Search results for "Calcium silicate"
showing 10 items of 55 documents
Onset of cohesion in cement paste
2004
It is generally agreed that the cohesion of cement paste occurs through the formation of a network of nanoparticles of a calcium-silicate-hydrate ("C-S-H"). However, the mechanism by which these particles develop this cohesion has not been established. Here we propose a dielectric continuum model which includes all ionic interactions within a dispersion of C-S-H particles. It takes into account all co-ions and counterions explicitly (with pure Coulomb interactions between ions and between ions and the surfaces) and makes no further assumptions concerning their hydration or their interactions with the surface sites. At high surface charge densities, the model shows that the surface charge of…
Post-tilleyite, a dense calcium silicate-carbonate phase
2019
Scientific reports 9(1), 7898 (2019). doi:10.1038/s41598-019-44326-9
Could the Calcium Silicate-Based Sealer Presentation Form Influence Dentinal Sealing? An In Vitro Confocal Laser Study on Tubular Penetration
2021
Dentinal tubule penetration influences root canal treatment sealing. The aim of this study was to compare dentinal penetration of two clinical presentations of silicate-based sealers using confocal laser. Sixty single-rooted human teeth from 50–70 year-old patients extracted for orthodontic/periodontal reasons were used. Canals were prepared using Mtwo system up to 35/0.04, with 5.25% NaOCl irrigation and final irrigation using 17% EDTA. Teeth were randomly assigned into study groups (ni = 20): EndoSequence BC sealer (ES, group 1), BioRoot RCS (BR, group 2); and a control group (nc = 20) with AH Plus (AHP). Root canals were obturated with 35/0.04 gutta-percha (single-cone technique). The sa…
Aqueous solubility diagrams for cementitious waste stabilization systems. 3. Mechanism of zinc immobilizaton by calcium silicate hydrate.
2002
Zinc oxide was added during hydration of alite (C3S) as an analogue for solidification/stabilization by cement of metal-bearing hazardous waste. Curing of samples was stopped at various intervals between 8 h and 100 d, and the reaction products were analyzed by both X-ray diffraction (XRD) and X-ray absorption spectroscopy (EXAFS at Zn, Ca, and Si K-edges). Calcium zincate hydrate (CaZn2(OH)6 x 2H2O) initially formed together with calcium silicate hydrate (CSH) vanishes from X-ray diffractograms after 14 d, and no other crystalline Zn-bearing phase could be detected thereafter. EXAFS Zn K-edge data analysis reveals that Zn(O,OH)4 tetrahedra continue to determine the first shell coordination…
From C–S–H to C–A–S–H: Experimental study and thermodynamic modelling
2015
Abstract It has long been known that the stoichiometry of C–S–H varies with the calcium hydroxide concentration in solution. However, this issue is still far from understood. We revisit it in both experimental and modelling aspects. A careful analysis of the solubility confirms the existence of three different C–S–H phases, defined as Ca 4 H 4 Si 5 O 16 , Ca 2 H 2 Si 2 O 7 and Ca 6 (HSi 2 O 7 ) 2 (OH) 2 , respectively. The variation of the Ca/Si ratio of the three phases has been described by surface reactions: the increase of the Si content is accounted for by silicate bridging, the increase of calcium content and the surface charge are accounted for by reactions involving silanol groups v…
The Structure, Stoichiometry and Properties of C-S-H Prepared by C3S Hydration Under Controlled Condition
1998
Hydrations of tricalcium silicate undertaken by keeping constant lime concentration in solution in an open system and in diluted suspensions for different values of [CaO] ranging between 6.5 and 30 mmol/1 show that the lime concentration in solution is the parameter which determines the main characteristics of the reaction and products. The stoichiometry of C3S hydration products vanes with lime concentration in the same way as synthetic C-S-H until C/S c.a. 1.5 corresponding to about [CaO] =20 mmol/1. Beyond this concentration, single phase C-S-H samples were obtained with 1.8<C/S<2. The discontinuity of the variation of stoichiometry with concentration is characteristic of an invariant po…
Solubility of Zn(II) in Association with Calcium Silicate Hydrates in Alkaline Solutions
1999
The binding of Zn(II) to the cement mineral calcium silicate hydrate (CSH) was investigated in a well-defined laboratory system. CSH (Ca:Si = 1:1) was synthesized by coprecipitation with varying contents of Zn(II). Zn(II) was added in the proportions 0, 0.1, 1.0, 5.0, and 10% in exchange for Ca. The resulting CSH was characterized by X-ray diffraction. The solid phases were then equilibrated in aqueous suspensions, and the solubilities of Ca, Si, and of Zn(II) were determined as a function of pH and Zn(II) content in the solid phase. The solubility of Ca and Si in equilibrium with the CSH phases was in agreement with that predicted by thermodynamic calculations. Dissolved Zn(II) concentrati…
Triple-Quantum Two-Dimensional 27Al Magic Angle Nuclear Magnetic Resonance Study of the Aluminum Incorporation in Calcium Silicate Hydrates
1998
Triple-quantum two-dimensional 27Al magic angle spinning nuclear magnetic resonance (27Al 3Q-MAS NMR) was used to characterize the substitution of Si4+ by Al3+ into the Te−Oc−Te structure of calcium silicate hydrates (C−S−H). This substitution was studied with C−S−H having an Oc/Te ratio of 1 and in equilibrium with Al(OH)3 in aqueous suspensions. In the absence of NaOH, no substitution into the C−S−H structure occurred. Addition of NaOH in the preparation increased the concentration of Al(OH)4- and favored substitution. The deficit of charge resulting from this substitution was compensated by the accommodation of sodium in the interlayer space of the C−S−H. Increasing levels of substituted…
Zeta-Potential Study of Calcium Silicate Hydrates Interacting with Alkaline Cations
2001
An investigation into the interaction between alkaline cations and calcium silicate hydrates (CSH) was conducted by electrokinetic measurements, which provided information on the nature of the interface between the solid and its equilibrium solution. Calcium constitutes for the CSH surface a potential-determining cation. A model of the CSH surface could be proposed, accounting for the experimental evolution of the CSH zeta potential. The necessity of studying the zeta-potential evolution of the system as a function of the calcium activity, instead of its concentration, was underlined. The results obtained suggest a specific interaction between cesium and the CSH surface, whereas sodium and …
Experimental study of Si–Al substitution in calcium-silicate-hydrate (C-S-H) prepared under equilibrium conditions.
2009
International audience; C-A-S-H of varying Al/Si and Ca/(Al+Si) ratios have been prepared introducing C-S-H (Ca/Si=0.66 and 0.95) at different weight concentrations in a solution coming from the hydration of tricalcium aluminate (Ca3Al2O6) in water. XRD and EDX (TEM) analyses show that using this typical synthesise procedure, pure C-A-S-H is obtained only for calcium hydroxide concentrations below 4.5 mmol L−1. Otherwise, calcium carboaluminate or strätlingite is also present beside C-A-S-H. The tobermorite-like structure is maintained for C-A-S-H. A kinetic study has shown that the formation of C-A-S-H is a fast reaction, typically less than a few hours. The Ca/(Al+Si) ratio of C-A-S-H mat…