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……的合成、光谱学及催化作用 (原文表述不完整,只能大致翻译到这种程度)

Synthesis, spectroscopy and catalysis of.

作者信息

Weckhuysen BM, Pelgrims J, Schoonheydt RA, Bodart P, Debras G, Collart O, Vansant EF

机构信息

Centrum voor Oppervlaktechemie en Katalyse, Department Interfasechemie, K.U.Leuven, Heverlee, Belgium.

出版信息

Chemistry. 2000 Aug 18;6(16):2960-70. doi: 10.1002/1521-3765(20000818)6:16<2960::aid-chem2960>3.0.co;2-7.

Abstract

Chromium acetyl acetonate [Cr(acac)3] complexes have been grafted onto the surface of two mesoporous crystalline materials; pure silica MCM-41 (SiMCM-41) and Al-containing silica MCM-41 with an Si:Al ratio of 27 (AlMCM-41). The materials were characterized with X-ray diffraction, N2 adsorption, thermogravimetrical analysis, diffuse reflectance spectroscopy in the UV-Vis-NIR region (DRS), electron spin resonance (ESR) and Fourier transform infrared spectroscopy. Hydrogen bonding between surface hydroxyls and the acetylacetonate (acac) ligands is the only type of interaction between [Cr(acac)3] complexes and SiMCM-41, while the deposition of [Cr(acac)3] onto the surface of AlMCM-41 takes place through either a ligand exchange reaction or a hydrogen-bonding mechanism. In the as-synthesized materials, Cr3+ is present as a surface species in pseudo-octahedral coordination. This species is characterized by high zero-field ESR parameters D and E, indicating a strong distortion from O(h), symmetry. After calcination, Cr3+ is almost completely oxidized to Cr6+, which is anchored onto the surface as dichromate, some chromate and traces of small amorphous Cr2O3 clusters and square pyramidal Cr5+ ions. These materials are active in the gas-phase and slurry-phase polymerization of ethylene at 100 degrees C. The polymerization activity is dependent on the Cr loading, precalcination temperature and the support characteristics: a 1 wt % [Cr(acac)3]-AlMCM-41 catalyst pretreated at high temperatures was found to be the most active material with a polymerization rate of 14000 g polyethylene per gram of Cr per hour. Combined DRS-ESR spectroscopies were used to monitor the reduction process of Cr(6+/5+) and the oxidation and coordination environment of Cr(n+) species during catalytic action. It will be shown that the polymer chains initially produced within the mesopores of the Cr-MCM-41 material form nanofibres of polyethylene with a length of several microns and a diameter of 50 to 100 nanometers. These nanofibres (partially) cover the outer surface of the MCM-41 material. The catalyst particles also gradually break up during ethylene polymerization resulting in the formation of crystalline and amorphous polyethylene with a low bulk density and a melt flow index between 0.56 and 1.38g per 10 min; this indicates the very high molecular weight of the polymer.

摘要

乙酰丙酮铬(III)[Cr(acac)₃]配合物已接枝到两种介孔晶体材料的表面;纯硅MCM-41(SiMCM-41)和硅铝比为27的含铝硅MCM-41(AlMCM-41)。通过X射线衍射、N₂吸附、热重分析、紫外-可见-近红外区域的漫反射光谱(DRS)、电子自旋共振(ESR)和傅里叶变换红外光谱对材料进行了表征。表面羟基与乙酰丙酮(acac)配体之间的氢键是[Cr(acac)₃]配合物与SiMCM-41之间唯一的相互作用类型,而[Cr(acac)₃]在AlMCM-41表面的沉积是通过配体交换反应或氢键机制进行的。在合成后的材料中,Cr³⁺以伪八面体配位的表面物种形式存在。该物种的特征是具有高的零场ESR参数D和E,表明其与O(h)对称性有很大偏差。煅烧后,Cr³⁺几乎完全氧化为Cr⁶⁺,以重铬酸盐、一些铬酸盐以及少量无定形Cr₂O₃簇和四方锥Cr⁵⁺离子的形式锚定在表面。这些材料在100℃下对乙烯的气相和淤浆相聚合具有活性。聚合活性取决于Cr负载量、预煅烧温度和载体特性:发现一种在高温下预处理的1 wt%[Cr(acac)₃]-AlMCM-41催化剂是活性最高的材料,聚合速率为每克Cr每小时14000 g聚乙烯。结合DRS-ESR光谱用于监测催化作用过程中Cr(6+/5+)的还原过程以及Cr(n+)物种的氧化和配位环境。结果表明,最初在Cr-MCM-41材料介孔内生成的聚合物链形成了长度为几微米、直径为50至100纳米的聚乙烯纳米纤维。这些纳米纤维(部分)覆盖了MCM-41材料的外表面。在乙烯聚合过程中,催化剂颗粒也逐渐破碎,导致形成结晶和无定形聚乙烯,其堆积密度低,熔体流动指数在0.56至1.38 g/10 min之间;这表明聚合物的分子量非常高。

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