Core-Shell Au@Nanoplastics as a Quantitative Tracer to Investigate the Bioaccumulation of Nanoplastics in Freshwater Ecosystems.

Studies on the adverse effects of nanoplastics (NPs, particle diameter <1000 nm) including physical damage, oxidative stress, impaired cell signaling, altered metabolism, developmental defects, and possible genetic damage have intensified in recent years. However, the analytical detection of NPs is still a bottleneck. To overcome this bottleneck and obtain a reliable and quantitative distribution analysis in complex freshwater ecosystems, an easily applicable NP tracer to simulate their fate and behavior is needed. Here, size- and surface charge-tunable core-shell Au@Nanoplastics (Au@NPs) were synthesized to study the environmental fate of NPs in an artificial freshwater system. The Au core enables the quantitative detection of NPs, while the polystyrene shell exhibits NP properties. The Au@NPs showed excellent resistance to environmental factors (e.g., 1% hydrogen peroxide solution, simulating gastric fluid, acids, and alkalis) and high recovery rates (>80%) from seawater, lake water, sewage, waste sludge, soil, and sediment. Both positively and negatively charged NPs significantly inhibited the growth of duckweed (Lemna minor L.) but had little effect on the growth of cyanobacteria (Microcystis aeruginosa). In addition, the accumulation of positively and negatively charged NPs in cyanobacteria occurred in a concentration-dependent manner, with positively charged NPs more easily taken up by cyanobacteria. In contrast, negatively charged NPs were more readily internalized in duckweed. This study developed a model using a core-shell Au@NP tracer to study the environmental fate and behavior of NPs in various complex environmental systems.

Effects of size and surface charge on the sedimentation of nanoplastics in freshwater.

The environmental issues caused by nanoplastics (NPs) are increasingly noticeable. Environmental behavior study of the NPs could provide vital information for their environmental impact assessment. However, associations between NPs' inherent properties and their sedimentation behaviors were seldom investigated. In this study, six types of PSNPs (polystyrene nanoplastics) with different charges (positive and negative) and particle sizes (20-50 nm, 150-190 nm and 220-250 nm) were synthesized, and their sedimentations under different environmental factors, (e.g., pH value, ionic strength (IS), electrolyte type and natural organic matter) were investigated. Results displayed that both particle size and surface charge would affect the sedimentation of PSNPs. The maximum sedimentation ratio of 26.48% was obtained in positive charged PSNPs with size of 20-50 nm, while the minimum sedimentation ratio of 1.02% was obtained in negative charged PSNPs with size of 220-250 nm at pH 7.6. The pH value shift (range of 5-10) triggered negligible changes of sedimentation ratio, the average particle size and the Zeta potential. Small size PSNPs (20-50 nm) showed higher sensitivity to IS, electrolyte type and HA condition than large size PSNPs. At high IS value ( [Formula: see text]  = 30 mM or ISNaCl = 100 mM), the sedimentation ratios of the PSNPs all increased differently according to their properties, and the sedimentation promoting effect of CaCl2 was more significant on negative charged PSNPs than positive charged PSNPs. When [Formula: see text] increased from 0.9 to 9 mM, the sedimentation ratios of negative charged PSNPs increased by 0.53%-23.49%, while that of positive charged PSNPs increased by less than 10%. Besides, humic acid (HA) addition (1-10 mg/L) would lead to a stable suspension status for PSNPs in water with different degree and perhaps different mechanism due to their charge characteristics. These results showed new light on influence factor studies of NPs' sedimentation and would be helpful for further knowledge of NPs' environmental behaviors.

Improved methane elimination by methane-oxidizing bacteria immobilized on modified oil shale semicoke.

Methane is a greenhouse gas with significant global warming potential. The methane-oxidizing bacteria (MOB) immobilized on biocarrier could perform effectively and environmentally in methane elimination. To further improve the efficiencies of MOB immobilization and methane elimination, the surface biocompatibility of biocarrier needs to be improved. In this work, the oil shale semicoke (SC) was chemically modified by sodium p-styrenesulfonate hydrate (SS) and 2-(methacryloyloxy)ethyltrimethylammonium chloride (DMC) to promote surface hydrophilicity and positive charge, respectively. Results revealed that, under methane concentrations of ~10% (v/v) and ~0.5% (v/v), the MOB immobilized on semicoke modified with 1.0 mol L-1 of SS permitted improved methane elimination capacities (ECs), which were 15.02% and 11.11% higher than that on SC, respectively. Additionally, under methane concentrations of ~10% (v/v) and ~0.5% (v/v), the MOB immobilized on semicoke modified with 0.4 mol L-1 of DMC held superior ECs, which were 17.88% and 11.29% higher than that on SC, respectively. The qPCR analysis indicated that the MOB abundance on modified semicoke were higher than that on SC. In consequence, the surface biocompatibility of semicoke could be promoted by SS and DMC modifications, which potentially provided methods for other biocarriers to improve surface biocompatibility.

Bioaugmentation with an acetate-type fermentation bacterium Acetobacteroides hydrogenigenes improves methane production from corn straw.

The effect of bioaugmentation with an acetate-type fermentation bacterium in the phylum Bacteroidetes on the anaerobic digestion of corn straw was evaluated by batch experiments. Acetobacteroides hydrogenigenes is a promising strain for bioaugmentation with relatively high growth rate, hydrogen yields and acetate tolerance, which ferments a broad spectrum of pentoses, hexoses and polyoses mainly into acetate and hydrogen. During corn straw digestion, bioaugmentation with A. hydrogenigenes led to 19-23% increase of the methane yield, with maximum of 258.1 mL/g-corn straw achieved by 10% inoculation (control, 209.3 mL/g-corn straw). Analysis of lignocellulosic composition indicated that A. hydrogenigenes could increase removal rates of cellulose and hemicelluloses in corn straw residue by 12% and 5%, respectively. Further experiment verified that the addition of A. hydrogenigenes could improve the methane yields of methyl cellulose and xylan (models for cellulose and hemicelluloses, respectively) by 16.8% and 7.0%.