Abstract:The paper discusses a possibility of using an ultrasonic wave transmission method to study the influence of superplasticizers on the formation of structure of cement pastes at early ages. When compared to mixtures without additives, lower P-wave velocity was found through superplasticized cement pastes, indicating that superplasticizers prevent formation of a solid network frame. Comparing to sulfonate naphthalene-formaldehyde superplasticizers, polycarboxylate ether (PCE) admixtures retarded the solid network… Show more
“…Interestingly, the delaying effect of superplasticizers was compensated by increasing the final mixing speed (compare Figures 16 (a), (b), and (c)). Retardation of cement hydration due to superplasticizers has been commonly reported, and could be due to adsorption of the polymer molecules of the superplasticizer onto cement particles inhibiting subsequent topochemical reactions from occurring [50,[55][56][57][58][59] and/or an increase in the time needed to reach the percolation threshold due to the particles being initially dispersed further apart from the superplasticizer [53]. It was seen that the apparent viscosity of the 045_SP mixture was lower than of the 045 mixture (see Figure 5) at all the sample preparation mixing speeds that were used in this research.…”
Section: Changes In the Chemical Environment Of Cement Pastementioning
From both the fundamental and applied points of view, there is a growing interest in characterizing the rheological properties of concentrated suspensions, such as cement paste. When a cement paste is sheared, its intrinsic network structure will respond to the shear induced stresses. The influence of mixing intensity on the rheological properties of fresh state cement paste is studied. The results showed that contrary to what is popularly believed, when subjected to a high mixing intensity the rheological properties of cement paste can increase once a certain threshold mixing intensity is achieved. This increase in rheological properties was associated with changes in the chemical nature and physical nature of the cement pastes.
“…Interestingly, the delaying effect of superplasticizers was compensated by increasing the final mixing speed (compare Figures 16 (a), (b), and (c)). Retardation of cement hydration due to superplasticizers has been commonly reported, and could be due to adsorption of the polymer molecules of the superplasticizer onto cement particles inhibiting subsequent topochemical reactions from occurring [50,[55][56][57][58][59] and/or an increase in the time needed to reach the percolation threshold due to the particles being initially dispersed further apart from the superplasticizer [53]. It was seen that the apparent viscosity of the 045_SP mixture was lower than of the 045 mixture (see Figure 5) at all the sample preparation mixing speeds that were used in this research.…”
Section: Changes In the Chemical Environment Of Cement Pastementioning
From both the fundamental and applied points of view, there is a growing interest in characterizing the rheological properties of concentrated suspensions, such as cement paste. When a cement paste is sheared, its intrinsic network structure will respond to the shear induced stresses. The influence of mixing intensity on the rheological properties of fresh state cement paste is studied. The results showed that contrary to what is popularly believed, when subjected to a high mixing intensity the rheological properties of cement paste can increase once a certain threshold mixing intensity is achieved. This increase in rheological properties was associated with changes in the chemical nature and physical nature of the cement pastes.
“…This period lasted for up to ~300 h of hydration for the TiO 2 -containing samples (between lines C and D) and up to ~ 700 h for the reference sample (between lines C and E). The data show a nonlinear behavior for the TiO 2 -containing specimens and a linear behavior for the reference sample, a characteristic of adding fine aggregates to cement [ 66 , 67 , 68 , 69 , 70 ]. The addition of fine aggregates accelerates the evolution of the microstructure [ 51 ].…”
Titanium dioxide (TiO2) is an excellent photocatalytic material that imparts biocidal, self-cleaning and smog-abating functionalities when added to cement-based materials. The presence of TiO2 influences the hydration process of cement and the development of its internal structure. In this article, the hydration process and development of a pore network of cement pastes containing different ratios of TiO2 were studied using two noninvasive techniques (ultrasonic and NMR). Ultrasonic results show that the addition of TiO2 enhances the mechanical properties of cement paste during early-age hydration, while an opposite behavior is observed at later hydration stages. Calorimetry and NMR spin–lattice relaxation time T1 results indicated an enhancement of the early hydration reaction. Two pore size distributions were identified to evolve separately from each other during hydration: small gel pores exhibiting short T1 values and large capillary pores with long T1 values. During early hydration times, TiO2 is shown to accelerate the formation of cement gel and reduce capillary porosity. At late hydration times, TiO2 appears to hamper hydration, presumably by hindering the transfer of water molecules to access unhydrated cement grains. The percolation thresholds were calculated from both NMR and ultrasonic data with a good agreement between both results.
“…Several ultrasound techniques have been used to evaluate the setting process [1][2][3], mechanical strength [4,5], porosity [6][7][8][9], permeability [6][7][8][9] and durability [10,11] of pastes, mortars and concrete during the past years. The influence of different superplasticizers and additions on early strength development has been analyzed by [12][13][14][15].…”
This paper focuses on the characterization of setting and hardening of accelerated cementitious matrices by ultrasound propagation velocity, correlating these processes with chemical parameters and the phase evolution obtained by in situ XRD. Evolution of temperature and determination of setting times complemented this analysis. The technique employed provided a continuous monitoring of the setting and hardening of the hydrating matrix and was susceptible to changes in accelerator reactivity and phase composition. Results showed that ettringite formed by accelerator reaction improves the solid-phase interconnectivity and increases initial ultrasound velocity. P-wave propagation during the acceleration period is directly proportional to alite and C3A degrees of hydration. The influence of AFm phases to increase ultrasound velocity is stronger than ettringite and C-S-H. Based on an extensive statistical analysis, multivariate linear regressions were established between ultrasound velocity and the main chemical properties influencing its evolution, leading to a better comprehension of how these parameters are related.Peer ReviewedPostprint (author's final draft
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.