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Determination of Field Chemicals: Corrosion Inhibitor (CI) and Kinetic Hydrate Inhibitor (KHI) in Produced Water

机译:田间化学品的测定:生产水中腐蚀抑制剂(CI)和动力学水合物抑制剂(KHI)

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Corrosion inhibitors (CI) and hydrate inhibitors are among the few but essential field chemicals added in oil and gas production operations as a part of fluid flow assurance. While CI is added regularly to prevent corrosion, hydrate inhibitors are used only during cold season in order to prevent the formation of gas hydrates. A new generation of hydrate inhibitors, namely kinetic hydrate inhibitors (KHI), is becoming more attractive than thermodynamic inhibitors, since lower dosage of KHI is typically needed. Monitoring of residual field chemicals in produced water is essential for flow assurance issues; and is also of particular concern to better understand the needs for water treatment options, and to evaluate their environmental impacts. The corrosion and hydrate inhibitors bring several challenges associated with their determination and characterization in produced water. The challenges include identification of the interferences and enhancing the selectivity and sensitivity for these chemicals. This paper evaluates selective analytical methodologies for the analyses of CI and KHI in produced water. The paper also addresses improvements in enhanced detection and accuracy of these field chemicals. The CI is analyzed by high performance liquid chromatography (HPLC) with UV detection. The brine composition and pH of the eluting solutions have to be adjusted to minimize the associated matrix effects. Besides, CI analyses suffer from low UV-absorption of key components, which limits their quantitation. The use of a Corona detector in conjunction with HPLC to achieve desired sensitivity is evaluated, with emphasis on peak separation of key CI components. The methods evaluated for KHI analyses are colorimetric, iodine complexation, and size exclusion chromatography (SEC). The colorimetric method is subject to intense interference by CI, limiting its application for KHI determination in the presence of CI blends. The iodine complexation method is chosen as a practical wet chemical method for KHI analysis.lt is modified to minimize the interferences due to brine concentration, corrosion inhibitor, condensate, and sulfide. However, the selectivity of the iodine complexation method is still not at the desired level. As an improvement to selectivity and accuracy, the SEC method is evaluated. The SEC method offers better selectivity and characterization of KHI. The characterization of molecular weight distribution is critical in the evaluation of treatment and removal efficiency of KHI in produced water streams.
机译:腐蚀抑制剂(CI)和水合物抑制剂是石油和天然气生产作业中添加的少数但必需的田间化学品中,作为流体流动保证的一部分。虽然CI定期加入以防止腐蚀,但水合物抑制剂仅在寒冷季节使用,以防止液体水合物的形成。新一代水合物抑制剂即动力学水合物抑制剂(KHI),比热力学抑制剂更具吸引力,因为通常需要较低剂量的khi。制作水中的残留场化学品监测对于流量保证问题至关重要;并且还特别关注更好地了解水处理选择的需求,并评估其环境影响。腐蚀和水合物抑制剂带来了几种与生产水中的测定和表征相关的若干挑战。挑战包括鉴定干扰和增强这些化学品的选择性和敏感性。本文评估了生产水中CI和KHI分析的选择性分析方法。本文还解决了这些现场化学品的增强检测和准确性的改进。通过具有UV检测的高效液相色谱(HPLC)分析CI。必须调整洗脱溶液的盐水组合物和pH以最小化相关的基质效应。此外,CI分析患有关键部件的低紫外线吸收,这限制了它们的定量。评估使用电晕检测器与HPLC一起获得所需灵敏度,重点是关键CI组分的峰值分离。评估对KHI分析的方法是比色,碘络合和尺寸排阻色谱(SEC)。比色法受Ci的强烈干扰,限制了其在存在CI混合物中的KHI测定的应用。选择碘络合方法作为KHI分析的实用湿化学方法。改性以最小化由于盐水浓度,腐蚀抑制剂,冷凝物和硫化物引起的干扰。然而,碘络合方法的选择性仍然不处于所需的水平。作为选择性和准确性的改进,评估SEC方法。 SEC方法提供更好的选择性和khi的表征。分子量分布的表征对于在生产的水流中的KHI治疗和去除效率评估中至关重要。

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