화학공학소재연구정보센터
Korean Chemical Engineering Research, Vol.43, No.5, 560-565, October, 2005
제올라이트 Beta, USY, Mordenite 촉매를 이용한 Methylnaphthalene의 트랜스메틸화 반응
Transmethylation of Methylnaphthalene Over Beta, USY and Mordenite Zeolite Catalysts
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초록
1-methylnaphthalene(1-MN)과 2-methylnaphthalene(2-MN) 사이에서의 트랜스메틸화 반응을 제올라이트, H-mordenite (HM), H-Beta(Hβ), H-USY(HUSY) 촉매를 이용한 고정층 반응기에서 수행하였다. Hβ25(SiO2/Al2O3=25) 촉매는 다음 과 같은 조건, 반응온도 350 oC, 반응압력 1.5Mpa, 전체 액상 반응물의 WHSV 2.7gfeed /gcat · h, 반응물 1-MN과 2-MN 의 몰비 1:1, 반응 1시간에서 2-MN/1-MN 비=2.3와 2,6-DMN/2,7-DMN 비=1.3을 보이면서 다른 촉매보다 높은 전환 율과 안정성을 나타내었다. 촉매의 세공구조, 산성도와 관련하여 촉매성능을 해석하였다.
Catalytic performances of zeolite catalysts such as H-mordenite(HM), H-Beta(Hβ), H-USY(HUSY) for the transmethylation between 1-methylnaphthalene(1-MN) and 2-methylnaphthalene(2-MN) were investigated in a fixed-bed flow reactor. Hβ showed higher and more stable conversion than others to exhibit a high and stable 2-MN/1-MN ratio of 2.3 and 2,6-DMN/2,7-DMN ratio of 1.3 at the 1st hour of time on stream under the reaction conditions as follows: reaction temperature of 350 oC, reaction pressure of 1.5 MPa, WHSV of 2.7 gfeed /gcat·h and the molar ratio of 1-MN and 2-MN of 1:1. The catalytic behavior has been discussed in relation with the catalyst pore structure and acidity.
  1. Song C, Schobert HH, Fuel Process. Technol., 34(2), 157 (1993) 
  2. Inui T, Pu SB, Sep. Technol., 5(4), 229 (1995) 
  3. Tanabe K, Holderich WF, Appl. Catal. A: Gen., 181(2), 399 (1999) 
  4. Hagen GP, Hung DT, "Selective Production of 2,6-dimethylnaphthalene", U.S. Patent No. 5,670,704 (1997)
  5. Pu SB, Inui T, Appl. Catal. A: Gen., 146(2), 305 (1996) 
  6. Fraenkel D, Cherniavsky M, Ittah B, Levy M, J. Catal., 101(2), 273 (1986) 
  7. Komatsu T, Araki Y, Namba S, Yashima T, Stud. Surf. Sci. Catal., 84(1), 1821 (1994)
  8. Inui T, Pu SB, Kugai JI, Appl. Catal. A: Gen., 146(2), 285 (1996) 
  9. Park JN, Wang J, Lee CW, Park SE, Bull. Korean Chem. Soc., 23(7), 1011 (2002)
  10. Pazzuconi G, Terzoni G, Perego C, Bellussi G, Stud. Surf. Sci. Catal., 135(1) (2001)
  11. Tsutsui T, Ijichi K, Inomata T, Setiadi, Kojima T, Sato K, Chem. Eng. Sci., 59(19), 3993 (2004) 
  12. Weitkamp J, Neuber M, Stud. Surf. Sci. Catal., 60(1), 291 (1991)
  13. Park JN, Wang J, Kim HY, Lee JK, Lee CW, "Gas Phase Methylation of 2-Methylnaphthalene by 1,2,4-Trimethylbenzene/Methanol Over Various Zeolitic Catalysts", Prog. Catal. Res., Chapter 3, Nova Science Publisher (2005)
  14. Park JN, Wang J, Hong SI, Lee CW, Appl. Catal. A: Gen., 292(1), 68 (2005)
  15. Santilli DS, Chen CY, "Method of Making 2,6-dimethylnaphthalene from Other Dimethylnaphthalene Isomers and from Dimethyltetralins/Dimethyldecalins with a Methyl Group on Each Ring", U.S. patent No. 6,015,930 (2000)
  16. Chen T, Kang NY, Lee CW, Kim HY, Hong SB, Roh HD, Park YK, Catal. Today, 93(1), 371 (2004) 
  17. Motoyuki M, Yamamoto K, Sapre AV, Williams JPM, Donnelly SP, "Process for Preparing 2,6-dialkylnaphthalene", U.S. Patent No. 6,121,501 (2000)