Abstract
The effects of solvent and concentration in the radical copolymerization of styrene (ST) and methacrylic acid (MAA) on the nature of intramolecular hydrogen bonding in the prepared copolymers were investigated. The copolymerizations at lower monomer concentration in benzene gave copolymers with exceedingly higher intramolecular association ability compared to the copolymerizations in dioxane and at higher monomer concentration in benzene. This result could be explained. assuning an intrachain reaction of the end radical with MAA monomers hydrogen-bonded to MAA segments in he macroradical.
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 callDisclaimer: 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.
