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Synthesis and Characterization of Fe3O4 Nanoparticles using Polyvinyl Alcohol (PVA) as Capping Agent and Glutaraldehyde (GA) as Crosslinker

机译:使用聚乙烯醇(PVA)作为封端剂和戊二醛(GA)作为交联剂的合成与表征

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The use of polyvinyl alcohol (PVA) as a capping agent and glutaraldehyde (GA) as a crosslinker for a synthesis of magnetite (Fe3O4) nanoparticles is able to reduce agglomeration of produced Fe3O4. Additionally, oxidation of Fe3O4 by air could be avoided. The synthesis is carried out in two steps: first step, magnetite (Fe3O4) nanoparticles were prepared by dissolving the FeCl3.6H2O and FeCl2.4H2O in alkaline media (NH3.H2O). The second step, magnetite nanoparticles were coated with polyvinyl alcohol (PVA) and glutaraldehyde (GA) to obtain Fe3O4-PVA-GA. The latter material was then characterized by FTIR to determine the typical functional groups of magnetite coated with PVA-GA. X-ray Diffraction analysis was used to determine structure and size of crystal as well as the percentage of magnetite produced. It was found that the produced nanoparticles have crystal sizes around 4-9 nm with the cubic crystal structure. The percentage of magnetite phase increases when the amount of glutaraldehyde increased. SEM-EDX was employed to assess the surface morphology and elemental composition of the resulted nanoparticles. The magnetic character of the magnetite and Fe3O4-PVA-GA were studied using Electron Spin Resonance.
机译:使用聚乙烯醇(PVA)作为封端剂和戊二醛(GA)作为合成磁铁矿(Fe3O4)纳米颗粒的交联剂,可以减少产生的Fe3O4的附聚。另外,可以避免通过空气氧化Fe3O4。合成在两个步骤中进行:通过将FECL3.6H2O和FECL2.4H 2 O溶解在碱性培养基(NH3.H2O)中,制备第一步,磁铁矿(Fe3O4)纳米颗粒。第二步,用聚乙烯醇(PVA)和戊二醛(GA)涂覆磁铁矿纳米颗粒,得到Fe3O4-PVA-Ga。然后通过FTIR表征后一种材料,以确定涂有PVA-GA的典型磁岩典型官能团。使用X射线衍射分析来确定晶体的结构和尺寸以及所产生的磁铁矿的百分比。发现产生的纳米颗粒具有约4-9nm的晶体尺寸,具有立方晶体结构。当戊二醛的量增加时,磁铁液相增加的百分比增加。使用SEM-EDX来评估所得纳米颗粒的表面形态和元素组成。使用电子旋转共振研究磁铁矿和Fe3O4-PVA-Ga的磁性。

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