کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
61009 47558 2014 11 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
From natural aluminosilicate minerals to hierarchical ZSM-5 zeolites: A nanoscale depolymerization–reorganization approach
موضوعات مرتبط
مهندسی و علوم پایه مهندسی شیمی کاتالیزور
پیش نمایش صفحه اول مقاله
From natural aluminosilicate minerals to hierarchical ZSM-5 zeolites: A nanoscale depolymerization–reorganization approach
چکیده انگلیسی


• A top-down method to efficiently depolymerize natural minerals was developed.
• The reorganization of depolymerized intermediates into hierarchical ZSM-5 zeolite was achieved.
• Neither inorganic aluminum and silicon salts nor mesoscale template and post-treatment were used.
• The resulting hierarchical ZSM-5 zeolite showed superior catalytic performance.

In this article, we describe a novel strategy for synthesizing hierarchical ZSM-5 zeolites via the nanoscale depolymerization–reorganization of natural aluminosilicate minerals. This strategy involves two important steps: the first is the top-down depolymerization of one aluminum-rich aluminosilicate mineral via a novel submolten salt system and one silicon-rich aluminosilicate mineral via conventional thermal treatment into nanoscale building blocks, and the second is the bottom-up rearrangement and reorganization of nanoscale building blocks in the synthesis system into hierarchical ZSM-5 zeolites. When used as a fluid catalytic cracking catalyst additive, the resulting ZSM-5 zeolite with hierarchical micro–mesoporous structure exhibited high activity and selectivity for valuable products in preliminary oil refining tests. The salient features of the strategy lie in that it neither involves any inorganic aluminum and silicon salts as precursors nor uses any secondary mesoscale template and post-treatment to create mesopores, thus demonstrating itself to be a green route to synthesizing hierarchical zeolites.

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ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Catalysis - Volume 319, November 2014, Pages 200–210
نویسندگان
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