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Hydromagnesite from the efflorescence of the Stone Town Nature Reserve in Ciężkowice, the Western Carpathians, Poland Cover

Hydromagnesite from the efflorescence of the Stone Town Nature Reserve in Ciężkowice, the Western Carpathians, Poland

Open Access
|Nov 2025

Abstract

Hydromagnesite, Mg5(CO3)4(OH)2⋅4H2O, is a naturally occurring mineral belonging to the group of hydrated magnesium carbonates containing hydroxyl groups, part of the MgO–CO2–H2O system. Its formation requires high Mg/Ca ratios, typically linked to ultramafic rock weathering, and is influenced by pH, with alkaline conditions being favorable. Hydromagnesite commonly forms in alkaline lakes, as efflorescences on carbonate rocks, and even in meteorites, and plays a key role in CO2 capture and storage. This study characterizes natural hydromagnesite forming as spring efflorescences on a sandstone tor in the Stone Town Nature Reserve, Ciężkowice, Poland. The site hosts pickeringite, MgAl2(SO4)4⋅22⋅H2O, and alunogen, Al2(SO4)3∙17⋅H2O, rich efflorescences during summer, reflecting significant seasonal pH variations. This represents perhaps the first discovery of hydromagnesite on such rocks in Poland. The paper describes mineralogical and geochemical characteristics of the efflorescence and hydromagnesite itself, using methods SEM-EDS, XRPD, EPMA, Raman spectroscopy, and STA coupled with QMS for the analysis of evolved gases. Hydromagnesite crystals exhibit an acicular to flame-bladed habit, often with irregular surfaces covered by flaky and flocculent grains, clustering in aggregates. The calculated formula is Mg5(CO3)4(OH)2⋅5.14 H2O (based on five cations). Crystals of hydromagnesite are monoclinic (space group P21/c) with: a = 10.050(8) Å, b = 8.921(7) Å, c = 8.384(6) Å, β = 114.291(25)°. Raman spectra reveal intense bands at 1119 cm−11 CO32−), weaker bands at 710, 732, 762 cm−14 CO32−), 646 cm−14 HCO3), and OH-stretching vibrations at 3515, 3445, and 3373 cm−1. Thermal effects associated with hydromagnesite occur at 270°C and 390°C, corresponding to dehydration and overlapping dehydroxylation and decarbonation, respectively. The relatively low decarbonation temperature likely results from crystal morphology enhancing heat transfer and earlier CO2 release. Although the efflorescence contains minor hexahydrite, gypsum, and quartz, the above parameters for the predominant hydromagnesite are consistent with literature values.

DOI: https://doi.org/10.2478/mipo-2025-0009 | Journal eISSN: 1899-8526 | Journal ISSN: 1899-8291
Language: English
Page range: 74 - 93
Submitted on: Jul 29, 2025
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Accepted on: Oct 10, 2025
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Published on: Nov 10, 2025
In partnership with: Paradigm Publishing Services
Publication frequency: 1 issue per year

© 2025 Mariola Marszałek, published by Mineralogical Society of Poland
This work is licensed under the Creative Commons Attribution 4.0 License.