In English

Abstract

The effect of microstructural changes caused by chemical modification of diatomite with aluminosilicate nanoparticles on its adsorption properties with respect to fluorine has been elucidated. The surface modification of diatomite with aluminosilicate is accompanied with significant changes in its structure and chemical properties – a growth of specific surface area, a shift of electro-superficial properties and an increase of adsorption capacity for fluorine. Moreover, some kind of synergism takes place after modification: adsorption capacity of aluminosilicate species grafted on the diatomite surface is higher than that of bulk aluminosilicate. The surface-chemical modification of diatomite has been carried out by heating it in a NaOH solution and subsequent treatment with a solution of aluminum salt and after that with ammonia. Amorphous surface silica partially dissolves during the treatment with NaOH and due to addition of an aluminum salt it forms an aluminosilicate compound. The obtained product is further denoted as DMA. The increase in the specific surface area of DMA is connected with variation of the ratio of the micro- and mesopores through the filling of the large mesopores with aluminosilicate and its own microporous structure increment; the specific surface area gets 81.8 m 2 /g, which is 2.5 times larger than the corresponding value of the initial unprocessed diatomite (37.5 m 2 /g). Partial substitution of Si atoms in silicates of diatomite surface by Al atoms creates as a result of their different valences an excess negative charge, and pH PZC of the sorbent surface shifts to higher values compared to initial diatomite sample that facilitates the attraction of more negatively charged ions from solution. Both these phenomena lead to that adsorption capacity of modified diatomite (DMA) with respect to fluorine is considerably increased from 10 to 58 mmol/g. Aluminosilicate in the DMA composition has 1.3 times greater adsorption capacity with respect to fluorine compared to bulk synthetic aluminosilicate. Since the reactive sites responsible for the adsorption are essentially surface aluminum ions, it is expected that their concentration is closely associated with the content of Al 2 O 3 in aluminosilicate. I t is easy to understand that not all the silica in diatomite matrix, but the surface only was subjected to the substitution of Si atoms with Al, so the surface aluminosilicate composition must contain the increased ratio of Al 2 O 3 / SiO 2 ; it is 0.5 according to some calculation compared to the volume ratio which is 0.33; besides, t he surface aluminosilicate is more or less uniformly distributed on the pore material surface, so more aluminum sites are accessible for interaction with fluoride ions. Furthermore, molecular aluminum and silicon precursors are preferentially grafted on sites that enable the formation of Al(IV) coordination form, and deposited aluminum species on silica are Al(IV) tetrahedrally coordinated species. This specific surface site connectivity eventually enables the formation of Brønsted acid sites. Such acid sites may be formulated as bridging hydroxyls in connection with Al(IV) species, such as pseudo-bridging silanol in Al/SiO 2 , therefore more fluorine is involved in complexes with Al. Apparently, all of the above facts together should be responsible for an increased adsorption capacity of the surface aluminosilicate in the DMA composition.