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EN
TiO2 attracts much interest because of its many potential applications. The use of titanium dioxide strongly depends on its polymorphic form: brookite, anatase, or rutile. Only rutile and anatase play an important role in industry. Anatase as a metastable form undergoes a non-reversible transformation into rutile. Understanding the kinetics of phase transformation and the processes of crystal growth of a material is essential for controlling its structure and, thus, its specific properties. The main purpose of this paper is to explain the anatase to rutile recrystallization kinetics in the modified TiO2 calcined from industrial hydrated titanium dioxide. The apparent activation energy of anatase to rutile transformation and the average size of titanium dioxide crystallites were determined for the unmodified TiO2 and TiO2 modified with P, K, Al, B, Zn, Zr, Ce, Sn, or Sb introduced in the amount of 0.5 mol% and 1.0 mol% when recalculated for their oxides. The growth of TiO2 crystallites during calcination was strongly inhibited by P, Ce and Zr, and inhibited to a lesser degree by Al, Sn and Sb. B and Zn did not affect the investigated process and K accelerated crystallites growth. The values of apparent activation energy depending on a modifier formed a relationship: Al
EN
Chitosan is naturally abundant biopolymer that could be used as chelating sorbent for removal of metal ions from aqueous solutions. In this study the uniform-sized chitosan microspheres and their modified derivatives were prepared by using the one stage membrane emulsification process. The obtained sorbents were used for removal of chromium VI ions. The sorption evaluation was carried out at different initial ion concentrations and allowed to fit the experimental data to Langmuir isotherm in the case of unmodified materials and to Freundlich isotherm in the case of modified microspheres. The highest sorption towards chromium has been shown by unmodified chitosan with medium molecular weight. The calculated maximum sorption capacity for this polymer was found to be 1.6 mmol/g.
EN
The aim of this work was to study the activity of unmodified and modified ZnO in the peroxide crosslinking of hydrogenated acrylonitrile-butadiene elastomer (HNBR) and ethylene-propylene copolymer (EPM). In the first step, zinc oxide was obtained by emulsion precipitation. Maleic acid was introduced onto the surface of ZnO using an in situ method. The unmodified and modified zinc oxide was characterized using dispersive and morphological analysis, BET surface area analysis, and elemental, spectroscopic and thermal analysis. In the second stage of the research, the ZnO/MA systems were incorporated into the structure of elastomer compounds improving the kinetic and mechanical properties of vulcanizates. The proposed modification method had a favorable effect on the physicochemical properties of the zinc oxide and on the kinetic and mechanical properties of the vulcanizates. This study demonstrated that modification of zinc oxide by maleic acid is a promising technique.
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