Polymer brushes quartz crystal microbalance with

The present study aims to understand the influence of solvent quality on the molecular-level friction mechanism of tethered, brushlike polymers. It involves complementary adsorption studies of PLL-,g-PEG by means of optical waveguide lightmode spectroscopy (OWLS) and quartz crystal microbalance with dissipation (QCM-D) as well as friction studies performed on the nanoscale using colloidal-probe lateral force microscopy (LFM). The adsorbed mass measured by QGM-D includes a contribution from solvent molecules absorbed within the surface-bound polymer fllm. This is in contrast to optical techniques, such as OWLS, which are sensitive only to the dry mass of a polymer adsorbed onto the surface of the waveguide.By subtracting the dry mass , derived from OWLS measurements, from the wet mass , derived from QCM-D measurements, it is therefore possible to determine the mass of the solvent per unit substrate area absorbed in the brushlike structure of PLL- -PEG, expressed as areal solvation, P. Areal solvation was varied by choosing solvents (aqueous buffer solution, methanol, ethanol, and 2-propanol) of different quality with respect to the PEG brush. The solvents were characterized in terms of the three-component Hansen solubility parameters, and these values were compared with measured areal solvation of the PEG brush. 

In a non-electrochemical method with N4 type complexes, Kimura et al. [50] detected volatile organic compounds using a Quartz Crystal Microbalance coated with SAM s of nanostructured macromolecular metal complexes of Co-Pc, Ni-Pc, Cu-Pc or Zn-Pc in the form of polymer brushes. The method was based on the highly hydrophilic character of the brushes and on their good performance as anion exchangers... 

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