Search results for "aluminate"
showing 10 items of 38 documents
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…
Mechanisms and parameters controlling the tricalcium aluminate reactivity in the presence of gypsum.
2007
International audience; To understand the mechanisms and the parameters controlling the reactivity of tricalcium aluminate in the presence of gypsum at an early age, a study of the hydration of the “C3A–sulphate” system by isothermal microcalorimetry, conductimetry and a monitoring of the ionic concentrations of diluted system suspensions have been carried out with various gypsum quantities. The role of C3A source and its fineness were also studied. This work shows the fast initial formation of AFm phase followed by ettringite formation during the period when the sulphate is consumed. It has been highlighted that the time necessary to consume all the gypsum varies with the type of C3A and i…
Composite Polymer Electrolytes with Improved Lithium Metal Electrode Interfacial Properties: I. Elechtrochemical Properties of Dry PEO‐LiX Systems
1998
Several types of lithium ion conducting polymer electrolytes have been synthesized by hot-pressing homogeneous mixtures of the components, namely, poly(ethylene oxide) (PEO) as the polymer matrix, lithium trifluoromethane sulfonate (LiCF{sub 3}SO{sub 3}), and lithium tetrafluoroborate (LiBF{sub 4}), respectively, as the lithium salt, and lithium gamma-aluminate {gamma}-LiAlO{sub 2}, as a ceramic filler. This preparation procedure avoids any step including liquids so that plasticizer-free, composite polymer electrolytes can be obtained. These electrolyte have enhanced electrochemical properties, such as an ionic conductivity of the order of 10{sup {minus}4} S/cm at 80--90 C and an anodic bre…
Mechanism of Anionic Polymerization of (Meth)acrylates in the Presence of Aluminium Alkyls IV. Formation of a Co-ordinative Polymer Network via the L…
1996
The polymerization of methyl methacrylate in the presence of aluminium alkyls in toluene deviates from conventional kinetics. This results predominantly from the formation and precipitation of a co-ordinative polymer gel or network. Due to the lower reactivity and accessibility of the living chains in the gel, they are regarded as ’dormant’ and thus the concentration of active species decreases during polymerization. The network formation occurs via co-ordination of the living aluminate chain end group with in-chain ester carbonyl groups. Part of the chains are deactivated by a termination process but they are free of cyclic β-ketoesters which would result from the common ’back-biting’ reac…
Interlamellar Reactions of Tetracalcium Aluminate Hydrates with Water and Organic Compounds
1967
Tetracalcium aluminate hydrates are the first example of layer-structured crystals containing neutral sheets, which are highly capable of interlamellar adsorption of water and neutral organic compounds. In this respect tetracalcium aluminate hydrates present new aspects of the phenomenon of swelling, and bring about the challenge of comparison with the frequently examined clay-organic compounds. This report is concerned with the probable monolayer structure of tetracalcium aluminate hydrate which forms five hydration stages. A summary concerning configuration and properties of adsorption complexes with approximately 500 selected organic substances follows. As far as these substances are hom…
Phase evolution by thermal treatment of equimolar cobalt–magnesium cordierite glass powders
2004
Abstract The structural evolution with annealing time at temperatures between 900 and 1100 °C of loosely compacted equimolar cobalt–magnesium cordierite glass powder was reported. The glass, with composition MgCoAl4Si5O18, was prepared by melting a glass precursor, previously synthesized by a semiwet method, at 1650 °C. Field emission scanning electron microscopy (FESEM) of isothermally heated glasses at 900 and 950 °C revealed increased phase separation with thermal treatment. X-ray diffraction (XRD) results of these powders indicated that the first crystalline phase formed was μ cobalt-containing cordierite which transformed to α cordierite with longer annealing. At the beginning of the μ…
Early C3A hydration in the presence of different kinds of calcium sulfate.
2009
International audience; Hydration reactions of C3A with various amounts of calcium sulfate hemihydrate, gypsum or a mixture of two, were investigated by isothermal microcalorimetry, and a monitoring of the ionic concentrations of diluted suspensions. This study shows that sulfate type used modifies the early C3A-CaSO4 hydration products and the rate of this hydration. The fast initial AFm formation observed before ettringite precipitation in the C3A-gypsum system is avoided as soon as hemihydrate is present in the suspension. This was attributed to.higher super saturation degrees and then higher nucleation frequency with regard to the ettringite obtained in the presence of hemihydrate. More…
Hydration of tricalcium aluminate in the presence of various amounts of calcium sulphite hemihydrate : Conductivity tests.
2006
Abstract Hydration of calcium aluminate C3A (3CaO·Al2O3) in the presence of calcium sulphite hemihydrate (CaSO3·0.5H2O), with the molar ratio of substrates close to 1, produces the C3A·CaSO3·11H2O calcium monosulphite aluminate phase. Small amounts of calcium sulphite added to calcium aluminate (the ratio of CaSO3·0.5H2O / C3A equalling 0 : 1) change the rate of C3A hydration and influence the whole reaction. Reaction processes for various ratios of the C3A–CaSO3·0.5H2O mixture were examined in pure distilled water with a considerable amount of liquid W / S = 38–50 (constant W / C3A). Processes in the liquid phase were monitored with conductivity equipment, and the XRD analysis was used to …
SHORT-TERM PROCESSES OF RADIONUCLIDE IMMOBILIZATION IN CEMENT - A CHEMICAL APPROACH
1992
Abstract The ions released in solution by the constituents of cement (principally silicate, aluminate, OH and Ca ions) can combine with the anions and cations from nuclear wastes present in the mixing water to give very insoluble compounds that can fix these ions in the concrete matrix. In order to understand some of the particular physico-chemical processes involved in cement hydration in the presence of analogue elements, tricalcium silicate (C 3 S) was used instead of cement, which is too complex a mixture. It was found that the salt of a chemical analogue, a lanthanide salt, showed some accelerating effects when present in dilute amounts but resulted in large accelerating effects on QS …
Novel method of phosphorescent strontium aluminate coating preparation on aluminum
2018
This work was supported by the ERDF , European-Union Project No. 1.1.1.1/16/A/182 .