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Synthesis And Preparation Of Magnetic Nanocomposites And Its Functionalization Research

Posted on:2024-07-25Degree:MasterType:Thesis
Country:ChinaCandidate:C N LiuFull Text:PDF
GTID:2531307157994789Subject:Chemistry
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In this thesis,the composite photocatalyst Fe3O4@SiO2@MoS2/Bi VO4with semiconductor p-n heterogeneous structure and recyclable was prepared by loading the magnetic Fe3O4@SiO2@MoS2complex onto the surface of Bi VO4.The catalytic ability of Fe3O4@SiO2@MoS2/Bi VO4to pollutants such as dyes,antibiotics and herbicide under visible light was studied.The possible catalytic mechanism of Fe3O4@SiO2@MoS2/Bi VO4was analyzed based on the experimental results.(1)Hydrophobic OA-Fe3O4 and hydrophilic Na3Cit-Fe3O4 were prepared by Chemical coprecipitation method and Solvothermal method,respectively.The experiment also explored the effect of reaction conditions on product size,morphology,magnetic saturation strength and crystal form.Through characterization,it can be seen that both methods can synthesize pure phase and uniform morphology of magnetic Fe3O4 nanoparticles.(2)The main step in the preparation of Fe3O4@SiO2 material is to coat a SiO2 shell on the surface of Fe3O4 by sol-gel method.The SiO2 layer can effectively improve biocompatibility,prevent corrosion and agglomeration of Fe3O4nanoparticles.It′s also improve its stability in aqueous solution.CTAB is added as a mesoporous template in sol-gel reactions during preparation,and can be used as a stable surfactant for the transfer of Fe3O4nanoparticles into the aqueous phase.(3)The MoS2 was grown in situ on the surface layer of OA-Fe3O4@SiO2 by Hydrothermal method.And a double-layer shell material Fe3O4@SiO2@MoS2 was prepared.In the preparation process,OA-Fe3O4@SiO2 is put into dilute HNO3 solution for surface protonation to positively charge the SiO2 surface,so that negatively charged MoS2can grow to the SiO2 surface.Through degradation experiments,it can be seen that Fe3O4@SiO2@MoS2has the best degradation effect on antibiotics.At 100 min,the degradation efficiency of tetracycline hydrochloride reached 77.83%,and at 80 min,the degradation efficiency of norfloxacin reached 68.39%.(4)The experimental results of Bi VO4 degradation of cationic dyes,norfloxacin and Cr(VI)further proved that the best conditions for the preparation of Bi VO4 were p H=5modification and reaction for 12 h.Specifically,the degradation rate of MB was 73.25%at80 min.The degradation rate of norfloxacin at 100 min was72.43%.The degradation rate of glyphosate isopropylamine salt in 100 minutes is 72.05%.The degradation rate of Cr(VI)was 67.00%at 100 min.(5)It can be seen from photocatalytic experiments that when the load capacity of MoS2is 5%,the photocatalyst has the best degradation efficiency for the target pollutants after modification in the p H value of 5.Specifically,the maximum adsorption efficiency of methylene blue reached 97.22%at 100 min.The degradation rate of methyl orange at 120min was 97.99%.(6)The optimal dosage of Fe3O4@SiO2@MoS2/Bi VO4 for composite photocatalysts is20 mg.At 80 min,the maximum degradation efficiency of 20 mg dosage for norfloxacin was83.27%;The maximum degradation efficiency of Cr(VI)with 20 mg was 69.31%at 90 min.(7)Fe3O4@SiO2@MoS2/Bi VO4had the largest degradation rate within the p H=5-7range of norfloxacin solution,indicating that it met the acidity environment of human urine metabolites and norfloxacin in medical wastewater.At 80 min,the maximum degradation efficiency was 76.34%.At the solution acidity of p H=3,the degradation efficiency of Cr(VI)reached 75.00%at 90 min.
Keywords/Search Tags:Composite photocatalyst, Core-shell material, p-n Heterojunction, Magnetic nanomaterials, Glyphosate isopropylamine salt, Norfloxacin
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