Static Adsorption of Surfactants on Bakken Rock Surfaces in High Temperature, High Salinity Conditions

Xun Zhong, H. Pu, Yanxia Zhou, J. Zhao
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引用次数: 6

Abstract

Surfactant EOR received attraction due to its extreme capability to increase displacement efficiency by altering the wettability, lowering the oil/water interfacial tension and ultimately mobilizing the residual oil. However, surfactant systems are widely acknowledged to have large adsorption on rock/clay/sediment solid surfaces, which may result in concentration loss, thus impair the effectiveness of the chemical solution and turn the process into an economically unfeasible case. Surfactant adsorption can be affected by the adsorbents, surfactant structure, experimental temperature and some other factors. Also, the driving force for adsorption varies with different surfactants types. Generally speaking, electrostatic interaction is more prominent for those anionic surfactants, while hydrophobic interaction is more common for nonionic type. In this paper, the static adsorption behaviors of two surfactants (A1 and N1) on Bakken minerals and Berea sandstone in high salinity and high temperature Bakken conditions (salinity≈290,000 mg/L, temperature=80~105 °C) were studied using spectrometric iodine method, where 0.1 mM I2-0.2 mM KI solution was used as a color developing agent. The primary stability indicated that both surfactants have high compatibility with the Bakken formation brine at high temperature, and their critical micelle concentrations showed a small decrease in the presence of high saline brine. Bakken mineral is relatively complicate, which is composed of quartz, dolomite, calcite and clay, while Berea sandstone contains over 75 wt% quartz. Herein, the effects of surfactant concentration, surfactant type, temperature, adsorbents and salinity on adsorption density were covered, and the impacts of surfactant concentration and adsorbents were found to be more significant. Due to the higher specific surface area and high clay content of Bakken minerals, both anionic surfactant blend A1 and nonionic surfactant blend N1 have pretty high adsorption on Bakken minerals, and the specific adsorption densities of 1000 mg/L surfactant solution were calculated to be 1.74 mg/m2 and 1.69 mg/m2, respectively. Meanwhile, the results also indicated that though the applied surfactant concentration is relatively low, the concentration loss due to adsorption should never be overlooked. Future study on how to effectively reduce the adsorption of surfactant especially in those clay-rich formations is of great significance.
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高温、高盐条件下Bakken岩石表面表面活性剂的静态吸附
表面活性剂提高采收率受到青睐,因为它能够通过改变润湿性、降低油水界面张力并最终动员残余油来提高驱油效率。然而,表面活性剂体系被广泛认为在岩石/粘土/沉积物固体表面有很大的吸附作用,这可能导致浓度损失,从而影响化学溶液的有效性,并使该工艺在经济上不可行。表面活性剂的吸附受吸附剂、表面活性剂结构、实验温度等因素的影响。不同表面活性剂的吸附驱动力也不同。一般来说,阴离子型表面活性剂的静电相互作用更为突出,而非离子型表面活性剂的疏水相互作用更为常见。本文以0.1 mM i2 ~ 0.2 mM KI溶液为显色剂,采用光谱碘法研究了高盐高温Bakken条件下(盐度≈290,000 mg/L,温度=80~105℃)两种表面活性剂A1和N1在Bakken矿物和Berea砂岩上的静态吸附行为。初级稳定性表明,两种表面活性剂在高温下与Bakken地层盐水具有较高的相容性,且在高盐盐水存在下,其临界胶束浓度略有下降。巴肯的矿物相对复杂,主要由石英、白云岩、方解石和粘土组成,而伯里亚砂岩的石英含量超过75%。研究了表面活性剂浓度、表面活性剂类型、温度、吸附剂和盐度对吸附密度的影响,发现表面活性剂浓度和吸附剂对吸附密度的影响更为显著。由于巴肯矿物具有较高的比表面积和较高的粘粒含量,阴离子表面活性剂混配A1和非离子表面活性剂混配N1对巴肯矿物均具有较高的吸附性能,计算出1000 mg/L表面活性剂溶液的比吸附密度分别为1.74 mg/m2和1.69 mg/m2。同时,研究结果还表明,虽然表面活性剂的使用浓度较低,但由于吸附而造成的浓度损失不容忽视。今后研究如何有效地减少表面活性剂的吸附,特别是在富粘土地层中,具有重要的意义。
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