{"title":"Crystallization process of LTA zeolite from alkoxides assisted by microwave heating","authors":"Kazuumi Ito , Yuji Jinbo , Wataru Fujiwara , Takeshi Higuchi","doi":"10.1016/j.micromeso.2024.113343","DOIUrl":null,"url":null,"abstract":"<div><div>Microwave heating (MH) is a promising way for zeolite synthesis in terms of rapid and uniform reaction. However, detail process of the synthesis reaction and mechanism of its promotion by microwave are still under investigation. In the present study, LTA (Linde Type-A) zeolite was hydrothermally synthesized by 300 W of MH from hydrolyzed Al and Si alkoxides. The formation process of LTA was elucidated by nuclear magnetic resonance spectroscopy (<sup>29</sup>Si NMR), small angle X-ray scattering (SAXS), X-ray diffraction (XRD), transmission electron microscopy (TEM), dynamic light scattering (DLS) and scanning electron microscopy (SEM). <sup>29</sup>Si NMR and SAXS analyses suggest that linear polycondensates of aluminosilicate in the precursor solution was immediately transformed into densely packed structure by MH. TEM observations reveals that crystalline phase with several nanometers was already formed in amorphous aluminosilicate nanoparticles prior to the MH while XRD shows that the amorphous phase had been transformed to LTA phase until 400 min of MH. It is basically consistent with the previous studies among zeolite synthesis assisted by both of conventional heating and MH. The aluminosilicate/LTA particle size was measured by DLS and SEM image as well as the yield was calculated from weight of the reaction products. The particle gradually grew up to 242 nm in diameter until 36 h while the yield sharply increased to nearly 100 % during 6.7 h and 12 h. In other words, all aluminosilicate in the solution once had polycondensed to form insoluble particle until 12 h followed by particle growth by dissolution-reprecipitation or agglomeration until 36 h.</div></div>","PeriodicalId":392,"journal":{"name":"Microporous and Mesoporous Materials","volume":"381 ","pages":"Article 113343"},"PeriodicalIF":4.8000,"publicationDate":"2024-09-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Microporous and Mesoporous Materials","FirstCategoryId":"88","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1387181124003652","RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
引用次数: 0
Abstract
Microwave heating (MH) is a promising way for zeolite synthesis in terms of rapid and uniform reaction. However, detail process of the synthesis reaction and mechanism of its promotion by microwave are still under investigation. In the present study, LTA (Linde Type-A) zeolite was hydrothermally synthesized by 300 W of MH from hydrolyzed Al and Si alkoxides. The formation process of LTA was elucidated by nuclear magnetic resonance spectroscopy (29Si NMR), small angle X-ray scattering (SAXS), X-ray diffraction (XRD), transmission electron microscopy (TEM), dynamic light scattering (DLS) and scanning electron microscopy (SEM). 29Si NMR and SAXS analyses suggest that linear polycondensates of aluminosilicate in the precursor solution was immediately transformed into densely packed structure by MH. TEM observations reveals that crystalline phase with several nanometers was already formed in amorphous aluminosilicate nanoparticles prior to the MH while XRD shows that the amorphous phase had been transformed to LTA phase until 400 min of MH. It is basically consistent with the previous studies among zeolite synthesis assisted by both of conventional heating and MH. The aluminosilicate/LTA particle size was measured by DLS and SEM image as well as the yield was calculated from weight of the reaction products. The particle gradually grew up to 242 nm in diameter until 36 h while the yield sharply increased to nearly 100 % during 6.7 h and 12 h. In other words, all aluminosilicate in the solution once had polycondensed to form insoluble particle until 12 h followed by particle growth by dissolution-reprecipitation or agglomeration until 36 h.
期刊介绍:
Microporous and Mesoporous Materials covers novel and significant aspects of porous solids classified as either microporous (pore size up to 2 nm) or mesoporous (pore size 2 to 50 nm). The porosity should have a specific impact on the material properties or application. Typical examples are zeolites and zeolite-like materials, pillared materials, clathrasils and clathrates, carbon molecular sieves, ordered mesoporous materials, organic/inorganic porous hybrid materials, or porous metal oxides. Both natural and synthetic porous materials are within the scope of the journal.
Topics which are particularly of interest include:
All aspects of natural microporous and mesoporous solids
The synthesis of crystalline or amorphous porous materials
The physico-chemical characterization of microporous and mesoporous solids, especially spectroscopic and microscopic
The modification of microporous and mesoporous solids, for example by ion exchange or solid-state reactions
All topics related to diffusion of mobile species in the pores of microporous and mesoporous materials
Adsorption (and other separation techniques) using microporous or mesoporous adsorbents
Catalysis by microporous and mesoporous materials
Host/guest interactions
Theoretical chemistry and modelling of host/guest interactions
All topics related to the application of microporous and mesoporous materials in industrial catalysis, separation technology, environmental protection, electrochemistry, membranes, sensors, optical devices, etc.