Adsorption de polycarboxylates et de lignosulfonates sur poudre modèle et ciments

Placing concrete requires much more water than the cement needs for its hydration. This results in an important porosity in the hardened concrete, which accentuates the degradation of this material. By adding small amounts of polymeric admixtures, called superplasticizers, to the fresh concrete one can significantly reduce the amount of water required to obtain the suitable workability. The plasticizing effect of superplasticizers has been studied for many years, and remains today, an ongoing field of research. This research led to a better understanding of the forces that act during the deflocculation and dispersion of cement grains induced by superplasticizers. This research work was performed within the framework of the "Superplast" European project. Its main objective has been to determine which parameters (molecular structure, induced charge, adsorption mode, molar mass) influence the plasticizing effects of superplasticizers. The results of this study will allow synthesis new polymeric admixtures with better performances than those currently available. For this study, two types of superplasticizers were selected: lignosulfonates and polycarboxylates. For each one, different samples were synthesised and characterised. For each sample, adsorption, rheological and interaction forces measurements were performed by our partners while we have performed adsorption and electroacoustic measurements on model powder suspensions. Different cement model powders were investigated and a magnesium oxide was selected. The particle size distribution and reactivity were carefully characterized. The inert model system (MgO) allowed us to study adsorption mechanisms without the complexity linked to cement hydration reactions that modify surface and solution of the suspension. Particle surface charge and pH are the two main parameters that influence the polymer adsorption and the polymer conformation. Magnesium oxide which has a high isoelectric point (around at pH 12.4) allows a surface charge similar to cement suspensions at high pH. First, we have measured the adsorption isotherms of all superplasticizers on model suspensions in NaOH (0.01M). This study allowed us to evaluate the affinity of each polymer for MgO and its adsorption plateau. These measurements showed that the lignosulfonates have a higher affinity than the polycarboxylates. They also showed that lignosulfonate adsorption is mainly influenced by their molar mass and their carboxylic group content (for similar sulfonate group content) while polycarboxylate adsorption is mainly driven by the backbone length, the side chain length and the carboxylic group content. Adsorption plateaux allowed us to calculate the surface coverage ratio and to estimate the superplasticizer conformation on the surface. Adsorption isotherms were finally measured on a Portland cement. The polymer adsorption is influenced by the same parameters as on MgO. The model system MgO is representative for the polymer adsorption on cement. In a second step, different electrolytes were added to model suspensions. This practice allowed us to study separately the effect of the main ions present in cement suspensions (Na+, Ca2+, SO42-, OH-) and to mimic the ionic composition of the aqueous phase of the cement suspension. Lignosulfonate adsorption is neither influenced by the studied ions or the pH. Only an increase of ionic strength increases the adsorbed polymer mass. Polycarboxylate adsorption is influenced by calcium and sulfate ions and by the particle surface charge. Finally, superplasticizer adsorption was studied on different cements by our partners and on a fly ash and a silica fume by ourselves. Lignosulfonate adsorption isotherms on cements showed that affinity and adsorbed polymer mass increases with the C3A content and decreases with the alkalis content. The isotherms measured on industrial by-products showed that superplasticizers adsorb on fly ash, but not on silica fume.

Autogenous Shrinkage and Hydration Kinetics of SH-UHPFRC under Moderate to Low Temperature Curing Conditions

Mohammadhadi Kazemi Kamyab

Strain Hardening Ultra High Performance Fiber Reinforced Concrete (SH-UHPFRC) were used successfully over the last 8 years in numerous cast in place rehabilitation applications as long lasting waterproofing layers (20 to 30 mm thickness) and, combined with rebar, to increase the structural load bearing capacity of existing bridge decks or building slabs (50 to 70 mm thickness). In composite applications on reinforced concrete substrates, SH-UHPFRC provide a deformation capability (strain hardening) larger than their free shrinkage which makes localized macro cracking at service state very unlikely. On the other hand some specific conditions of microclimatic state of the substrate (moisture and thermal conditions) and climatological (temperature and humidity) of the site such as casting at low temperatures (winter conditions) might increase the autogenous shrinkage and thus eigenstresses of the freshly cast SH-UHPFRC and hinder the development of its tensile strength or/and deformability. Combination of these specific circumstances could compromise the SH-UHPFRC protective functions due to the occurrence of localized macro cracks, making the objective of using SH-UHPFRC as a onetime intervention strategy in rehabilitation application obsolete. Advancement in hydration at early age leads to formation of partially emptied capillary spaces contributing to self-desiccation, decrease of the relative humidity and increase of the capillary depression. Since water is under depression, the solid porous material is under compression forcing the material to shrink. From the aforementioned, it can be deduced that the autogenous shrinkage is a force driven phenomenon: a force is applied on the ageing viscoelastic porous skeleton and the apparent structural response of the bulk cementitious material is the autogenous shrinkage strain. Based on the aforementioned two levels of investigation were considered in this thesis: I. Material level: ageing viscoelastic porous skeleton of hydrating cementitious material II. Structural level: autogenous shrinkage development under the action of its driving forces The objective of this thesis was to study the development of the autogenous shrinkage and its relation with the development of microstructure and mechanical properties in SH-UHPFRC cured at moderate and low temperature conditions (1 to 20°C). Focus was put on: (1) kinetics and magnitude of hydration of silica fume and cement, (2) activation energy of the processes, (3) stiffness (E modulus and Poisson ratio) development, and (4) states of water and pore development. Finally a cross link analysis of information obtained from material and structural level was carried out to better highlight the mechanisms and driving forces of autogenous shrinkage. CM22-TKK, a SH-UHPFRC developed at MCS for rehabilitation applications, on the basis of CEMTECmultiscale® fibrous mixes, was used. Silica fume is one of the major constituents of CM22-TKK (26% by mass of cement). Extent of the silica fume pozzolanic reaction significantly affects the pore size distribution of the UHPFRC matrix which then influences the development of the relative humidity, self-desiccation and finally autogenous deformation. Detailed experimental investigation performed showed that only maximum 8% by mass of cement out of 26% silica fume used in the recipe reacts in moderate and low temperature curing conditions. Finally, a model of silica-fume degree of reaction as a function of curing temperature (5 to 250 °C) was proposed on the basis of a detailed literature survey of existing works with low W/B mixes. The activation energy of the thermo-mechanical properties was evaluated for thermo (cumulative heat of hydration) and mechanical properties development (such as dynamic Elastic modulus, dynamic Poisson’s ratio and compressive strength). A single activation energy Ea of 27.4 KJ/mol could successfully model the activation of all properties. Since maturity was not a proper reference to compare the autogenous deformations at various temperatures, a more fundamental reference such as degree of hydration was used. Experimental investigation was carried out using different techniques such as isothermal calorimetry and 29Si solid NMR to evaluate the development of the degree of hydration of cement and silica fume in UHPFRC at moderate and low temperature curing conditions. The ultimate degree of hydration of cement in CM22-TKK for a closed system was 0.34. There was a close correspondence between the experimental results and the predictions of the volumetric phase distribution models of Waller (0.28) and Jensen (0.32). Finally, the De Schutter et al. 1996 model was used to describe the mechanical properties (Emodulus and Poisson ratio) as function of degree of hydration. Nondestructive and non-invasive 1H-NMR was used to evaluate volumetric phase distribution development at 20°C, especially the classification of the water types (capillary, gel and C-S-H interlayer water) which brought fully new and valuable information about the hydration kinetics and pore size development. The results were also compared with Jensen volumetric phase distribution model to check the advantages and limitation of both approaches. Finally experimental investigation was carried out to follow the development of autogenous shrinkage and eigenstresses (in case of restrained shrinkage) of CM22-TKK cured in isotherm conditions (1 to 20°C). Eigenstresses were obtained and used to highlight the effect of the viscous response of the material at the different temperatures investigated. The previously mentioned results on the kinetics of the silica fume reaction, cement hydration and evolution of states of water and development of stiffness were then put into perspective with the trends observed on the autogenous shrinkage and eigenstresses development.

EPFL2013

Impact of water activity on the mineralogy of hydrated cement

Luis Guillermo Baquerizo Ibarra

Cement hydrates and their chemically bound water content are sensitive to changes in relative humidity (RH) and temperature. This may cause specific solid volume changes affecting dimensional properties of hydrated cement paste such as shrinkage, swelling and expansion, and therefore impact the performance and the transport properties of cementitious materials. The present thesis studies the impact of drying conditions on the structure and thermodynamic properties of crystalline cement hydrates in different hydration states (i.e. varying molar water contents). The cement hydrates studied include the most important AFm and AFt phases present in different types of cements. A novel multi method approach, including XRD, TGA, DSC, sorption balance measurements, sorption calorimetry and the hydrate pair ¿ humidity buffer method, was used to derive physico-chemical boundary conditions and the thermodynamic properties of the studied hydrated phases. The stability and hydration states of AFm phases depend on the anion content and the exposure conditions. Some phases such as monosulfoaluminate and hydroxy-AFm are very sensitive to different relative humidities. On the other hand monocarboaluminate and strätlingite present very good volume stability with varying RH. Ettringite shows a strong hysteresis during desorption/adsorption, and the thermodynamic properties associated with its decomposition and reformation were determined. The experimental results were included into a thermodynamic model capable of predicting the response of cementitious systems considering the ¿true¿ crystal water content on the final phase assemblage in two different scenarios: i) during hydration, even at conditions where the amount of water added was insufficient for complete hydration, and ii) during drying and re-wetting processes in already hydrated systems. Our work hence opens the possibility to model the response of various cement materials exposed to different climatic conditions and to engineer cementitious systems with respect to minimizing volume changes in the course of drying, which may positively impact properties like drying shrinkage and total porosity.

EPFL2015

Modified poly(carboxylate ether)-based superplasticizer for enhanced flowability of calcined clay-limestone-gypsum blended Portland cement

Tunahan Aytas, Aurélie Rosine Favier, Amin Hodaei, Karen Scrivener, Buse Tatli

Supplementary materials that are utilized to replace ordinary Portland cement (OPC) decrease the workability of the cementitious mixtures and superplasticizers are usually added to cement to control their fluidity. In general, current superplasticizers are solely optimized for single component systems such as OPC. Here, we report the performance of a series of a modified poly(carboxylate ether)-based superplasticizers (PCEs) in a ternary OPC-calcined clay-limestone blend. We have utilized: i) a co-monomer with high ionic character, 2-acrylamido-2-methylpropane sulfonic acid (AMPS) to be incorporated into the acrylic acid backbone of PCEs and ii) low density of polyethylene glycol (PEG) grafted chains < 0.01 mol/mol. The optimized polymer does not intercalate into the layered structure of calcined clay and preserves its steric size in the presence of high concentration of sulfate ions.