Einfluss der elektrochemischen Doppelschicht auf die Sorption und den Transport von Chlorionen im Zementstein / Influence of the electrochemical double layer on sorption and transport of chlorides in hardened cement paste

Abstract

Abstract Besides the formation of Friedel salt the transport and binding of chlorides in concrete is mainly defined by the electrochemical double layer at the interface between cement matrix and pore solution. Due to the alkaline pore solution the surface of hardened cement paste is negatively charged which may change to positive values by the potential regulating calcium ions. Inverting of the surface charge leads to an attraction of anions and therefore, to an adsorption of chloride ions in the diffuse part of the electrochemical double layer. Influence from outside like sulphates and carbon dioxide may lead to a decomposition of Friedel salt. Apart from these effect temperature, pH-value and certain environmental conditions affects the electrochemical double layer as well. The chloride equilibrium is mainly controlled by adsorbed ions in the electrochemical double layer. The model presented here is relevant for the assessment of ion transport processes in mineral building materials. Continuing investigations may lead to optimize transport models and a better evaluation of the critical chloride threshold value in reinforced concrete.