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Development of microfluidic technology for in-situ determination of iron and manganese in natural aquatic systems

机译:微流控技术在天然水生系统中原位测定铁和锰的研究进展

摘要

In-situ sensors are crucially important for understanding the physico-chemical processes that occur in natural water environments. Manual sampling with laboratory analysis cannot provide the temporal and spatial resolution required to characterize marine and fresh water ecosystems, and this approach is both expensive and time consuming, and may also be affected by artefacts during handling and storage. In-situ sensors minimize these drawbacks and provide a tool to obtain long-term data banks which will allow a more synoptic interpretation of the biogeochemical cycles of key elements in water systems. The trace metals iron and manganese are examples of key elements that shape thebiogeochemistry of aquatic systems. Processes influenced by them include phytoplankton growth, deep-sea vent chemistry and redox equilibria in environments with strong oxygen concentration gradients.This thesis describes the development, optimisation and application in environment of two sequential prototypes of a Lab-On-A-Chip microfluidic autonomous analyser for the in-situ determination iron and manganese in aquatic environments. A first prototype (Prototype 1,P1) of the device existed at the beginning of this project. It was labtested and deployed at depth in the Lucky Strike Vents Field (Mid Atlantic Ridge) for the determination of Fe(II). An operative fault during the deployment triggered a trouble shooting process which highlighted some weak points in the device. Those weaknesses were addressed and solved in a second version of the device (Prototype 2, P2) whose novel feature was the in-line mixing by diffusion of reagents and samples. Total Fe, Fe(II) and Mn could be measured with a frequency of up to 12 and 6 samples per hour respectively, with limits of detection of 35 nM and 27 nM for Total Fe and Fe(II) and 28 nM for Mn.The robustness and reliability of P2 was tested in the laboratory and in the environment in both marine (Baltic Sea) and fresh (Beaulieu River) waters. The results of these deployments are presented and directions for further developments of the technology are proposed.
机译:现场传感器对于理解天然水环境中发生的物理化学过程至关重要。带有实验室分析的手动采样无法提供表征海洋和淡水生态系统所需的时间和空间分辨率,这种方法既昂贵又费时,并且在处理和存储过程中还会受到人工制品的影响。原位传感器可最大程度地减少这些弊端,并提供一种获取长期数据库的工具,从而可以对水系统中关键元素的生物地球化学循环进行更概括的解释。微量金属铁和锰是塑造水生系统生物地球化学的关键元素。受它们影响的过程包括在氧气浓度梯度强烈的环境中的浮游植物生长,深海通风化学和氧化还原平衡。本文描述了两个芯片实验室芯片微流控自主模型的开发,优化和在环境中的应用。分析仪,用于在水生环境中现场测定铁和锰。该设备的第一个原型(原型1,P1)存在于该项目的开始。它经过了实验室测试,并在“幸运打击通风口”油田(大西洋中脊)中进行了深入测定,用于测定Fe(II)。部署期间的操作故障触发了故障排除过程,突出了设备中的某些薄弱环节。这些弱点在设备的第二个版本(Prototype 2,P2)中得以解决,其新功能是通过试剂和样品的扩散进行在线混合。总Fe,Fe(II)和Mn的测量频率分别为每小时最多12个和6个样品,总Fe和Fe(II)的检出限分别为35 nM和27 nM,Mn的检出限为28 nM。在海水(波罗的海)和淡水(波琉河)的实验室和环境中,都对P2的耐用性和可靠性进行了测试。介绍了这些部署的结果,并提出了进一步发展该技术的方向。

著录项

  • 作者

    Milani Ambra;

  • 作者单位
  • 年度 2014
  • 总页数
  • 原文格式 PDF
  • 正文语种 {"code":"en","name":"English","id":9}
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