Effect of double chain anionic surfactant on the dynamic interfacial tensions of betaine solutions

IF 5.3 2区 化学 Q2 CHEMISTRY, PHYSICAL Journal of Molecular Liquids Pub Date : 2023-07-15 DOI:10.1016/j.molliq.2023.121866
Lu Han , Huoxin Luan , Jia Ren , Qun Zhang , Chongjun Xu , Gen Li , Hongyan Xiao , Zhaohui Zhou , Lei Zhang , Lu Zhang
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Abstract

To clarify the effect of the anionic surfactant with double alkyl chains on the interfacial tension (IFT) of betaine solutions, the IFT values of the sodium dialkyl sulfosuccinates (AOT) mixed with different betaines (alkyl sulphobetaine (ASB) and benzyl substituted alkyl sulphobetaine (BSB)) against n-alkanes and crude oil were detected by the spinning drop method. Additionally, molecular dynamics (MD) simulation was employed to verify the interaction mechanism between AOT and different betaine molecules. The results demonstrate that AOT molecules reach hydrophilic-lipophilic balance and form a relatively compacted interfacial film at the dodecane-water interface. Owing to the flexible double alkyl chains, AOT molecules possess a robust self-regulating ability at the oil–water interface. It is the self-regulating ability of AOT molecules and the electrostatic attraction between betaines and AOT molecules that achieve superior synergistic effects between AOT and betaine molecules with different molecular sizes. Besides, mixed adsorption and hydrophilic-lipophilic balance (HLB) reduce the IFT values of mixed systems containing AOT and different betaines effectively. The equilibrium IFT of the AOT-ASB system and the AOT-BSB system can be reduced to ultralow vales of 5.7 × 10−3 mN/m and 8.2 × 10−3 mN/m, respectively. At the crude oil–water interface, active components in crude oil compete with AOT molecules, which results in a significant increase in IFT values for AOT solution alone. Despite the different molecular sizes of ASB and BSB molecules, the flexible double alkyl chains of AOT molecules enable AOT to have synergistic effects with both ASB and BSB molecules at crude oil–water interface. Ultralow IFTs against crude oil can be obtained at optimized ratio of AOT to betaines, which is meaningful for the application of mixed solutions containing betaines and anionic surfactants in enhanced oil recovery.

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双链阴离子表面活性剂对甜菜碱溶液动态界面张力的影响
为明确双烷基链阴离子表面活性剂对甜菜碱溶液界面张力(IFT)的影响,采用纺丝滴法测定了二烷基磺基琥珀酸钠(AOT)与不同甜菜碱(烷基亚砜碱(ASB)和苄基取代烷基亚砜碱(BSB))混合后对正构烷烃和原油的界面张力(IFT)值。此外,采用分子动力学(MD)模拟验证了AOT与不同甜菜碱分子的相互作用机理。结果表明,AOT分子达到亲水亲脂平衡,并在十二烷-水界面形成相对致密的界面膜。由于具有柔性的双烷基链,AOT分子在油水界面具有很强的自调节能力。正是AOT分子的自我调节能力和甜菜碱与AOT分子之间的静电吸引力,使得AOT与不同分子大小的甜菜碱分子之间实现了优越的协同效应。此外,混合吸附和亲水-亲脂平衡(HLB)可以有效降低AOT与不同甜菜碱混合体系的IFT值。AOT-ASB体系和AOT-BSB体系的平衡IFT可分别降至5.7 × 10−3 mN/m和8.2 × 10−3 mN/m的超低值。在原油-水界面,原油中的活性成分与AOT分子竞争,导致单独AOT溶液的IFT值显著增加。尽管ASB和BSB分子的分子大小不同,但AOT分子的柔性双烷基链使得AOT在原油-水界面上与ASB和BSB分子都有协同作用。优化AOT与甜菜碱的配比可获得对原油的超低IFTs,这对甜菜碱与阴离子表面活性剂混合溶液在提高原油采收率方面的应用具有重要意义。
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来源期刊
Journal of Molecular Liquids
Journal of Molecular Liquids 化学-物理:原子、分子和化学物理
CiteScore
10.30
自引率
16.70%
发文量
2597
审稿时长
78 days
期刊介绍: The journal includes papers in the following areas: – Simple organic liquids and mixtures – Ionic liquids – Surfactant solutions (including micelles and vesicles) and liquid interfaces – Colloidal solutions and nanoparticles – Thermotropic and lyotropic liquid crystals – Ferrofluids – Water, aqueous solutions and other hydrogen-bonded liquids – Lubricants, polymer solutions and melts – Molten metals and salts – Phase transitions and critical phenomena in liquids and confined fluids – Self assembly in complex liquids.– Biomolecules in solution The emphasis is on the molecular (or microscopic) understanding of particular liquids or liquid systems, especially concerning structure, dynamics and intermolecular forces. The experimental techniques used may include: – Conventional spectroscopy (mid-IR and far-IR, Raman, NMR, etc.) – Non-linear optics and time resolved spectroscopy (psec, fsec, asec, ISRS, etc.) – Light scattering (Rayleigh, Brillouin, PCS, etc.) – Dielectric relaxation – X-ray and neutron scattering and diffraction. Experimental studies, computer simulations (MD or MC) and analytical theory will be considered for publication; papers just reporting experimental results that do not contribute to the understanding of the fundamentals of molecular and ionic liquids will not be accepted. Only papers of a non-routine nature and advancing the field will be considered for publication.
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