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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.
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.
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.