21 research outputs found

    Understanding the growth mechanism of stabilizer-free Ag nanoparticles on reduced graphene oxide: the role of CO

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    International audienceIn this study, one-step approach to prepare stabilizer-free Ag-graphene nanocomposites using DMAc-assisted thermal reduction method with uniform distribution of "near spherical'' Ag nanoparticles (Ag NPs) in the range of 16-20 nm is reported. Interestingly, from the change of absorption spectrum as a function of reaction time, we observed that the characteristic absorption peak of Ag NPs shows no peak position shift in a quite long time without extra stabilizer while red-shift and broaden after continuous reaction. To explain this phenomenon, we further proposed a growth mechanism that CO, which is generated from reduction of functional groups on GO, adsorbed on the surface of Ag NPs and leaded to growth cease of Ag NPs into a narrow size distribution during the reduction of GO. Meanwhile, Ag NPs can catalyze the oxidation of adsorbed-CO to CO2 in the presence of O-2 which can easily desorb from Ag surfaces. Hence, after fully removal of functional groups on GO, continuous supply of CO was cutoff while the desorption of adsorbed-CO was still happening continually, so Ag NPs start to gradually grow and resulting in aggregation. Moreover, the dosage of less DMAc or more AgNO3 would cause the anisotropic growth and form multiply twinned structure of Ag NPs. Our study presents a useful understanding on the growth of Ag NPs on graphene

    Phosphorus migration from sediment to phosphorus-inactivating material: A key process neglected by common phosphorus immobilization assessments for lake geoengineering

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    Various phosphorus (P)-inactivating materials with a strong capability of immobilizing P in sediment have been developed for lake geoengineering purposes to control internal P pollution. However, unsatisfactory applications have raised concerns about the reliability of the method. This study hypothesized that P migration from sediment to material is a key process regulating the immobilization, which is often neglected by common assessment procedures that assume that the material is closely in contact with sediment (e.g., as mixtures). To verify this hypothesis, 90-day incubation tests were conducted using drinking water treatment residue (DWTR). The results showed that the soluble P in the overlying water of sediment–DWTR mixtures and the mobile P in the mixtures were substantially reduced from the initial period and remained low during the whole incubation tests. However, assessment based on separated samples indicated a gradual P migration from sediment to DWTR for immobilization. Even after 90 days of incubation, mobile P still accounted for ∼5.33% of total P in the separated sediment. Further analysis suggested that using mixtures of sediment with DWTR accelerated P migration during the assessment, leading to a faster P immobilization assessment. Considering the relatively low levels of mobile P in the separated DWTR during incubation, the gradual decrease in mobile P in the separated sediment indicates that sediment P release regulates P immobilization efficiency. Therefore, designing a proper strategy to ensure sufficient time for the material to remain in close contact with the target sediment is critical to reducing uncertainties in lake geoengineering

    One-pot synthesis of Ag/r-GO/TiO2 nanocomposites with high solar absorption and enhanced anti-recombination in photocatalytic applications.

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    International audienceIn this paper, we reported a simple one-pot solvothermal approach to fabricate Ag/reduced graphene oxide (r-GO)/TiO2 composite photocatalyst under atmospheric pressure. Based on the experimental data, we concluded that the introduction of Ag into classical graphene-TiO2 system (i) efficiently enlarges the absorption range, (ii) improves photogenerated electron separation and (iii) increases photocatalysis reaction sites. The optimized sample exhibits prominent photocatalysis ability as compared to pure TiO2 under simulated sunlight. We further proposed that besides the above three advantages of Ag, a different size of Ag nanoparticles is also responsible for the improved photocatalysis ability, where small size Ag nanoparticles (2-5 nm) could store a photoexcited electron that was generated from TiO2, while large-size Ag nanoparticles could utilize visible light due to their localized surface plasmon resonance (LSPR) absorption. Our present work gives new insights into the photocatalysis mechanism of noble metal/r-GO/TiO2 composites and provides a new pathway into the design of TiO2-based photocatalysts and promote their practical application in various environmental and energy issues

    OMC-YOLO: A Lightweight Grading Detection Method for Oyster Mushrooms

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    In this paper, a lightweight model—OMC-YOLO, improved based on YOLOv8n—is proposed for the automated detection and grading of oyster mushrooms. Aiming at the problems of low efficiency, high costs, and the difficult quality assurance of manual operations in traditional oyster mushroom cultivation, OMC-YOLO was improved based on the YOLOv8n model. Specifically, the model introduces deeply separable convolution (DWConv) into the backbone network, integrates the large separated convolution kernel attention mechanism (LSKA) and Slim-Neck structure into the Neck part, and adopts the DIoU loss function for optimization. The experimental results show that on the oyster mushroom dataset, the OMC-YOLO model had a higher detection effect compared to mainstream target detection models such as Faster R-CNN, SSD, YOLOv3-tiny, YOLOv5n, YOLOv6, YOLOv7-tiny, YOLOv8n, YOLOv9-gelan, YOLOv10n, etc., and that the mAP50 value reached 94.95%, which is an improvement of 2.62%. The number of parameters and the computational amount were also reduced by 26%. The model provides technical support for the automatic detection of oyster mushroom grades, which helps in realizing quality control and reducing labor costs and has positive significance for the construction of smart agriculture

    Facile Formation of Anatase Nanoparticles on H-Titanate Nanotubes at Low Temperature for Efficient Visible Light-Driven Degradation of Organic Pollutants

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    Anatase nanoparticles (5–10 nm) generated on H-titanate nanotube surface (H-titanate/anatase) were prepared by an ingenious and simple method. H-titanate tubes were prepared by a hydrothermal reaction of Ti powder in concentrated NaOH solution and an ion exchange process with HNO3 solution. After that, at a relatively low drying temperature (100 °C), a small quantity of anatase nanoparticles were in-situ formed on the H-titanate tubes surface by a surface dehydration reaction. In-situ transformation can form a strong interface coupling between H-titanate and anatase, which is conducive to accelerating charge transfer and improving its photocatalytic activity. In addition, the smaller average crystal size, the large specific surface areas (BET), the nanotubed and layered structure and the synergistic effect of dual phases would be beneficial to improving the photocatalytic efficiency

    Preparation and Tribological Behaviors of Antigorite and Wollastonite Mineral Dual-Phase-Reinforced Polytetrafluoroethylene Matrix Composites

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    Research on polymer matrix composites with excellent tribological properties has received increasing attention in recent years. In this study, antigorite and wollastonite mineral dual-phase-reinforced polytetrafluoroethylene (PTFE) matrix composites were prepared by filling PTFE with mineral powders using ball-milling, cold-pressing, and pressureless sintering methods. The phase structure, microstructure, chemical composition, Shore hardness, and tribological behavior of the composites rubbed against steel balls under dry friction conditions were investigated. The results show that the composites have a dense structure and uniform distribution of mineral phases, with a Shore hardness of 62–68.8, an increase of 18.7–23.7% compared to pure PTFE. Compared with the addition of mono antigorite or wollastonite, the composites prepared by simultaneously filling the two minerals exhibited excellent tribological properties. The average friction coefficient and wear volume of the (10Atg + 20Wl)/PTFE composites were reduced by 44.2% and 71.4%, respectively, compared to those of pure PTFE. A dense and continuous tribofilm composed mainly of SiO2, MgSiO3, Mg2SiO4, MgO, CaO, CaMg(SiO3)2, and CaF2 was formed on the worn surfaces of both the dual-phase-reinforced PTFE matrix composites and counterpart steel balls during the friction process. The reduction in friction and wear is attributed to the reinforcement effect of the minerals on the PTFE matrix as well as the complex physical and chemical reactions at the friction interface stimulated by the synergistic effects between the two minerals. The addition of wollastonite reduced the phase transition temperature of antigorite, promoting more tribochemical reaction products with good abrasion resistance and friction-reducing properties, which contributed to the excellent tribological behavior of the composites

    Toward Quantitative Understanding of the Bioavailability of Dissolved Organic Matter in Freshwater Lake during Cyanobacteria Blooming

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    Occurrence of cyanobacterial harmful algal blooms (CyanoHAB) can induce considerable patchiness in the concentration and bioavailability of dissolved organic matter (DOM), which could influence biogeochemical processes and fuel microbial metabolism. In the present study, a laboratory 4-stage plug-flow bioreactor was used to successfully separate the CyanoHAB-derived DOM isolated from the eutrophic Lake Taihu (China) into continuum classes of bioavailable compounds. A combination of new state-of-the-art tools borrowed from analytical chemistry and microbial ecology were used to characterize quantitatively the temporary evolution of DOM and to get deeper insights into its bioavailability. The results showed a total 79% dissolved organic carbon loss over time accompanied by depletion of protein-like fluorescent components, especially the relatively hydrophilic ones. However, hydrophilic humic-like fluorescent components exhibited bioresistant behavior. Consistently, ultrahigh resolution mass spectrometry (FTICR-MS) revealed that smaller, less aromatic, more oxygenated, and nitrogen-rich molecules were preferentially consumed by microorganisms with the production of lipid-like species, whereas recalcitrant molecules were primarily composed of carboxylic-rich alicyclic compounds. Moreover, the bioavailability of DOM was negatively correlated with microbial community diversity in the bioreactor. Results from this study provide deeper insights into the fate of DOM and relevant biogeochemical processes in eutrophic lakes
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