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Collaborative Research: Coupled effects of particle shape/flexibility and pore morphology on membrane rejection: theory and experiment

Collaborative Research: Coupled effects of particle shape/flexibility and pore morphology on membrane rejection: theory and experiment
合作研究:颗粒形状/柔韧性和孔形态对膜排斥的耦合影响:理论与实验
批准号:
1604715
负责人:
Ruth Baltus
金额:
$15.34万
依托单位:
依托单位国家:
美国
项目类别:
Standard Grant
财政年份:
2016
资助国家:
美国
项目状态:
已结题
起止时间:
2016-08-15 至 2021-07-31

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中文摘要
翻译
提案编号:1604715(电极导线)/1605088 PI:Baltus,R.E./合作研究:颗粒形状/柔性和孔形态对膜排斥的耦合效应:理论和实验这项研究的动机在于,到2025年,预计将有近20亿人生活在缺水地区。这些驱动因素表明,需要先进的水和废水处理技术来缓解不断增长的水需求。低压液-固膜分离技术如微滤和超滤直接去除贾第虫和隐孢子虫等难以消毒的寄生虫,沿着大多数细菌、浊度和其他胶体物质。然而,微滤器和超滤器在去除病毒和某些细菌方面并不有效。本研究的总体目标是检查非理想的孔几何形状和颗粒形状和柔性对多孔膜的微生物截留的影响。该合作研究项目将进行数学建模和实验工作,以定量研究更接近真实世界分离的复杂系统。该项目产生的结果对于微滤和超滤系统的优化设计以及与水和废水处理以及食品,生物技术和制药操作相关的实际应用非常重要。更广泛的教育影响包括面向德克萨斯州学院站和纽约州波茨坦邻近社区的小学、初中和高中开展科学推广活动,以吸引代表性不足的少数民族进入STEM领域。目前可用的膜系统设计策略基于简单的孔几何形状和微生物形状。因此,它们不能完全解释在实践中观察到的不完全微生物去除。这个合作项目将产生基础知识,以表征尾病毒,丝状病毒,可变形细菌和刚性合成纳米棒在具有曲折互连孔网络的多孔膜上的受阻对流。该项目紧密结合了实验和理论的努力。该项目将重点关注使用具有毛细孔的低压膜以及具有复杂孔形态的膜系统分离尾部和柔性病毒和细菌颗粒。这项研究的技术影响的一个例子是,它解决了去除环境中最丰富的生物体之一的尾病毒的困难,并已被证明可以穿透所谓的无菌过滤器。该研究将检查柔性颗粒是否能够在孔隙弯曲处导航,以及缺乏刚性细胞壁的细菌是否可以通过孔隙。为了从理论上研究颗粒的形状和灵活性,将开发单个圆柱形孔中颗粒传输的详细模型。具体而言,将纳入病毒和细菌的非球形形状和灵活性的物理学。实验验证这些模型的预测将使用轨道蚀刻膜。为了检查膜形态的影响,包括孔互连性,将使用开发的模型来描述这些系统进行2D渗透测量和解释。这个项目将产生一个定量的了解复杂的孔几何形状和微生物特性的作用,管理从多孔膜的微生物排斥。阐明这些考虑因素将改进现有的过滤模型,以更准确地描述现实世界中的膜分离的排斥。
英文摘要
Proposal Numbers: 1604715 (Lead)/1605088 PIs: Baltus, R.E./Chellam, S.Collaborative Research: Coupled effects of particle shape/flexibility and pore morphology on membrane rejection: theory and experimentThe motivation for this research lies in the fact that by the year 2025, nearly 2 billion people are projected to live in areas of water scarcity. These drivers point to the need for advanced water and wastewater treatment technologies to alleviate ever-increasing water demand. Low-pressure liquid-solid membrane separation technologies such as microfiltration and ultrafiltration directly remove difficult-to disinfect parasites such as Giardia and Cryptosporidium, along with most bacteria, turbidity, and other colloidal materials. However, micro- and ultrafilters are not effective in removing viruses and some bacteria. The overall goal of this research is to examine the impact of non-ideal pore geometry and particle shape and flexibility on microbial rejection by porous membranes. This collaborative research project will perform both mathematical modeling and experimental work to quantitatively examine complex systems that more closely represent real-world separations. Results generated from this project will be important for the optimal design of micro- and ultrafiltration systems and for practical applications related to water and wastewater treatment and food, biotechnological, and pharmaceutical operations. Educational broader impacts include the development of science outreach activities geared towards elementary, middle, and high schools in neighboring communities in College Station, TX and Potsdam, NY to attract underrepresented minorities into STEM fields. Currently available membrane system design strategies are based on simple pore geometries and microbial shapes. Consequently, they cannot fully explain incomplete microbial removal observed in practice. This collaborative project will generate fundamental knowledge to characterize the hindered convection of tailed viruses, filamentous viruses, deformable bacteria, and rigid synthetic nanorods across porous membranes with tortuous interconnected pore networks. The project tightly integrates the experimental and theoretical efforts. The project will focus on separations of tailed and flexible viral and bacterial particles using low-pressure membranes with capillary pores as well as membrane systems with complex pore morphology. One example of the technological impact of this research is that it is addressing the difficulty in removing tailed viruses that are among the most abundant organisms in the environment and have been shown to penetrate so-called sterile filters. The research will examine whether flexible particles will be able to navigate around pore bends and whether bacteria that lack rigid cell walls can squeeze through pores. To theoretically examine particle shape and flexibility, detailed models of particle transport in a single cylindrical pore will be developed. Specifically, the physics of the non-spherical shape and flexibility of the viruses and bacteria will be incorporated. Experiments to validate these model predictions will be performed using track-etched membranes. To examine effects of membrane morphology including pore interconnectivity, 2D permeation measurements will be performed and interpreted using models developed to describe these systems. This project will generate a quantitative understanding of the role of complex pore geometries and microbial characteristics that govern rejection of microorganism from porous membranes. Incorporating such considerations will improve existing filtration models to more accurately describe rejection in real-world membrane separations.
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Collaborative Research: Shape Effects on Microorganism Removal by Microfiltration and Ultrafiltration Membranes
  • 批准号:
    0966934
  • 项目类别:
    Standard Grant
  • 资助金额:
    $14.77万
  • 财政年份:
    2010
  • 负责人:
    Ruth Baltus
  • 依托单位:
Transport Characteristics of Gases and Organic Solutes in Room Temperature Ionic Liquids
  • 批准号:
    0522589
  • 项目类别:
    Standard Grant
  • 资助金额:
    $0.0万
  • 财政年份:
    2005
  • 负责人:
    Ruth Baltus
  • 依托单位:
The Development of Procedures for the Fabrication of Alumina Porous Membranes by Anodic Oxidation
  • 批准号:
    9409441
  • 项目类别:
    Standard Grant
  • 资助金额:
    $3.81万
  • 财政年份:
    1994
  • 负责人:
    Ruth Baltus
  • 依托单位:
Immobilizaton of Enzymes on Porous Membranes
  • 批准号:
    8808490
  • 项目类别:
    Standard Grant
  • 资助金额:
    $4.45万
  • 财政年份:
    1988
  • 负责人:
    Ruth Baltus
  • 依托单位:
国内基金
海外基金
Research on Quantum Field Theory without a Lagrangian Description
  • 批准号:
    24ZR1403900
  • 项目类别:
    省市级项目
  • 资助金额:
    --
  • 批准年份:
    2024
  • 负责人:
    SATOSHI NAWATA
  • 依托单位:
Cell Research
Cell Research
Cell Research (细胞研究)