极性添加剂膨胀微凝胶在液-液界面上的组装和堵塞:从反皮克林乳液到功能材料。

IF 9.4 1区 化学 Q1 CHEMISTRY, PHYSICAL Journal of Colloid and Interface Science Pub Date : 2024-10-16 DOI:10.1016/j.jcis.2024.10.051
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引用次数: 0

摘要

假设:基于聚-N-异丙基丙烯酰胺(PNIPAM)的微凝胶因其可变形性和功能性而成为有效的软颗粒稳定剂,引起了人们的极大兴趣。然而,微凝胶固有的亲水性限制了其在稳定油包水型(W/O)皮克林乳液中的潜在用途。使用不同的极性添加剂可以改善微凝胶的疏水性,从而为反向皮克林乳液的形成和材料制造提供新的可能性:实验:利用自由基沉淀聚合生成了不同类型的微凝胶,这些微凝胶具有量身定制的理化特性。实验:采用自由基沉淀聚合法生成了不同类型的微凝胶,这些微凝胶具有量身定制的理化特性。系统研究了各种极性添加剂对微凝胶的润湿性、吸附动力学和界面覆盖率的影响。利用添加剂溶胀的微凝胶稳定了反向 W/O 皮克林乳液,并以此为模板开发出了具有刺激响应性和分层结构的功能材料:添加剂溶胀的 PNIPAM 基微凝胶具有更强的疏水性和更优越的乳化能力,能在油水界面自发聚集和堵塞,从而显著降低界面能。添加剂膨胀后的微凝胶形成了一个紧密堆积、富有弹性和反应灵敏的微凝胶单层。通过制备各种反向 W/O 皮克林乳液和高内相皮克林乳液(HIPPE),验证了该策略的可行性。更重要的是,这种直接形成微凝胶稳定的反向 W/O 皮克林乳液的策略提供了一个新颖的平台,可用于创建具有定制内部结构的功能材料,从微观尺度(如响应性核壳水凝胶微球和胶体)到宏观尺度(如分层多孔材料),这些材料可用于可回收的污染物去除和液滴操纵等潜在应用。
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Assembly and jamming of polar additive-swollen microgels at liquid–liquid interfaces: From inverse Pickering emulsions to functional materials

Hypothesis

Poly-N-isopropylacrylamide (PNIPAM)-based microgels have garnered significant interest as effective soft particulate stabilizers because of their deformability and functionality. However, the inherent hydrophilic nature of microgel restricts their potential use in stabilizing water-in-oil (W/O) Pickering emulsions. Employing diverse polar additives can improve the hydrophobicity of microgels, thus unlocking new possibilities in inverse Pickering emulsion formation and materials fabrication.

Experiments

Different types of microgels were generated using free-radical precipitation polymerization with tailored physiochemical properties. The effect of various polar additives on the wettability, adsorption kinetics, and interfacial coverage of microgels was systematically investigated. Additive-swollen microgels were utilized to stabilize inverse W/O Pickering emulsions, which served as templates to develop functional materials with stimuli responsiveness and hierarchical structures.

Findings

Additive-swollen PNIPAM-based microgels exhibited enhanced hydrophobicity and superior emulsifying capability, which spontaneously assembled and jammed at oil–water interfaces, resulting in a significant interfacial energy decrease. The additive-swollen microgels formed a tightly packed, elastic, and responsive microgel monolayer. The feasibility of the strategy was verified by preparing various inverse W/O Pickering emulsions and high internal phase Pickering emulsions (HIPPEs). More importantly, this straightforward formation strategy of microgel-stabilized inverse W/O Pickering emulsions offered a novel platform to create functional materials with customized inner structures from microscale (e.g., responsive core–shell hydrogel microspheres and colloidosomes) to macroscale (e.g., hierarchical porous materials) that can be used for potential applications, such as recyclable contaminant removal and droplet manipulation.
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来源期刊
CiteScore
16.10
自引率
7.10%
发文量
2568
审稿时长
2 months
期刊介绍: The Journal of Colloid and Interface Science publishes original research findings on the fundamental principles of colloid and interface science, as well as innovative applications in various fields. The criteria for publication include impact, quality, novelty, and originality. Emphasis: The journal emphasizes fundamental scientific innovation within the following categories: A.Colloidal Materials and Nanomaterials B.Soft Colloidal and Self-Assembly Systems C.Adsorption, Catalysis, and Electrochemistry D.Interfacial Processes, Capillarity, and Wetting E.Biomaterials and Nanomedicine F.Energy Conversion and Storage, and Environmental Technologies
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