Abstract

The pH response and mechanical properties of copolymer-based hydrogels such aspoly(acrylonitrile-co-acrylic acid) are usually attributed to their chemical composition. In thisstudy, it has been shown that the architecture of the polymer chains, i.e. the distribution ofcomonomers in the macromolecules, also plays a major role in controlling these properties.A series of four poly(acrylonitrile-co-acrylic acids) with fixed composition (i.e. ∼30 mol% acrylic acid moieties) were synthesized, where the block lengths of both AN(acrylonitrile) and AAc (acrylic acid) moieties in the copolymers were varied by controllingthe feeding pattern of the monomers during free radical copolymerization. Thesecopolymers were then converted into fine fibers of the same dimensions. The monomerdistribution in the four copolymers was estimated using quantitative carbon 13C nuclear magnetic resonance (NMR) and related to the mechanical and pH responseproperties of the resultant fibers. The pH response of the fibers with similar compositionincreased dramatically as the block length of the AAc moiety was increased, while themechanical properties increased as a direct function of the block length of the AN moieties.The fiber’s response at pH 10 in terms of the change in length increased by∼four times while its responserate increased by ∼50 times with the increase in block length of the AAc moiety. On theother hand, the tensile properties and retractive stress increased by∼four times with the increase in the block length of the AN moiety.

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.