2O, 6 mL concentrated sulfuric acid (Merck Millipore, USA) and one L of deionized water. Every L of samples was added 80 mL of Fe (II) solution and 80 mL 35% hydrogen peroxide (Merck Millipore, USA) [14, 3840]. Afterward, One L Erlenmeyer flasks containing samples were placed on a stirring plate at 60 °C at 300 rpm for 30 min to boost the digestion. Subsequently, samples were kept at room temperature for 24 h before filtration. Then they were filtered via a vacuum pump through cellulose nitrate membrane filters with a pore size of 0.2 µm and 47 mm diameter. To remove clay and other inorganic particles from the filters, a density separation was applied. Hence, a zinc chloride solution (Merck Millipore, 5 M, 1.55 g cm−3) [31, 41, 42] was added to 20 mL centrifuge tubes and the filters were placed into the solution. Subsequently, the tubes were treated with an ultrasonic bath for 10 min to detach the particles from the filter. Without removing the filters, the tubes were centrifuged at 4000 rpm for 5 min and supernatants were filtered again to have almost pure MPs. Afterward, filters were placed in Petri dishes and dried in an oven at 60 °C for 1 h. Afterward, the Petri dishes containing the samples were covered by aluminum foil and placed in a desiccator for further quantitative and qualitative analysis.

Quality assurance/quality control (QA/QC)

Cotton laboratory outfit and nitrile gloves were utilized to minimize the risk of pollution. A negative-pressure ventilation system was functioning during the sample processing to eliminate the risk of depositing airborne MPs on the filters. Working surfaces on which the experiments were conducted were repeatedly cleaned with 1 M NaOH (Merck Millipore, USA). Furthermore, all the glassware for the sample processing were rinsed three times with filtered deionized water to remove potential MPs on their surfaces. For the sampling, dark glass bottles were used to lower the effect of photo-degradation. Plastic bottles were abstained from using in order to minimize the risk of the addition of MPs from the bottles. To minimize sample pollution, a layer of aluminum foil was placed between the bottles and screw caps. Additionally, one blank sample was carried out to ensure if there was sample contamination. The preparation method was applied on one L of previously filtered deionized water.

Quantitative analysis

A scanning electron microscope (Thermo Fisher Scientific, FEI Quanta 200, USA) with an accelerating voltage of 30 kV and detector working distance of 10 mm was used to image the filter surface in order to enumerate and identify the shape and size of MPs. The filters were cut in half and three cut-outs (3 mm × 8 mm) from one of the halves (one in the center, one in the edge and one in the middle) were scanned by SEM [40]. Before imaging, a gold layer was sputtered onto the samples to create electrical conductivity. Approximately 60 images from each cut-out were taken (13 mm2 in total, 1.25% of the whole filter; Fig. S1) and the number, size and shape of detected MPs were extrapolated to the whole area of the filter. The number, size and shape (fiber, fragment and sphere) of MPs were verified by ImageJ software (Version 1.50e, National Institute of Health, USA) based on one-L samples. Fibers were verified as thin and long MPs and were measured by their thickness, while fragments are particles that have been created by breaking down of larger pieces of plastic via fragmentation that were measured by their longest ends and spherical MPs have an appearance of a sphere. The particles were divided into 5 categories in terms of their size (1–5 μm; 5–10 μm; 10–50 μm; 50–100 μm; > 100 μm).

Qualitative analysis

To identify the chemical properties of MPs, a previously cleaned needle was used to transfer MPs on another half of the filter onto a conductive adhesive copper tape using a light microscope (N-120, Hinotek, China). In total, 107 suspected MP particles ranging from approximately 120 to 50 µm and various shapes, were carefully transferred onto the copper tape and sent for analysis. Since Fourier Transform Infrared (FTIR) spectroscopy is used for detecting the spectrum of particles greater than 500 µm and µ-FTIR is utilized for the particles down to the size of 20 µm [43] and the fact that the majority of the MPs in this study were comprised of particles smaller than 20 µm, µ-Raman spectroscopy (Horiba Scientific, XploRA ONE™, Japan) was used to detect the chemical composition of MPs by Labspecs 6 Software (Horiba Scientific, Japan) and the obtained spectra were compared with Infrared and Raman Users Group (IRUG) library. The frequency of excitation laser of micro-Raman spectroscopy was 785 nm, 1 accumulation and 100 × objective at 10 mW. The grating was 1200 1 mm−1, instrument aperture 100-μm slit, acquisition time 2 s and spectral range was set to 500–3500 cm−1. The match factor threshold of the detected MPs was set to 80%. In qualitative analysis, 62% of suspected particles were MPs, so this amount was subtracted from the MP numbers in quantitative analysis.

Statistical analysis

All statistical analyses were computed using Statistical Package for Social Science (version 16.0, SPSS, Inc.) and the figures were created with Microsoft Excel 2016 for Windows. Prior to statistical analysis, all data were tested for the basic assumptions for normality and homogeneity of variance. The Kolmogorov–Smirnov test was applied to analyze the normality of the data distribution. P < 0.05 was considered statistically significant (Tables S1S3, Supplementary Data).

Results and discussion

MP abundance and size

Three DWTPs are fed from three different rivers and there are no industrial areas in the vicinity of them. However, these rivers pass through the city of Tehran, so MP pollution is expected to be originated by people activity [44] and deposition of airborne MPs [45]. Therefore, in all of the samples, both in raw water and treated water of DWTPs, MPs were detected in various numbers. The average number of MPs in raw water of DWTPs are 2808 ± 80, 1996 ± 268 and 2172 ± 119 particles L−1 in DWTP 1, DWTP 2 and DWTP 3, respectively. The difference in the number of MPs can be attributed to the variation in water sources, precipitation and density of population in the proximity of the rivers [4648]. Kankanige and Babel [48] investigated a conventional DWTP in Thailand for MP removal and they reported that raw water samples of rainy seasons are 30% more polluted with MPs than in dry seasons. Moreover, source of water supply may influence MP abundance. For instance, Jajrud River (source of DWTP 1) originates from Latyan Dam, where is a hotspot for people's recreation. While Lar dam (source of DWTP 3) is almost free of people's activity and water is transferred by a tunnel with a diameter of 3.6 m to the DWTP 3. Moreover, DWTP 1 is fed from Karaj River which is also a hotspot for people's recreation and Kan River that flows through the city of Tehran. The quality of raw and treated water in this study is described in Table S4 and S5, supplementary data. Turbidity of water in three assessed DWTPs ranged from 4.32 to 7.91 in raw water and from 0.28 to 0.78 in treated water and no direct relation was observed with MP abundance. This may be due to low levels of turbidity in three DWTPs of Tehran. However, Sarkar et al. [37] revealed a strong relation between turbidity and MP abundance. This implies that more detailed studies need to be conducted to evaluate the relation between water quality parameters and abundance of MPs.

Regarding treated water samples, the average number of MPs are 1401 ± 86, 1042 ± 269 and 971 ± 103 particles L−1 for DWTP 1, DWTP 2 and DWTP 3, respectively. The function of all three DWTPs is the same with the same coagulant—ferric chloride—and the same purification system. Table 1 represents the number of MPs in both raw and treated water samples. Failure in desirable removal of MPs can be observed in all the DWTPs—an average decrease of 50.1, 48.4 and 55.2 in DWTP 1, DWTP 2, and DWTP 3, respectively. The rate of removal in this study is comparable to that of Kankanige and Babel [48] with 57.2% and 67.6% in rainy and dry seasons, respectively. In this study, performance of three DWTPs in the reduction of MPs is almost the same which can be attributed to the same functionality of them. Table 2 compares the result of this study to that of other similar studies. According to the Table 2, lower removal rate in this study can also be attributed to lower efficiency in coagulation and flocculation process of three analyzed DWTPs in comparison with that of Table 2. For example, Polyacrylamide (PAM) or any other efficient coagulant aid is not used in these facilities. However, Pivokonsky et al. [40] indicated that more than 20% of MPs in their WTP 1 are comprised of PAM due to its usage in coagulation process. They also demonstrated that two WTPs that operate granular activated carbon (GAC) filtration, remove more than 80% of MPs, while the other one without this filtration system can remove 70% of these particles. Therefore, presence of GAC filtration or pulse clarifiers [37] in three analyzed DWTPs could increase the removal rate of MPs. According to Fig. 1, 65% to 87% of MPs are comprised of particles smaller than 10 µm. This implies that the findings in this study are comparable to other similar studies investigating MPs in drinking and bottled water [40, 49, 50, 52]. Although the diminishment of larger MP particles was significant, most of the smaller MPs were not removed due to low solidification efficiency in coagulation and flocculation process and the fact that sand filtration systems are comprised of larger particles (0.9–1.3 mm) which can be more efficient to trap larger MPs. However, almost all of the particles greater than 50 µm were removed in the treatment process. Additionally, a significant portion of MPs are smaller than 1 µm, but due to the difficulty in the enumeration process and the fact that those particles cannot be analyzed qualitatively, they were disregarded in quantitative analysis.

Table 1.

Number of MPs in each sample (L−1)

MPs in raw water (L−1) MPs in treated water (L−1) Removal (%)
DWTP 1
 Day 1 2725 1312 51.8
 Day 2 2814 1407 50
 Day 3 2884 1484 48.5
 Average 2808 ± 80 1401 ± 86 50.1
DWTP 2
 Day 1 1911 895 53.2
 Day 2 2297 1352 41.2
 Day 3 1781 878 50.7
 Average 1996 ± 268 1042 ± 269 48.4
DWTP 3
 Day 1 2045 891 56.4
 Day 2 2280 934 59
 Day 3 2191 1088 50.3
 Average 2172 ± 119 971 ± 103 55.2

Removal rate of each sampling day was calculated by the difference in the abundance of MPs in water and treated water (L−1). The average number of MPs in each DWTP is recorded above

Table 2.

Comparison of other similar studies to the findings of this study

Type of Water Size range of MP particles (µm) MP abundance (L−1) References
Mean Range
WTP 1, raw water > 1 1473 ± 34 1383–1575 Pivokonsky et al. [40]
WTP 2, raw water > 1 1812 ± 35 1648–2040 Pivokonsky et al. [40]
WTP 3, raw water > 1 3605 ± 497 3123–4464 Pivokonsky et al. [40]
WTP 1, treated water > 1 443 ± 10 369–485 Pivokonsky et al. [40]
WTP 2, treated water > 1 338 ± 76 243–466 Pivokonsky et al. [40]
WTP 3, treated water > 1 628 ± 28 562–684 Pivokonsky et al. [40]
38 tap water samples > 1 440 0–1247 Tong et al. [49]
ADWTPb > 1 6614 ± 1132 930 ± 72 Wang et al. [50]
Influent of 10 WWTPs 10–500 7216a 2223–18,285 Simon et al. [51]
Effluent of 10 WWTPs 10–500 54a 19–447 Simon et al. [51]
Influent of a conventional WTP > 6.5 1590.8 ± 148.8 Kankanige and Babel [48]
Effluent of a conventional WTP > 6.5 609.1 ± 84.7 Kankanige and Babel [48]
DWTP 1, raw water > 1 2255 ± 383 1867–2665 This study
DWTP 2, raw water > 1 1588 ± 313 1434–1699 This study
DWTP 3, raw water > 1 1933 ± 381 1899–1966 This study
DWTP 1, treated water > 1 1356 ± 264 1201–1600 This study
DWTP 2, treated water > 1 1022 ± 259 900–1167 This study
DWTP 3, treated water > 1 1222 ± 288 1133–1368 This study

aMedian

bThis ADWTP contains GAC filtration system

Fig. 1.

Fig. 1

Average size distribution and number of MPs detected in each L of a raw water samples and b treated water samples

MPs shapes

Regarding the shape of MPs, fibers outnumbered the other two categories with 51.1% in raw water samples, while fragments comprised 35.6% of the MPs. However, fibers were removed higher in comparison with fragments, comprising 38% of MPs in treated water samples. That may be attributed to their long ends which can be trapped in sand filtration process. These microfibers can be originated from washing fabric garments [53]. Moreover, fragments were more abundant in treated water than in raw water. These particles are created through the breakdown of larger plastic debris and plastic products including packaging materials, plastic bottles and washing synthetic materials [50, 54, 55]. Figure 2 represents the different shapes of MPs detected in samples. Figure 2a and d depicts fragments in various sizes, Fig. 2b, c, f and g illustrate fibers in different diameters and 2e represents a microsphere. Finally, spherical MPs were the least abundant among detected MPs (13.3% and 5.3% in raw water and treated water samples, respectively). These particles originate from personal care and cosmetic products [54]. Wang et al. [54] also demonstrated that sand filtration is able to remove 60–80% of microspheres which is comparable to that of this study (60.2%). Figure 3 illustrates three different shape of detected MPs in both raw and treated water samples.

Fig. 2.

Fig. 2

Images a and d depicts fragments in various sizes, b, c, f and g illustrate fibers in different diameters and e represents a microsphere

Fig. 3.

Fig. 3

Abundance of MPs in three different shapes in raw and treated water. Standard error bars are presented in the chart

Qualitative analysis

In qualitative analysis of MPs, 10 different polymers were detected by µ-Raman spectroscopy (PP, Polyethylene Terephthalate (PET), PE, Polystyrene (PS), Polytetrafluoroethylene (PTFE), Polyurethane (PU), Polyamide (PA), Polybutylene terephthalate (PBT), Polyvinylidene Fluoride (PVDF), Polyvinyl Chloride (PVC) and polycarbonate (PC)). Figure 4 represents the average composition of MPs in raw and treated water samples. PP was the most abundant polymer in both raw and treated water samples with 27.3% and 24.8%, respectively. The high presence of these polymers can be attributed to the widespread consumption of food packaging materials, including cereal, flour, biscuits, dried fruit and vegetables, dried pasta [56]. PET is the second common polymer detected by µ-Raman spectroscopy with 15.1% in raw water samples. However, it is the third common polymer in treated water samples (14.2%), following PE with 12.1% and 14.4% of raw and treated water samples, respectively. Decrease in PET MPs can be attributed to its high density (1.38 g cm−3) versus other abundant MPs. PET is also consumed considerably as beverage bottles and bottled water [57], PE is usually used for bags, packaging and houseware [36]. The result from qualitative analysis in this study is consistent with other similar studies. For instance, Tong et al. [49] demonstrated that 26.7% and 24.4% of MPs from tap water in China are PE and PP, respectively. Wang Z. et al. [50], by investigating an advanced drinking water treatment plant (ADWTP) in China, showed that 55.4–63.1%, 15.1–23.8% and 8.4–18.2% of MPs in raw water samples are comprised of PET, PE and PP, respectively. Likewise, they indicated that PAM, prior to PET (47.2–58.8%), is the most abundant MPs in treated water samples, comprising 10.1–14.7% of MPs.

Fig. 4.

Fig. 4

Average composition of MPs detected by µ-Raman spectroscopy in both raw water and treated water samples. Standard error bars are presented in the chart

Further study

In this study, we demonstrated that treated water from conventional DWTPs contains a significant amount of MPs, so people are exposed to MP ingestion from drinking water. Mortensen [58] also indicated that drinking water is one of the main sources of ingestion of MP smaller than 50 μm. PP, PET and PE MPs that are the most abundant in treated water samples, are recognized to pose human health risks [59, 60]. These particles can also adsorb and transfer chemical to humans [6163]. Therefore, further studies are recommended to boost the efficiency of DWTPs to remove MP particles. In this regard, addition of GAC filtration needs to be investigated to increase MPs removal. Increasing depth of sand filtration and using finer particles in these systems can also trap more MPs, especially microfibers. Usage of PAM which can better remove MPs in coagulation/flocculation process is recommended [64]. However, it can be a source of pollution in treated water, so an alternative coagulant aid is suggested. Moreover, sources for DWTPs water supply can be managed to be free of human activity and transferring water in a tunnel can lower MP pollution of raw water. Additionally, plastic pipes are better to be disregarded for water transfer—whether from source to DWTP or DWTP to household consumption—or be checked up regularly in case of potential degradation.

Conclusion

This study investigated MPs in three different conventional DWTPs of Tehran through quantitative and qualitative analysis. MPs were abundant both in raw and treated water samples. On average, 1996 ± 268 to 2808 ± 80 MPs L−1 and 971 ± 103 to 1401 ± 86 MPs L−1 were identified in raw and treated water samples, respectively. Accordingly, conventional DWTPs are not successful to efficiently eliminate MPs. Moreover, 65–87% of MPs are smaller than 10 µm that were more abundant in treated water than in raw water which indicates that conventional DWTPs are incapable of removing MPs in this size. Generally, the ability of MPs removal by the investigated DWTPs ranges from 41.2 to 59.0%. Additionally, PP was the most abundant type of MPs in three detected DWTPs, both in raw and treated water samples, comprising 27.3% and 24.8%, respectively. Furthermore, fibers were more abundant than fragments and spheres in raw water (51.1%), while in treated water, fragments were more abundant than other two categories (56.7%).

Supplementary Information

Below is the link to the electronic supplementary material.

Acknowledgements

This work was conducted in the laboratory of Islamic Azad University, West Tehran Branch by the authors with no funding support.

Funding

All the expenditures on the findings of this study were provided by the authors.

Data availability

Not applicable.

Declarations

Conflict of interest

This manuscript has not been submitted to, nor is under review at, another journal or other publishing venue. The following authors have affiliations with organizations with no financial support in the subject matter discussed in the manuscript.

Footnotes

Publisher’s note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

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