TY - JOUR
T1 - Chemically activated microporous carbons derived from petroleum coke
T2 - Performance evaluation for CF4 adsorption
AU - Yuan, Xiang Zhou
AU - Choi, Seung Wan
AU - Jang, Eunji
AU - Lee, Ki Bong
N1 - Funding Information:
This work was supported by the R&D Center for Reduction of Non-CO 2 Greenhouse Gases (2013001690013) as the Global Top Environment R&D Program and by the “Public Technology Program based on Environment Policy” (Grant number E416-00070-0604-0). Both programs were funded by the Korean Ministry of Environment (MOE).
Publisher Copyright:
© 2017 Elsevier B.V.
PY - 2018/3/15
Y1 - 2018/3/15
N2 - CF4 is considered to be a significant global-warming compound and has a fairly long atmospheric lifetime, which exacerbates climate change. Adsorption is considered a promising technology for capturing CF4 and appropriate adsorbent is one of key factors for successful development of adsorption method. In this study, CF4 adsorption using microporous carbon materials was investigated from both equilibrium and kinetic perspectives. Petroleum coke (PC) was utilized for developing CF4 adsorbents by carbonization and KOH-activation processes. The carbonization temperature and KOH/PC mass ratio were varied from 300 to 600 °C and from 1 to 3, respectively. Varying the carbonization temperature and KOH/PC mass ratio had a dramatic effect on the textual properties of the prepared samples. CF4 adsorption was well fitted by the Langmuir isotherm model, and the CF4 uptake was remarkably dominated by the surface area and pore volume of narrow micropores below 0.8 nm in diameter. The experimental CF4 adsorption data were well described by the pseudo-second-order kinetic model, compared with the Elovich and intra-particle-diffusion models, and CF4 adsorption appeared to be mainly controlled by physisorption. The PC450-K2 adsorbent, prepared using a carbonization temperature of 450 °C and a KOH/PC mass ratio of 2, exhibited the highest CF4 adsorption uptake of 2.79 mol kg−1 at 25 °C and 1 atm, in addition to good CF4/N2 selectivity at relatively low CF4 pressures, excellent recyclability, easy regeneration, and rapid adsorption-desorption kinetics.
AB - CF4 is considered to be a significant global-warming compound and has a fairly long atmospheric lifetime, which exacerbates climate change. Adsorption is considered a promising technology for capturing CF4 and appropriate adsorbent is one of key factors for successful development of adsorption method. In this study, CF4 adsorption using microporous carbon materials was investigated from both equilibrium and kinetic perspectives. Petroleum coke (PC) was utilized for developing CF4 adsorbents by carbonization and KOH-activation processes. The carbonization temperature and KOH/PC mass ratio were varied from 300 to 600 °C and from 1 to 3, respectively. Varying the carbonization temperature and KOH/PC mass ratio had a dramatic effect on the textual properties of the prepared samples. CF4 adsorption was well fitted by the Langmuir isotherm model, and the CF4 uptake was remarkably dominated by the surface area and pore volume of narrow micropores below 0.8 nm in diameter. The experimental CF4 adsorption data were well described by the pseudo-second-order kinetic model, compared with the Elovich and intra-particle-diffusion models, and CF4 adsorption appeared to be mainly controlled by physisorption. The PC450-K2 adsorbent, prepared using a carbonization temperature of 450 °C and a KOH/PC mass ratio of 2, exhibited the highest CF4 adsorption uptake of 2.79 mol kg−1 at 25 °C and 1 atm, in addition to good CF4/N2 selectivity at relatively low CF4 pressures, excellent recyclability, easy regeneration, and rapid adsorption-desorption kinetics.
KW - CF adsorption
KW - KOH activation
KW - Kinetics
KW - Microporous carbon
KW - Petroleum coke
UR - http://www.scopus.com/inward/record.url?scp=85037547216&partnerID=8YFLogxK
U2 - 10.1016/j.cej.2017.11.168
DO - 10.1016/j.cej.2017.11.168
M3 - Article
AN - SCOPUS:85037547216
VL - 336
SP - 297
EP - 305
JO - Chemical Engineering Journal
JF - Chemical Engineering Journal
SN - 1385-8947
ER -
