Adsorption of Cu2+ by UV aged polystyrene in aqueous solution.

Microplastics are the critical carriers of heavy metals in the environment. Thus, investigating the adsorption mechanisms between the microplastics and heavy metals is helpful to understand the migration and transformation pattern of the heavy metals in the environment. The adsorption of microplastics towards heavy metals can be largely affected by natural aging (e.g., UV-aging), environmental pH, and salinity. In this study, the adsorption of polystyrene (PS) towards Cu2+ and the effects of UV-aging, environment pH, and salinity on the adsorption were systematically investigated. The results show that the adsorption capacity of PS towards Cu2+ increased with the UV-aging time, as UV-aging increased the microcracks and oxygen-containing functional groups on the surface of the PS. Adsorption kinetics data followed the pseudo-second-order model, indicating that the interaction between PS and Cu2+ is chemical adsorption. Adsorption isotherms data could be well-described by both the Langmuir and Freundlich models, indicating that the adsorption was multilayer adsorption. As the solution pH and salinity can influence the surface charge of the PS, they could also affect the performance of the PS on Cu2+ adsorption. High pH facilitated the adsorption of PS towards Cu2+, while high salinity (above 1‰) inhibited the adsorption.

Effects of complex pollution by microplastics and heavy metals on soil physicochemical properties and microbial communities under alternate wetting and drying conditions.

Microplastics (MPs) broadly coexist with heavy metals (HMs) in soil, Cd and Cu are the main types of soil HMs contamination, in addition to polystyrene (PS), which is also widely present in the environment and prone to aging. However, differences in the effects of MPs and HMs on soil properties and microbial characteristics under alternating wetting and drying (AWD) remain unclear. Thus, this study investigated the effects of four conventional (0.2% (w/w)) and aged MPs in indoor incubation experiments on soil properties under desiccation (Dry) and AWD. We found that with the influence of the "enzyme lock" theory, the coexistence of MPs and HMs under Dry had a more pronounced effect on soil physicochemical properties, whereas the effects on soil enzyme activity under AWD were more significant. In addition, MPs decreased the available Cu by 4.27% and, conversely, increased the available Cd by 8.55%. Under Dry, MPs affected microbial function mainly through physicochemical properties, with a contribution of approximately 72.4%, whereas under AWD enzyme activity and HMs were significantly greater, with increases of 28.2% and 7.9%, respectively. These results indicate that the effects of MPs on environmental variation and microbial profiles under AWD conditions differed significantly from those under Dry.

Tetracycline adsorption trajectories on aged polystyrene in a simulated aquatic environment: A mechanistic investigation.

Microplastics (MPs) have attracted widespread attention as an organic class of pollutants as well as pollutant carriers in recipient aquatic ecosystems. In this study, tetracycline (TC) adsorption by polystyrene (PS), with multiple aging-based temporal changes in the adsorption mechanism, was observed. The results revealed that the pseudo-second-order model accurately predicted the TC adsorption kinetics for different types of PS. In addition, the isothermal adsorption processes fit the Freundlich model; however, their interactions were drastically weakened at lower temperatures or increasing salinities. Corresponding to the electrostatic interactions, adsorption TC was largely pH-dependent, with the maximum adsorbed TC content on the PS surface at a pH of 5 in an aqueous environment. More importantly, mechanistic studies have revealed that, compared to virgin PS, TC complexes with aged PS are principally controlled by hydrogen bonding and ionic interactions, followed by π-π, polar-polar, and van der Waals interactions. These findings will aid in understanding the insights of TC and aged PS interactions and the underlying interactive molecular forces, which will be advantageous for comprehending the real case scenario of inter-pollutant interactions and related environmental pollution.

Distribution of microplastics in the sludge of wastewater treatment plants in chengdu, China.

Large amounts of microplastics can accumulate in wastewater treatment plants (WWTPs), and sludge disposal is suspected to be a major source of microplastics pollution in the environment. It is therefore important to investigate the distribution of microplastics in the sludge of each processing unit of WWTPs. However, little information is available on this topic in China. Accordingly, in this study, the abundance and characteristics of microplastics in the sludge of two WWTPs in Chengdu were investigated. The abundance of microplastics in the sludge samples ranged from 44.4 n·kg-1 to 750.0 n·kg-1. Microplastics were mainly divided into particles (32.16%), debris (28.14%) and fibers (17.08%) according to their shape, and the colors of the microplastics were mainly green (35.19%) and translucent (18.06%). The particle sizes were mainly larger than 1 mm in dimension. Polyethylene, polypropylene and polystyrene were the prevalent types of microplastics analyzed. Our results provide basic information for better understanding the characteristics of microplastics in sludge and for improving sludge treatment.

Fabrication of spherical lignin nanoparticles using acid-catalyzed condensed lignins.

Valorization of lignin by-products enhances the overall economics of current lignocellulose biorefinery. This work showed the high potential of fabricating acid-catalyzed condensed lignin fragments into high-value lignin nanoparticles (LNPs) with spherical structure. Four condensed lignins, i.e., liquid hot water pretreated hardwood aspen and eucalyptus lignin, steam pretreated softwood lodgepole pine and herbaceous corn stover lignin, were assessed for their abilities for LNPs using facile self-assembly method. Results showed the contents of condensed aromatics (0.20-0.67 mmol g-1) were varied with biomass species and hydrothermal pretreatment methods selected. Those resulting LNPs exhibited yields from 17.5 to 29.4%, particle sizes ranging from 20 to 100 nm and considerable suspension stabilities at pH 4-10. It was proposed that higher content of condensed lignin aromatics could provide more anchors available for their self-assembly through enhanced hydrophobic interactions, thus LNPs with more uniform particle size could be obtained. This work showed the technical opportunity to enhance the value of intractable condensed lignin through LNPs production towards a multi-product lignocellulose biorefinery.

Acidic deep eutectic solvents pretreatment for selective lignocellulosic biomass fractionation with enhanced cellulose reactivity.

This work tailored a promising two-step pretreatment, i.e., liquid hot water extraction followed by mild acidic deep eutectic solvents pretreatment for clean lignocellulose fractionation while enhancing cellulose reactivity for its subsequent utilization. The abilities of three acidic deep eutectic solvents (formic acid-, acetic acid- and lactic acid-choline chloride) to selectively extract poplar wood lignin and enhance cellulose reactivity were comparatively assessed. Results showed that rather high lignin selectivity of 6.3-7.9 was obtained while the available area and porosity of the resulting cellulose were significantly increased. The resulting cellulose pulps exhibited comparable chemical reactivity to commercial bleached Kraft pulp when cellulose acetate was selected as testing cellulose derivative for demonstrating purpose, showing their great promise for high-value use. It was proposed that the unique ionic properties of these acidic deep eutectic solvents were responsible for their selective lignin removal and cellulose swelling/deconstruction to enhance cellulose chemical reactivity.

Nitrogen addition significantly affects forest litter decomposition under high levels of ambient nitrogen deposition.

BACKGROUND: Forest litter decomposition is a major component of the global carbon (C) budget, and is greatly affected by the atmospheric nitrogen (N) deposition observed globally. However, the effects of N addition on forest litter decomposition, in ecosystems receiving increasingly higher levels of ambient N deposition, are poorly understood. METHODOLOGY/PRINCIPAL FINDINGS: We conducted a two-year field experiment in five forests along the western edge of the Sichuan Basin in China, where atmospheric N deposition was up to 82-114 kg N ha(-1) in the study sites. Four levels of N treatments were applied: (1) control (no N added), (2) low-N (50 kg N ha(-1) year(-1)), (3) medium-N (150 kg N ha(-1) year(-1)), and (4) high-N (300 kg N ha(-1) year(-1)), N additions ranging from 40% to 370% of ambient N deposition. The decomposition processes of ten types of forest litters were then studied. Nitrogen additions significantly decreased the decomposition rates of six types of forest litters. N additions decreased forest litter decomposition, and the mass of residual litter was closely correlated to residual lignin during the decomposition process over the study period. The inhibitory effect of N addition on litter decomposition can be primarily explained by the inhibition of lignin decomposition by exogenous inorganic N. The overall decomposition rate of ten investigated substrates exhibited a significant negative linear relationship with initial tissue C/N and lignin/N, and significant positive relationships with initial tissue K and N concentrations; these relationships exhibited linear and logarithmic curves, respectively. CONCLUSIONS/SIGNIFICANCE: This study suggests that the expected progressive increases in N deposition may have a potential important impact on forest litter decomposition in the study area in the presence of high levels of ambient N deposition.