LaFeO3 nanoparticle immobilized on DFNS-graphene oxide for the production of polymer and biopolyurethanes from carbon dioxide

Abstract

Dendritic fibrous nano silica (DFNS) was functionalized through the utilization of graphene oxide (GO) as a long-lasting anchoring agent. Consequently, the LaFeO3 nanoparticles were evenly spread out without clumping over the DFNS/GO. The supramolecular polymerized GO served the dual purpose of preventing the restacking of graphene sheets and functioned as a supplier of nitrogen to create active sites for the bonding of LaFeO3 nanoparticles. The nitrogen content above the extent of the GO films was modified by LaCl3·7H2O and Fe(NO3)3·9H2O ions to synthesize LaFeO3 nanoparticles. The catalytic properties of DFNS/GO-LaFeO3 was observed in the reaction between CO2 and oxetane and epoxide, leading to the production of the corresponding polycarbonates. The results indicated that DFNS/GO-LaFeO3 significantly enhanced the efficiency of synthesizing poly(propylene carbonate) and poly(trimethylene carbonate) from carbon dioxide. This approach offers substantial benefits, including high economic efficiency. The union reaction of CO2 and highly substituted epoxides sourced from sustainable sources such as discarded vegetable oils and fatty acids resulted in the production of novel cyclic carbonates of bio-origin. This reaction occurred under gentle and solvent-free conditions using DFNS/GO-LaFeO3 as a catalyst. The DFNS/GO-LaFeO3 exhibited a high capacity for CO2 uptake with exceptionally rapid kinetics. The nanoplate morphology of DFNS/GO-LaFeO3 facilitated the formation of a satisfactory outer layer for carbon dioxide uptake at each metal site. Consequently, the nanoplate morphology of DFNS/GO-LaFeO3 ensured systematic carbon dioxide emission, guaranteeing a complete reaction with the entire sheet and enabling rapid CO2 adsorption kinetics.