کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
61199 47569 2013 13 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Opportunities for selective catalysis within discrete portions of zeolites: The case for SSZ-57LP
موضوعات مرتبط
مهندسی و علوم پایه مهندسی شیمی کاتالیزور
پیش نمایش صفحه اول مقاله
Opportunities for selective catalysis within discrete portions of zeolites: The case for SSZ-57LP
چکیده انگلیسی


• New zeolite catalyst has been created where only a portion is developed for strong acid sites.
• Selective creation of strong acid sites occurs via Al replacement for B in parts of the structure.
• The novel large pore (but short path) zeolite is contrasted with ZSM-11 and SSZ-57.
• Reactions studied are Constraint Index, hydroisomerization of n-hexane, and isomerization and disproportionation of diethylbenzene.

We describe a new zeolite catalyst where we develop only a portion of the structure for strong acid sites. This is achieved using zeolite SSZ-57 in boron lattice substitution (weak acid sites) and then replacing the boron sites in the large pore segments of this novel zeolite, while the intermediate pores (with MEL topology) remain unchanged. We can achieve the creation of such a novel catalyst system due to the inherent structure of SSZ-57 (repeat domains of MEL topology, periodically interrupted by a short segment of large pores) because the re-insertion of aluminum for boron requires that the pores be large to effect substitution. In this work, we describe the preparation and characterization of the novel material designated as SSZ-57LP. We use three model compound reactions to demonstrate the unique behavior for this novel large pore (but short path) zeolite and contrast it with intermediate pore zeolite Al-ZSM-11 (MEL topology) and the Al-SSZ-57 where the strong acid sites are in both intermediate and large pore regions (from direct zeolite synthesis with aluminum in the gel). The reactions studied are the Constraint Index probing reactant selectivity for cracking n-hexane and 3-methylpentane, the hydroisomerization of n-hexane where the formation of dimethylbutanes is examined for large pore space within a zeolite, and then finally, the isomerization and disproportionation of 1,3-diethylbenzene, again as a probe for large enough transition state selectivity within a given zeolite.

SSZ-57LP shown with color contrast of the 12-ring portion bonded adjacent to the 10-ring MEL segments in a rendering that shortens the repeat distance for image clarity.Figure optionsDownload high-quality image (95 K)Download as PowerPoint slide

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Catalysis - Volume 308, December 2013, Pages 213–225
نویسندگان
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