Sources Of Phthalate Esters Research Articles

Occurrence of phthalate esters in the yellow and Yangtze rivers of china: Risk assessment and source apportionment

Phthalate esters (PAEs), recognized as endocrine disruptors, are released into the environment during usage, thereby exerting adverse ecological effects. This study investigates the occurrence, sources, and risk assessment of PAEs in surface water obtained from 36 sampling points within the Yellow River and Yangtze River basins. The total concentration of PAEs in the Yellow River spans from 124.5 to 836.5 ng/L, with Dimethyl phthalate (DMP) (75.4 ± 102.7 ng/L) and Diisobutyl phthalate (DiBP) (263.4 ± 103.1 ng/L) emerging as the predominant types. Concentrations exhibit a pattern of upstream (512.9 ± 202.1 ng/L) > midstream (344.5 ± 135.3 ng/L) > downstream (177.8 ± 46.7 ng/L). In the Yangtze River, the total concentration ranges from 81.9 to 441.6 ng/L, with DMP (46.1 ± 23.4 ng/L), Diethyl phthalate (DEP) (93.3 ± 45.2 ng/L), and DiBP (174.2 ± 67.6 ng/L) as the primary components. Concentration levels follow a midstream (324.8 ± 107.3 ng/L) > upstream (200.8 ± 51.8 ng/L) > downstream (165.8 ± 71.6 ng/L) pattern. Attention should be directed towards the moderate ecological risks of DiBP in the upstream of HH, and both the upstream and midstream of CJ need consideration for the moderate ecological risks associated with Di-n-octyl phthalate (DNOP). Conversely, in other regions, the associated risk with PAEs is either low or negligible. The main source of PAEs in Yellow River is attributed to the release of construction land, while in the Yangtze River Basin, it stems from the accumulation of pollutants in lakes and forests discharged into the river. These findings are instrumental for pinpointing sources of PAEs pollution and formulating control strategies in the Yellow and Yangtze Rivers, providing valuable insights for global PAEs research in other major rivers.

Occurrence, ecological and health risk assessment of phthalates in a polluted urban river used for agricultural land irrigation in central Mexico

The escalating global concern on phthalate esters (PAEs) stems from their status as emerging contaminants, marked by their toxicity and their potential to harm both the environment and human health. Consequently, this study aimed to evaluate the occurrence, spatial distribution, and ecological and health risks associated with PAEs in the Atoyac River, an urban waterway in central Mexico that receives untreated and poorly treated urban and industrial wastewater. Of the 14 PAEs analyzed in surface water samples collected along the river mainstream, nine were detected and quantified by GC-MS. The concentration of each detected PAE ranged from non-detected values to 25.7 μg L−1. Di (2-ethylhexyl) phthalate (DEHP) and di-n-hexyl phthalate (DnHP) were detected in all sampling sites, with concentrations ranging from 8.1 to 19.4 μg L−1 and from 6.3 to 15.6 μg L−1, respectively. The cumulative Σ9PAEs concentrations reached up to 81.1 μg L−1 and 96.0 μg L−1 in sites downstream to high-tech industrial parks, pinpointing industrial wastewater as the primary source of PAEs. Given that the river water is stored in a reservoir and used for cropland irrigation, this study also assessed the ecological and human health risks posed by PAEs. The findings disclosed a high ecological risk to aquatic organisms exposed to di-n-octyl phthalate (DOP), dicyclohexyl phthalate (DCHP), benzyl butyl phthalate (BBP), DEHP, and DnHP. Additionally, a high carcinogenic (CR > 10−4) and noncarcinogenic (HQ > 10) risk for the DEHP exposure through ingestion of crops irrigated with river water was identified for both children and adults. These data on PAEs provide valuable insights for the Mexican government's future strategies in regulating these pollutants in water bodies, thereby minimizing the environmental and human health risks that they pose.

Phthalate esters delivery to the largest European lagoon: Sources, partitioning and seasonal variations

Phthalate esters (PAEs) due to their ability to leach from plastics, widely used in our daily life, are intensely accumulating in wastewater water treatment plants (WWTP) and rivers, before being exported to downstream situated estuarine systems. This study aimed to investigate the external sources of eight plasticizers to the largest European lagoon (the Curonian Lagoon, south-east Baltic Sea), focusing on their seasonal variation and transport behaviour through the partitioning between dissolved and particulate phases. The obtained results were later combined with hydrological inputs at the inlet and outlet of the lagoon to estimate system role in regulating the transport of pollutants to the sea. Plasticizers were detected during all sampling events with a total concentration ranging from 0.01 to 6.17 μg L−1. Di(2-ethylhexyl) phthalate (DEHP) was the most abundant PAEs and was mainly found attached to particulate matter, highlighting the importance of this matrix in the transport of such contaminant. Dibutyl phthalate (DnBP) and diisobutyl phthalate (DiBP) were the other two dominant PAEs found in the area, mainly detected in dissolved phase. Meteorological conditions appeared to be an important factor regulating the distribution of PAEs in environment. During the river ice-covered season, PAEs concentration showed the highest value suggesting the importance of ice in the retention of PAEs. While heavy rainfall impacts the amount of water delivered to WWTP, there is an increase of PAEs concentration supporting the hypothesis of their transport via soil leaching and infiltration into wastewater networks. Rainfall could also be a direct source of PAEs to the lagoon resulting in net surplus export of PAEs to the Baltic Sea.

Residual status and source analysis of phthalate esters in Ulungur Lake, China.

Ulungur Lake is the largest lake in northern Xinjiang and undertakes important aquatic tasks. It is the No. 1 fishing ground in northern Xinjiang, and the problem of persistent organic pollution in the water has received much attention. However, there are few studies on phthalate esters (PAEs) in the water of Ulungur Lake. Understanding the pollution levels, distribution characteristics and sources of PAEs is of great significance for the protection and prevention of water. Fifteen sampling sites are established in Ulungur Lake to collect water samples during flood and dry periods, then seventeen PAEs are extracted from the water samples and purified by liquid-liquid extraction-solid-phase purification. Gas chromatography-mass spectrometry is used to detect the pollution levels and distribution characteristics of the 17 PAEs and analyse their sources. Results show that the concentrations of PAEs in the dry and flood periods are 0.451-9.97µg/L and 0.0490-6.38µg/L, respectively. The concentration of ∑PAEs with time is characterised by the dry period > the flood period. The change in flow is the main reason for the diverse concentration distributions of PAEs in different periods. The concentration of ΣPAEs in the dry period is much lower on the side near the lake entrance of the Ulungur River and Irtysh River. In the dry period, PAEs mainly come from chemical production and the use of cosmetics and personal care products; in the flood period, they mainly come from chemical production. River input and atmospheric sedimentation are the main sources of PAEs in the lake.

Atmospheric phthalate esters in a multi-function area of Hangzhou: Temporal variation, gas/particle phase distribution, and population exposure risk

Phthalate esters (PAEs) are prevalent in both indoor and outdoor environments. However, there are relatively few studies on phthalate contamination in the air of multi-function areas. Experiments were conducted to analyze the concentrations of 14 distinct PAEs in outdoor air in the college town of Hangzhou throughout both the warm and cold seasons. Correlation and principal component analyses were performed to investigate the influence and source factors of PAEs. This study also focused on the relationship between the gas/particle partition coefficient Kp and temperature, as well as the application of the gas/particle partition model. The risk of exposure to PAEs via inhalation was predicted for four groups of the general population: toddlers, adolescents, adults, and older adults. The results indicated that the concentration levels of Σ14PAEs in outdoor air were 1573 ng/m3 in the gaseous phase and 126 ng/m3 in the particulate phase. Additionally, this study indicated three primary sources of PAEs: indoor diffuse sources, industrial emission sources, and building construction sources. The gas/particle partitioning of PAEs also revealed that low-molecular-weight PAEs are more prevalent in gas, whereas high-molecular-weight PAEs are more predominant in the particle phase. A health risk analysis revealed high estimations of daily intakes (EDI) for toddlers and adolescents and high lifetime average daily doses (LADD) for older adults. This study establishes a solid foundation for formulating scientific and effective air pollution control measures by analyzing the characteristics and assessing the health risks of PAEs.

Riverine inputs, spatiotemporal variations, and potential sources of phthalate esters transported into the Bohai Sea from an urban river in northern China

The effects of anthropogenic activities on pollutant transport and inputs to the sea remain unclear. This study aimed to evaluate the impacts of sewage discharge and dam interception on riverine inputs, spatiotemporal variations, and potential sources of phthalate esters (PAEs) throughout the Haihe River, one of the largest rivers in northern China. Based on seasonal observations, the yearly inputs of the total concentrations of 24 PAE species (Σ24PAEs) from the Haihe River to the adjacent Bohai Sea were in the range of 5.28–19.52 tons, a considerable amount compared with those of other large rivers worldwide. The value of Σ24PAEs in the water column ranged from 1.17 to 15.46 μg/L and showed the following overall seasonal pattern: normal season > wet season > dry season, with dibutyl phthalate (DBP) (31.0 ± 11.9 %), di (2-ethylhexyl) phthalate (DEHP) (23.4 ± 14.1 %), and diisobutyl phthalate (DIBP) (17.2 ± 5.4 %) as the dominant components. Σ24PAEs were higher in the surface layer, slightly lower in the intermediate layer, and higher in the bottom layer. Σ24PAEs increased from the suburban section to the urban and industrial sections, which may indicate the effects of runoff, biodegradation, regional urbanization, and industrialization levels. The Erdaozha Dam intercepted 0.29–1.27 tons of Σ24PAEs inputs into the sea, but induced a substantial quantity accumulated behind the dam. The dominant sources of PAEs were the basic residential necessities (18.2–25.5 %) and industrial production (29.1–53.0 %). This study provides insights into the direct effects of sewage discharge and river dams on the inputs and variations in the PAEs entering the sea, which can be leveraged to manage and control PAEs in megacities.

Spatiotemporal occurrence of phthalate esters in stormwater drains of Hong Kong, China: Mass loading and source identification

Urban stormwater is an important pathway for transporting anthropogenic pollutants to water bodies. Phthalate esters (PAEs) are endocrine disruptors owing to their estrogenic activity and potential carcinogenicity and their ubiquitous presence has garnered global interest. However, their transportation by urban stormwater has been largely overlooked. This study, for the first time, investigated 15 PAEs in stormwater from six major stormwater drains in the highly urbanized Hong Kong, a major metropolitan city in China. The results showed that PAEs were ubiquitous in the stormwater of Hong Kong, with total concentrations (∑15PAEs) spanning from 195 to 80,500 ng/L. Bis(2-n-butoxyethyl) phthalate (DBEP), diisopentyl phthalate (DiPP), dicyclohexyl phthalate (DCHP) and di-n-pentyl phthalate (DnPP) were detected in stormwater for the first time. Spatial variations in PAEs were observed among different stormwater drains, possibly due to the different land use patterns and intensities of human activities in their respective catchments. The highest and lowest levels of ∑15PAEs were found in Kwai Chung (3860 ± 1960 ng/L) and the Ng Tung River (672 ± 557 ng/L), respectively. Additionally, significantly higher concentrations of ∑15PAEs in stormwater were found in the wet season (2520 ± 2050 ng/L) than in the dry season (947 ± 904 ng/L). Principal component analysis classified domestic and industrial origins as two important sources of PAEs in the stormwater of Hong Kong. Stormwater played a crucial role in transporting PAEs, with an estimated annual flux of 0.705–29.4 kg. Thus, possible stormwater management measures were proposed to protect the receiving environment and local ecosystems from stormwater.

Distribution, source apportionment and health risk assessment of phthalate esters in outdoor dust samples on Tibetan Plateau, China

The urbanization of Tibetan Plateau (TP) probably results in a significant contamination of organic pollutants in the area, such as phthalate esters (PAEs). However, there is a lack of monitoring and evaluation of their occurrence and risks in the outdoor dust on TP. This study for the first time investigated the concentrations, distributions and health risk of PAEs in outdoor dust samples on TP, China. A total of 132 outdoor dust samples were collected from five different functional areas, and results showed the ubiquitous detection of all PAEs in the samples. The Σ6PAEs concentrations ranged from 0.08 to 31.49 μg·g−1 with a mean of 3.57 μg·g−1. High concentrations of Σ6PAEs in the outdoor dust were found in commercial districts, which were attributed to the heavy use of PAEs in the public commerce such as consumer products, commodities, and building materials. Di-n-butyl phthalate (DBP) and bis(2-ethylhexyl) phthalate (DEHP) were the dominant components accounting for 30.65% and 53.19% of the Σ6PAEs. Principal component analysis, positive matrix factorization, and correlation analysis were used to apportion the potential sources of PAEs in outdoor dust samples. The PAEs in the outdoor dust originated mainly from wide application of plasticizers as well as cosmetics and personal care products. The main pathways of human exposure to PAEs in the outdoor dust were ingestion and dermal absorption of dust particles. The total intakes of PAEs from outdoor dusts for children and adults were 1.50 × 10−5 and 2.47 × 10−6 mg·kg−1·d−1, respectively. Children were more susceptible to the PAEs intake than the adults. Although the estimated health risks of the six PAEs are currently acceptable, caution is needed given the likely future increase in use of these PAEs and the currently unknown contribution to human exposure by other medium.

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.

Phthalate esters in surface sediments from fishing ports in Circum-Bohai-Sea region, China

The concentration, composition, distribution, and possible sources of phthalate esters (PAEs) in surface sediments from fishing ports in the Circum-Bohai-Sea region were investigated. The potential ecological risks of PAEs on three sensitive aquatic organisms (algae, crustacean, and fish) were assessed based on the risk quotient. The concentrations of 16 PAEs were in the range of 8.53–86.13 μg/g. Six PAEs, which were considered as priority pollutants by the United States Environmental Protection Agency, were main congeners. Fishing ports with high PAE concentration were located near the eastern area of the Shandong Peninsula, the southern area of the Liaodong Peninsula, and the estuary of the Yellow River. Wastewater, atmospheric deposition, plastic, and rubber products were possible sources of PAEs. The PAEs showed medium to high ecological risks on the three aquatic organisms, and the ecological risks were attributed to four PAEs, including dimethyl phthalate, diethyl phthalate, dibutyl phthalate, and benzylbutyl phthalate.

Evaluating the spatial distribution and source of phthalate esters in the surface water of Xingkai Lake, China during summer

Increasing production and usage of phthalate esters (PAEs) has made them ubiquitous in the environment. In this study, the distribution and source of PAEs in the surface water of Xingkai Lake, China were analyzed. The concentration of ΣPAEs in the water of Xingkai Lake ranged from 0.26 to 3.83 μg/L with a median of 1.28 μg/L. It was observed that the difference in the concentration of ƩPAEs between the small and large Xingkai Lakes is not significant (p > 0.05). Agriculturally dominated land use types in the Xingkai Lake watershed may be mainly responsible for the occurrence of PAEs in this Lake. The distribution of butyl benzyl phthalate (BBP) in small and large Xingkai Lakes showed a significant difference (p < 0.05) which may be related to anthropogenic activities. ƩPAEs in the water of Xingkai Lake demonstrated significant positive correlations with the ratio of total nitrogen (TN) to concentration of TP (rp = 0.697, p < 0.01) and the concentration of suspended particulate organic matter (SPOM) (rp = 0.345, p < 0.05). These results further indicate that the concentration of nutrients from agricultural activity had an impact on the concentrations of PAE in the lakes. Furthermore, the more SPOM would lead to more suspension of PAEs in the water phase. The source analysis of PAEs showed that high molecular weight PAEs were dominant in the Xingkai Lake which may be arising from the combustion of plastics or from building materials and household furnishing.

Occurrence of phthalate esters and microplastics in urban secondary effluents, receiving water bodies and reclaimed water treatment processes

The occurrence of phthalate esters (PAEs) and microplastics (MPs) was simultaneously investigated in four wastewater treatment plants (WWTPs), receiving water bodies and reclaimed water treatment processes (RWTPs) in winter and spring. Four PAEs (dimethyl phthalate, dibutyl phthalate, diisobutyl phthalate, and di(2-ethylhexyl)phthalate) were detected. The total concentrations of PAEs were 568.9–1847.5 ng/L in the four WWTP effluents and 39.9–1847.5 ng/L in the four receiving water bodies. Di(2-ethylhexyl)phthalate had the highest concentration among the PAEs. MPs were mostly in the form of granules and fragments with size <0.01 mm in the four WWTP effluents (276–1030 items/L) and receiving water bodies (103–4458 items/L). The four WWTP effluents were important sources of PAEs to the receiving water bodies in spring but were not likely to be the sources of MPs. The overall removal rates of PAEs and MPs were 47.7%–81.6% and 63.5%–95.4% in the four RWTPs. Low or negative removal rates of PAEs were observed in chlorination and ozonation. Clarification, filtration (except ultrafiltration) and reverse osmosis were the dominant processes, contributing 42.7%–69.2%, 25.3%–59.3%, and 22.6%–51.0%, respectively, of the MP removal in the RWTPs. According to the Spearman analysis results, the levels of PAEs and MPs had more significant correlations with the physicochemical parameters of water samples from the RWTPs (including the WWTP effluents) than those of the receiving water bodies. The results indicated that the levels of PAEs and MPs in surface waters could be significantly influenced by the surrounding environment.

Distribution, source, and environmental risk assessment of phthalate esters (PAEs) in water, suspended particulate matter, and sediment of a typical Yangtze River Delta City, China.

Phthalates (PAEs) in drinking water sources such as the Yangtze River in developing countries had aroused widespread concern. Here, the water, suspended particulate matter (SPM), and sediment samples were collected from 15 sites in wet and dry seasons in Zhenjiang, for the determination of six PAEs (DMP, DEP, DIBP, DBP, DEHP, and DOP) using the solid-phase extraction (SPE) or ultrasonic extraction coupled with gas chromatography-mass spectrometry (GC-MS). The total concentrations of six PAEs (Σ6PAEs) spanned a range of 2.65-39.31 μg L-1 in water, 1.97-34.10 μg g-1 in SPM, and 0.93-34.70 μg g-1 in sediment. The partition coefficients (Kd1) of PAEs in water and SPM phase ranged from 0.004 to 3.36 L g-1 in the wet season and from 0.12 to 2.84 L g-1 in the dry season. Kd2 of PAEs in water and sediment phase was 0.001-9.75 L g-1 in the wet season and 0.006-8.05 L g-1 in the dry season. The dominant PAEs were DIBP, DBP, and DEHP in water and SPM, DIBP, DEHP, and DOP in sediment. The concentration of DBP in water exceeded the China Surface Water Standard. The discharge of domestic sewage and industrial wastewater might be the main potential sources of PAEs. The risk quotient (RQ) method used for the risk assessment revealed that DBP (0.01 < RQ < 1) posed a medium risk, while DIBP and DEHP (RQ > 1) posed a high environmental risk in water, DIBP (RQ > 1) also showed a high risk in sediment.

Phthalate esters (PAEs) in atmospheric particles around a large shallow natural lake (Lake Chaohu, China)

The pollution of phthalate esters (PAEs) remains an important issue in the world. Current studies mainly focused on atmospheric PAEs in urban area with strong anthropogenic activities, but there were no studies on PAEs in the ambient air around large natural lake. This paper focused on two sites around Lake Chaohu to investigate the monthly occurrence, composition and source of PAEs in the atmospheric particles around large shallow natural lake. New insights into atmospheric PAEs in large shallow natural lake and the overall fate of PAEs in lake ecosystem were given. The concentrations of the Σ13PAEs in atmospheric particles were at a significantly low level ranging from 2740 to 11,890 pg·m−3 and 2622 to 15,331 pg·m−3 in ZM (the lakeshore site) and HB (the downtown site), respectively. There were no statistically significant differences of PAEs between ZM and HB. The highest atmospheric PAE concentrations in August were likely related to the long-range transport from Guangdong Province. Di(2-ethylhexyl) phthalate (DEHP), diisobutyl phthalate (DIBP) and dibutyl phthalate (DBP) were the main PAE congeners. Temporally, DIBP and DBP had the highest fractions in winter and the lowest fractions in summer. It might be justified by the condensation of DIBP and DBP from gas phase to particulate phase at low temperature. Multimedia comparison of PAE profiles in Lake Choahu revealed that low molecular weight (LMW) congeners were transported mainly through water while high molecular weight (HMW) congeners were transported mainly through atmosphere.

Concentrations and distribution of phthalate esters in the seamount area of the Tropical Western Pacific Ocean

A total of 14 phthalate esters (PAEs) were analysed by gas chromatography–mass spectrometry (GC–MS) to better understand its occurrence and distribution in seawater samples of M2 seamount in the Tropical Western Pacific Ocean (TWPO). The concentrations of ΣPAEs in the seawater ranged from 12.13 ng L−1 to 60.69 ng L−1 (av. 28.86 ng L−1), dominated by dibutyl phthalate (DBP), di(2‑ethylhexyl) phthalate (DEHP) and diisobutyl phthalate (DiBP). ΣPAEs concentrations in the southwest of the seamount were lower than those in the northeast, with the minima appearing above the seamount summit. Current-seamount interaction was reckoned to be the principal driving factors in the distribution of PAEs. DEHP posed a medium risk in seawater, suggesting that marine plastic pollution has become an urgent environmental issue that calls for more attention and actions. Microplastics leaching and atmospheric deposition might be the potential sources of PAEs.

The occurrence, composition and partitioning of phthalate esters (PAEs) in the water-suspended particulate matter (SPM) system of Lake Chaohu, China

The occurrence, composition, and partitioning of six phthalate esters (PAEs) (dimethyl phthalate (DMP), diethyl phthalate (DEP), diisobutyl phthalate (DIBP), dibutyl phthalate (DBP), butyl benzyl phthalate (BBP) and di(2-ethylhexyl) phthalate (DEHP)) in the water-suspended particulate matter (SPM) system of Lake Chaohu were investigated in this study. Our results showed that PAEs were ubiquitous contaminants in Lake Chaohu. The concentration of the Σ6 PAEs in dissolved and particulate phases ranged from 0.370 to 13.2 μg·L−1 and from 14.4 to 7129 μg·L−1, respectively. The Σ6 PAEs in water and SPM phases exhibited different seasonal trends. PAEs with different degrees of hydrophobicity demonstrated different temporal distributions in the dissolved phase. In particulate phase, all PAEs exhibited the same temporal distribution. Regarding the occurrence of PAEs, significant spatial differences exist between lake and estuary. However, there were no specific differences in PAEs across lake zones and river types of Lake Chaohu. River input should be considered an important source of PAEs in Lake Chaohu. DIBP and DBP were the most abundant PAEs in Lake Chaohu, and DIBP should attract more attention in the future. The organic carbon normalized partitioning coefficient (logKoc) ranged from an average of 2.38 ± 0.86 L·g−1 for BBP to 3.98 ± 0.66 L·g−1 for DEHP, and approximately 2 to 3 unit variations of logKoc existed for the individual PAEs. It was difficult to ascertain whether the partitioning of PAEs was in, near or far from the equilibrium. No linear relationship was found between logKoc and the octanol-water partitioning coefficient (logKow) for PAEs. Koc might not be suitable for describing the partitioning of PAEs in the water-SPM system. The hydrophobicity of PAEs may have little impact on their partitioning in the complex environmental system, and the Kow model may be inappropriate to predict the partitioning of PAEs in natural large lakes.

Application of catastrophe theory in comprehensive ecological security assessment of plastic greenhouse soil contaminated by phthalate esters.

Large amount of phthalate esters (PAEs) used as plasticizers in polyvinyl chloride (PVC) products has caused ubiquitous contamination to the environment and potential ecology security risk all around the world, especially in places plastic films were indispensably utilized due to the widely proposing of facility agriculture in China. A case of PAEs contamination in four suburb areas of Nanjing was analyzed and discussed in this study. A new frame work has been put forward based on multi-criteria evaluation model and mathematical method of catastrophe theory, using farming work, laboratory determination and relevant environmental standards to measure the ecology security risk of PAEs in study areas. The factors were selected based on the availability of the data and the local conditions. The assessment model involves the contamination status of PAEs in soil and vegetables, the contamination effects of PAEs to human and soil organisms and the contamination source of PAEs from plastic films and other products in the four study facility agriculture areas. An evaluation system of the model was composed of thirteen mesosphere indicators and twenty-five underlying indicators including total PAEs concentration in soils, single PAE concentration in soils, total PAEs concentrations in roots, leafy, solanaceous and stem vegetables, PAE human risks, soil microbial counts, microorganism diversity indices, atmospheric deposition of PAEs, whether sewage wastewater irrigation, planting mode of the facility agriculture areas and climate condition of study areas. The modified evaluation system was used in the assessment of ecology security of the same place based on the data of 2012, and the results suggested that the ecology security indicators were reliable and were agree well with the practical situation of the study areas. The results could provide guidance for the application of health risk assessment of soil environment for the strong objectivity of catastrophe theory compared with other evaluation methods.

Contamination Levels and Ecological Risk Assessment of Phthalate Esters (PAEs) in the Aquatic Environment of Key Areas of Taihu Lake

To better understand phthalate esters (PAEs) pollution in key areas of Taihu Lake, water and sediment samples were collected for content analysis. The concentrations of ∑PAEs in water samples from wet, dry, and normal seasons ranged 1.6-11.2 μg·L-1 (mean:3.68 μg·L-1), nd-6.21 μg·L-1 (mean:1.3 μg·L-1), and nd-1.72 μg·L-1 (mean:0.48 μg·L-1), respectively. No differences were found between upstream and downstream samples. DEHP was the predominant component in water samples, whereas DBP exceeded the national surface water environmental quality standards. The total PAE concentration in the sediment ranged between 0.74 and 6.90 μg·g-1 (mean:2.64 μg·g-1), with DBP and DEHP the predominant PAEs. The risk quotient (RQ) results showed that DBP and DEHP contributed the most potentially adverse effects to the aquatic environment in the key areas. The contents of PAEs in sediment were all less than the ERLs, thus posing no significant threat to aquatic organisms. The overall level of PAEs in the study area was moderate compared to those in other areas, including rivers, lakes, and estuaries from cities worldwide. Industrial pollution and urban activities are the major sources of PAEs in the aquatic environment of key areas of Taihu Lake.

Occurrence of phthalate esters around the major plastic industrial area in southern Taiwan

The increasing usage and disposal of plastic products could cause the wide distribution of phthalate esters (PAEs) in various environmental media. In this study, six PAE compounds, namely dimethyl phthalate, diethyl phthalate, di-n-butyl phthalate, benzyl butyl phthalate, di(2-ethylhexyl) phthalate (DEHP), di-n-octyl phthalate, were analyzed in various samples collected from the major plastic industrial area of southern Taiwan, including soil, fertilizer and plastic products, for the purposes of identifying of the possible sources of PAEs and assessing the related health risk. The results show that PAEs in soil samples was dominated by DEHP, with the total concentrations in the range of 0.7 ± 0.5, 0.2 ± 0.1, and 0.3 ± 0.2 mg kg−1 for soil samples from farmland, household back gardens and the roadside, respectively. Contents of PAEs in chemical fertilizer (ND—0 0.87 mg kg−1) were higher than that in organic fertilizer (ND—0.08 mg kg−1), and PAEs concentrations (ND—316 mg kg−1) in plastic mulching films were much less than those in the other types of plastic products (ND—1719 mg kg−1), implying that major sources of PAEs in agricultural soil could be the use of chemical fertilizer and plastic products other than plastic mulching films. Health risk assessment suggested that, via the exposure to PAEs in soil, the potential non-cancer and carcinogenic risks for adults and children are minimal in most cases, except that a “moderate” carcinogenic risk for children exposure to DEHP. The results of this study can serve as a reference for further pollution prevention and environmental protection plans in relation to the industrial operation and discharge as well as the farming practices.

Estimated daily intake and cumulative risk assessment of phthalates in Taiwan military personnel

Background: Phthalate esters (PAEs), which may have potential adverse health effects, are widely used in industrial and consumer products. The public raised concerns of exposure to PAEs after di-2-ethylhexyl PAE (DEHP) had been illegally used in food products in Taiwan in 2011. However, there is little information regarding the exposure levels of PAEs among Taiwanese military personnel. Objective: Health risk assessment indicators, including daily intake (DI), hazard quotient (HQ), and hazard index (HI), were used to assess the distribution and trends of PAEs and cumulative risk in Taiwanese military personnel. Materials and Methods: We recruited 503 participants who participated in northern voluntary military service from June to August 2017. We calculated the DI of five PAEs, namely dimethyl PAE, diethyl PAE, dibutyl PAE (DBP), benzyl butyl phthalate, and DEHP, and selected the reference dose (RfD) described by the US Environmental Protection Agency (EPA) as an acceptable exposure reference value to compute the HQ and HI. We used statistical analysis to examine the differences and trends of PAE metabolites in urine and investigated the possible primary sources of PAEs with principal component analysis. Results: The detection rates of 7 PAE metabolite concentrations were ≥72.2%. All DIs, HQRfDs, and HIRfDs were not over the standard EPA RfD. For all participants, two principal components (PC) were extracted. Three DEHP metabolites and MBP were correlated with PC1, and MiBP and MnBP were correlated with PC2. Conclusions: The main potential sources of PAE exposure for Taiwanese military personnel are DEHP and DBP. Efforts to reduce exposure to environmental PAEs are necessary to maintain health within the military.