26 research outputs found

    Transcriptome and UPLC-MS/MS reveal mechanisms of amino acid biosynthesis in sweet orange ‘Newhall’ after different rootstocks grafting

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    Sweet orange ‘Newhall’ (C. sinensis) is a popular fruit in high demand all over the world. Its peel and pulp are rich in a variety of nutrients and are widely used in catering, medicine, food and other industries. Grafting is commonly practiced in citrus production. Different rootstock types directly affect the fruit quality and nutritional flavor of citrus. However, the studies on citrus metabolites by grafting with different rootstocks are very limited, especially for amino acids (AAs). The preliminary test showed that there were significant differences in total amino acid content of two rootstocks (Poncirus trifoliata (CT) and C. junos Siebold ex Tanaka (CJ)) after grafting, and total amino acid content in the peel was higher than flesh. However, the molecular mechanism affecting amino acid differential accumulation remains unclear. Therefore, this study selected peel as the experimental material to reveal the amino acid components and differential accumulation mechanism of sweet orange ‘Newhall’ grafted with different rootstocks through combined transcriptome and metabolome analysis. Metabolome analysis identified 110 amino acids (AAs) and their derivatives in sweet orange ‘Newhall’ peels, with L-valine being the most abundant. L-asparagine was observed to be affected by both developmental periods and rootstock grafting. Weighted gene co-expression network analysis (WGCNA) combined with Redundancy Analysis (RDA) revealed eight hub structural genes and 41 transcription factors (TFs) that significantly influenced amino acid biosynthesis in sweet orange ‘Newhall’ peels. Our findings further highlight the significance of rootstock selection in enhancing the nutritional value of citrus fruits and might contribute to the development of functional citrus foods and nutritional amino acid supplements

    Mechanically Robust and Repairable Superhydrophobic Zinc Coating via a Fast and Facile Method for Corrosion Resisting

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    Zinc coatings and superhydrophobic surfaces have their own characteristics in terms of metal corrosion resistance. Herein, we have prepared a robust and repairable superhydrophobic zinc coating (SZC) based on a widely commercially available cold galvanized paint via a fast (within 10 min) and facile process for corrosion resistance. Specifically, the cold galvanized paint was sprayed onto the iron substrate, followed by acetic acid (HAc) etching and stearic acid (STA) hydrophobizing. The as-obtained sample was coded as Fe-Zn-HAc-STA and possessed an apparent contact angle of 168.4 ± 1.5° as well as a sliding angle of 3.5 ± 1.2°. The Fe-Zn-HAc-STA sample was mechanically durable and easily repairable. After being ultrasonicated in ethanol for 100 min, the superhydrophobicity was still retained. The Fe-Zn-HAc-STA sample lost its superhydrophobicity after being abraded against sandpaper with a load of 100 g and regained its superhydrophobicity after HAc etching and subsequent STA hydrophobizing. The corrosion resistance of the SZC was investigated by immersing the Fe-Zn-HAc-STA sample into the static or dynamic aqueous solution of NaCl (3.5 wt.%) and the lasting life of the entrapped underwater air layer (EUAL) was roughly determined by the turning point at the variation curve of surface wettability against immersion time. The lasting life of the EUAL iwas 8 to 10 days for the SZC in the static NaCl solution and it decreased sharply to 12 h in a dynamic one with the flow rate of 2 and 4 m/s. This suggests that the superhydrophobic surface provided extra corrosion protection of 8 to 10 days or 12 h to the zinc coating. We hope that the SZC may find its practical application due to the facile and fast fabrication procedure, the good mechanical durability, the easy repairability, and the good corrosion protection

    J. Nanosci. Nanotechnol.

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    At the room temperature, a novel and environmental friendly approach for synthesizing polyaniline (PANI) nanofibers on a large scale is presented firstly in the aqueous phase by ultraviolet (UV)-assisted polymerization using cetyltrimethylammonium bromide (CTAB) as the "soft-template." It is obvious that the polymerization process can be accelerated under the illumination of UV light and the preliminary mechanism has been pointed out. Furthermore, it also can be noted that the lower concentrations of CTAB and HCl are helpful for the fabrication of smooth and uniform PANI nanofibers. As observed with FE-SEM and TEM, the as-synthesized PANI nanostructures under the appropriate conditions are composed of uniform nanofibers with the average diameter of about 100 nm and the length of several micrometers. Subsequently, the synthesized PANI nanostructures are characterized with UV-vis, FTIR, XRD spectra, and the typical physical and chemical properties of PANI are displayed. In addition, the conductivity of the synthesized PANI nanofibers was also measured with the four probe method and the excellent conductivity was presented. In summary, the procedure presented here only involving exposure of an acidic aqueous solution of aniline to UV light illumination is so simple and the needed equipment is so low cost, from the viewpoint of technological applications, that the large-scale UV-assisted polymerization of PANI nanofibers from the monomer solution is feasible and promising.At the room temperature, a novel and environmental friendly approach for synthesizing polyaniline (PANI) nanofibers on a large scale is presented firstly in the aqueous phase by ultraviolet (UV)-assisted polymerization using cetyltrimethylammonium bromide (CTAB) as the "soft-template." It is obvious that the polymerization process can be accelerated under the illumination of UV light and the preliminary mechanism has been pointed out. Furthermore, it also can be noted that the lower concentrations of CTAB and HCl are helpful for the fabrication of smooth and uniform PANI nanofibers. As observed with FE-SEM and TEM, the as-synthesized PANI nanostructures under the appropriate conditions are composed of uniform nanofibers with the average diameter of about 100 nm and the length of several micrometers. Subsequently, the synthesized PANI nanostructures are characterized with UV-vis, FTIR, XRD spectra, and the typical physical and chemical properties of PANI are displayed. In addition, the conductivity of the synthesized PANI nanofibers was also measured with the four probe method and the excellent conductivity was presented. In summary, the procedure presented here only involving exposure of an acidic aqueous solution of aniline to UV light illumination is so simple and the needed equipment is so low cost, from the viewpoint of technological applications, that the large-scale UV-assisted polymerization of PANI nanofibers from the monomer solution is feasible and promising

    A Facile Route to Fabricate Superhydrophobic Cu2O Surface for Efficient Oil–Water Separation

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    The mixture of insoluble organics and water seriously affects human health and environmental safety. Therefore, it is important to develop an efficient material to remove oil from water. In this work, we report a superhydrophobic Cu2O mesh that can effectively separate oil and water. The superhydrophobic Cu2O surface was fabricated by a facile chemical reaction between copper mesh and hydrogen peroxide solution without any low surface reagents treatment. With the advantages of simple operation, short reaction time, and low cost, the as-synthesized superhydrophobic Cu2O mesh has excellent oil–water selectivity for many insoluble organic solvents. In addition, it could be reused for oil–water separation with a high separation ability of above 95%, which demonstrated excellent durability and reusability. We expect that this fabrication technique will have great application prospects in the application of oil–water separation

    Porous Ultrahigh Molecular Weight Polyethylene/Functionalized Activated Nanocarbon Composites with Improved Biocompatibility

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    Ultrahigh molecular weight polyethylene (UHMWPE) materials have been prevalent joint replacement materials for more than 45 years because of their excellent biocompatibility and wear resistance. In this study, functionalized activated nanocarbon (FANC) was prepared by grafting maleic anhydride polyethylene onto acid-treated activated nanocarbon. A novel porous UHMWPE composite was prepared by incorporating the appropriate amount of FANC and pore-forming agents during the hot-pressing process for medical UHMWPE powder. The experimental results showed that the best prepared porous UHMWPE/FANC exhibited appropriate tensile strength, porosity, and excellent hydrophilicity, with a contact angle of 65.9°. In vitro experiments showed that the porous UHMWPE/FANC had excellent biocompatibility, which is due to its porous structure and hydrophilicity caused by FANC. This study demonstrates the potential viability for our porous UHMWPE/FANC to be used as cartilage replacement material for biomedical applications

    In Situ Separation and Collection of Oil from Water Surface via a Novel Superoleophilic and Superhydrophobic Oil Containment Boom

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    We have prepared a porous, superoleophilic and superhydrophobic miniature oil containment boom (MOCB) for the in situ separation and collection of oils from the surface of water. The MOCB was fabricated by a one-step electrodepositing of Cu<sub>2</sub>O film on Cu mesh surface without using low surface energy materials. Oils on water surface could be fast contained in the MOCB while water was completely repelled out of the MOCB, thus achieving the separation of oil from water surface. In addition, the contained oil in the MOCB could be in situ collected easily by a dropper, thus achieving the collection of oil. Moreover, the MOCB could be reused for many times in the oil–water separating process with large separation abilities more than 90%. The MOCB also possessed excellent water pressure resistance for about 164 mm water column and good corrosion resistance in simulating seawater. Therefore, the findings in the present study might offer a simple, fast, and low-cost method for the in situ separation and collection of oil spills on seawater surface
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