The Corning Archaeological Reference Glasses are widely used as standards in the analysis of archaeological and historical glasses, as their compositions were designed to approximate those of major glass types in antiquity. Scientific analysis of glass has played an important role in archaeology in recent years, in the study of raw materials, provenance determination, glass-making technology, the organisation of production and the recycling of glass (cf. Rehren and Freestone, 2015). Reference standards are used in chemical analysis to calibrate the equipment, to test the performance of the analytical equipment and the quality of the data generated, and to indicate the degree to which data are comparable with other data. To achieve this, the reference material must be homogeneous and its composition well-characterised.
Since the development of the Corning glasses, their elemental compositions have been re-evaluated and new updated values suggested, most recently by Wagner et al (2012). However, the concentrations of three elements were not re-examined in that study and the values are still based on theoretical values. This paper provides a brief overview of the Corning reference glasses and recommendations for new values for the concentrations of two of these elements; sulphur and chlorine. These elements can be studied to understand technological processes involved in the making of glass. Sulphur concentrations can be an indicator of the chemical properties giving the glass its colour and the redox conditions of the furnace (Schreurs and Brill, 1984; Beerkens, 2003; Freestone and Stapleton, 2015), whereas chlorine concentrations serve as a marker of repeated melting or recycling (Al-Bashaireh et al., 2016), the addition of salt as a raw material (Gerth, Wedepohl and Heide, 1998; Wedepohl, 2003), and the melting temperature of the glass (Rehren, 2000). Both elements are also related to deterioration processes (Schreiner et al., 1999).
Overview of the Corning Archaeological Reference Glasses
Robert Brill and The Corning Museum of Glass initiated, and were central to, a project to improve the analysis of archaeological glass by developing four reference glasses with compositions similar to those of common ancient glasses: Corning A and B are soda-lime silicate glasses that were designed to resemble ancient Egyptian, Mesopotamian, Roman, Byzantine and Islamic plant ash and natron glasses; Corning C is a high-lead, high-barium glass, similar to some East Asian glasses; and Corning D is a potash-lime silicate glass based on Medieval European compositions (Brill, 1965, 1972).
The glasses were prepared using chemicals of known purity that were weighed out according to the target compositions and ball-milled for 16 hours to ensure homogeneous mixing before melting (details of the procedure described in Brill 1965 and in Brill 1972). Theoretical compositions were calculated based upon the mixtures (published in Brill, 1972). Sulphur and chlorine were added to the mixtures using sodium sulphate and sodium chloride, and their ultimate concentrations estimated assuming 70% retention of SO3 and 80% retention of Cl. The glasses were distributed to multiple laboratories (cf. Brill, 1972 Appendix I) for analysis by numerous methods without prior knowledge of their theoretical composition, and “tentative” compositions were then recommended (Brill, 1972 Appendix IV). In 1999, Brill published new recommended values for the four glasses based upon replicate analyses by inductively coupled plasma optical emission spectrometry (ICP-OES), though the traces were still based upon the theoretical compositions (Brill, 1999: analytical procedure detailed in Appendix A, theoretical compositions in Appendix B, and recommended reference compositions in Appendix D).
Vicenzi and colleagues (2002) evaluated the usefulness of the Corning glasses as secondary standards, focusing on the minor and trace elements and impurities, and using the analytical methods of electron probe microanalysis (EPMA), laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) and secondary ion mass spectrometry (SIMS). The primary focus of this paper was the spatial heterogeneity of the glasses (and thus their basic suitability as secondary standards) rather than the confirmation or re-evaluation of the recommended values from Brill (1999), and they concluded that the Corning glasses were suitably homogeneous for use as secondary standards.
However, various published articles reported some discrepancies between their measured analyses of some elements in the Corning glasses and the published recommended compositions (including Kuisma-Kursula and Räisänen, 1999; Kuisma-Kursula, 2000; Bronk and Freestone, 2001; Falcone et al, 2002; Vicenzi et al., 2002; Shortland et al, 2007; Dussubieux et al., 2008; Wagner et al., 2008; Dussubieux et al, 2009). This prompted the study by Wagner et al. (2012) with the purpose of testing the published recommended compositions of the Corning glasses and where needed, suggesting new values for some elements. Using LA-ICP-MS with three different laser systems, they suggested new values for elements whose results were separated by 3σ from the previously recommended values. The concentrations of sulphur, chlorine and silver were not tested by Wagner and colleagues.
Re-evaluation of Sulphur and Chlorine Concentrations
The impetus for this paper came from an observation that, firstly, the measured values for SO3 and Cl in some of the Corning glasses in analytical work at the UCL Institute of Archaeology consistently differed from the recommended values, and secondly, many published papers also reported similar disagreement (see references listed in Table 2). The theoretical concentrations of SO3 and Cl in the Corning glasses were admittedly approximate due to the unpredictable loss of these elements during the glass melting process (described in detail in Brill, 1972). That it is unsurprising that measured results for these elements shows poor agreement with the theoretical recommended values is explicitly acknowledged by Vicenzi (et al 2002: 722); however, the low degree of confidence in these concentrations make it highly important to re-evaluate those values in order to better characterise the composition of these glasses and to further their usefulness as reference standards.
|A (n = 80)||B (n = 91)||D (n = 97)|
|Kuisma-Kursula & Räisänen 1999||SEM-EDS||–||–||–||–||0.28||0.15|
|Bronk & Freestone 2001||SEM-EDS||0.17||0.09||0.55||0.17||–||–|
|Vicenzi et al. 2002||EPMA-WDS||0.13||0.09||0.45||0.16||0.19||0.16|
|Schoer & Rehren 2007||EPMA-WDS||0.09||0.09||0.41||0.15||–||–|
|Freestone et al. 2010||SEM-EDS||–||–||–||–||0.32||0.17|
|Freestone et al. 2015||EPMA-WDS||0.14||0.09||0.50||0.16||–||–|
|Cholakova, Rehren and Freestone 2015||EPMA-WDS||0.15||0.09||0.51||0.17||–||–|
|Previously recommended values (Brill 1999)||0.10||0.10||0.50||0.20||0.30||0.40|
The concentrations for Ag in the Corning glasses, which are also currently based upon theoretical values, will not be addressed here, as it is present in concentrations below the limits of detection of the equipment (see below); also Corning C will not be addressed as this high-lead, high-barium glass is not used in most glass analysis in these laboratories and therefore no data was available.
The Corning Archaeological Reference Glasses A, B and D are used as secondary standards for electron microprobe analysis in the UCL Institute of Archaeology Wolfson Archaeological Science Laboratories. The data used for this paper has been collected by the author over the past two years (2015–2016) as part of research involving the analysis of medieval glass. Samples of the Corning glasses were embedded in epoxy resin, polished to 1μm with diamond paste, and vacuum-coated in carbon. Analyses were carried out using a JEOL JXA-8100 Electron Probe Microanalyser with attached wavelength dispersive spectrometers (EPMA-WDS). Standard procedure for glass analysis in the Wolfson Archaeological Science Laboratories is to take area measurements with magnifications of 800x and a working distance of 11mm giving a raster area of 150 x 110 μm, with an accelerating voltage of 15kV and a beam current of 50nA, and with 30s count time on each element peak and 10s count time per background measurement. Analytical totals had a mean of 99.5%, and the data were not normalised.
Data compiled from several publications were also used. This was limited by the fact that some publications using the Corning glasses do not publish their measurements of the standards and others did not report values for the elements of interest. The data taken from published works were generated using EPMA or scanning electron microscopy (SEM) with either attached WDS or energy dispersive spectrometers (EDS). For a comparative study of WDS and EDS systems in the analysis of glass, see Verità et al (1994).
As the previously accepted values are based on theoretical compositions, a statistical test for difference is not considered appropriate. The recommended values in this paper, calculated as the mean average of nine publications, are the first based upon actual measurement.
New Values for Chlorine and Sulphur Concentrations
The mean and standard deviation of the results for SO3 and Cl in Corning A, B and D as measured by the author using EPMA-WDS are given in Table 1, and it is also noted that the standard deviation of the results for SO3 in all three Corning glasses are greater than those for Cl. These results are compared with data from eight other publications (Table 2). The Cl concentrations are in good agreement, whereas the SO3 results are more variable. This variability is largely due to the convention of reporting sulphur as an oxide rather than the measured element, resulting in a reported standard deviation that has been multiplied by 2.497 (the conversion factor of S to SO3), and furthermore means that the concentrations are closer to detection limits than the oxide concentration suggests. The sulphur concentrations as measured by EDS tend to be higher than those by WDS; the overlapping S-Kα and Pb-Mα lines may have had a small effect on those results. Variation between laboratories and machines is also evident, for example in the consistently lower SO3 values reported by Schoer & Rehren (2007) and Kuisma-Kursula (2000).
The best agreement with the recommended values (Brill, 1999) is for SO3 in Corning B and Cl in Corning A; the most significant disagreement is found in Cl concentrations in Corning D. Estimated retention rates were assumed to be the same for all three glasses (Brill, 1972), but instead the solubility would be dependent on the composition of each glass; for example, the soda concentrations (Freestone et al., 2015).
The lack of a complete up-to-date list of concentrations for the Corning glasses has meant that some papers use recommended concentrations based upon the initial theoretical values published by Brill (1972) and reiterated again in Brill (1999), others use the “tentative recommended compositions” also published in Brill (1972), whereas others are using values whose origins are not known to this author and are presumably based upon unpublished work shared between researchers. To address this problem, a full list of elements for the four Corning glasses has been compiled with the most up-to-date recommended concentrations and with references to the published origin of each value, reported in Table 3; it is suggested that these values are used in future work.
a Brill 1972. Theoretical values, nominal compositions calculated from precursor mass fractions (uncontested by Wagner et al. 2012); a’ Ag2O concentrations were not addressed by Wagner and colleagues.
b Brill 1999.
c Brill unpublished data, reported in Vicenzi et al. 2002
d Wagner et al. 2012 data.
e Adlington 2017 (current paper).
The Corning Archaeological Reference Glasses are important secondary standards used in the analysis of archaeological and historical glass, and so it has been important to verify their usefulness as standards (cf. Vicenzi et al., 2002) and corroborate their compositions (cf. Wagner et al., 2012). The compositions of three elements in these glasses have not been re-examined and are theoretical values based upon batch calculations. This paper revisited the concentrations of sulphur and chlorine in Corning A, B and D, after the author observed consistent disagreement with the recommended values both in her own analytical work and in published research, and new values were recommended based on a mean average of published and new results. These results here are tentative and are expected to be revised again when a more thorough, directed approach can be taken; in particular, results for SO3 in all glasses, especially Corning D, vary widely in the published data used in this paper. However, the contribution of this work will give analysts a better understanding of the composition of these standards and of the performance of their equipment. Finally, a complete, up-to-date list of compositions has been compiled for the benefit of other analysts using the Corning glasses.
I am grateful to Ian Freestone, Tom Gregory, and other members of the UCL Wolfson Archaeological Science Laboratories, as well as to the reviewers, for their help and advice. This research is supported by the UCL Graduate Research Scholarship and the UCL Overseas Research Scholarship.
The author has no competing interests to declare.
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