Condensation and growth of amorphous aluminosilicate nanoparticles via an aggregation process
Author(s) -
Romain Dupuis,
Seung Ho Hahn,
Adri C. T. van Duin,
Roland J.M. Pellenq,
Arnaud Poulesquen
Publication year - 2022
Publication title -
physical chemistry chemical physics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.053
H-Index - 239
eISSN - 1463-9084
pISSN - 1463-9076
DOI - 10.1039/d1cp05412k
Subject(s) - aluminosilicate , nucleation , silanol , silicate , amorphous solid , chemical engineering , nanoparticle , metastability , precipitation , crystallization , materials science , aluminate , chemistry , crystallography , organic chemistry , nanotechnology , catalysis , physics , cement , meteorology , engineering , metallurgy
The precipitation of zeolite nanoparticles involves the initial formation of metastable precursors, such as amorphous entities, that crystallize through non-classical pathways. Here, using reactive force field-based simulations, we reveal how aluminosilicate oligomers grow concomitantly to the decondensation of silicate entities during the initial step of the reaction. Aluminate clusters first form in the solution, thus violating the Loewenstein rule in the first instant of the reaction, which is then followed by their connection with silicate oligomers at the terminal silanol groups before reorganization to finally diffuse within the silicate oligomers to form stable amorphous aluminosilicate nanoparticles that do obey the Loewenstein rule. Our results clearly indicate that aluminate does not serve as the nucleation center for the growth of aluminosilicates in a nucleation-like process but rather proceeds via an aggregation process. The coexistence of aluminosilicate oligomers and small silicate entities induces a phase separation that promotes the precipitation of zeolites with aging.
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