About: Selective synthesis of linear alkylbenzene by alkylation of benzene with 1-dodecene over desilicated zeolites     Goto   Sponge   NotDistinct   Permalink

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  • 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).
  • 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). (en)
Title
  • Selective synthesis of linear alkylbenzene by alkylation of benzene with 1-dodecene over desilicated zeolites
  • Selective synthesis of linear alkylbenzene by alkylation of benzene with 1-dodecene over desilicated zeolites (en)
skos:prefLabel
  • Selective synthesis of linear alkylbenzene by alkylation of benzene with 1-dodecene over desilicated zeolites
  • Selective synthesis of linear alkylbenzene by alkylation of benzene with 1-dodecene over desilicated zeolites (en)
skos:notation
  • RIV/61388955:_____/14:00427874!RIV15-GA0-61388955
http://linked.open...avai/riv/aktivita
http://linked.open...avai/riv/aktivity
  • I, P(GBP106/12/G015)
http://linked.open...iv/cisloPeriodika
  • MAY 2014
http://linked.open...vai/riv/dodaniDat
http://linked.open...aciTvurceVysledku
http://linked.open.../riv/druhVysledku
http://linked.open...iv/duvernostUdaju
http://linked.open...titaPredkladatele
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  • 44302
http://linked.open...ai/riv/idVysledku
  • RIV/61388955:_____/14:00427874
http://linked.open...riv/jazykVysledku
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  • zeolites; benzene alkylation; long-chain olefin (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • NL - Nizozemsko
http://linked.open...ontrolniKodProRIV
  • [8B3D40570EC4]
http://linked.open...i/riv/nazevZdroje
  • Catalysis Today
http://linked.open...in/vavai/riv/obor
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http://linked.open...vavai/riv/projekt
http://linked.open...UplatneniVysledku
http://linked.open...v/svazekPeriodika
  • 227
http://linked.open...iv/tvurceVysledku
  • Aitani, A.
  • Al-Khattaf, S.
  • Čejka, Jiří
  • Aslam, W.
  • Jermy, B. R.
  • Siddiqui, M. A. B.
http://linked.open...ain/vavai/riv/wos
  • 000332412900026
issn
  • 0920-5861
number of pages
http://bibframe.org/vocab/doi
  • 10.1016/j.cattod.2013.10.015
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