Michael Rapp

Surface acoustic wave-based (SAW) sensors are of great interest due to their high sensibility and fast and stable responses. They can be obtained at an overall low cost and with an intuitive and easy-to-use method. The chemical sensitization of a piezoelectric transducer plays a key role in defining the properties of SAW sensors. In this study, we investigate the structural and adhesion properties of a new class of coating material based on polyurethane polymeric composites. We used dark-field microscopy (DFM) and scanning electron microscopy (SEM) to observe the microstructure of polyurethane composite coatings on piezoelectric sensor elements and to analyze the effects of the chemical resistance and adhesion test (CAT) on the coating layers obtained with the polyurethane polymeric composites. The results of the microscopy showed that all polyurethane composite coatings exhibited excellent uniformity and stability after chemical adherence testing (CAT). All of the observations were correlated with the results of the ultrasonic analysis, which demonstrated the role of polyurethane as a binder to form the stable structure of the composites and, at the same time, as an adhesion promoter, increasing the chemical resistance and the adherence of the coating layer to the complex surface of the piezoelectric sensor element.

The chemical sensitization of surface acoustic wave (SAW) sensors plays a key role for this technology. The analysis of the resulting nanometric sensing layer is crucial for the development of new sensing materials as well as for the quality control of SAW sensors systems for commercial applications. In the previous works, the resulting coating layers using new coating materials based on polyurethane-polymer composites were evaluated considering the ultrasonic analysis, the adhesion, and the sensor responses. In this work, the characterization of the coating process, Bright Field Microscopy (BFM) and Dark Field Microscopy (DFM) were used to evaluate the quality of the material distribution and homogeneity of the obtained sensing layers. The sensing materials analyzed were the four polymers used in the previous works and their respective new composites with polyurethane (PU). The combination of BFM and DFM allows the characterization of the resulting material distribution obtained by the coating process, providing inferences about the interaction of each coating material with the surface of the SAW sensor element as well as about the correlation between the results of the ultrasonic parameters, the real material distribution and the homogeneity of the obtained coating layer of each coating material.

This work presents the application of the methodology for the sensitization of surface acoustic wave-based sensors (SAW), developed in the first part of this work. The strategy of the method is the obtention of sensing layers with tailored chemical environments by taking advantage of the wide variety of chemical composition of the organic polymers, which have been used as sensing polymers, and combining them with polyurethane (PU) to form polymeric composites that show enhanced properties as sensing materials for the SAW sensor technology. In the first part of this work, the ultrasonic and adhesion characterization was correlated to the sensor responses of PU-polybutylmethacrylate (PBMA) composites of different relative concentrations of the sensing polymer (PBMA) and PU. The resulting coating layers obtained with the PU polymer composites improved the chemical and mechanical properties of the sensing layer without interfering with the quality of their sensor responses in comparison to those with the pristine polymer as the sensing material. In this second part of this work, three new polyurethane polymeric composites were analyzed. The new sensing materials were produced using polylaurylmetacrylate (PLMA), polyisobutene (PIB), and poly(chlorotrifluoroethylene-co-vinylidene fluoride) (PCTFE) as the sensing polymers combined with PU. The results of the new PU polymer composites showed consequently different properties depending on the type of sensing polymer used, reproducing, however, the previous features achieved with PU and polybutylmetacrylate (PBMA) composites, like the improvements in the adhesion and the resistance against an organic solvent and preserving, in each case, the sensor response characteristic of each sensing polymer used, as was also observed for the PU-PBMA polymeric composites. The results obtained with the new sensing materials validated the strategy and confirmed its generalization as a very suitable methodology for the sensitization of SAW sensors, strongly indicating the applicability and reliability of the method, which makes possible the choice of virtually any chemical environments for the sensitization of SAW sensor systems.

A surface acoustic wave (SAW) resonator chip setup is presented that eliminates interfering signal responses caused by changes in the electrical environment of the surrounding media. When using a two-port resonator, applying electrically shielding layers between the interdigital transducers (IDTs) can be challenging due to the limited dimensions. Therefore, a layered setup consisting of an insulating polymer layer and a conductive gold layer was preferred. The SAW resonators were provided with polycarbonate housings, resulting in SAW resonator chips. This setup enables easy application of a wide range of coatings to the active part of the resonator surface, while ensuring subsequent electrical and fluidic integration of the resonator chips into a microfluidic array for measurements. The signal responses of uncoated SAW resonators and those with polymer coatings with and without a gold layer were tested with aqueous potassium chloride (KCl) solutions up to 3 mol/L, corresponding to conductivities up to 308 mS/cm. The use of a polymer coating at the thickness of the first Love mode resonance and a conductive gold layer completely reduced the electrical impact on the SAW resonator signal response, making small signals resulting from changes in viscosity and density of the KCl solutions visible.