Abstract

The reactivity ratios, thermal behavior, and the bacteriocidal properties of the resins prepared from substituted acetophenones, i.e., m-aminoacetophenone, o-hydroxyacetophenone, and m-hydroxyacetophenone, have been investigated. The results obtained from the bacteriocidal studies are found to be quite interesting. Some of the resins synthesized are potent bacteriocides. The simple Kelen—Tüdös linear graphical method was used to determine the order of reactivity of substituted acetophenones when they are copolymerized with halogen-substituted anilines, i.e., o-chloroaniline, m-chloroaniline, and p-chloroaniline. The resins are found to be thermally stable and the energy of activation have been evaluated from TG curve by applying the Freeman—Anderson and Broido methods.

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.