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Methods for the Self-integration of Megamolecular Biopolymers on the Drying Air-LC Interface
Published on: April 7, 2017
Moisture changes inside hydrogel particles during their drying process investigated with fluorescence lifetime
1Institute of Physical Chemistry, RWTH Aachen University, Landoltweg 2, 52074 Aachen, Germany. woell@pc.rwth-aachen.de.
Abstract:
The properties of hydrogels and microgels, i.e. hydrogel particles, depend strongly on their water content. Based on our previously developed method to access the local water content in microgels, we performed fluorescence lifetime microscopy measurements at different stages of drying poly(N-isopropylacrylamide) (PNIPAM) microgels under ambient conditions. For this purpose, the red-emitting dye ATTO 655 was covalently attached to the microgels. Its emission is quenched by water molecules due to an energy transfer from the first excited state of the dye to a vibrational level of the water molecules. The quenching constant or, equivalently, the fluorescence lifetime, gives direct access to the local water concentration. We measured the fluorescence lifetime after spin-coating, reswelling and at different times of subsequent drying to follow the changes of water content during this process. We found that the microgels are not totally dry after spin coating, but drying them to their equilibrium moisture under ambient temperature and humidity conditions requires several hours. Additionally, we determined the moisture inside microgels in equilibrium at different air humidities. In summary, the method allows for a detailed investigation of the moisture inside hydrogels and gives straight-forward access to in situ and operando measurements of hydrogel systems.
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