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Received March 9, 2017
Accepted May 24, 2017
articles This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/bync/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
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Enhanced CO methanation over Ni-based catalyst using a support with 3D-mesopores

Low Carbon Energy Institute, China University of Mining and Technology, Xuzhou 221008, China 1School of Electrical and Power Engineering, China University of Mining and Technology, Xuzhou 221116, China
clguo@cumt.edu.cn
Korean Journal of Chemical Engineering, September 2017, 34(9), 2374-2382(9), 10.1007/s11814-017-0148-4
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Abstract

Ni-based catalysts supported on a support with 3D-mesopores, including Ni/KIT-6(EG), Ni/KIT-6(PS) and Ni/KIT-6(DS), were prepared by adding ethylene glycol, direct synthesis and post synthesis methods, respectively, and their catalytic properties were investigated for CO methanation as one of the core technologies of synthetic natural gas production in a continuous flow fixed-bed reactor. The catalysts were characterized by N2 adsorption-desorption, X-ray diffraction (XRD), transmission electron microscope (TEM), energy-dispersive X-ray spectroscopy (EDS), hydrogen temperature-programmed reduction (H2-TPR), hydrogen temperature-programmed desorption (H2-TPD) and thermal gravimetric analysis (TGA), respectively. The results showed that Ni/KIT-6(EG) exhibited the best catalytic performance with CO conversion of almost 100% and CH4 yield of 75% at 450 °C, atmospheric pressure and 60,000 mL/g/h due to the higher dispersion of Ni species, stronger reducibility of NiO and formation of smaller Ni nanoparticles fixed into 3D-mesopores, indicating that adding ethylene glycol was effective to improve catalytic performance of Ni-based catalyst for CO methanation. Moreover, compared with Ni/Al2O3(EG) prepared using Al2O3 as a support, Ni/KIT- 6(EG) showed better catalytic performance owing to the higher specific surface area, stronger reducibility of NiO and confinement effect of 3D-mesopores promoting to produce more active sites. After 60h lifetime test of Ni/KIT-6(EG) at 500 °C, atmospheric pressure and 60,000mL/g/h, 3D-mesopores were still maintained and no obvious agglomeration of Ni nanoparticles was observed, meaning that Ni species were still well dispersed into 3D-mesopores. As a consequence, Ni/KIT-6(EG) exhibited superior catalytic performance and stability, which makes it a promising candidate for CO methanation.

References

Gotz M, Lefebvre J, Mors F, Koch AM, Graf F, Bajohr S, Reimert R, Kolb T, Renew. Energy, 85, 1371 (2016)
Gao J, Liu Q, Gu F, Liu B, Zhong Z, Su F, RSC Adv., 5, 22759 (2015)
Barrientos J, Lualdi M, Paris RS, Montes V, Boutonnet M, Jaras S, Appl. Catal. A: Gen., 502, 276 (2015)
Goula MA, Charisiou ND, Papageridis KN, Delimitis A, Pachatouridou E, Iliopoulou EF, Int. J. Hydrog. Energy, 40(30), 9183 (2015)
Galletti C, Specchia S, Specchia V, Chem. Eng. J., 167(2-3), 616 (2011)
Kustov AL, Frey AM, Larsen KE, Johannessen T, Norskov JK, Christensen CH, Appl. Catal. A: Gen., 320, 98 (2007)
Yao ZW, Zhang XH, Peng F, Yu H, Wang HJ, Yang JA, Int. J. Hydrog. Energy, 36(3), 1955 (2011)
Liu Q, Gu FN, Lu XP, Liu YJ, Li HF, Zhong ZY, Xu GW, Su FB, Appl. Catal. A: Gen., 488, 37 (2014)
Sehested J, Dahl S, Jacobsen J, Rostrup-Nielsen JR, J. Phys. Chem. B, 109(6), 2432 (2005)
Mok YS, Kang HC, Lee HJ, Koh DJ, Shin DN, Plasma Chem. Plasma Process., 30(4), 437 (2010)
Liu Q, Gu F, Gao J, Li H, Xu G, Su F, J. Energy Chem., 23, 761 (2014)
Zyryanova MM, Snytnikov PV, Gulyaev RV, Amosov YI, Boronin AI, Sobyanin VA, Chem. Eng. J., 238, 189 (2014)
Shinde VM, Madras G, AIChE J., 60(3), 1027 (2014)
Li XQ, Tong DM, Hu CW, J. Energy Chem., 24, 463 (2015)
Ma SL, Tan YS, Han YZ, J. Nat. Gas Chem., 20, 435 (2011)
Struis RPWJ, Schildhauer TJ, Czekaj I, Janousch M, Biollaz SMA, Ludwig C, Appl. Catal. A: Gen., 362(1-2), 121 (2009)
Li HD, Ren J, Qin X, Qin ZF, Lin JY, Li Z, RSC Adv., 5, 96504 (2015)
Liu Q, Gu F, Zhong Z, Xu G, Su F, Korean J. Chem. Eng., 33(5), 1599 (2016)
Tao M, Meng X, Lv YH, Bian ZC, Xin Z, Fuel, 165, 289 (2016)
Bian ZC, Meng X, Tao M, Lv YH, Xin Z, Fuel, 179, 193 (2016)
Zhang JY, Xin Z, Meng X, Tao M, Fuel, 109, 693 (2013)
Xie T, Shi LY, Zhang JP, Zhang DS, Chem. Commun., 50, 7250 (2014)
Kleitz F, Berube F, Guillet-Nicolas R, Yang C, Thommes M, J. Phys. Chem., 114, 9344 (2010)
Subramaniyan K, Arumugam P, J. Porous Mat., 23, 639 (2016)
He F, Luo JQ, Liu ST, Chem. Eng. J., 294, 362 (2016)
Lv XY, Chen JF, Tan YS, Zhang Y, Catal. Commun., 20, 6 (2012)
Lu BW, Kawamoto K, RSC Adv., 2, 6800 (2012)
Lu BW, Kawamoto K, Fuel, 103, 699 (2013)
Kleitz F, Choi SH, Ryoo R, Chem. Commun., 17, 2136 (2003)
Liu Q, Gao J, Zhang MJ, Li HF, Gu FN, Xu GW, Zhong ZY, Su FB, RSC Adv., 4, 16094 (2014)
Jin G, Gu F, Liu Q, Wang X, Jia L, Xu G, Zhong ZY, Su FB, RSC Adv., 6, 9631 (2016)
Sanchez-Cantu M, Perez-Diaz LM, Maubert AM, Valente JS, Catal. Today, 150(3-4), 332 (2010)
Guo CL, Wu YY, Qin HY, Zhang JL, Fuel Process. Technol., 124, 61 (2014)

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