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Title: Hydration characteristics of tricalcium aluminate phase in mixes containing {beta}-hemihydate and phosphogypsum

Journal Article · · Cement and Concrete Research
 [1];  [2]
  1. National Research Center, Dokki, Cairo (Egypt)
  2. Chemistry Department, Faculty of Science, Zagazig University, Benha Branch, Benha (Egypt)

The tricalcium aluminte phase was prepared from pure chemicals on a laboratory scale. Five mixes were formulated from the prepared C{sub 3}A phase, {beta}-hemihydate, phosphogypsum, calcium hydroxide and quartz. Different mixes were hydrated at various time intervals, namely, 6, 24, 72 and 168 h. The kinetics of hydration was measured from chemically combined water and combined lime contents. The phase compositions and microstructures of the hydrated products were studied by X-ray diffraction (XRD), differential thermal analysis (DTA)/TG, scanning electron microscopy (SEM) techniques and FT-IR spectroscopy. This work aimed to study the effect of partial to full substitution of phosphogypsum by {beta}-hemihydate on the hydration characteristics and microstructures of tricalcium aluminte phase. The results showed that the combined lime slightly increases with the increase of amounts of phosphogypsum. The XRD patterns showed the increase in the intensities of monosulphate and different forms of calcium aluminate (C{sub 4}AH{sub 13} and C{sub 4}AH{sub 19}) with phosphogypsum content. Ettringite is less stable than monosulphoaluminate, so it transformed into monosulpho-aluminate after 24 h, which persisted up to 168 h. The mechanism of the hydration process of C{sub 3}A phase in the presence of phosphogypsum proceeds in a similar path as with {beta}-hemihydate. Phosphogypsum reacts with C{sub 3}A in the presence of Ca(OH){sub 2} forming sulphoaluminate hydrates, which are responsible for setting regulation in cementitious system.

OSTI ID:
20706229
Journal Information:
Cement and Concrete Research, Vol. 35, Issue 8; Other Information: DOI: 10.1016/j.cemconres.2004.06.037; PII: S0008-8846(04)00302-3; Copyright (c) 2004 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved; Country of input: International Atomic Energy Agency (IAEA); ISSN 0008-8846
Country of Publication:
United States
Language:
English