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Catalytic reactors performing continuously are an important step towards more efficient and controllable processes compared to the batch operation mode. For this purpose, homogenous high internal phase emulsion polymer materials with an immobilized silver catalyst were prepared and used as a continuous plug flow reactor. Porous material with epoxide groups was functionalized to bear aldehyde groups which were used to reduce silver ions using Tollens reagent. Investigation of various parameters revealed that the mass of deposited silver depends on the aldehyde concentration as well as the composition of Tollens reagent. Nanoparticles formed on the pore surface showed high crystallinity with a cuboctahedra crystal shape and highly uniform surface coverage. The example of the 4-nitrophenol catalytic reduction in a continuous process was studied and demonstrated to be dependent on the mass of deposited silver. Furthermore, productivity increased with the volumetric silver density and flow rate, and it was preserved during prolonged usage and storage.

The role of bacteriophage therapy in medicine has recently regained an important place. Oral phage delivery for gastrointestinal treatment, transport through the stomach, and fast release in the duodenum is one of such applications. In this work, an efficient polyHIPE/hydrogel system for targeted delivery of bacteriophages with rapid release at the target site is presented. T7 bacteriophages were encapsulated in low crosslinked anionic nanocellulose-based hydrogels, which successfully protected phages at pH < 3.9 (stomach) and completely lost the hydrogel network at a pH above 3.9 (duodenum), allowing their release. Hydrogels with entrapped phages were crosslinked within highly porous spherical polyHIPE particles with an average diameter of 24 μm. PolyHIPE scaffold protects the hydrogels from mechanical stimuli during transport, preventing the collapse of the hydrogel structure and the unwanted phage release. On the other hand, small particle size, due to the large surface-to-volume ratio, enables rapid release at the target site. As a consequence, a fast zero-order release was achieved, providing improved patient compliance and reduced frequency of drug administration. The proposed system therefore exhibits significant potential for a targeted drug delivery in medicine and pharmacy.

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Due to plasmonic and catalytic properties, silver nanoplates are of significant interest; therefore, their simple preparation in gram quantities is required. Preferably, the method is seedless, consists of few reagents, enables preparation of silver nanoplates with desired optical properties in high concentration, is scalable, and allows their long-term storage. The developed method is based on silver nitrate, sodium borohydride, polyvinylpyrrolidone, and H 2 O 2 as the main reagents, while antifoam A204 is implemented to achieve better product quality on a larger scale. The effect of each component was evaluated and optimized. Solution volumes from 3 to 450 mL and concentrations of silver nanoplates from 0.88 to 4.8 g/L were tested. Their size was tailored from 25 nm to 8 μm simply by H 2 O 2 addition, covering the entire visible plasmon spectra and beyond. They can be dried and spontaneously dispersed after at least one month of storage in the dark without any change in plasmonic properties. Their potential use in modern art was demonstrated by drying silver colloids on different surfaces in the presence of reagents or purified, resulting in a variety of colors but, more importantly, patterns of varying complexity, from simple multi-coffee-rings structures to dendritic forms and complex multilevel Sierpinśki triangle fractals.

Purifications of biologics can be improved using 3D printed stationary phases with perfectly ordered morphology. However, limited spatial resolution and lack of porous materials have hindered application of additive manufacturing in bioprocessing. To bridge this gap, digital light processing and polymerization‐induced phase separation are combined to fabricate platform materials with bed morphology at the micrometer scale, and porous network in the nanometer scale. Four different porous inks are developed, 3D printed, and characterized in terms of their rheological behaviour, polymerization kinetics, and printing resolution. Rapid 3D printing (down to 1 h) is achieved at scale (up to 100 mL column) of porous supports (50% porosity) at high resolution (up to 50 µm for linear features and 200 µm for complex geometries). 3D‐printed gyroids are chemically functionalized with various ion exchange ligands. These are successfully challenged for i) the separation of model proteins in dynamic conditions and ii) protein capture from a clarified cell harvest, demonstrating dynamic binding capacities between 5 and 16 mg mL−1 and up to 86% purity in a single run. This work introduces a rapid and facile approach to 3D printing porous inks to fabricate perfectly ordered stationary phases for downstream processing.