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Received May 12, 2016
Accepted June 30, 2016
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CO2 decomposition using metal ferrites prepared by co-precipitation method
Department of Environmental Engineering, Kyung Hee University, Yongin-si, Gyeonggi 17104, Korea 1Green Process and Material R&D Group, KITECH, Chungcheongnam-do 31056, Korea
Korean Journal of Chemical Engineering, November 2016, 33(11), 3162-3168(7), 10.1007/s11814-016-0192-5
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Abstract
To catalytically decompose the greenhouse gas, CO2, spinel structure M-ferrites (M=Co, Ni, Cu, Zn) were synthesized by chemical co-precipitation using metal salts and sodium hydroxide as starting materials. The crystallite size of the newly-prepared M-ferrites increased and the BET surface area decreased with increasing calcination temperature. A thermal analysis of the reduction and reoxidation of M-ferrites indicated that substitution of divalent transition metals (i.e., Cu, Ni and Co) into Fe3O4 improved the reduction kinetics in the order of Cu>Ni>Co. ZnFe2O4 was the most difficult compound to completely reduce due to its stable structure. Commercial samples of the reduced Fe3O4, CoFe2O4 and ZnFe2O4 showed an increase in mass through the reoxidation process, but it was much more difficult for oxygen atoms to enter the structure of the reduced samples of NiFe2O4 and CuFe2O4. The M-ferrites in a batch type reactor showed better efficiency than the commercial Fe3O4. Also found was that CoFe2O4 showed a high regeneration potential, although it required a higher critical reaction temperature. NiFe2O4 and CuFe2O4 were excellent candidate materials for CO2 decomposition at lower temperatures.
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Lv WZ, Liu B, Luo ZK, Ren XZ, Zhang PX, J. Alloy. Compd., 465, 261 (2008)
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Hwang CS, Wang NC, Mater. Chem. Phys., 88(2-3), 258 (2004)
Kobayashi M, Shirai H, Nunokawa M, Ind. Eng. Chem. Res., 39(6), 1934 (2000)
Khedr MH, Omar AA, Abdel-Moaty SA, Colloids Surf. A: Physicochem. Eng. Asp., 281, 8 (2006)
Ma LJ, Chen LS, Chen SY, Solid State Sci., 11, 176 (2009)
Tamaura Y, Tahata M, Nature, 346, 255 (1990)
Kodama T, Tabata M, Tominaga K, Yoshida T, Tamaura Y, J. Mater. Sci., 28, 547 (1993)
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Kato H, Kodama T, Tsuji M, Tamaura Y, Chang SG, J. Mater. Sci., 28, 5689 (1994)
Chen LS, Chen SY, Lu GL, J. Mater. Sci., 41(19), 6465 (2006)
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Shen JW, Lim YH, Jo YM, Appl. Chem. Eng., 22(2), 185 (2011)
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Lv WZ, Liu B, Luo ZK, Ren XZ, Zhang PX, J. Alloy. Compd., 465, 261 (2008)
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Hwang CS, Wang NC, Mater. Chem. Phys., 88(2-3), 258 (2004)
Kobayashi M, Shirai H, Nunokawa M, Ind. Eng. Chem. Res., 39(6), 1934 (2000)
Khedr MH, Omar AA, Abdel-Moaty SA, Colloids Surf. A: Physicochem. Eng. Asp., 281, 8 (2006)
Ma LJ, Chen LS, Chen SY, Sol. State Sci, 11, 176 (2009)
Sacco A, Reid RC, Carbon, 17, 459 (1979)
Tamaura T, Tahata M, Nature, 346, 255 (1990)
Kodama T, Tabata M, Tominaga K, Yoshida T, Tamaura Y, J. Mater. Sci., 28, 547 (1993)
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Kato H, Kodama T, Tsuji M, Tamaura Y, Chang SG, J. Mater. Sci., 29(21), 5689 (1994)
Chen LS, Chen SY, Lu GL, J. Mater. Sci., 41(19), 6465 (2006)
Ma LJ, Chen LS, Chen SY, J. Phys. Chem. Solids, 68, 6459 (2007)
Shen JW, Lim YH, Jo YM, Appl. Chem. Eng., 22(2), 185 (2011)
Khedr MH, Omar AA, Abdel-Moaty SA, Colloids Surf. A: Physicochem. Eng. Asp., 281, 8 (2006)
Lv WZ, Liu B, Luo ZK, Ren XZ, Zhang PX, J. Alloy. Compd., 465, 261 (2008)
Ko JH, Park RS, Jeon JK, Kim DH, Jung SC, Kim SC, Park YK, J. Ind. Eng. Chem., 32, 109 (2015)
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Hwang CS, Wang NC, Mater. Chem. Phys., 88(2-3), 258 (2004)
Kobayashi M, Shirai H, Nunokawa M, Ind. Eng. Chem. Res., 39(6), 1934 (2000)
Khedr MH, Omar AA, Abdel-Moaty SA, Colloids Surf. A: Physicochem. Eng. Asp., 281, 8 (2006)
Ma LJ, Chen LS, Chen SY, Solid State Sci., 11, 176 (2009)