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|Title:||Room temperature synthesis of diphenylmethane over MCM-41 supported AlCl3 and other Lewis acids||Authors:||Hu, X.
|Issue Date:||3-Sep-2001||Citation:||Hu, X., Chuah, G.K., Jaenicke, S. (2001-09-03). Room temperature synthesis of diphenylmethane over MCM-41 supported AlCl3 and other Lewis acids. Applied Catalysis A: General 217 (1-2) : 1-9. ScholarBank@NUS Repository. https://doi.org/10.1016/S0926-860X(01)00574-9||Abstract:||The catalytic properties of MCM-41 activated with AlCl3, ZnCl2 and other Lewis acids, such as FeCl3, NiCl2 and CuCl2 were investigated for room temperature Friedel-Crafts benzylation in the liquid phase. The catalysts were studied under batch-wise as well as continuous operation conditions. AlCl3/MCM-41 showed higher activity than ZnCl2/MCM-41, while FeCl3/MCM-41, CuCl2/MCM-41 and NiCl2/MCM-41 were inactive under identical conditions. ZnCl2 offered some advantages due to reduced hydrolytic sensitivity and better selectivity. The optimized ZnCl2 loading of ZnCl2/MCM-41 was 4 mmol g-1. For AlCl3/MCM-41, the pore size of MCM-41 did not affect the activity nor the selectivity in the benzylation of benzene. Very low selectivity was observed in the benzylation of substituted aromatics using AlCl3/MCM-41 as catalyst due to a tendency for migration or transfer of the substituent group. With its inherently lower activity, ZnCl2/MCM-41 did not catalyze this reaction. In a continuous trickle bed reactor, sustained activity of the AlCl3/MCM-41 catalyst could be demonstrated. Hence, MCM-41 supported with AlCl3 or ZnCl2 may be promising candidates to replace AlCl3 in the industrial manufacture of diphenylmethanes. © 2001 Elsevier Science B.V.||Source Title:||Applied Catalysis A: General||URI:||http://scholarbank.nus.edu.sg/handle/10635/94733||ISSN:||0926860X||DOI:||10.1016/S0926-860X(01)00574-9|
|Appears in Collections:||Staff Publications|
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