Recycling Site Research Articles

Catalytic N‐Formylation of CO2 by Atomically Precise Au8Pd1(DPPF)42+ Clusters into a Two‐Dimensional Metal–Organic Framework

AbstractBy highly efficient ligand‐exchange strategy, atomically precise Au8Pd1(PPh3)82+ (PPh3=triphenylphosphine) cluster can be transformed into a Au8Pd1(DPPF)42+ (DPPF=1,1′‐bis(diphenylphosphino)ferrocene) cluster that can maintain the atomic‐packing structure but overcome the lability of Au8Pd1(PPh3)82+. Catalytic evaluation for the CO2 hydrogenation coupled with o‐phenylenediamine demonstrates that the Au8Pd1(DPPF)42+ catalyst can remarkably enhance both activity and stability compared to the Au8Pd1(PPh3)82+ catalyst. More notably, the direct construction of a two‐dimensional metal–organic framework (2D MOF) can be elaborately accomplished in the formylation process of o‐phenylenediamine, CO2 and H2 with zinc nitrate enabled by the Au8Pd1(DPPF)42+ catalyst. The 2D MOF further enables the capture and transformation of CO2 to combine in the organic synthesis with epoxides under mild conditions. This work provides opportunities for creating highly active cluster sites for the chemical recycling of CO2.

Catalytic N-Formylation of CO2 by Atomically Precise Au8Pd1(DPPF)4 2+ Clusters into a Two-Dimensional Metal-Organic Framework.

By highly efficient ligand-exchange strategy, atomically precise Au8Pd1(PPh3)8 2+ (PPh3=triphenylphosphine) cluster can be transformed into a Au8Pd1(DPPF)4 2+ (DPPF=1,1'-bis(diphenylphosphino)ferrocene) cluster that can maintain the atomic-packing structure but overcome the lability of Au8Pd1(PPh3)8 2+. Catalytic evaluation for the CO2 hydrogenation coupled with o-phenylenediamine demonstrates that the Au8Pd1(DPPF)4 2+ catalyst can remarkably enhance both activity and stability compared to the Au8Pd1(PPh3)8 2+ catalyst. More notably, the direct construction of a two-dimensional metal-organic framework (2D MOF) can be elaborately accomplished in the formylation process of o-phenylenediamine, CO2 and H2 with zinc nitrate enabled by the Au8Pd1(DPPF)4 2+ catalyst. The 2D MOF further enables the capture and transformation of CO2 to combine in the organic synthesis with epoxides under mild conditions. This work provides opportunities for creating highly active cluster sites for the chemical recycling of CO2.

Ascorbic acid export from human donor lenses: Is the lens a source of ascorbic acid in the ocular humors?

In previous work, we have shown that the lens acts a reservoir of the antioxidant glutathione (GSH), capable of exporting this antioxidant into the ocular humors and potentially protecting the tissues of the eye that interface with these humors from oxidative stress. In this study, we have extended this work by examining whether the lens acts as a source of ascorbic acid (AsA) to maintain the high levels of AsA known to be present in the ocular humors either by the direct export of AsA into the humors and/or by functioning as a recycling site for AsA, via the direct uptake of oxidised ascorbate (DHA) from the humors, its regeneration to AsA in the lens and then its subsequent export back into the humors. To test this, human lenses of varying ages were cultured for 1 h under hypoxic conditions and AsA/DHA levels measured in the media and in the lens. Human lenses were also cultured in compartmentalised chambers to determine whether efflux of AsA/DHA occurs at the anterior or posterior surface. Immunohistochemistry was performed on human donor lenses and sections labelled with antibodies against GLUT1, a putative DHA uptake transporter. Vitreous humor was collected from patients undergoing vitrectomy who either had a natural clear lens, an artificial intraocular implant (IOL) or a cataractous lens, and AsA/DHA and GSH and oxidised GSH (GSSG) measured. We found that cultured human donor lenses released both AsA and DHA into the media. Culturing of lenses in a compartmentalised chamber revealed that AsA and DHA efflux occurs at both surfaces, with relatively equal amounts of AsA and DHA released from each surface. The posterior surface of the lens was shown to express the GLUT1 transporter. Analysis of vitreous samples from patients undergoing vitrectomy revealed that vitreous GSH and AsA levels were similar between the natural lens group, IOL and cataractous lens group. Taken together, while human donor lenses were shown to export AsA and DHA into the surrounding media, the amount of AsA and DHA released from donor lenses was low and not sufficient to sustain the high levels of total AsA normally present in the humors. This suggests that although the lens is not the main source for maintaining high levels of AsA in the ocular humors, the lens may help to support local AsA levels close to the lens.

The Detection of Propionate Utilization by Bacteria Isolated from a Plastic Recycling Site

(1) The study aims to utilize a reported approach for culturing mesophilic bacteria from a plastic waste environment; (2) The work revived mesophilic microbial population from an aged PET recycling site using a culture-based approach, and determined the purified isolates in genus level in 16S identification; (3) A total of 59 bacterial isolates were obtained, in which microbial species, including Pseudomonas spp, Rhodococcus spp, and Burkholderia spp were identified as abundance. It was observed that the surviving microbes favoured sodium propionate as a short-chain carbon source for growth, rather than the intended plastic substrate, PET. The preference of sodium propionate utilization by several bacterial isolates, including 5601W (detected as Rhodococcus spp.), 5601Y, 7801, and 7802 (detected as Burkholderia spp.), was confirmed through growth curve analysis and cell enumeration conducted in a medium where sodium propionate served as the sole carbon source.; (4) The microbial demonstration revealed the metabolic complex of microbial communities in the environment and indicated the challenges associated with bacterial isolation from environments with accumulated plastic waste.

Understanding the Occurrence and Fate of Atmospheric Microplastics and Their Potential Risks to Human Health: Protocol for a Cross-Sectional Analysis.

Plastic pollution has reached an alarming magnitude, defining the contemporary era as the "Plastic Age." Uncontrolled plastic production and inadequate recycling processes have led to widespread contamination of the environment with micro and nanoplastics. The study aims to assess the environmental and human health consequences of exposure to microplastic particles (MPs) and their additives among plastic recycling workers in Dhaka. Specifically, it focuses on mapping the management pathways of plastic waste from collection to disposal, analyzing the types of MPs in the environment, and assessing the potential health impacts on plastic recycling workers. A cross-sectional exploratory study design was used, consisting of exposed and nonexposed groups in plastic recycling sites in Dhaka, Bangladesh. The study will establish possible associations between different health consequences and microplastic particle exposure with a systematic approach involving plastic recycling hot spot detection, management pathway mapping, and detecting the presence of environmental MP. MPs and heavy metals will be detected from environmental samples using fluorescence microscopy, Fourier-transform infrared spectroscopy, and inductively coupled plasma mass spectrometry. Human exposure will be assessed by detecting the metabolites of bisphenol and phthalates from urine samples using liquid chromatography-tandem mass spectrometry and thoroughly evaluating endocrine, reproductive, respiratory, and renal functions. The sample size was derived from the mean concentrations of urinary bisphenol and phthalates metabolites, requiring the participation of 168 respondents. A 1:1 exposure to nonexposed stratification would be sufficient to meet our study objectives, considering the conventional level of power and confidence interval. This study protocol (PR#22111) has received approval from the Research Review Committee and Ethical Review Committee of the icddr,b. The project was funded in August 2022. We started collecting environmental samples in January 2023 and completed participant enrollment, exposure survey, and biological sample collection by December 2023. We enrolled 84 adult plastic recycling workers with at least 5 years of exposure history and 84 nonexposed participants who were not involved with plastic recycling activities. Data analysis is currently underway, and the first results are expected to be submitted for publication in November 2024. The findings would provide valuable insights into the adverse impacts of microplastic pollution on both the environment and human health, aiding in better understanding the extent of the issue. DERR1-10.2196/60289.

High-efficiency combination washing agents with eco-friendliness simultaneously removing Cd, Cu and Ni from soil of e-waste recycling site: A lab-scale experiment

Soil washing technology plays an important role in the removal of heavy metals, and the efficacy of this process depends on the washing agent used. Due to the difficulty in treating soils contaminated by multiple heavy metals, there is still a need for further exploration of efficient washing agents with low environmental impact. Although single washing agents, such as chelators, can also effectively remove heavy metals from soil, combining efficient washing agents and determining their optimal washing conditions can effectively improve their removal efficiency for multiple heavy metals in soil simultaneously. Based on the previous research, the present study was carried out to combine different types of washing agents to remediate contaminated soils at a commonly e-waste recycling site. The objectives were to investigate their efficient washing conditions and assess the impact of the washing process on the speciation distribution and pollution level associated with heavy metals in soil. The results showed that the combination of HEDP (1-hydroxyethylidene-1,1-diphosphonic acid) and FeCl3 at a ratio of 6:4 exhibited the most effective removal of Cd, Cu and Ni from the contaminated soil at an e-waste recycling site. Under optimal washing conditions, with a soil-to-liquid ratio of 1:20 and a washing time of 48 h, the removal rates of Cd, Cu and Ni were 96.72%, 69.91% and 76.08%, respectively. It needed to be emphasized that the combination washing agents were able to remove most of the acid-soluble, reducible and oxidizable fractions of heavy metals, and even the removal rates of the stable residual fraction (e.g., of Cd) was at a relatively high level. In addition, the washing process significantly reduced the pollution level associated with heavy metals in soil. This study aid in the development of combined efficient washing agents and explores optimal washing strategies for the remediation of Cd, Cu, and Ni-contaminated soil at e-waste recycling sites. The findings may play a role in enhancing the remediation capabilities for soils contaminated with multiple heavy metals, due to its characteristics of and high-efficiency and environmental friendliness.

Concentrations and influencing factors of 17 elements in placenta, cord blood, and maternal blood of women from an e-waste recycling area

BackgroundThe effects of prenatal element exposure on mothers and fetuses have generated concern. Profiles of trace and toxic elements in biological material are urgently desired, especially for women who reside near e-waste recycling facilities. The aim of this study was to investigate elements concentrations in placenta, cord blood, and maternal blood of women and to evaluate the influencing factors. MethodsA group of 48 women from an e-waste recycling site and a group of 31 women from a non-e-waste recycling site were recruited. Basic characteristics were collected by questionnaire and the concentrations of 17 elements in placenta, cord blood, and maternal blood samples were analyzed by inductively coupled plasma mass spectrometry (ICP-MS). Finally, the generalized linear model regression analysis (GLM) was used to test the association between element concentrations and possible factors. ResultsCompared to the control group, the exposed group had significantly elevated cadmium (Cd), zinc (Zn), nickel (Ni), and antimony (Sb) in placenta, and higher lead (Pb) in maternal blood and cord blood (P<0.05). Sb concentration in maternal blood was significantly lower than in the control group (P<0.05). GLM analysis showed that element concentrations were mainly associated with maternal age [chromium (Cr), iron (Fe), selenium (Se), cobalt (Co), mercury (Hg) in placenta, copper (Cu) in maternal blood], education (Se, Sb in placenta), family income (Cu in maternal blood and Ni in placenta), passive smoking [Cu and Zn in placenta, Pb in maternal blood], and e-waste contact history (Hg in cord blood, Cu, Zn, and Cd in maternal blood). ConclusionsWomen in the e-waste recycling area had higher toxic element levels in the placenta and blood samples. More preventive measures were needed to reduce the risk of element exposure for mothers and fetuses in these areas.

Tetrabromobisphenol-A/S and their derivatives in surface particulates from workshop floors of three representative e-waste recycling sites in China

Surface particulates collected from the workshop floors of three major e-waste recycling sites (Taizhou, Qingyuan, and Guiyu) in China were analyzed for tetrabromobisphenol A/S (TBBPA/S) and their derivatives to investigate the environmental pollution caused by e-waste recycling activities. Mean concentrations of total TBBPA/S analogs in surface particulates were 31,471–116,059 ng/g dry weight (dw). TBBPA, TBBPA-BGE, and TBBPA-BDBPE were the most frequently detected in particulates with average concentration ranges of 17,929–78,406, 5601–15,842, and 5929–21,383 ng/g dw, respectively. Meanwhile, TBBPA, TBBPA-BGE, and TBBPA-BDBPE were the most abundant TBBPA/S analogs, accounting for around 96% of the total. The composition profiles of TBBPA/S analogs differed significantly among three e-waste sites. Similarly, principal component analysis uncovered different pollution patterns among different sites. The discrepancy in the profiles of TBBPA/S analogs largely relied on the e-waste types recycled in different areas. E-waste recycling led to the release of TBBPA/S analogs, and TBBPA/S analogs produced differentiation during migration from source (surface particulates) to nearby soil. More researches are necessary to find a definite relationship between pollution status and e-waste types and study differentiation behavior of TBBPA/S analogs in migration and diffusion from source to environmental medium.

Effects of transient flow conditions on colloid-facilitated release of decabromodiphenyl ether: Implications for contaminant mobility at e-waste recycling sites

Polybrominated diphenyl ethers (PBDEs) are ubiquitous contaminants, especially in the soil and groundwater of contaminated sites and landfills. Notably, 2,2′,3,3′,4,4′,5,5′,6,6′-decabromodiphenyl ether (BDE-209), one of the most frequently and abundantly detected PBDE congeners in the environment, has recently been designated as a new pollutant subject to rigorous control in China. Colloid-facilitated transport is a key mechanism for the release of PBDEs from surface soils and their migration in the aquifer, but the effects of hydrodynamic conditions, particularly transient flow, on colloid-facilitated release of PBDEs are not well understood. Herein, we examined the effects of typical transient flow conditions on the release characteristics of colloids and BDE-209 from surface soil collected from an e-waste recycling site by undisturbed soil core leaching tests involving multiple dry–wet cycles (with different drying durations) and freeze–thaw cycles. We observed significant positive correlations between BDE-209 and colloid concentrations in the leachate in both the dry–wet and freeze–thaw leaching experiments, highlighting the critical role of colloids in facilitating BDE-209 release. However, colloids mobilized during the dry–wet cycles contained higher contents of BDE-209 than those in the freeze–thaw cycle tests, and the difference was primarily due to the more intensive disintegration of soil aggregates and elution of newly formed inorganic colloidal particles (mainly primary silicate minerals such as quartz and albite) with low BDE-209 content during the freeze–thaw process. These findings underscore the necessity of considering transient flow conditions when assessing the fate and risks of PBDEs at contaminated sites.

Preferential association of PBDEs and PAHs with mineral particles vs. dissolved organic carbon: Implications for groundwater contamination at e-waste sites

Polybrominated biphenyl ethers (PBDEs) and polycyclic aromatic hydrocarbons (PAHs) are commonly detected contaminants at e-waste recycling sites. Against the conventional wisdom that PBDEs and PAHs are highly immobile and persist primarily in shallow surface soils, increasing evidence shows that these compounds can leach into the groundwater. Herein, we compare the leachabilities of PBDEs vs. PAHs from contaminated soils collected at an e-waste recycling site in Tianjin, China. Considerable amounts of BDE-209 (0.3–2 ng/L) and phenanthrene (42–106 ng/L), the most abundant PBDE and PAH at the site, are detected in the effluents of columns packed with contaminated soils, with the specific concentrations varying with hydrodynamic and solution chemistry conditions. Interestingly, the leaching potential of BDE-209 appears to be closely related to the release of colloidal mineral particles, whereas the leachability of phenanthrene correlates well with the concentration of dissolved organic carbon in the effluent, but showing essentially no correlation with the concentration of mineral particles. The surprisingly different trends of the leachability observed between BDE-209 and phenanthrene is counterintuitive, as PBDEs and PAHs often co-exist at e-waste recycling sites (particularly at the sites wherein incineration is being practiced) and share many similarities in terms of physicochemical properties. One possible explanation is that due to its extremely low solubility, BDE-209 predominantly exists in free-phase (i.e., as solid (nano)particles), whereas the more soluble phenanthrene is mainly sorbed to soil organic matter. Findings in this study underscore the need to better understand the mobility of highly hydrophobic organic contaminants at contaminated sites for improved risk management.

Heavy Metals Analysis and Physicochemical Characterization of Groundwater at a Battery Recycling Site in South-western Nigeria

Indiscriminate dumping of battery waste is a huge issue that endangers human health and the environment. This study aimed at analysing the health impacts of exposure to pollution from spent battery recycling in Ogun State, which houses a diverse range of battery recycling industries. At this study site, forty water samples were studied over the Wet and Dry seasons to assess the impact of battery recycling waste on groundwater. Except for the TSS, the physiochemical parameters of the groundwater vary with season and are within the permissible limits. The electrical conductivity (EC), turbidity, Phosphorus, Biochemical oxygen demand (BOD), Dissolve oxygen (DO), and Total suspended solid (TSS) within the study year ranges from 51.00 - 178.22 S/cm, 2.26 - 2.36 NTU, 0.089 - 0.66 mg/L, 13.3 - 14.2 mg/L, 5.06 - 5.67 mg/L, and 78.0 - 88.4 mg/L, respectively. Furthermore, the average concentrations (in ppm) obtained for Mn, Cu, Zn, Ni, Cd, As, Fe, Pb, Cr, and Co are 0.407 – 0.42, 0.355 – 0.369, 0.179 – 0.225, 0.061 – 0.265, 0.366 – 0.464, 0.488 – 0.631, 0.544 – 0.601, 0.481 – 0.576, 0.284 – 0.334, 0.3 – 0.382. The Heavy Metal Pollution Index (HPI) values ranging from 3.880 to 4.528 indicate minimal levels of heavy metal contamination, but water quality index (WQI) scores ranging from 124.68 to 131.46 indicate potential environmental hazards.

Historical Occurrence and Composition of Novel Brominated Flame Retardants and Dechlorane Plus in Sediments from an Electronic Waste Recycling Site in South China.

Novel brominated flame retardants (NBFRs) and dechlorane plus (DP) have been widely used as alternatives to traditional BFRs. However, little is known about the temporal trends of NBFR and DP pollution in e-waste recycling sites. In the current study, three composite sediment cores were collected from an e-waste-polluted pond located in a typical e-waste recycling site in South China to investigate the historical occurrence and composition of NBFRs and DP. The NBFRs and DP were detected in all layers of the sediment cores with concentration ranges of 5.71~180,895 and 4.95~109,847 ng/g dw, respectively. Except for 2,3,5,6-tetrabromo-p-xylene (pTBX) and 2,3,4,5,6-pentabromoethylbenzene (PBEB), all the NBFR compounds and DP showed a clear increasing trend from the bottom to top layers. These results implied the long-term and severe contamination of NBFRs and DP. Decabromodiphenyl ethane (DBDPE) was the most abundant NBFR with the contribution proportions of 58 ± 15%, 73 ± 15%, and 71 ± 18% in three sediment cores, followed by 1,2-bis(2,4,6-tribromophenoxy) ethane (BTBPE) and pentabromobenzene (HBB). The ratios of BTBPE/Octa-BDEs and DBDPE/Deca-BDEs varied from 0.12 to 60 and from 0.03 to 0.49, respectively, which had no clear increase trends with a decrease in sediment depth. As for DP, the fanti values (the concentration ratios of anti-DP to the sum of anti-DP and syn-DP) in sediment cores ranged from 0.41 to 0.83, almost falling in the range of those in DP technical products, suggesting that DP degradation did not occur in sediment cores. The environmental burdens of DBDPE, BTBPE, HBB, PBT, PBEB, pTBX, and DP were estimated to be 34.0, 5.67, 10.1, 0.02, 0.02, 0.01, and 34.8 kg, respectively. This work provides the first insight into the historical contamination status of NBFRs and DP in the sediments of an e-waste recycling site.

An extracellular matrix-mimicking magnetic microrobot for targeted elimination of circulating cancer cells.

Cancer cells disseminate through the bloodstream, leading to metastasis in distant sites within the body. One promising strategy to prevent metastasis is to eliminate circulating tumor cells. However, this remains challenging due to the lack of an active and targeted biomedical tool for efficient cancer cell elimination. Here, we developed a magnetic microrobot by using natural materials derived from the extracellular matrix (ECM) to mimic the ligand-receptor interaction between cancer cells and the ECM, offering targeted elimination of cancer cells. The ECM-mimicking microrobot is designed with a biodegradable hydrogel matrix, incorporating a cancer cell ligand and magnetic microparticles for cancer cell capture and active locomotion. This microrobot was fabricated based on an interface-shearing method, enabling controllable magnetic response and size scalability (30 μm-500 μm). The presented ECM-mimicking microrobot can actively approach and capture single cancer cells and cell clusters under the control of specific magnetic fields. The experiment was conducted in a blood vessel-mimicking simulator. The microrobot demonstrates an outstanding elimination efficacy of 92.3% on MDA-MB-231 cancer cells and a stable transport capability of the captured cells over long distances to a designed recycling site, inhibiting cell metastasis. This magnetic ECM-mimicking microrobot based on a bioinspired binding mechanism represents a promising candidate for the efficient elimination of cancer cells and other biological waste in the blood.

A comprehensive assessment of external exposure to persistent halogenated organic pollutants for residents in an e-waste recycling site, South China

Human skin wipes from 30 participants, air, dust, and food items were collected from a former electronic waste site in South China to provide a comprehensive understanding of residents' exposure to halogenated flame retardants (HFRs) and polychlorinated biphenyls (PCBs). The total concentration of halogenated organic pollutants (HOPs) in the dust, air, food and skin wipes ranged 240–25000 ng/g, 130–2500 pg/m3, 0.08–590 ng/g wet weight, and 69–28000 ng/m2, respectively. Wild fish, vegetables, and air were dominated by PCBs, whereas dust, livestock, and poultry were dominated by HFRs. The HOP concentrations were several orders of magnitude higher in local foodstuffs than in market foodstuffs. The chemical composition on the forehead was remarkably different from that on the hand. The importance of different exposure routes depends on the residents’ food choices, except decabromodiphenyl ethane (DBDPE). For residents who consumed a 100-foot diet (mainly egg) and local wild fish, diet ingestion overwhelmed other exposure routes, and PCBs were mainly contributed by fish and HFRs by egg. For residents who consumed market food, the dermal absorption of most PCB congeners and dust ingestion of highly brominated flame retardants were relatively prominent. Inhalation was found to be a crucial route for pentabromoethylbenzene (PBEB).

Liquid crystal monomers in soils near the e-waste recycling site and liquid crystal display manufacturer: Exponential decrease with distance

Liquid crystal monomers (LCMs) have been recognized as contaminants of emerging concerns. E-waste recycling sites and liquid crystal displays (LCDs) manufacturers are supposed to be critical sources. However, information regarding LCM contaminations in soils surrounding these sites are currently unavailable. In this study, soil samples were collected from two distinct areas in South China: e-waste recycling area (n = 36) and LCD manufacturer (n = 41), and 60 target LCMs (including 13 biphenyl and analogs (BAs), 10 cyanobiphenyl and analogs (CBAs), and 37 fluorinated biphenyl and analogs (FBAs)) were determined. The concentrations of LCMs in the soils from near the e-waste recycling area (0.32–18 ng/g, average: 4.2 ng/g) were higher than those surrounding the LCD manufacturer (ND – 7.2 ng/g, average: 1.5 ng/g). The compositional profiles of LCMs in soil samples from these two typical point sources were considerably different. The concentrations of FBAs exponentially decreased with distance from the e-waste recycling park, by >90 % within 2 km. The levels of BAs exhibited a similar exponential decrease with distance from the LCD manufacturer. The inventories of LCMs were estimated to be 21.0 kg in the e-waste recycling area and 10.8 kg in the LCD manufacturer area. Remarkably, the inventory of LCMs in soils from e-waste recycling area was one order of magnitude larger than that of hexabromocyclododecanes (HBCDs) in the same region, and 0.2 to 20 times the annual global emissions of LCMs from discarded LCD panels. More studies are required to elucidate the environmental occurrence, behavior, and fate of LCMs in multimedia environment surrounding typical point sources.

Concentrations and biomagnification of persistent organic pollutants in three granivorous food chains from an abandoned e-waste recycling site.

The distinct accumulation patterns of persistent organic pollutants (POPs) among granivorous groups and the biomagnification of POPs from crops to granivorous species are still unclear. In this study, occurrence and biomagnification of POPs in three granivorous species including spotted dove (Spilopelia chinensis), scaly-breasted munia (Lonchura punctulata), and reed vole (Microtus fortis Buechner) from a former e-waste recycling site were investigated. Concentrations of polychlorinated biphenyls (PCBs) and polybrominated diphenyl ethers (PBDEs) in granivorous species ranged from 41.5 to 1370 and 21.1 to 3890ng/g lipid weight, respectively. PCBs and PBDEs were the main POPs in birds and vole, while decabromodiphenyl ethane (DBDPE) and PBDEs were predominant POPs in crops. The dominance of BDE 209 was observed in samples, with few exceptions. Biomagnification factors (BMFs) of POPs in birds and vole were measured. BMFs of most POPs in vole were higher than those in birds, indicating that POPs had greater biomagnification potential in vole. Species-specific biomagnification of POPs might be affected by many factors, such as physiochemical properties and metabolic capability of POPs. There was significant correlation between concentration ratios of POPs in muscle/air and log KOA, which demonstrated that respiratory elimination to air affects biomagnification of POPs in granivorous birds and vole.

Soil colloids can significantly enhance spreading of polybromodiphenyl ethers in groundwater by serving as an effective carrier

Polybromodiphenyl ethers (PBDEs), the widely used flame retardants, are common contaminants in surface soils at e-waste recycling sites. The association of PBDEs with soil colloids has been observed, indicating the potential risk to groundwater due to colloid-facilitated transport. However, the extent to which soil colloids may enhance the spreading of PBDEs in groundwater is largely unknown. Herein, we report the co-transport of decabromodiphenyl ester (BDE-209) and soil colloids in saturated porous media. The colloids released from a soil sample collected at an e-waste recycling site in Tianjin, China, contain high concentration of PBDEs, with BDE-209 being the most abundant conger (320 ± 30 mg/kg). The colloids exhibit relatively high mobility in saturated sand columns, under conditions commonly observed in groundwater environments. Notably, under all the tested conditions (i.e., varying flow velocity, pH, ionic species and ionic strength), the mass of eluted BDE-209 correlates linearly with that of eluted soil colloids, even though the mobility of the colloids varies markedly depending on the specific hydrodynamic and solution chemistry conditions involved. Additionally, the mass of BDE-209 retained in the columns also correlates strongly with the mass of retained colloids. Apparently, the PBDEs remain bound to soil colloids during transport in porous media. Findings in this study indicate that soil colloids may significantly promote the transport of PBDEs in groundwater by serving as an effective carrier. This might be the reason why the highly insoluble and adsorptive PBDEs are found in groundwater at some PBDE-contaminated sites.

Risk assessment and partitioning behavior of PFASs in environmental matrices from an e-waste recycling area

ObjectivePerfluoroalkyl and polyfluoroalkyl substance (PFAS) contamination and their human exposure risks are a major concern. However, knowledge of PFAS contamination in environments near e-waste recycling sites and their health risk assessment are scarce. MethodsWe measured the concentrations of PFASs in soil (n = 12), water (n = 12) and atmospheric samples (n = 26) by LCP-MS/MS, analyzed the source apportionment of PFASs by PCA, and investigated the child health risk assessment from an e-waste recycling area (Guiyu) and a reference area (Haojiang). ResultsWe found high concentrations of PFASs in the atmosphere and low concentrations of PFASs in soil. The average concentration of perfluoro-n-heptanoic acid (PFHpA) (9.43 ng/L) was highest among PFASs in water. The concentrations PFASs in the atmosphere and water were higher in the e-waste recycling area than in the reference area (p < 0.05). According to Multi-Linear regression model, we found that daily intake doses for PFASs in air of PFODA [β (95 % CI): −0.217 (−0.332, −0.048), p < 0.05] and PFBS [β (95 % CI): −0.064 (−0.106, −0.006), p < 0.05] were negatively associated with child BMI. PFBA [β (95 % CI: −1.039 (−2.454, −0.010), p < 0.05] was negatively correlated with child head circumference. ConclusionThe concentrations of PFASs in the water and atmosphere are higher in the e-waste recycling site than in the reference area. We found that their intake affected growth and development in children. We need to reduce pollution from PFASs in the e-waste recycling area while maintaining a focus on their impact on child health.

Colloid-facilitated release of polybrominated diphenyl ethers at an e-waste recycling site: evidence from undisturbed soil core leaching experiments

Colloid-facilitated release of polybrominated diphenyl ethers at an e-waste recycling site: evidence from undisturbed soil core leaching experiments

Optimization of carton recycling site selection using particle swarm optimization algorithm considering residents' recycling willingness.

With the development of the express delivery industry, how to increase the recycling rate of waste cartons has become a problem that needs to be solved. Recycling enterprises began to provide the new recycling mode, door-to-door recycling services, to residents with waste cartons. In this article, we constructed a site selection model for a carton recycling site with the aim of maximizing total profits. Considering the residents' recycling willingness and the government subsidy earned through the contribution to carbon emission reduction, this model achieves the task of site selection and unit price fixation for carton recycling. We used the particle swarm optimization (PSO) algorithm to solve the model and compared it with the genetic algorithm (GA) for validity testing. PSO algorithm was also used to carry out sensitivity analysis in this model. The proposed model and the results of the sensitivity analysis can be used for decision-making in recycling enterprises as well as for further research on waste recycling and reverse logistics.