Issue 5, 2018

A solvent-free, one-step synthesis of sulfonic acid group-functionalized mesoporous organosilica with ultra-high acid concentrations and excellent catalytic activities

Abstract

We demonstrate herein a novel solvent-free technique for the synthesis of sulfonic acid group-functionalized mesoporous organosilica, which was achieved from the self-assembly of a block copolymer template using mercaptopropyltrimethoxysilane (MPTS) and tetramethoxysilane (TMOS) under melting conditions without using additional solvents and subsequent condensation at high temperature (up to 140 °C). The resultant samples were designated as SMS-xs, where x stands for molar ratio of MPTS/(MPTS + TMOS). SMS-xs have relatively large BET surface areas, highly cross-linked frameworks, and abundant and uniform mesopores with wormhole-like characteristics. Interestingly, MPTS could be used as the solo precursor to prepare mesoporous organosilica (SMS-1.0), which had controllable acidity and an ultra-high concentration of sulfur (5.51 mmol g−1, the highest acid density to date), which was even higher than those of commercial Amberlyst 15 (4.7 mmol g−1), HS-JLU-20-0.8 (4.61 mmol g−1) and sulfonated carbon (CH0.30O0.33S0.16, 4.90 mmol g−1). These structural characteristics give SMS-xs excellent activities and good reusability in biomass conversions and fine chemicals synthesis, which are much better than various solid acids, such as Amberlyst 15, H-form USY zeolite, and sulfonic acid group-functionalized ordered mesoporous silica.

Graphical abstract: A solvent-free, one-step synthesis of sulfonic acid group-functionalized mesoporous organosilica with ultra-high acid concentrations and excellent catalytic activities

Supplementary files

Article information

Article type
Paper
Submitted
01 Jan 2018
Accepted
23 Jan 2018
First published
23 Jan 2018

Green Chem., 2018,20, 1020-1030

A solvent-free, one-step synthesis of sulfonic acid group-functionalized mesoporous organosilica with ultra-high acid concentrations and excellent catalytic activities

Q. Wu, F. Liu, X. Yi, Y. Zou and L. Jiang, Green Chem., 2018, 20, 1020 DOI: 10.1039/C8GC00002F

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