UNS: Diffusion of Strongly Interacting Species in Microemulsions and Gels

UNS：强相互作用物质在微乳液和凝胶中的扩散

• 批准号: 1506474
• 负责人: Ronald Phillips
• 金额: $ 35.67万
• 依托单位: University of California-Davis
• 依托单位国家: 美国
• 项目类别: Standard Grant
• 财政年份: 2015
• 资助国家: 美国
• 起止时间: 2015-09-15 至 2020-08-31
• 项目状态: 已结题
• 来源: https://www.nsf.gov/awardsearch/showAward?AWD_ID=1506474&HistoricalAwards=false
• 关键词: UNS; Diffusion; Strongly; Interacting; Species

CBET - 1506474PI: Phillips, Ronald J.The goal of this project is to understand molecular diffusion in two types of complex media - microemulsions and polymer gels. Microemulsions are solutions of aggregated surfactants in water, and they are used in pharmaceutical drug delivery to increase solubility, reduce toxicity, and control the rate of drug release. Polymer gels are water-filled networks of thread-like molecules, and they are used in gel chromatography and membrane filtration to separate molecules. Fibrous gels shrink or swell in response to changes in the liquid between the fibers, which strongly affects their function in ways that are not understood. The investigators will use an optical technique to measure rates of molecular movement in microemulsions and polymer gels. Data will be compared with theory to improve theoretical models for these complex systems.The diffusion of a hydrophobic solute in the presence of micelles or surfactant aggregates will be measured. In such systems, localized interactions in the interior of the aggregates strongly affect diffusion rates of the solute and the surfactant. Strong solute-matrix interactions also occur in polymer gels, in which polymer fibers hinder solute motion, and solute molecules may induce gel swelling or shrinkage. Diffusion rates in microemulsions and shrinking and swelling in polymer hydrogels will be measured by holographic interferometry, an optical method for monitoring changes in concentration in transparent solutions and gels. Taylor diffusiometry, solid phase microextraction, single-photon counting fluorescence spectroscopy, and osmometry will also be used to measure physical properties needed to compare data to theoretical descriptions of these processes.

CBET -1506474 PI：菲利普斯，罗纳德J.该项目的目标是了解分子扩散在两种类型的复杂介质-微乳液和聚合物凝胶。 微乳液是聚集的表面活性剂在水中的溶液，并且它们用于药物递送以增加溶解度、降低毒性和控制药物释放速率。 聚合物凝胶是线状分子的水填充网络，它们用于凝胶色谱和膜过滤以分离分子。 纤维状凝胶会随着纤维之间液体的变化而收缩或膨胀，这会以尚不清楚的方式强烈影响它们的功能。 研究人员将使用光学技术来测量微乳液和聚合物凝胶中的分子运动速率。 将数据与理论进行比较，以改进这些复杂系统的理论模型。将测量胶束或表面活性剂聚集体存在下疏水溶质的扩散。 在这样的系统中，聚集体内部的局部相互作用强烈影响溶质和表面活性剂的扩散速率。 强溶质-基质相互作用也发生在聚合物凝胶中，其中聚合物纤维阻碍溶质运动，并且溶质分子可诱导凝胶溶胀或收缩。 微乳液中的扩散速率和聚合物水凝胶中的收缩和溶胀将通过全息干涉测量法测量，全息干涉测量法是一种用于监测透明溶液和凝胶中浓度变化的光学方法。 泰勒扩散法，固相微萃取，单光子计数荧光光谱法，和渗透压测定法也将用于测量所需的物理性质，比较数据的理论描述这些过程。