Improving the yield and selectivity of chemical reactions is one of the challenging tasks in paving the way for a more sustainable and climate-friendly economy. For the industrially highly relevant gas–liquid reactions, this can be achieved by tailoring the timescales of mixing to the requirements of the reaction. Although this has long been known for idealized reactors and time- and space-averaged processes, considerable progress has been made recently on the influence of local mixing processes. This progress has become possible through joint research between chemists, mathematicians, and engineers. We present the reaction systems with adjustable kinetics that have been developed, which are easy to handle and analyze. We show examples of how the selectivity of competitive-consecutive reactions can be controlled via local bubble wake structures. This is demonstrated for Taylor bubbles and bubbly flows under technical conditions. Highly resolvednumerical simulations confirm the importance of the bubble wake structure for the performance of a particular chemical reaction and indicate tremendous potential for future process improvements.

Neutralization of acid and base to produce electricity in the process of reverse electrodialysis with bipolar membranes (REDBP) presents an interesting but until now fairly overlooked flow battery concept. Previously, we presented single-cell experiments, which explain the principle and discuss the potential of this process. In this contribution, we discuss experiments with REDBP stacks at lab scale, consisting of 5 to 20 repeating cell units. They demonstrate that the single-cell results can be extrapolated to respective stacks, although additional losses have to be considered. As in other flow battery stacks, losses by shunt currents through the parallel electrolyte feed/exit lines increases with the number of connected cell units, whereas the relative importance of electrode losses decreases with increasing cell number. Experimental results are presented with 1 mole L⁻¹ acid (HCl) and base (NaOH) for open circuit as well as for charge and discharge with up to 18 mA/cm² current density. Measures to further increase the efficiency of this novel flow battery concept are discussed.

Surface science methods originating from analysis of noble metal catalysts are increasingly applied to metal oxides. These methods provide direct access to fundamental structural properties and phase equilibria governing the catalytic properties of metal oxide surfaces. However, no systematic way existed so far for transferring this knowledge to technical catalysts. The aim of this paper is to combine surface science with chemical engineering methods to bridge this gap. Styrene synthesis over pure and K-doped iron oxides is used as an example to develop and to explain the methodology. Single crystal films (SCF), grown epitaxially on a Pt-carrier are considered as ideal model surfaces. Comprehensive UHV analyses yield the structural properties of SCF as well as their interaction with relevant components of the reaction mixture. Their results are combined with conversion experiments to derive a mechanistic catalyst model along with quantitative information on the reaction rates. The activity of SCF as well as their phase transitions under reactive conditions can be described with a continuum model depending on the macroscopic properties of the system. This model forms the crucial link towards technical catalysts. It is shown that the behaviour of a powder catalyst can be described as a superposition of the above kinetic model and an appropriate porous model. In this paper we review the developed methodology and conclude with the evaluation of the concept.