Short-chain Chlorinated Paraffins Levels Research Articles

Removal Efficiency and Fate of Chlorinated Paraffins (CPs) in a Municipal Sewage Treatment Plant near a Typical Petrochemical Park

Water resources play an important role in industrial, agricultural, and public activities. Chlorinated paraffins (CPs) in wastewater generated by these activities provide an important source of CP contamination. In this study, the occurrences of short-chain chlorinated paraffins (SCCPs) and medium-chain chlorinated paraffins (MCCPs) were simultaneously studied in a typical sewage treatment plant (STP) near China’s second-largest oil production base over a 1-year period. High levels of SCCPs and MCCPs (3809 ± 670 and 4803 ± 478 ng/L) were found in the influent due to receiving 75% of industrial wastewater. C14-CPs was the predominant congener group, accounting for 37% of the total CP concentrations. The dissolved removal efficiency of CPs was 83.5%. Mass balance results demonstrated that 3.2% of the initial CPs was found in the final effluent, and 66.3% of the initial CPs was found in the dehydrated sludge, while 30.4% of the initial CPs was lost due to the biodegradation and volatilization. This indicated that sorption onto sludge was the main fate of CPs in wastewater treatment. High mass fractions of CPs were found in the final effluent and dewatered sludge in the winter season due to the low biodegradation, biotransformation, and volatilization.

Physical and chemical processes driving remote seasonal atmospheric exposure to cyclic volatile methysiloxanes and short-chain chlorinated paraffins

Cyclic volatile methylsiloxanes (cVMS) and short-chain chlorinated paraffins (SCCPs) use has been restricted in recent years due to environmental health concerns. Both of these classes of emerging contaminants possess long range transport potential (LRTP), highlighting the need for continuous monitoring to assess effectiveness of implemented regulations. However, emission source elucidation and understanding processes affecting atmospheric transport remain challenging. Atmospheric levels of cVMSs and SCCPs were simultaneously monitored at a background monitoring site in Norway from January–July 2020. Concentrations obtained from active air samplers ranged from 49.9 to 845 (mean: 208) pg/m3 for ƩSCCPs and from 0.4 to 3.5 (mean: 1.5), 1.1–15 (mean: 5.6) and 0.1–0.9 (mean: 0.4) ng/m3 for octamethylcyclotetrasiloxane (D4), decamethylcyclopentasiloxane (D5) and dodecamethylcyclohexasiloxane (D6), respectively. As SCCPs pose several challenges to analysts, different quantification methodologies and blank handling procedures were investigated to ensure reliable environmental measurements. Simulations using a Lagrangian atmospheric transport model (FLEXPART) revealed air masses impacting sampling measurements were of Oceanic origin, but periodic emission events from Europe and Russia were also observed. Seasonal pattern in cVMS concentrations was mainly driven by atmospheric degradation via hydroxyl radical reaction, whereas SCCP concentrations were more influenced by periodic anthropogenic inputs from local and continental Europe. No clear correlation could be observed with SCCP atmospheric concentrations and temperature over the entire sampling campaign. However, increased volatilization at elevated temperatures may be important with emissions originating from local sources. Higher chlorinated homologue groups dominated during the winter season and declined towards spring and summer, whereas reverse was found for the lower and more volatile chlorinated homologue groups.

Human exposure to short-chain chlorinated paraffins and organophosphate flame retardants in relation to paired multiple sources

In this study, the levels and distributions of short chain chlorinated paraffins (SCCPs) and organophosphate flame retardants (OPFRs) were determined in 10–88 aged human serum/hair and their paired multiple exposure sources, including one-day composite food, drinking water, and house dust. The average concentration of SCCPs and OPFRs were respectively 6313 and 176 ng/g lipid weight (lw) in serum, 1008 and 108 ng/g dry weight (dw) in hair, 1131 and 27.2 ng/g dw in food, not detected and 45.1 ng/L in drinking water, and 2405 and 864 ng/g in house dust. The levels of SCCPs in serum of adults were significantly higher than those of juvenile (Mann-Whitney U test, p < 0.05), whereas gender showed no statistically significant difference in SCCPs and OPFRs levels. In addition, there were significant relationships of OPFR concentrations between serum and drinking water as well as hair and food using the multiple linear regression analysis, whereas no correlation was observed for SCCPs. Based on the estimated daily intake, the major exposure pathway for SCCPs was food, while for OPFRs, it was food and drinking water with three order magnitude safety margin.

Spatiotemporal distribution and risk assessment of short-chain chlorinated paraffins in 30 major rivers in Taiwan

Because of their highly persistent, bioaccumulative and toxic properties, short-chain chlorinated paraffins (SCCPs) have become emerging contaminants and have been included in Annex A (elimination) of the Stockholm Convention since 2017. The contamination of SCCPs has been observed in the environment and biota worldwide but has not been detected in Taiwanese river ecosystems. Thus, this study aimed to determine the occurrence of SCCPs in sediments and fish from 30 major rivers in Taiwan and to evaluate the risk of SCCPs to river ecosystems and human health. The concentrations of SCCPs in sediments and fish ranged from ND (not detected) to 12.6 mg/kg dw and ND to 2.07 mg/kg ww, respectively. The concentrations of SCCPs in sediments were significantly correlated with some indicators of the discharge sources and water quality variables, indicating that SCCPs were released via human activities and various discharges into rivers and accumulated in sediments. The bioaccumulation of SCCPs in fish exhibited species-specific profiles and was related to environmental contamination levels and the living pattern and trophic level of the fish. The SCCP levels in sediments from 20 major rivers in Taiwan might pose a potential ecological risk to river ecosystems according to the criteria of the Federal Environmental Quality Guidelines in Canada, the biota–sediment accumulation factor and the risk quotient. Consumption of SCCP-contaminated river fish by different gender and age groups showed no significant health risk to residents in Taiwan evaluated by the estimated daily intake and hazard quotient. However, there was a health concern for the 0- to 3-year-old group due to the consumption of contaminated river fish at a bioaccessibility of 100% for SCCPs by the margin of exposure. Routine monitoring of SCCPs in river ecosystems is needed to protect aquatic organisms and human health.

Metabolomic mechanisms of short chain chlorinated paraffins toxicity in rats

Short chain chlorinated paraffins (SCCPs) have received increased interest worldwide since they were added to the list of controlled POPs in Annex A of the Stockholm Convention in 2017. Although many toxicological studies have already shown that SCCPs are hepatotoxic, nephrotoxic, and thyrotoxic to rodents, there have been few studies to date that have characterized changes in the metabolic pathways targeted by SCCPs. In this study, a UPLC-Q-TOF-MS based plasma metabolomics approach was used to investigate the toxicity of SCCPs in rats. Liver and kidney injury occurred rapidly after high-dose SCCP exposure, and the most relevant pathways affected were energy metabolism, amino acid metabolism, glycerophospholipid metabolism, nucleotide metabolism, and vitamin B metabolism. Exposure to SCCPs inhibited the tricarboxylic acid cycle and accelerated degradation. Fluctuating levels of phospholipids and nucleotides may have contributed to the neurotoxicity of SCCPs. In addition, the down regulation of folic acid induced by SCCPs may have led to malformations during the early development of laboratory animals. These results suggested that high exposure levels of SCCPs may have serious health risks and more research is needed to assess the health status of relevant occupational groups.

Highly elevated levels, infant dietary exposure and health risks of medium-chain chlorinated paraffins in breast milk from China: Comparison with short-chain chlorinated paraffins.

Short-chain chlorinated paraffins (SCCPs) are persistent organic pollutants which are toxic to human. Median-chain chlorinated paraffins (MCCPs) have similar toxicity to SCCPs. The productions of chlorinated paraffins (CPs) in China were 1 million tons in 2013 and remained high after that, which may lead to high risks for human exposure to CPs. To investigate temporal trends and health risks of SCCPs and MCCPs in breast milk in China, samples (n=2020) were collected from urban and rural areas of 11 Chinese provinces in 2017 and mixed into 42 pooled samples. SCCPs and MCCPs were analyzed by two-dimensional gas chromatography with electron-capture negative-ionization mass spectrometry (GC×GC-ECNI-MS). The MCCP concentrations (median (range)) were 472 (94-1714) and 567 (211-1089) ng g-1 lipid in urban and rural areas, respectively, which showed continuously rapidly increasing during 2007-2017. The SCCP concentrations (median (range)) were 393 (131-808) and 525 (139-1543) ng g-1 lipid in urban and rural areas, respectively. The results showed SCCP levels decreased in urban areas between 2007 and 2017. Significant increases in MCCP/SCCP ratios might arise from extensive manufacturing and use of MCCPs. The median estimated dietary intake via breast milk in urban and rural samples were 1230 and 2510ngkg-1d-1, respectively, for SCCPs and 2150 and 1890ngkg-1d-1, respectively, for MCCPs. Preliminarily risk assessment showed that SCCPs posed a significant health risk to infants via breastfeeding. The high MCCP levels should also be of concern because of continuous growth and negative effect on infants. Correspondence analysis indicated congeners with higher carbon and chlorine numbers in dietary tend to accumulate in breast milk.

Short- and Medium-Chain Chlorinated Paraffins in Polyvinylchloride and Rubber Consumer Products and Toys Purchased on the Belgian Market.

This study investigates the presence of Stockholm Convention listed short-chain chlorinated paraffins (SCCPs) and their replacement medium-chain chlorinated paraffins (MCCPs) counterparts in polyvinyl chloride and rubber consumer products and toys purchased on the Belgian market in 2019. SCCPs were detected in 27/28 samples at concentrations ranging from <LOQ–130,000 µg/g with a median level of 2.5 µg/g, while MCCPs were detected in only five samples ranging <LOQ–3500 µg/g. Levels of SCCPs in all but one of the samples were below the European Union’s guideline limit of 0.15%, by weight, and concentrations of both SCCPs and MCCPs in the majority of products suggested unintentional incorporation to the polymeric materials. The homologue distribution of SCCPs was generally dissimilar to known commercial formulations and appeared to be indicative of contamination during manufacture or via recycling of previously treated goods. MCCP patterns, conversely, were broadly representative of those reported for industrial mixtures and may have been inadvertently incorporated via the application of mixed carbon-chain length CP formulations or recycled goods. This research suggests that overall SCCP presence has decreased in goods on the European market compared with previous reports and that both SCCPs and MCCPs may still enter EU marketplaces from unintentional sources.

Short-chain chlorinated paraffins in soils indicate landfills as local sources in the Tibetan Plateau

Background contamination levels of contemporary persistent organic pollutants (POPs) may be elevated due to local discharges, and hence it is of high importance to assess and monitor them in alpine and Polar Regions. This study investigated the role of waste disposal in the Tibetan plateau as the local source of short-chain chlorinated paraffins (SCCPs). SCCPs were determined in soils from the urban landfill and rural dumpsites, with a concentration range of 56.8–1348 ng/g dw. The gradient descent of SCCP levels from Lhasa landfill to the surrounding soils with increasing distances suggested a significant SCCP release from waste disposal. The transport pattern was well fitted by the Boltzmann equation after normalization in terms of soil organic carbon contents. Compared to the landfill cells closed in early years, the recently closed cells contained higher concentrations but lower proportions of the short-chain congener groups, likely reflecting the SCCP use history in Tibet. In open-burning dumpsites, higher SCCP levels and dominance of lighter congener groups indicates that such crude waste treatment process might cause an extra release of volatile SCCPs. This study elucidates local SCCP inputs to the background environment, and demonstrates that both urbanization and badly-managed landfill have been contributing to the presence of contemporary POPs in the Tibetan Plateau.

Integrated Monitoring with Moss-Bag and Mussel Transplants in Reservoirs

For the first time, transplants with moss-bags and mussels together were applied to study the water quality in standing water bodies. The tested species: Fontinalis antipyretica Hedw. and Sinanodonta woodiana (Lea, 1834) were collected from unpolluted sites and analyzed to obtain background levels. Then, the moss and mussels were left in cages for a period of 30 days in three reservoirs where both are not present naturally. Two of the reservoirs suffer from old industrial contamination and one is affected by untreated wastes. Twenty-four compounds were studied, among them trace elements Al, As, Cd, Co, Cr, Cu, Fe, Hg, Mn, Ni, Pb, Zn and organic priority substances: six polybrominated diphenyl ethers (PBDEs) congeners and short-chain chlorinated paraffins (SCCPs). The trace element accumulation was significant after the exposition period in all studied stations. PBDEs and SCCPs were also accumulated up to two times more in the moss tissues. PBDEs in the mussels exceeded the environmental quality standard (EQS). The applied combined transplants, and especially the moss-bags, revealed severe contamination with heavy metals not detected by the water samples. The moss and the mussel followed a different model of trace element and PBDEs accumulation. The SCCPs levels were alarmingly high in all plant samples. The study confirmed PBDEs and SCCPs as bioaccumulative compounds and suggested that an EQS for SCCPs in biota needs to be established.

Bioaccumulation of short-chain chlorinated paraffins in chicken (Gallus domesticus): Comparison to fish

Short chain chlorinated paraffins (SCCPs) are a complex group of chlorinated organic pollutants that have raised an increasing public attention. However, limited information is currently available on the bioaccumulation of SCCPs in terrestrial birds which are abundant and widely distributed around the world. In the present study, chicken (Gallus domesticus) was used as a model organism to provide significant implications for other avian species. We investigated the transfer of SCCPs from dietary sources (feed and topsoil) to chicken and their tissue distribution behavior. SCCPs were detected in chicken feed (54−170 ng/g, dry weight), topsoil (170−860 ng/g, dry weight), and adult chicken tissues (460−13000 ng/g, lipid weight). Adult chicken tended to accumulate SCCP congeners with lower n-octanol-water partition coefficients (KOW) and octanol-air partition coefficients (KOA). The accumulation ratio values for SCCPs of the chicken were more influenced by KOA than by KOW, which was contrary to those for aquatic fish. Levels and homologue profiles of SCCPs varied among chicken tissues. SCCP levels in the livers were significantly lower than those in the other tissues (p < 0.05). The accumulation potential for SCCP congeners with higher KOW increased in the order of muscle < liver < fat.

Spatial distribution and profile of atmospheric short-chain chlorinated paraffins in the Yangtze River Delta

Research on the atmospheric occurrence of short chain chlorinated paraffins (SCCPs) in industrialized areas is scarce. In this study, we investigated the concentrations, profile, and spatial distribution of SCCPs in the highly industrialized and developed areas of the Yangtze River Delta (YRD) in China using polyurethane foam passive air samplers. Sampling was performed during two separate periods in 2011. The concentrations of atmospheric SCCPs ranged from 6.1 to 63 ng m−3 in summer and 6.2–42 ng m−3 in winter. The C10 and C11 groups were the predominant carbon groups in all the samples. Different congener patterns between summer and winter were found, indicating that congeners in the air in winter may be influenced by local and external sources. The highest level of SCCPs was found in Suzhou, which is a highly industrialized area with many manufactories including electronic industries and plastic factories. Higher levels of SCCPs were found in the air than polychlorinated biphenyls (PCBs), organochlorine pesticides (OCPs), and polybrominated diphenyl ether (PBDEs), suggesting that the production and use of SCCPs were much higher than prohibited or restricted persistent organic pollutants (e.g., PCBs, OCPs, and PBDEs). Future studies should investigate the different sources of atmospheric SCCPs by conducting a comprehensive assessment of SCCP exposure.

The underlying challenges that arise when analysing short-chain chlorinated paraffins in environmental matrices

As short-chain chlorinated paraffins (SCCPs) are listed on several monitoring programs, validated methods are essential. However, their complexity and the lack of commercially available certified reference materials (RMs) hinder a proper validation of methods. Instead, one method is usually ‘validated’ by evaluating performances and results of spiked materials with that of one other method, which could easily lead to unreliable results.This study evaluated four analytical methods with different principles (i.e. comprehensive two dimensional GC coupled to a micro electron capture detector, developed for this study, chloride enhanced atmospheric pressure chemical ionization triple quadrupole time of flight MS (APCI-QToF-HRMS), GC coupled to an electron capture negative ion low resolution MS (GC–ECNI–LRMS) and carbon skeleton GC–MS), investigated the comparability in SCCP determination in spiked and naturally contaminated samples and determined SCCP amounts in candidate RMs for possible certification.The results cast doubt on the use of the most commonly applied method (i.e. GC–ECNI–LRMS), as well as using spiked materials for method validation. The APCI-QToF-HRMS method was found most promising as it achieves the required MS resolution (>21,000), is relatively fast and can detect also other CPs. The suitable identified SCCP levels in the candidate RMs and the agreement in results between the methods bring the first certification of a RM for SCCPs within reach.

Congener-Specific Mother-Fetus Distribution, Placental Retention, and Transport of C10-13 and C14-17 Chlorinated Paraffins in Pregnant Women.

Short-chain chlorinated paraffins (SCCPs) and medium-chain chlorinated paraffins (MCCPs) are high-production-volume persistent and toxic industrial chemicals found ubiquitously in various environmental matrices. However, information is scarce regarding human internal exposure. The congener-specific SCCP and MCCP levels in matched maternal serum (n = 31), umbilical cord serum (n = 31), and placenta (n = 31) were studied to investigate the maternal-placenta-fetus distribution and the placental transport mechanisms of SCCPs and MCCPs. The results indicated that lower chlorinated and shorter carbon chain CPs were efficiently transported across placenta compared to highly chlorinated and longer carbon chain CPs. Meanwhile, ∑MCCP concentration followed the order of maternal sera > placentas > cord sera. The cord/maternal concentration fraction ratios (RCM) of CPs exhibited similar values from C10 to C14, and then from C15, a decreasing trend was observed with increasing carbon chain length. The log-normalized maternal SCCP concentrations were positively correlated (P < 0.01) with that in the cord, suggesting fetus exposure to SCCPs during pregnancy. Furthermore, the placenta/maternal concentration fraction ratio (RPM) values for MCCPs were relatively higher than those for SCCPs, demonstrating that MCCPs were not efficiently transported and effectively retained in placenta tissues. These findings provide a better understanding of the maternal-fetal transmission and neonatal exposure to CPs.

Short-chain chlorinated paraffins in fish from two developed regions of China: Occurrence, influencing factors and implication for human exposure via consumption

The risk associated with human exposure to short-chain chlorinated paraffins (SCCPs) via dietary intake are of great concern because of the bioaccumulation potential of SCCPs in biota and adverse effects. Fish are an important food source for human beings. However, there is a paucity of studies on human exposure to SCCPs via fish consumption. In this study, SCCPs were measured in frequently consumed river fish from the Pearl River Delta, and farmed freshwater fish and wild sea fish from the Yangtze River Delta. Lipid-normalized SCCP levels in river fish ranged from 3000 to 41,000 ng/g lipid weight (lw), with an average of 16,000 ± 12,000 ng/g lw. SCCP concentrations in farmed fish were significantly lower than those in river fish (p < 0.05), but significantly higher than those in sea fish (p < 0.05). Homologue patterns of SCCPs in river fish, farmed fish and sea fish were similar, with C10-11Cl6-7 SCCPs being the predominant homologues. SCCP concentrations in river fish increased significantly with increasing lipid content (p < 0.01), indicating that lipid content was a controlling factor influencing SCCP concentrations. Body length and weight also played important roles in SCCP concentrations in river fish, as SCCP concentrations decreased with the increase of body length and weight of breams, keeled mullets and tilapias. Although risk assessment implied no significant risk for human exposure to SCCPs via consuming fish collected in this study, the estimated daily intakes indicated that the consumption of sea fish was safer than farmed freshwater fish.

Tagged sources of short-chain chlorinated paraffins in China's marine environment and fish

Most emitters of short chain chlorinated paraffins (SCCPs) in China are located in eastern China, posing potential risks to the marine environment and food web. Here we employed a comprehensive atmospheric transport model combined with multiple environmental compartment exchange modules and a marine food web model to simulate levels and risks of SCCPs in the marine environment and fish in the Yellow Sea (YS), East China Sea (ECS), and South China Sea (SCS). Results unveiled a decreasing SCCP level in seawaters and sediments towards offshore. The modeled SCCP total (dry + wet) loadings to the three seawater bodies ranged from 0.0013 to 0.1635 mg/m2/season and gaseous diffusive deposition ranged from 43 to 4443 kg/month. The meteorological factors and secondary emission contributing to seasonal changes in SCCPs were also discussed. A tagging technique was used to trace origins of SCCPs, demonstrating that source proximity contributes most in SCCP contamination to these seawater bodies. Modeled SCCP levels in 5 marine fish in the YS, ECS, and SCS ranged from 23 to 111 ng/g. Our results showed the current SCCP levels in the marine environment and fish did not pose exposure risks to fish consumers for different age groups and genders. However, if consumed fish were harvested and imported from more seriously contaminated seawaters by SCCPs, the estimated dietary intake (EDI) would considerably increase.

First detection of short-chain chlorinated paraffins (SCCPs) in humpback whales (Megaptera novaeangliae) foraging in Antarctic waters

Short-chain chlorinated paraffins (SCCPs) are particularly prone to environmental dispersal through long range atmospheric transport. Consequently, they have been detected in biota and environmental matrices at both the North Pole and South Pole. This study shows the first detection of SCCPs in southern hemisphere humpback whales feeding in Antarctic waters. Blubber of specimens stranded along the Australian coastline was analysed and SCCPs were detected in 7 out of 9 individuals. Levels of SCCPs detected in this study were generally low with concentrations up to only 46 ng/g lw. These results were significantly lower than those detected in Northern Hemisphere odontocetes from previous studies, although no reported burdens in northern hemisphere baleen whales are available for comparison. Both the highest level and lowest (<MDL) were measured in calves-of-the-year. Congener group profile in the samples showed that the predominant carbon chain length was C11, followed by C10 = C12 > C13. Further investigation is needed in order to evaluate the presence and distribution of SCCPs in the remote Antarctica ecosystem, and delineate longer term environmental consequences of recent inclusion of SCCPs under Annex A of the Stockholm Convention, securing their phase out in ratifying nations.

Altitude-dependent accumulation of short chain chlorinated paraffins in fish from alpine lakes and Lhasa river on the Tibetan Plateau

High mountain cold-trapping effects can play important roles in the global long-range transport of persistent organic pollutants (POPs). Short chain chlorinated paraffins (SCCPs) have recently been included into the Stockholm Convention as a new class of POPs. However, the long-range transport behavior and environmental fate of SCCPs still remain largely unknown in high-altitude mountain areas. In this study, a total of 51 fish samples were collected from five high-altitude mountain lakes and Lasha river across the Tibetan Plateau. SCCPs were positively detected in all fish samples, and the concentrations ranged from 3.9 to 107 ng g−1 dry weight (dw) with an average of 26.6 ng g−1 dw. Compared to aquatic organisms from the Artic and Antarctica, the SCCP levels found in alpine fish from the Tibetan Plateau were lower. A significant increasing trend in accumulation levels of SCCPs in alpine fish with the increasing altitude was found on the Tibetan Plateau (r = 0.98, p < 0.001). Shorter chain congener group C10 showed a significant increase in percentage contribution to total SCCPs with increasing altitude, but a contrary tendency was found for longer chain congener group C13. The widespread occurrence of SCCPs in Tibetan fish was mainly sourced from the long-range atmospheric transport, and the altitude-dependent distribution of SCCPs was due to the mountain cold-trapping effects and potential susceptibility to bioaccumulation. To our knowledge, this is the first report regarding the altitude-dependent accumulation of SCCPs in biota in the polar environment.

Concentrations of selected chemicals in indoor air from Norwegian homes and schools

Both building materials and consumer products have been identified as possible sources for potentially hazardous substances like phthalates, polychlorinated biphenyls (PCBs), organophosphorous flame retardants (OPFRs), polybrominated diphenyl ethers (PBDEs) and short chain chlorinated paraffins (SCCPs) in indoor air. Thus, indoor air has been suggested to contribute significantly to human exposure to these chemicals. There is lack of data on the occurrence of several of the aforementioned chemicals in indoor air. Therefore, indoor air (gas and particulate phase) was collected from 48 households and 6 classrooms in two counties in Norway. In both the households and schools, median levels of low molecular weight phthalates (785 ng/m3), OPFRs (55 ng/m3) and SCCPs (128 ng/m3) were up to 1000 times higher than the levels of PCBs (829 pg/m3) and PBDEs (167 pg/m3). Median concentrations of dimethyl phthalate (DMP), diethyl phthalate (DEP), di-isobutyl phthalate (DiBP) and SCCPs were 3–6 times higher in households compared to schools. The levels of OPFRs, PCBs and PBDEs were similar in households and schools. In univariate analysis, the indoor concentrations of different environmental chemicals were significantly affected by location of households (OPFRs), airing of living room (some PCBs and PBDEs), presence of upholstered chair/couch (OPFRs), pet animal hold (some PBDEs) and presence of electrical heaters (selected PCBs and PBDEs). Significant correlations were also detected for the total size of households with OPFRs, frequency of vacuuming the living room with selected PCBs and PBDEs, frequency of washing the living room with selected PCBs and the total number of TVs in the households with selected phthalates and SCCPs. Finally, intake estimates indicated that indoor air contributed more or equally to low molecular weight phthalates and SCCPs exposure compared to food consumption, whereas the contribution from indoor air was smaller than the dietary intake for the other groups of chemicals.

Elimination of short-chain chlorinated paraffins in diet after Chinese traditional cooking-a cooking case study

Short-chain chlorinated paraffins (SCCPs) were listed in the Stockholm Convention in 2017 yet are still used in large-tonnage in China. Diet is the main external exposure pathway of many persistent organic pollutants (POPs), but SCCP diet exposure has not been studied completely thus far. In this study, samples of 122 raw foods were collected from markets in Beijing, cooked with Chinese traditional cooking methods, and analyzed for SCCPs. Overall, SCCP levels in the raw food materials ranged from0.67 to 5100 ng g−1 wet weight (ww). SCCP elimination was found in six out of seven kinds in the cooking case study. Concentrations in the raw food used for cooking ranged from 3.6 to 52 ng g−1 ww, while the corresponding values in the cooked food ranged from 0.67 to 10.8 ng g−1 ww. The SCCP elimination rate ranged from 12% to 93%. The daily average intake of SCCPs for the general population through raw food and cooked food was assessed. The total daily SCCP intake via these foods was 403 and 145 ng kg−1 bw d−1, which suggests that different assessing approaches may result in different estimated SCCP diet exposure amounts.

Mass Fractions, Congener Group Patterns, and Placental Transfer of Short- and Medium-Chain Chlorinated Paraffins in Paired Maternal and Cord Serum.

Multiple studies have demonstrated the occurrences of short-chain chlorinated paraffins (SCCPs) and medium-chain chlorinated paraffins (MCCPs) in environmental matrixes, but human internal exposure to them has been studied rarely. Mass fractions and congener group patterns of SCCPs and MCCPs in paired maternal and cord serum were studied for the first time to investigate the placental transport mechanism and prenatal exposure risks of CPs. Samples were collected in Beijing, China, and analyzed using two-dimensional gas chromatography coupled to time-of-flight mass spectrometry. SCCP and MCCP mass fractions in maternal serum were 21.7-373 and 3.76-31.8 ng/g ww, respectively. They were 8.51-107 and 1.33-12.9 ng/g ww, respectively, in cord serum. Significant positive correlation between SCCP and MCCP levels in maternal serum was found ( p < 0.01), suggesting SCCPs and MCCPs may undergo similar accumulation, transfer, and transformation pathways. The predominant congener groups for SCCP and MCCP in maternal serum were C10-11Cl6-7 and C14Cl7-8. The homologue profiles of CPs in cord serum were similar but with varied contribution percentage compared with those in maternal serum. By calculating and comparing cord-maternal serum ratios for each individual congener group, passive diffusion was recognized to be the possible placental transport form. The relationships between CP and thyroid hormone concentrations (THs) indicated that exposure to CPs might affect circulating TSHs. C9-CPs were also detected, improving our understanding of CPs in human serum.