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  4. Interaction of metallic cations between the inter face of SiO2(s)/solution
 
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Interaction of metallic cations between the inter face of SiO2(s)/solution

Date Issued
2000-07-31
Date
2000-07-31
Author(s)
駱尚廉  
DOI
892211E002018
URI
http://ntur.lib.ntu.edu.tw//handle/246246/22048
Abstract
The transport and fate of metallic cations are issues of concern with regard to the natural environment, such as rivers, lakes, groundwater, and soil in waste disposal sites. When cations exist in an oxide suspension system, it has been proposed that a transition takes place from mononuclear adsorption to hydrolysis to multinuclear adsorption and, finally, to precipitation on the oxide surface or in bulk solution with increasing system pH or cation concentration. SiO2 is the most abundant oxide in the earth crust and can significantly influence a variety of nutrients and pollutants in aquatic and soil environments. Moreover, SiO2 is widely applied to many industrial processes including use as filtration medium in water treatment plants and base substrate in catalysts. Thus, the objectives of this study are to explore the interaction of various metallic cations (Al(III) and Fe(III)) between the interface of SiO2 and aqueous solution. The TEM images show that pure silica particles are aggregate and that the diameter of a primary particle is around 15-25 nm. It is obviously shown from the results that discrete Fe(OH)3 precipitate forms both at low pH (2.40) and at high pH (7.00) around the unchanged size of base SiO2 particle. However, no discrete Al(OH)3 phase is evident in the Al(III)/SiO2 systems. The invisibility of discrete Al(OH)3 precipitate suggests a strong association between Al- (hyro)oxide and the SiO2 surface. With an increasing system pH, the Al(OH)3 precipitate gradually forms on the surface ofthe base SiO2 particle and the particle size becomes larger. The charge reversals (CR) observed in the Al(III)/SiO2 system represent, in order of increasing pH, the point-of-zero charge (PZC) on the SiO2 substrate (CR1), the pH of surface nucleation of Al(OH)3 (CR2), and, at high pH, the PZC of the Al(OH)3 coating (CR3). The observed electrophoresis mobility of Fe(III)/SiO2 is the overall result contributed by negatively charged SiO2 and positively charged Fe(OH)3.
Subjects
SiO2
Al(III)
Fe(III)
Surface
reactions
TEM
Electrophoresis
Publisher
臺北市:國立臺灣大學環境工程學研究所
Type
report
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