Phosphonate Speciation - Challenges and Solutions

S. J. Ewing, N. Hunter, Kirsty MacKinnon, Kelly Whittingham, G. Graham, S. Heath
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引用次数: 1

Abstract

Reliable and accurate analysis of inhibitors is vital for decisions on efficiency and cost-effectiveness of scale inhibitor squeeze treatments. Recent developments have resolved issues for residual sulphonated polymer chemistries which were previously difficult to isolate. Attention now is directed to challenges associated with phosphonate based inhibitors, particularly when assay is required from a multi-component produced water sample containing other P based inhibitor species which currently poses a significant challenge. This paper describes the advantages and limitations of techniques used for phosphorus assay including inductively coupled plasma spectroscopy, ion chromatography and wet chemical methods (e.g. Phospho-molybdenum blue, PMB) approaches. Field examples are discussed to emphasize the analytical challenge with cases whereby speciation is readily achieved and others where this is not the case. To overcome the limitations of these methods, novel approaches for analysis of P – containing inhibitors (in the presence of other –containing additives) include time resolved fluorescence spectroscopy (TRF) and mass spectrometry (MS) detection (which also require development) are considered with potential benefits and limitations / interferences highlighted. These are discussed with highlights of TRF development presented. This technique shows significant scope and potential with promising results showing speciation and discrimination of both polymeric and phosphonate based scale inhibitors as well as a phosphate ester based corrosion inhibitor. This paper highlights the concept that for residual scale inhibitor assay, one analytical approach does not fit all environments and applications. However the availability of a range of techniques, some of which are still in development, allows for effective monitoring in complex, multi-component environments. The paper highlights development opportunities for some of the newer approaches such as TRF and MS as well as discussing their limitations in complex produced fluids.
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磷酸盐的形成-挑战和解决方案
可靠和准确的抑制剂分析对于决定阻垢剂挤压处理的效率和成本效益至关重要。最近的发展已经解决了以前难以分离的残留磺化聚合物化学物质的问题。现在的注意力集中在与膦酸盐抑制剂相关的挑战上,特别是当需要对含有其他P基抑制剂的多组分采出水样进行分析时,这目前构成了重大挑战。本文描述了用于磷测定的技术的优点和局限性,包括电感耦合等离子体光谱,离子色谱和湿化学方法(例如磷钼蓝,PMB)方法。本文讨论了实地的例子,以强调分析的挑战,在这些例子中,物种形成很容易实现,而在其他情况下,情况并非如此。为了克服这些方法的局限性,考虑了分析含P抑制剂(在其他含添加剂存在的情况下)的新方法,包括时间分辨荧光光谱(TRF)和质谱(MS)检测(也需要开发),并强调了潜在的好处和局限性/干扰。这些都将被讨论,并提出扶轮基金会发展的重点。该技术显示了巨大的应用范围和潜力,并取得了令人满意的结果,显示了聚合物和膦酸盐基阻垢剂以及磷酸酯基缓蚀剂的形成和区分。本文强调了残留阻垢剂测定的概念,一种分析方法不适合所有的环境和应用。然而,一系列技术的可用性(其中一些仍在开发中)允许在复杂的多组件环境中进行有效监测。本文重点介绍了一些新方法的发展机会,如TRF和MS,并讨论了它们在复杂采出流体中的局限性。
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