Issue 10, 2019

Mechanochemically-assisted solvent-free and template-free synthesis of zeolites ZSM-5 and mordenite

Abstract

Aluminosilicate-based zeolite materials, such as ZSM-5 and mordenite, are well-studied as catalysts. Typical approaches to synthesize these zeolites require either templates or seeds to direct ordered crystal growth and both of these are expensive and add to the complexity of zeolite synthesis. In this paper, we describe a solvent-free and template-free method to synthesize crystalline ZSM-5 and mordenite zeolites without any added seed crystals. Key to the success of this approach is a mechanochemical precursor pre-reaction step. High-energy ball-milling is used to initiate a solid-state metathesis (exchange) reaction between Na2SiO3 and Al2(SO4)3 reagents, forming crystalline Na2SO4 and well-mixed aluminosilicate precursor. The solid precursor mixture is thermally converted to crystalline ZSM-5 or mordenite at moderate 180 °C temperatures without solvents or an organic amine structure directing template. Variations in Si/Al ratios in the precursor mixture and additions of solid NaOH to the mechanochemical reaction were found to influence the subsequent growth of either crystalline ZSM-5 or mordenite zeolites. The crystalline zeolites from this solvent-free and template free method have high ∼300 m2 g−1 surface areas directly from the synthesis without requiring high-temperature calcination. These materials are also comparably active to their commercial counterparts in cellulose and glucose biomass catalytic conversion to hydroxymethylfurfural.

Graphical abstract: Mechanochemically-assisted solvent-free and template-free synthesis of zeolites ZSM-5 and mordenite

Supplementary files

Article information

Article type
Paper
Submitted
24 Jun 2019
Accepted
22 Aug 2019
First published
03 Sep 2019
This article is Open Access
Creative Commons BY-NC license

Nanoscale Adv., 2019,1, 3918-3928

Mechanochemically-assisted solvent-free and template-free synthesis of zeolites ZSM-5 and mordenite

M. H. Nada, S. C. Larsen and E. G. Gillan, Nanoscale Adv., 2019, 1, 3918 DOI: 10.1039/C9NA00399A

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