非离子表面活性剂对卤水中FR水化的促进作用

Allen Kelley, Kristina Fontenot, Christinna Becktold, Carla Morgan, C. Stanciu, Jorge Fernandez
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摘要

探讨了聚丙烯酰胺聚合物(PAM和PHPA)水化动力学的理论模型,重点研究了盐度对传统PAM和PHPA聚合物水化动力学的影响。通过在分子水平上了解聚合物和溶剂体系之间的相互作用,预计聚合物作为增粘剂的可用性可以扩展到微咸水和可能的采出水中。在这项研究中,粘度与时间的关系图被用来找出PAM和PHPA乳剂在淡水和各种盐水中的水化率。设计了含铁(III)的特殊卤水。该研究是通过使用普通的商业粘度计完成的,利用R1 B1 bob配置加热杯。在整个运行过程中产生的混合剪切量很小,并保持恒定。运行的温度和长度也保持不变。这允许确定速率限制水化步骤,最大粘度和水化率的各种非离子表面活性剂的探索。通过对纯卤水、自来水和添加非离子表面活性剂的卤水的PAM和PHPA水化率的比较表明,选择正确的非离子表面活性剂可使盐水溶液的水化率提高3500%以上,自来水的水化率提高10-50%以上。结果表明,盐水溶液可使最大粘度增加700%以上,自来水可使最大粘度增加27%以上。使用纳米纯水也证明了这一趋势。结果支持了我们提出的理论水化动力学,显示了非离子表面活性剂对限速水化步骤和不同水化步骤之间的过渡的影响。这些数据有力地证明,通过了解聚合物水化过程,可以利用各种TDS中的微咸水和可能的产出水成功地水化聚合物。该测试的新颖之处在于,它提供了进一步的例子,说明如何成功地使用非离子表面活性剂,使PAM和PHPA聚合物在各种成分的盐水中水化而不损害其性能。注意使用非常常用的仪器,并制定简单明了的测试程序,使不一定拥有最先进设备的实地实验室能够轻松可靠地使用该方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Non-Ionic Surfactants as Boosters for FR Hydration in Brines
A theoretical model of polyacrylamide polymers (PAM and PHPA) hydration dynamics is explored, with emphasis on the effect pf salinity on the hydration dynamics of traditional PAM and PHPA polymers. By understanding the interactions at a molecular level between the polymer and the solvent system it is expected that the polymer’s usability as a viscosifying agent can be extended into brackish and possibly produced water. In this study, viscosity vs. time plots are used to find the hydration rates for PAM and PHPA emulsions in fresh water and various brines. Special brines were designed, including one with Fe(III) among components. The study is done by using common, commercial viscometers, utilizing an R1 B1 bob configuration with heated cup. The overall mixing shear generated is low and kept constant throughout the runs. The temperature and length of runs are also kept constant. This allows the determination of the rate limiting hydration step, maximum viscosity and the hydration rates of a wide variety of nonionic surfactants to be explored. By comparing the PAM and PHPA hydration rates for the neat brine, tap water and brine with non-ionic surfactant it is shown that by choosing the correct nonionic surfactant the hydration rates can be increased by over 3500% from the brine solution and more than 10-50% from tap water. It is also shown that the maximum viscosity can be increased by over 700% from the brine solution and 27% from tap water. This trend was also shown to be true using Nano pure water. The results support the theoretical hydration dynamics we propose, showing the effect the nonionic surfactants have on the rate limiting hydration step and transitions between different hydration steps. The data is strong proof that by understanding the processes of polymer hydration, brackish and possibly produced water in a wide range of TDS can be used to successfully hydrate the polymer. The novelty of this testing is that it provides further examples of how non-ionic surfactants can be used successfully to allow PAM and PHPA polymers to be hydrated in brine waters of various compositions with no damage to performance. Care was taken to utilize very common instrumentation and to develop simple and clear procedures for testing, to make the method easy and reliable to use by field labs that may not necessarily have state-of-the-art equipment available.
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