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Nickel oligomerization catalysts heterogenized on zeolites obtained using ionic liquids as templates
Synthesis of zeolites using 1-butyl-3-methylimidazolium chloride (BMI.Cl) as a template yields highly crystalline materials after a few days reaction time. Depending on the Si/Al ratio the system crystallizes differently, giving selectively ZSM-5 or β-zeolite structures. The β-zeolite was used as su...
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Published in: | Applied catalysis. A, General General, 2010-02, Vol.374 (1), p.26-30 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Synthesis of zeolites using 1-butyl-3-methylimidazolium chloride (BMI.Cl) as a template yields highly crystalline materials after a few days reaction time. Depending on the Si/Al ratio the system crystallizes differently, giving selectively ZSM-5 or β-zeolite structures. The β-zeolite was used as support for a nickel-β-diimine complex and the system used in ethylene catalytic oligomerization reactions.
Synthesis of zeolites using 1-butyl-3-methylimidazolium chloride (BMI.Cl) as a template yields highly crystalline materials after a 3-day reaction time. SEM micrographs of material obtained with a Si/Al molar ratio of 50 showed formation of very regular microspherical agglomerates with approximate diameters of 30
μm composed of ZSM-5 crystallites with 3–5
μm long edges. The regular format of these crystallites has been attributed to the formation of micellar aggregates due to the ionic liquid. Decreasing the Si/Al molar ratio to 20 reduces the diameter of the microspheres to less than 1
μm. The ZSM-5 zeolites show a specific area of 384
m
2
g
−1 and a microporous volume of 0.10
cm
3
g
−1, and the β-zeolite, obtained after 7 days of crystallization, shows a specific area of 418
m
2
g
−1 and a microporous volume of 0.11
cm
3
g
−1. The β-zeolite was used as support for a nickel β-diimine complex and the system used in ethylene catalytic oligomerization reactions. |
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ISSN: | 0926-860X 1873-3875 |
DOI: | 10.1016/j.apcata.2009.11.017 |