addenda and errata\(\def\hfill{\hskip 5em}\def\hfil{\hskip 3em}\def\eqno#1{\hfil {#1}}\)

Journal logoJOURNAL OF
APPLIED
CRYSTALLOGRAPHY
ISSN: 1600-5767

The crystal structure of dypingite: understanding the long-range disorder. Corrigendum

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aDepartment of Technology Systems, University of Oslo, Gunnar Randers vei 19, Kjeller 2007, Norway, bNatural History Museum, University of Oslo, Blindern, Oslo 1172, Norway, cSINTEF Industry, Forskningsveien 1, Oslo 0374, Norway, dCELLS-ALBA Synchrotron, Carrer de la Llum 2-26, Barcelona 08290, Spain, and eDepartment of Geosciences, University of Oslo, Sem Saelands vei 1, Oslo 0371, Norway
*Correspondence e-mail: [email protected]

Edited by H. Brand, Australian Synchrotron, ANSTO, Australia (Received 6 March 2026; accepted 6 March 2026; online 11 March 2026)

An error in the article by Sednev-Lugovets et al. [J. Appl. Cryst. (2025), 58, 1908–1919] is corrected.

The article by Sednev-Lugovets et al. (2025View full citation) contains a factual error in the description of the TGA–DSC results: in the discussion of Fig. 6, the thermal effect at approximately 62 °C is described as exothermic, whereas it is in fact endothermic. The second paragraph of Section 3.2 should read as follows:

The compositional difference between the hydrated and dehydrated samples of synthetic dypingite was studied by thermogravimetric analysis, coupled with differential scanning calorimetry (TGA–DSC). On heating, the two samples underwent similar decomposition stages (Fig. 6) with peak temperature (Tp) events at 120 and 245 °C, corresponding to the release of water from the material. The third process at Tp = 433 °C was associated with the sample decarbonation. While these findings are consistent with previous reports, the TGA–DSC curve of the hydrated sample demonstrated an additional decomposition step, with a pronounced endothermic effect at Tp = 62 °C (Raade, 1970; Suzuki & Ito, 1973; Canterford et al., 1984; Yamamoto et al., 2022; Frost et al., 2008). This was associated with desorption of water previously accommodated by the sample during the hydration process.

References

Return to citationSednev-Lugovets, A., Lu, Y., Vistad, Ø., Carvalho, P. A., Missyul, A., Austrheim, H., Friis, H. & Guzik, M. N. (2025). J. Appl. Cryst. 58, 1908–1919.   CrossRef ICSD CAS IUCr Journals Google Scholar

This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.

Journal logoJOURNAL OF
APPLIED
CRYSTALLOGRAPHY
ISSN: 1600-5767
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