Oxidative dissolution of silver nanoparticles: A new theoretical approach

被引:56
作者
Adamczyk, Zbigniew [1 ]
Ocwieja, Magdalena [1 ]
Mrowiec, Halina [2 ]
Walas, Stanislaw [2 ]
Lupa, Dawid [1 ]
机构
[1] Polish Acad Sci, Jerzy Haber Inst Catalysis & Surface Chem, Niezapominajek 8, PL-30239 Krakow, Poland
[2] Jagiellonian Univ, Fac Chem, Ingardena 3, PL-30060 Krakow, Poland
关键词
Kinetics of silver nanoparticle dissolution; Oxidative dissolution of silver nanoparticles; Silver nanoparticle dissolution; Silver ion release; Theoretical model of silver nanoparticle dissolution; ANTIBACTERIAL ACTIVITY; RELEASE; MONOLAYERS; STABILITY; TOXICITY; KINETICS; CELLS; IONS;
D O I
10.1016/j.jcis.2015.12.051
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A general model of an oxidative dissolution of silver particle suspensions was developed that rigorously considers the bulk and surface solute transport. A two-step surface reaction scheme was proposed that comprises the formation of the silver oxide phase by direct oxidation and the acidic dissolution of this phase leading to silver ion release. By considering this, a complete set of equations is formulated describing oxygen and silver ion transport to and from particles' surfaces. These equations are solved in some limiting cases of nanoparticle dissolution in dilute suspensions. The obtained kinetic equations were used for the interpretation of experimental data pertinent to the dissolution kinetics of citrate-stabilized silver nanoparticles. In these kinetic measurements the role of pH and bulk suspension concentration was quantitatively evaluated by using the atomic absorption spectrometry (AAS). It was shown that the theoretical model adequately reflects the main features of the experimental results, especially the significant increase in the dissolution rate for lower pH. Also the presence of two kinetic regimes was quantitatively explained in terms of the decrease in the coverage of the fast dissolving oxide layer. The overall silver dissolution rate constants characterizing these two regimes were determined. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:355 / 364
页数:10
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