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On the synthesis of copper-nickel binary alloy nanoparticles and binding silane coupling agents to magnetic ferrite nanoparticles.

机译:关于铜镍二元合金纳米粒子的合成以及将硅烷偶联剂结合到磁性铁氧体纳米粒子上。

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摘要

This dissertation addresses the creation of a multifunctional nanoplatform for cancer targeting, imaging, and therapy. Magnetic oxide nanoparticles were labeled with silane coupling agents that could be used for targeting. The magnetic oxides have application as contrast enhancing agents for magnetic resonance imaging. Copper-nickel binary alloy nanoparticles were prepared for possible use in Curie temperature limited hyperthermia therapy.;Spherical, single crystal iron oxide nanoparticles with average diameters of 4 nm, 6 nm, 8 nm, 11 nm, or 16 nm were prepared using published procedures. The iron oxide particle chemistry was extended to synthesize 13 nm diameter CoFe2O4, 9 nm diameter MnFe2O4, and 12 nm diameter NiFe2O4. The particles had a coating of oleic acid and oleylamine ligands. Silane coupling chemistry was used to displace these ligands with either beta-aminoethyl-gamma-aminopropyl-trimethoxysilane, triethoxysilane-PEG, or triethoxysilane-biotin. The silane ligands would allow the particles to be conjugated with a targeting group.;New chemistry was developed to synthesize fcc CuNi nanoparticles with the objective of finding methods that give particles with an average size less than 50 nm, a narrow distribution of particle sizes, and control of particle composition. The particle synthesis involves the reduction of a mixture of copper(II) and nickel(II) and the reduction conditions included diol reduction, polyol synthesis, seeding by diol reduction, and oleate reduction. One of the main issues is the formation of hcp nickel particles as a containment in the method. The factors that avoided the formation of hcp nickel particles and allow only fcc particles to form were the choice of reducing agent, ratio of surfactants, and heating time. Both the oleate reduction and diol reduction gave a mixture of the hcp and fcc phases. By controlling certain reaction conditions, such as keeping the ratio of oleic acid to oleylamine 1:1 and slowly heating to reflux for 30 minutes, only fcc nanoparticles were formed. The method of making CuNi nanoparticles by diol reduction gave the best result and it consisted of a total amount of 1 mmol of Cu(acac)2 and Ni(acac) 2, 5 mmol of 1,2 hexadecanediol, 1.5 mL of oleic acid, 1.5 mL of oleylamine and 15 mL of benzyl ether. It made fcc CuNi, provided control of composition, and gave particles with average size smaller than 100 nm.
机译:本论文致力于癌症靶向,成像和治疗的多功能纳米平台的创建。磁性氧化物纳米颗粒用可用于靶向的硅烷偶联剂标记。磁性氧化物可用作磁共振成像的造影剂。制备了铜-镍二元合金纳米颗粒,可用于居里温度有限的高温疗法;使用公开程序制备了平均直径为4 nm,6 nm,8 nm,11 nm或16 nm的球形单晶氧化铁纳米颗粒。扩展了氧化铁颗粒的化学性质,以合成直径为13 nm的CoFe2O4,直径为9 nm的MnFe2O4和直径为12 nm的NiFe2O4。该颗粒具有油酸和油胺配体的涂层。硅烷偶联化学用于用β-氨基乙基-γ-氨基丙基-三甲氧基硅烷,三乙氧基硅烷-PEG或三乙氧基硅烷-生物素置换这些配体。硅烷配体可以使颗粒与靶向基团结合。开发了一种新的化学方法来合成fcc CuNi纳米颗粒,其目的是找到一种方法,使平均粒径小于50 nm,粒径分布窄,和控制颗粒成分。颗粒合成涉及还原铜(II)和镍(II)的混合物,并且还原条件包括二醇还原,多元醇合成,通过二醇还原的晶种和油酸酯的还原。主要问题之一是在该方法中形成六聚氰胺镍颗粒作为遏制物。避免形成hcp镍颗粒而仅允许形成fcc颗粒的因素是还原剂的选择,表面活性剂的比例和加热时间。油酸酯还原和二醇还原均得到hcp和fcc相的混合物。通过控制某些反应条件,例如保持油酸与油胺的比例为1:1,并缓慢加热至回流30分钟,仅形成了fcc纳米颗粒。通过二醇还原制备CuNi纳米颗粒的方法获得了最佳效果,该方法包括总量为1 mmol的Cu(acac)2和Ni(acac)2、5 mmol的1,2十六烷二醇,1.5 mL的油酸, 1.5 mL油胺和15 mL苄基醚。它制备了fcc CuNi,提供了组成控制,并提供了平均尺寸小于100 nm的颗粒。

著录项

  • 作者

    Pritchett, Jeremy Scott.;

  • 作者单位

    The University of Alabama.;

  • 授予单位 The University of Alabama.;
  • 学科 Chemistry General.;Chemistry Inorganic.;Nanotechnology.;Chemistry Analytical.
  • 学位 Ph.D.
  • 年度 2011
  • 页码 210 p.
  • 总页数 210
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

  • 入库时间 2022-08-17 11:45:15

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