Abstract.1 The kinetics of copper ions adsorption by natural zeolite has been investigated in the apparatus with mechanical stirrer. The presence of external diffusion and pore diffusion area was established. For the external diffusive area, the dependence of mass transfer coefficient on stirrer rotation speed was confirmed; the dependence was described using a criterial equation. For the pore diffusion area, the equation is adduced by means of which the effective coefficient of pore diffusion was calculated.
The mechanism of phosphates sorption process on clinoptilolite was determined. The significant increase in zeolite sorption capacity was observed while interaction of zeolite and wastewaters with acid reaction. New active centers of zeolite are formed due to disalumination of its surface.
The statics and kinetics of albumin adsorption on natural zeolite of clinoptilolite structure have been investigated. The basic characteristics of zeolite have been determined. The method of albumin in a solution analysis was given. An isotherm of albumin adsorption was plotted and the Langmuir equation describing this isotherm was given. The presence of an external and pore diffusion adsorption mechanism has been experimentally established during the study of kinetics in a machine with mechanical stirring. The mass-transfer coefficient for external diffusion and the molecular diffusion constant for the pore diffusion are determined.
1 The adsorption of ammonium ions by natural zeolite and Al 2 O 3 under static conditions has been investigated. The reason for changing the investigated solution pH during adsorption of ammonium ions on Al 2 O 3 has been grounded. A phase diagram of the twocomponent system has been constructed and the composition of the adsorption system in the state of equilibrium has been determined. The thermodynamic calculations of the adsorption system Al 2 O 3-NH 4 Cl-H 2 O have been carried out. It was established that the adsorption of ammonium with aluminum oxide occurs via the mechanism of physical adsorption.
In the paper, the assessment of the impact of heavy metals on water objects, namely copper and chromium was performed, and the methods for their neutralization were defined. A scientifically grounded method for the selection of natural zeolite for the purification of wastewater from heavy metals has been developed, provided that they are jointly present. The physicochemical characteristics of two metals related to heavy metals are presented: copper and chromium. The methods for determining the sorption capacity of natural zeolite for copper and chromium compounds, as well as the methods of analytical control of the wastewater components were presented. The results of the experimental studies on the combined adsorption of copper and chromium cations by natural zeolite under static conditions were presented. The changes in the chemical composition of the zeolite surface as a result of heavy metal sorption have been investigated. The influence of the nature of the ions and the pH of the adsorption medium on the selectivity of the heavy metal ions extraction by zeolite was analyzed. A diagram of the composition of the solution, depending on the pH values, was constructed. The pH of the beginning of deposition of the corresponding heavy metal hydroxides on the zeolite surface was calculated. While analyzing the results of experimental studies on the combined adsorption of copper and chromium ions, it was found that the copper ions are significantly better adsorbed by the sorbent than the chromium ions. Despite the same concentration of the chromium and copper ions in solution, Cu 2+ is extracted selectively. As can be seen from the results of experimental studies, the concentration of copper on the surface of the sorbent increases from 0.628% mass at a concentration of 0.01 g/dm 3 to 47.380% mass at a concentration of 1 g/dm 3 . The studies on the static activity of clinoptilolite for the copper and chromium ions indicate a simultaneous mechanism of the process, which involves ion exchange and physical adsorption. The concentration of the chromium ions on the surface of the sorbent after adsorption depends on the increase of the concentration of Cr 3+ in the original solution to a lesser extent. The results of the studies on the combined adsorption of the Cu 2+ and Cr 3+ ions indicate the possibility of their chromatographic separation, which makes their further use possible.
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