화학공학소재연구정보센터
Korean Journal of Chemical Engineering, Vol.33, No.12, 3417-3424, December, 2016
Production of butene and butadiene by oxidative dehydrogenation of butane over carbon nanomaterial catalysts
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C4 alkenes are generally used to produce synthetic rubbers, plastics, and other important chemicals. Transition metal oxides are traditionally used as catalysts to produce C4 alkenes from n-butane by oxidative dehydrogenation (ODH). On the other hand, metal-free carbon nanomaterials are receiving much attention as catalysts for ODH due to their environmental benignity, corrosion resistance, and unique surface properties. In this work, a systematic methodology was designed to measure conversion of the reactants, selectivity to main products, and other catalytic performances of a set of carbon catalysts, including graphite and activated carbon. The experiments were carried out under a wide range of reaction conditions, and the reaction mechanism and kinetics were developed based on Marsvan Krevelen interpretation of the experimental results.
  1. Makshina EV, Dusselier M, Janssens W, Degreve J, Jacobs PA, Sels BF, Chem. Soc. Rev., 43, 7917 (2014)
  2. Yoshimura Y, Kijima N, Hayakawa T, Murata K, Suzuki K, Mizukami F, Shiojima T, Catal. Surv. Jpn, 4, 157 (2001)
  3. Worrell E, Price L, Neelis M, Galitsky C, Zhou N, World best practice energy intensity values for selected industrial sectors, Lawrence Berkeley National Laboratory (2007).
  4. Lim H, Choi J, Realff M, Lee JH, Park S, Ind. Eng. Chem. Res., 45(16), 5738 (2006)
  5. James DH, Castor WM, Styrene, Ullmann’s Encyclopedia of Industrial Chemistry (1994).
  6. Bhasin MM, McCain JH, Vora BV, Imai T, Pujado PR, Appl. Catal. A: Gen., 221(1-2), 397 (2001)
  7. Gascon J, Tellez C, Herguido J, Menendez M, Appl. Catal. A: Gen., 248(1-2), 105 (2003)
  8. Setnicka M, Cicmanec P, Tvaruzkova E, Bulanek R, Top. Catal., 56, 662 (2013)
  9. Weyten H, Keizer K, Kinoo A, Luyten J, Leysen R, AIChE J., 43(7), 1819 (1997)
  10. Batist PA, Bouwens JFH, Schuit GCA, Bouwens JFH, Schuit GCA, J. Catal., 25, 1 (1972)
  11. Vajda S, Pellin MJ, Greeley JP, Marshall CL, Curtiss LA, Ballentine GA, Elam JW, Catillon-Mucherie S, Redfern PC, Mehmood F, Zapol P, Nat. Mater., 8(3), 213 (2009)
  12. Batist PA, Kinderen AHWM, Leeuwenburgh Y, Metz FA, Schuit GCA, J. Catal., 12, 45 (1968)
  13. Park JH, Noh H, Park JW, Row K, Jung KD, Shin CH, Appl. Catal. A: Gen., 431, 137 (2012)
  14. Schraut A, Emig G, Sockel HG, Appl. Catal., 29, 311 (1987)
  15. Zhang J, Liu X, Blume R, Zhang A, Schlogl R, Su DS, Science, 322, 73 (2008)
  16. Pereira MFR, Figueiredo JL, Orfao JJ, Serp P, Kalck P, Kihn Y, Carbon, 42, 2807 (2004)
  17. Pereira MFR, Orfao JJM, Figueiredo JL, Appl. Catal. A: Gen., 196(1), 43 (2000)
  18. Mars P, Van Krevelen DW, Chem. Eng. Sci., 3, 41 (1954)
  19. Yang CN, Rev. Mod. Phys., 34, 694 (1962)
  20. Schwaab M, Pinto JC, Chem. Eng. Sci., 62(10), 2750 (2007)