Kumar Sugam, Ganguly Rajib, Honecker Dirk, Aswal Vinod K
Solid State Physics Division, Bhabha Atomic Research Centre, Mumbai-400085, India.
Homi Bhabha National Institute, Anushakti Nagar, Mumbai-400094, India.
Soft Matter. 2025 Jul 16;21(28):5752-5763. doi: 10.1039/d5sm00312a.
Phase behaviour and wetting properties of negatively charged silica nanosuspensions are influenced strongly by polyethylene oxide-polypropylene oxide-polyethylene oxide based non-ionic surfactants, known popularly as Pluronics. These triblock copolymers are adsorbed at silica nanoparticle surfaces and impart inter-particle attraction driven re-entrant liquid-liquid phase separations in silica nanosuspensions. The association characteristics of Pluronics at silica surfaces that lead to such behaviours are, however, not clearly understood yet. To shed light on this, we carried out dynamic light scattering (DLS), small-angle neutron scattering (SANS) and rheological studies on Ludox® LS-Pluronic systems comprising both hydrophobic Pluronic P123 and its hydrophilic counterpart, Pluronic F127. Our contrast matched SANS studies show that micelles formed by Pluronics in these systems remain correlated even at Pluronic concentrations as low as 1-2 wt%, which has not been observed hitherto in non-ionic micellar systems. Our DLS, SANS and rheological studies also show that evolutions of Pluronics induced inter particle attractions in LS nanosuspensions with Pluronic concentration and temperature differ significantly for the two Pluronics due to their widely different hydrophilic-lipophilic balances (HLB). Re-entrant transitions of repulsive-to-attractive-to-repulsive (or less attractive) state of inter particle interactions are thus observed as a function of temperature in the case of hydrophobic Pluronic P123 but as a function of Pluronic concentration in the case of hydrophilic Pluronic F127. The results give a comprehensive idea about the role of the association characteristics of Pluronics at the silica nanoparticle surface in influencing the properties of silica nanosuspensions.
带负电荷的二氧化硅纳米悬浮液的相行为和润湿性受到基于聚环氧乙烷-聚环氧丙烷-聚环氧乙烷的非离子表面活性剂(俗称普朗尼克)的强烈影响。这些三嵌段共聚物吸附在二氧化硅纳米颗粒表面,并在二氧化硅纳米悬浮液中引发颗粒间吸引力驱动的再入式液-液相分离。然而,导致这种行为的普朗尼克在二氧化硅表面的缔合特性尚未完全清楚。为了阐明这一点,我们对包含疏水性普朗尼克P123及其亲水性对应物普朗尼克F127的Ludox® LS-普朗尼克体系进行了动态光散射(DLS)、小角中子散射(SANS)和流变学研究。我们的对比匹配SANS研究表明,即使在普朗尼克浓度低至1-2 wt%时,这些体系中由普朗尼克形成的胶束仍保持相关性,这在非离子胶束体系中迄今尚未观察到。我们的DLS、SANS和流变学研究还表明,由于两种普朗尼克的亲水-亲油平衡(HLB)差异很大,普朗尼克诱导的LS纳米悬浮液中颗粒间吸引力随普朗尼克浓度和温度的变化在两种普朗尼克中存在显著差异。因此,在疏水性普朗尼克P123的情况下,观察到颗粒间相互作用从排斥到吸引再到排斥(或吸引力较小)状态的再入转变是温度的函数,而在亲水性普朗尼克F127的情况下,是普朗尼克浓度的函数。这些结果全面地揭示了普朗尼克在二氧化硅纳米颗粒表面的缔合特性在影响二氧化硅纳米悬浮液性质方面的作用。