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Bioinspired synthesis of magnetic nanoparticles.

机译:生物启发的磁性纳米粒子合成。

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摘要

High quality magnetite crystals have previously been synthesized in a pluronic medium using a biomineralization protein, mms6, derived from magnetotactic bacteria. However, until present these studies have been conducted only in the solution phase, for which particle aggregation and movement of particles to the bottom of the pluronic medium limit characterization opportunities, including how the particles affect the pluronic structure. In this study, magnetite synthesis is completed in a solid pluronic gel phase for which magnetite particles are suspended and can be characterized using small-angle x-ray scattering (SAXS). This study has shown that the proteins alone do not affect the Pluronic structure, except slightly for the case of the highest concentration of His-mms6. In addition, mixed chlorides may act to stabilize the self-organization of the Pluronic due in electrostatic interactions. This study has shown that magnetite synthesis in Pluronic is a function of several parameters including the concentration and size of the protein used for templating, the concentration of the magnetite, and the viscosity of the Pluronic gel. Our results indicate that magnetite particle synthesis in Pluronic causes the inter-micellar distance to decrease, most notably for the case of the highest concentration of His-mms6. This may be attributed to an apparent compression in the gel because of the magnetite particles and the large size of His-mms6. Large magnetite particles can be formed in solid Pluronic gel in the absence of protein, indicating that Pluronic alone may template particle synthesis. This is in contrast to magnetite formation in the solution phase, for which either the His-mms6 or C25 protein is required for templating. Disruption in the FCC structure is observed for the case of the highest His-mms6 concentration, which is consistent with the larger size of the His-mms6 protein. Disruption of the FCC structure may eliminate the possible templating ability of the Pluronic gel, as evidenced by the lack of large particles present in the case of the highest His-mms6 concentration. The large scattering due to the magnetite particles suggests the use of a lower concentration of iron chlorides so as to be able to resolve all the higher order peaks in the gel. Compared to the solution phase experiments, the solid gel phase synthesis method results in a gel with a much higher viscosity, which is likely to impede particle growth. Thus, the viscosity of the gel may be used to control the particle size in the biomineralization synthesis platform.
机译:先前已经在普朗尼克培养基中使用源自趋磁细菌的生物矿化蛋白mms6合成了高质量的磁铁矿晶体。但是,到目前为止,这些研究仅在固溶阶段进行,对于固溶阶段,颗粒的聚集和颗粒向普朗尼克介质底部的移动限制了表征机会,包括颗粒如何影响普朗尼克结构。在这项研究中,磁铁矿的合成是在固态普卢尼克凝胶相中完成的,在该相中悬浮了磁铁矿颗粒,可以使用小角度X射线散射(SAXS)对其进行表征。这项研究表明,单独的蛋白质不会影响Pluronic的结构,但对于His-mms6最高浓度的情况除外。另外,由于静电相互作用,混合的氯化物可以起到稳定Pluronic的自组织的作用。这项研究表明,Pluronic中磁铁矿的合成是几个参数的函数,包括用于模板化的蛋白质的浓度和大小,磁铁矿的浓度以及Pluronic凝胶的粘度。我们的结果表明,Pluronic中磁铁矿颗粒的合成导致胶束间距离减小,尤其是在His-mms6浓度最高的情况下。这可能是由于磁铁矿颗粒和His-mms6的大尺寸导致凝胶中明显的压缩。在不存在蛋白质的情况下,可以在固体Pluronic凝胶中形成大的磁铁矿颗粒,这表明仅Pluronic可以作为模板合成颗粒。这与在固溶相中形成磁铁矿相反,在固溶相中需要His-mms6或C25蛋白进行模板化。对于最高的His-mms6浓度,观察到了FCC结构的破坏,这与His-mms6蛋白的较大尺寸一致。 FCC结构的破坏可能会消除Pluronic凝胶的可能的模板能力,这在His-mms6浓度最高的情况下,由于缺少大颗粒而证明了这一点。由于磁铁矿颗粒引起的大散射表明使用较低浓度的氯化铁,以便能够解析凝胶中所有较高阶的峰。与溶液相实验相比,固体凝胶相合成方法得到的凝胶的粘度要高得多,这很可能会阻碍颗粒的生长。因此,凝胶的粘度可用于控制生物矿化合成平台中的粒度。

著录项

  • 作者

    David, Anand.;

  • 作者单位

    Iowa State University.;

  • 授予单位 Iowa State University.;
  • 学科 Chemistry Inorganic.
  • 学位 M.S.
  • 年度 2009
  • 页码 62 p.
  • 总页数 62
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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