The effect on chalk recrystallisation after treatment with oxidizing agents

Dina Belova, Anna Margit Susanne Johnsson, Nicolas Emile Bovet, Leonid Lakstanov, Susan Louise Svane Stipp

18 Citationer (Scopus)

Abstract

Chalk consists of the fossilized remains of the hard parts from some species of unicellular algae. These algae use polysaccharides to control the morphology of their shields, called coccoliths, which are made of from 20 to 60 individual, sub-micrometer size calcite crystals. This biogenic calcite has resisted recrystallization during the more than 65millionyears of diagenesis. In this study, we examined the effect of oxidizing agents on the ability of the chalk to recrystallize. Samples from a North Sea drill core that had never been exposed to oil and Rørdal chalk from the Ålborg Portland quarry, north Jutland, Denmark, were treated with oxidizing agents to remove organic material and the recrystallization rates were determined. We treated the chalk with solutions of NaOCl and H 2O 2 with and without 0.1M NaCl and monitored recrystallization in CaCO 3 saturated 0.1M NaCl solutions using H 14CO 3 - as a tracer. X-ray photoelectron spectroscopy (XPS) showed that initially, the North Sea chalk had a higher surface concentration of organic carbon than the Ålborg sample, but it decreased significantly after the oxidizing treatment. Loss of CO correlated with higher recrystallization rates; rate increase was highest (~50%) after H 2O 2 treatment. Our results demonstrate that through geological time, miniscule amounts of organic material remain associated with the chalk surface and act as an inhibitor for chalk recrystallization. This implies that the polysaccharides originally made by the algae to control coccolith morphology have contributed to hindering chalk diagenesis to limestone, keeping the biogenic particles much smaller, even after 65millionyears, than inorganic calcite grown in the lab for a few days.

OriginalsprogEngelsk
TidsskriftChemical Geology
Vol/bind291
Sider (fra-til)217-223
Antal sider7
ISSN0009-2541
DOI
StatusUdgivet - 6 jan. 2012

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