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CO 开关型表面活性剂调控十二烷-盐水体系可逆乳化/破乳过程的分子动力学模拟。

Molecular dynamics simulation of CO-switchable surfactant regulated reversible emulsification/demulsification processes of a dodecane-saline system.

机构信息

State Key Laboratory for Ore Deposits Research, School of Earth Sciences and Engineering, Nanjing University, Nanjing, Jiangsu 210023, P. R. China.

State Key Laboratory of Enhanced Oil Recovery, Research Institute of Petroleum Exploration and Development, China National Petroleum Corporation (CNPC), Beijing 100083, P. R. China.

出版信息

Phys Chem Chem Phys. 2020 Oct 28;22(41):23574-23585. doi: 10.1039/d0cp03904g.

Abstract

CO2-Switchable surfactants are of great potential in a wide range of industrial applications related to their ability to stabilize and destabilize emulsions upon command. Molecular dynamics simulations have been performed to reveal the fundamental mechanism of the reversible emulsification/demulsification processes of a dodecane-saline system by a CO2-switchable surfactant that switches between active (i.e., N'-dodecyl-N,N-dimethylacetamidinium (DMAAH+)) and inactive (i.e., N'-dodecyl-N,N-dimethylacetamidine (DMAA)) forms. The density profiles indicate that DMAAH+ could increase the oil-water interfacial thickness to a greater extent compared to DMAA. DMAAH+ could sharply reduce the interfacial tension of the dodecane-saline system, while DMAA only exhibits a limited decrease, which is in accordance with the experimental observation that DMAAH+/DMAA can reversibly emulsify/demulsify alkane-water systems. Our simulations showed that both the number and lifetime of hydrogen bonds (HBs) between DMAA and water are almost equal to those between DMAAH+ and water. In DMAA, the N atom connecting with the alkyl tail acted as a HB acceptor, while the N atom attached by a proton in DMAAH+ acted as a HB donor. Furthermore, the HBs between DMAAH+ and HCO3- at the interfaces are relatively limited. Hence, it is deduced that the HBs are insufficient to achieve the CO2-switchability of DMAA/DMAAH+. The Lennard Jones and coulombic potentials between DMAA/DMAAH+ and other species show that the coulombic potentials between DMAAH+ and water or anions (i.e., Cl- and HCO3-) sharply decrease with the increase of DMAAH+ and are much lower than those in models with DMAA. The enhanced coulombic interactions between DMAAH+ and anions lead to a remarkable reduction in interfacial tension and the emulsification of the alkane-saline system. Therefore, coulombic interactions are of crucial importance to the reversible emulsification/demulsification processes regulated by CO2-switchable surfactants, namely DMAAH+/DMAA.

摘要

CO2 可切换表面活性剂在与乳液的稳定和去稳定相关的广泛工业应用中具有巨大的潜力,因为它们能够根据指令进行控制。通过分子动力学模拟,揭示了一种 CO2 可切换表面活性剂在正构烷烃-盐水体系中的可逆乳化/破乳过程的基本机理,该表面活性剂在活性(即 N'-十二烷基-N,N-二甲基乙酰胺基(DMAAH+))和非活性(即 N'-十二烷基-N,N-二甲基乙酰胺基(DMAA))形式之间切换。密度分布表明,与 DMAA 相比,DMAAH+ 可以更大程度地增加油-水界面厚度。DMAAH+ 可以显著降低正构烷烃-盐水体系的界面张力,而 DMAA 仅表现出有限的降低,这与实验观察到的 DMAAH+/DMAA 可以可逆地乳化/破乳烷烃-水体系的情况一致。我们的模拟表明,DMAA 与水之间以及 DMAAH+与水之间氢键(HBs)的数量和寿命几乎相等。在 DMAA 中,与烷基尾相连的 N 原子充当 HB 受体,而在 DMAAH+中连接质子的 N 原子充当 HB 供体。此外,界面处 DMAAH+与 HCO3-之间的 HBs 相对有限。因此,可以推断出 HBs 不足以实现 DMAA/DMAAH+的 CO2 切换性。DMAA/DMAAH+与其他物质之间的 Lennard-Jones 和库仑势表明,DMAAH+与水或阴离子(即 Cl-和 HCO3-)之间的库仑势随着 DMAAH+的增加而急剧下降,并且远低于具有 DMAA 的模型中的库仑势。DMAAH+与阴离子之间增强的库仑相互作用导致界面张力显著降低和烷烃-盐水体系的乳化。因此,库仑相互作用对于 CO2 可切换表面活性剂(即 DMAAH+/DMAA)调节的可逆乳化/破乳过程至关重要。

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