SYNTHESES AND CRYSTAL-STRUCTURES OF TITANIUM-OXIDE SULFATES

Citation
Mak. Ahmed et al., SYNTHESES AND CRYSTAL-STRUCTURES OF TITANIUM-OXIDE SULFATES, Acta chemica Scandinavica, 50(3), 1996, pp. 275-283
Citations number
24
Categorie Soggetti
Chemistry,Biology
Journal title
ISSN journal
0904213X
Volume
50
Issue
3
Year of publication
1996
Pages
275 - 283
Database
ISI
SICI code
0904-213X(1996)50:3<275:SACOTS>2.0.ZU;2-S
Abstract
When titanium dioxide, metatitanic acid or iron titanate (ilmenite) is heated with 65-95 wt% H2SO4, TiOSO4 or TiOSO4 . H2O is formed dependi ng on the water content of the sulfuric acid. The contours of reaction mechanisms are discussed. TiOSO4 and TiOSO4 . H2O dissolve slightly i n cold or hot water during short-term treatment. On longer contact wit h water the solubility becomes more appreciable. The undissolved remai nder, as well as the dissolved fraction after removal of the water pha se, proves to have been converted into X-ray amorphous products with c omposition TiOSO4 . xH(2)O, x approximate to 1. The crystal structure of TiOSO4 [orthorhombic, a = 1095.3(3), b = 515.2(1) and c = 642.6(1) pm] has been determined on the basis of powder X-ray diffraction data. The structure of TiOSO4 . H2O has been redetermined. Both structures contain...-O-Ti-...zigzag chains with short Ti-O distances. The chains are connected via sulfate groups, and the structures probably suffer from some disorder. For both structures the possibility of deviations from the centrosymmetric space group Pnma is discussed. The close stru ctural relationship between TiOSO4 and TiOSO4 . H2O is discussed. On h eating, TiOSO4 undergoes a reversible phase transition at around 330 d egrees C and decomposes into TiO2-a (anatas) at ca. 525 degrees C. TiO SO4 . H2O looses its crystal water at ca. 310 degrees C. However, libe ration of SO3 starts at about 40 degrees C lower temperature than for TiOSO4, and the decomposition shows a two-step character in TG, DTG an d DTA. Attempts to isolate intermediate decomposition product(s) have so far not been successful.