Silver Adsorption on the Low Temperature Activated Alumina Grades. I. Adsorption Capacity and Kinetics

Abstract

Aluminum hydroxide is a key product for the industrial production of alumiana and aluminium, ceramics insulator and refractories, desiccants, absorbents, flame retardants, filers for plastics and rubbers, catalysts, and various construction materials. The production of these arrays of useful material products is grounded on the multiple thermal decomposition pathways of Al(OH)3, which involve major crystallographic dislocations and many microstructure reconfigurations on variable lines of phase transitions, from the raw material up to large varieties of precursors and commercial grade products. A wide range of literature on this subject is available, and recent reviews cover suitable information about preparation and characterization of different activated alumina products with specific properties and applications. In our previous papers, there was studied the mechanisms of aluminum hydroxide phase transitions, during low temperature calcination, namely, at 260ºC, 300ºC, 400ºC and 600 ºC, under chosen particularly conditions, for promoting the nucleation of the amorphous phases. Collected data suggest that raw aluminum hydroxide; dried, milled and classified is a precursor for the new low temperature activated alumina transition phases, carrying distinctive characteristics and properties, due to products enrichment in amorphous phases. Accordingly, as effects of the main driving factors (temperature and rate of heating, and initial particle size dimension) on the aluminum hydroxide as new precursor, notable changes were observed in products mineral composition, morphology and specific surface area, pore size, pore distribution, and the particle size distribution. Beside, some other secondary effects have to be apprehended. For example, the main phase transition process dinamic factors control over some physical and technical properties of the new products, like: absolute density, brightness, oil absorption capacity and water absorption capacity. The purpose of this work was to continue the characterization of low temperature activation alumina products, and also, to measure the adsorption capacity and to reveal adsorption kinetics mechanisms. Thus, the first step of survey was silver adsorption maximum capacity measurements for all sample prepared by heating the precursor alumina hydroxide, milled and classified as 5 different dimension size fractions to 260, 300, 400 and 600ºC. Hereinafter, four samples, carefully selected as representative for the entire lot of samples, were used for the study of kinetics mechanism and data fitting to the adequate kinetic equations. Confident data validate the pseudo second order kinetic model for the entire activation process, independently of samples heating temperature and particles dimension.