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Journal ArticleDOI

The alkali-silica reaction, part I: Use of the double-layer theory to explain the behavior of reaction-product gels

Monica Prezzi, +2 more
- 01 Jan 1997 - 
- Vol. 94, Iss: 1, pp 10-17
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TLDR
In this paper, a double-layer model is proposed to explain the volume change behavior of mortar bars containing a reactive aggregate, and the expansion of the reaction-product gels is attributed to swelling caused by electrical double layer repulsive forces.
Abstract
An understanding of the expansion mechanisms resulting from alkali-silica reaction is necessary to assess the susceptibility of a concrete structure to deterioration by these processes and to the planning and implementation of preventive measures. As a result of the alkali-silica reaction between certain reactive aggregates and the highly alkaline pore fluids in a cement paste, a reaction-product gel develops that, in the presence of water, expands and may cause cracking of mortar or concrete. To explain the volume change behavior of mortar bars containing a reactive aggregate, a theoretical model is proposed in this paper. The expansion of the alkali-silica reaction-product gels is attributed to swelling caused by electrical double-layer repulsive forces. For a given colloidal system, double-layer theory indicates that the larger the valence of the counterions in the double layer, or the larger the concentration of these ions, the smaller the double-layer thickness and the repulsive forces that may be generated in the presence of water. Results of experiments from the literature support the double-layer model. According to these results, the expansion of mortar bars in the American Society for Testing and Materials (ASTM) C 1260 test is related to the composition of the reaction product gels. The reaction-product gels containing larger amounts of equivalent sodium oxide (Na2Oe) and smaller CaO/Na2Oe cause larger expansions in the mortar bars.

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Journal ArticleDOI

Alkali-silica reaction: Current understanding of the reaction mechanisms and the knowledge gaps

TL;DR: In this article, the authors summarize the current state of understanding and the existing knowledge gaps with respect to reaction mechanisms and the roles of aggregate properties (e.g., composition, mineralogy, size, and surface characteristics), pore solution composition, pH, alkalis, calcium, aluminum, and exposure conditions, such as temperature, humidity) on the rate and magnitude of alkali-silica reaction.
Journal ArticleDOI

Mathematical model for kinetics of alkali-silica reaction in concrete

TL;DR: In this paper, a model for the chemical reaction of the alkali-silica reaction (ASR) in concrete is presented, where a spherical layer of basic ASR gel grows radially inward into the particle, controlled by diffusion of water toward the reaction front.
Journal ArticleDOI

Use of waste glass as sand in mortar: Part II – Alkali–silica reaction and mitigation methods

TL;DR: In this article, the influence of glass content, color and particle size on ASR expansion of mortar was determined by the accelerated mortar bar method, and two approaches were investigated for green, brown and clear glass sand mortar, and they were: (1) replacing cement with pozzolans, that is, 30% fly ash, 60% GGBS, 10% silica fume, or 20% glass powder; (2) adding a suppressor, that are, plain steel fibers, and lithium chloride and lithium carbonate compounds.
Journal ArticleDOI

Modified model of alkali-silica reaction

TL;DR: In this article, an experimental study has been carried out for understanding why soft and fluid hydrated alkali silicate generated by the alkali-silica reaction (ASR) of aggregate with alkaline pore solution accumulates the expansive pressure for cracking the aggregate and the surrounding concrete.
Journal ArticleDOI

The Behavior of Zeta Potential of Silica Suspensions

TL;DR: In this article, it was observed that for pH values below the isoelectric point (IEP), the positive value of zeta potential of water suspensions of α-quartz and α-cristobalite, experiences a sudden steep increase with the increase in specific surface area of the powders.
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