A Study on the Stability of Carbon Nanoforms-Polyimidazolium Network Hybrids in the Conversion of CO2 into Cyclic Carbonates: Increase in Catalytic Activity after Reuse

Three different carbon nanoforms (CNFs), single-walled and multi-walled carbon nanotubes (SWCNTs, MWCNTs) and carbon nanohorns (CNHs), have been used as supports for the direct polymerization of variable amounts of a bis-vinylimidazolium salt. Transmission electron microscopy confirmed that all CNFs act as templates on the growth of the polymeric network, which perfectly covers the nanocarbons forming a cylindrical (SWCNTs, MWCNTs) or spherical (CNHs) coating. The stability of these hybrid materials was investigated in the conversion of CO2 into cyclic carbonate under high temperature and CO2 pressure. Compared with the homopolymerized monomer, nanotube-based materials display an improved catalytic activity. Beside the low catalytic loading (0.05-0.09 mol%) and the absence of Lewis acid co-catalysts, all the materials showed high TON values (up to 1154 for epichlorohydrin with SW-1:2). Interestingly, despite the loss of part of the polymeric coating for crumbling or peeling, the activity increases upon recycling of the materials, and this behaviour was ascribed to their change in morphology, which led to materials with higher surface areas and with more accessible catalytic sites. Transmission electron microscopy analysis, along with different experiments, have been carried out in order to elucidate these findings.

Automated summary

Three different carbon nanoforms were used as supports for the direct polymerization of a bis-vinylimidazolium salt, showing that nanotube-based materials have improved catalytic activity with high TON values. These materials successfully converted CO2 into cyclic carbonate under high temperature and CO2 pressure. Interestingly, the materials exhibited increased activity upon recycling due to changes in morphology, leading to materials with higher surface areas and more accessible catalytic sites.