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AbstractAbstract
[en] Lime mortar and plaster were sampled from Roman, medieval and early modern buildings in Styria. The historical lime mortar and plaster consist of calcite formed in the matrix during setting and various aggregates. The stable C and O isotopic composition of the calcite matrix was analyzed to get knowledge about the environmental conditions during calcite formation. The δ13Cmatrix and δ18Omatrix values range from -31 to 0 per mille and -26 to -3 per mille (VPDB), respectively. Obviously, such a range of isotope values does not represent the local natural limestone assumed to be used for producing the mortar and plaster. In an ideal case, the calcite matrix in lime mortar and plaster is isotopically lighter in the exterior vs. the interior mortar layer according to the relationship δ18Omatrix = 0.61 . δ13Cmatrix - 3.3 (VPDB). Calcite precipitation by uptake of gaseous CO2 into alkaline Ca(OH)2 solutions shows a similar relationship, δ18Ocalcite = 0.67 . δ13Ccalcite - 6.4 (VPDB). Both relationships indicate that the 13C/12C and 18O/16O values of the calcite reflect the setting behaviour of the lime mortar and plaster. Initially, CO2 from the atmosphere is fixed as calcite, which is accompanied by kinetic isotope fractionation mostly due to the hydroxylation of CO2 (δ13Cmatrix ∼ -25 per mille and δ18Omatrix ∼ -20 per mille ). As calcite formation continued the remaining gaseous CO2 is subsequently enriched in 13C and 18O causing later formed calcite to be isotopically heavier along the setting path in the matrix. Deviations from such an ideal isotopic behaviour may be due to the evolution of H2O, e.g. evaporation, the source of CO2, e.g. from biogenic origin, relicts of the natural limestone, and secondary effects, such as recrystallization of calcite. The results of the field and experimental study suggest that isotope values can be used as overall proxies to decipher the origin of carbonate and the formation conditions of calcite in the matrix of ancient and recent lime mortar and plaster. Moreover, these proxies can be used to select calcite matrix from historical lime mortar and plaster for 14C dating
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S0883-2927(08)00184-4; Available from http://dx.doi.org/10.1016/j.apgeochem.2008.05.003; Copyright (c) 2008 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.; Country of input: International Atomic Energy Agency (IAEA)
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Journal Article
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ALKALINE EARTH METAL COMPOUNDS, BETA DECAY RADIOISOTOPES, BETA-MINUS DECAY RADIOISOTOPES, CALCIUM COMPOUNDS, CARBON COMPOUNDS, CARBON ISOTOPES, CARBON OXIDES, CARBONATE MINERALS, CARBONATE ROCKS, CHALCOGENIDES, CHEMICAL REACTIONS, DIMENSIONLESS NUMBERS, EVEN-EVEN NUCLEI, EVEN-ODD NUCLEI, HYDROGEN COMPOUNDS, HYDROXIDES, ISOTOPES, LIGHT NUCLEI, MILLISECONDS LIVING RADIOISOTOPES, MINERALS, NUCLEI, OXIDES, OXYGEN COMPOUNDS, OXYGEN ISOTOPES, PHASE TRANSFORMATIONS, PROTON DECAY RADIOISOTOPES, RADIOISOTOPES, ROCKS, SEDIMENTARY ROCKS, SEPARATION PROCESSES, STABLE ISOTOPES, SULFUR ISOTOPES, YEARS LIVING RADIOISOTOPES
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