6 research outputs found
Release of Silicon and Aluminum from Montmorillonite Surfaces in Aqueous Systems
The release of silicon and aluminum from purified Na-montmorillonite surfaces in aqueous
systems was investigated in dependence of pH at 25 Ā°C. This study has shown that the dissolution
of montmorillonite solid involves several parallel and sequential physico-chemical processes.
The initial fast exchange of surface cations by hydrogen ions is followed by the release
of aluminum and silicon. The dissolution rate of Si is higher than that of Al and influenced by
the relative ratios of basal siloxane and edge surfaces. It is quantitatively described by the dissolution
rate constants depending on pH. These results are in agreement with the heterogeneity
of montmorillonite surfaces and the dominant presence of the siloxane basal surface. The shift
of pH to more basic values by the ion exchange processes, and the hydrolysis of dissolved species,
induces the formation of secondary amorphous solids, which may serve as precursors for
the formation of amorphous aluminosilicates
INTERACTIONS AT INORGANIC/ORGANIC INTERFACES - FROM BIOMINERALIZATION TO HARD TISSUE IMPLANT MATERIALS
Osnova veÄine prirodnih procesa taloženja jesu meÄudjelovanja na meÄupovrÅ”ini organsko/anorgansko. Kosti i bubrežni kamenci su dvije vrste tkiva koja privlaÄe veliku pažnju zbog medicinskih problema vezanih uz njih. U ovom radu, kroz prikaz istraživanja meÄudjelovanja organskih molekula s kristalima kalcijevih fosfata u naÅ”oj grupi, pokazat Äemo kako se spoznaje dobivene i opisane u istraživanjima pojednostavljenih modelnih sustava mogu primijeniti na osmiÅ”ljavanje i priptavu novih biomimetiÄkih presvlaka za metalne implante.Interactions at organic/inoiganic interfaces underly many natural precipitation processes. Bones and urinary stones are two types of mineralized tissue in human organism that attract special attention due to the medical problems connected with them. In this paper, through the review of the investigations of interactions between organic additives and calcium phosphate crystalls performed in our group, it is shown how results obtained in these model systems can be applied in design and preparation of novel biomimetic coatings for bone metal implants
Interactions at inorganic/organic interfaces - from biomineralization to hard tissue implant materials
Osnova veÄine prirodnih procesa taloženja jesu meÄudjelovanja na meÄupovrÅ”ini organsko/anorgansko. Kosti i bubrežni kamenci su dvije vrste tkiva koja privlaÄe veliku pažnju zbog medicinskih problema vezanih uz njih. U ovom radu, kroz prikaz istraživanja meÄudjelovanja organskih molekula s kristalima kalcijevih fosfata u naÅ”oj grupi, pokazat Äemo kako se spoznaje dobivene i opisane u istraživanjima pojednostavljenih modelnih sustava mogu primijeniti na osmiÅ”ljavanje i priptavu novih biomimetiÄkih presvlaka za metalne implante.Interactions at organic/inoiganic interfaces underly many natural precipitation processes. Bones and urinary stones are two types of mineralized tissue in human organism that attract special attention due to the medical problems connected with them. In this paper, through the review of the investigations of interactions between organic additives and calcium phosphate crystalls performed in our group, it is shown how results obtained in these model systems can be applied in design and preparation of novel biomimetic coatings for bone metal implants
Interactions of Sodium Dodecylbenzenesulfonate and Calcite in 0.55 M NaCl Solution
Complex mutual interactions of calcite and sodium dodecylbenzene sulfonate (NaDBS) were studied in 0.55 M NaCl solution, using several complementary techniques.
Adsorption of NaDBS on calcite could be resolved from other processes such as adsorption onto the reaction vessel and/or formation of solid crystalline phase, when a special a.c. voltammetric procedure was used below the critical micelle concentration (c.m.c. = = 9 x 10-5 mol/L). A two-plateau type isotherm was obtained. Initial adsorption of NaDBS occurs at Ca2+ ions on the calcite/solution interface through electrostatic interactions. The second stage of adsorption was described as hydrophobic interaction between hydrocarbon chains from bulk solution and those electrostatically adsorbed on calcite, forming surface aggregates.
The results of adsorption were analyzed by a two-step adsorption model. The equilibrium constants and &2 for the first and second adsorption step, the surface aggregation number, re, the amount of adsorbed monomer, the saturated adsorption, rm and the standard free energy of surface aggregate formation for one mole of surfactant, AG^m, were calculated