Liu Siyuan, Lai Beibei, James Stuart L
School of Chemistry and Chemical Engineering, Queen's University Belfast, David Keir Building, Stranmillis Road, Belfast BT9 5AG, U.K.
ACS Appl Mater Interfaces. 2024 Apr 3;16(13):16436-16444. doi: 10.1021/acsami.3c18998. Epub 2024 Mar 21.
Type III porous liquids (PLs) consist of porous solid particles dispersed in a size-excluded liquid phase and are attracting much attention as novel media for applications such as gas separation. However, the effects of fundamental variables such as particle size on their physical properties are currently largely unknown. Here we study the effects of particle size in a series of porous liquids based on solid Al(OH)(fumarate) (a microporous metal-organic framework, MOF) with particle sizes of 60 nm, 200-600 nm, or 800-1000 dispersed in liquid polydimethylsiloxane (PDMS). Properties examined include physical stability of the dispersion, viscosity, total CO uptake, and kinetics of CO uptake. As expected, both physical stability and viscosity decreased with increasing particle size. Unexpectedly, total gravimetric gas uptake also varied with particle size, being greatest for the largest particles, which we ascribe to larger particles having a lower relative content of surface-bound FMA ligands. Various models for the gas uptake kinetic data were considered, specifically adsorption reaction models such as pseudo-first-order, pseudo-second-order, and Elovich models. In contrast to pure PDMS, which showed first-order kinetics, all PLs fit best to the Elovich model confirming that their uptake mechanism is more complex than for a simple liquid. Adsorption diffusion models, specifically Weber and Morris' intraparticle model and Boyd's model, were also applied which revealed a three-step process in which a combination of diffusion through a surface layer and intraparticle diffusion were rate-limiting. The rate of gas uptake follows the order PDMS < PL1 < PL2 < PL3, showing that the porous liquids take up gas more rapidly than does PDMS and that this rate increases with particle size. Overall, the study suggests that for high gas uptake and fast uptake kinetics, large particles may be preferred. Also, the fact that large particles resulted in low viscosity may be advantageous in reducing the pumping energy needed in flow separation systems. Therefore, the work suggests that finding ways to stabilize PLs with large particles against phase separation could be advantageous for optimizing the properties of PLs toward applications.
III型多孔液体(PLs)由分散在尺寸排阻液相中的多孔固体颗粒组成,作为气体分离等应用的新型介质正备受关注。然而,诸如粒径等基本变量对其物理性质的影响目前在很大程度上尚不清楚。在此,我们研究了一系列基于固体富马酸铝(氢氧化铝)(一种微孔金属有机框架,MOF)的多孔液体中粒径的影响,这些多孔液体的粒径分别为60纳米、200 - 600纳米或800 - 1000纳米,分散在液体聚二甲基硅氧烷(PDMS)中。所研究的性质包括分散体的物理稳定性、粘度、总CO吸收量以及CO吸收动力学。正如预期的那样,物理稳定性和粘度均随粒径增大而降低。出乎意料的是,总重量气体吸收量也随粒径而变化,最大粒径的颗粒吸收量最大,我们将其归因于较大颗粒表面结合的FMA配体相对含量较低。考虑了各种气体吸收动力学数据模型,特别是诸如伪一级、伪二级和埃洛维奇模型等吸附反应模型。与表现出一级动力学的纯PDMS不同,所有PLs最符合埃洛维奇模型,这证实了它们的吸收机制比简单液体更为复杂。还应用了吸附扩散模型,特别是韦伯和莫里斯的颗粒内模型以及博伊德模型,这些模型揭示了一个三步过程,其中通过表面层的扩散和颗粒内扩散的组合是限速步骤。气体吸收速率遵循PDMS < PL1 < PL2 < PL3的顺序,表明多孔液体比PDMS吸收气体更快,且该速率随粒径增加。总体而言,该研究表明,对于高气体吸收量和快速吸收动力学,较大颗粒可能更具优势。此外,大颗粒导致低粘度这一事实在降低流分离系统所需的泵送能量方面可能具有优势。因此,这项工作表明,找到使大颗粒PLs稳定以防止相分离的方法可能有利于优化PLs在应用中的性能。