Stability of Biopolymer and Partially Hydrolyzed Polyacrylamide in Presence of H2S and Oxygen

M. T. Al-Murayri, Dawood S. Kamal, J. G. Garcia, N. Al-Tameemi, J. Driver, Richard Hernandez, R. Fortenberry, Christopher Britton
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引用次数: 3

Abstract

There are many oil reservoirs worldwide with substantial amount of H2S but otherwise very favorable conditions for polymer flooding such as low temperature, high permeability, and moderate to high oil viscosity. However, there is a legitimate concern about the chemical stability of polymers when there is dissolved oxygen in the injection water or injection facility and its high concentrations of H2S in the reservoir. Several synthetic polymers and biopolymers were selected for stability testing under a wide range of conditions. We focused on identifying the concentration limits for co-presence of H2S and oxygen for which the synthetic and biopolymers are stable for an extended period, using different, widely available brine compositions. Experiments were conducted with and without standard polymer protection packages to evaluate their effects on stability and degradation under sour conditions. Viscosity of polymer solutions with varying concentrations of H2S and oxygen were measured and compared with the oxygen free or H2S free solution viscosities for a period of 6 months. Several methods of safely introducing H2S to the polymer solution were investigated and compared. The laboratory results indicated that biopolymers were stable at all the concentrations of oxygen and H2S concentrations studied. Three synthetic polymers tested showed some degradation in the presence of oxygen and H2S but were stable when either species is absent. The results indicated that oxygen is the limiting reagent in the degradation reaction with partially hydrolyzed polyacrylamide (HPAM) polymers under normal reservoir conditions. We observed little-to-no difference in degradation between samples with 10 or 100 ppm H2S at 500 ppb oxygen concentration, so H2S is not the limiting reagent under these conditions. Additionally, HPAM exposed to 10 ppm H2S and intermediate levels of oxygen (~0.5 ppm) only partially degrades, while samples exposed to H2S and ambient oxygen completely degrade. We anticipate these results will be useful for operators evaluating the potential of polymer flooding in sour reservoirs to follow a stricter polymer preparation at the surface facility to minimize oxygen concenration.
生物聚合物和部分水解聚丙烯酰胺在H2S和氧气存在下的稳定性
世界上有许多具有大量H2S的油藏,但它们具有低温、高渗透、中高油粘度等非常有利的聚合物驱条件。然而,当注入水或注入设备中存在溶解氧以及储层中高浓度的H2S时,人们有理由担心聚合物的化学稳定性。选择几种合成聚合物和生物聚合物在各种条件下进行稳定性测试。我们专注于确定H2S和氧气共存的浓度限制,在这种情况下,合成聚合物和生物聚合物可以使用不同的、广泛可用的盐水成分长时间保持稳定。采用标准聚合物保护包和无标准聚合物保护包进行了实验,以评估其在酸性条件下的稳定性和降解效果。在6个月的时间里,测量了不同浓度H2S和氧的聚合物溶液的粘度,并与无氧溶液或无H2S溶液的粘度进行了比较。研究并比较了几种将H2S安全引入聚合物溶液的方法。实验结果表明,生物聚合物在所有氧和H2S浓度下都是稳定的。测试的三种合成聚合物在氧气和H2S存在时表现出一定的降解,但在两种物质都不存在时表现稳定。结果表明,在正常储层条件下,氧是部分水解聚丙烯酰胺(HPAM)聚合物降解反应的限制试剂。我们观察到,在氧气浓度为500 ppb时,含10 ppm或100 ppm H2S的样品在降解方面几乎没有差异,因此在这些条件下H2S不是限制试剂。此外,HPAM暴露于10ppm H2S和中等水平的氧气(~0.5 ppm)中只能部分降解,而暴露于H2S和环境氧气中的样品则完全降解。我们预计这些结果将有助于作业者评估含硫油藏中聚合物驱的潜力,以便在地面设施中进行更严格的聚合物制备,以尽量减少氧浓度。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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