Abstract
A new type of hyperbranched aromatic poly(ether ketone) terminated with carboxylic acid groups (P2) was synthesized via a one-step polycondensation of a symmetric AB2 monomer, 4,4′-(m-phenylenedioxy)-bis(benzenecarboxylic acid), using phosphorous pentoxide-methanesulfonic acid (PPMA) as a condensing agent and solvent. Subsequently, the terminal carboxylic acid functional group of P2 was converted to an ethyl ester functional group by treatment with thionyl chloride followed by ethanol in the presence of triethylamine. The weight-average molecular weight (Mw) of the ethyl ester-terminated hyperbranched poly(ether ketone) (P3) was measured by gel permeation chromatography. By changing the reaction time and the amount of PPMA, Mw can be controlled in the range of 4.2 × 104 to 1.6 × 105. P2 was soluble in polar solvents, and P3 was soluble in less-polar solvents. The thermal stabilities of the poly(ether ketone)s were investigated using thermogravimetric analysis, which indicated that the decompositions of P2 and P3 start at around 150 and 200 °C, respectively. The inherent viscosities of P2 were in the range of 0.101–0.171, while those of P3 ranged from 0.067 to 0.112. The ion exchange capacities calculated by titration were in the range of 2.2–2.8 mol kg−1 according to the difference in molecular weights. P2 was tested as a weak-acid catalyst and exhibited a certain catalytic activity for the hydrolysis of cellulose to glucose. A new type of hyperbranched aromatic polyetherketone terminated with carboxylic acid group was synthesized by one-step polycondensation of a symmetric AB2 monomer, 4,4′-(m-phenylenedioxy)-bis(benzenecarboxylic acid), using phosphorous pentoxide/methanesulfonic acid (PPMA) as condensing agent and solvent. By changing the reaction time and the amount of PPMA, Mw can be controlled in the range of 4.2 × 104 to 1.6 × 105. The polymer has been tested as a weak-acid catalyst and shows a certain catalytic activity for the hydrolysis of cellulose to glucose.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
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.