Surface Investigation and Morphological Analysis of Structurally Disordered MgCl2 and MgCl2/TiCl4 Ziegler–Natta Catalysts

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• 作者：Maddalena D’Amore ; K. S. Thushara ; Alessandro Piovano ; Mauro Causà ; Silvia Bordiga ; Elena Groppo
• 刊名：ACS Catalysis
• 出版年：2016
• 出版时间：September 2, 2016
• 年：2016
• 卷：6
• 期：9
• 页码：5786-5796
• 全文大小：545K
• 年卷期：0
• ISSN：2155-5435

文摘

Activated MgCl₂ nanocrystals were prepared by controlled dealcoholation of the MgCl₂·6CH₃OH adduct, mimicking the routinely adopted methods to synthesize industrial heterogeneous Ziegler–Natta catalysts. The effect of the alcohol in driving the morphology of MgCl₂ crystals, i.e., the type and extension of the exposed surfaces, was investigated by integrating a detailed structural, morphological, and surface characterization with a state-of-the-art computational modeling. FT-IR spectroscopy of CO adsorbed at 100 K emerged as a feasible, simple, and powerful method to characterize the surface of structurally disordered MgCl₂ and MgCl₂-based Ziegler–Natta catalysts. Our computational morphological analysis revealed that the (012), (015), and (110) surfaces are highly stabilized by methanol as an electron donor, especially at the temperature typically adopted in the preparation of the precatalysts. FT-IR spectroscopy of adsorbed CO allows distinguishing these surfaces from the other penta-coordinated ones and provides a clear experimental evidence that TiCl₄ binds to the (110) and (015) surfaces. The (015) surface was never considered in the past and is characterized by an unusual flexibility in the presence of adsorbates, which detach the Mg cations from the Cl underneath, leaving a coordination vacancy available for the binding of asymmetric titanium sites. Since the recent literature identified a tetra-coordinated Mg as a site of election for the deposition of the Ti species relevant in olefin polymerization, the presence of two eligible Mg sites for Ziegler–Natta catalysis is highly interesting.