Abstract
The porous alumina catalysts with different acidity were prepared and tested for dehydrofluorination of 1,1,1,2-tetrafluoroethane to synthesize trifluoroethylene. The XRD, BET, SEM, NH3-TPD and py-IR techniques were used to characterize the alumina catalysts with different calcination temperatures. The porous θ-Al2O3 showed the excellent catalytic performance, with 35.1 % conversion and the selectivity to trifluoroethylene of 99.0 %. The active sites of catalysts for formation of trifluoroethylene are appropriate weak Lewis acid sites, and the strong Lewis acid sites may result in its rapid deactivation, due to the coke or polymerization of trifluoroethylene.
Graphical Abstract
Dehydrofluorination of 1,1,1,2-tetrafluoroethane (CF3CFH2) is a promising route to synthesize trifluoroethylene over θ-Al2O3, the conversion is 35.1 % and the selectivity to trifluoroethylene is 99 % at 450 °C. It was suggested that appropriate number of weak Lewis acid sites was beneficial to the catalysis for dehydrofluorination of CF3CFH2, the weak Lewis acid sites as the active sites of synthesis of trifluoroethylene. On the other hand, the strong Lewis acid sites easily result in deactivation of catalysts derived from the coke or polymerization of trifluoroethylene.
Similar content being viewed by others
References
Meng BC, Sun ZY, Ma JP, Cao GP, Yuan WK (2010) Catal Lett 138:68
Ohnishi R, Wang WL, Ichikawa M (1994) Appl Catal A General 113:29
Scott SP, Sweetman M, Thomson J, Fitzgerald AG, Sturrocky EJ (1997) J Catal 168:501
Ueda W, Tomioka S, Morinkawa Y, Sudo M, Ikawa T (1990) Chem Lett 19:879
Shekar SC, Venugopal A, Rama Rao KS, Sai Prasad PS, Srinivas R, Kanta Rao P (1998) Stud Surf Sci Catal 113:391
Mori T, Yasuoka T, Morikawa Y (2004) Catal Today 88:111
Liu ZT, Liu L, Wu J, Lu J, Sun P, Song LP, Liu ZW, Dong WS, Gao ZW (2007) Ind Eng Chem Res 46:22
Shine KP, Sturges WT (2007) Science 315:1804
Henne S, Shallcross DE, Reimann S, Xiao P, Brunner D, O’Doherty S, Buchmann B (2012) Environ Sci Technol 46:1650
Qin LB, Han J, Liu L, Yang XL, Kim HJ, Yu F (2013) Fresenius Environ Bull 22:1919
Huang CQ, Yang B, Yang R, Wei LX, Wang SS, Shan XB, Oi F, Zhang YW, Sheng LS, Hao LQ, Zhou SK, Wang ZY (2005) Chem J Chin Univ 26:2314
Wu XY, Cong PH, Nanao H, Kobayashi K, Mori S (2002) Langmuir 18:10122
Wu XY, Cong PH, Mori S (2002) Appl Surf Sci 201:115
Cong PH, Imai J, Mori S (2001) Wear 24:143
Li GL, Nishiguchi H, Ishihara T, Moro-oka Y, Takita Y (1998) Appl Catal B Environ 16:309
Li GL, Ishihara T, Nishiguchi H, Moro-oka Y, Takita Y (1996) Chem Lett 7:507
Okazaki S, Toyota S (1972) Nikkashi 1615
Sirlibaev TS, Akramkhodzhaev A, Usmanov KU (1985) J Appl Chem USSR 58:1541
Tojo M, Fukuoka S, Tsukube H (2011) Bull Chem Soc Japan 84:333
Teinz K, Wuttke S, Börno F, Eicher J, Kemnitz E (2011) J Catal 282:175
Busca G (2014) Catal Today 226:2
Jia WZ, Jin LY, Wang YJ, Lu JQ, Luo MF (2011) J Ind Eng Chem 17:615
Sung DM, Ha Kim Y, Park ED, Yie JE (2010) Res Chem Intermed 36:653
Kuo J, Bourell DL (1997) J Mater Sci 32:2687
Du XL, Wang YQ, Su XH, Li JG (2009) Powder Technol 192:40
Morterra C, Magnacca G (1996) Catal Today 27:497
Ramis G, Yi L, Busca G (1996) Catal Today 28:373
Busca G (1999) Phys Chem Chem Phys 1:723
Sharanda LF, Shimansky AP, Kulik TV, Chuiko AA (1995) Colloids Surf 105:167
Carre S, Tapin B, Gnep NS, Revel R, Magnoux P (2010) Appl Catal A 372:26
Weingarten R, Tompsett GA, Conner JWC, Huber GW (2011) J Catal 279:174
Digne M, Sautet P, Raybaud P, Euzen P, Toulhoat H (2002) J Catal 211:1
Satsuma A, Kamiya Y, Westi Y, Hattori T (2000) Appl Catal A General 194:253
Dambournet D, Eltanamy G, Vimont A, Lavalley JC, Goupil JM, Demourgues A, Durand E, Majimel J, Rudiger S, Kemnitz E, Winfield JM, Tressaud A (2008) Chem Eur J 14:6205
Neely BD, Carmichael H (1973) J Phys Chem 77:307
Noble B, Carmichael H, Bumgardner CL (1972) J Phys Chem 76:1680
Dumesic JA, Fripiat JJ (1997) Top Catal 4:1
Schekler-Nahama F, Clause O, Commereuc D, Saussey J (1998) Appl Catal A General 167:237
Ishida S, Imamura S, Ren F, Tatematsu Y, Fujimura Y (1992) React Kinet Catal Lett 46:199
Bi QY, Qian L, Xing LQ, Tao LP, Lu JQ, Luo MF (2009) J Fluorine Chem 130:528
Macias O, Largo J, Pesquera C, Blanco C, González F (2006) Appl Catal A General 314:23
Acknowledgments
This work was financially supported by Shanghai Key Basic Research (Grant No. 11JC1412500), CNPC Inovation Research Funds (2012D-5006-0505) and National Natural Science Foundation of China (51174277).
Author information
Authors and Affiliations
Corresponding author
Electronic supplementary material
Below is the link to the electronic supplementary material.
Rights and permissions
About this article
Cite this article
Jia, W., Wu, Q., Lang, X. et al. Influence of Lewis Acidity on Catalytic Activity of the Porous Alumina for Dehydrofluorination of 1,1,1,2-Tetrafluoroethane to Trifluoroethylene. Catal Lett 145, 654–661 (2015). https://doi.org/10.1007/s10562-014-1409-z
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s10562-014-1409-z