Grafting polysulfonamide from cellulose paper through organocatalytic ring-opening polymerization of N-sulfonyl aziridines

Carbohydr Polym. 2021 Jun 1:261:117903. doi: 10.1016/j.carbpol.2021.117903. Epub 2021 Mar 5.

Abstract

A facile and effective "grafting from" method by ROP of N-sulfonyl aziridines toward cellulose-g-polysulfonamides has been developed for efficient oil/water separation. The cellulose paper was initially succinylated to transform the hydroxyl to carboxyl acid groups, which act as the initiating sites for the ring-opening copolymerization of fluorescent 2-methyl-1-dansylaziridine and 2-methyl-1-tosylaziridine (TsMAz) towards the grafted cellulose. Both steps are catalyzed by the same compound, 7-methyl-1,5,7-triazabicyclo[4.4.0]dec-5-ene (MTBD). The grafted polysulfonamide ratio was up to 136 wt%, and the surface contact angle up to 147°. A one-pot tandem strategy was applied to produce the grafted cellulose paper with a grafting ratio ranging from 96 to 150 % and a contact angle over 127°. The modified cellulose paper material showed promising properties for efficient oil/water separations.

Keywords: Cellulose paper; N-Sulfonyl aziridine; Oil/water separation; Ring-opening polymerization.