Thermo-photo catalysis: a whole greater than the sum of its parts.

Thermo-photo catalysis, which is the catalysis with the participation of both thermal and photo energies, not only reduces the large energy consumption of thermal catalysis but also addresses the low efficiency of photocatalysis. As a whole greater than the sum of its parts, thermo-photo catalysis has been proven as an effective and promising technology to drive chemical reactions. In this review, we first clarify the definition (beyond photo-thermal catalysis and plasmonic catalysis), classification, and principles of thermo-photo catalysis and then reveal its superiority over individual thermal catalysis and photocatalysis. After elucidating the design principles and strategies toward highly efficient thermo-photo catalytic systems, an ample discussion on the synergetic effects of thermal and photo energies is provided from two perspectives, namely, the promotion of photocatalysis by thermal energy and the promotion of thermal catalysis by photo energy. Subsequently, state-of-the-art techniques applied to explore thermo-photo catalytic mechanisms are reviewed, followed by a summary on the broad applications of thermo-photo catalysis and its energy management toward industrialization. In the end, current challenges and potential research directions related to thermo-photo catalysis are outlined.

3D Graphene Materials: From Understanding to Design and Synthesis Control.

Carbon materials, with their diverse allotropes, have played significant roles in our daily life and the development of material science. Following 0D C60 and 1D carbon nanotube, 2D graphene materials, with their distinctively fascinating properties, have been receiving tremendous attention since 2004. To fulfill the efficient utilization of 2D graphene sheets in applications such as energy storage and conversion, electrochemical catalysis, and environmental remediation, 3D structures constructed by graphene sheets have been attempted over the past decade, giving birth to a new generation of graphene materials called 3D graphene materials. This review starts with the definition, classifications, brief history, and basic synthesis chemistries of 3D graphene materials. Then a critical discussion on the design considerations of 3D graphene materials for diverse applications is provided. Subsequently, after emphasizing the importance of normalized property characterization for the 3D structures, approaches for 3D graphene material synthesis from three major types of carbon sources (GO, hydrocarbons and inorganic carbon compounds) based on GO chemistry, hydrocarbon chemistry, and new alkali-metal chemistry, respectively, are comprehensively reviewed with a focus on their synthesis mechanisms, controllable aspects, and scalability. At last, current challenges and future perspectives for the development of 3D graphene materials are addressed.

Effects of early florfenicol exposure on glutathione signaling pathway and PPAR signaling pathway in chick liver.

Florfenicol (FFC) is a common antibiotic for animals. The nonstandard and excessive use of FFC can cause veterinary drug residues in animals, pollute soil and marine environment, and even threaten human health. Therefore, it is necessary to study the toxicity and side effects of FFC on animals. Our previous studies have proved that FFC can cause liver injury in chicks, but there are few in-depth studies on the mechanism of FFC causing liver injury at the level of signaling pathway in chicks. Therefore, transcriptome and proteome sequencing were performed and combined analysis was performed. Sequencing results showed that 1989 genes and 917 proteins were significantly changed in chick livers after FFC exposure. These genes and proteins are related to redox, glutathione transferase activity and lipid metabolism. There are 9 significantly different genes and 7 significantly different proteins in glutathione signaling pathway. Oxidative stress may occur in the liver of chicks through the change of activation state of glutathione signaling pathway. And there are 13 significantly different genes and 18 significantly different proteins in PPAR signaling pathway. The changes of PPAR signaling pathway may induce lipid metabolism disorder in liver. The verification results of qPCR and PRM were consistent with the sequencing results. We also detected GSH-Px, GSH, GST, TG, TC and ANDP levels in liver. These changes of biochemical indicators directly confirmed oxidative stress and lipid metabolism disorders were occurred in the livers of chicks treated by FFC. In conclusion, FFC could induce liver injury in chicks by regulating the expression levels of significantly different genes and proteins in glutathione signaling pathway and PPAR signaling pathway.

Compact passively Q-switched single-frequency distributed Bragg reflector fiber laser at 2.0 µm.

Based mainly on the distributed Bragg reflector (DBR) short linear cavity with a 1.6-cm-long heavily Tm3+-doped germanate glass fiber and semiconductor saturable absorber mirror (SESAM), a compact passively Q-switched single-frequency fiber laser at around 1950 nm is demonstrated experimentally. By comparing pulse characters of Q-switched operations fulfilled via SESAMs with different parameters, a stable output pulse is optimized to deliver a maximum average power of 22.2 mW, a peak power of 0.67 W, and an optical signal-to-noise ratio over 61 dB. Moreover, the repetition rate of the output pulse can be tuned from 92 to 520 kHz with a narrowest pulse width of 64 ns. To the best of our knowledge, this is the first time a 2.0 µm passively Q-switched single-frequency DBR Tm3+-doped fiber laser has been realized, and it shows great potential application in remote sensing, biomedical science, and nonlinear optics.

Emerging approaches of utilizing trees to produce advanced structural and functional materials.

The global number of trees is approximately 3 trillion, covering 31% of the land area. Trees are considered a cheap, abundant, renewable, and environmentally friendly feedstock for producing advanced structural and functional materials toward a widespread application in sustainable energy and environment. In this highlight, we reveal the structure and composition of wood, leaves, and tree extracts, and then highlight the strategies to control their hierarchical structures and properties. Moreover, we provide an up-to-date overview of their emerging applications in sustainable buildings, ionic nanofluidics, batteries, capacitors, solar cells, environmental remediation, biodegradable packaging, and nanomaterial synthesis. Finally, we outline the challenges and opportunities in valorizing trees for creating a sustainable future.

Structural transition and chemical reactivity of atomic carbon chains.

The sp-hybridized carbon chain (carbyne) is a representative 1D atomic material, whose bonding structure and chemical reactivity have remained a mystery for a century. Here, we report the unexpected alternating bond orders of 1.4 and 2.6 for the most stable carbon chain and the in situ diffuse reflectance infrared Fourier-transform spectroscopy (DRIFTS) detection of the temperature-dependent reversible change of the bond order alternation. Moreover, we revealed its reactivities with O2, H2, and CO2 at temperatures up to 600 °C and created an end-group-protection strategy to stabilize it. These observations open a new door to the chemistry of atomic materials.

3D meso/macroporous carbon from MgO-templated pyrolysis of waste plastic as an efficient electrode for supercapacitors.

Converting waste plastic into valuable carbon materials as the electrode for supercapacitors represents a sustainable way to deal with the severe waste plastic-related environmental issues. However, ideal carbon materials for supercapacitors require not only a large specific surface area but also abundant meso/macropores, which is still challenging for conventional synthesis methods. Herein, MgO-templated pyrolysis with chemical activation was demonstrated as an effective approach to convert waste polyethylene terephthalate (PET) plastic bottles into 3D meso/macroporous carbon (MMPC) with both large total surface area (1863.55 m2/g) and meso/macropore surface area (1478.46 m2/g). Furthermore, it exhibited a high capacitance of 191.4 F/g and an excellent rate capability (86.3% retention from 0.5 to 10 A/g) for supercapacitor. This work provides not only a facile approach to synthesize 3D meso/macroporous carbon materials but also a sustainable way to mitigate plastic-derived pollution.

Cross-Linked and Doped Graphene Oxide Membranes with Excellent Antifouling Capacity for Rejection of Antibiotics and Salts.

Graphene oxide (GO) membranes have suffered from the instability of water permeability and low rejection of pollutant separation. In this paper, a reasonable modification protocol for GO nanosheets at the molecular level was proposed. A molecular cross-linking strategy was adopted to regulate the interlayer spacing of GO nanosheets, and nanofiltration membranes with high water stability and excellent antifouling capacity were prepared, which could effectively reject antibiotics and salts. The GO1-MPD0.5 (the mass ratio of GO nanosheets to MPD is 1:0.5) and GO/GO1-MPD0.5-0.25 (the doping ratio of GO1-MPD0.5 is 25%) membranes had stable water permeability of 4.22 ± 0.06 and 3.65 ± 0.11 L m-2 h-1 bar-1, and the rejection rates for ciprofloxacin (CIP) and ofloxacin (OFX) were 93.35 ± 3.62 and 95.48 ± 2.97 and 85.89 ± 6.52 and 88.21 ± 3.67%, respectively. Molecular dynamics simulations well explained the high water stability of membranes, and the cross-linked hydrophobic benzene ring played a role in the rejection of pollutant molecules. Moreover, the GO1-MPD0.5 membrane showed excellent antifouling capacity and the flux recovery ratio (FRR) was more than 98%. This paper provides a new idea for the design of nanofiltration membranes with high stability and good rejection permeability at the molecular level and provides a prospect for the application of nanofiltration membranes in practical water treatment and water purification.

Turning dead leaves into an active multifunctional material as evaporator, photocatalyst, and bioplastic.

Large numbers of leaves fall on the earth each autumn. The current treatments of dead leaves mainly involve completely destroying the biocomponents, which causes considerable energy consumption and environmental issues. It remains a challenge to convert waste leaves into useful materials without breaking down their biocomponents. Here, we turn red maple dead leaves into an active three-component multifunctional material by exploiting the role of whewellite biomineral for binding lignin and cellulose. Owing to its intense optical absorption spanning the full solar spectrum and the heterogeneous architecture for effective charge separation, films of this material show high performance in solar water evaporation, photocatalytic hydrogen production, and photocatalytic degradation of antibiotics. Furthermore, it also acts as a bioplastic with high mechanical strength, high-temperature tolerance, and biodegradable features. These findings pave the way for the efficient utilization of waste biomass and innovations of advanced materials.

Double-charged self-assembled rGO/g-C3N4 membrane prepared by "functional group substitution" for heavy metal ions rejection at low pressure.

Heavy metals are still the critical pollutants in industrial wastewater and there is an urgent need for efficient and environmentally friendly treatment technologies. Reduced graphene oxide (rGO) is widely used for preparations of nanofiltration (NF) membranes but suffers from poor hydrophilicity and electronegativity. In this work, a double-charged rGO/g-C3N4-P membrane was prepared for removal of heavy metals at low pressure. Graphitic carbon nitride (g-C3N4) assisted reduction of GO membranes under ultraviolet (UV) irradiation, and the modification of functional groups with high polarity improved the hydrophilicity of membrane surface. The filtration performance for heavy metals of rGO/g-C3N4-P membrane was evaluated under low pressure (1-2 bar). The rejection rates of Cu2+, Cr3+, Mn2+, Cd2+, and Pb2+ by membranes reduced by UV for 18 h (rGO/g-C3N4-18-P membrane) reached 94.72 %, 98.05 %, 82.32 %, 88.2 % and 77.15 %, respectively. In the experiment of mixed simulated wastewater, the rejection rates of NO3- and SO42- both reached >95 %. Outstanding rejection rates were attributed to the interaction and the synergy effect of double-charged layers as well as steric effects. Meanwhile, the water flux of rGO/g-C3N4-18-P membrane was as high as 37.14-50.16 L m-2h-1bar-1 (1-2 bar). The high flux was due to the reduced degree of oxidation so that water molecules transported between GO nanochannels more smoothly and the transport path was shortened through the nanopores of g-C3N4. Obviously, flux and heavy metal rejection of rGO/g-C3N4-18-P membrane were simultaneously improved, breaking "trade-off" effect. Furthermore, rGO/g-C3N4-18-P membrane showed excellent antifouling ability and the potential for heavy metal wastewater filtration in comparison with other NF membranes reported in literature.

Direct Observation of Twin van der Waals Molecular Chains.

The van der Waals (vdW) assemblies are the most common structures of materials. However, direct mapping of intermolecular electron clouds of a vdW assembly has never been obtained, even though the intramolecular electron clouds were visualized by atomic-resolution techniques. In this report, we unprecedentedly mapped the intermolecular electron cloud of the assemblies of ethanol molecules via ethyl groups with high-resolution atomic force microscopy and scanning tunneling microscopy at 5 K, leading to the first visualization of vdW molecular chains, in which ethanol molecules assemble into twin vdW molecular chains in a reverse parallel configuration on the Ag(111) plane. Furthermore, spontaneous order-disorder transitions in the chain were dynamically observed, suggesting its unusual properties different from those of 2D vdW materials. These findings provide an "eye" to see the atomic world of vdW materials.

Antifouling and Chemical-Resistant Nanofiltration Membrane Modulated by a Functionalized MWCNT Interlayer for Efficient Dye/Salt Separation at High Salinity.

Dye/salt separation in textile wastewater is of great importance. Membrane filtration technology is an environmentally friendly and effective approach to solve this issue. In this study, a thin-film composite membrane with a tannic acid (TA)-modified carboxylic multiwalled carbon nanotube (MWCNT) interlayer (M-TA) was prepared by interfacial polymerization with amino-functionalized graphene quantum dots (NGQDs) acting as aqueous monomers. The addition of the M-TA interlayer favored the formation of a thinner, more hydrophilic, and smoother selective skin layer for the composite membrane. The pure water permeability of the M-TA-NGQDs membrane was ∼9.32 L m-2 h-1 bar-1, which was higher than that of the NGQDs membrane without the interlayer. Meanwhile, the M-TA-NGQDs membrane presented better methyl orange (MO) rejection (97.79%) than the NGQDs membrane (87.51%). The optimal M-TA-NGQDs membrane exhibited excellent dye rejection (Congo red (CR): 99.61%; brilliant green (BG): 96.04%) and low salt rejection (NaCl < 15%). Noticeably, the M-TA-NGQDs membrane displayed effective selective separation performance (CR and BG > 99%) for dye/NaCl mixed solutions even at a high NaCl concentration of 50,000 mg/L. Furthermore, the M-TA-NGQDs membrane presented high water permeability recovery ratio values (91.02-98.20%). Importantly, the M-TA-NGQDs membrane showed excellent chemical stability (acid/alkali resistance). Generally, the fabricated M-TA-NGQDs membrane exhibited a great prospect for applications in dye wastewater treatment and water recycling, especially for the effective selective separation of dye/salt mixtures for high-salinity textile dyeing wastewater.

Thin-Film Nanocomposite Membranes with Nature-Inspired MOFs Incorporated for Removing Fluoroquinolone Antibiotics.

A nanofiltration membrane functionalized with metal-organic frameworks (MOFs) is promising to enhance micropollutant removal and realize wastewater reclamation. However, the current MOF-based nanofiltration membranes still suffer from severe fouling problems with an indefinable mechanism when used for antibiotic wastewater treatment. Hence, we report a nature-inspired MOF-based thin-film nanocomposite (TFN-CU) membrane to explore its rejection and antifouling behavior. Compared with unmodified membranes, the optimal TFN-CU5 membrane (with 5 mg·mL-1 C-UiO-66-NH2) had high water permeance (17.66 ± 1.19 L·m-2·h-1·bar-1), exceptional rejection for norfloxacin (97.92 ± 2.28%) and ofloxacin (95.36 ± 1.03%), and excellent long-term stability for treating synthetic secondary effluent with antibiotic rejection over 90%. Furthermore, it also showed superior antifouling capability (flux recovery up to 95.86 ± 1.28%) in bovine serum albumin (BSA) filtration after fouling cycles. Deriving from the extended Derjaguin-Landau-Verwey-Overbeek (XDLVO) approach, the antifouling mechanism between BSA and the TFN-CU5 membrane was mainly attributed to the inhibited adhesion forces because the growing short-ranged acid-base interaction caused repulsive interfacial interactions. It is further revealed that BSA fouling behavior is slightly retarded under an alkaline environment, while strengthened in the presence of calcium ions and humic acid, as well as high ionic strength. In short, the nature-inspired MOF-based TFN membranes possess exceptional rejection and organic fouling resistance, giving insights into the design of antifouling membranes during antibiotic wastewater reclamation.

Low-pressure thin-film composite nanofiltration membranes with enhanced selectivity and antifouling property for effective dye/salt separation.

For better sustainable resource recovery and elevating the separation efficiency of dye/salt mixture, it is essential to develop an appropriate nanofiltration membrane for the treatment of textile dyeing wastewater containing relatively smaller molecule dyes. In this work, a novel composite polyamide-polyester nanofiltration membrane was fabricated by tailoring amino functionalized quantum dots (NGQDs) and ß-cyclodextrin (CD). An in-situ interfacial polymerization occurred between the synthesized NGQDs-CD and trimesoyl chloride (TMC) on the modified multi-carbon nanotubes (MWCNTs) substrate. The incorporation of NGQDs significantly elevated the rejection (increased by âˆ¼ 45.08%) of the resultant membrane for small molecular dye (Methyl orange, MO) compared to the pristine CD membrane at low pressure (1.5 bar). The newly developed NGQDs-CD-MWCNTs membrane exhibited enhanced water permeability without compromising the dye rejection compared to the pure NGQDs membrane. The improved performance of the membrane was primarily attributed to the synergistic effect of functionalized NGQDs and the special hollow-bowl structure of CD. The optimal NGQDs-CD-MWCNTs-5 membrane expressed pure water permeability of 12.35 L m-2h-1 bar-1 at the pressure of 1.5 bar. Noteworthily, the NGQDs-CD-MWCNTs-5 membrane not only showed high rejection for the larger molecular dye of Congo Red (CR, 99.50%) but also for the smaller molecular dye of MO (96.01%) and Brilliant Green (BG, 95.60%) with the permeability of 8.81, 11.40, and 6.37 L m-2h-1 bar-1, respectively at low pressure (1.5 bar). The rejection of inorganic salts by the NGQDs-CD-MWCNTs-5 membrane was 17.20% for sodium chloride (NaCl), 14.30% for magnesium chloride (MgCl2), 24.63% for magnesium sulfate (MgSO4), and 54.58% for sodium sulfate (Na2SO4), respectively. The great rejection of dyes remained in the dye/salt binary mixed system (higher than 99% for BG and CR, <21% for NaCl). Importantly, the NGQDs-CD-MWCNTs-5 membrane exhibited favorable antifouling performance and potential good operation stability performance. Consequently, the fabricated NGQDs-CD-MWCNTs-5 membrane suggested a prospective application for the reuse of salts and water in textile wastewater treatment owing to the effective selective separation performance.

Facile and Scalable Synthesis of Metal- and Nitrogen-Doped Carbon Nanotubes for Efficient Electrochemical CO2 Reduction.

Metal- and nitrogen-doped carbon (M-N-C) is a promising material to catalyze electrochemical CO2 reduction reaction (CO2RR). However, most M-N-C catalysts in the literature require complicated synthesis procedures and produce small quantities per batch, limiting the commercialization potential. In this work, we developed a simple and scalable synthesis method to convert metal-impurity-containing commercial carbon nanotubes (CNTs) and nitrogen-containing organic precursors into M-N-C via one-step moderate-temperature (650 °C) pyrolysis without any other treatment nor the need to add metal precursors. Batches of catalysts in varied mass up to 10 g (150 mL in volume) per batch were synthesized, and repeatable catalytic performances were demonstrated. To the best of our knowledge, the 10 g batch is one of the largest batches of CO2RR catalysts synthesized in the literature while requiring minimal synthesis steps. The catalyst possessed single-atomic iron-nitrogen (Fe-N) sites, enabling a high performance of >95% CO product selectivity at a high current density of 400 mA/cm2 and high stability for 45 h at 100 mA/cm2 in a flow cell testing. The catalyst outperformed a benchmark noble-metal nanoparticle catalyst and achieved longer stability than many other reported M-N-C catalysts in the literature. The scalable and cost-effective synthesis developed in this work paves a pathway toward practical CO2RR applications. The direct utilization of metal impurities from raw CNTs for efficient catalyst synthesis with minimal treatment is a green and sustainable engineering approach.

Thin-water-film-enhanced TiO2-based catalyst for CO2 hydrogenation to formic acid.

Carbon dioxide (CO2) hydrogenation can not only mitigate global warming, but also produce value-added chemicals. Herein, we report a novel three-phase catalytic system with an in situ generated and dynamically updated thin water film covered on the noble-metal-free TiO2-based catalyst for highly efficient CO2 hydrogenation, realizing a four-time enhancement compared with that with the catalyst suspended in water. The water film plays dual roles by directly participating in the reaction and removing the produced oxygenates (mainly formic acid) from the catalyst surface by dissolution. These results demonstrate an effective design for CO2 hydrogenation, which will open a new door to three-phase catalysis.

Salvia miltiorrhiza polysaccharides alleviates florfenicol-induced liver metabolic disorder in chicks by regulating drug and amino acid metabolic signaling pathways.

Excessive and nonstandard use of florfenicol (FFC) can damage animal body, pollute ecological environment, and even harm human health. The toxic and side effects of FFC directly affect the production performance of poultry and the safe supply of chicken-related food. Salvia miltiorrhaza polysaccharides (SMPs) are natural macromolecular compounds, and were proved to have the effect of protecting animal liver. We used transcriptome and proteome sequencing technologies to study the effect of FFC on specific signal transduction pathways in chick livers and further explored the regulatory effect of SMPs on the above same signal pathways, and finally revealed the intervention effect and mechanism of SMPs on FFC-induced changes of liver function. The screened sequencing results were verified by qPCR and PRM methods. The results showed that FFC changed significantly 9 genes and 5 proteins in drug metabolism-cytochrome P450 signaling pathway, and the intervention of SMPs adjusted the expression levels of 5 genes and 4 proteins of the above factors. In glycine, serine and threonine metabolism signaling pathway, 8 genes and 8 proteins were significantly changed due to FFC exposure, and SMPs corrected the expression levels of 5 genes and 6 proteins to a certain extent. In conclusion, SMPs alleviated FFC-induced liver metabolic disorder in chicks by regulating the drug and amino acid metabolism pathway. This study is of great significance for promoting the healthy breeding of broilers and ensuring the safe supply of chicken-related products.

Impacts of typical engineering nanomaterials on the response of rhizobacteria communities and rice (Oryza sativa L.) growths in waterlogged antimony-contaminated soils.

The combined eco-risks of Sb (widely presented in soils, especially nearing mining areas) and the engineering nanomaterials (ENMs) (applied in agriculture and soil remediation) still remain uncovered. The current study investigated the impacts of single and combined exposure of CuO, CeO2 nanoparticles (NPs) and multi-walled carbon nanotube (MWCNTs) with Sb on rice growths and rhizosphere bacterial communities. The results showed that co-exposure of CuO NPs (0.075 wt%) with Sb (III) posed the most adverse impacts on root biomass and branches (up to 66.59% and 70.00% compared to other treatments, respectively). Treatments containing MWCNTs showed insignificant dose-dependent effects, while CeO2 NPs combined with Sb (III) showed significant synergistic stimulating effects on the fresh weights of root and shoot, by 68.30% and 73.48% (p < 0.05) compared to single Sb exposure, respectively. The rice planting increased the percentage of non-specifically sorbed Sb in soils by 1.50-14.49 than the no-planting stage. Analysis on microbial communities revealed that co-exposure of CuO NPs with Sb (III) induced the greatest adverse impacts on rhizobacteria abundances and community structures at both phylum and genus levels. Therein, significant decrease of Bacteroidetes, Acidobacteria and increase of Firmicutes abundance at the phylum level were observed. This study provided information about the risks of different ENMs released to Sb-contaminated soils under flooded condition on both crops and bacterial communities.

Critical role of tetracycline's self-promotion effects in its visible-light driven photocatalytic degradation over ZnO nanorods.

Zinc oxide (ZnO), which is widely applied for ultraviolet-light driven photocatalysis, has no activity in visible-light photocatalytic process due to its large band gap of ∼3.2 eV. Herein, however, we demonstrated the multiple self-promotion effects of tetracycline as band adjuster, photo-sensitizer, and charge transfer promoter for ZnO nanorods, realizing its visible-light photocatalytic degradation with an excellent removal efficiency up to 91.1% within only 2 h. Besides, the influence of complex realistic factors on this unique process was evaluated together with tests with realistic water matrices. Furthermore, the active species and degradation products were identified. Both acute and developmental toxicities were found to be reduced as the degradation proceeds. These results pave the path for the brand-new self-driven visible-light photocatalysis.

The effect of UV exposure on conventional and degradable microplastics adsorption for Pb (II) in sediment.

Plastic discharged into the environment would break down into microplastics (MPs). However, the possible impact of MPs on heavy metals in the aquatic sediment remains unknown. In order to evaluate the potential role of MPs as carriers of coexisting pollutants, the adsorption capacity of lead ions from sediment onto aged degradable and conventional MPs were investigated as a function of lead ions concentration, contact time, temperature, MPs dosage, aging time, and fulvic acid concentration. MPs were exposed to UV to obtain aged polyethylene (A-PE) and aged polylactic acid (A-PLA). The aging treatment increased the oxygen content, specific surface area and hydrophilicity of MPs. The adsorption capacity of A-PE for Pb(II) in sediment increased from 10.1525 to 10.4642 mg g-1 with the increasing aging time. However, the adsorption capacity of A-PLA for Pb(II) in sediment decreased from 9.3199 to 8.7231 mg g-1 with the increasing aging time. The adsorption capacity of MPs in sediment for Pb(II) was in the following order: A-PE > PLA > PE > A-PLA. Fulvic acid could promote the adsorption of Pb(II) by MPs in sediment. These results indicated that the aging process of the plastics in the environment would affect its role as a carrier of coexisting pollutants.