Ali Muhammad, Aftab Adnan, Arain Zain-Ul-Abedin, Al-Yaseri Ahmed, Roshan Hamid, Saeedi Ali, Iglauer Stefan, Sarmadivaleh Mohammad
Western Australia School of Mines, Minerals, Energy and Chemical Engineering, Curtin University, 26 Dick Perry Avenue, Kensington 6151, Western Australia, Australia.
Petroleum Engineering Discipline, School of Engineering, Edith Cowan University, 270 Joondalup Dr, Joondalup 6027, Western Australia, Australia.
ACS Appl Mater Interfaces. 2020 Sep 2;12(35):39850-39858. doi: 10.1021/acsami.0c10491. Epub 2020 Aug 20.
Every year, millions of tons of CO are stored in CO-storage formations (deep saline aquifers) containing traces of organic acids including hexanoic acid C (HA), lauric acid C (LuA), stearic acid C (SA), and lignoceric acid C (LiA). The presence of these molecules in deep saline aquifers is well documented in the literature; however, their impact on the structural trapping capacity and thus on containment security is not yet understood. In this study, we therefore investigate as to how an increase in organic acid concentration can alter mica water wettability through an extensive set of experiments. X-ray diffraction (Figure S2), field emission scanning electron microscopy, total organic carbon analysis, Fourier-transform infrared spectroscopy, atomic force microscopy, and energy-dispersive X-ray spectroscopy were utilized to perceive the variations in organic acid surface coverage with stepwise organic acid concentration increase and changes in surface roughness. Furthermore, thresholds of wettability that may indicate limits for structural trapping potential (θ < 90°) have been discussed. The experimental results show that even a minute concentration (∼10 mol/L for structural trapping) of lignoceric acid is enough to affect the CO trapping capacity at 323 K and 25 MPa. As higher concentrations exist in deep saline aquifers, it is necessary to account for these thresholds to derisk CO-geological storage projects.
每年,数百万吨的一氧化碳被存储在含有痕量有机酸(包括己酸C(HA)、月桂酸C(LuA)、硬脂酸C(SA)和木蜡酸C(LiA))的一氧化碳存储地层(深层盐水含水层)中。这些分子在深层盐水含水层中的存在在文献中有充分记载;然而,它们对结构捕集能力进而对封存安全性的影响尚不清楚。因此,在本研究中,我们通过一系列广泛的实验来研究有机酸浓度的增加如何改变云母的水润湿性。利用X射线衍射(图S2)、场发射扫描电子显微镜、总有机碳分析、傅里叶变换红外光谱、原子力显微镜和能量色散X射线光谱来观察随着有机酸浓度逐步增加有机酸表面覆盖率的变化以及表面粗糙度的变化。此外,还讨论了可能表明结构捕集潜力极限(θ < 90°)的润湿性阈值。实验结果表明,即使是微量浓度(对于结构捕集约为10 mol/L)的木蜡酸也足以在323 K和25 MPa下影响一氧化碳的捕集能力。由于深层盐水含水层中存在更高的浓度,有必要考虑这些阈值以降低一氧化碳地质存储项目的风险。