The aim of this review paper is to give an overview of the research activities of GKSS in the field of polymer based membranes. After summarizing the historic development of membrane science at GKSS, it describes different classes of polymeric materials for membranes, and the characterization of membranes. The design of membrane‐based separation processes followed by examples of applications will also be presented. In the last chapter we will try to give an outlook for the future activities in membrane research.

Gas permeation is increasingly considered for high capacity applications. This contribution discusses the commonly employed membrane module types for flat sheet membranes and suggests a new module concept. The applications considered are the separation of CO 2 from flue gas and hydrocarbon dewpointing of natural gas. Rigorous models for predicting the operating performance of the module types are described. Pilot plant experiments were conducted to validate the model for envelope type modules. Simulation studies were carried out to predict the performances of the different module types for the two examples and assess their advantages and disadvantages.

No abstract

Novel selective ceramic-supported thin polyimide films produced in a single dip coating step are proposed for membrane applications at elevated temperatures. Layers of the polyimides P84®, Matrimid 5218®, and 6FDA-6FpDA were successfully deposited onto porous alumina supports. In order to tackle the poor compatibility between ceramic support and polymer, and to get defect-free thin films, the effect of the viscosity of the polymer solution was studied, giving the entanglement concentration (C*) for each polymer. The C* values were 3.09 wt. % for the 6FDA-6FpDA, 3.52 wt. % for Matrimid®, and 4.30 wt. % for P84®. A minimum polymer solution concentration necessary for defect-free film formation was found for each polymer, with the inverse order to the intrinsic viscosities (P84® ≥ Matrimid® >> 6FDA-6FpDA). The effect of the temperature on the permeance of prepared membranes was studied for H2, CH4, N2, O2, and CO2. As expected, activation energy of permeance for hydrogen was higher than for CO2, resulting in H2/CO2 selectivity increase with temperature. More densely packed polymers lead to materials that are more selective at elevated temperatures.

No abstract