화학공학소재연구정보센터
Journal of Industrial and Engineering Chemistry, Vol.21, 1077-1088, January, 2015
Influence of toluene-tetramethylbenzene transalkylation on heavy aromatics conversion to xylenes
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Transalkylation of toluene.tetramethylbenzene (TeMB) over MOR and BEA was investigated at 250-400 ℃. Conversion of TeMB was higher than trimethylbenzene (TMB) and toluene. Xylene yield was in the following order: [toluene - TMB - TeMB]>[toluene - TeMB]>[toluene - TMB]≫[toluene]. Kinetic modeling for reaction network consisting of toluene.TeMB transalkylation; toluene disproportionation; and toluene-TMB transalkylation was carried out. Toluene-TeMB transalkylation rate was >50% higher than the toluene-TMB transalkylation while the toluene disproportionation was an order of magnitude slower than transalkylation reactions. An addition of 5-10 wt.% TeMBs to the heavy reformate caused minor impact on the xylene yield but an improvement in xylene selectivity.
  1. Tsai TC, Liu S, Wang I, Catal. Surv. Asia, 13, 94 (2009)
  2. Tsai TC, Chen WH, Liu SB, Tsai CH, Wang I, Catal. Today, 73(1-2), 39 (2002)
  3. Dave D, New routes to styrene and paraxylene, in: IHS Chemical Process Economics Program, PEP Report 289, IHS, 2013.
  4. Ali SA, Ali MA, Al-Nawad K, Ercan C, Wang Y, Appl. Catal. A: Gen., 393(1-2), 96 (2011)
  5. Serra JM, Guillon E, Corma A, J. Catal., 232(2), 342 (2005)
  6. Oh SH, Lee SI, Seong KH, Kim YS, Lee JH, Woltermann J, Cormier WE, Chu YF, Stud. Surf. Sci. Catal., 145, 487 (2003)
  7. Krejci A, Al-Khattaf S, Ali MA, Bejblova M, Cejka J, Appl. Catal. A: Gen., 377(1-2), 99 (2010)
  8. Lee YK, Park SH, Rhee HK, Catal. Today, 44(1-4), 223 (1998)
  9. Wang I, Tsai TC, Huang ST, Ind. Eng. Chem. Res., 29, 2005 (1990)
  10. Tsai TC, Liu SB, Wang IK, Appl. Catal. A: Gen., 181(2), 355 (1999)
  11. Waziri SM, Aitani AM, Al-Khattaf S, Ind. Eng. Chem. Res., 49(14), 6376 (2010)
  12. Das J, Bhat YS, Bhardwaj AI, Halgeri AB, Appl. Catal. A: Gen., 116(1-2), 71 (1994)
  13. Cejka J, Krejci A, Stud. Surf. Sci. Catal., 130, 2627 (2000)
  14. Ali SA, Ogunronbi KE, Al-Khattaf SS, Chem. Eng. Res. Des., 91(12), 2601 (2013)
  15. Corma A, Costa-Vaya VI, Diaz-Cabanas MJ, Llopis FJ, J. Catal., 207(1), 46 (2002)
  16. Park SH, Rhee HK, Catal. Today, 63(2-4), 267 (2000)
  17. Al-Khattaf S, Tukur NM, Al-Amer A, Ind. Eng. Chem. Res., 46(13), 4459 (2007)
  18. de Lasa HI, Riser simulator, in: U.S. Patent No. 5,102,628A, 1992.
  19. Hastings SH, Nicholson DE, J. Chem. Eng. Data, 6, 1 (1961)
  20. Al-Mubaiyedh UA, Ali SA, Al-Khattaf SS, Chem. Eng. Res. Des., 90(11), 1943 (2012)
  21. Lonyi F, Valyon J, Microporous Mesoporous Mater., 47, 293 (2001)
  22. Ungureanu A, Hoang TV, On DT, Dumitriu E, Kaliaguine S, Appl. Catal. A: Gen., 294(1), 92 (2005)
  23. Al-Khattaf S, Tukur NM, Al-Amer A, Ind. Eng. Chem. Res., 46(13), 4459 (2007)
  24. Xu OG, Su HY, Ji JB, Jin XM, Chu J, Chin. J. Chem. Eng., 15(3), 326 (2007)
  25. Toch K, Thybaut JW, Vandegehuchte BD, Narasimhan CSL, Domokos L, Marin GB, Appl. Catal. A: Gen., 425-426, 130 (2012)
  26. Bhavikatti SS, Patwardhan SR, Ind. Eng. Chem. Prod. Res. Dev., 20, 106 (1981)
  27. Chang JR, Sheu FC, Cheng YM, Wu JC, Appl. Catal., 33, 39 (1987)