高温高盐条件下超低界面张力非离子表面活性剂配方研究

Shaohua Chen, M. Han, A. AlSofi, A. Fuseni
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引用次数: 0

摘要

非离子型烷基聚葡萄糖苷(APG)表面活性剂是一种环保、无毒、可生物降解的表面活性剂。本研究对两种APG表面活性剂在高温高盐度条件下的理化性质进行了评价。研究了表面活性剂作为渗吸剂提高碳酸盐岩储层产油量的效果。介绍了一种超低界面张力(IFT)配方,探讨了超低界面张力形成的机理。研究了两种APG表面活性剂。通过老化后在盐水溶液中的透明度来评价相容性。用表面活性剂/添加剂的配方测定了IFT。通过扫描电镜(SEM)观察了表面活性剂/添加剂形成的网状结构。用总有机碳(TOC)分析仪测定了APGs在碳酸盐粉末上的静态吸附。在表面活性剂溶液中测定了碳酸盐岩心表面油滴的接触角。采用阿莫特井进行了碳酸盐岩岩心水自吸采油试验。利用UTCHEM仿真器对渗吸模拟模型进行了验证。在储层温度下,表面活性剂APG-1和APG-2与模拟高矿化度水均表现出良好的相容性。它们在碳酸盐岩储层上也表现出较低的静态吸附。疏水碳链较大的表面活性剂(APG-1)比疏水链较短的表面活性剂(APG-2)具有更大的增产潜力。在浓度为0.2 wt%时,APG-1的IFT较低,约为10-2 mN/m;添加少量添加剂后,APG-1的IFT极低,约为10-3 mN/m。SEM图表明,与APG-1单独形成的聚集结构相比,APG-1与添加剂通过疏水部分的相互作用产生了更紧密的结构。这样的影响最终会导致油和水之间的IFT下降。APG-1略微改变了碳酸盐岩心表面的润湿性,使其趋向水湿性。自发渗吸实验结果表明,APG-1和APG-2的产油量分别为28%和21%。经参数调整后,UTCHEM模拟器的数值模拟所得曲线与实验数据吻合较好。一种新的基于apg的配方设计具有超低的IFT,从而使油水界面的两亲性结构更加紧凑。研究结果表明,APG表面活性剂及其衍生物在高温高矿化度碳酸盐岩油藏中具有很大的增产潜力。
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Non-Ionic Surfactant Formulation with Ultra-Low Interfacial Tension at High-Temperature and High-Salinity Conditions
Non-ionic alkyl polyglucoside (APG) surfactants have been considered as eco-friendly, nontoxic and biodegradable surfactants. In this study, the physicochemical properties of two APG surfactants under high-temperature and high-salinity conditions were evaluated. The effectiveness of the surfactants as imbibition agents on improving oil production in carbonate reservoirs was investigated. A formulation with ultra-low interfacial tension (IFT) was introduced and the mechanisms resulting in such low IFT were probed and discussed. Two APG surfactants were studied. Compatibility was evaluated by the transparency in brine solutions after aging. IFT was measured with the formulations of surfactant/additives. The morphology of network formed by surfactant/additives was observed via scanning electron microscope (SEM). The static adsorption of the APGs onto carbonate powder was determined by total organic carbon (TOC) analyzer. The contact angle of oil droplet on surface of carbonate core was measured in surfactant solution. The oil production via spontaneous imbibition of water in carbonate core was obtained using Amott cell. An imbibition simulation model was validated by the experimental results using UTCHEM simulator. Both surfactants APG-1 and APG-2 exhibited excellent compatibility with the simulated high salinity water at reservoir temperature. They also demonstrated low static adsorption on carbonate reservoir. The surfactant containing larger hydrophobic carbons (APG-1) showed more incremental oil production potential than the other one bearing shorter hydrophobic chain (APG-2). At a concentration of 0.2 wt%, APG-1 yielded a low IFT in the order of 10-2 mN/m and an ultra-low IFT in the order of 10-3 mN/m was obtained upon addition of a small amount of additives. SEM pictures indicated that APG-1 and the additives synergistically generated a more compact structure via interaction between hydrophobic moieties of the chemicals compared to the aggregated structure formed by APG-1 alone. Such an effect could eventually lead to a decrease in IFT between oil and water. APG-1 slightly altered the wettability of carbonate core surface toward water-wet. The experimental results of spontaneous imbibition tests showed an oil production of 28% and 21% by APG-1 and APG-2, respectively. After parameter tuning, the yielded curves from numerical simulation by UTCHEM simulator perfectly matched the experimental data. A new APG-based formulation was designed with an ultra-low IFT resulting in a much more compact amphiphilic structure along the oil-water interface. This study shows a great potential of APG surfactants and the relevant derivative formulations in improving oil production application for high-temperature and high-salinity carbonate reservoirs.
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