Dehydroxylation and rehydroxylation mechanisms in fired clay ceramic: A TG-MS and DRIFTS investigation

Francis Clegg, Chris Breen, Margaret A. Carter, Ceren Ince, Shaun D. Savage, Moira A. Wilson

    Research output: Contribution to journalArticlepeer-review


    Selected instrumental techniques [dilatometry, thermogravimetry - mass spectrometry (TG-MS), and variable temperature - diffuse reflectance infrared Fourier transform spectroscopy (VT-DRIFTS)] have been used to investigate the role of moisture in the rehydroxylation reaction which causes expansion and mass gain in fired clay ceramics. The temperature range over which adsorbed water molecules and structural hydroxyl groups are desorbed from fired clay ceramic as it is reheated, and the nature of the structural hydroxyls that are formed as the ceramic is cooled and then held under controlled conditions have been explored. The mass chromatogram for m/z = 18, supported by VT-DRIFTS, showed that physisorbed water molecules were removed from the ceramic at about 105°C, whereas strongly bound molecules of water and structural hydroxyls were held to °C. Dilatometry revealed a marked contraction of the ceramic between 200°C and 330°C which corresponded to loss of strongly bound molecules of water. The VT-DRIFTS also showed that the interaction of water molecules with the ceramic body following reheating occurred in two stages and confirmed the kinetic law previously derived from mass gain and moisture expansion in fired clay ceramics. © 2011 The American Ceramic Society.
    Original languageEnglish
    Pages (from-to)416-422
    Number of pages6
    JournalJournal of the American Ceramic Society
    Issue number1
    Publication statusPublished - Jan 2012


    Dive into the research topics of 'Dehydroxylation and rehydroxylation mechanisms in fired clay ceramic: A TG-MS and DRIFTS investigation'. Together they form a unique fingerprint.

    Cite this