کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
68601 48518 2006 8 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
An ONIOM2 study on pyridine adsorption in the main channels of Li- and Na-MOR
موضوعات مرتبط
مهندسی و علوم پایه مهندسی شیمی کاتالیزور
پیش نمایش صفحه اول مقاله
An ONIOM2 study on pyridine adsorption in the main channels of Li- and Na-MOR
چکیده انگلیسی

A 24T model containing a complete two-layered 12-membered ring connected by an 8-membered side pocket was used to represent the channel of the MOR framework. On the basis of this model, the structures of the acid sites in the main channels of Li- and Na-MOR as well as their interaction with pyridine probe molecule were investigated using the ONIOM2 (QM/QM; B3LYP/6-31G(d,p):HF/3-21G) and ONIOM2 (QM/MM; B3LYP/6-31G(d,p):UFF) methods. There are two stable structures for the Li-MOR cluster; one has Li+ interacting with two oxygen atoms around Al, and the other has Li+ interacting with four oxygen atoms belonging to a five-membered ring. This four-fold Li+ coordination is consistent with Na+ in Na-MOR, and is the same as the Na+ coordination in the intersection model of Na-ZSM-5. The ONIOM2 (QM/MM) method overestimates the adsorption energies of pyridine (195.0/192.8 and 170.6 kJ/mol for Li-MOR and Na-MOR, respectively), while the ONIOM2 (QM/QM) method gives reasonable results (171.6/154.7 and 131.3 kJ/mol, respectively) compared to the available experimental values (153–195 and 120 kJ/mol, respectively). The structural parameters of the adsorption complexes showed that coordination of the alkali ion to the nitrogen atom of pyridine dominates the overall interaction between the zeolite and pyridine, and the adsorption complexes were further stabilized by hydrogen bonding between the hydrogen atoms of pyridine and the lattice oxygen atoms of the zeolite framework.

The structures of Li- and Na-MOR as well as their interaction with pyridine were investigated with the help of a 24T model using the ONIOM2 (QM/QM) and (QM/MM) methods. The coordination of the alkali metal ion to the nitrogen atom of pyridine dominates the overall interaction between zeolite and pyridine, and the adsorption complexes were further stabilized by hydrogen bonding between the hydrogen atoms of pyridine and the lattice oxygen atoms of the zeolite framework. Figure optionsDownload as PowerPoint slide

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Molecular Catalysis A: Chemical - Volume 256, Issues 1–2, 18 August 2006, Pages 130–137
نویسندگان
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