TY - JOUR
T1 - A study on the stability of carbon nanoforms–polyimidazolium network hybrids in the conversion of co2 into cyclic carbonates
T2 - Increase in catalytic activity after reuse
AU - Morena, Anthony
AU - Campisciano, Vincenzo
AU - Comès, Adrien
AU - Liotta, Leonarda Francesca
AU - Gruttadauria, Michelangelo
AU - Aprile, Carmela
AU - Giacalone, Francesco
N1 - Funding Information:
Funding: This research was funded by University of Palermo and the Italian Ministry of Education (project no. 2017W8KNZW). This research is supported by the F.R.S-FNRS via funding grants GEQ U.G014.19 and EQP U.N034.17.
Funding Information:
Acknowledgments: The authors gratefully acknowledge the University of Palermo and the Italian Ministry of Education, University and Research (MIUR) for financial support through PRIN 2017 (project no. 2017W8KNZW). This research is supported by the F.R.S-FNRS via the funding grants GEQ U.G014.19 and EQP U.N034.17. This research used resources of the PC2 and the MORPH-IM platforms located at the University of Namur.
Publisher Copyright:
© 2021 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2021/9
Y1 - 2021/9
N2 - 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.
AB - 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.
KW - Carbon dioxide fixation
KW - Carbon nanotubes
KW - Cyclic carbonates
UR - http://www.scopus.com/inward/record.url?scp=85114389907&partnerID=8YFLogxK
U2 - 10.3390/nano11092243
DO - 10.3390/nano11092243
M3 - Article
AN - SCOPUS:85114389907
SN - 2079-4991
VL - 11
JO - Nanomaterials
JF - Nanomaterials
IS - 9
M1 - 2243
ER -