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Flow of Hydrophobically Modified Water-Soluble Polymers in Porous Media: Controlled Resistance Factors vs. Flow-Induced Gelation in the Semidilute Regime

机译:疏水改性的水溶性聚合物在多孔介质中的流动:在半稀释状态下受控的阻力因子与流动诱导的凝胶化

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摘要

The associative properties of hydrophobically modified water soluble polymers (HMWSPs) are attractive for improved oil recovery (IOR) because of both their enhanced thickening capability, compared with classical water-soluble polymers (for mobility-control applications), and their permeability-reduction, or plugging, ability (for well-treatment applications). In previous works, we have studied the injectivity of HMWSP made of sulfo-nated polyacrylamide backbones and alkyl side chains in the dilute regime and have shown, in particular, that it was largely governed by adsorption. In this paper, we report new experimental data on the injectivity of the same class of HMWSP solutions in the semidilute regime. From membrane filtration tests at imposed flow rate, we have first observed the formation of a filter cake made of HMWSP physical gel, which remained largely permeable to polymers. Our observations are compatible with the creation of channels within the gel. This leads to a gel-filtration process, entailing modifications of the solution's viscosimetric properties, which can be explained by a rearrangement of the intra- and interchain hydro-phobic bonds in the solution. The second part of our work consisted of injectivity tests in model granular packs. We have performed comparative experiments in porous media with variable permeabilities, but at the same shear rate in the pore throats. Results show that, above a critical permeability k~C, or a critical pore-throat radius r_P~C, HMWSP injection led to stable resistance factors, with values close to the solution's viscosity, and that, at less than k~C or r_P~C, the very high resistance factors observed suggest that flow-induced gelation of the HMWSP takes place. Furthermore, resistance factors measured over the core internal sections are compatible with an in-depth formation of the gel. These insights could be of use for designing HMWSP better suited to mobility-control operations and for tuning HMWSP-injection conditions for profile/conformance-control operations.
机译:疏水改性的水溶性聚合物(HMWSPs)的缔合特性对于提高采油率(IOR)具有吸引力,因为与传统的水溶性聚合物(用于流动性控制应用)相比,它们的增稠能力增强,并且降低了渗透率,或堵漏能力(用于良好处理的应用)。在以前的工作中,我们研究了由磺化聚丙烯酰胺主链和烷基侧链制成的HMWSP在稀释状态下的注入性,尤其表明它在很大程度上受吸附控制。在本文中,我们报告了有关在半稀释状态下相同类别的HMWSP解决方案的可注射性的新实验数据。通过施加流速的膜过滤测试,我们首先观察到了由HMWSP物理凝胶制成的滤饼的形成,该滤饼仍然对聚合物具有很大的渗透性。我们的观察结果与凝胶内通道的创建兼容。这导致凝胶过滤过程,导致溶液粘度特性的改变,这可以通过溶液中链内和链间疏水键的重排来解释。我们工作的第二部分包括模型颗粒包装中的注入性测试。我们已经在具有可变渗透率的多孔介质中进行了对比实验,但是在孔喉中的剪切速率相同。结果表明,在临界渗透率k〜C或临界孔喉半径r_P〜C之上,HMWSP注入导致稳定的阻力因子,其值接近溶液的粘度,并且小于k〜C或r_P大约C,观察到的非常高的抗性因子表明HMWSP发生了流动诱导的凝胶化。此外,在芯内部截面上测量的电阻系数与凝胶的深度形成相容。这些见解可用于设计更适合于流动性控制操作的HMWSP,以及用于调整轮廓/一致性控制操作的HMWSP注入条件。

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  • 来源
    《SPE journal》 |2012年第4期|1196-1206|共11页
  • 作者单位

    SPE, IPREM-EPCP and IFP Energies nouvelles;

    University of Strasbourg;

    SPE, IFP Energies nouvelles University of Paris;

    SPE, IPREM-EPCP University of Strasbourg;

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