To gain knowledge about cause–effect relationships for the adhesion of ice on surfaces with different chemical groups, we wanted to study the effect of thin polymer layers on the ice adhesion strength. To minimize the effect of roughness, smooth substrates that have generally relatively low ice adhesion strengths were chosen. To be able to obtain highly reproducible values for the region of low ice adhesion and to measure small differences of ice adhesion at surfaces with different chemical compositions, a new measuring system for the determination of the ice adhesion strength which is based on a modified spin-coater was developed. We show its technical potential on the basis of first results on pure silicon wafers and selected hydrophilic polymer layers. Furthermore, we investigated the effect of the water quality on the ice adhesion strength. The obtained data are discussed in the context of physicochemical properties of the layers and of the chemical characteristics of the used polymers.

The ferro-, pyro-and piezoelectric properties of poly(vinylidene fluoride-co-trifluoroethylene) P(VDF-TrFE) have created interest with regard to its application in aqueous and ambient surroundings for sensors, functional coatings, and in the field of life sciences. P(VDF-TrFE) thin films are usually applied via spin-coating, but dip-coating will be advantageous especially for irregularly shaped substrates. The morphology of dip-and spin-coated semi-crystalline thin films is studied as a function of both the film thickness and the annealing temperature. The characterization of the films is carried out by grazing incidence wide-angle X-ray scattering (GIWAXS), X-ray reflectometry (XRR), and infrared reflection absorption spectroscopy (IRRAS). Atomic force microscopy measurements (AFM) are used to examine the resulting topography. It is found that both spin-and dip-coated thin films crystallize in the desired edge-on orientation, but the overall crystallinity after dip-coating is decreased compared to the spin-coated films of comparable thickness and the resulting roughness is increased. The higher roughness is most probably caused by the slower evaporation of the solvents and a secondary crystallization process at the air-polymer interface.

For cleaning tests, which are important in many industrial processes, there are no test contaminations with which geometry‐independent homogeneous films can be produced. Polymer films can fill this gap when they are able to mimic the properties of reference contaminants. For this purpose, acrylic acid (AA) copolymers are prepared by conventional atom transfer radical copolymerization and subsequent acidolysis of the tert‐butyl acrylate (tBA) prepolymers. In this way polarity and adhesion can be adjusted by the amount of carboxy groups in the polymer. Dynamic contact angle measurements show that the advancing contact angle of acrylic acid/methyl(meth)acrylate statistical copolymer layers increase with decreasing carboxy group content. Cleaning experiments show accordingly that the amount of residual polymer of coatings made from these polymers is dependent on the absolute number of adhesive carboxy groups in the polymer. Therefore, for an adaption of the polymer layers to hydrophilic reference contaminants it is necessary to incorporate additional hydrophilic monomer components into the polymers, which lead to lower contact angles but also stronger adhesion of the layers. Hence, it is shown that the chosen polymer concept is delivering the leverages to adjust the properties of appropriate test contaminants.