Kwok Man-Hin, Ambreen Jaweria, Ngai To
Department of Chemistry, The Chinese University of Hong Kong, Shatin, N. T., Hong Kong.
Department of Chemistry, COMSATS University Islamabad, 45550 Park Road, Chak Shahzad, Pakistan.
J Colloid Interface Sci. 2019 Jun 15;546:293-302. doi: 10.1016/j.jcis.2019.03.072. Epub 2019 Mar 23.
This study presents the synthesis and characterization of Poly(N-isopropylacrylamide)-co-methacrylic acid (PNIPAM-co-MAA) based multi-responsive soft microgel particles employed as "smart emulsifiers" for controlled stabilization and breakage of the decane-in-water Pickering emulsions. These soft microgel particles can act as reversible stabilizers, i.e. they can either stay at the oil-water interface by supporting emulsion formation or preventing aggregates; while triggering demulsification can be controlled by varying the temperature, pH or ionic strength of the microgel system.
Dynamic light scattering was applied to observe the variation in hydrodynamic radius of the particles as a function of temperature and pH of the multi-responsive microgel system. Microgel composition was varied in terms of MAA-content and influence of this variation on their thermo-sensitivity and pH responsiveness as well as on the stability of corresponding emulsions was evaluated.
The microgel particles with highest MAA content showed a significant impact on multi-responsive behaviour. Thermal sensitivity is pH dependent under acidic conditions but this dependence is gradually reduced as the pH increases above 7.5. On the other hand, pH-responsiveness is enhanced with the rise in temperature and stable emulsions were formed under highly alkaline conditions even the temperature was far above the volume phase transition temperature (VPTT). Understanding the correlation of stimuli responsiveness at interface with the emulsion stability would help to fabricate and design novel smart Pickering emulsions with better control over desired properties.
本研究介绍了基于聚(N-异丙基丙烯酰胺)-共-甲基丙烯酸(PNIPAM-co-MAA)的多响应性软微凝胶颗粒的合成与表征,这些颗粒用作“智能乳化剂”,用于控制水包癸烷Pickering乳液的稳定和破乳。这些软微凝胶颗粒可作为可逆稳定剂,即它们可以通过支持乳液形成或防止聚集体而停留在油水界面;而触发破乳可通过改变微凝胶体系的温度、pH值或离子强度来控制。
应用动态光散射观察多响应性微凝胶体系中颗粒的流体动力学半径随温度和pH值的变化。微凝胶组成根据甲基丙烯酸(MAA)含量而变化,并评估了这种变化对其热敏感性和pH响应性以及相应乳液稳定性的影响。
具有最高MAA含量的微凝胶颗粒对多响应行为有显著影响。在酸性条件下,热敏感性取决于pH值,但随着pH值升高到7.5以上,这种依赖性逐渐降低。另一方面,pH响应性随着温度升高而增强,即使温度远高于体积相变温度(VPTT),在高碱性条件下也能形成稳定的乳液。了解界面处刺激响应性与乳液稳定性之间的相关性,将有助于制备和设计新型智能Pickering乳液,从而更好地控制所需性能。