Bram Zoetebier

Monovalent cation selective crown ether containing poly(arylene ether ketone)/SPEEK blend membranes

Blend membranes of sulfonated poly(ether ether ketone) (SPEEK) and poly(arylene ether ketone) (PAEK) derivatives containing crown ether units in the main chain (CPAEK) were prepared and characterized in terms of water swelling and ion exchange capacity (IEC). The miscibility of the polymers was verified by DSC and HR-SEM. Ion transport characteristics of the membranes were established for the monovalent ions Li+ and K+ and the separation of these ions by the cation exchange membranes was investigated. Diffusion experiments for aqueous KCl, LiCl and their mixtures were carried out with pure SPEEK membranes as well as with the CPAEK/SPEEK membranes. Blending significantly decreased the ion permeability due to cation-crown ether complexation and increased the hydrophobicity of the matrix. The K+ over Li+ selectivity of the SPEEK membrane was enhanced by blending SPEEK with CPAEK by a factor of nearly 4, indicating that the presence of a crown ether polymer changes the relative transport of the ions in the membrane.

Nanoemulsion-induced enzymatic crosslinking of tyramine-functionalized polymer droplets

In situ gelation of water-in-oil polymer emulsions is a key method to produce hydrogel particles. Although this approach is in principle ideal for encapsulating bioactive components such as cells, the oil phase can interfere with straightforward presentation of crosslinker molecules. Several approaches have been developed to induce in-emulsion gelation by exploiting the triggered generation or release of crosslinker molecules. However, these methods typically rely on photo- or acid-based reactions that are detrimental to cell survival and functioning. In this work, we demonstrate the diffusion-based supplementation of small molecules for the in-emulsion gelation of multiple tyramine-functionalized polymers via enzymatic crosslinking using a H2O2/oil nanoemulsion. This strategy is compatible with various emulsification techniques, thereby readily supporting the formation of monodisperse hydrogel particles spanning multiple length scales ranging from the nano- to the millimeter. As proof of principle, we leveraged droplet microfluidics in combination with the cytocompatible nature of enzymatic crosslinking to engineer hollow cell-laden hydrogel microcapsules that support the formation of viable and functional 3D microtissues. The straightforward, universal, and cytocompatible nature of nanoemulsion-induced enzymatic crosslinking facilitates its rapid and widespread use in numerous food, pharma, and life science applications.

Functional macromolecules and smart polymer networks for ion separation, reduction and delivery

In this thesis we tackle the synthesis, characterization and function of novel organometallic polyanions, polycations, and their corresponding hydrogels and explore the use of these redox-responsive water-soluble or water-swellable materials in applications where either their charge or their redox activity leads to new opportunities, such as in metal nanoparticle fabrication and transfection. In addition, crown ether-functionalized aromatic polymers and organometallic polymers will be explored for ion separation and – sensing.