Issue
Korean Journal of Chemical Engineering,
Vol.32, No.1, 51-61, 2015
Development of the Al2O3-supported NaNO3-Na2Mg(CO3)2 sorbent for CO2 capture with facilitated sorption kinetics at intermediate temperatures
For the development of a dry solid sorbent having quite fast CO2 sorption kinetics in an intermediate temperature range of 245-300 ℃ to be applicable to a riser-type fluidized bed carbonator, samples of Al2O3-supported MgCO3 (1.2mmol/g) promoted with different molar amounts of Na2CO3 (1.2, 1.8mmol/g) and/or NaNO3 (0.6mmol/g) were prepared by incipient wetness pore volume impregnation. For a reference, an unsupported bulk phase sorbent of NaNO3-Na2Mg(CO3)2 was also prepared. From the sorption reaction using a gas mixture containing CO2 by 2.5-10% at 1 bar for the sorbents after their activation to MgO, Al2O3-supported sorbents were featured by their rapid carbonation kinetics in contrast to the unsupported sorbent showing a quite slow carbonation behavior. The addition of Na2CO3 to the MgCO3/Al2O3 sorbent made MgO species more reactive for the carbonation, bringing about a markedly enhanced kinetic rate and conversion, as compared with the unpromoted MgCO3/Al2O3 sorbent having a small negligible reactivity. The addition of NaNO3 to MgCO3/Al2O3 or to Na2CO3-MgCO3/Al2O3 induced the same promotional effects, but to a lesser magnitude, as observed for the Na2CO3 addition. It was also characteristic for all these MgCO3-based sorbents that initial carbonation conversions with time appeared as sigmoid curves. For the Al2O3-supported sorbent comprised of NaNO3, Na2CO3, and MgCO3 by 0.6, 1.8, and 1.2mmols, respectively, per gram sorbent, showing the best kinetic performance, a kinetic equation capable of reflecting such sigmoid conversion behavior was established, and its applicability to a riser carbonator was examined throughout a simple model calculation based on the kinetics obtained.
[References]
  1. Samanta A, Zhao A, Shimizu GKH, Sarkar P, Gupta R, Ind. Eng. Chem. Res., 51(4), 1438, 2012
  2. Zaman M, Lee JH, Korean J. Chem. Eng., 30(8), 1497, 2013
  3. Hayashi H, Taniuchi J, Furuyashiki N, Sugiyama S, Hirano S, Shigemoto N, Nonaka T, Ind. Eng. Chem. Res., 37(1), 185, 1998
  4. Abanades JC, Anthony EJ, Lu DY, Salvador C, Alvarez D, AIChE J., 50(7), 1614, 2004
  5. Yu CH, Huang CH, Tan CS, Aerosol Air Quality Res., 12, 745, 2012
  6. Kim K, Kim D, Park YK, Lee KS, Int. J. Greenhous Gas Control, 26, 135, 2014
  7. Iijima M, Nagayasu T, Kamijyo T, Nakatani S, Mitsubishi Heavy Industries Technical Review, 48, 26, 2011
  8. Yi CK, Jo SH, Seo Y, Lee JB, Ryu CK, Int. J. Greenhouse Gas Control, 1, 31, 2007
  9. Choi JH, Yi CK, Jo SH, Korean J. Chem. Eng., 28(4), 1144, 2011
  10. Veneman R, Li ZS, Hogendoorn JA, Kersten SRA, Brilman DWF, Chem. Eng. J., 207, 18, 2012
  11. Lee DK, Min DY, Seo H, Kang NY, Choi WC, Park YK, Ind. Eng. Chem. Res., 52(26), 9323, 2013
  12. Monazam ER, Shadle LJ, Miller DC, Pennline HW, Fauth DJ, Hoffman JS, Gray ML, AIChE J., 59(3), 923, 2013
  13. Zhang K, Li XS, Duan Y, King DL, Singh P, Li L, Int. J. Greenhouse Gas Control, 12, 351, 2013
  14. Mayorga SG, Weigel SJ, Gaffney TR, Brzozowski JR, US Patent, 6,280,503 B1, 2001
  15. Bauer T, Laing D, Kroner U, Tamme R, Int. J. Thermophys., 33, 91, 2012
  16. Berg RW, Kerridge DH, Larsen PH, J. Chem. Eng. Data, 51(1), 34, 2006
  17. Zhao CW, Chen XP, Zhao CS, Ind. Eng. Chem. Res., 51(44), 14361, 2012
  18. Zhao CW, Chen XP, Zhao CS, Energy Fuels, 26(2), 1401, 2012
  19. Patience GS, Chaouki J, Berruti F, Wong SR, Powder Technol., 72, 31, 1992
  20. Geankoplis CJ, Transport processes and separation process principles, 4th Ed., Prentice Hall, U.S.A., 2003
  21. Kunii D, Levenspiel O, Fluidization Engineering, Wiley, N.Y., 1969