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At least 253 records · Page 14

Inhibition mechanisms of steel slag on the early-age hydration of cement

Steel slag inhibits the early-age hydration of cement. However, its mechanism is still unclear. In this paper, the early-age hydration kinetics and the evolution of the solid phases, aqueous species and microstructures in a cement-steel slag composite binder are investigated to explore how steel slag inhibits the early-age hydration of cement. Two novel phenomena are found: (1) steel slag slows the depletion of gypsum and reduces the formation of ettringite, and (2) steel slag significantly inhibits the precipitation of CH and CSH. The results show that the addition of steel slag increases the Ca concentration in the pore solution, reduces the supersaturation of the pore solution with respect to CH and inhibits the nucleation and growth of CSH. Based on the above results, the retardation mechanisms of steel slag on the initial setting of cement paste are explained.

36 MATERIALS SCIENCE↗

Long-term cement hydration studies with isothermal calorimetry

The purpose of this study was to investigate for how long the thermal power of hydration can be measured with isothermal calorimetry, which is a general measurement technique with stable properties that, in many cases, can detect low rates of processes. Measurements were conducted for 365 days on cement paste with Portland cement, fly ash blended Portland cement and different water-to-binder ratios. The results showed that all the tested systems still produced a measureable signal after one year. The samples with Portland cement were also analyzed by XRD after 365 days, and phase composition calculations were made with GEMS. Together with the calorimetric results, these results were used to determine the degree of hydration by five methods, the results of which showed good agreement.

36 MATERIALS SCIENCE↗

Influence of mixing on the generation of nanoparticles in cement systems

In this work, we study the effect of mixing intensity on the size and concentration of nanoparticles in quartz and cement systems. We vary the local shear rate in the studied suspensions induced by mixing by either changing solid volume fraction or mixing speed. Our results obtained on quartz, cement and quartz-cement suspensions provide a master curve relating the concentration of nanoparticles in the pore solution as a function of the local shearing conditions computed at a micromechanical level. Our results suggest, in accordance with literature, that high mixing intensity is at the origin of a detachment of nano-hydrates from the surface of cement particles. These nanoparticles can be stabilized and therefore detected in the pore-solution only in the presence of superplasticizers, which inhibit their agglomeration to other particles.

36 MATERIALS SCIENCE↗

Effects of anionic and nonionic surfactants on the dispersion and stability of nanoSiO2 in aqueous and cement pore solutions

It has been well recognized that the benefits and effectiveness of nanoparticles in cement-based materials could not be maximized if these are not well dispersed. To address this issue, in this study, different anionic (SDS and PCE) and nonionic surfactants (Tweens and Tritons) were used to disperse nanosilica (NS) in aqueous solution and cement pore solution. The results show that the dispersibility of NS in cement pore solution was improved, and the compressive strength of the cement-NS pastes increased linearly with critical micelle concentration (CMC) of nonionic surfactants. Among all surfactants studied, Triton X-405 led the paste to the highest increase in strength (33% at 1-day and 41% at 3-days) since it had the highest CMC. TEM and EDS analysis evidenced that this strength increase might be attributed to the nucleation of outer product CSH gel and its densification with calcite nanocrystals, attributed to Triton X-405 addition.

36 MATERIALS SCIENCE↗

Mechanisms of internal curing water release from retentive and non-retentive superabsorbent polymers in cement paste

This paper examines the mechanisms of desorption within cement pastes for superabsorbent polymers (SAP) with different sorption kinetics: retentive and non-retentive (self-releasing). Despite the different behavior in solution, both SAP types mitigated the autogenous shrinkage of cement pastes. {sup 1}H NMR and X-ray tomography showed that the cavities formed by both SAP types were saturated until 9–11 h after mixing, while the entrained water in the cavities redistributed to the cement matrix afterwards. In particular, the non-retentive SAP might have rapidly released the absorbed water, but the released water stayed in the original cavities. Therefore, the behavior of the SAP in the pore solution may not completely determine their internal curing performance in cement pastes. In particular, the initial absorption that forms the solution-filled cavities might be more important than whether the SAP are able to retain the solution for extended periods of time or not.

36 MATERIALS SCIENCE↗

Impact of limestone fineness on cement hydration at early age

This study compares the influence of two limestone fineness on strength development and cement hydration. The replacement of clinker by 20% of fine limestone (d{sub v,50} = 2 μm and SSA = 4,21 m{sup 2}/g) gives similar strength development to PC up to 7 days. Fine limestone enhances cement hydration and offsets the dilution effect caused by the decrease of clinker amount. The accelerating effect of the limestone was explained by a higher degree of undersaturation with respect to C{sub 3}S. The influence of coarse limestone (d{sub v,50} = 130 μm and SSA = 0,46 m{sup 2}/g) on cement hydration is limited to dilution effect. The combination of fine and coarse limestone was also studied. A linear correlation was obtained between strength and gel space ratio for all investigated systems. Furthermore, the results showed that despite the similarity of specific surface area, limestone is more effective than quartz for the enhancement of cement hydration.

36 MATERIALS SCIENCE↗

Cement hydration kinetics study in the temperature range from 15 °C to 95 °C

The heat evolution during the hydration of cement was examined by multiple calorimetric methods: isothermal, oscillating isothermal, as well as temperature scanning tests in the temperature range from 15 °C to 95 °C. The apparent activation energy (E{sub a}) of several different types of cements were all found to decrease significantly with temperature. Type of additives and water to cement ratio had little influence on the temperature dependence of E{sub a}. The correlation between E{sub a} and temperature may be mathematically simplified to a step function, where E{sub a} is a nonzero constant below a critical temperature (T{sub cr}) and reduces to zero above that temperature. The proposed model of E{sub a} was combined with a scale factor model to simulate the influence of curing temperature on the hydration kinetics of cement with significantly improved accuracy compared to an earlier model.

36 MATERIALS SCIENCE↗

Experimental evidence for the acceleration of slag hydration in blended cements by the addition of CaCl2

Cements with high substitution rates of ground granulated blast furnace slags (GGBS) have the potential to significantly lower CO{sub 2} emissions of concrete, but their early age strength is often below those of traditional OPC cements. One way of mitigating this drawback is to use accelerating admixtures. In this study, the effect of CaCl{sub 2} additions on the hydration of blended cements was investigated by measuring compressive strength, porosity, heat release and propagation of ultrasound in blends containing 70 wt% of GGBS. The onset of formation of aluminate phases was monitored using in-situ XRD. The effect of CaCl{sub 2} on slag hydration was isolated by replacing GGBS by an inert quartz filler. Results showed that compressive strength values at one, two and seven days were increased by 50% by the CaCl{sub 2} addition. The increases in compressive strength corresponded to a reduction in pore space. GGBS hydration contributed to the heat development, structuration and compressive strength of the blended cements from 15 h. The addition of CaCl{sub 2} led to an earlier onset of the GGBS reaction, at around 10 h, and increased the rate of GGBS hydration during the first seven days. The time of onset of the GGBS contribution was also the moment when AFm precipitation started. In CaCl{sub 2}-containing blends, Cl was incorporated in AFm.

36 MATERIALS SCIENCE↗

Investigation of aluminum nitrate as a set retarder of magnesium potassium phosphate cement: Mechanisms involved in diluted suspension

In this study, the influence of aluminum nitrate on the hydration process of magnesium potassium phosphate (MKP) cement was investigated experimentally and through thermodynamic modelling using diluted systems with Mg/PO{sub 4} molar ratio and water-to-cement ratio of 1 and 100 respectively. Three processes contributed to retard cement hydration: the acidic nature of aluminum nitrate which reduced the initial pH of the solution by two units, the early precipitation of a taranakite-like amorphous potassium aluminophosphate, which reduced the aqueous phosphate and potassium concentrations, and a salt effect due to the presence of soluble nitrate. Precipitation of potassium-containing magnesium phosphate hydrates, like Mg{sub 2}KH(PO{sub 4}){sub 2}⋅15H{sub 2}O and K-struvite, was prohibited, whereas precipitation of newberyite and cattiite was delayed. Furthermore, the modelled phase development with ongoing cement hydration agreed rather well with the experimental findings.

36 MATERIALS SCIENCE↗

Agglomeration and reactivity of nanoparticles of SiO 2 , TiO 2 , Al 2 O 3 , Fe 2 O 3 , and clays in cement pastes and effects on compressive strength at ambient and elevated temperatures

We report the agglomeration state of SiO 2 , TiO 2 , Al 2 O 3 , Fe 2 O 3 , bentonite, and halloysite nanoparticles (NPs) in solutions, including simulated cement environments, and their agglomeration and reactivity within the cement paste were evaluated. In water, all NPs formed agglomerates, while sonication and addition of polycarboxylate-based, high range water reducer generally decreased the agglomerate size. Agglomeration of NPs was observed in the chemical environment of hydrating cement paste. The bridging role of Ca 2+ , charge balancing, screening by K + , and pH were identified as factors controlling agglomeration. TiO 2 , bentonite, and halloysite NPs enhanced the cement paste residual compressive strength after exposure to elevated temperature.

36 MATERIALS SCIENCE↗

Visco-inertial gas flow through wellbore cement fractures

Understanding the nature of fluid flow through fractured wellbore cement is fundamental for evaluating the leakage potential and risk assessments of leaky wellbores. In this study, the conditions that require considering visco-inertial flow for describing the gas flow through wellbore cement fractures were investigated. Nitrogen gas flow tests were conducted on fractured cement samples under varying pressure conditions and flow rates, covering both viscous and visco-inertial flow regimes. The data substantially deviated from Darcy's law at higher flowrates and were well-fit to Forchheimer's equation for visco-inertial flow. The inertial coefficient and critical Reynolds number were expressed as a function of the hydraulic aperture. Finally, the empirical function obtained from the experiments was used as an input to numerical simulations which showed the significant role of visco-inertial flow in wellhead pressure build-up and leakage rates, and demonstrated the importance of visco-inertial flow when modeling gas flow through wellbore cement fractures.

03 NATURAL GAS↗

Marginal Gaps between 2 Calcium Silicate and Glass Ionomer Cements and Apical Root Dentin

Introduction: The outcome of periapical surgery has been directly improved with the introduction of novel material formulations. The aim of the study was to compare the retrograde obturation quality of the following materials: calcium silicate (Biodentine; Septodont, Saint-Maur-des-Fosses, France), mineral trioxide aggregate (MTA+; Cerkamed Company, Stalowa Wola, Poland), and glass ionomer cement (Fuji IX; GC Corporation, Tokyo, Japan). Methods: Materials' wettability was calculated concerning the contact angles of the cements measured using a glycerol drop. Cements' porosity was determined using mercury intrusion porosimetry and micro computed tomographic (mu CT) imaging. Extracted upper human incisors were retrofilled, and mu CT analysis was applied to calculate the volume of the gap between the retrograde filling material and root canal dentin. Experiments were performed before and after soaking the materials in simulated body fluid (SBF). Results: No statistically significant differences were found among the contact angles of the studied materials after being soaked in SBF. The material with the lowest nanoporosity (Fuji IX: 2.99% and 4.17% before and after SBF, respectively) showed the highest values of microporosity (4.2% and 3.1% before and after SBF, respectively). Biodentine had the lowest value of microporosity (1.2% and 0.8% before and after SBF, respectively) and the lowest value of microgap to the root canal wall ({[}10 +/- 30] x 10(-3) mm(3)). Conclusions: Biodentine and MTA possess certain advantages over Fuji IX for hermetic obturation of retrograde root canals. Biodentine shows a tendency toward the lowest marginal gap at the cement-to-dentin interface.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Influence of nano-dispersive modified additive on cement activity

In the work the influence of single-walled carbon nanotubes (SWCNT) on the cement activity and the processes of structure formation of the hardened cement paste in different periods of hydration are studied. The changes in the kinetic curves of the sample strength growth modified with SWCNT in amount of 0.01 and 0.0005 % are stipulated by the results of differential scanning colorimetry, scanning electronic and ionic microscopy, X-ray-phase analysis. It was found that the nano-modified additive may increase in the axis compressive strength of the system by 1.4–6.3 fold relatively to the reference samples and may reach 179.6 MPa. It may intensify the hydration process of calcium silicates as well as influence on the matrix of hardened cement paste. The studies are conducted on the structural changes in the hardened cement paste, the time periods of increase and decrease of the compressive strength of the samples, the amount of the calcium hydroxide and tobermorite-like gel as well as the degree of hydration C{sub 3}S and β-C{sub 2}S.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Quantifications of growth rate and particle size of magnesium silicate hydrate cement using small‐angle X‐ray scattering

The focus of recent research on cement binders has shifted to alternatives such as magnesium silicate hydrate (M-S-H) to mitigate the environmental impact of conventional concrete production. However, a detailed understanding of the morphology and growth rate of M-S-H, which informs its applicability as a cementing agent, is lacking. These properties are important as they influence cement hydration and consequently the development of macroscopic properties. Here, in this study, the particle size distribution and growth rate of M-S-H synthesized by mixing aqueous stock solutions were analyzed using synchrotron-based small-angle X-ray scattering. The reaction solutions contained dissolved magnesium and silicon with concentrations ranging from 2 to 500 mM, corresponding to saturation indices with respect to M-S-H endmembers, M 0.75 -S-H and M 1.50 -S-H, between 5.8 and 10.3. The precipitation rates of M-S-H align with affinity-based kinetic models and can be described by the following equations: For M 0.75 -S-H: 𝑟 M 0.75 −S−H =10 −9.54±0.70 ⁢(Ω$^{0.59±0.08}_{M_{0.75}⁢\textrm{SH}}$−1), and for M 1.50 -S-H: 𝑟 M 1.50 −S−H =10 −7.56±0.37 ⁢(Ω$^{0.34±0.04}_{M_{1.50}⁢\textrm{SH}}$−1), where 𝑟 is the rate in mol/L/s, and Ω represents the saturation ratio with respect to M-S-H. Moreover, we observed that changing the [Mg]/[Si] ratio affects particle size, a trend that cannot be fully explained by changes in the saturation index alone. These insights are critical for improving the predictability and control of cementation in concrete that utilizes M-S-H-based binders.

M-S-H↗

Dataset documenting reaction-induced changes to five fractured foamed wellbore cement cores during CO2 fluid flow

This dataset consists of reconstructed CT scans for four fractured foamed cement cores, generated in the lab using Portland Class H cement, and associated processed data. The cements were exposed to reactive brines, and CT scans were take at different time points through the experiment. The CT imaging allows for the tracking of dissolution-induced changes to fracture morphology, as well as alteration and dissolution in the cement matrix.

Computed Tomography↗

Design Guidelines for Predicting Stress in Cemented Doublets Undergoing Temperature Change, Part 2

This work builds on prior work that developed a methodology for evaluating thermal stress in cemented doublets. The prior studies were limited by a paucity of actual test data, particularly from thermally tested cemented doublets. This follow-on study uses the existing methodology to estimate stresses in cemented doublets that have been tested for a temperature range from –40°C to 85°C and establishes safe stress levels using actual data. We also discuss limitations and concerns that we need to address to improve our understanding of cemented doublet failure.

36 MATERIALS SCIENCE↗

Development of a nuclear mixing process for high performance cementation - 15064

In the CEA Project 'Cementation of LLW/ILW Slurry' EIRICH and CEA developed together a high performance mixing process matching the French security regulations for nuclear facilities. Since 2010 mixing tests had been carried out by CEA to develop and verify a new cementation process. In 2012 EIRICH started the development of the mixing equipment for the cementation plant together with CEA. This new cementation plant will be put into operation in 2016 at the CEA site in Marcoule. (authors)

12 MANAGEMENT OF RADIOACTIVE AND NON-RADIOACTIVE W↗

Influence of Particle Size on the Basic and Time-Dependent Rheological Behaviors of Cemented Paste Backfill

The rheological properties of cemented paste backfill (CPB) significantly influence the material’s transportability, and these properties are strongly affected by the material’s particle size. This paper mainly focuses on the influence of particles size on the basic and time-dependent rheological behaviors of CPB. The rheology tests and microstructure analysis were conducted using multiple CPB samples with different solid contents, cement contents, and particle sizes. Results show that the CPB samples with finer particle sizes have a lower apparent maximum packing density compared to the CPB samples with larger particle sizes. Fresh CPB mixture samples exhibit shear thinning characteristics which are more pronounced in samples with larger particle sizes and higher volume fraction to apparent maximum packing density (ϕ/ϕ{sub m}) ratios. When the ϕ/ϕ{sub m} ratio is lower than 0.875, the samples with finer particle sizes display a higher yield stress but less time-dependent rheological behavior than coarser samples. In all CPB samples that contained cement, the shear stress decreases first and then increases over the shearing time when samples are sheared at a constant shear rate. In the CPB samples without cement, samples with finer particle sizes show lower apparent viscosities, and it is observed in the sample with the finest particles that the shear stress only decreases over the shearing time. Moreover, it is found that the number of hydration products and the rate of particle sedimentation are both higher in samples with larger particle sizes, which result in these samples having higher apparent viscosities.

36 MATERIALS SCIENCE↗