74 research outputs found

    One-pot melamine derived nitrogen doped magnetic carbon nanoadsorbents with enhanced chromium removal

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    Novel nitrogen doped magnetic carbons (NMC), in-situ synthesized through facile pyrolysis-carbonization processes using Fe(NO3)3 and melamine as precursors, were demonstrated as excellent nanoadsorbents to remove Cr(VI) effectively. The achieved removal capacity in both neutral and acidic solution was 29.4 and 2001.4 mg g−1 respectively, much higher than the reported adsorbents so far. The unprecedented high adsorption performance can be attributed to the incorporation of the nitrogen dopant, which increased the negative charge density on the surface of adsorbent and thereby enhanced the interaction between the adsorbents and Cr(VI) ions. The density functional theory (DFT) calculation demonstrated that the nitrogen dopants can decrease the adsorption energy between the Cr(VI) ions and NMC (−3.456 kJ mol−1), lower than the undoped sample (−3.344 kJ mol−1), which boosted the adsorption behavior. Chemical rather than physical adsorption was followed for these magnetic nanoadsorbents as revealed from the pseudo-second-order kinetic study. Furthermore, the NMC showed high stability with recycling tests for the Cr(VI) removal

    Poly(vinylidene fluoride) derived fluorine-doped magnetic carbon nanoadsorbents for enhanced chromium removal

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    Newly designed fluorine-doped magnetic carbon (F-MC) was synthesized in situ though a facile one-step pyrolysis-carbonization method. Poly(vinylidene fluoride) (PVDF) served as the precursor for both carbon and fluorine. 2.5% F content with core-shell structure was obtained over F-MC, which was used as a adsorbent for the Cr(VI) removal. To our best knowledge, this is the first time to report that the fluorine doped material was applied for the Cr(VI) removal, demonstrating very high removal capacity (1423.4 mg g−1), higher than most reported adsorbents. The unexpected performance of F-MC can be attributed to the configuration of F dopants on the surface. The observed pseudo-second-order kinetic study indicated the dominance of chemical adsorption for this process. High stability of F-MC after 5 recycling test for the Cr(VI) removal was also observed, indicating that F-MC could be used as an excellent adsorbent for the toxic heavy metal removal from the wastewater

    An Ascorbic Acid-Imprinted Poly(o-phenylenediamine)/AuNPs@COFTFPB-NBPDA for Electrochemical Sensing Ascorbic Acid

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    An electrochemical sensor based on a molecularly imprinted polymer membrane (MIP) was developed. The electrochemical sensor was prepared by electropolymerization of o-phenylenediamine (O-PD) on the surface of glassy carbon electrode (GCE), modified by AuNPs@covalent organic framework (COF) microspheres with ascorbic acid (AA) as template molecule. First, ultrasmall polyvinylpyrrolidone (PVP)-coated AuNPs were prepared by a chemical reduction method. Then, 1,3,5-tri(p-formylphenyl)benzene (TFPB) and N-boc-1,4-phenylene diamine (NBPDA) underwent an ammonaldehyde condensation reaction on PVP-coated AuNPs to form AuNPs@COFTFPB-NBPDA microspheres. The porous spherical structure of AuNPs@ COFTFPB-NBPDA could accelerate the mass transfer, enlarge the specific surface area, and enhance the catalytic activity of PVP-coated AuNPs. The electrochemical sensors, based on AuNPs@ COFTFPB-NBPDA/GCE and nMIPs/AuNPs@COFTFPB-NBPDA/GCE, were applied for the detection of AA, with a detection limit of 1.69 and 2.57 μM, as well as linear ranges of 5.07 to 60 mM and 7.81 to 60 mM. The nMIPs/AuNPs@COFTFPB-NBPDA sensor had satisfactory stability, selectivity, and reproducibility for AA detection

    A Paper-Based Electrochemical Sensor Based on PtNP/COFTFPB−DHzDS@rGO for Sensitive Detection of Furazolidone

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    Herein, a paper-based electrochemical sensor based on PtNP/COFTFPB−DHzDS@rGO was developed for the sensitive detection of furazolidone. A cluster-like covalent organic framework (COFTFPB−DHzDS) was successfully grown on the surface of amino-functional reduced graphene oxide (rGO-NH2) to avoid serious self-aggregation, which was further loaded with platinum nanoparticles (PtNPs) with high catalytic activity as nanozyme to obtain PtNP/COFTFPB−DHzDS@rGO nanocomposites. The morphology of PtNP/COFTFPB−DHzDS@rGO nanocomposites was characterized, and the results showed that the smooth rGO surface became extremely rough after the modification of COFTFPB−DHzDS. Meanwhile, ultra-small PtNPs with sizes of around 1 nm were precisely anchored on COFTFPB−DHzDS to maintain their excellent catalytic activity. The conventional electrodes were used to detect furazolidone and showed a detection limit as low as 5 nM and a linear range from 15 nM to 110 μM. In contrast, the detection limit for the paper-based electrode was 0.23 μM, and the linear range was 0.69–110 μM. The results showed that the paper-based electrode can be used to detect furazolidone. This sensor is a potential candidate for the detection of furazolidone residue in human serum and fish samples

    An Ascorbic Acid-Imprinted Poly(o-phenylenediamine)/AuNPs@COF<sub>TFPB-NBPDA</sub> for Electrochemical Sensing Ascorbic Acid

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    An electrochemical sensor based on a molecularly imprinted polymer membrane (MIP) was developed. The electrochemical sensor was prepared by electropolymerization of o-phenylenediamine (O-PD) on the surface of glassy carbon electrode (GCE), modified by AuNPs@covalent organic framework (COF) microspheres with ascorbic acid (AA) as template molecule. First, ultrasmall polyvinylpyrrolidone (PVP)-coated AuNPs were prepared by a chemical reduction method. Then, 1,3,5-tri(p-formylphenyl)benzene (TFPB) and N-boc-1,4-phenylene diamine (NBPDA) underwent an ammonaldehyde condensation reaction on PVP-coated AuNPs to form AuNPs@COFTFPB-NBPDA microspheres. The porous spherical structure of AuNPs@ COFTFPB-NBPDA could accelerate the mass transfer, enlarge the specific surface area, and enhance the catalytic activity of PVP-coated AuNPs. The electrochemical sensors, based on AuNPs@ COFTFPB-NBPDA/GCE and nMIPs/AuNPs@COFTFPB-NBPDA/GCE, were applied for the detection of AA, with a detection limit of 1.69 and 2.57 μM, as well as linear ranges of 5.07 to 60 mM and 7.81 to 60 mM. The nMIPs/AuNPs@COFTFPB-NBPDA sensor had satisfactory stability, selectivity, and reproducibility for AA detection
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