Collaborative Research: Deciphering the nanoscale interactions during mineral nucleation and scale formation on polymer surfaces
合作研究:破译聚合物表面矿物成核和结垢过程中的纳米级相互作用
基本信息
- 批准号:2232687
- 负责人:
- 金额:$ 28.17万
- 依托单位:
- 依托单位国家:美国
- 项目类别:Standard Grant
- 财政年份:2023
- 资助国家:美国
- 起止时间:2023-08-01 至 2026-07-31
- 项目状态:未结题
- 来源:
- 关键词:
项目摘要
Mineral precipitation, or the formation of solid mineral phases from solutions, is a process of great importance in the natural environment and engineered systems. Mineral scaling on surfaces, or the unwanted deposition of mineral precipitates, poses a technological challenge to many industrial processes. In membrane-based water treatment, mineral scaling of polymer membranes decreases membrane flux, diminishes energy efficiency, and shortens membrane module lifespan. In the oil and gas industry, mineral scale deposition on the interior surface of pipes can result in complete blockage of pipelines and disrupt oil and gas production. Despite its importance, the role of polymeric solid substrates on mineral scaling is poorly understood. This research aims to understand how the surface characteristics of polymers impact the formation of mineral scales. The investigators will employ combined experimental characterization and theoretical analysis to examine the nanoscale interactions that drive mineral scale formation on polymeric substrates. The findings of this work will inform design of anti-scaling polymer surfaces in submerged aqueous environments, which will bring significant economic benefits to industries in which mineral scaling plagues system performance and long-term durability. This research project will provide outreach activities through public engagement at both George Washington University and University of Maryland. The investigators will host a yearly student-run symposium on environmental nanoscience, and host high school student interns and deliver guest lectures to local high school students. Mineral scaling on surfaces, or the unwanted deposition of mineral precipitates, is a ubiquitous yet unwanted phenomenon in many industrial processes including reverse osmosis, water desalination, heat exchangers, and oil and gas production. One promising strategy for mitigating scaling is to modify polymer surface characteristics or apply polymer coatings to non-polymer surfaces to render the surface scaling resistant. Currently, there is a significant knowledge gap in understanding the nanoscale interactions and physicochemical processes in the initial stages of scale formation on polymers. This knowledge gap limits rational development of scaling-resistant membranes and surface polymer coatings. In this research, the investigators will integrate liquid phase transmission electron microscopy, real-time measurement of scale formation dynamics using quartz crystal microbalance, and theoretical modeling to establish nucleation mechanisms during scaling of silica and gypsum on polyamide surfaces. The research objectives are to 1) investigate the effect of surface charge and hydrophobicity of polyamide films prepared via molecular layer-by-layer assembly on mineral scaling rate, 2) employ liquid phase transmission electron microscopy to visualize and quantify mineral nucleation dynamics on polyamide surfaces in real time at the nanometer length scale and 3) derive theoretical models for nanoparticle attachment and nucleation kinetics to identify the nanoscale interactions involved in scale formation as a function of polymer surface chemistry. The results of this work will facilitate rational manipulation of nanoscale mineral-membrane interactions to prevent mineral scaling on engineering polymers in the aqueous environment. Educational and outreach aspects of the project will incorporate research findings into undergraduate and graduate course materials, host joint student-run nanomaterial and water symposia, and enhance the participation of underrepresented students in research.This award reflects NSF's statutory mission and has been deemed worthy of support through evaluation using the Foundation's intellectual merit and broader impacts review criteria.
矿物沉淀,即从溶液中形成固体矿物相,在自然环境和工程系统中是一个非常重要的过程。表面的矿物结垢,或不必要的矿物沉淀物的沉积,给许多工业过程带来了技术挑战。在膜基水处理中,聚合物膜的矿物结垢会降低膜通量,降低能效,缩短膜组件的使用寿命。在石油和天然气工业中,管道内表面的矿垢沉积会导致管道完全堵塞,扰乱油气生产。尽管聚合物固体基质很重要,但它对矿物结垢的作用却知之甚少。这项研究旨在了解聚合物的表面特性如何影响矿物结垢的形成。研究人员将采用实验表征和理论分析相结合的方法,研究在聚合物衬底上形成矿物鳞片的纳米级相互作用。这项工作的发现将为水下水环境中防垢聚合物表面的设计提供参考,这将为矿物结垢困扰系统性能和长期耐用性的行业带来显著的经济效益。这一研究项目将通过乔治华盛顿大学和马里兰大学的公众参与提供外联活动。研究人员将每年举办一次由学生举办的关于环境纳米科学的研讨会,并主办高中生实习生,并为当地高中生提供客座讲座。在许多工业过程中,包括反渗透、海水淡化、热交换器和石油和天然气生产中,表面的矿物结垢或矿物沉淀物的有害沉积是一种普遍但不受欢迎的现象。减轻结垢的一个有希望的策略是改变聚合物表面特性或在非聚合物表面涂覆聚合物涂层以使表面抗结垢。目前,在理解聚合物结膜初期的纳米尺度相互作用和物理化学过程方面存在着显著的知识差距。这一知识差距限制了防结垢膜和表面聚合物涂层的合理开发。在这项研究中,研究人员将结合液相透射电子显微镜、使用石英晶体微天平实时测量结垢动力学和理论建模来建立聚酰胺表面二氧化硅和石膏结垢的成核机理。研究目的:1)研究分子层层组装聚酰胺薄膜的表面电荷和疏水性对矿物结垢速率的影响;2)利用液相电子显微镜在纳米尺度上实时观察和量化聚酰胺表面的矿物成核动力学;3)推导纳米粒子附着和成核动力学的理论模型,以确定作为聚合物表面化学函数的纳米尺度上的相互作用。这项工作的结果将有助于合理操纵纳米级矿物-膜相互作用,以防止水环境中工程聚合物上的矿物结垢。该项目的教育和推广方面将把研究成果纳入本科生和研究生课程材料,主办由学生联合举办的纳米材料和水研讨会,并加强未被充分代表的学生参与研究。该奖项反映了NSF的法定使命,并通过使用基金会的智力优势和更广泛的影响审查标准进行评估,被认为值得支持。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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Taylor Woehl其他文献
Transient colloidal crystals fueled by electrochemical reaction products
由电化学反应产物驱动的瞬态胶体晶体
- DOI:
10.1038/s41467-025-57333-4 - 发表时间:
2025-02-28 - 期刊:
- 影响因子:15.700
- 作者:
Medha Rath;Satyam Srivastava;Eric Carmona;Sarangua Battumur;Shakti Arumugam;Paul Albertus;Taylor Woehl - 通讯作者:
Taylor Woehl
Taylor Woehl的其他文献
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{{ truncateString('Taylor Woehl', 18)}}的其他基金
CAREER: Single Particle Visualization of Chemical Processes During Multimetallic Nanocrystal Synthesis
职业:多金属纳米晶体合成过程中化学过程的单粒子可视化
- 批准号:
2045258 - 财政年份:2021
- 资助金额:
$ 28.17万 - 项目类别:
Continuing Grant
Mechanistic Understanding and Control over Electrokinetic Assembly and Separation of Colloids in pH Gradients
pH 梯度下胶体动电组装和分离的机理理解和控制
- 批准号:
2025249 - 财政年份:2020
- 资助金额:
$ 28.17万 - 项目类别:
Standard Grant
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