The aim of this work was to study the influence of tannate concentration (tannic acid/Al molar ratio [R] of 0.01 -0.1), pH (5.0 and 8.0), order of aluminum, hydroxyl, and tannate addition, and prolonged ageing at different temperatures (10 months at 50degreesC and 5 y at room temperature and further ageing for 3-15 days at 140degreesC) on the nature and crystallinity of synthetic boehmite. Tannate facilitated the formation of boehmite relative to Al(OH)(3) polymorphs when coprecipitated with Al and also when added to Al(OH)(x) phases already formed at pH 4.5 or 8.0. However, the organic ligand was more effective in preventing or perturbing the growth of the crystals of boehmite when coprecipitated with Al than when added to soluble Al(OH), species or preformed Al precipitates. Boehmite aged at temperatures less than or equal to50degreesC typically showed a fibrous morphology. Crystals with a rhombic habit were observed in some treatments after ageing at 140degreesC. Significant amounts (15-30% C) of tannate were present in the precipitates after prolonged ageing. This tannate was only partly (<50%) oxidized by repeated treatments with H2O2. With further ageing at 140degreesC, the crystallite size of selected samples increased only slightly, suggesting that much of the remaining tannate was present in the internal structure of these samples and not simply adsorbed to their surfaces. Atomic force microscopy observation showed the presence of globular nanoparticles (probably Al tannate precipitates) attached to the elongated crystals of boehmite. Taken together, our results demonstrate that the crystalline phases that formed under mild conditions in the presence of low concentrations (R = 0.01) of foreign ligands have the same structure as boehmite, but with a poorly ordered and defective ion arrangement. At higher ligand concentrations (R greater than or equal to 0.05), mixtures of materials are formed having varying degrees of order, particle size and morphology.
|Digital Object Identifier (DOI):||10.1346/CCMN.2004.0520607|
|Codice identificativo ISI:||000225808100007|
|Codice identificativo Scopus:||2-s2.0-11144338377|
|Appare nelle tipologie:||1.1 Articolo in rivista|