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原位流动MAS NMR光谱和同步加速器PDF分析高温水合过程中SAPO-34中布朗斯台德酸性位点的局部响应

In Situ Flow MAS NMR Spectroscopy and Synchrotron PDF Analyses of the Local Response of the Brønsted Acidic Site in SAPO-34 during Hydration at Elevated Temperatures.

作者信息

Kalantzopoulos Georgios N, Lundvall Fredrik, Checchia Stefano, Lind Anna, Wragg David S, Fjellvåg Helmer, Arstad Bjørnar

机构信息

Centre for Materials Science and Nanotechnology (SMN), Department of Chemistry, University of Oslo, Sem Saelands vei 26, 0371, Oslo, Norway.

The European Synchrotron (ESRF), 71 Avenue des Martyrs, Grenoble, 38000, France.

出版信息

Chemphyschem. 2018 Feb 19;19(4):519-528. doi: 10.1002/cphc.201700973. Epub 2017 Dec 12.

Abstract

In situ flow magic-angle spinning nuclear magnetic resonance (MAS NMR) spectroscopy and synchrotron-based pair distribution function (PDF) analyses were applied to study water's interactions with the Brønsted acidic site and the surrounding framework in the SAPO-34 catalyst at temperatures up to 300 °C for NMR spectroscopy and 700 °C for PDF. Si enrichment of the sample enabled detailed NMR spectroscopy investigations of the T-atom generating the Brønsted site. By NMR spectroscopy, we observed dehydration above 100 °C and a coalescence of Si peaks due to local framework adjustments. Towards 300 °C, the NMR spectroscopy data indicated highly mobile acidic protons. In situ total X-ray scattering measurements analyzed by PDF showed clear changes in the Al local environment in the 250-300 °C region, as the Al-O bond lengths showed a sudden change. This fell within the same temperature range as the increased Brønsted proton mobility. We suggest that the active site in this catalyst under industrial conditions comprises not only the Brønsted proton but also SiO . To the best of our knowledge, this is the first work proposing a structural model of a SAPO catalyst by atomic PDF analysis. The combination of synchrotron PDF analysis with in situ NMR spectroscopy is promising in revealing the dynamic features of a working catalyst.

摘要

采用原位流动魔角旋转核磁共振(MAS NMR)光谱和基于同步加速器的对分布函数(PDF)分析,研究了在高达300 °C(NMR光谱)和700 °C(PDF)的温度下,水与SAPO-34催化剂中布朗斯台德酸性位点及周围骨架的相互作用。样品的硅富集使得能够对产生布朗斯台德位点的T原子进行详细的NMR光谱研究。通过NMR光谱,我们观察到在100 °C以上发生脱水,并且由于局部骨架调整导致硅峰合并。在接近300 °C时,NMR光谱数据表明酸性质子具有高度流动性。通过PDF分析的原位全X射线散射测量表明,在250 - 300 °C区域,Al的局部环境发生了明显变化,因为Al - O键长出现了突然变化。这与布朗斯台德质子流动性增加的温度范围相同。我们认为,在工业条件下,该催化剂的活性位点不仅包括布朗斯台德质子,还包括SiO。据我们所知,这是第一项通过原子PDF分析提出SAPO催化剂结构模型的工作。同步加速器PDF分析与原位NMR光谱的结合,有望揭示工作催化剂的动态特征。

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