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Since its invention in the early 1990’s, self-consolidating concrete has never become well established in the ready-mix sectors worldwide. The reason for this can be mainly found in the fact that the sophisticated compositions are sensitive against changing environments. This lack of robustness can be attributed to the interaction between cement hydration reaction and high range water reducing agent (HRWRA). Understanding the relevant mechanisms that control the initial flow performance as well as the flow retention helps optimizing SCC mixtures that perform either steadily in one specific environment or that perform largely similarly at steadily changing environments.
This paper depicts how HRWRAs interact with clinker and hydration phases and discusses the important role of the charge density of a polycarboxylic HRWRA in the way the rheology is affected. Based on rheometric results and observations of the Vicat setting times, it is shown that increasing charge densities of the HRWRA and decreasing water to powder ratios (w/p) reduce the flow retention and have lesser retarding effect on the setting. Based on the discussion, optimization procedures for the mixture composition and the HRWRA modification are suggested to achieve optimized performance for varying environmental situations or highest robustness for specific conditions.
Todays superplasticizers for self-compacting concrete and high Performance cementitious materials are very versatile. Typically superplasticizers are composed of a polycarboxylic backbone equipped with polyethylene oxide graft chains of variable length and grafting degree. The mode of operation of these admixtures is based on the steric repulsion of the particles upon adsorption. The adsorption is strongly depending upon the charge density of a superplasticizer and the time dependent Adsorption processes control the retention of the flow performance – an important issue particularly for ready-mix and construction site concrete. However, the properties of polycarboxylic superplasticizers typically remain a black box for users. The paper suggests a simple and rapid test method, which can be conducted without sophisticated equipment, to qualitatively distinguish between two types of superplasticizers based on the adsorption mechanism. Interpreting the results in the right way provides a powerful tool to choose the right admixture for individual time dependent flow specifications.
Chemical admixtures like superplasticisers or stabilising agents are of ever increasing importance for modern concrete technology. They liberate the workability of concrete from its dependency on water content, and thus, open the gate towards innovative and future oriented concrete technologies such as selfcompacting concrete. Meanwhile admixtures have become common practice in concrete technology, but the understanding of these highly complex polymers in the entire concrete system lags far behind their application. Due to its complex time-dependent, multi-phase and multi-scale behaviour, flowable concrete systems are highly complicated and cannot be described comprehensively by simple models. It is therefore extremely challenging to identify the relevant parameters that predominantly control flow phenomena on different size scales, since these may occur on any scale between the nano scale (e.g. superplasticizer adsorption) and macro scale (e.g. grading of the aggregates). The present study discusses fundamental mechanisms at the interface between particle or hydrate surfaces and the fluid phase at a very early stage of concrete formation, and links these effects to macroscopic flow phenomena. Methods are discussed that appear promising interdisciplinary tools for enhancement of the understanding of the relevant interactions that are responsible for the macroscopic flow of flowable concrete.
Viscosity-modifying agent (VMA) are used in several applications of concrete, such as underwater concrete, Self-Compacting Concrete (SCC) or Self-Levelling Underlayments (SLU) in order to improve the washout resistance and the stability. The study focuses on the modifications of cement pastes properties implied when a VMA (hydroxypropyl guars or HPG) and a superplasticizer are introduced together. For reaching this objective, two chemically different polycarboxylate-based superplasticizers (PCE) and two HPGs exhibiting different molar substitution ratios (MSHP), were studied. A method, combining total organic carbon and size exclusion chromatography, was developed in order to quantify the adsorption of the both admixtures. The adsorption of HPGs appears being significantly lowered by the presence of PCE, while only the adsorption of the less charged PCE is slightly affected by the HPG. As consequence, strong modifications of the rheological properties of cement pastes were noticed when HPG and PCE are combined. The desorption of HPG leads to higher yield stress and residual viscosity than with PCE alone.
Effect of Polycarboxylate Superplasticizer in Ordinary Portland Cement and Sulfate Resistant Cement
(2023)
Polycarboxylate superplasticizers (PCE) are the most widely used admixtures in today’s cementitious construction materials. The molecular structure has a decisive influence on the effectiveness of PCE, which also can be tailored to serve in a different cementitious system.
The current study investigates the influence of the backbone charge density of PCE on the rheology, hydration kinetics, and adsorption behavior of ordinary Portland cement (OPC) and sulfate-resistant cement (SRC). The results indicate that regardless of the PCE type, OPC requires a higher amount of PCE to be adsorbed to induce changing of rheological parameters and hydration kinetics. Regardless of the cement type, the PCE with a higher charge density exhibits higher adsorption behavior, corresponding to lower viscosity measurement.
Compared to OPC, SRC is more sensitive to the introduction of both PCEs and has a lower saturation dosage, indicating that SRC generally provides better workability properties regardless of the PCE.