On the Order and Orientation in Liquid Crystalline Polymer Membranes for Gas Separation

Joey Kloos; Nico Jansen; Menno Houben; Anna Casimiro; Johan Lub; Zandrie Borneman; Albert P H J Schenning; Kitty Nijmeijer

doi:10.1021/acs.chemmater.1c02526

On the Order and Orientation in Liquid Crystalline Polymer Membranes for Gas Separation

Chem Mater. 2021 Nov 9;33(21):8323-8333. doi: 10.1021/acs.chemmater.1c02526. Epub 2021 Oct 25.

Authors

Joey Kloos¹, Nico Jansen¹, Menno Houben¹, Anna Casimiro¹, Johan Lub², Zandrie Borneman¹, Albert P H J Schenning², Kitty Nijmeijer¹

Affiliations

¹ Membrane Materials and Processes, Department of Chemical Engineering and Chemistry, Eindhoven University of Technology, P.O. Box 513, 5600 MB Eindhoven, The Netherlands.
² Stimuli-Responsive Functional Materials and Devices, Department of Chemical Engineering and Chemistry, Eindhoven University of Technology, P.O. Box 513, 5600 MB Eindhoven, The Netherlands.

Abstract

To prevent greenhouse emissions into the atmosphere, separations like CO₂/CH₄ and CO₂/N₂ from natural gas, biogas, and flue gasses are crucial. Polymer membranes gained a key role in gas separations over the past decades, but these polymers are often not organized at a molecular level, which results in a trade-off between permeability and selectivity. In this work, the effect of molecular order and orientation in liquid crystals (LCs) polymer membranes for gas permeation is demonstrated. Using the self-assembly of polymerizable LCs to prepare membranes ensures control over the supramolecular organization and alignment of the building blocks at a molecular level. Robust freestanding LC membranes were fabricated that have various, distinct morphologies (isotropic, nematic cybotactic, and smectic C) and alignment (planar and homeotropic), while using the same chemical composition. Single gas permeation data show that the permeability decreases with increasing molecular order while the ideal gas selectivity of He and CO₂ over N₂ increases tremendously (36-fold for He/N₂ and 21-fold for CO₂/N₂) when going from randomly ordered to the highly ordered smectic C morphology. The calculated diffusion coefficients showed a 10-fold decrease when going from randomly ordered membranes to ordered smectic C membranes. It is proposed that with increasing molecular order, the free volume elements in the membrane become smaller, which hinders gasses with larger kinetic diameters (Ar, N₂) more than gasses with smaller kinetic diameters (He, CO₂), inducing selectivity. Comparison of gas sorption and permeation performances of planar and homeotropic aligned smectic C membranes shows the effect of molecular orientation by a 3-fold decrease of the diffusion coefficient of homeotropic aligned smectic C membranes resulting in a diminished gas permeation and increased ideal gas selectivities. These results strongly highlight the importance of molecular order and orientation in LC polymer membranes for gas separation.