TY - JOUR
T1 - Copper-doped activated carbon from amorphous cellulose for hydrogen, methane and carbon dioxide storage
AU - Conte, Giuseppe
AU - Policicchio, Alfonso
AU - De Luca, Oreste
AU - Rudolf, Petra
AU - Desiderio, Giovanni
AU - Agostino, Raffaele G.
N1 - Funding Information:
This research was supported by PON03PE_00092_1 ( EOMAT ) and benefitted from financial support by the Advanced Materials research program of the Zernike National Research Centre under the Bonus Incentive Scheme of Ministry for Education, Culture and Science (The Netherlands).
Publisher Copyright:
© 2022
PY - 2022/5/15
Y1 - 2022/5/15
N2 - The transition away from fossil fuel and ultimately to a carbon-neutral energy sector requires new storage materials for hydrogen and methane as well as new solutions for carbon capture and storage. Among the investigated adsorbents, activated carbons are considered especially promising because they have a high specific surface area, are lightweight, thermally and chemically stable, and easy to produce. Moreover, their porosity can be tuned and they can be produced from inexpensive and environmentally friendly raw materials. This study reports on the development and characterization of activated carbons synthesized starting from amorphous cellulose with and without the inclusion of copper nanoparticles. The aim was to investigate how the presence of different concentrations of metal nanoparticles affects porosity and gas storage properties. Therefore, the research work focused on synthesis and characterization of physical and chemical properties of pristine and metal-doped activated carbons materials and on further investigation to analyze their hydrogen, methane and carbon dioxide adsorption capacity. For an optimized Cu content the microporosity is improved, resulting in a specific surface area increase of 25%, which leads to a H2 uptake (at 77 K) higher than the theoretical value predicted by the Chahine Rule. For CH4, the storage capacity is improved by the addition of Cu but less importantly because the size of the molecule hampers easy access of the smaller pores. For CO2 a 26% increase in adsorption capacity compared to pure activated carbon was achieved, which translated with an absolute value of over 48 wt% at 298 K and 15 bar of pressure.
AB - The transition away from fossil fuel and ultimately to a carbon-neutral energy sector requires new storage materials for hydrogen and methane as well as new solutions for carbon capture and storage. Among the investigated adsorbents, activated carbons are considered especially promising because they have a high specific surface area, are lightweight, thermally and chemically stable, and easy to produce. Moreover, their porosity can be tuned and they can be produced from inexpensive and environmentally friendly raw materials. This study reports on the development and characterization of activated carbons synthesized starting from amorphous cellulose with and without the inclusion of copper nanoparticles. The aim was to investigate how the presence of different concentrations of metal nanoparticles affects porosity and gas storage properties. Therefore, the research work focused on synthesis and characterization of physical and chemical properties of pristine and metal-doped activated carbons materials and on further investigation to analyze their hydrogen, methane and carbon dioxide adsorption capacity. For an optimized Cu content the microporosity is improved, resulting in a specific surface area increase of 25%, which leads to a H2 uptake (at 77 K) higher than the theoretical value predicted by the Chahine Rule. For CH4, the storage capacity is improved by the addition of Cu but less importantly because the size of the molecule hampers easy access of the smaller pores. For CO2 a 26% increase in adsorption capacity compared to pure activated carbon was achieved, which translated with an absolute value of over 48 wt% at 298 K and 15 bar of pressure.
KW - Activated carbon
KW - Carbon capture
KW - Hydrogen storage
KW - Metal doping
KW - Methane storage
KW - Microporosity
UR - http://www.scopus.com/inward/record.url?scp=85129947627&partnerID=8YFLogxK
U2 - 10.1016/j.ijhydene.2022.04.029
DO - 10.1016/j.ijhydene.2022.04.029
M3 - Article
AN - SCOPUS:85129947627
SN - 0360-3199
VL - 47
SP - 18384
EP - 18395
JO - International Journal of Hydrogen Energy
JF - International Journal of Hydrogen Energy
IS - 42
ER -