Self-Assembly at Oil–Water Interfaces Driven by Solubility Differences and Polar–Hydrophobic Interactions: An Insight into a Highly Mechanical Performance Gel with Gradients

IF 3.9 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Ruoxin Zhang, Hongsheng Lu*, Lingyan Wei, Xingyu Lin, Ziteng Yang, Jie Qi and Zheng Zhang*, 
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Abstract

Interfacial self-assembly offers a promising route to fabricate functional materials, yet achieving robust mechanical performance remains challenging. Here, the self-assembly of nonionic surfactant polyoxyethylene monoalkyl ether (AEO-9) at oil–water interfaces was systematically investigated to form a high-strength interfacial gel. During the self-assembly process, the mechanical strength of the interfacial gel progressively increased, reaching a maximum equilibrium value of 4200 Pa after 24 h. Furthermore, significant gradients in the composition, microstructure, and micromechanical properties of the interfacial gel along the sample height were revealed by fluorescence microscopy, small-angle X-ray scattering (SAXS), and atomic force microscopy (AFM). This unique interfacial self-assembly behavior was further studied via dynamic light scattering and molecular simulations. The solubility differences and polar–hydrophobic interactions are the key factors. Directional migration of AEO-9 from the oil phase (low solubility) to the aqueous phase (high solubility), driven by solubility differences, was found to establish a transient interfacial concentration gradient. This gradient facilitated interfacial enrichment of AEO-9, which was subsequently organized into gradient lamellar liquid crystals (LC) through compositional heterogeneity and polar–hydrophobic interactions. The gradient variations in micromechanical properties were correlated with the gradient structural packing. Moreover, the effects of AEO-9 concentration, brine, temperature, and oil type on the gel’s mechanical properties were examined, highlighting their roles in modulating the polar–hydrophobic balance. This study reveals the dual control of solubility-driven migration and interfacial interactions on gradient formation, establishing a framework for the design of high-performance interfacial materials.

Abstract Image

由溶解度差异和极性疏水相互作用驱动的油水界面自组装:对具有梯度的高机械性能凝胶的洞察
界面自组装为制造功能材料提供了一条很有前途的途径,但实现强大的机械性能仍然具有挑战性。本文系统地研究了非离子表面活性剂聚氧乙烯单烷基醚(AEO-9)在油水界面的自组装形成高强度界面凝胶。在自组装过程中,界面凝胶的机械强度逐渐增加,在24 h后达到最大平衡值4200 Pa。此外,荧光显微镜、小角度x射线散射(SAXS)和原子力显微镜(AFM)显示,界面凝胶的组成、微观结构和微观力学性能沿样品高度呈显著的梯度变化。通过动态光散射和分子模拟进一步研究了这种独特的界面自组装行为。溶解度差异和极性-疏水相互作用是关键因素。在溶解度差异的驱动下,AEO-9从油相(低溶解度)向水相(高溶解度)定向迁移,建立了瞬态界面浓度梯度。这种梯度促进了AEO-9的界面富集,随后通过成分非均质性和极性疏水相互作用被组织成梯度层状液晶(LC)。微力学性能的梯度变化与梯度结构堆积有关。此外,研究了AEO-9浓度、盐水、温度和油类型对凝胶力学性能的影响,强调了它们在调节极性-疏水平衡中的作用。本研究揭示了溶解度驱动迁移和界面相互作用对梯度形成的双重控制,为高性能界面材料的设计建立了框架。
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来源期刊
Langmuir
Langmuir 化学-材料科学:综合
CiteScore
6.50
自引率
10.30%
发文量
1464
审稿时长
2.1 months
期刊介绍: Langmuir is an interdisciplinary journal publishing articles in the following subject categories: Colloids: surfactants and self-assembly, dispersions, emulsions, foams Interfaces: adsorption, reactions, films, forces Biological Interfaces: biocolloids, biomolecular and biomimetic materials Materials: nano- and mesostructured materials, polymers, gels, liquid crystals Electrochemistry: interfacial charge transfer, charge transport, electrocatalysis, electrokinetic phenomena, bioelectrochemistry Devices and Applications: sensors, fluidics, patterning, catalysis, photonic crystals However, when high-impact, original work is submitted that does not fit within the above categories, decisions to accept or decline such papers will be based on one criteria: What Would Irving Do? Langmuir ranks #2 in citations out of 136 journals in the category of Physical Chemistry with 113,157 total citations. The journal received an Impact Factor of 4.384*. This journal is also indexed in the categories of Materials Science (ranked #1) and Multidisciplinary Chemistry (ranked #5).
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