Concentrations Of Phthalate Esters Research Articles

Combination of a Highly Efficient Biological System and Visible-Light Photocatalysis Pretreatment System for the Removal of Phthalate Esters from Wastewater

To save energy and increase treatment efficiency, a visible-light photocatalysis system was coupled with a biological treatment system for the continuous removal of phthalate esters (PAEs) from synthetic wastewater. Di-(2-ethylhexyl) phthalate (DEHP), dibutyl phthalate (DBP), and dimethyl phthalate (DMP) were treated using an iodine-doped TiO2 photocatalyst, and the reactions followed first-order kinetics (similar to ultraviolet TiO2 photocatalysis) to produce phthalic acid as an intermediate product. The effects of various operating factors, such as PAE concentrations, pH, light intensity, retention time (RT), and the coexistence of PAEs, on individual PAE removal were investigated. DEHP-degrading bacteria were isolated from DEHP-contaminated soil, purified through serial dilution, and then identified through DNA sequencing. The results indicated that the optimal operating conditions for PAE removal with a visible-light photoreactor were a pH of 5, a temperature of 30 °C, a light intensity of 300 W, and an RT of 5.5 min. DEHP, which contains long and branched chains, was more difficult to degrade than DMP, which contains short alkyl side chains. Pseudomonas sp. was the most dominant bacteria in the DEHP-contaminated soil and was inoculated in a packed bed reactor (PBR) for complete PAE degradation. The effluent containing PAEs was pretreated using the visible-light photoreactor under a short RT. This treatment resulted in the effluent becoming biodegradable, and PAEs could be completely removed from the treated effluent by using the PBR. The coupled photobiological system achieved removal efficiencies of 99.6%, 99.9%, and 100% for DEHP, DBP, and DMP, respectively, during the continuous treatment. The results of this study indicate that the developed coupled system is an effective, energy-saving, and cost-efficient tool for treating wastewater containing PAEs.

Co-occurrence of phthalate esters and perfluoroalkyl substances affected bacterial community and pathogenic bacteria growth in rural drinking water distribution systems

The adverse health effects of phthalate esters (PAEs) and perfluoroalkyl substances (PFAS) in drinking water have attracted considerable attention. Our study investigated the effects of PAEs and PFAS on the bacterial community and the growth of potential human pathogenic bacteria in rural drinking water distribution systems. Our results showed that the total concentration of PAEs and PFAS ranged from 1.02 × 102 to 1.65 × 104 ng/L, from 4.40 to 1.84 × 102 ng/L in rural drinking water of China, respectively. PAEs concentration gradually increased and PFAS slowly decreased along the pipeline distribution, compared to concentrations in the effluents of rural drinking water treatment plants. The co-occurrence of higher concentrations of PAEs and PFAS changed the structure and function of the bacterial communities found within these environments. The bacterial community enhanced their ability to respond to fluctuating environmental conditions through up-regulation of functional genes related to extracellular signaling and interaction, as well as genes related to replication and repair. Under these conditions, co-occurrence of PAEs and PFAS promoted the growth of potential human pathogenic bacteria (HPB), therefore increasing the risk of the development of associated diseases among exposed persons. The main HPB observed in this study included Burkholderia mallei, Mycobacterium tuberculosis, Klebsiella pneumoniae, Acinetobacter calcoaceticus, Escherichia coli, and Pseudomonas aeruginosa. Contaminants including particles, microorganisms, PAEs and PFAS were found to be released from corrosion scales and deposits of pipes and taps, resulting in the increase of the cytotoxicity and microbial risk of rural tap water. These results are important to efforts to improve the safety of rural drinking water.

Pollution characteristics and health risk assessment of phthalate esters in household dust in Chengdu, China

The characteristics and health risks of 15 phthalate esters in household dust and the association with household attributes were investigated in Chengdu, China. The concentrations of total phthalate esters ranged from 87.9 to 3623 μg/g. Di (2-ethylhexyl) phthalate (DEHP) was the dominant compound of phthalate esters with a median of 151 μg/g. The statistical analysis result showed that household products and synthetic polymer emission were the main sources of phthalate esters. Smoking, cooking, keeping pets and the use of wooden floor and plastic wallpaper might increase the concentrations of phthalate esters in household dust, but opening windows frequently, and increasing the sweeping frequency might cause the decrease of phthalate esters in the indoor environment. The hazard indexes (HI) values of phthalate esters were all below 1, indicated that there are not non-carcinogenic of phthalate esters in household dust for the residents in Chengdu. However, the carcinogenic risk of DEHP was 2.54 × 10−6, implying that the carcinogenic risks via exposure to DEHP from Chengdu household dust were noticeable.

Occurrence and distribution of phthalate esters and microplastics in wastewater treatment plants in Taiwan and their toxicological risks

Phthalate esters (PAEs) are fat soluble synthetic chemicals, usually regarded as plasticizers for being added in numerous plastic products. Thus, environmental and health hazards of PAEs are associated with increasing plastic pollution. In this study, PAEs from sludge samples collected from water, sewage, and industrial treatment plants (N = 17) were analyzed using Gas Chromatography/Mass Spectrometry. Microplastics (MPs) were also quantified and correlated with PAEs. Results showed the highest average PAE concentrations in sewage treatment plants. The greatest ΣPAEs concentration were found in sewage treatment plant (STP4) with 32,414 μg/kg dw, while the lowest found in water treatment plant (WTP3) with 2062 μg/kg dw. Among different PAEs, di-(2-ethyl hexyl) phthalate (DEHP) contributes the highest. Similarly, DEHP, di-n-octyl phthalate (DnOP) and diisononyl phthalate (DiNP) significantly correlated with the total PAEs indicating their large contribution to sludge contamination. The abundance of microplastics in sludge ranged between 1 and 7 MP/g, highest at ITP6, but not detected in some stations. While microplastics may potentially increase PAEs, there was no significant relationship between ΣPAEs and MP abundance. The estimated human daily intake of DEHP and di-n-butyl phthalate (DnBP) when contaminated sludge be used showed low toxicological risks to exposed adults. This research presents the sludge characteristics, PAEs, and microplastic concentrations in different wastewater treatment plants in Taiwan. PAE contamination was highly contributed by domestic and industrial wastes shown by their significant amounts in STP and ITP. Results further provide evidence for potential sludge recycling (WTP sludge) and application to soil.

Characteristics and Health Risks of Phthalate Ester Contamination in Soil and Plants in Coastal Areas of South China.

Phthalate esters (PAEs) are widely used as plasticizers in industrial and commercial products, and are classified as endocrine-disrupting compounds. In this study, we investigated the contamination characteristics and health risks of PAEs in the soil–plant system in coastal areas of South China. PAEs were detected in soil and plant samples at all 37 sampling sites. The total concentration of the 15 PAEs in soil samples ranged from 0.445 to 4.437 mg/kg, and the mean concentration was 1.582 ± 0.937 mg/kg. The total concentration of the 15 PAEs in plant samples ranged from 2.176 to 30.276 mg/kg, and the mean concentration was 8.712 ± 5.840 mg/kg. Di(2-Ethylhexyl) phthalate (DEHP) and di-n-butyl phthalate (DnBP) were the major PAEs compounds in all samples. The selected contaminants exhibited completely different spatial distributions within the study area. Notably, higher concentrations of PAEs were found in the coastal Guangdong Province of South China. The average noncarcinogenic risks of Σ6 PAEs were at acceptable levels via dietary and nondietary routes. However, the noncarcinogenic risks posed by DEHP and DBP at some sampling sites were relatively high. Furthermore, dietary and nondietary carcinogenic risks were very low for BBP, but carcinogenic risks posed by DEHP via diet. The results suggest that PAEs in the coastal soil–plant system in South China, through human risk assessment, will induce some adverse effects on human health, especially in children. This study provides an important basis for risk management of PAEs in agriculture, and safety in coastal areas of South China.

Freeze-thaw alternations accelerate plasticizers release and pose a risk for exposed organisms

The application of plastic mulch films brings convenience to agricultural production, but also causes plastic waste that can be degraded into microplastics (MPs). However, little is known about the fate of plastic waste in agricultural ecosystem under freeze-thaw alternation in middle and high latitudes, as well as in highlands around the world. Whether the release of plasticizers, i.e. phthalate esters (PAEs), under such conditions would pose a potential risk to exposed organisms due to bioaccumulation is also unknown. To fill these data gaps, the agricultural fields in Liaoning of China with typical freeze-thaw alternation was selected as the study area. The transformation of plastic film was demonstrated by simulation freeze-thaw alternating from −30 to 20 ℃. Soil samples were collected to investigate the patterns of MP composition, abundance, and distribution. Concurrently, the concentrations of two PAEs including bis(2-ethylhexyl) phthalate (DEHP) and diethyl phthalate (DEP) in soils were analyzed to provide information on the correlation between MPs abundance and PAEs concentrations as well as potential risks. The results showed that freeze-thaw alternating can accelerate the formation of MPs and release of PAEs from plastic waste. The abundance of MPs was positively correlated with the concentration of PAEs. Soil PAEs ranged from 3268 ± 213–6351 ± 110 μg/kg, indicating that over 40 % of the PAEs were transferred from plastic films to soils. Such residual amounts could pose risk for exposed organisms. Hence, the current study suggested that special concerns should be given to the release plasticizers in plastic waste of agricultural soils.

Biotransformation of phthalate plasticisers and bisphenol A by marine and freshwater fungi

Phthalate esters (PEs) are environmentally ubiquitous micropollutants that are used as plasticizers and additives in diverse consumer products. Considerable concern relates to their reported xenoestrogenicity and the microbial-based attenuation of environmental PE concentrations is of interest to combat harmful downstream effects. Fungal PE catabolism has received less attention than that by bacteria, and particularly marine fungal species remain largely overlooked in this respect. We have compared the biocatalytic and biosorptive removal rates of di-n-butyl phthalate (DBP) and diethyl phthalate (DEP), chosen as two environmentally prominent PE representatives (exhibiting differing structures and hydrophobicities), by marine- and freshwater fungal strains. Bisphenol A, both an extensively used plastic additive and prominent environmental xenoestrogen, was included as a reference compound due to its previously well-documented fungal degradation. Partial pathways for DBP metabolization by these ecophysiologically diverse ascomycetes were proposed with the help of UPLC-QTOF-MS analysis. Species-specific biochemical reaction steps contributing to DBP metabolism were also observed. The involved reactions include initial cytochrome P450-dependent monohydroxylations of DBP with subsequent further oxidation of related metabolites, de-esterification via either hydrolytic cleavage or cytochrome P450-dependent oxidative O-dealkylation, transesterification, and demethylation steps - finally yielding phthalic acid as a central intermediate in all pathways. Beyond previous research into fungal PE metabolism which emphasises hydrolytic de-esterification as the primary catabolic step, a prominent role of cytochrome P450 monooxygenase-catalysed reactions is established.

Microplastics: A major source of phthalate esters in aquatic environments

Phthalate esters (PAEs) are predominant additives in plastics, their widespread contamination in aquatic environments has raised global concern. Here, twelve plastic products were prepared as microplastics to investigate their release behaviors of PAEs. Six out of 15 PAEs were quantified after 14 days of incubation in water. The leaching potentials were plastic type-specific, where the pencil case (polyvinyl chloride, PVC) represented the highest migrations with total ∑15 PAEs concentration of 6660 ± 513 ng/g, followed by the cleaning brush-1 (polyamide, PA, ~1830 ng/g) and rubber glove (1390 ± 57.5 ng/g). Conversely, the straw (polypropylene, PP), cleaning brush-2 (polyethylene terephthalate, PET) and shampoo bottle (PET) released the lowest amounts of PAEs, with 50.3 ± 8.21, 93.9 ± 91.8 and 104.35 ng/g, respectively. The release patterns of PAE congeners were polymer type-related, where di-n-butyl phthalate (DBP) dominated the leaching from PA, PP and PET microplastics (47–84%), diethyl phthalate leached the most from PVC and rubber microplastics (45–92%), while diisobutyl phthalate and DBP dominated the leaching from PE microplastics (68–94%). Water chemical properties could affect PAEs migration and the kinetic leaching process was well fitted with the pseudo-first-order model. Approximately 57.8–16,100 kg/year of PAEs were estimated to be released into oceans from microplastics.

Levels of phthalates and bisphenol in toys from Brazilian markets: Migration rate into children's saliva and daily exposure

Bisphenols (BPs) and phthalate esters (PAEs) are extensively used in toys and childcare products. Therefore, children may be exposed to these compounds, causing potential adverse effects. Despite the strict control of the levels of these contaminants in toys by some nations, routine testing in Brazil is very scarce. The present study was aimed at determining the concentrations of PAEs and BPs in toys commercialized in Brazil, employing GC–MS and LC-MS/MS, respectively. Furthermore, the migration capacity of PAEs into saliva and the daily intake (EDI) were also estimated. Di-2-ethylhexyl phthalate (DEHP) was the PAE with the highest detection rate (93%) and migration rate (0.26 μg/min). Moreover, the levels of DEHP in some samples were above the threshold values set by the European Commission and the Brazilian Institute of Metrology, Standardization, and Industrial Quality. Among the BPs analogs, BPA and BPS presented the highest positive detection rates (72% and 30%, respectively). However, their levels were below the permitted values in all analyzed samples. A daily intake of DEHP was estimated at 29.8 μg/kg bw/day, being this exposure similar to those found in other countries and below the EFSA acceptable intake limit (50 μg/kg bw/day). However, our data are referred to exposure through oral contact with the analyzed toys, while the contribution of other potential sources, such as food consumption, were not here considered. To the best of our knowledge, this is the first study estimating the exposure of Brazilian children to PAEs and BPs, considering toys as the exposure source. These preliminary data may become a valuable guide for the control of EDC levels in toys commercialized in Brazil, as well as for future studies regarding estimation of exposure to EDCs by children taking into account multiple potential sources.

Occurrence and dietary exposure risk assessment of phthalate esters in Chinese mitten crabs (Eriocheir sinensis) from Hubei, central China

ABSTRACT: Recently, the wide existence of phthalate esters (PAEs) in aquatic environment has drawn great public attention, due to their negative health impacts on human and aquatic organisms. Chinese mitten crab is a major aquaculture economic resource in Hubei, feeding a world population of more than 10 million. Due to their wide consumption and great economic value, it's imperative to study the dietary risks of PAEs in mitten crabs ensuring food safety. In this study, a simple and selective method based on matrix matched calibration strategy coupled with gas chromatography-tandem mass spectrometry (GC-MS/MS) was developed to quantify 17 PAEs in Chinese mitten crabs (Eriocheir sinensis) from Hubei, central China and their dietary exposure risks were investigated. Recoveries were in the range of 56.9–131.2%. The limits of detection and quantification were 0.01–0.2 μg kg−1 and 0.5–7.5 μg kg−1, respectively. The PAEs were found to be present in both juvenile and adult mitten crabs in the study area. The mean concentration of total PAEs (∑17 PAEs) was 495.73–2033.39 μg kg−1 in crab muscles, and 159.69–651.69 μg kg−1 in hepatopancreas and gonad, respectively. The highest detection frequency of PAEs in all samples was di(2-ethylhexyl) phthalate (DEHP), and followed by dibutyl phthalate (DBP) and diisobutyl phthalate (DiBP). The estimated daily intakes of DEHP, DBP and DiBP, were more than ten times greater than any other PAEs. Calculated hazard ratio of PAEs were all below 0.1, suggesting that intake of PAEs by dietary of mitten crabs had non-cancer risk for both adults and children. Overall, this study provides a reliable method to evaluate PAEs pollution in aquatic food and critical data on the occurrence of PAEs in Chinese mitten crabs (Eriocheir sinensis) from Hubei, central China, which is a key part of PAEs pollution prevention in food source.

Distribution Dynamics of Phthalate Esters in Surface Water and Sediment of the Middle-Lower Hanjiang River, China.

Phthalate esters (PAEs) are endocrine-disrupting chemicals that pose potential risks to human health. Water and sediments are crucial carriers and storage media for the migration and transformation of PAEs. In this study, six congeners of PAEs were measured in water and sediment samples to elucidate their spatial distribution, congener profiles, and ecological risks in the middle-lower Hanjiang River during the wet and dry seasons. The concentration of the Σ6PAEs ranged from 592 to 2.75 × 103 ng/L with an average of 1.47 × 103 ng/L in surface water, while the concentration of the Σ6PAEs ranged from 1.12 × 103 to 6.61 × 103 ng/g with an average of 2.69 × 103 ng/g in sediments. In general, PAE concentrations were ranked as sediment > water, and dry season > wet season. DEHP and DBP were the dominant PAEs in the middle-lower Hanjiang River in surface water and sediments. SPSS analysis showed that dissolved organic carbon (DOC) in surface water was significantly correlated with the concentration of DBP, DEHP, and the ∑6PAEs, while organic matter (OM) was significantly correlated with the concentration of the ∑6PAEs in sediments. The concentrations of PAEs were irregularly distributed and varied significantly in surface water and sediments. Compared with other regions at home and abroad, the pollution levels of surface water and sediments in the middle-lower Hanjiang River were relatively low and not enough to have a negative impact on the local water’s ecological environment. However, the supervision of land-based discharge should still be strengthened.

Impact of Storage on Levels of Phthalates in Sachet and Bottled Water Brands in Enugu State, Nigeria

ABSTRACT The determination of phthalate ester concentrations in stored packaged water brands produced in Enugu State was carried out and the health risks evaluated. Packaged water samples were obtained in four batches from six sachet water and six bottled water factories, and stored outdoor for 1 month before analysis, while control samples were obtained and analysed immediately after purchase. Solvent extraction was carried out using dichloromethane, and phthalates concentrations were determined using Gas Chromatography-Mass Spectrometry. The range of limit of detection, recovery analysis and limit of quantitation were 0.001-0.002 mg/L, 81.26–91.47% and 0.003-0.006 mg/L respectively. The concentrations (µg/L) of DMP, BBP, MEHP, DBP and PADHE were<0.002–0.13, 0.41–1.84, <0.002–19.66, 0.76–4.22 and <0.002–0.81 in the bottled water and 0.11–0.36, <0.002–0.43, 0.21–5.75, 0.87–3.28 and <0.002–0.57 in the sachet water. Dimethyl phthalate (DMP) concentrations in the exposed and stored sachet water were significantly higher (P˂0.05) than that obtained from bottled water. There were also significantly higher (P<0.05) concentrations of Diethyl phthalate (DEP), Butyl benzyl phthalate (BBP), Di-butyl phthalate (DBP) and phthalic acid decyl hept-2-yl ester (PADHE), and pH in exposed sachet water than the control. Non-carcinogenic hazard quotient for phthalate esters in the packaged water samples was ˂1, which indicates no carcinogenic health risk. The contribution of individual phthalates to drinking water for Mono-2-ethylhexyl phthalate in both adults and toddlers exceeded the 0.5% TDI in some of the packaged water brands. Results suggest that increased concentrations of phthalate esters in the exposed packaged water samples were as a result of storage temperature, while the presence of phthalate esters in few of the control samples was probably from the packaging process. Although the levels of phthalates were low, regular consumption of packaged water could be detrimental to health of the general populace.

Phthalate Esters in Tap Water, Southern Thailand: Daily Exposure and Cumulative Health Risk in Infants, Lactating Mothers, Pregnant and Nonpregnant Women.

Human exposure to phthalate esters (PAEs) via drinking water has generated public health concerns due to their endocrine disruptive abilities. This study reports on the occurrence and fate of six PAEs in raw and tap water samples collected from provincial waterworks located in Songkhla Province, Southern Thailand. In addition, the daily exposure and cumulative health risk of susceptible populations due to drinking tap water were evaluated by using four different reference dose (RfDs) sources. The maximum concentrations of PAEs in raw water were between 1.68 and 4.84 and 0.52 and 1.24 µg/L in tap water. Moreover, the levels of PAEs in the tap water samples indicated the poor PAEs removal efficiency of the conventional treatment process (59.9–69.1%). The contribution of water to the daily intake of PAEs did not exceed 0.37% in all the groups. Furthermore, both the individual and cumulative risk assessment showed negligible noncarcinogenic and antiandrogenic risk for all the groups. Nevertheless, the cumulative risk showed an increasing trend in the order of infants > lactating mothers > pregnant women > nonpregnant women, suggesting that infants are more vulnerable. In additional, the newly proposed RfDAA yielded higher hazard quotient and hazard index estimates, which indicates it is a more sensitive tool than other RfDs for the assessment of the individual and mixture risk of pollutants. The carcinogenic risk of DEHP was acceptable in every group. However, we recommend a future cumulative risk assessment of vulnerable groups considering their simultaneous exposure to all chemicals that have antiandrogenic effects via tap water.

Phthalate Esters Released from Plastics Promote Biofilm Formation and Chlorine Resistance.

Phthalate esters (PAEs) are commonly released from plastic pipes in some water distribution systems. Here, we show that exposure to a low concentration (1-10 μg/L) of three PAEs (dimethyl phthalate (DMP), di-n-hexyl phthalate (DnHP), and di-(2-ethylhexyl) phthalate (DEHP)) promotes Pseudomonas biofilm formation and resistance to free chlorine. At PAE concentrations ranging from 1 to 5 μg/L, genes coding for quorum sensing, extracellular polymeric substances excretion, and oxidative stress resistance were upregulated by 2.7- to 16.8-fold, 2.1- to 18.9-fold, and 1.6- to 9.9-fold, respectively. Accordingly, more biofilm matrix was produced and the polysaccharide and eDNA contents increased by 30.3-82.3 and 10.3-39.3%, respectively, relative to the unexposed controls. Confocal laser scanning microscopy showed that PAE exposure stimulated biofilm densification (volumetric fraction increased from 27.1 to 38.0-50.6%), which would hinder disinfectant diffusion. Biofilm densification was verified by atomic force microscopy, which measured an increase of elastic modulus by 2.0- to 3.2-fold. PAE exposure also stimulated the antioxidative system, with cell-normalized superoxide dismutase, catalase, and glutathione activities increasing by 1.8- to 3.0-fold, 1.0- to 2.0-fold, and 1.2- to 1.6-fold, respectively. This likely protected cells against oxidative damage by chlorine. Overall, we demonstrate that biofilm exposure to environmentally relevant levels of PAEs can upregulate molecular processes and physiologic changes that promote biofilm densification and antioxidative system expression, which enhance biofilm resistance to disinfectants.

Seasonal Variation of Phthalate Esters in Urban River Sediments: A Case Study of Fengshan River System in Taiwan

The Fengshan River system is one of the major rivers in Kaohsiung City, Taiwan. This study investigated the concentration of eight phthalate esters (PAEs) in sediments of the river and the impact of potential ecological risks during the dry and wet seasons. The potential risk assessment of sediment PAEs was evaluated by adopting the total risk quotient (TRQ) method. The total PAEs concentrations (∑PAEs) in the sediments of the Fengshan River system are between 490–40,190 ng/g dw, with an average of 8418 ± 11,812 ng/g dw. Diisononyl phthalate (38.1%), bis(2-ethylhexyl) phthalate (36.9%) and di-isodecyl phthalate (24.3%) accounted for more than 99.3% of ∑PAEs. The concentration of ∑PAEs in sediments at the river channel stations is higher during the wet season (616–15,281 ng/g dw) than that during the dry season (490–1535 ng/g dw). However, in the downstream and estuary stations, the wet season (3975–6768 ng/g dw) is lower than the dry season (20,216–40,190 ng/g dw). The PAEs in sediments of the Fengshan River may have low to moderate potential risks to aquatic organisms. The TQR of PAEs in sediments at the downstream and estuary (TQR = 0.13) is higher than that in the upstream (TQR = 0.04). In addition, during the wet season, rainfall transported a large amount of land-sourced PAEs to rivers, leading to increased PAEs concentration and potential ecological risks in the upper reaches of the river.

The effect of heavy rainfall on the exposure risks of sedimentary phthalate esters to aquatic organisms

Phthalate esters (PAEs) have known widely being used in plastic products leading to being ubiquitous in the environment by easy to release from those products. This study aims to understand the impact of heavy rainfall on the concentration of PAEs in surface sediments of the Salt River in Kaohsiung, Taiwan, and its potential ecological risks on aquatic organisms. The potential ecological risk assessment of sediment PAEs is based on the total risk quotient (TRQ) method. The total concentration of 10 PAEs (∑PAE10) in sediments of the Salt River is 333–13,615 ng/g dw, with an average of 4212 ± 3753 ng/g dw. Before the rainy season, the ∑PAE10 concentration in sediments at the outlets of domestic sewage in upstream was 9768–13,615 ng/g dw, which were relatively higher than other sites (542–3721 ng/g dw). During the rainy season, the ∑PAE10 concentration was 2820–12,041 ng/g dw, which was 1–11 times higher than that determined before the rainy season. After the rainy season, the ∑PAE10 concentration recorded was 530–6652 ng/g dw, which is 1–11 times lower than the value obtained during the rainy season. PAEs in sediments of the Salt River may have low to moderate potential risks to algae, crustaceans, and fish. Bis(2-ethylhexyl) phthalate (DEHP) and diisobutyl phthalate (DiBP) are the main PAE that poses a potential risk to algae and crustaceans, and to fish respectively, whose values of risk quotient accounts for 40–69% of the TRQ value. The distribution of TRQ values for these aquatic organisms show a decreasing trend of PAEs level with respect to the rainy season: during the rainy season > after the rainy season > before the rainy season. Heavy rainfall may cause more serious pollution in sediments and increase the exposure risk of PAEs to aquatic organisms.

Dynamic variations of phthalate esters in PM2.5 during a pollution episode

Phthalate esters (PAEs) as hazardous air pollutants can be easily released during the life cycle of plastic products. In this study, a thermal desorption aerosol comprehensive two-dimensional gas chromatography mass spectrometer coupled with a dual-trap was developed and used to measure the hourly-resolved PAEs characteristics in atmospheric PM2.5 at an urban site. Dimethyl phthalate (DMP), diethyl (DEP), dibutyl (DnBP), benzyl butyl (BBP), di(2-ethylhexyl) (DEHP), and di-n-octyl phthalate (DnOP) in PM2.5 were analyzed. The most abundant compounds were DEHP and DMP, followed by DnBP and DEP. The mass concentrations of the detected PAEs are comparable to those at other urban sites measured using offline methods with a lower time resolution. The concentrations of PAEs showed intense change with the variation of PM2.5 mass concentration. The proportion of DEHP increased while that of DMP decreased with the increase in PM2.5 pollution. Positive correlations between PAEs and PM2.5, organic carbon, and elemental carbon were observed, while PAEs had negative correlation with the ambient temperature. Our observation provides evidences on understanding the volatile and semi-volatile PAEs in the ambient aerosols.

Phthalate esters in seawater and sediment of the northern South China Sea: Occurrence, distribution, and ecological risks

In this study, the occurrence and distribution of 15 phthalate esters (PAEs) in seawater and sediment from the northern South China Sea (NSCS) were investigated for the first time to improve understanding on the contamination status of PAEs in this region. The concentrations of total PAEs (∑15 PAEs) were found to range from 68.8 to 1500 ng/L, 46.0 to 7800 ng/L, and 49.2 to 440 ng/g dry weight in surface seawater, bottom seawater, and sediment, respectively. Among the 15 PAEs, dibutyl phthalate (DBP) and bis(2-ethylhexyl) phthalate (DEHP) were the predominant PAE congeners, with mean contributions of 44.7% and 24.0% in surface water, and 42.7% and 25.8% in bottom water, respectively. Moreover, diisobutyl phthalate (DiBP) constituted the majority of ∑15 PAEs in the sediment (61.3%). Comparatively high concentrations of Σ15 PAEs were observed in seawater at the sites within the western NSCS, whereas relatively higher concentrations of Σ15 PAEs were detected in sediments at the eastern NSCS. River input and atmospheric deposition could be the main sources of PAEs in the NSCS. Preliminary risk assessment implied that DBP, DiBP, and DEHP posed low to high potential risks for marine organisms at different trophic levels. These results would be valuable for implementing effective control measures and remediation strategies for PAEs contamination in the region.

Release of phthalate esters from a local landfill in the Tibetan Plateau: Importance of soil particle-size specific association

High loads of phthalate esters (PAEs) in background regions can be directly attributed to the local sources, and their association with soil particles may determine the environment behaviors. However, little is known about the particle-size specific distributions of PAEs in soils from point source to the surroundings. In this study, 12 PAE congeners were measured in clay (< 2 μm), silt (2–63 μm) and sand fractions (63–250 μm) from surficial soils and soil profiles (0–200 cm) around the Lhasa landfill. The total concentrations of PAEs in bulk soils varied from 0.44 to 22.3 μg/g, with a dominance of bis(2-ethylhexyl) phthalate (DEHP). The clay-sorbed PAEs exhibited a decreasing trend with the increasing distance from landfill. This distribution pattern was well described by the Gaussian air pollution model, suggesting the airborne particles/gaseous transport of clay-sorbed PAEs. The Boltzmann equation explained the spatial variation of silt-sorbed PAEs, reflecting the atmospheric dispersion of silt-sorbed PAEs. In comparison, the sand-sorbed PAEs in surrounding soils showed downslope accumulation possibly due to the aeolian transport of sand particles. Half-life of the most abundant PAE congener DEHP was assumed based on the soil inventories from observed concentration and the Level III fugacity model simulations, and the results indicated significant longer half-life of DEHP in deeper soils (~24,000 h) than in surficial soils (5500 h). This study elucidates that the distribution and fate of soil PAEs would depend on their association with particles in the source area, and the relative stability of DEHP in deeper soils would further increase PAE inventory in soil compartment.

Occurrence and cross-interface transfer of phthalate esters in the mangrove wetland in Dongzhai Harbor, China

Phthalate esters (PAEs), the most widely used plasticizers, are extensively present in various environmental media, and are continuously transported from land to sea. However, PAEs have not been well characterized in multiple media in mangrove wetlands, an important land-sea interface. This study investigated the distribution and transfer of six PAEs in water, sediment, mangroves, and fish in Dongzhai Harbor. The mangrove forest in Dongzhai Harbor is the largest in China and is surrounded by shrimp ponds and villages. PAEs are ubiquitous in the study area. The mean concentration range of ∑6PAEs was 0.31–1.52 μg/L in water, 450–2096 μg/kg dry weight (dw) in sediment, 210–937 μg/kg dw in mangrove plants, and not detected (n.d.) -205 μg/kg in fish. Among the six PAEs, di-n-butyl phthalate (DBP) and di-ethylhexyl phthalate (DEHP) were predominant. The concentrations of the PAEs in mangrove plants tended to decrease from the river and coast to tidal gullies, which might be related to the periodic inundation of tides. A study of PAEs bioaccumulation showed that the concentration of PAEs in herbivorous fish was higher than that in carnivorous fish. In the same species, larger individuals had a lower concentration of ∑6PAEs. Di-n-octyl phthalate (DnOP) and DEHP tended to transfer from water to sediments, while the four less-hydrophobic PAEs, such as DBP, were more likely to be released from sediments to water. Our results can provide important information of the distribution and fate of PAEs in mangrove wetlands.