Occurrence Of Phthalates Research Articles

Occurrence and Health Risk Assessment of Phthalates in Municipal Drinking Water Supply of a Central Indian City.

In this study, the occurrence of phthalates in the municipal water supply of Nagpur City, India, was studied for the first time. The study aimed to provide insights into the extent of phthalate contamination and identify potential sources of contamination in thecity's tap water. We analyzed fifteen phthalates and the total concentration (∑15phthalates) ranged from 0.27 to 76.36µgL-1. Prominent phthalates identified were di-n-butyl phthalate (DBP), di-isobutyl phthalate (DIBP), benzyl butyl phthalate (BBP), di (2-ethylhexyl) phthalate (DEHP), di-n-octyl phthalate (DNOP), and di-nonyl phthalate (DNP). Out of the fifteen phthalates analyzed, DEHP showed the highest concentration in all the samples with the median concentration of 2.27µgL-1, 1.39µgL-1, 1.83µgL-1, 2.02µgL-1, respectively in Butibori, Gandhibaag, Civil Lines, and Kalmeshwar areas of the city. In 30% of the tap water samples, DEHP was found higher than the EPA maximum contaminant level of 6µgL-1. The average daily intake (ADI) of phthalates via consumption of tap water was higher for adults (median: 0.25µgkg-1day-1) compared to children (median: 0.07µgkg-1day-1). The hazard index (HI) calculated for both adults and children was below the threshold level, indicating no significant health risks from chronic toxic risk. However, the maximum carcinogenic risk (CR) for adults (8.44 × 10-3) and children (7.73 × 10-3) was higher than the threshold level. Knowledge of the sources and distribution of phthalate contamination in municipal drinking water is crucial for effective contamination control and management strategies.

Occurrence of phthalates and 2,6-diisopropylnaphthalene in dry foods packed in cellulosic materials

Occurrence of phthalates and 2,6-diisopropylnaphthalene in dry foods packed in cellulosic materials

Occurrence of Phthalates in common effluent treatment plants and removal by using Nano Titania-Graphene based photo-catalyst for tertiary treated effluent

The occurrence and effectiveness of common effluent treatment plants (CETPs) for the removal of phthalates, as well as the fate of DEHP, are demonstrated in this study using a nano TiO2-Graphene-based photo-catalyst and photolytic system. Full-scale CETPs were selected at SIDCUL, Haridwar, and Unnao, Uttar Pradesh, along with installing a lab-scale photocatalytic reactor. Solid phase extraction (SPE) and gas chromatography-mass spectrometry (GCMS) was used to extract and quantify four phthalates, namely DEP, DBP, BBP, and DEHP, and byproducts.The average concentration of DEP, DBP, BBP, and DEHP in the mixed industrial effluent of CETP Haridwar exceeded by around ten folds than the literature value. Still, it was removed significantly by 77.9%, 32.8%, 97.5%, and 41.8%, respectively.The average influent concentration was eventually lower than the treated effluent at CETP Unnao, and phthalates were not removed during the process. During process optimization, the distinct ability of each method to remove DEHP during photolysis and photo-catalysis was discovered. The UV-TiO2-GO had removal effectiveness of 98% in 30 min at pH-6. However, at a dose of 500 mg, UV and UV-TiO2-GO had removal efficacy of 73% and 86%, respectively, for 180 min. After de-esterification, the UV system only cleaved the aliphatic chain, leaving the aromatic ring intact and producing a variety of byproducts. The superoxide ions (O2°−) and hydroxyl radicals produced in the photocatalytic process attacked not only the aliphatic chain but also the benzene ring.

Occurrence of phthalates in facemasks used in India and its implications for human exposure

ABSTRACT Synthetic polymers with additives are used in the manufacturing of face masks (FMs); hence, FMs could be a potential source of exposure to phthalic acid esters (PAEs). India stands second in the world in terms of the FMs usage since the beginning of Covid-19 pandemic. However, little is known about the PAEs content of FMs used in India. Some PAEs, such as DEHP and DBP are suspected endocrine disrupting chemicals (EDCs); hence, wearing FM may increase the risk of exposure to these EDCs. In this study, we collected 91 samples of FMs from eight Indian cities and analyzed for five PAEs viz. DMP, DEP, DBP, BBP, and DEHP. The PAEs contents in FMs ranged from 101.79 to 27,948.64 ng/g. The carcinogenic risk of N 95 with filter, N-95, and cloth masks was higher than the threshold levels. The findings indicate the need to control PAEs in FMs through regulatory actions.

Occurrence of Phthalates in Bottled Drinks in the Chinese Market and Its Implications for Dietary Exposure.

Ubiquitous occurrences of phthalic acid esters (PAEs) or phthalates in a variety of consumer products have been demonstrated. Nevertheless, studies on their occurrence in various types of bottled drinks are limited. In this study, fifteen PAEs were analyzed in six categories of bottled drinks (n = 105) collected from the Chinese market, including mineral water, tea drinks, energy drinks, juice drinks, soft drinks, and beer. Among the 15 PAEs measured, DEHP was the most abundant phthalate with concentrations ranging from below the limit of quantification (LOQ) to 41,000 ng/L at a detection rate (DR) of 96%, followed by DIBP (DR: 88%) and DBP (DR: 84%) with respective concentration ranges of below LOQ to 16,000 and to 4900 ng/L. At least one PAE was detected in each drink sample, and the sum concentrations of 15 PAEs ranged from 770 to 48,004 ng/L (median: 6286 ng/L). Significant differences with respect to both PAE concentrations and composition profiles were observed between different types of bottled drinks. The median sum concentration of 15 PAEs in soft drinks was over five times higher than that detected in mineral water; different from other drink types. Besides DEHP, DBIP, and DBP, a high concentration of BMEP was also detected in a tea drink. The estimated daily dietary intake of phthalates (EDIdrink) through the consumption of bottled drinks was calculated based on the concentrations measured and the daily ingestion rates of bottled drink items. The EDIdrink values for DMP, DEP, DIBP, DBP, BMEP, DAP, BEEP, BBP, DCP, DHP, BMPP, BBEP, DEHP, DOP, and DNP through the consumption of bottled mineral water (based on mean concentrations) were 0.45, 0.33, 12.5, 3.67, 2.10, 0.06, 0.32, 0.16, 0.10, 0.09, 0.05, 0.81, 112, 0.13, and 0.20 ng/kg-bw/d, respectively, for Chinese adults. Overall, the EDIdrink values calculated for phthalates through the consumption of bottled drinks were below the oral reference doses suggested by the United States Environmental Protection Agency (U.S. EPA).

Semi-Volatile Organic Compounds in Car Dust: A Pilot Study in Jeddah, Saudi Arabia.

People may spend a significant amount of their daily time in cars and thus be exposed to chemicals present in car dust. Various chemicals are emitted from during car use, contaminating the car dust. In this study, we compiled published and unpublished data on the occurrence of phthalates, flame retardants (FRs), polycyclic aromatic hydrocarbons (PAHs), and polychlorinated biphenyls (PCBs) in Saudi car dust. Phthalates, a class of chemical commonly used as plasticizers in different car parts, were the major pollutants found in car dust, with a median value of ∑phthalates 1,279,000 ng/g. Among other chemicals, organophosphate flame retardants (OPFRs) were found to be between 1500–90,500 ng/g, which indicates their use as alternative FRs in the car industry. The daily exposure to Saudi drivers (regular and taxi drivers) was below the respective reference dose (RfD) values of the individual chemicals. However, the estimated incremental lifetime cancer risk (ILCR) values due to chronic exposure to these chemicals was >1 × 10−5 for taxi drivers for phthalates and PAHs, indicating that the long-term exposure to these chemicals is a cause of concern for drivers who spend considerable time in cars. The study has some limitations, due to the small number of samples, lack of updated RfD values, and missing cancer slope factors for many studied chemicals. Despite these limitations, this study indicates the possible range of exposure to drivers from chemicals in car dust and warrants further extensive studies to confirm these patterns.

GC-MS Analysis of Phthalates and Di-(2-thylhexyl) Adipate in Canadian Human Milk for Exposure Assessment of Infant Population.

Although more information has become available on the occurrence of phthalates and di(2-ethylhexyl) adipate (DEHA) in foods including cow's milk, information on their presence in human milk, the important and recommended sole diet for infants up to six months of age, is very limited, especially for DEHA. To develop a GC-MS method for simultaneous analysis of DEHA and phthalates in human milk samples and generate occurrence data for exposure assessment. Human milk samples were extracted with acetonitrile followed by dispersive solid-phase extraction and GC-MS analysis. Among the 305 human milk samples collected from the Canadian Maternal-Infant Research on Environmental Chemicals Study, some phthalates (DHxP, BBzP, and DOP) were not detected in any of the samples, while DEHA and the other phthalates (DMP, DEP, DBP, DiBP, and DEHP) were detected at low frequencies with levels from 30.4-237 ng/g in up to 31 of the 305 human milk samples. In general, DEHA and phthalates were detected at low frequencies and low levels in the 305 human milk samples. A GC-MS method based on dispersive solid phase extraction was developed for analysis of DEHA and eight phthalates in 305 human milk samples for exposure assessment.

Occurrence and emission of phthalates and non-phthalate plasticizers in sludge from wastewater treatment plants in Korea.

Phthalates are endocrine-disrupting chemicals that cause adverse health effects in wildlife and humans. Due to domestic and global regulations of phthalates in commercial products, non-phthalate plasticizers (NPPs) have been introduced into industrial markets. Few studies have been conducted on the occurrence of phthalates and NPPs in sludge from wastewater treatment plants (WWTPs). In this study, sludge samples were collected from 40 WWTPs in Korea to investigate the occurrence, compositional profiles, and emission flux of phthalates and NPPs. Total concentrations of phthalates and NPPs in sludge ranged from 4.7 to 1400 (mean: 110) μg/g dry weight and from 0.17 to 780 (mean: 28.0) μg/g dry weight, respectively. Di(2-ethylhexyl)phthalate (DEHP) was a predominant compound, suggesting widespread consumption in Korea. Di(2-ethylhexyl)terephthalate (DEHT) was dominant in industrial sludge samples, whereas di-isononyl cyclohexane-1,2-dicarboxylate (DINCH) and trioctyl trimellitate (TOTM) were dominant in domestic sludge. This implies different consumption patterns of phthalate alternatives by industry and domestic activities. Concentrations of NPPs were significantly correlated with those of high-molecular-weight (HMW) phthalates, indicating that HMW phthalates were preferentially replaced by NPPs. The emission fluxes of phthalates via domestic WWTP activities were higher than those measured for industrial WWTPs, while the emission fluxes of NPPs via industrial WWTPs were higher than those found for domestic and industrial WWTPs. This indicates that phthalate emissions are associated with household activities, while NPP emissions are associated with industrial activities.

A Review of Biomonitoring of Phthalate Exposures.

Phthalates (diesters of phthalic acid) are widely used as plasticizers and additives in many consumer products. Laboratory animal studies have reported the endocrine-disrupting and reproductive effects of phthalates, and human exposure to this class of chemicals is a concern. Several phthalates have been recognized as substances of high concern. Human exposure to phthalates occurs mainly via dietary sources, dermal absorption, and air inhalation. Phthalates are excreted as conjugated monoesters in urine, and some phthalates, such as di-2-ethylhexyl phthalate (DEHP), undergo secondary metabolism, including oxidative transformation, prior to urinary excretion. The occurrence of phthalates and their metabolites in urine, serum, breast milk, and semen has been widely reported. Urine has been the preferred matrix in human biomonitoring studies, and concentrations on the order of several tens to hundreds of nanograms per milliliter have been reported for several phthalate metabolites. Metabolites of diethyl phthalate (DEP), dibutyl- (DBP) and diisobutyl- (DiBP) phthalates, and DEHP were the most abundant compounds measured in urine. Temporal trends in phthalate exposures varied among countries. In the United States (US), DEHP exposure has declined since 2005, whereas DiNP exposure has increased. In China, DEHP exposure has increased since 2000. For many phthalates, exposures in children are higher than those in adults. Human epidemiological studies have shown a significant association between phthalate exposures and adverse reproductive outcomes in women and men, type II diabetes and insulin resistance, overweight/obesity, allergy, and asthma. This review compiles biomonitoring studies of phthalates and exposure doses to assess health risks from phthalate exposures in populations across the globe.

Health risk of phthalates in water environment: Occurrence in water resources, bottled water, and tap water, and burden of disease from exposure through drinking water in tehran, Iran

Occurrence of phthalates in water resources, bottled water, and tap water, and health risk of exposure to the phthalates through drinking water in Tehran, Iran, 2018 were studied. The six phthalates with the most health and environmental concerns, including di-(2-ethylhexyl) phthalate (DEHP), butyl benzyl phthalate (BBP), di-n-butyl phthalate (DBP), diethyl phthalate (DEP), dimethyl phthalate (DMP), and di-n-octyl phthalate (DNOP) were monitored in drinking water and water resources. The average levels (±standard deviation: SD) of the total phthalates in drinking water from the water distribution system, bottled water, surface waters, and ground waters were determined to be 0.76 ± 0.19, 0.96 ± 0.10, 1.06 ± 0.23, and 0.77 ± 0.06 μg/L, respectively. The dominant compounds in the phthalates were DMP and DEHP causing a contribution to the total phthalate levels higher than 60% in all the water sources. The phthalate levels of drinking water significantly increased by contact of hot water with disposable plastic and paper cups and by sunlight exposure of bottled water (p value < 0.05). The hazard quotients (HQs) of DEHP, BBP, DBP, and DEP for all ages both sexes combined were determined to be 1.56 × 10−4, 1.01 × 10−5, 1.80 × 10−5, and 1.29 × 10−6, respectively that were much lower than the boundary value of 1.0. The disability-adjusted life years (DALYs) and DALY rate (per 100,000 people) attributable to DEHP intake through drinking water for all ages both sexes combined were estimated to be 6.385 (uncertainty interval: UI 95% 1.892 to 22.133), and 0.073 (0.022–0.255), respectively. The proportion of mortality in the attributable DALYs was over 96%. The attributable DALY rate exhibited no significant difference by sex, but was considerably affected by age in a manner that the DALY rates ranged from 0.052 (0.015–0.175) in the age group 65 y plus to 0.099 (0.026–0.304) in the age group 5 to 9 y. Both the carcinogenic and non-carcinogenic health risks of the phthalates in drinking water were considered to be very low. The results can also be of importance in terms of developing frameworks to expand the domain of burden of disease study to the other environmental risks.

Occurrence of phthalates in aquatic environment and their removal during wastewater treatment processes: a review.

Phthalates are plasticizers and are concerned environmental endocrine-disrupting compounds. Due to their extensive usage in plastic manufacturing and personal care products as well as the potential to leach out from these products, phthalates have been detected in various aquatic environments including drinking water, groundwater, surface water, and wastewater. The primary source of their environmental occurrence is the discharge of phthalate-laden wastewater and sludge. This review focuses on recent knowledge on the occurrence of phthalate in different aquatic environments and their fate in conventional and advanced wastewater treatment processes. This review also summarizes recent advances in biological removal and degradation mechanisms of phthalates, identifies knowledge gaps, and suggests future research directions.

Elevated levels of urinary 17-ketosteroids in central Indian children residing near sewage treatment plant and solid waste disposal plant: A preliminary study

ABSTRACTUrinary excretion of 17-ketosteroid (17-KS) was assessed in male pre-pubertal subjects aged (8–11 years; n = 90). Children living near sewage treatment plant and solid waste disposal plant (Group P) showed significantly higher levels of urinary 17-KS (Group P: 3.27 ± 1.63 µg/mL/CRE; p < 0.01) than children living in cleaner area (0.50 ± 0.53 µg/mL/CRE; Group C). Occurrence of urinary dibutyl phthalate in representative subjects of Group P (odds ratio: 9; p < 0.05; 95% of Confidence interval (CI) 1.93–72.99) was higher compared to Group C. Urinary concentrations of Cd (0.85 µg/g CRE ± 0.11), Mn (24.25 µg/g CRE ± 6.11) and Pb (12.39 µg/g CRE ± 2.86) in Group P were significantly (p < 0.01) higher than those found in Group C (Cd (0.28 µg/g CRE ± 0.03), Mn (13.33 µg/g CRE ± 3.20) and Pb (5.67 µg/g CRE ± 0.53)). Analyses of ambient air samples (PM10) in polluted area revealed major occurrence of phthalates, whereas derivatives of trifluoromethyl, dione, etc. were identified in PM2.5 fraction. Metal (Cd, Co, Mn and Pb) concentrations in ambient air (24 h, PM10) were higher in polluted area compared to cleaner area. We conclude that elevated levels of urinary 17-KS in Group P could be attributed to higher exposure of these subjects to Endocrine disrupting chemicals (EDCs) compared to Group C.

Effects of plastic film residues on occurrence of phthalates and microbial activity in soils

Plastic film mulching has played an important role in Chinese agriculture, especially in vegetable production, but large amounts of film residues can accumulate in the soil. The present study investigated the effects of plastic film residues on the occurrence of soil PAEs and microbial activities using a batch pot experiment. PAE concentrations increased with increasing plastic film residues but the soil microbial carbon and nitrogen, enzyme activities and microbial diversity decreased significantly. At the end of the experiment the PAE concentrations were 0–2.02 mg kg−1 in the different treatments. Soil microbial C and N, enzyme activities, AWCD value, and Shannon-Weaver and Simpson indices declined by about 28.9–76.2%, 14.9–59.0%, 4.9–22.7%, 23.0–42.0% and 1.8–18.7%, respectively. Soil microbial activity was positively correlated with soil PAE concentration, and soil PAE concentrations were impacted by plastic color and residue volume. Correlations among, and molecular mechanisms of, plastic film residues, PAE occurrence and microbial activity require further study.

Occurrence of Phthalates in Sewage Sludge from Three Wastewater Treatment Plants in Istanbul, Turkey

AbstractPhthalates are considered priority pollutants because of their potential adverse effects on ecosystems and human health. The objectives of this study were to determine the occurrence of five phthalates (DMP, DEP, DBP, BBP, and DEHP) in sewage sludge and to determine the seasonal variability of these contaminants at three (Bahçeşehir, Paşaköy, and Tuzla) full‐scale municipal and domestic wastewater treatment plants (WWTP) in Istanbul, Turkey. Mass balance was also calculated for DEHP at Tuzla WWTP sludge treatment units. DMP, DEP, DBP, BBP, and DEHP concentrations in sewage sludge ranged from 1.4 to 2.7 mg/kg dry weight (dw), 1.1 to 2.8, 0.6 to 4.6, 2.8 to 6.2, 18 to 490 mg/kg dw, respectively. Phthalate concentrations from the Bahçeşehir and Paşaköy WWTPs met the limit (100 mg/kg dw) of Turkey national sludge regulation and the Europe Union draft of sludge directive for land application, whereas phthalate concentrations from Tuzla WWTP exceeded the maximum permissible concentration. Phthalate concentrations did not show seasonal variations for Bahçeşehir and Paşaköy WWTPs, which receive mainly household wastewater while some fluctuations were observed DEP, DBP, and DEHP at Tuzla WWTP which has a lot of industrial wastewater contribution. The mass balance showed that approximately 17% of DEHP in the primary and secondary sludge was removed by anaerobic digestion, while 43% returned back to the beginning of the WWTP and 40% remained in the dewatered sludge. This study suggests that phthalates in sludge from WWTPs with industrial wastewater contribution may limit the use of sludge for land application.

Occurrence of phthalates in surface runoff, untreated and treated wastewater and fate during wastewater treatment

Dimethyl phthalate, diethyl phthalate, dibuthyl phthalate, butylbenzyl phthalate, bis(2-ethylbenzyl) phthalate (DEHP) and dioctyl phthalate were analysed in raw and treated wastewater as well as in surface runoff samples from traffic roads. All six investigated phthalates have been detected in all raw sewage samples, in nearly all wastewater treatment plant (WWTP) effluent samples and in all road runoff samples, with DEHP being the most abundant compound. DEHP inflow concentrations ranged 3.4–34 μg L −1 and effluent concentrations 0.083–6.6 μg L −1. In two WWTPs the fate of the phthalates was assessed by performing mass balances. Overall removal efficiencies of approx 95% were calculated. Removal is attributed to biotransformation and adsorption and the relevance of the removal via adsorption to sludge increased with increasing molecular weight and increasing lipophilic character of the compound. Except DEHP phthalate concentrations were higher in treated effluent samples than in road runoff. The environmental quality standard (EQS) for DEHP in surface waters is exceeded only in a few effluent samples, whereas nearly all road runoff samples were higher than the EQS. An assessment based on pure concentrations is not feasible and a mass balance based approach is required. Nevertheless the observations highlight the relevance of stormwater emissions and direct emissions from separated sewer systems to surface waters in relation to emissions from WWTPs and the necessity to consider all potential influences in the assessment of the status of surface water bodies with reference to xenobiotics.

Occurrence of Phthalates in Indoor Dust from Children's Facilities and Apartments in Seoul

The aim of the study was to assess the levels in typical central borough of phthalate exposure by monitoring children's facilities (19 kindergartens and 21 elementary schools) and households (17 old apartments and 22 new apartments) via sampling indoor floor dust. A vacuum cleaner specifically prepared for sampling dust was attached to a filter of a vacuum cleaner dust collecting container. During the sample preparation process, containers made of glass were used and analysis was performed using GC-MSD. The mean concentration of DEHP was <TEX>$412{\mu}g/g$</TEX>, DnBP was <TEX>$24{\mu}g/g$</TEX>, and BBzP was <TEX>$10{\mu}g/g$</TEX> dust. The indoor characteristics including floor, wall materials, years after construction, water leakage history for the past three years, and ventilation were also examined to categorize phthalate esters from the dust samples. From the flooring and wallpaper materials of kindergartens and elementary schools, DEHP in the dust sample appeared at a statistically significant level (p<0.05) when PVC materials were present. DEHP in the indoor dust also increased significantly (p<0.01) during the construction period. The daily intake of DEHP measured from indoor dust was 0.08~<TEX>$19.7{\mu}g/kg/day$</TEX> for children and 0.02~<TEX>$1.1{\mu}g/kg/day$</TEX> for adults (women). The results clearly revealed that phthalate exposure is greater in children than in adults (women) due to the indoor dust.

Determination and occurrence of phthalates, alkylphenols, bisphenol A, PBDEs, PCBs and PAHs in an industrial sewage grid discharging to a Municipal Wastewater Treatment Plant

Industrial and urban discharges release organic contaminants which might affect the quality of receiving waters if not properly eliminated in Wastewater Treatment Plants (WWTP). This study is aimed to evaluate the source, transport and fate of contaminants of industrial origin in a sewage grid discharging to a WWTP and finally to the sea. The sampling network covered an industrial and urban area and wastewaters, influents and effluents of a WWTP were analyzed using a newly developed multiresidual method to capture a wide range contaminants (phthalates, alkylphenols, bisphenol A, PBDEs, PCBs and PAHs). Alkylphenols and phthalates followed by PAHs were the main compounds detected at levels between 0.01 to 698 µg l − 1 in the sewage pipelines. At the WWTP influent they were detected at concentrations up to 345 µg l − 1 . The contaminant load was eliminated in a 64–92% during the primary and secondary treatment of the plant. However, alkylphenols, phthalates bisphenol A and traces of PAHs were discharged with the effluent, producing a total net input of 825 g d − 1 to the sea. The study of wastewaters herein proposed can be used to better predict the loads into WWTP to improve treatment conditions according to specific sewage inputs and to assess the risks associated with the continuous discharge of contaminants to receiving plants.

Occurrence of phthalates in sediment and biota: Relationship to aquatic factors and the biota-sediment accumulation factor

Phthalate compounds in sediments and fishes were investigated in 17 Taiwan’s rivers to determine the relationships between phthalate levels in sediment and aquatic factors, and biota-sediment accumulation factor (BSAF) for phthalates. Mean concentrations (range) of di(2-ethylhexyl) phthalate (DEHP), butyl benzyl phthalate (BBzP) and di- n-butyl phthalate (DBP) in sediment at low-flow season were 4.1 (<0.05–46.5), 0.22 (<0.05–3.1) and 0.14 (<0.05–1.3) mg kg −1 dw; those at high-flow season were 1.2 (<0.05–13.1), 0.13 (<0.05–0.27) and 0.09 (<0.05–0.22) mg kg −1 dw, respectively. Trace levels of dimethyl phthalate (DMP), diethyl phthalate (DEP) and di- n-octyl phthalate (DOP) in sediment were found in both seasons. Concentrations of DEHP in sediments were significantly affected by temperature, suspended solids, ammonia–nitrogen, and chemical oxygen demand. The highest concentration of DEHP in fish samples were found in Liza subviridis (253.9 mg kg −1 dw) and Oreochromis miloticus niloticus (129.5 mg kg −1 dw). BSAF of DEHP in L. subviridis (13.8–40.9) and O. miloticus niloticus (2.4–28.5) were higher than those in other fish species, indicating that the living habits of fish and physical–chemical properties of phthalates, like log K ow, may influence the bioavailability of phthalates in fish. Our data suggested that DEHP level in river sediments were influenced by water quality parameters due to their effects on the biodegradation processes, and that the DEHP level in fish was affected by fish habitat and physiochemical properties of polluted contaminants.

Occurrence of phthalates and musk fragrances in indoor air and dust from apartments and kindergartens in Berlin (Germany).

In this study, the occurrence of persistent environmental contaminants room air samples from 59 apartments and 74 kindergartens in Berlin were tested in 2000 and 2001 for the presence of phthalates and musk fragrances (polycyclic musks in particular). These substances were also measured in household dust from 30 apartments. The aim of the study was to measure exposure levels in typical central borough apartments, kindergartens and estimate their effects on health. Of phthalates, dibutyl phthalate had the highest concentrations in room air, with median values of 1083 ng/m(3) in apartments and 1188 ng/m(3) in kindergartens. With around 80% of all values, the main phthalate in house dust was diethylhexyl phthalate, with median values of 703 mg/kg (range: 231-1763 mg/kg). No statistically significant correlation could be found between air and dust concentration. Musk compounds were detected in the indoor air of kindergartens with median values of 101 ng/m(3) [1,3,4,6,7,8-hexahydro-4,6,6,7,8,8- hexamethylcyclopenta-(g) 2-benzopyrane (HHCB)] and 44 ng/m(3) [7-acetyl-1,1,3,4,4,6-hexamethyl-tetraline (AHTN)] and maximum concentrations of up to 299 and 107 ng/m(3) respectively. In household dust HHCB and AHTN were detected in 63 and 83% of the samples with median values of 0.7 and 0.9 mg/kg (Maximum: 11.4 and 3.1 mg/kg) each. On comparing the above phthalate concentrations with presently acceptable tolerable daily intake values (TDI), we are talking about only a small average intake [di(2-ethylhexyl) phthalate and diethyl phthalate less than 1 and 8% of the TDI] by indoor air for children. The dominant intake path was the ingestion of foodstuffs. For certain subsets of the population, notably premature infants (through migration from soft polyvinyl chloride products), children and other patients undergoing medical treatment like dialysis, exchange transfusion, an important additional intake of phthalates must taken into account. The phthalate and musk compounds load in a sample of apartments and kindergartens were low with a typical distribution pattern in air and household dust, but without a significant correlation between air and dust concentration. The largest source of general population exposure to phthalates is dietary. For certain subsets of the general population non-dietary ingestion (medical and occupational) is important.

Occurrence of phthalates and bisphenol A and F in the environment

Certain xenoestrogens, namely bisphenol A (BPA), bisphenol F (BPF), butylbenzyl phthalate (BBP), dibutyl phthalate (DBP), and di(2-ethylhexyl)phthalate (DEHP), were measured in various compartments (surface water, sediments, sewage treatment plant effluents, sewage sludge, dump water, liquid manure) in order to contribute to a better understanding of exposure to these compounds in different environments.Hundred and sixteen surface-water samples and 35 sediments from rivers, lakes and channels, 39 sewage effluents, and 38 sewage sludges were collected in Germany. Furthermore, ten liquid manure, two waste-dump and two compost-runoff water samples were also analysed.BPA measurements showed low concentrations from 0.0005 to 0.41μgL−1 in surface water, in sewage effluents from 0.018 to 0.702μgL−1, in sediments from 0.01 to 0.19mgkg−1 and in sewage sludge from 0.004 to 1.363mgkg−1 dw. Measured concentrations of BPF were clearly lower than BPA in all environmental media.DEHP dominated the phthalate concentrations, which ranged from 0.33 to 97.8μgL−1 (surface water), 1.74 to 182μgL−1 (sewage effluents), 27.9 to 154mgkg−1 dw (sewage sludge) and 0.21 to 8.44mgkg−1 (sediment). DBP was found only in minor concentrations and BBP, only in a few samples in low amounts. Very high concentrations of BPA and phthalates were confirmed in waste dump water and compost water samples as well as in the liquid manure samples.