4.5 Article

Transformation of Discrete Amorphous Aluminosilicate Nanoparticles into Nanosized Zeolites

Journal

ADVANCED MATERIALS INTERFACES
Volume 8, Issue 4, Pages -

Publisher

WILEY
DOI: 10.1002/admi.202000634

Keywords

alkali suspensions; amorphous nanoparticles; inorganic cations; nanosized zeolites; selective transformation

Funding

  1. Thousand Talents Program for Foreign Experts [WQ20152100284]
  2. French-China Science Foundation (FFCSA)
  3. National Natural Science Foundation of China [21975285, U1862118]
  4. Fundamental Research Funds for the Central Universities [18CX05018A]
  5. State Key Laboratory of Advanced Technology for Materials Synthesis and Processing (Wuhan University of Technology) [2018-KF-13]
  6. International Associated Laboratory (LIA)-Zeolites
  7. CNRS [IR-RMN-THC Fr3050]

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The study demonstrates the impact of amorphous aluminosilicate precursor nanoparticles on the formation of nanosized zeolites with faujasite (FAU) and sodalite (SOD) frameworks. The two-step synthesis procedure involves the transformation of amorphous nanoparticles into FAU and SOD nanosized crystals, with the presence of sodalite cages confirmed by Na-23-H-1 D-HMQC NMR spectroscopy. The subsequent treatment with aqueous sodium hydroxide stabilizes the sodalite cages during long-range ordering in the amorphous particles.
The effect of amorphous aluminosilicate precursor nanoparticles on the formation of nanosized zeolites with faujasite (FAU) and sodalite (SOD) type frameworks is illustrated using a new synthetic strategy to prepare nanosized zeolites with tailored particle size distribution, morphology, and structure. This two-step synthesis procedure includes the formation of colloidal suspensions followed by separation of the amorphous precursor nanoparticles, and their subsequent transformation into nanosized crystals by treatment with alkali suspensions (NaOH) solutions only. The selective transformation of the amorphous nanoparticles into FAU and SOD nanosized crystals is studied at atomistic and microscopic levels using Si-29 and Na-23 nuclear magnetic resonanse (NMR) spectroscopy, X-ray powder diffraction, and N-2 physisorption, respectively. The presence of sodalite cages occluding highly mobile sodium in the amorphous nanoparticles is confirmed by Na-23-H-1 D-HMQC NMR spectroscopy. The subsequent treatment of these amorphous precursor particles with aqueous sodium hydroxide illustrates that the cations are not only charge compensators but also inorganic templates stabilizing sodalite cages during the long-range ordering in the amorphous particles.

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