pling is required, tide-lines are created due to the application of water. A micro-electrode was used in order to minimize the amount of water needed and consequently, related damage induced by the measurement (Strlic 2005). The electrode is so far not commercially available. Considering the damage which is induced using the above described methods, a non-destructive method which does not require addition of water would be desirable. Recently, a good correlation (R = 0.9573) between measured and predicted pH values were obtained using a scientific bench-top spectrometer described earlier. Using a portable Ocean Optics spectrometer and the above mentioned software, prediction model for all kinds of independent paper samples is characterised by R = 0.8802 and RMSEP = 0.73. Although in use for decades, the standard methodology involving pH determination after 1hr of cold extraction does not provide information on whether gelatine sized rag paper is acidic or alkaline, when equilibrium pH is reached. Our study of 150 historical rag samples showed that pH of most of the rag papers with acidic pH, as determined using the standard method, stabilised in alkaline region. This was observed also in our earlier study (Strlic 2004). Determination of the equilibrium pH value would thus be useful in the assessment of the stability of paper. The latter is difficult to determine, as several weeks of measurements may be needed for paper pH to reach equilibrium, while the recently proposed method where the sample in water is stirred at 250 r.p.m. (Strlic 2004) is difficult to implement. Although not as accurate as the determination using a pH meter, NIR spectroscopy may be useful also in this case offering a prediction for the equilibrium pH with R = 0.8123 and RMSEP = 0.76. Prediction is based on all kinds of paper. Conclusions Inherent features of cultural heritage require a specific approach to its characterisation. It is imperative that the data is collected non-destructively or at worst, micro-destructively. Also, the instrumentation should be portable in order to minimize risks to the heritage due to the transport. The method employed should be characterised by high sensitivity and low detection limits, which reveal the condition, enable determination of provenance, or point to possible future problems and thus allow preservation actions to be taken in time. It is also preferable that the methods are simple, reliable and accessible. While we know what we want, none of the existing methods for determination of pH and the condition of paper addresses all of the above mentioned requirements. DP determination is sensitive, affordable and reproducible, yet destructive. Size exclusion chromatography of carbanilated cellulose leaves no visible damage to the artefact, but is instrumentally demanding and expensive. Near infra-red spectroscopy with accompanying software can be simple, fast, portable, relatively affordable, but is associated with a larger uncertainty. The choice of the analytical method will remain subject to the nature of the artefact and the conservation problem, among others. While size exclusion chromatography, when available, may be the method of choice in case of a precious artefact or a limited number of samples to be analysed, NIR spectroscopy may be more appropriate for characterisation of larger sets of artefacts, as well as for rapid characterisation of the artefacts during daily work in conservation departments. References Henniges, U., Reibke, R., Banik, G., Huhsmann, E., Hähner, U., Prohaska, T., Potthast, A. 2008. ‚Iron gall ink-induced corrosion of cellulose: aging, degradation and stabilization. Part 2: application on historic sample material‘. Cellulose, 15(6):861-870. Kolar, J., Malesic, J., Kocar, D., Strlic, M., De Bruin, G., and Kolesa, D. 2012. ‘Characterisation of paper containing iron gall ink using size exclusion chromatography’. Polym. Deg. Stab., 97(11):2212–2216. Lichtblau, D., Strlic, M., Trafela, T., Kolar, J., & Anders, M. 2008. ‚Determination of mechanical properties of historical paper based on NIR spectroscopy and chemometrics – a new instrument‘. Applied Physics A, 92(1):191-195. Lojewski, T., Zieba, K., & Lojewska, J. 2010. ‘Size exclusion chromatography and viscometry in paper degradation studies. New Mark-Houwink coefficients for cellulose in cupri-ethylenediamine’. Journal of chromatography. A, 1217(42):6462-8. Stôl, R., Pedersoli Jr., J.L, Poppe, H., Kok, W.Th. 2002. ‘Application of Size Exclusion Electrochromatography to the Microanalytical Determination of the Molecular Mass from Objects of Cultural and Historical Value’. Anal. Chem., 74:2314-2320. Strlic, M., Pihlar, B., Mauko, L., Kolar, J., Hocevar, S., Ogorevc, B. 2005. ‘A New Elec- ICOM-CC Graphic Documents Working Group Interim Meeting | Vienna 17 – 19 April 2013 44
trode for Micro Determination of <strong>Paper</strong> pH’. Restaurator, 26(3):159-171. Strlic, M., Kolar, J., Kocar, D., Drnovsek, T., Selih, V.-S., Susic, R., Pihlar, B. 2004. ‘What is the pH of alkaline paper?’. e-PS, 1:35-47. Zou, X., Uesaka, T., Gurnagul, N. 1996. ‘Prediction of paper permanence by accelerated aging Part I: Kinetic analysis of the aging process’. Cellulose, 3:243-267. Acknowledgement The support by the Slovenian Research Agency (grant L1-2401), Nationaal Archief, NL and FP7 project Nano for Art, ref. no. 282816 is acknowledged. Author’s Jana Kolar, Morana RTD, Oslica 1b, 1295 Ivancna Gorica, Slovenia, fax: +38617876334 jana.kolar@morana-rtd.com info@morana-rtd.com Gerrit de Bruin, Natonaal Archief, Prins Willem-Alexanderhof 20, 2595 BE Haagse Hout, The Netherlands Vilma Sustar, Univerza v Mariboru, Faculty of Agriculture and Life Sciences, Pivola 10, 2311 Hoce, Slovenia ICOM-CC Graphic Documents Working Group Interim Meeting | Vienna 17 – 19 April 2013 45
- Page 1 and 2: Paper Conservation: Decisions & Com
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Microorganisms in Books - First Res
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Deconstructing the Reconstruction E
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Applications of Image Processing So
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Analysing Deterioration Artifacts i
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