Characterization of microplastic-derived dissolved organic matter in freshwater: Effects of light irradiation and polymer types.

This study investigated the impacts of light irradiation and polymer types on the leaching behavior of dissolved organic matter (DOM) from microplastics (MPs) in freshwater. Polypropylene had the highest leaching capacity of DOM after photoaging, followed by polystyrene (PS), polyamide (PA) and polyethylene terephthalate (PET). While similarly low levels of DOM were observed in the remaining 5 MP suspensions under UV irradiation and in almost all MP suspensions (except PA) under darkness. These suggest that the photooxidation of some buoyant plastics may influence the carbon cycling of nature waters. Among 9 MP-derived leachates, PET leachates had the highest chromophoric DOM concentration and aromaticity, probably owing to the special benzene rings and carbonyl groups in PET structures and its fast degradation rate. Protein-like substances were the primary fluorescent DOM in MP suspensions (except PS), especially in darkness no other fluorescent substances were found. Considering the bio-labile properties of proteins together, MPs regardless of floating or suspended in an aquatic environment may have prevalent long-term effects on microbial activities. Besides, from monomers to hexamers with newly formed chemical bonds were identified in UV-irradiated MP suspensions. These results will contribute to a deep insight into the potential ecological effects related to MP degradation.

Determination of organotin compounds in marine sediments from Arctic Svalbard and West Antarctic Fildes Peninsula.

This study investigated the contamination levels of five typical organotin compounds in Arctic and Antarctic marine sediments. Organotin total concentrations ranged from not detected (ND) to 37.9 ng Sn/g dw and from ND to 34.0 ng Sn/g dw in surface sediments of Svalbard and Fildes Peninsula, respectively. Dibutyltin accounted for 11.3 %-100 % of butyltins in Arctic sediments, whilst diphenyltin was the predominant phenyltin species in both Arctic and Antarctic. However, the concentrations of tributyltin and triphenyltin were lower than low-substituted organotins in the study areas, indicating the effectiveness of international ban on the use of triorganotin-based antifouling paints. No significant difference in organotin contamination was found between Arctic and Antarctic, although the time suffered from human interference was shorter in the Antarctic. Overall, these data can provide a diagnosis of recent organotin inputs in polar regions and serve as a baseline for future study assessing their local applications.

A syndromic diagnostic assay on a macrochannel-to-digital microfluidic platform for automatic identification of multiple respiratory pathogens.

The worldwide COVID-19 pandemic has changed people's lives and the diagnostic landscape. The nucleic acid amplification test (NAT) as the gold standard for SARS-CoV-2 detection has been applied in containing its transmission. However, there remains a lack of an affordable on-site detection system at resource-limited areas. In this study, a low cost "sample-in-answer-out" system incorporating nucleic acid extraction, purification, and amplification was developed on a single macrochannel-to-digital microfluidic chip. The macrochannel fluidic subsystem worked as a world-to-chip interface receiving 500-1000 µL raw samples, which then underwent bead-based extraction and purification processes before being delivered to DMF. Electrodes actuate an eluent dispensed to eight independent droplets for reverse transcription quantitative polymerase chain reaction (RT-qPCR). By reading with 4 florescence channels, the system can accommodate a maximum of 32 detection targets. To evaluate the proposed platform, a comprehensive assessment was conducted on the microfluidic chip as well as its functional components (i.e., extraction and amplification). The platform demonstrated a superior performance. In particular, using clinical specimens, the chip targeting SARS-CoV-2 and Flu A/B exhibited 100% agreement with off-chip diagnoses. Furthermore, the fabrication of chips is ready for scaled-up manufacturing and they are cost-effective for disposable use since they are assembled using a printed circuit board (PCB) and prefabricated blocks. Overall, the macrochannel-to-digital microfluidic platform coincides with the requirements of point-of-care testing (POCT) because of its advantages: low-cost, ease of use, comparable sensitivity and specificity, and availability for mass production.

Microplastics in the Bronchoalveolar Lavage Fluid of Chinese Children: Associations with Age, City Development, and Disease Features.

This study characterized the occurrence patterns of microplastics (MPs) in the bronchoalveolar lavage fluid (BALF) of children with pulmonary diseases. MPs were detected in 89.6% of BALF samples with an average of 4.31 ± 2.77 items/10 mL, supporting the hypothesis that inhalation is a significant pathway of airborne MP exposure to pediatric lungs. Inhaled MPs were predominantly composed of 10 polymer types [e.g., polypropylene (41.9%), polyethylene (19.4%), and polyester (13.6%)], with the majority being smaller than 20 µm. MP levels in BALF exhibited a negative correlation with children's age, probably owing to the preferential crawling and tumbling actions in indoor environments and underdeveloped immune systems of young children. Participants living in urban areas suffered from higher pulmonary MP exposure, likely due to higher environmental levels, compared with suburban/rural residents (P < 0.05). Although no significant differences were found between MP levels in pediatric lungs with community-acquired pneumonia (CAP) and asthma (P > 0.05), the severe CAP group displayed significantly higher MP contamination than the nonsevere group (P < 0.05), indicating that some yet undiscovered relationship(s) between inhaled MPs and pediatric pulmonary diseases may exist.

Pulsed distribution of organotins in the turbidity maximum zone of the Yangtze Estuary throughout a tidal cycle.

This study investigated the concentration fluctuation of organotin compounds in the Turbidity Maximum Zone (TMZ) of the Yangtze Estuary within a tidal cycle. Organotin concentrations varied greatly during the tidal cycle with dissolved organotins ranged from 39 to 682 ng Sn·L-1 and 40-1588 ng Sn·L-1, and particulate organotins ranged from 59 to 467 ng Sn·g-1 dw and 21-429 ng Sn·g-1 dw in TMZ water close to Hengsha Island and Jiuduansha Island, respectively. Meanwhile, the maximum levels of organotins appeared at each period of tidal transition, suggesting the tidal-driven pulsed exposure of organotins was prevalent in the estuaries. Besides, the organic carbon-normalized partition coefficients (Koc) of tri-organotins between suspended particulate matter (SPM) and aqueous phase were correlated with the phase distribution of natural organic matter (NOM). The dissolved tri-organotins were also associated with the properties of dissolved organic carbon (DOC) including aromaticity, hydrophobicity, and chromophoricity. Hence, pulsed exposure on organotins in the TMZ are highly dictated by the dynamic environmental conditions (i.e., SPM and NOM) with the tidal currents, which could further provide information to assess organotin ecological risks accurately in estuaries.

Impacts of microplastics on organotins' photodegradation in aquatic environments.

Microplastics are ubiquitous in natural waters and affect the environmental fate of hydrophobic organic micropollutants. This study evaluated the impacts of four microplastics, polypropylene (PP), polyethylene (PE), polystyrene (PS) and polymethyl methacrylate (PMMA), on the photodegradation of organotin compounds (OTCs) under UV365 irradiation (2.3 ± 0.1 W m-2). The experiments were performed by mixing PP, PE, PS or PMMA microparticles with tri-organotins in artificial seawater. The photodegradation of OTCs in microplastic suspensions was influenced by the absorptivity onto microplastics. The decomposition rate of tributyltin (TBT) in UV-irradiated PP suspensions was greater than trimethyltin (TMT) and triphenyltin (TPhT) (p < 0.01). The adsorption capacities of OTCs (e.g., TBT) on PP particle surfaces were significantly lower than those on PE surfaces (p < 0.05) but similar with those on PMMA due to the different surface areas, shapes, and surface hydrophobicity of microplastics. TBT degraded faster (9.1%) in PS than in PMMA suspension (11.2%) within 240 min, respectively. However, only less than 5.4% was photodegraded in PP suspension due to the light scattering or absorption of the large sized PP particles. This study provided new insight into the impacts of microplastics on photodegradation of micropollutants in natural waters.

The source apportionment, pollution characteristic and mobility of Sb in roadside soils affected by traffic and industrial activities.

Antimony (Sb), as an emerging pollutant, has aroused people's concerns for its wide usage in industrial production. In this study, we identify and quantify the traffic-derived Sb and investigate its mobility in roadside soils affected by traffic and industrial activities. 73 surface roadside soils and 5 transects in three areas nearby different industries (smelting, power and refining, and waste incineration) were collected and analyzed. Results showed that the Sb concentration ranged between 0.54 and 9.32 mg/kg, and the mean EFs value was 4.63, which indicated moderate to significant Sb enrichment. Significantly high concentrations of Sb occurred at locations with heavy traffic and frequent braking process, with an average concentration of 4.13 mg/kg, compared to the control sites (2.01 mg/kg). Moreover, Sb diffused exponentially with increasing distance from road edges. These results suggested that traffic activities were the main source of Sb in roadside soils. According to the quantitative calculation, the average contributions from traffic, industrial activities and soil parent material to Sb accumulation in roadside soils were 50.73%, 21.38% and 27.88%, respectively. Even though Sb was slightly mobile, roadside soils was a persistent source of potentially mobile Sb which may release into water and cause long-term environmental risk.

Organotin Release from Polyvinyl Chloride Microplastics and Concurrent Photodegradation in Water: Impacts from Salinity, Dissolved Organic Matter, and Light Exposure.

Photochemical weathering leads to degradation of microplastics and releases chemical additives, polymeric fragments, and/or byproducts. This study evaluated the release kinetics of organotin compounds (OTCs) from three different sized (10-300 µm) polyvinyl chloride (PVC) microplastics under UV- and visible light irradiation. Four OTCs, dimethyltin (DMT), monomethyltin (MMT), dibutyltin (DBT), and monobutyltin (MBT), were found to release from PVC particles after 24 h leaching in darkness ranging from 2 to 20 µg·g-PVC-1. Under UV/visible light irradiation, only DMT and DBT were detectable, whereas MMT and MBT were not detected due to rapid photodegradation. The total tin concentrations (including organic and inorganic tins) in the aqueous phase monotonically increased under light exposure. By contrast, they reached plateaus after 24 h in darkness, confirming the photodegradation of OTCs. A release kinetics model was established and correctly interpreted the microplastics size effect on the OTC release process. Finally, the impacts of salinity and dissolved organic matter (DOM) were investigated. The release and photodegradation of OTCs were both inhibited at high salinity conditions, probably due to the enhanced readsorption of OTCs on PVC microplastics and the formation of halogen radicals that were less reactive toward neutral OTCs. The presence of DOM, however, increased OTCs release probably because the excited state triplet DOM (3DOM*) formed and reacted with OTCs from PVC microplastics.

Urgent caution to trace organometal pollution: Occurrence, distribution and sources of methyltins, butyltins and phenyltins in sediments from South Hangzhou Bay, China.

The concentrations of seven organotin compounds (OTCs) were determined seasonally in 22 sediment samples (brackish, freshwater and shrimp pond sediments) in South Hangzhou Bay, China. For the brackish and freshwater sediments, methyltins of up to 43.0 ng Sn g-1 dw showed no significant variation with seasons or locations (p > 0.05). However, butyltin levels in summer (44.0 ±â€¯30.2 ng Sn g-1 dw) were about two folds higher than those in spring (20.4 ±â€¯18.7 ng Sn g-1 dw) and four folds higher than in autumn or winter (both≈10 ng Sn g-1 dw), which is mainly attributed to the heavy contamination near the shipyard, mariculture and textile plants in summer. Phenyltins in spring reached the peak level of 28.4 ng Sn g-1 dw, about three times of other seasons. Meanwhile, there was a significant variation of phenyltins in summer with high-value sites also in the vicinity of mariculture. Thus, excepting the contribution of agricultural activities to phenyltins, mariculture is likely to be a potential source of butyltins and phenyltins into the marine environment (particularly in summer). This hypothesis has been partly validated by determining adjacent shrimp pond sediments, which showed ubiquitous contamination of butyltins and phenyltins in summer and spring (14.2-44.2 ng Sn g-1 dw and 2.2-16.9 ng Sn g-1 dw), but only one sample had the detectable methyltin levels with 8.8 ng Sn g-1 dw of momomethyl-tin. On the other hand, seven OTCs showed a stronger affinity to brackish sediments than the adjacent freshwater sediments, probably owing to the differences of physicochemical parameters and microbial activities in sediments. Overall, OTC contaminants have become more diversified and complicated in coastal zones, suggesting that future studies should pay attention to other OTC species like phenyltins and methyltins, not only the butyltins.

Organotin contamination in commercial and wild oysters from China: Increasing occurrence of triphenyltin.

Organotin contamination in marine environment has been a public concern for many years due to its adverse impacts on biota and human health. This study investigated levels, distribution and health risks of six organotin compounds: tributyltin (TBT), dibutyltin (DBT), monobutyltin (MBT), triphenyltin (TPhT), diphenyltin (DPhT) and monophenyltin (MPhT) in commercial and wild oysters in China. The total organotin in commercial oysters ranged from 251 to 1949 ng Sn g-1 dw (dry weight) >. Two endocrine disruptors TBT and TPhT were detected in these samples with the highest level of 68.1 ±â€¯20.1 ng Sn g-1 dw and 747 ±â€¯7.3 ng Sn g-1 dw, respectively. For wild oysters, the concentrations of total organotins varied from 33.3 to 2671 ng Sn g-1 dw. Butyltins were dominated by TBT with the mean level of 26.1 ±â€¯30.0 ng Sn·g-1 dw and showed no significant spatial variation between the southern and northern coastal zones (p > 0.05). However, compared with the north, phenyltin levels especially TPhT were much higher in the south coastline (246-1484 ng Sn·g-1 dw) due to the wider use of TPhT-based biocides in local mariculture and agriculture. Health risk assessment indicated that a daily exposure of TPhT-contaminated oysters (including commercial and wild ones) may pose adverse threats to human particularly children as the risk quotients (RQ) were higher than 1. Organotin contamination (e.g., TPhT) still occurs in the South China's coastal zones after the TBT ban, which deserves future research and effective measures to protect the marine ecosystem and human health.

On the optimization of a rolling-force model for a hot strip finishing line.

This paper starts with a profound analysis of rolling-force calculation models of two hot strip rolling product lines. According to classical theory of rolling-force calculation, the structure of rolling-force calculation model is firstly optimized. Then with application of data mining techniques, including clustering sampling approach and optimization algorithm, to the field data from product line, the value of key coefficients of the model is adjusted. By the proposed optimization scheme, a better rolling-force prediction is achieved.