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Sol–Gel Route to Nanocrystalline Lithium Metasilicate Particles
Author(s) -
Zhang Bo,
Nieuwoudt Michel,
Easteal Allan J.
Publication year - 2008
Publication title -
journal of the american ceramic society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.9
H-Index - 196
eISSN - 1551-2916
pISSN - 0002-7820
DOI - 10.1111/j.1551-2916.2008.02389.x
Subject(s) - calcination , nanocrystalline material , thermogravimetric analysis , materials science , lithium (medication) , differential scanning calorimetry , fourier transform infrared spectroscopy , sol gel , chemical engineering , particle size , specific surface area , bet theory , mineralogy , nuclear chemistry , chemistry , adsorption , nanotechnology , organic chemistry , medicine , physics , endocrinology , engineering , thermodynamics , catalysis
Crystalline lithium metasilicate (Li 2 SiO 3 ) nanoparticles have been synthesized using a sol–gel process with tetraethylorthosilicate and lithium ethoxide as precursors. The particle size examined by using transmission electron microscopy and BET‐specific surface area techniques is in the range 5–50 nm, depending on the temperature at which the material is calcined. The crystalline Li 2 SiO 3 forms at ambient temperature (∼40°C), and it remains in this phase after calcination at temperatures up to 850°C. The BET‐specific surface area is ∼110 m 2 /g for material calcined at temperatures below 500°C, decreasing to ∼29 and ∼0.7 m 2 /g following calcination at 700° and 850°C, respectively. Solid‐state 29 Si NMR spectroscopy shows the presence of only Q 2 structural units in the material. The lithium metasilicate is further characterized using differential scanning calorimetry and thermogravimetric analysis, and Fourier transform infrared spectroscopy.