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NSF-DFG Confine: Plasma-Catalysis in Confined Spaces for Cold Start NOx Abatement in Automotive Exhaust

NSF-DFG Confine: Plasma-Catalysis in Confined Spaces for Cold Start NOx Abatement in Automotive Exhaust
NSF-DFG Confine:密闭空间中的等离子体催化用于冷启动汽车尾气中的氮氧化物减排
批准号:
2234270
负责人:
Peter Bruggeman
金额:
$60.0万
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
项目状态:
未结题
起止时间:
2023-01-01 至 2025-12-31

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中文摘要
翻译
该项目寻求改变传统的化学加工,以确保可持续的未来。催化能促进理想的化学反应,在确定现代污染减排标准、高能量密度燃料以及熟练和安全的燃料和化肥方面发挥了关键作用。该项目旨在通过非平衡等离子体与表面催化反应的耦合来发展对化学催化实践中的新概念的理解。在接近环境温度的情况下,模拟现代催化转化器中的“蜂窝状整体”,在毛细管微反应器中减少NOx,作为一个试验台系统。在危害人类健康和环境的NOx污染中,交通尾气排放占了很大一部分。最先进的汽车尾气后处理系统在473 K(200摄氏度)的起燃阈值温度以上有效地修复NOx,足以克服催化过程中固有的动力学限制。该项目利用受限几何结构中等离子体化学和热催化过程之间的相互作用,使汽车在接近环境温度的情况下能够减少NOx。这解决了发动机预热过程中的“冷启动”汽车尾气排放问题,这些尾气排放占机动车NOx污染的80%。该项目进一步促进了美国和德国在STEM方面的科学合作和培训。等离子体化学以体积计发生,涉及短暂的活性中间体--离子、自由基、电子和振动激发的物种--当它们撞击到选择性催化表面时,可能会影响化学转化和常规催化无法达到的途径。等离子体(小于10^-6到10 S)和催化化学(10^-1到10 S)在反应时间上的差异以及等离子体(体积)和催化(表面)化学的不同长度尺度意味着,只有当表面与体积比较大时,才能实现等离子体与表面催化化学之间的有效耦合,从而使短暂的等离子体衍生中间体能够高通量地进入催化剂表面。因此,能够实现非常高的表面体积比的限制是将体积和快速等离子体化学与选择性的、较慢的表面催化过程相结合的关键。该项目结合了反应器设计、先进的光谱和光谱诊断技术以及多尺度建模,以检查在受限反应环境中影响等离子体-催化化学耦合的反应和传输现象。这包括(1)探索毛细微反应器内等离子体和热催化过程联合操作中反应物种的特征扩散时间尺度和寿命,(2)开发光谱和光谱工具来识别和计数气相和催化剂表面上的短期反应中间体,以及(3)开发描述这些受限反应环境中支撑过程的多尺度模型。这将有助于阐明反应和传输现象如何影响等离子体-催化耦合,并描述新的催化物种和还原NOx的途径。该项目是通过“受限空间中的化学和运输(NSF-DFG Confine)”机会获得的,这是一个由国家科学基金会和德国科学基金会(DFG)参与的合作征集活动。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。
英文摘要
This project seeks to transform traditional chemical processing to ensure a sustainable future. Catalysis, which facilitates desired chemical reactions, has played a key role in defining the modern standard of pollution abatement, high-energy density fuels, and proficient and safe fuels and fertilizers. This project aims to develop an understanding of new concepts in the practice of chemical catalysis enabled by coupling of non-equilibrium plasma with surface catalyzed reactions. NOx abatement in capillary microreactors, mimicking “honeycomb monoliths” in modern-day catalytic converters, at near ambient temperatures serve as a testbed system. Tailpipe emissions in transportation account for a majority of NOx pollution harming human health and the environment. State-of-the-art automobile exhaust after-treatment systems remediate NOx efficiently above a threshold light-off temperature 473 K (200 degrees C), sufficient to overcome kinetic limitations inherent in catalytic processes. The project harnesses interactions among plasma chemistry and thermocatalytic processes in confined geometries to enable NOx reduction in automobiles at near ambient temperatures. This addresses “cold start” automotive emissions during engine warm up, which account for 80% of NOx vehicular pollution. This project furthers US-German scientific collaboration and training in STEM.Plasma chemistry occurs volumetrically and involves short-lived reactive intermediates—ions, radicals, electronically- and vibrationally-excited species—which when impinged on a selective catalytic surface could effect chemical transformations and pathways inaccessible to conventional catalysis. The disparity in reaction timescales of plasma (sub-10^-6 to 10 s) and catalytic chemistry (10^-1 to 10 s) and the different length scales for plasma (volume) and catalytic (surface) chemistry implies that effective coupling between plasma and surface catalytic chemistry can only be achieved if surface-to-volume ratios are large to enable a high flux of short-lived plasma-derived intermediates to the catalyst surface. Hence, confinement, enabling very high surface-to-volume ratios, is key to coupling volumetric and fast plasma chemistry with selective, slower surface-based catalytic processes. The project combines reactor design, advanced spectroscopic and spectrometric diagnostics, and multiscale modeling to examine reaction and transport phenomena impacting plasma-catalytic chemistry coupling in confined reaction environments. This includes (1) probing characteristic diffusion time scales and lifetimes of reactive species in combined operation of plasma- and thermocatalytic processes within capillary microreactors, (2) developing spectroscopic and spectrometric tools to identify and enumerate short-lived reactive intermediates in the gas phase and on catalyst surfaces and (3) developing multiscale models describing the underpinning processes in these confined reaction environments. This will allow to elucidate how reaction and transport phenomena impact plasma-catalytical coupling and describe new catalytic species and pathways for NOx reduction. This project was awarded through the “Chemistry and Transport in Confined Spaces (NSF-DFG Confine)" opportunity, a collaborative solicitation that involves the National Science Foundation and Deutsche Forschungsgemeinschaft (DFG).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.
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Collaborative Research: ECO-CBET: Plasma-Assisted Dehalogenation of Persistent Halogen-Containing Waste Streams
  • 批准号:
    2318493
  • 项目类别:
    Standard Grant
  • 资助金额:
    $84.99万
  • 财政年份:
    2023
  • 负责人:
    Peter Bruggeman
  • 依托单位:
GCR: Collaborative Research: Plasma-Biofilm Interactions at the Intersection of Physics, Chemistry, Biology and Engineering
  • 批准号:
    2020695
  • 项目类别:
    Continuing Grant
  • 资助金额:
    $281.0万
  • 财政年份:
    2020
  • 负责人:
    Peter Bruggeman
  • 依托单位:
Collaborative Research: Understanding Plasma-Liquid Interactions Through Controlled Plasma-Microdroplet Experiments and Modeling
  • 批准号:
    1903151
  • 项目类别:
    Standard Grant
  • 资助金额:
    $20.0万
  • 财政年份:
    2019
  • 负责人:
    Peter Bruggeman
  • 依托单位:
2018 Plasma Processing Science: Fundamental Insights in Plasma Processes
  • 批准号:
    1824150
  • 项目类别:
    Standard Grant
  • 资助金额:
    $1.0万
  • 财政年份:
    2018
  • 负责人:
    Peter Bruggeman
  • 依托单位:
国内基金
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  • 批准号:
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  • 项目类别:
    面上项目
  • 资助金额:
    60.0万元
  • 批准年份:
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  • 负责人:
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