Silicalite-1分子筛氢键诱导晶化机制的固体核磁共振研究

Hydrogen-Bond Induced Crystallization of Silicalite-1 Zeolite as Revealed by Solid-State NMR Spectroscopy

The flexible chemical composition of the frameworks with tunable pore size and geometry of molecular dimensions makes zeolites widely used in chemical and petrochemical industry fields. The understanding of crystallization mechanism is important for a rational design of new zeolite with target structure and property, which however is still a big challenge in the field of material science. In this work, the specific spatial correlations/interactions between the SiO^-···HO―Si hydrogen bonds within the charged framework of silicalite-1 (MFI topology) zeolite and the alkyl chains of tetrapropylammonium ion (TPA⁺) organic structure direction agents (OSDAs) were studied by one-dimensional (1D) and two-dimensional (2D) solid state-NMR spectroscopy in combination with other techniques, with the aim to shed light into the crystallization mechanism of silicalite-1. The "solvent-free" route was used to study the crystallization process. Silicalite-1 crystals were also prepared following the hydrothermal synthesis route. The structural properties of as-synthesized TPA-silicalite-1 samples during the crystallization were characterized by XRD and scanning electron microscopy (SEM) images, which showed the evolution of long-range periodic structure and cyrtal growth. The ¹H-²⁹Si CP/MAS NMR experiments showed that the reorganization of the silica or silicates occurred in the crystallization process. The ^lH-¹³C CP/MAS NMR experiments performed on the samples synthesized with different time indicated that the TPA⁺ ions in the amorphous samples experienced a constrained environment, forming the inorganic-organic composites. The splitting of the methyl carbon signal from TPA⁺ ions was observed in the ¹³C NMR spectra, which is the direct reflection of the interactions between the methyl groups and the silicate framework in the straight and zig-zag channels of silicalite-1. Two types of SiO^-···H―OSi hydrogen bonds (SiO^-···H―OSi hydrogen bond in-cage and SiO^-···H―OSi hydrogen bond between lamellae) have been identified by 2D ¹H double quantum (DQ)-single quantum (SQ) MAS NMR and ²H MAS NMR during the crystallization of silicalite-1. The SiO^-···H―OSi hydrogen bonds between lamellae are formed and gradually transformed into the in-cage ones during the crystallization process. Their functions have been revealed in the formation of silicalite-1: the SiO^-···H―OSi hydrogen bond in-cage provides the stereoscopic counterbalance for the positive charges from TPA⁺ ions and this stereoscopic electrostatic interaction is the key factor to transform inorganic-organic composites with the MFI structure property, even though the long-range periodic MFI structures have not been established yet; the SiO^-···H―OSi hydrogen bond between lamellae acts as a connector to assemble the silicate species together to generate the zeolite framework. ²H MAS NMR spectra show that the SiOH nests exist in the zeolite framework even though the long-range periodic structures have been fully established.