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用于寻找分级沸石的合成策略。

Synthesis strategies in the search for hierarchical zeolites.

机构信息

Department of Chemical and Energy Technology, ESCET, Rey Juan Carlos University, c/Tulipán s/n, 28933, Móstoles, Madrid, Spain.

出版信息

Chem Soc Rev. 2013 May 7;42(9):4004-35. doi: 10.1039/c2cs35330j. Epub 2012 Nov 9.

Abstract

Great interest has arisen in the past years in the development of hierarchical zeolites, having at least two levels of porosities. Hierarchical zeolites show an enhanced accessibility, leading to improved catalytic activity in reactions suffering from steric and/or diffusional limitations. Moreover, the secondary porosity offers an ideal space for the deposition of additional active phases and for functionalization with organic moieties. However, the secondary surface represents a discontinuity of the crystalline framework, with a low connectivity and a high concentration of silanols. Consequently, hierarchical zeolites exhibit a less "zeolitic behaviour" than conventional ones in terms of acidity, hydrophobic/hydrophilic character, confinement effects, shape-selectivity and hydrothermal stability. Nevertheless, this secondary surface is far from being amorphous, which provides hierarchical zeolites with a set of novel features. A wide variety of innovative strategies have been developed for generating a secondary porosity in zeolites. In the present review, the different synthetic routes leading to hierarchical zeolites have been classified into five categories: removal of framework atoms, surfactant-assisted procedures, hard-templating, zeolitization of preformed solids and organosilane-based methods. Significant advances have been achieved recently in several of these alternatives. These include desilication, due to its versatility, dual templating with polyquaternary ammonium surfactants and framework reorganization by treatment with surfactant-containing basic solutions. In the last two cases, the materials so prepared show both mesoscopic ordering and zeolitic lattice planes. Likewise, interesting results have been obtained with the incorporation of different types of organosilanes into the zeolite crystallization gels, taking advantage of their high affinity for silicate and aluminosilicate species. Crystallization of organofunctionalized species favours the formation of organic-inorganic composites that, upon calcination, are transformed into hierarchical zeolites. However, in spite of this impressive progress in novel strategies for the preparation of hierarchical zeolites, significant challenges are still ahead. The overall one is the development of methods that are versatile in terms of zeolite structures and compositions, capable of tuning the secondary porosity properties, and being scaled up in a cost-effective way. Recent works have demonstrated that it is possible to scale-up easily the synthesis of hierarchical zeolites by desilication. Economic aspects may become a significant bottleneck for the commercial application of hierarchical zeolites since most of the synthesis strategies so far developed imply the use of more expensive procedures and reagents compared to conventional zeolites. Nevertheless, the use of hierarchical zeolites as efficient catalysts for the production of high value-added compounds could greatly compensate these increased manufacturing costs.

摘要

近年来,人们对具有至少两个层次孔隙率的分级沸石的开发产生了极大的兴趣。分级沸石具有更高的可及性,从而在受空间位阻和/或扩散限制的反应中提高了催化活性。此外,次级孔隙为沉积额外的活性相和官能化提供了理想的空间。然而,次级表面代表了晶体骨架的不连续性,具有低连接性和高硅醇浓度。因此,在酸度、疏水性/亲水性、限域效应、形状选择性和水热稳定性方面,分级沸石的“沸石行为”比传统沸石差。然而,这种次级表面远非无定形,这为分级沸石提供了一系列新的特性。人们已经开发出多种创新策略来在沸石中产生次级孔隙。在本综述中,将导致分级沸石的不同合成途径分为五类:骨架原子的去除、表面活性剂辅助方法、硬模板、预成型固体的沸石化和有机硅烷方法。最近,这些替代方案中的许多都取得了重大进展。这些方法包括脱硅,由于其多功能性,与聚季铵盐表面活性剂的双重模板化以及用含有表面活性剂的碱性溶液处理的骨架重组。在后两种情况下,如此制备的材料既具有介观有序性又具有沸石晶格平面。同样,通过将不同类型的有机硅烷掺入沸石结晶凝胶中,利用其对硅酸盐和硅铝酸盐物种的高亲和力,也获得了有趣的结果。有机官能化物种的结晶有利于形成有机-无机复合材料,这些复合材料在煅烧后转化为分级沸石。然而,尽管在制备分级沸石的新策略方面取得了令人瞩目的进展,但仍面临着重大挑战。总的来说,就是要开发出一种对沸石结构和组成具有多功能性的方法,能够调整次级孔隙率的性质,并以具有成本效益的方式进行放大。最近的工作表明,通过脱硅很容易实现分级沸石的放大合成。对于分级沸石的商业应用,经济方面可能成为一个重大瓶颈,因为迄今为止开发的大多数合成策略都需要使用比传统沸石更昂贵的程序和试剂。然而,将分级沸石用作生产高附加值化合物的高效催化剂,可以大大弥补这些增加的制造成本。

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