Ajumobi Oluwole, Su Yang, Farinmade Azeem, Yu Lei, He Jibao, Valla Julia A, John Vijay T
Department of Chemical & Biomolecular Engineering, Tulane University, 6823 St. Charles Avenue, New Orleans, Louisiana 70118, United States.
Department of Chemical & Biomolecular Engineering, University of Connecticut, Storrs, Connecticut 06269, United States.
ACS Appl Nano Mater. 2021 Aug 27;4(8):8455-8464. doi: 10.1021/acsanm.1c01678. Epub 2021 Aug 6.
In many porous catalyst supports, the accessibility of interior catalytic sites to reactant species could be restricted due to limitations of reactant transport through pores comparable to reactant dimensions. The interplay between reaction and diffusion in porous catalysts is defined through the Thiele modulus and the effectiveness factor, with diffusional restrictions leading to high Thiele moduli, reduced effectivess factors, and a reduction in the observed reaction rate. We demonstrate a method to integrate ceramic nanostraws into the interior of ordered mesoporous silica MCM-41 to mitigate diffusional restrictions. The nanostraws are the natural aluminosilicate tubular clay minerals known as halloysite. Such halloysite nanotubes (HNTs) have a lumen diameter of 15-30 nm, which is significantly larger than the 2-4 nm pores of MCM-41, thus facilitating entry and egress of larger molecules to the interior of the pellet. The method of integrating HNT nanostraws into MCM-41 is through a ship-in-a-bottle approach of synthesizing MCM-41 in the confined volume of an aerosol droplet that contains HNT nanotubes. The concept is applied to a system in which microcrystallites of Ni@ZSM-5 are incorporated into MCM-41. Using the liquid phase reduction of nitrophenol as a model reaction catalyzed by Ni@ZSM-5, we show that the insertion of HNT nanostraws into this composite leads to a 50% increase in the effectiveness factor. The process of integrating nanostraws into MCM-41 through the aerosol-assisted approach is a one-step facile method that complements traditional catalyst preparation techniques. The facile and scalable synthesis technique toward the mitigation of diffusional restrictions has implications to catalysis and separation technologies.
在许多多孔催化剂载体中,由于反应物通过与反应物尺寸相当的孔隙进行传输时存在限制,内部催化位点对反应物的可及性可能会受到限制。多孔催化剂中反应与扩散之间的相互作用通过西勒模数和有效因子来定义,扩散限制会导致高西勒模数、降低有效因子,并使观察到的反应速率降低。我们展示了一种将陶瓷纳米管整合到有序介孔二氧化硅MCM - 41内部以减轻扩散限制的方法。这些纳米管是天然的铝硅酸盐管状粘土矿物,称为埃洛石。这种埃洛石纳米管(HNTs)的内腔直径为15 - 30纳米,明显大于MCM - 41的2 - 4纳米孔隙,从而便于较大分子进出颗粒内部。将HNT纳米管整合到MCM - 41中的方法是通过在含有HNT纳米管的气溶胶液滴的受限体积内合成MCM - 41的瓶中造船法。该概念应用于将Ni@ZSM - 5微晶掺入MCM - 41的体系。以Ni@ZSM - 5催化的硝基苯酚的液相还原作为模型反应,我们表明将HNT纳米管插入该复合材料中会使有效因子提高50%。通过气溶胶辅助方法将纳米管整合到MCM - 41中的过程是一种一步简便方法,可补充传统的催化剂制备技术。这种简便且可扩展的用于减轻扩散限制的合成技术对催化和分离技术具有重要意义。