Abstract

The present study aims at investigating the properties of pH/thermo-responsive polyelectrolyte microgels intended for surface functionalisation of textiles. Microgels were prepared to have their pH/thermo-responsiveness expressed within the physiological pH and temperature range. They consisted of pH/thermo-responsive microparticles of poly(N-isopropylacrylamide-co-acrylic acid) either alone or complexed with the pH-responsive natural polysaccharide chitosan. Basic characterisation included observation of the microgel morphology and determination of the polyelectrolyte isoelectric points and of the lower critical solution temperatures of the microgels. The analyses were performed by means of scanning electron microscopy, potentiometric titration and differential scanning calorimetry, respectively. Further physicochemical characterisation was conducted using bulk rheology, UV–vis spectroscopy, dynamic light scattering and electrophoresis. These analyses revealed that the studied thermo-responsive microparticles and their complexes with chitosan undergo a volume-phase transition from swollen and hydrophilic to de-swollen and hydrophobic at temperatures close to the average human body temperature. Kinetics measurements showed that this transition is completed in approximately 15min. Furthermore, the polyelectrolyte complexes exhibit a change of surface charge from positive to negative values at pH 6, i.e. within the physiological pH range. It was, therefore, confirmed that the polyelectrolyte microgels investigated in this study were successfully prepared to have pH/thermo-responsive properties suitable for textile functionalisation.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.