Side-chain Alkylation of Toluene with Methanol, Modification and Deactivation of Zeolite Catalysts of the Reaction

Y. Voloshyna, O. Pertko
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Abstract

The review deals with main aspects of the toluene methylation reaction on basic catalysts. The side reactions of decomposition of methanol to CO and H2 on strong basic sites and ring alkylation of toluene on Lewis acid sites (cations of high polarizing ability) hinder obtaining high yields of the target products – styrene and ethylbenzene. Both types of sites are necessary for the course of the target reaction. So optimizing their strength and quantity is an important prerequisite for the selectivity of the side-chain alkylation catalysts. The advantage of fojasite-based systems for this reaction was confirmed by the works of many researchers. However, the possibilities of use of zeolites of other structural types and representatives of a new generation of molecular sieves are being studied, as well as ways of modifying such materials to increase their catalytic efficiency. The main direction of modification is to regulate the balance of acidity and basicity. Effective charge of framework oxygen atoms, which determines basicity of zeolite framework, increases due to the introduction of guest compounds into the catalyst, and this effect is more significant than influence on basicity of ion exchange for cations of elements of low electronegativity. However, the role of this method of modifying in increasing the selectivity remains crucial due to potentiality to decrease the Lewis acidity of cations. Compounds of other elements and transition metals also are used for modification, as well as promotion with metallic copper and silver. Techniques are applied, but not widely, to deprive the external surface of crystallites of active sites. This method of modification is effective for slowing down their deactivation by coke. Acid sites, in particular BAS, are most often distinguished among the sites responsible for coke formation. The mechanism of coke formation in the absence of such centers is also proposed. On the whole, this issue not fully disclosed and requires a deeper study.
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甲苯与甲醇侧链烷基化反应及其沸石催化剂的改性和失活
综述了在碱性催化剂上甲苯甲基化反应的主要方面。甲醇在强碱位分解为CO和H2的副反应和甲苯在Lewis酸位(高极化能力的阳离子)上的环烷基化反应阻碍了目标产物苯乙烯和乙苯的高产率。这两种位点对于目标反应的过程都是必需的。因此,优化侧链烷基化催化剂的强度和数量是保证侧链烷基化催化剂选择性的重要前提。许多研究人员的工作证实了fojasite基体系在该反应中的优势。然而,目前正在研究使用其他结构类型的沸石和新一代分子筛的代表的可能性,以及对这些材料进行改性以提高其催化效率的方法。改性的主要方向是调节酸碱度的平衡。由于客体化合物的引入,分子筛骨架氧原子的有效电荷增加,决定分子筛骨架的碱度,这种影响比低电负性元素的阳离子对离子交换碱度的影响更显著。然而,这种修饰方法在提高选择性方面的作用仍然是至关重要的,因为它有可能降低阳离子的刘易斯酸度。其他元素和过渡金属的化合物也用于改性,以及金属铜和银的促进。技术被应用,但不广泛,以剥夺活性位点的晶体的外表面。这种改性方法对减缓焦炭使其失活是有效的。酸位点,特别是BAS,在负责焦炭形成的位点中最常被区分开来。并提出了在没有这些中心的情况下焦炭形成的机理。总的来说,这个问题还没有完全揭示出来,需要深入研究。
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