Abstract
Fossil fuels are dominant as an energy source, typically producing carbon dioxide (CO2) and enhancing global climate change. The present work reports the application of low-cost tri-sodium phosphate (TSP) to capture CO2 from model flue gas (CO2 + N-2) mixture, in a batch mode and fixed-bed setup. It is observed that TSP has a high CO2 capture capacity as well as high CO2 selectivity. At ambient temperature, TSP shows a maximum CO2 capture capacity of 198 mg CO2/g of TSP. Furthermore, the CO2 capture efficiency of TSP over a flue gas mixture was found to be more than 90%. Fresh and spent materials were characterized using powder X-ray diffraction (PXRD), scanning electron microscopy (SEM), and Fourier transformed infrared spectroscopy (FTIR). Preliminary experiments were also conducted to evaluate the performance of regenerated TSP. The spent TSP was regenerated using sodium hydroxide (NaOH) and its recyclability was tested for three consecutive cycles. A conceptual prototype for post-combustion CO2 capture based on TSP material has also been discussed.
Original language | English |
---|---|
Article number | 2889 |
Number of pages | 16 |
Journal | Energies |
Volume | 12 |
Issue number | 15 |
DOIs | |
Publication status | Published - 1 Aug 2019 |
Cite this
}
Carbon Dioxide Capture from Flue Gas Using Tri-Sodium Phosphate as an Effective Sorbent. / Sakpal, Tushar; Kumar, Asheesh; Aman, Zachary M.; Kumar, Rajnish.
In: Energies, Vol. 12, No. 15, 2889, 01.08.2019.Research output: Contribution to journal › Article
TY - JOUR
T1 - Carbon Dioxide Capture from Flue Gas Using Tri-Sodium Phosphate as an Effective Sorbent
AU - Sakpal, Tushar
AU - Kumar, Asheesh
AU - Aman, Zachary M.
AU - Kumar, Rajnish
PY - 2019/8/1
Y1 - 2019/8/1
N2 - Fossil fuels are dominant as an energy source, typically producing carbon dioxide (CO2) and enhancing global climate change. The present work reports the application of low-cost tri-sodium phosphate (TSP) to capture CO2 from model flue gas (CO2 + N-2) mixture, in a batch mode and fixed-bed setup. It is observed that TSP has a high CO2 capture capacity as well as high CO2 selectivity. At ambient temperature, TSP shows a maximum CO2 capture capacity of 198 mg CO2/g of TSP. Furthermore, the CO2 capture efficiency of TSP over a flue gas mixture was found to be more than 90%. Fresh and spent materials were characterized using powder X-ray diffraction (PXRD), scanning electron microscopy (SEM), and Fourier transformed infrared spectroscopy (FTIR). Preliminary experiments were also conducted to evaluate the performance of regenerated TSP. The spent TSP was regenerated using sodium hydroxide (NaOH) and its recyclability was tested for three consecutive cycles. A conceptual prototype for post-combustion CO2 capture based on TSP material has also been discussed.
AB - Fossil fuels are dominant as an energy source, typically producing carbon dioxide (CO2) and enhancing global climate change. The present work reports the application of low-cost tri-sodium phosphate (TSP) to capture CO2 from model flue gas (CO2 + N-2) mixture, in a batch mode and fixed-bed setup. It is observed that TSP has a high CO2 capture capacity as well as high CO2 selectivity. At ambient temperature, TSP shows a maximum CO2 capture capacity of 198 mg CO2/g of TSP. Furthermore, the CO2 capture efficiency of TSP over a flue gas mixture was found to be more than 90%. Fresh and spent materials were characterized using powder X-ray diffraction (PXRD), scanning electron microscopy (SEM), and Fourier transformed infrared spectroscopy (FTIR). Preliminary experiments were also conducted to evaluate the performance of regenerated TSP. The spent TSP was regenerated using sodium hydroxide (NaOH) and its recyclability was tested for three consecutive cycles. A conceptual prototype for post-combustion CO2 capture based on TSP material has also been discussed.
KW - CO2 capture
KW - tri-sodium phosphate
KW - inorganic sorbent
KW - gas separation
KW - flue gas mixture
KW - POSTCOMBUSTION CO2 CAPTURE
KW - MESOPOROUS MOLECULAR-SIEVE
KW - ADSORPTION
KW - SILICA
KW - ADSORBENTS
KW - SOLUBILITY
KW - SEPARATION
KW - CAPACITY
KW - MCM-48
U2 - 10.3390/en12152889
DO - 10.3390/en12152889
M3 - Article
VL - 12
JO - Energies
JF - Energies
SN - 1996-1073
IS - 15
M1 - 2889
ER -