Amirmoshiri Mohammadreza, Zhang Leilei, Puerto Maura C, Tewari Raj D, Bahrim Ridhwan Zhafri B Kamarul, Farajzadeh Rouhi, Hirasaki George J, Biswal Sibani Lisa
Department of Chemical and Biomolecular Engineering, Rice University, 6100 Main St., MS-362, Houston, Texas 77005, United States.
Petronas Research Sdn Bhd, alan Ayer Itam, Kawasan Institusi Bangi, 43000 Bandar Baru Bangi, Selangor, Malaysia.
Langmuir. 2020 Sep 15;36(36):10725-10738. doi: 10.1021/acs.langmuir.0c01521. Epub 2020 Sep 1.
We investigate the dynamic adsorption of anionic surfactant C alpha olefin sulfonate on Berea sandstone cores with different surface wettability and redox states under high temperature that represents reservoir conditions. Surfactant adsorption levels are determined by analyzing the effluent history data with a dynamic adsorption model assuming Langmuir isotherm. A variety of analyses, including surface chemistry, ionic composition, and chromatography, is performed. It is found that the surfactant breakthrough in the neutral-wet core is delayed more compared to that in the water-wet core because the deposited crude oil components on the rock surface increase the surfactant adsorption via hydrophobic interactions. As the surfactant adsorption is satisfied, the crude oil components are solubilized by surfactant micelles and some of the adsorbed surfactants are released from the rock surface. The released surfactant dissolves in the flowing surfactant solution, thereby resulting in an overshoot of the produced surfactant concentration with respect to the injection value. Furthermore, under water-wet conditions, changing the surface redox potential from an oxidized to a reduced state decreases the surfactant adsorption level by 40%. We find that the decrease in surfactant adsorption is caused not only by removing the iron oxide but also by changing the calcium concentration after the core restoration process (calcite dissolution and ion exchange as a result of using EDTA). Findings from this study suggest that laboratory surfactant adsorption tests need to be conducted by considering the wettability and redox state of the rock surface while recognizing how core restoration methods could significantly alter the ionic composition during surfactant flooding.
我们研究了在代表油藏条件的高温下,阴离子表面活性剂α-烯烃磺酸盐在具有不同表面润湿性和氧化还原状态的 Berea 砂岩岩心上的动态吸附。通过使用假设 Langmuir 等温线的动态吸附模型分析流出物历史数据来确定表面活性剂的吸附水平。进行了包括表面化学、离子组成和色谱分析在内的各种分析。结果发现,与水湿岩心相比,中性湿岩心中表面活性剂的突破延迟更多,因为岩石表面沉积的原油成分通过疏水相互作用增加了表面活性剂的吸附。当表面活性剂吸附达到饱和时,原油成分被表面活性剂胶束增溶,一些吸附的表面活性剂从岩石表面释放出来。释放的表面活性剂溶解在流动的表面活性剂溶液中,从而导致产出的表面活性剂浓度相对于注入值出现过冲。此外,在水湿条件下,将表面氧化还原电位从氧化态变为还原态可使表面活性剂的吸附水平降低 40%。我们发现表面活性剂吸附的降低不仅是由于去除了氧化铁,还由于岩心恢复过程(使用 EDTA 导致方解石溶解和离子交换)后钙浓度的变化。本研究的结果表明,在进行实验室表面活性剂吸附试验时,需要考虑岩石表面的润湿性和氧化还原状态,同时要认识到岩心恢复方法在表面活性剂驱油过程中如何显著改变离子组成。