ettringite and calcium-aluminate

ettringite has been researched along with calcium-aluminate* in 3 studies

Other Studies

3 other study(ies) available for ettringite and calcium-aluminate

ArticleYear
Immobilization of MSWI fly ash through geopolymerization: effects of water-wash.
    Waste management (New York, N.Y.), 2011, Volume: 31, Issue:2

    The present research explored the role played by water-wash on geopolymerization for the immobilization and solidification of municipal solid waste incineration (MSWI) fly ash. The water-wash pretreatment substantially promoted the early strength of geopolymer and resulted in a higher ultimate strength compared to the counterpart without water-wash. XRD pattern of water-washed fly ash (WFA) revealed that NaCl and KCl were nearly eliminated in the WFA. Aside from geopolymer, ettringite (Ca(6)Al(2)(SO(4))(3)(OH)(12)·26H(2)O) was formed in MSWI fly ash-based geopolymer (Geo-FA). Meanwhile, calcium aluminate hydrate (Ca(2)Al(OH)(7)·3H(2)O), not ettringite, appeared in geopolymer that was synthesized with water-washed fly ash (Geo-WFA). Leached Geo-WFA (Geo-WFA-L) did not exhibit any signs of deterioration, while there was visual cracking on the surface of leached Geo-FA (Geo-FA-L). The crack may be caused by the migration of K(+), Na(+), and Cl(-) ions outside Geo-FA and the negative effect from crystallization of expansive compounds can not be excluded. Furthermore, transformation of calcium aluminate hydrate in Geo-WFA to ettringite in Geo-WFA-L allowed the reduction of the pore size of the specimen. IR spectrums suggested that Geo-WFA can supply more stable chemical encapsulation for heavy metals. Static monolithic leaching tests were conducted for geopolymers to estimate the immobilization efficiency. Heavy metal leaching was elucidated using the first-order reaction/diffusion model. Combined with the results from compressive strength and microstructure of samples, the effects of water-wash on immobilization were inferred in this study.

    Topics: Aluminum Compounds; Calcium Compounds; Carbon; China; Coal Ash; Compressive Strength; Incineration; Kinetics; Metals, Heavy; Minerals; Particulate Matter; Polymerization; Refuse Disposal; Water; Water Pollutants, Chemical; X-Ray Diffraction

2011
Hydration mechanisms of mineral trioxide aggregate.
    International endodontic journal, 2007, Volume: 40, Issue:6

    To report the hydration mechanism of white mineral trioxide aggregate (White MTA, Dentsply, Tulsa Dental Products, Tulsa, OK, USA).. The chemical constitution of white MTA was studied by viewing the powder in polished sections under the scanning electron microscope (SEM). The hydration of both white MTA and white Portland cement (PC) was studied by characterizing cement hydrates viewed under the SEM, plotting atomic ratios, performing quantitative energy dispersive analyses with X-ray (EDAX) and by calculation of the amount of anhydrous clinker minerals using the Bogue calculation.. Un-hydrated MTA was composed of impure tri-calcium and di-calcium silicate and bismuth oxide. The aluminate phase was scarce. On hydration the white PC produced a dense structure made up of calcium silicate hydrate, calcium hydroxide, monosulphate and ettringite as the main hydration products. The un-reacted cement grain was coated with a layer of hydrated cement. In contrast MTA produced a porous structure on hydration. Levels of ettringite and monosulphate were low. Bismuth oxide was present as un-reacted powder but also incorporated with the calcium silicate hydrate.. White MTA was deficient in alumina suggesting that the material was not prepared in a rotary kiln. On hydration this affected the production of ettringite and monosulphate usually formed on hydration of PC. The bismuth affected the hydration mechanism of MTA; it formed part of the structure of C-S-H and also affected the precipitation of calcium hydroxide in the hydrated paste. The microstructure of hydrated MTA would likely be weaker when compared with that of PC.

    Topics: Aluminum; Aluminum Compounds; Bismuth; Calcium; Calcium Compounds; Calcium Hydroxide; Chemical Precipitation; Drug Combinations; Electron Probe Microanalysis; Ferric Compounds; Humans; Materials Testing; Microscopy, Electron, Scanning; Minerals; Oxides; Porosity; Powders; Root Canal Filling Materials; Silicates; Surface Properties; Water

2007
Synthesis of ettringite: a way to deal with the acid wastewaters of aluminium anodising industry.
    Water research, 2005, Volume: 39, Issue:1

    Synthesis of ettringite from acid wastewaters of the aluminium anodising industry has been studied as a possible route of reducing the emissions to the environment, recovering at the same time resource materials as a useful marketable mineral. Wastewaters of different concentrations have been subjected to the process of synthesis suspending calcium oxide and calcium aluminate powders at different time and pH conditions. High caustic alkalinity (pH approximately 12) and low sulphate concentrations (<0.1 M) are the most suitable conditions to synthesise ettringite. The mineral characterisation has been performed using X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA) and differential thermal analysis (DTA), proving the high purity of the pursued solid product when hydrated in the appropriate sodium hydroxide concentrations. In such conditions, around 90% of the aluminium initially present in the wastewater solutions is recovered in the form of ettringite.

    Topics: Aluminum; Aluminum Compounds; Calcium Compounds; Chemical Precipitation; Differential Thermal Analysis; Electrochemistry; Hydrogen-Ion Concentration; Industrial Waste; Metallurgy; Minerals; Oxides; Spectroscopy, Fourier Transform Infrared; Thermogravimetry; Water Pollutants, Chemical; Water Purification; X-Ray Diffraction

2005