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首页> 外文期刊>Journal of Catalysis >Solid-state MAS NMR studies on the hydrothermal stability of the zeolite catalysts for residual oil selective catalytic cracking
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Solid-state MAS NMR studies on the hydrothermal stability of the zeolite catalysts for residual oil selective catalytic cracking

机译:固态MAS NMR研究残油选择性催化裂化的沸石催化剂的水热稳定性

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By using the solid-state MAS NMR technique, the hydrothermal stabilities (under 100% steam at 1073 K) of HZSM-5 zeolites modified by lanthanum and phosphorus have been studied. They are excellent zeolite catalysts for residual oil selective catalytic cracking (RSCC) processes. It was indicated that the introduction of phosphorus to the zeolite via impregnation with orthophosphoric acid led to dealumination as well as formation of different Al species, which were well distinguished by Al-27 3Q MAS NMR. Meanwhile, the hydrothermal stabilities of the zeolites (P/HZSM-5, La-P/HZSM-5) were enhanced even after the samples were treated under severe conditions for a prolonged time. It was found that the Si-O-Al bonds were broken under hydrothermal conditions, while at the same time the phosphorous compounds would occupy the silicon sites to form (SiO)(x)Al(OP)(4 - x) species. With increasing time, more silicon sites around the tetrahedral coordinated Al in the lattice can be replaced till the aluminum is completely expelled from the framework. The existence of lanthanum can partially restrict the breaking of the Si-O-Al bonds and the replacement of the silicon sites by phosphorus, thus preventing dealumination under hydrothermal conditions. This was also proved by P-31 MAS NMR spectra. (C) 2004 Elsevier Inc. All rights reserved.
机译:通过使用固态MAS NMR技术,研究了镧和磷改性的HZSM-5沸石的水热稳定性(在100%蒸汽和1073 K下)。它们是用于残油选择性催化裂化(RSCC)工艺的优秀沸石催化剂。结果表明,通过用正磷酸浸渍将磷引入沸石可导致脱铝以及形成不同的Al,Al-27 3Q MAS NMR可以很好地区分磷。同时,即使在苛刻条件下长时间处理后,沸石(P / HZSM-5,La-P / HZSM-5)的水热稳定性也得到增强。发现在水热条件下Si-O-Al键断裂,而同时磷化合物将占据硅位点以形成(SiO)(x)Al(OP)(4-x)物质。随着时间的增加,晶格中四面体配位Al周围的更多硅位点可以被置换,直到铝完全从骨架中排出。镧的存在可以部分限制Si-O-Al键的断裂和磷取代硅位点,从而防止在水热条件下脱铝。 P-31 MAS NMR光谱也证明了这一点。 (C)2004 Elsevier Inc.保留所有权利。

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