- Research article
- Open Access
Material properties of Islamic paper
© The Author(s) 2016
- Received: 13 April 2016
- Accepted: 11 August 2016
- Published: 7 November 2016
- Near infrared spectroscopy
- Non-destructive characterization
As an information carrier, paper has a significant role in history and culture [1, 2]. Yet, although the craft originated in China, the focus of much of recent research has been on Western papermaking. Material properties of paper changed as the knowledge of its production travelled from China through central Asia until it reached the West [1–4]. It is well known that Islamic papermakers utilized techniques and processes not often used elsewhere, such as surface polishing, starch sizing or dyeing and decoration, which appear to make Islamic paper distinct from Indic, Sino-Asian or European [2, 4–8]. However, it is as yet unknown how geographically distinct and widespread these techniques were and whether they affect paper stability.
For the purpose of this paper, we define ‘Islamic paper’ as paper that has been produced in the Islamic cultural realm, i.e. in Arab, Persian or Turkic territories. There could well be regional differences in the history and techniques of papermaking; however, there is currently insufficient knowledge to distinguish them. There is a significant gap in the knowledge of what Islamic paper is, as provenancing can only be achieved by historical, palaeographical and codicological research , and scientific understanding of Islamic paper is almost entirely lacking.
We also know little about what proportion of Islamic paper constitutes manuscripts in Islamic library collections, especially since intensive trade led to significant imports of European paper into Islamic countries from the 17th century on [2, 4, 6, 8]. There is a strong relationship between the durability of paper and the materials and techniques used in its production, e.g. the effect of alum-rosin sizing on European paper [9, 10], widely used as a sizing material since the second half of the 19th century [11, 12]. Gaining such knowledge would help custodians of Islamic paper collections to understand the materials and develop more sustainable preservation plans .
Palaeography is important in this analysis, however, dating and provenancing of text may not reveal any information about its carrier due to trade, although a manuscript dated to the 11th century CE or earlier could not have been produced in Europe. Paper morphology, particularly watermarks, is an aspect of European papermaking that is often used for identification, however, in Islamic papermaking watermarks were not common. On the other hand, physical features such as sheet dimension, thickness, colour and paper mould construction [4, 5, 8, 13] are sometimes found to be specific to a geographic region and era. It is as yet unknown how such features could be used to identify Islamic paper in libraries and archives and if their absence is a conclusive proof of non-Islamic origin.
Paper fibres can be of decisive importance, as was shown, e.g. for Tibetan paper . However, we currently have no knowledge of, or historical information on, the use of particular fibres in Islamic papermaking, although bast and cotton have been used, as was the case of European papermaking [4, 7, 8, 13, 15]. More fibre furnish studies might reveal the presence of less usual fibres such as papyrus, rice, or silk.
Numerous scientific methods are used to study paper and pulp [10, 20, 21] although non-destructive techniques requiring neither sampling nor sample preparation are preferred when dealing with historic objects [20, 22, 23]. Near infrared (NIR) spectroscopy has been successfully used in studies of a variety of heritage materials [23, 24] as it reflects combination and overtone vibrations associated with C–H, O–H and N–H chemical bonds [20, 25]. Spectral data can be used to classify or estimate properties of unknown samples when combined with multivariate data analysis based on a correlation with physical properties obtained from reference analytical methods applied to well-characterized and representative samples [23–26].
Summary of the techniques used in this paper, with the corresponding number of samples
No. of samples analysed
Visual assessment for polishing
Specular/diffuse reflectance ratio
A substantial collection of 228 papers was collected at UCL Institute for Sustainable Heritage from different sources in Central Asia, Near East and North Africa (15th–19th century) for the purpose of material analysis (ref-collection). Most of the samples are written in Arabic (168), several in Coptic script or Persian and Turkic languages. 31 samples are from Samarqand (Uzbekistan). For the majority of papers (133), the date is unknown, while 83 are from 18th to 19th century and 10 are older. Unfortunately, no clear information is available about the provenance, date or history of the storage environment for these samples. Samples without ink or soiling were cut from the paper sheets, away from the margins, for investigation.
The collection was visually examined and digitally documented before sampling. For digitization and morphological measurements, a light table, rulers, digital calliper and a Nikon-D300s DSLR camera were used. All measurements, observations and images were recorded per catalogue number (Arabic paper—AP) thus building a reference database. All samples were given a unique ID, consisting of “AP” followed by an incremental number. Sheets from the same bound volume were considered as sub-samples e.g. AP 1-1 and AP 1-2.
The iodine test [6, 27] was used to establish the presence of starch. The I2 solution was prepared by adding 5 g of I2 (≥99.8 %, Sigma Aldrich, Dorset) to 10 g of KI (crystals, Sigma Aldrich, Dorset) dissolved in 100 ml of deionized water. After dissolution, the prepared solution was diluted 1:4 before use. One drop of the diluted solution was then added to ~0.5 cm2 of paper sample. Colour change was observed under low magnification.
The presence of rosin was tested using the Raspail test [27, 28] for samples that tested negatively for starch. In addition, 35 starch-sized samples were randomly selected to explore the possibility of rosin and starch being present in the same sample.
One drop of a sucrose solution (35 g sucrose, ≥99.5 %, Sigma Aldrich, Dorset, in 20 ml deionized water) was added to ~0.5 cm2 of paper sample and left for 3 min to allow for the solution to penetrate into the sample. Any excess was removed using filter paper. A drop of concentrated H2SO4 (95–97 %, Merck, Darmstadt) was then added. Colour change was observed under low magnification.
Surface polishing of Islamic papers was executed to different levels of quality and shine [4, 7, 8] and occasionally, a polished surface is difficult to assess by appearance (sheen, or occasionally only sheen marks) or by touch. Polishing was assessed visually and the ref-collection was divided into ‘Polished’, ‘Unpolished’ and ‘Uncertain’ categories. Reflection of light from surfaces depends on surface roughness , which can be measured in a variety of ways. Thus, in addition to visual assessment, roughness and gloss measurements were carried out, the ratio between specular and diffusely reflected light was determined, and scanning electron microscopy (SEM) was used, in order to find an instrumental method to reduce the subjectivity of visual assessment.
Roughness is a good indication of surface texture and irregularities . A TRACEiT profilometer (Innowep, Würzburg) was used. The topographic roughness parameter R a  was determined in both directions (x and y) with the resolution of 1536 lines per 5 mm. The arithmetic average was calculated.
Novo-Gloss Lite 45o glossmeter (Rhopoint Instruments, St Leonards) with a resolution of 0.1 gloss units (GU) was used. The measurements were collected at 20o. The average gloss value was calculated from ~10 random measurements, on both sides of each sheet.
Specular/diffuse reflectance ratio
Similarly to gloss, the principle of this method is to assess the relation between the reflectance of a surface and its roughness [29, 31, 32]. The ratio of intensity of reflected light at 457 nm was determined using a LabSpec-5000 spectrometer (ASD, Boulder) at two different angles relative to the incident beam (0o, 45o). This wavelength was selected as it is used to measure paper brightness [33, 34]. Using the ratio rather than absolute values also corrected for any influence of potential chromophores.
Scanning electron microscopy (SEM) imaging
TM3030 tabletop scanning electron microscope (Hitachi, Tokyo) in charge-up reduction mode was used to obtain surface topography images. A 5 × 5 mm piece was used without any sample preparation. Images were collected using low accelerating voltage (5 kV) and magnification of 100×.
Fourier transform infrared (FTIR) spectroscopy
Bruker (Coventry) Alpha ATR-FTIR spectrometer with OPUS software (version 6.5) was used to identify egg white and gum tragacanth as polishing materials [4, 7, 13, 18, 19]. 64 scans were acquired with a resolution of 4 cm−1 over the range 4000–400 cm−1, and averaged to produce the absorbance spectrum. Laboratory-made reference samples of Whatman No. 1 paper (Whatman, Maidstone) sized with egg white (from fresh eggs) and gum tragacanth (Cornelissen & Son, London) were prepared.
List of 15 samples from the ref-collection and their properties, selected randomly for fibre furnish analysis
Laid with no chain lines (hand-made)
Laid + chain lines (hand-made)
Laid + chain lines (hand-made)
Laid + chain lines (hand-made)
Laid + chain lines (hand-made)
Laid with no chain lines (hand-made)
Persian + Arabic
Laid + chain lines (hand-made)
Laid + chain lines (hand-made)
Laid with no chain lines (hand-made)
Y one side only
Laid with no chain lines (hand-made)
A modified standard cold extraction procedure  was used to measure the pH of 70 samples from the ref-collection. Mettler Toledo (Leicester) SevenGo pH/Ion Meter with a micro-combined glass electrode (diameter 3 mm, InLab® Micro, 51343160) was used. Samples (~1.14 mg in ~0.1 ml water) were taken out of the extraction liquid during measurement. All values were rounded to the nearest 0.1 pH unit [38, 39].
Degree of polymerization
The standard method  was used. For each sample, 3–5 repeated measurements of effluent time were performed and the average was used for calculating the DP using Mark–Houwink–Sakurada equation . The uncertainty of DP determination of a Whatman No. 1 filter paper (Maidstone) sample was <1 % (n = 3).
Due to the limited availability of historic samples, it was not possible to determine either water content or the content of non-cellulosic additives in each sample individually. As in previous publications [10, 23, 24], we assumed an average content of non-cellulosic compounds (including water) of 5 % knowing that an error of 1 % in this estimation (i.e. 5 % ± 1 %) would lead to ΔDP of 1 %. This could be considered negligible in relation to the observed differences in DP across the collection as discussed later.
PHAZIR NIR analyzer (Polychromix, now Thermo Fisher, Hemel Hempstead) in the interval of 1600–2400 nm (average of 10 scans), resolution 8 nm, was used. The measurements were carried out using single sheets with a Spectralon target as the background, in areas that contained no inks or visible soiling and away from the margins.
The same samples were measured using the SurveNIR instrument (Lichtblau, Dresden) in the interval of 1100-2200 nm (with 2 nm resolution, average of 8 spectra per sheet with 300 scans each) and the collected data was analysed based on models developed for European paper to explore their applicability.
Multivariate data analysis
Two different multivariate data analysis (MVA) methods have been used to analyse the NIR spectra. For classification, linear discriminant analysis (LDA) was used for several historic materials with good results [20, 25, 42–44], therefore this method was used to estimate the presence of starch-sizing and polishing. XLSTAT 2013 v.5.01 software was used to model the presence of starch using spectra of 228 samples and also to develop a model to identify polishing on 104 samples. No spectral pre-processing was used for these models. Calibration and validation datasets were selected randomly.
For quantitative calibration, multivariate regression methods such as partial least squares (PLS) [42–44] have been used to develop NIR-based models for characterization of heritage materials extensively. Models were developed to study different materials properties, e.g. European paper [23, 24, 45], textiles [46, 47], parchment  and easel paintings . Polychromix method generator v. 3.101 R2-64 software was used to build two PLS regression models for the determination of pH and DP using the reference data as measured using the traditional methods described above.
Different spectral pre-processing methods have been used to optimize the quality of calibration for the regression models. Standard normal variate (SNV) and Savitzky–Golay algorithm of the third polynomial order and a nine-point window second derivative were used for the pH model in the interval 1600-2400 nm. Only Savitzky–Golay algorithm of the third polynomial order and a seven-point window second derivative was applied to the spectra used for DP model. A dataset of 70 samples was used for the pH model, while 60 samples were used for the DP model as lignin-containing samples could not be measured using viscometry. Validation was performed with an independent dataset. Root mean square error of calibration (RMSEC), cross-validation (RMSECV) and prediction (RMSEP) were calculated to evaluate the models.
Characterization of the reference collection
Evidence of sheet-forming techniques for papers in the ref-collection
Laid and chain lines
Laid with no chain lines
Starch sizing could be seen as one of the defining characteristics of Islamic paper [4, 6, 15, 18]. Almost half of the samples (110) contain starch, although variation in the reaction to iodine was visible, which could indicate differences in the source and quantity of starch .
The Raspail test for rosin gave a positive reaction in only 5 samples out of 146 that were tested. One starch-sized sample (AP125-2) reacted positively to rosin as well. Since the test gives false positives for casein, ATR-FTIR was used to ensure the absence of peptide bonds. As a result of this analysis, two samples were found to contain protein (AP125-2, AP129-2). Consequently, only three out of the five samples reacting positively to the Raspail test were undoubtedly sized with rosin (AP98, AP105, AP128), i.e. ~2 %. All three are written in Arabic, have no starch or polishing, and no watermark. All are mechanically produced (2 wove and 1 wire-mesh).
It is worth noting that both visual and instrumental methods of assessment of polishing are still subject to error as many papers are not uniformly polished and the result may therefore depend on the sampled area. Quantitative imaging tools could be developed to estimate the homogeneity of polishing and visualise its application, as was developed for some European paper properties .
As shown in Fig. 7, the peaks at ~1533 and ~1639 cm−1 (amide group bands), indicate the presence of proteins [20, 53, 54]. However, the cellulose peak at ~1630 cm−1 may obscure the nearby amide peak and not allow for gelatine, casein or egg white [20, 53] to be distinguished. Similarly, it would be difficult to distinguish between gums using FTIR alone , although the spectrum of the gum tragacanth-coated sample shows a peak at ~1720-1740 cm−1.
To identify the polishing material, spectra of the ref-collection samples (n = 37) were peak-normalized at ~1026 cm−1. Almost half of the measured samples contained well-identifiable proteinaceous peaks. Samples sized with starch could have been polished with egg white or casein, while gelatine was not used in Islamic countries due to “high temperature”, though there is no clear rationale given for this in the literature [6, 16].
Several test samples (~10) have shown peaks in the region ~1720–1740 cm−1, which could indicate the presence of gums. However, none were as strong as the gum tragacanth peak in Fig. 7, which makes gums more difficult to identify than proteins, since this peak could also indicate the presence of oxidised degradation products .
Two polished samples (AP48, AP131) showed no protein or gum tragacanth peaks.
15 samples were randomly selected and investigated for fibre furnish. Only bast (hemp and flax), cotton and wood-based (both hardwood and softwood) fibres were found. All of the identified fibre types are common to European and Islamic papermaking [4, 7, 8, 13, 15]. However, an interesting finding is that most of the samples that were made from wood-pulp are not starch-sized, which might mean that these papers were imported.
Acidity and degree of polymerization
It is well known that acidity in paper negatively affects its permanence [55, 56], however it cannot be directly linked to loss of mechanical properties and degree of polymerization, as the rate of degradation also depends on temperature and RH .
The samples show a distribution of DP values that is strongly biased towards low values, peaking in the interval of 500–750. While the collection under study may not reflect an average library or archival collection of Islamic paper, the low values of DP may be a concern if this is encountered in real collections, especially since according to a study performed on papers of European origin, for DP <300, the risk of paper accumulating mechanical degradation due to handling increases substantially . Surveys in real collections would show whether such low DP values are typical of Islamic paper collections and would also enable us to observe whether the same DP value of 300 is also representative of higher risk of mechanical degradation with handling for Islamic paper.
The low observed average DP could be the result of high temperature during storage in the past. Considering that the average apparent Ea for historical paper is ~119 kJ/mol, a 4 °C higher average temperature would double the rate of degradation  as observed in more temperate climates.
Non-destructive characterization methodology
Due to the destructive nature of most of the characterization methods used in the previous section, methods need to be developed that allow us to characterize historically valuable collections non-destructively. Using NIR, two classification methods were developed to identify the presence of starch and polishing, and two regression methods to estimate the degree of polymerization and the content of acidity.
Presence of starch and polishing
Validation matrices for LDA models for identification of starch and polishing. 138 and 74 samples were used for calibration, respectively
A similarly well-performing model was built for the identification of polishing. 74 out of 104 samples were selected randomly for calibration and 30 samples were used for independent validation. Spectra in the interval of 1600–2400 nm were used. 86.7 % of validation samples were correctly identified. Although validation is highly satisfactory, it is worth emphasizing that the model was built based on visual (and thus subjective) assessment of the presence of polishing. It might be possible to improve the predictive value of this classification model by confirming the presence of polishing with SEM and FTIR; however, as it is, the model is useful for collection surveys where visual assessment of the presence of polishing is too time consuming in comparison with the NIR method.
Regression models for pH and DP
PLS calibration and validation parameters for regression models for pH and DP using NIR spectra obtained with the PHAZIR hand-held spectrometer; n-number of samples
Validation of the models using independent data sets shows that the model for pH does not perform very well, with the root mean square error of prediction (RMSEP) of 0.7, which is useful for a broad classification of samples, but 2–3-times larger than the uncertainty of the experimental method. The errors in DP determination are satisfactory and comparable with models as determined previously for European paper . This indicates that the methods developed here could be useful for collection surveys, however, particularly for the pH model, more samples might improve the quality of prediction.
Finally, it was of interest to explore whether the PLS regression models as applied to European papers could be of use for Islamic papers. For this purpose, the SurveNIR instrument with the associated software and database for European papers was used. NIR spectra of 70 samples from the Ref-Collection were collected using the SurveNIR Instrument and values of pH and DP were predicted.
To explore whether this reflects the composition of Islamic paper, we plotted points representing starch-containing papers in a different colour in Fig. 10. While the less satisfactory performance of the pH model for European paper cannot be explained by the presence of starch, it is evident that this compound strongly affects the predictions of DP with SurveNIR.
With the non-destructive NIR methods, it is now possible to survey well-dated and provenanced historically valuable Islamic paper collections in libraries and archives, which would give us a much clearer view of how widespread specific papermaking practices were through time and geographically. Additionally, we would gain a better insight into the state of conservation of such collections, as well as develop collection-specific preservation advice. This is the focus of our future work.
We investigated the properties of Islamic paper by exploring the material evidence presented by a reference historic materials database of 228 Islamic paper samples from north Africa, the near East and central Asia, mostly from the 18th and 19th century. For the majority of the documents neither their age nor exact provenance can be established with certainty, however, the collection presents a range of historic material typologies that have not been researched scientifically before. Given that the collection represents a random cross-section of paper production from the Islamic cultural realm, we explored whether typical material properties of Islamic paper could be defined.
The presence of polishing was evaluated visually, although it was found that polishing is often applied unevenly and to different qualities of shine. Since the process of visual evaluation was time consuming, instrumental methods were explored, of which the specular/diffuse reflectance ratio at 457 nm gave results that were most consistent with visual observation.
Due to the semi-transparent properties of paper, optical methods may not be performing optimally and SEM was found to be a reliable technique, albeit destructive. With ATR FTIR, the presence of proteinaceous coatings (casein, egg white) can easily be detected, while the presence of gums is difficult to establish due to the absence of specific absorption bands.
48 % of the collection contains starch and 64 % are polished. 28 samples are neither polished nor contain starch (~12 %), 90 samples are polished, but do not contain starch, 53 contain starch, but are not polished, and 57 are both polished and contain starch.
The majority of samples that are neither polished nor contain starch, are written in Arabic (n = 23), of these, a small proportion (~2 %) are rosin-sized and mechanically produced. It could be hypothesised that these papers were imported; however, it is clear that rosin sizing or the absence of both polishing and starch are not typical of Islamic papermaking practice.
Of the 15 samples of which fibre furnish was determined, none contained fibres that would be considered unusual for European paper making: all were bast, cotton, or wood-derived.
With respect to acidity, samples show a non-normal distribution, with two peaks in the distribution in the intervals of 6.5–7.0 and 5.5–6. Since only 4 samples are very acidic (pH < 5), 2 of which contain lignin, and 1 is rosin-sized, the observed bi-modality cannot be explained as a reflection of different papermaking practices as is the case in European collections where rosin-sized paper represents the acidic peak, and gelatin-sized and post-1990 papers represent the alkaline peak in distribution.
The DP of samples is mostly low, with 69 % having DP < 1000. Given that the typical fibres are bast and cotton with high initial DP, these results might be a reflection of high temperatures during past storage.
In the studied collection, the polished samples are typically associated with higher pH and DP, however, this could also be a reflection of age or past storage. Further research is needed to establish how polishing and the presence of starch affect paper stability.
On the basis of NIR spectra, linear discriminant analysis (LDA) and partial least squares (PLS) regression methods were developed for identification of the presence of starch and polishing and for determination of pH and DP. The validation and prediction errors are considered satisfactory for collection surveys, which would enable the collection of relevant data in well dated and provenanced collections.
NIR methods for the characterization of European paper were found unsuitable for application to Islamic paper. While determination of pH gave a larger prediction error, the NIR method for determination of DP of European paper gave inaccurate results due to the presence of starch in Islamic paper.
Scientific evidence of Islamic papermaking practices
For the first time, our research systematically reviewed the evidence of specific papermaking practices associated with paper used in the Islamic cultural realm. We used established or developed new techniques that could be useful to establish the presence of starch and polishing, and developed techniques that could now be used to survey large Islamic paper collections and establish material properties of well dated and provenanced collections, and thus add a layer of scientific data to codicological, historical and palaeographical research.
Since textual evidence alone is not a proof of provenance of the writing support, and the presence of polishing or even starch is not either (both could be applied to imported paper, prior to writing), and since the majority of Islamic paper has no watermarks, or does not contain fibres that cannot be found in European paper, there can be no unequivocal evidence for what should or should not be considered as Islamic paper. The literature reports specific cases of sieve patterning, the use of rice or papyrus fibres, but there is no evidence of these in the studied collection.
However, ~88 % of the studied collection contained starch and/or were polished, and these two practices could be considered typical of Islamic paper of the 18th, 19th and early 20th century.
HM, and MS jointly developed the concept of this work. HM, TB and MS carried out the experiments, produced samples, developed the computational model and analysed the data. TF contributed to data interpretation. DL contributed to the SurveNIR experiment. All co-authors contributed to the manuscript. All authors read and approved the final manuscript.
The authors gratefully acknowledge the financial support of the EPSRC Centre for Doctoral Training in Science and Engineering in Arts, Heritage and Archaeology (SEAHA), Lichtblau e.K., and EU Horizon 2020 project Nanorestart.
Particular thanks go to Jan Wouters for his help with this research and useful advice.
The authors declare that they have no competing interests.
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- Hunter D. Papermaking: the history and technique of an ancient craft. New York: Dover Publications; 1947.Google Scholar
- Bloom J. Paper before print: the history and impact of paper in the Islamic world. New Haven: Yale University Press; 2001.Google Scholar
- Pedersen J. The Arabic book. French G, translator. Hillenbrand R, editor. New Jersey: Princeton University Press; 1984.Google Scholar
- Loveday H. Islamic paper: a study of the ancient craft. London: Don Baker Memorial Fund; 2001.Google Scholar
- Baker D. A note on the expression. A manuscript on oriental paper Manuscripts of the Middle East, vol. 4. Leiden: Ter Lugt Press; 1989. p. 67–8.Google Scholar
- Baker D. ARAB PARERMAKING. Pap Conserv. 1991;15(1):28–35.View ArticleGoogle Scholar
- Karabacek J, Baker D, Dittmar S. Arab Paper, trans. London: Don Baker Memorial Fund and Archetype Publications; 2001.Google Scholar
- Déroche F. Islamic codicology—an introduction to the study of manuscripts in Arabic script. London: Al-Furqan Islamic Heritage Foundation; 2005.Google Scholar
- Hubbe M. Acidic and alkaline sizings for printing, writing, and drawing papers. Book Pap Gr Annu. 2004;23:139–51.Google Scholar
- Strlič M, Kolar J. Ageing and stabilization of paper. Ljubljana: National and University Library; 2005.Google Scholar
- Barrow WJ. Permanence/durability of the book-VII physical and chemical properties of book papers. Richmond: W. J. Barrow Research Laboratory Inc; 1974. p. 1507–949.Google Scholar
- Au C, Thorn I. Applications of wet-end paper chemistry. Glasgow: Chapman & Hall; 1995.View ArticleGoogle Scholar
- Al-Sāmarrāʼī Q. Arabic Islamic palaeography & codicology = ʻIlm al-iktināh al-ʻArabī al-Islāmī’. Riyadh: King Faisal Centre for research and Islamic studies; 2001.Google Scholar
- Helman-Ważny A, Van-Schaik S. Witnesses for Tibetan craftsmanship: bringing together paper analysis, palaeography and codicology in the examination of the earliest Tibetan manuscripts. Archaeometry. 2012;55(4):707–41.View ArticleGoogle Scholar
- Al-Hassan A. The different aspects of Islamic culture: science and technology in Islam. Technol Appl Sci Part II. 2011;4:155–8.Google Scholar
- Garlick K. A brief review of the history of sizing and resizing practices [internet]. The book and paper group-annual meeting, Vol.5. The American Institute for Conservation of Art and Historic Artifacts. 1986. http://cool.conservation-us.org/coolaic/sg/bpg/annual/v05/bp05-11.html. Accessed 5 Apr 2016.
- Kolbe G. Gelatine in historical paper production and as inhibiting agent for iron-gall ink corrosion on paper. Restaurator. 2004;25(1):26–39.Google Scholar
- Ibn Bādīs M. The staff of the scribes and implement of the discerning with a description of the line, the pens, soot inks, Līq, gall inks, dyeing, and details of bookbinding = ’Umdat Al-kuttab Wa’uddat Dhawi Al-albab’. Iran: Islamic Research Center; Ca. 1025.Google Scholar
- Levey M. Mediaeval Arabic bookmaking and its relation to early chemistry and pharmacology. Trans Am Philos Soc. 1962;52(4):1–79.View ArticleGoogle Scholar
- Stuart B. Analytical techniques in materials conservation, vol. 4. Molecular spectroscopy. Chichester: Wiley; 2007.Google Scholar
- Zervos S. Evaluating treatments of paper using statistically valid test methods. Part II: experimental setup and protocol. Restaurator. 2007;28(4):256–88.Google Scholar
- Derrick M, Stulik D, Landry J. Infrared spectroscopy in conservation science. Los Angeles: Getty Conservation Institute; 1999.Google Scholar
- Trafela T, Strlič M, Kolar J, Lichtblau D, Anders M, Mencigar D, Pihlar B. Non-destructive analysis and dating of historical paper based on ir spectroscopy and chemometric data evaluation. Anal Chem. 2007;79(16):6319–23.View ArticleGoogle Scholar
- Strlič M, Kolar J, Lichtblau D. The SurveNIR project—a dedicated near infrared instrument for paper characterization. In: Padfield T, Borchersen K, editors. Museum microclimates. Copenhagen: National Museum of Denmark; 2007. p. 81–4.Google Scholar
- Blanco M, Villarroya I. NIR spectroscopy: a rapid-response analytical tool. TrAC Trends Anal Chem. 2002;21(4):240–50.View ArticleGoogle Scholar
- Small G. Chemometrics and near-infrared spectroscopy: avoiding the pitfalls. TrAC Trends Anal Chem. 2006;25(11):1057–66.View ArticleGoogle Scholar
- Isenberg I. Pulp and paper microscopy. 3rd ed. Appleton: Institute of Paper Chemistry; 1967.Google Scholar
- AIC. Paper conservation catalog [internet]. 7th ed. Washington, D.C.: American Institute for Conservation of Historic and Artistic Works, Book and Paper Group. Chapter 10: Spot tests; 1990. http://cool.conservation-us.org/coolaic/sg/bpg/pcc/10_spot-tests.pdf. Accessed 5 Apr 2016.
- Bhushan B. Modern tribology handbook. Boca Raton: CRC Press; 2001. Chapter 2: Surface roughness analysis and measurement techniques.Google Scholar
- Leising C. Paper surface roughness with 3D profilometry [internet]. Irvine, USA; 2010. http://nanovea.com/wp-content/themes/wp-nanovea/Application%20Notes/paperroughness.pdf. Accessed 5 Apr 2016.
- Bennett H, Porteus J. Relation between surface roughness and specular reflectance at normal incidence. J Optic Soc Am. 1961;51(2):123–9.View ArticleGoogle Scholar
- Huynh V, Fan Y. Surface-texture measurement and characterisation with applications to machine-tool monitoring. Int J Adv Manuf Technol. 1992;7(1):2–10.View ArticleGoogle Scholar
- TAPPI-452-om. Brightness of pulp, paper and paperboard (Directional Reflectance at 457 nm). 1998.Google Scholar
- BS-ISO-2470-1. Paper, board and pulps. Measurement of diffuse blue reflectance factor. Indoor daylight conditions (ISO brightness). London: British Standardization Institute-BSI; 2009.Google Scholar
- BS-7463. Fiber furnish analysis of paper, board and pulps. London: British Standardization Institute-BSI; 1991.Google Scholar
- Ilvessalo-Pfäffli M. Fiber atlas: identification of papermaking fibers. Germany: Springer-Verlag; 1995.View ArticleGoogle Scholar
- Cornell University Library. Paper, the nature of materials [internet]. Tutorial- Iraq and Middle East, library preservation and conservation. 2005. https://www.library.cornell.edu/preservation/librarypreservation/mee/preservation/paper.html. Accesssed 4 Apr 2016.
- ASTM-D778-97. Standard test methods for hydrogen ion concentration (pH) of paper extracts (hot-extraction and cold-extraction procedures). USA: ASTM International; 2002.Google Scholar
- Strlič M, Kolar J, Kočar D, Drnovšek T, Šelih V, Susič R, Pihlar B. What is the pH of alkaline paper? [internet]. E-preservation science, MORANA RTD. 2004;1:35–47. http://www.morana-rtd.com/e-preservationscience/2004/Strlic-03-06-2004.pdf. Accessed 5 Apr 2016.
- BS-ISO-5351. Pulps —determination of limiting viscosity number in cupriethylenediamine (CED) solution, 2nd ed. London: British Standardization Institute-BSI; 2010.Google Scholar
- Evans R, Wallis A. Comparison of cellulose molecular weights determined by high performance size exclusion chromatography and viscometry. Paris: fourth international symposium on wood and pulping chemistry. 1987;1:201–5.Google Scholar
- Miller JN, Miller JC. Statistics and chemometrics for analytical chemistry. 6th ed. Upper Saddle River: Prentice Hall/Pearson; 2010.Google Scholar
- Brereton R. Chemometrics for Pattern Recognition. Chichester: Wiley; 2009.View ArticleGoogle Scholar
- Brereton R, Lloyd G. Partial least squares discriminant analysis: taking the magic away. J Chemom. 2014; 2609.Google Scholar
- SurveNIR, Near infrared tool for collection surveying [internet]. 2000. http://www.science4heritage.org/survenir/. Accessed 8 Jun 2016.
- Richardson E, Garside P. The use of near infrared spectroscopy as a diagnostic tool for historic silk artefacts. e-Preserv Sci. 2009;6:68–74.Google Scholar
- Garside P, Howard S, Loubser K, Wyeth P. On-site categorisation and condition assessment of silks in textile collections. Portugal: ICOM-CC 16th triennial conference preprints. 2011;1–10.Google Scholar
- Možir A, Strlič M, Trafela T, Cigić IK, Kolar J, Deselnicu V, De Bruin G. On oxidative degradation of parchment and its non-destructive characterisation and dating. Applied physics A: materials science & processing, vol. 104. Berlin: Springer; 2011. p. 211–7.Google Scholar
- Oriola M, Možir A, Garside P, Campo G, Nualart-Torroja A, Civil I, Odlyha M, Cassar M, Strlič M. Looking beneath Dalí’s paint: non-destructive canvas analysis. Anal Methods. 2014;6:86.View ArticleGoogle Scholar
- Wiesmüller B. The watermarks from the Refaiya library. Trans. from the German by Steven Black. [internet]. Between 2008–2012 (N.D.). http://www.refaiya.uni-leipzig.de/texts/Watermarks_Refaiya.pdf. Accessed 4 Apr 2016.
- Cséfalvayová L, Strlič M, Karjalainen H. Quantitative NIR chemical imaging in heritage science. Anal Chem. 2011;83(13):5101–6.View ArticleGoogle Scholar
- IRUG. Infrared and Raman Users Group, IRUG spectral database [Internet]. 2000. http://www.irug.org/. Accessed 5 Apr 2016.
- Baker M, Reyden D, Ravenel N. FTIR analysis of coated papers [internet]. Cincinnati: The book and paper group-Annual meeting, Vol. 8. The American Institute for Conservation of Art and Historic Artifacts. 1989. http://cool.conservation-us.org/coolaic/sg/bpg/annual/v08/bp08-01.html. Accessed 5 Apr 2016.
- Gorassini A, Calvini P, Baldin A. Fourier transform infrared spectroscopy (FTIR) analysis of historic paper documents as a preliminary step for chemometrical analysis. Italy: CMA4CH 2nd Mediterraneum meeting on multivariate analysis and chemometry for cultural heritage and environment. 2008;2:47–8.Google Scholar
- Zou X, Uesaka T, Gurnagul N. Prediction of paper permanence by accelerated aging I. Kinetic analysis of the aging process. Cellulose. 1996;3(1):243–67.View ArticleGoogle Scholar
- Zou X, Uesaka T, Gurnagul N. Prediction of paper permanence by accelerated aging II. Comparison of the predictions with natural aging results. Cellulose. 1996;3(1):269–79.View ArticleGoogle Scholar
- Strlič M, Grossi-Sampedro C, Dillon C, Bell N, Fouseki K, Brimblecombe P, Menart E, Ntanos K, Lindsay W, Thickett D, France F, de Bruin G. Damage function for historic paper. Part III: isochrones and demography of collections. Herit Sci. 2015;3(1):1.View ArticleGoogle Scholar
- Strlič M, Grossi-Sampedro C, Dillon C, Bell N, Fouseki K, Brimblecombe P, Menart E, Ntanos K, Lindsay W, Thickett D, France F, De Bruin, G. Damage function for historic paper. Part II: Wear and tear. Herit Sci. 2015;3(1).Google Scholar