Selective synthesis of linear alkylbenzene by alkylation of benzene with 1-dodecene over desilicated zeolites

0427874 - ÚFCH JH 2015 RIV NL eng J - Článek v odborném periodiku
Aslam, W. - Siddiqui, M. A. B. - Jermy, B. R. - Aitani, A. - Čejka, Jiří - Al-Khattaf, S.
Selective synthesis of linear alkylbenzene by alkylation of benzene with 1-dodecene over desilicated zeolites.
Catalysis Today. Roč. 227, MAY 2014 (2014), s. 187-197. ISSN 0920-5861. E-ISSN 1873-4308
Grant CEP: GA ČR GBP106/12/G015
Institucionální podpora: RVO:61388955
Klíčová slova: zeolites * benzene alkylation * long-chain olefin
Kód oboru RIV: CF - Fyzikální chemie a teoretická chemie
Impakt faktor: 3.893, rok: 2014

The alkylation of benzene with 1-dodecene to linear alkylbenzenes (LAB) was investigated over 12-ring zeolites MOR, BEA, and FAU with varying framework topologies and Si/Alratios. The reaction was carried out under a high-pressure, 20 bar, in a fixed-bed flow reactor at 140 degrees C, using WHSV 4 h-1, benzene/1 dodecene molar ratio of 6.0 and time-on-stream of 6.0 h. In contrast to MOR and BEA zeolites, FAU exhibited the lowest selectivity (24%) to the desired 2-phenyl dodecane (2-LAB) due to its large cavities. The MOR and BEA with different Si/Alratios were further desilicated using alkali-metal treatments (0.2 M and 0.05 M NaOH) to create hierarchical porous structure. The desilication of both zeolites improved the conversion of 1-dodecene and the selectivity to 2-LAB. The excellent stability resulting from desilication is attributed to a better diffusivity of the LAB isomers, shortening of real contact time, due to the enhanced mesporous structure in both zeolites and the higher Lewis acidity. The selectivity to 2-LAB increased to 70% over desilicated MOR (Si/Al ratio = 20) compared with a selectivity of 35% over desilicated BEA (Si/Al ratio = 24).
Trvalý link: http://hdl.handle.net/11104/0233319