首页> 外文学位 >Synthesis, characterization, and kinetic studies of ionizing radiation-induced intra- and inter-crosslinked poly(vinyl pyrrolidone) nanohydrogels.
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Synthesis, characterization, and kinetic studies of ionizing radiation-induced intra- and inter-crosslinked poly(vinyl pyrrolidone) nanohydrogels.

机译:电离辐射诱导的内部和内部交联的聚乙烯吡咯烷酮纳米水凝胶的合成,表征和动力学研究。

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摘要

A polymer nanohydrogel can be defined as a three-dimensional polymer network composed of hydrophilic crosslinked macromolecular chains filled with liquid and possessing a diameter of 1-102 nanometers. Nanohydrogels have drawn huge interest due to their potential applications, such as target-specific drug delivery carriers, absorbents, chemical/biological sensors, and bio-mimetic materials. However, the conventional methods of nanohydrogel synthesis require toxic chemicals (e.g., initiators, crosslinking agents) to form the gel structure. The additional steps required to remove unreacted or residual (undesired) substances cause nanohydrogel fabrication to be complicated, environmentally unfriendly, and unsuitable for biomedical use.;This study aims to develop simple and efficient methods of producing nanohydrogels from polymeric, aqueous solutions using ionizing radiation. Poly(vinyl pyrrolidone) (PVP) nanohydrogels of various sizes and molecular weights were prepared by pulsed electron beam and steady-state gamma irradiation at different doses (5 and 10 kGy; 1Gy = 1 J kg-1) and temperatures (20 to 77°C). The pervaded volume of the PVP chains becomes smaller at high temperatures (above 50°C) due to the disruption of hydrogen bonds between water and PVP molecules which reduces the size and the molecular weight of the synthesized PVP nanohydrogels. The synthesis parameters (e.g., irradiation temperature, pulse repetition rate, dose rate, and solution concentration) were varied in order to control the size and the average molecular weight of the irradiated sample. In the absence of oxygen, the radiolytically produced free radicals of the thermally collapsed PVP molecules primarily underwent intra-crosslinking reactions, along with a minor contribution from inter-crosslinking reactions. The predominance of the intra-crosslinking mechanism was exhibited at high irradiation temperature (77°C) in dilute solutions (c = 0.9 x 10-2 mol L-1). The formation of carbon-centered free radicals along the backbone of the PVP chain at higher pulse repetition rate (300 pulses per second) was found to enhance the intra-crosslinking reaction, thereby leading to the formation of smaller nanohydrogel molecules containing an average hydrodynamic radius (Rh) of 9.9 +/- 0.1 nm.
机译:聚合物纳米水凝胶可定义为三维亲水网络,由填充有液体且直径为1-102纳米的亲水性交联大分子链组成。纳米水凝胶由于其潜在的应用而引起了极大的兴趣,例如目标特异性的药物输送载体,吸收剂,化学/生物传感器和仿生材料。然而,纳米水凝胶合成的常规方法需要有毒化学物质(例如引发剂,交联剂)以形成凝胶结构。去除未反应的或残留的(多余的)物质所需的额外步骤导致纳米水凝胶的制造复杂,对环境不利且不适用于生物医学。本研究旨在开发简单有效的方法,利用电离辐射从聚合物水溶液中制备纳米水凝胶。 。通过脉冲电子束和稳态γ射线在不同剂量(5和10 kGy; 1Gy = 1 J kg-1)和温度(20至77)下制备各种尺寸和分子量的聚乙烯吡咯烷酮(PVP)纳米水凝胶°C)。由于水和PVP分子之间的氢键断裂,PVP链的渗透体积在高温(高于50°C)下变小,从而减小了合成PVP纳米水凝胶的尺寸和分子量。改变合成参数(例如辐照温度,脉冲重复率,剂量率和溶液浓度)以控制辐照样品的大小和平均分子量。在不存在氧气的情况下,热塌陷的PVP分子的辐射分解产生的自由基主要经历内部交联反应,而来自内部交联反应的贡献很小。在稀溶液(c = 0.9 x 10-2 mol L-1)的高辐照温度(77°C)下,内交联机理占优势。发现以较高的脉冲重复频率(每秒300个脉冲)沿着PVP链的骨架形成以碳为中心的自由基会增强内部交联反应,从而导致形成包含平均流体动力学半径的较小的纳米水凝胶分子(Rh)为9.9 +/- 0.1 nm。

著录项

  • 作者

    An, Jung-Chul.;

  • 作者单位

    University of Maryland, College Park.;

  • 授予单位 University of Maryland, College Park.;
  • 学科 Chemistry Polymer.;Engineering Materials Science.
  • 学位 Ph.D.
  • 年度 2007
  • 页码 166 p.
  • 总页数 166
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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