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Article

A Study on the Materials Used in the Ancient Architectural Paintings from the Qing Dynasty Tibetan Buddhist Monastery of Puren, China

1
Engineering Research Center of Historical Cultural Heritage Conservation, Ministry of Education, School of Materials Science and Engineering, Shaanxi Normal University, Xi’an 710119, China
2
Shaanxi Institute for the Preservation of Culture Heritage, Xi’an 710075, China
*
Authors to whom correspondence should be addressed.
Submission received: 31 August 2023 / Revised: 19 September 2023 / Accepted: 22 September 2023 / Published: 26 September 2023

Abstract

:
Situated in the village of Lama Temple on the eastern bank of the Wulie River in Chengde, Puren Temple stands as one of the few remaining royal temples of great importance from the Kangxi era (1662–1722 AD). This ancient edifice has greatly contributed to the advancement of our comprehension regarding the art of royal temple painting. The present study undertakes a comprehensive analysis and identification of nine samples obtained from the beams and ceiling paintings within the main hall of Puren Temple. Furthermore, a systematic examination of their mineral pigments and adhesives is conducted. The findings from polarized light microscopy (PLM), energy-type X-ray fluorescence spectrometer (ED-XRF), micro-Raman spectroscopy (m-RS), and X-ray diffractometer (XRD) analyses reveal that the pigments present in the main hall beams of Puren Temple are cinnabar, lead white, lapis lazuli, and lime green, while the pigments in the ceiling paintings consist of cinnabar, staghorn, lead white, lapis lazuli, and lime green. The use of animal glue as a binder for these pigments on both the main hall beams and ceiling paintings is confirmed via pyrolysis-gas chromatography–mass spectrometry (Py-Gc/Ms) results. These findings hold significant implications for the future restoration of Puren Temple, as they provide valuable guidance for the selection of appropriate restoration materials.

1. Introduction

The Puren Temple of the Qing dynasty (in 1713 AD), situated in the village of Lama Temple on the eastern bank of the Wulie River in Chengde City, holds significant meaning as it embodies the Emperor Kangxi’s profound benevolence and universal love (Figure 1a). Notably, among the eight outer temples of Chengde, the Puren Temple stands as the sole royal temple of the Kangxi Dynasty. During the early Qing dynasty, Tibetan Buddhism held considerable influence in the Mongolian and Tibetan regions of China, attracting devout followers. The teachings of Buddhism served as a vital spiritual foundation for the Mongolian and Tibetan communities. Puren Temple, similar to its counterparts within the Summer Resort, exemplifies the amalgamation of diverse nationalities in China and serves as a historical testament to the unification, consolidation, and progress of the nation during the Qing dynasty. Moreover, it stands as an exemplar of the early Qing dynasty’s royal temple architecture. The architectural design of Puren Temple seamlessly integrates numerous Tibetan decorative styles, adopting the structural layout reminiscent of a traditional Chinese temple known as the “seven halls of the Garan” (Figure 1b). Enclosed by a surrounding retaining wall, the temple prominently showcases Qing dynasty paintings, predominantly housed within the central hall, Ciyun Puyin Hall (Figure 1c), and the inner eaves of the newly constructed Bao Xiang Chang in the third courtyard. This sacred site boasts an extensive collection of culturally significant paintings, predominantly featuring Sanskrit and seal painting motifs. The extant paintings from the Qing dynasty, originating from the Kangxi period (1662–1722 AD), exhibit a remarkable and unadorned style, while also encapsulating a wealth of historical knowledge (Figure 1d,e).
Ancient painted architectural relics, as a distinct subset of architectural artifacts, serve as a testament, custodian, and transmitter for Chinese civilization. The depiction of ancient structures in paintings exhibits significant variations in terms of materials, patterns, and production techniques, which are contingent upon the architectural grade of the edifice [1]. The colorful paintings adorning ancient buildings have endured extensive weathering over the course of three centuries, particularly due to the persistent fluctuations in light, oxidation, temperature, humidity, dust, micro-organisms (including mold and bird droppings), and various other external factors. Consequently, these paintings have suffered from hollowing of the underlying structure, detachment of the pigment layer, warping, pollution, and other afflictions [2]. However, there is a dearth of scholarly research on the Qing dynasty paintings housed in Puren Temple, and the pressing issue of addressing the aforementioned ailments afflicting these artworks necessitates immediate attention. Moreover, it is imperative that the restoration process employ pigments and adhesives that faithfully replicate the original materials. Consequently, the significance of this study lies in its profound practical implications, providing data support for pigment and adhesive material for subsequent repair.
The composition of color paintings primarily comprises pigments and glues, wherein the pigments are responsible for the vibrancy of the artwork and hold paramount importance in the study of color painting [3,4,5]. Additionally, the glues serve to securely bind the pigments to the underlying substrate. The utilization of pigments and glues is intricately linked to the specific artistic themes conveyed in color paintings, the contextual factors specific to the locality, and the prevalent production techniques of the era. These pigments can be broadly classified into two categories: mineral pigments and organic dyes. The choice of selecting mineral pigments in color painting exhibits substantial similarities, primarily determined by color, composition, and expense, albeit with minor deviations in binders [4,6,7]. Prominent mineral pigments frequently employ encompass cinnabar, lead red, iron oxide, carbon black, stone green, lead white, malachite, and stone blue [2,8,9,10,11]. Hitherto, professionals in the field of heritage conservation have employed diverse techniques to scrutinize and ascertain the constituents of heritage pigments, including visible light microscopy, polarized light microscopy, energy-based X-ray fluorescence spectrometry (SEM-EDX), X-ray diffraction (XRD) [12,13,14], X-ray energy spectrometry (EDS) [9,10,15,16], X-ray emission spectroscopy (XPS) [17], and micro-Raman spectroscopy (m-RS) [18,19,20,21,22]. For example, m-RS was used for pigment identification of the Arshai cave murals [18] and the Santa Maria de Lem-On-Iz murals [23]; Fu Peng et al. used Raman combined with XRD for a series of explorations of pigments from the Qing Xi Ling paintings, and Wang Xin et al. used Raman combined with SEM-EDS for the analysis and identification of pigments from the Huayan Temple paintings of the Liao Dynasty, generally in the context of when analyzing heritage pigments for testing, researchers use a combination of methods.
The gum serves as a binding agent for the pigments on the surface of mortars, while hydrophilic pigments typically utilize fish glue, bone glue, or similar substances [24]. For oil-based pigments, castor oil, linseed oil, and tung oil are selected as binders [25]. Emulsion pigments often incorporate eggs or egg whites, used either alone or mixed with other materials [26]. Various techniques are employed for adhesive detection, including infrared spectroscopy [27,28], Raman spectroscopy [29,30,31], nuclear magnetic resonance spectroscopy [32], gas chromatography–mass spectrometry [33,34,35,36], and immunoassay. Notably, chromatography offers a rapid means of identifying animal glue, linseed oil, and casein, etc. [37], the results of which are less affected by other factors and can be applied to the detection of various types of painted artefacts, and therefore the pyrolysis–gas chromatography–mass spectrometry (Py-GC/MS) method was used in this paper to analyze the adhesive [14,38,39,40].
This study aims to examine the pigments and adhesive layers used in the architectural paintings of Puren Temple. By analyzing painted samples using various scientific analytical techniques including PLM, ED-XRF, XRD, micro-Raman spectroscopy, and Py-GC/MS, the research aims to enhance our understanding of the official Qing dynasty paintings of Puren Temple and offer valuable insights for future restoration.

2. Materials and Methods

2.1. Samples

Samples were obtained from the color painting on the southeast beam and the indoor ceiling of the main hall, Ciyun Puyin, in the PuRen Temple. In order to keep the painting as intact as possible, we used tools such as tweezers and scalpels to extract small amounts, making up 9 samples, from the flaking pigments (Table 1 and Figure 2).

2.2. Experimental Methods and Instrumentation

Polarized light microscopy (PLM; BX53M, Olympus, Tokyo, Japan) was used to visualize the macroscopic morphology of different samples. This instrument possesses an objective lens from 20 to 1000× at 5400 pixels.
Pigment element composition was analyzed using an electron microscope coupled with an energy-dispersive X-ray spectrometer (ED-XRF, Shimadzu, Kyoto, Japan) with a high-performance silicon drift detector and X-ray tube (Rh target) in the range of 11Na-92U.
The Renishaw InVia Reflection Spectrometer (Via Reflex, Wotton-under-Edge, Renishaw, Gloucestershire, UK) equipped with a Leica microscope, argon ion laser, charge-coupled detector, and 50× objective has two excitation wavelengths of 532 nm and 785 nm. The collection range is 100–2000 wavenumber. The pigment was carefully removed using a scalpel and subsequently transferred onto a slide for Raman analysis.
A Rigaku Corporation Smart Lab 9 high resolution X-ray diffractometer (XRD, Smart lab, Rigaku Corporation, Tokyo, Japan) with test conditions for Cu Kα rays (λ = 1.54056 A), 2θ range of 20–80°, acceleration voltage of 45 kV, a tube current of 200 mA, and a scanning speed of 5°/min was also employed.
Pyrolysis–gas chromatography–mass spectrometry (Py-GC/MS) was performed using a combination of a pyrolysis unit (EGA/PY-3030D, Frontier Labs, Koriyama, Japan) and a gas chromatograph mass spectrometer (GC/MS-QP2010 Ultra, Shimadzu, Kyoto, Japan). SLB-5MS (5% diphenyl/95% dimethyl siloxane) was a 30 m-long chromatography column with an internal diameter of 0.25 mm and a film thickness of 0.25 mm (Supelco, Bellefonte, PA, USA). An amount of 0.2 mg of the sample was taken, powdered, and placed in a thermally cracked sample cup. In order to achieve sufficient contact, tetramethylammonium hydroxide solution (2 μL) (TMAH, Aladdin, Shanghai, China) with a mass fraction of 25% was added and allowed to settle for 1 h. Subsequently, it was placed under an infrared lamp and allowed to lyse after the evaporation of water.
Temperatures were set at 600 °C for the thermal cracking, 300 °C for the cracking interface, and 250 °C for the cracking inlet. A 40 °C chromatographic column was ramped up to 280 °C at a rate of 10 °C/min, and the temperature was maintained for 20 min. A high-purity helium carrier gas with an inlet pressure of 15.4 kPa and a splitting ratio of 1:100 was used in the GC-MS. The electronic pressure control system was maintained in constant flow mode. The mass spectrometer was operated using EI ionization at an ionization energy of 70 eV. Within a scan range of (m/z) 50 to 750 and over a cycle time of 0.5 s, isolated chemical compounds were subsequently identified using NIST14 and corresponding mass spectrometers.

3. Results

3.1. Analysis of the Pigments

3.1.1. Red Pigment Analysis

Red is a prevalent color in ancient Chinese painting, with vermilion, lead red, iron red, and other common pigments being used. The element analysis of red samples P1 and P2, as presented in Table 2, reveals the presence of Hg, Pb, and Ca. Considering the relevant literature, it is plausible to infer that the red pigments might be either vermilion or lead red. The Raman spectrum and XRD analysis data of the red samples are depicted in Figure 3, respectively. Notably, the Raman peaks of the red pigments were observed at 255 cm−1 (vs) and 345 cm−1 (w) (Figure 3a,b). A comparison of the red sample Raman spectrum with the standard spectrum reveals that the peak at 255 cm−1 is attributed to a Hg-S stretching vibrational band. Additionally, the bands at 349 cm−1 (w) were identified as the degenerate E modes, which can be assigned to the normal modes ELO and ETO [41,42,43,44]. This finding confirms that the red pigment is cinnabar, which aligns with the results obtained from the ED-XRF analysis (Table 2). In the XRD analysis of the red sample, strong peaks can be seen at angles of 26.5°, 28.2°, and 31.2°. These three peaks exhibit conformity with the primary XRD peaks observed in the standard HgS product, suggesting that the sample a/b corresponds to vermilion, a finding that aligns with the conclusions drawn from ED-XRF analysis. Vermilion, a pigment extensively employed in ancient Chinese painting, traces its origins to the Yang-shao culture and was frequently utilized in various forms of artwork, including ancient architectural painting [42]. As investigated by Wang Shoudao et al., the examination of the patterned pigments found in silk weavings (N-5) recovered from the Mawangdui No. 1 Han tomb in Changsha revealed the presence of pure vermilion [42]. Additionally, vermilion pigment was identified in oracle bone inscriptions unearthed from the Yin Market in China, dating back to the Shang dynasty [45].

3.1.2. Blue Pigment Analysis

Following a thorough examination of the two blue samples (P3, P4), the ED-XRF data is presented in Table 2. The predominant elements found in the blue pigment are Ca, Si, and Cu. Despite the significant presence of Al and Si, it is postulated that these elements may originate from mortars. Subsequently, Raman spectroscopy was employed for additional analysis. Figure 4a illustrates the prominent peaks observed at 848 cm−1 (s), 1431 cm−1 (s), and 1583 cm−1 (s) in the blue pigment. The Raman spectrum in Figure 4b shows a noticeable peak at 1100 cm−1, which suggests the presence of C-O symmetric stretching vibration [46]. Additionally, the Raman spectrum displays a solitary peak at 1583 cm−1, representing the carbonate (υ3) asymmetric stretching vibration. In addition, we observe a band at 848 cm−1, which indicates the nonphase bending mode of the carbonate. Moreover, the intense band at 403 cm−1 is a distinctive feature of 2CuCO3·Cu(OH)2 [42]. The XRD analysis of the blue sample revealed diffraction peaks at 17.5°, 24.2°, and 35.3°, which aligned with the diffraction peaks observed in the 2CuCO3·Cu(OH)2 specimen. This correspondence suggests that the sample possesses a lime coloration. This finding is in agreement with the outcomes obtained from the energy-dispersive X-ray fluorescence (ED-XRF) and Raman spectroscopy analyses. The color blue held significant prominence in the realm of Qing dynasty color painting, resulting in a diverse array of blue pigments. Consequently, the identification of azurite as the mineral pigment in the blue samples is supported by these findings. Ancient structures such as the Bezeklik Grottoes [47] and the Longju Temple [8] used azurite widely as a blue pigment. Notably, these samples exhibited no discernible signs of aging, with the original composition largely preserved [47,48].

3.1.3. Green Pigment Analysis

Based on the ED-XRF data, it is evident that the primary elements present in the green samples P5 and P6 are Cu, Si, and Ca, although Si and Ca were also found in higher quantities. We hypothesize that these elements may originate from the mortars used. However, the specific type of green pigment cannot be determined solely via elemental analysis. Figure 5a,b displays the Raman spectra of P5 and P6, respectively, revealing prominent peaks at 155 cm−1, 178 cm−1, 354 cm−1, and 433 cm−1. Specifically, the Raman peaks at positions 155 cm−1, 178 cm−1, and 354 cm−1 signify the vibrational band of the Cu-O group [49]. The peak detected at 1100 cm−1 was determined to come from the (CO3)2− cluster, whereas the peak at 1066 cm−1 was linked to the symmetrical stretching motion of C-O [44]. Malachite has characteristic Raman peaks [50]. The XRD spectra of P5 and P6 are depicted in Figure 5c,d. The diffraction peaks observed at 31.3°, 24.1°, 17.6°, and 14.8° are in agreement with the diffraction spectrum of Cu2(OH)2CO3 (JCPDS no. 74-0660), suggesting that the pigment present in P5 and P6 is likely to be malachite. Green was a prominent hue in architectural painting during the Qing dynasty, encompassing stone green, green copper ore, and Parisian green [8]. However, it is worth noting that the extensive use of Parisian green did not occur until the latter part of the 19th century [11]. In ancient China, malachite emerged as the prevailing green mineral pigment, with its earliest known usage discovered on murals dating back to the Sixteen Kingdoms period (304–439 AD) [51].

3.1.4. White Pigment Analysis

The elemental composition of P7 and P8 exhibits notable similarities, as both white pigments primarily consist of Pb, Ca, and Si, albeit with relatively low concentrations of Ca and Si. Consequently, it is plausible to hypothesize that these elements originated either from the underlying soil layer or surface dust contaminants. In ancient China, various white pigments containing elemental Pb, such as lead white, cerussite, and phosgenite, were commonly employed. The main Raman peaks (Figure 6a,b) at 173 cm−1, 403 cm−1, 1058 cm−1, and 1380 cm−1 indicate that the white pigment was anglesite [Pb3(OH)4CO3] [52,53,54,55,56,57]. To ascertain the specific nature of P7 and P8, we conducted a comprehensive analysis utilizing XRD in conjunction with other techniques. The white pigment’s X-ray diffraction pattern is shown in Figure 6c,d. The most prominent peak in the XRD pattern occurs at 26.4°, which corresponds to the diffraction peak of quartz. This observation suggests the presence of quartz in the sample, potentially originating from the ground pillar layer or surface dust pollutants containing Ca and Si elements. Consequently, based on the identification of diffraction peaks at 24.6° and 36.1°, corresponding to the diffraction peaks of Pb3(OH)4CO3 (JCPDS no. 13-0131), it can be concluded that the white pigments P7 and P8 are lead white. Lead white, a synthetic pigment, was produced in China starting from the fourth century BC and found extensive application, such as in the Jiangxue Palace located within the Imperial Museum at the Mogao Grottoes and on the canvas oil painting Rebecca at the Well of Neapolitan anonymous [58].

3.1.5. Yellow Pigment Analysis

Based on the ED-XRF results and Raman spectra data, P9 is a yellow pigment commonly used for ceiling color painting. The analysis reveals that the main elements present in P9 are As, S, Ca, and Si, with a significant concentration of arsenic and sulfur, suggesting the presence of orpiment (As2S3). In conjunction with the examination of the Raman spectra data (Figure 7a), it is observed that the Raman spectra largely align with the customary distinctive Raman peaks associated with As2S3, specifically at 138, 154, 179, 202, 292, 311, 353, and 382 cm−1 [59]. Furthermore, the presence of the asymmetric and symmetric vibrations of As-S is manifested in the Raman spectra, which manifest as two distinct bands at 382 and 353 cm−1, respectively. Consequently, it can be deduced that the P9 pigment is indeed orpiment (As2S3) [41]. The X-ray diffraction (XRD) pattern (Figure 7b)depicted in the figure aligns with the standard diffraction peak of orpiment (As2S3) (JCPDS no. 71-2435), thereby providing additional evidence that the P9 yellow pigment is indeed orpiment (As2S3). This finding corroborates the results obtained from both ED-XRF and Raman spectroscopy, further supporting the identification of the yellow pigment as orpiment.

3.2. Analysis of Adhesives

Ancient architectural paintings are artifacts that contain a combination of organic and inorganic materials. In order to ensure the longevity of these paintings, ancient craftsmen utilized binders to create adhesive properties for the mineral pigments, thus preventing their detachment. The binders serve a crucial bridging function within the paintings, making the analysis of these binders indispensable. Py-GC/MS was applied to nine samples (Figure 8), and the resulting total ion chromatograms for these samples are presented in Figure 9. The pyrolysis analysis of the samples revealed the presence of various pyrolysis products commonly associated with proteins, including 1H-Pyrrole, 1-methyl, pyridine, valine, alanine, glycine (found in glue and egg white), and methyl ester. This suggests that the glues used in these samples contained proteins [60]. Additionally, certain samples exhibited the characteristic amino acids hydroxyproline (Hyp) and glycine (Gly), which are typically found in animal glue. Therefore, it can be inferred that the adhesive in these samples may consist of a combination of animal glue and egg whites [61,62,63,64,65]. Furthermore, the detection of low levels of these substances in some samples indicates that natural aging processes over time may have caused degradation, potentially rendering them undetectable (P3, P7).
For example, the samples P1-P9 exhibited the presence of monocarboxylic and dicarboxylic acids, which are commonly observed byproducts of pyrolysis of dry oils [66,67,68,69]. Moreover, certain samples showed the presence of APAs, which are characteristic pyrolysis products of cooked tung oil. According to Table 3, the ratio of palmitic to stearic acid (P/S) varied from 0.5 to 2.6 among the samples analyzed. This finding suggests the presence of dry oil components (mono-versus di-carboxylic acids) in the samples.
In the realm of academic discourse, researchers frequently distinguish between different dry oils based on their respective concentrations of palmitic and stearic acids. Specifically, the P/S values for cooked tung oil vary from 0.9 to 1.1, whereas raw tung oil displays P/S values ranging from 1.3 to 1.6. Conversely, linseed oil demonstrates P/S values ranging from 1.2 to 1.5, while poppy oil falls within the range of 1.6 to 1.8. Lastly, walnut oil exhibits P/S values between 1.8 and 2.0 [70]. It is worth noting that although the P/S values for dry oils may differ slightly between colored and non-colored in the literature, the presence of pigments tends to elevate the P/S values. The co-existence of raw and cooked tung oil in the sample can be attributed to the historical production techniques employed in ancient Chinese architectural paintings [71]. These techniques reached a high level of sophistication and standardization during the Qing dynasty, encompassing three distinct components: the pigment layer, the ground layer, and the wooden elements. The mortar used in these paintings typically consisted of brick ash, lime water, fiber, blood, and tung oil. The presumed correlation between the presence of raw tung oil and the painting process suggests that the application of an oil layer to the wood preceded the groundwork, facilitating a smoother surface and enhancing adhesion to the groundwork. Given this information, it is plausible to hypothesize that the presence of raw tung oil and cooked tung oil in the sample can be attributed to its infiltration from the painted ground layer.

4. Conclusions

Based on an examination of representative painted samples derived from Puren Temple, it can be deduced that the architectural paintings of Puren Temple exhibit exceptional preservation, exquisite craftsmanship, and a vibrant color palette. Consequently, the ensuing deductions are as follows:
The crossbeam painting at Puren Temple has been analyzed using PLM, ED-XRF, m-RS, and XRD techniques, revealing that the employed pigments are cinnabar, lead white, azurite, and malachite for the red, white, blue, and green colors, respectively. Similarly, the ceiling painting incorporates cinnabar, lead white, stone blue, stone green, and starch yellow pigments for the red, white, blue, green, and yellow hues, respectively. Notably, all the pigments examined in this study are classified as inorganic mineral pigments. The application of Py-GC/MS detection in the analysis demonstrated the utilization of animal glue as a binding agent for the pigments in the examined samples. Additionally, the presence of both raw and cooked tung oil were detected, likely indicating its penetration from the mortar material.
The paintings depicting ancient buildings possess significant historical, cultural, and artistic worth. The examination of extant paintings of ancient buildings offers data and evidence to bolster the preservation and improved administration of such artwork in the future. The restored paintings’ artistic value offers valuable guidance for the study of Qing dynasty royal paintings.

Author Contributions

Y.L. (Yuhu Li); Data curation, G.T., K.H. and D.H.; Formal analysis, G.T. and Z.J.; Funding acquisition, Z.J.; Investigation, Y.T., Y.L. (Yanli Li), X.C. and P.F.; Methodology, Y.L. (Yuhu Li); Project administration, Y.L. (Yuhu Li); Writing—original draft, G.T. and Z.J.; Writing—review & editing, Z.J. All authors have read and agreed to the published version of the manuscript.

Funding

This work was supported by the National Natural Science Foundation of China (Grant No. 22002080), Key Research and Development Program of Shaanxi Province, China (Grant No. 2021GY-172), Fundamental Research Funds for the Central Universities (Grant No. GK 202103060).

Institutional Review Board Statement

The study did not require ethical approval.

Informed Consent Statement

The study did not involve humans.

Data Availability Statement

Not applicable.

Acknowledgments

This work is supported by the project of Chengde Cultural Heritage Bureau, Hebei, China.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Lei, Z.B.; Wu, W.; Shang, G.H.; Wu, Y.Q.; Wang, J.L. Study on colored pattern pigments of a royal Taoist temple beside the Forbidden City (Beijing, China). Vib. Spectrosc. 2017, 92, 234–244. [Google Scholar] [CrossRef]
  2. Fu, P.; Teri, G.; Li, J.; Huo, Y.; Yang, H.; Li, Y. Analysis of an Ancient Architectural Painting from the Jiangxue Palace in the Imperial Museum, Beijing, China. Anal. Lett. 2021, 54, 684–697. [Google Scholar] [CrossRef]
  3. Rao, H.Y.; Li, B.; Yang, Y.M.; Ma, Q.L.; Wang, C.S. Proteomic identification of organic additives in the mortars of ancient Chinese wooden buildings. Anal. Methods 2015, 7, 143–149. [Google Scholar] [CrossRef]
  4. Wang, L.Q.; Yang, L.; Zhou, W.H.; Yan, J.; Guo, R. Analysis of the techniques and materials of the coloured paintings in the Renshou Hall in the Summer Palace. Anal. Methods 2015, 7, 5334–5337. [Google Scholar] [CrossRef]
  5. Yan, X.; Liu, Y.; Liu, C.; Jing, B. A Technological Analysis of Fish Pattern Painted Pottery from the Neolithic Site of Banpo. Bull. Chin. Ceram. Soc. 2014, 33, 1389–1393. [Google Scholar]
  6. Mazzeo, R.; Cam, D.; Chiavari, G.; Fabbri, D.; Ling, H.; Prati, S. Analytical study of traditional decorative materials and techniques used in Ming Dynasty wooden architecture. The case of the Drum Tower in Xi’an, P.R. of China. J. Cult. Herit. 2004, 5, 273–283. [Google Scholar] [CrossRef]
  7. Wang, L.Q.; Yang, L.; Zhou, W.H.; He, Q.J. Study on the Analytical Methods of Component Materials and Making Techniques of Painting and Colored Drawing in Ancient Architectures. Relics Museol. 2009, 6, 451–454. [Google Scholar]
  8. Chen, E.; Zhang, B.; Zhao, F.; Wang, C. Pigments and binding media of polychrome relics from the central hall of Longju temple in Sichuan, China. Herit. Sci. 2019, 7, 45. [Google Scholar] [CrossRef]
  9. Li, Y.; Wang, F.; Ma, J.; He, K.; Zhang, M. Study on the pigments of Chinese architectural colored drawings in the Altar of Agriculture (Beijing, China) by portable Raman spectroscopy and ED-XRF spectrometers. Vib. Spectrosc. 2021, 116, 103291. [Google Scholar] [CrossRef]
  10. Liu, L.; Zhang, B.; Yang, H. The Analysis of the colored paintings from the Tanxi Hall in the Forbidden City. Spectrosc. Spectr. Anal. 2018, 38, 68–77. [Google Scholar]
  11. Shen, A.G.; Wang, X.H.; Xie, W.; Shen, J.; Li, H.Y.; Liu, Z.A.; Hu, J.M. Pigment identification of colored drawings from Wuying Hall of the Imperial Palace by micro-Raman spectroscopy and energy dispersive X-ray spectroscopy. J. Raman Spectrosc. 2006, 37, 230–234. [Google Scholar] [CrossRef]
  12. del Río, M.S.; Martinetto, P.; Somogyi, A.; Reyes-Valerio, C.; Dooryhée, E.; Peltier, N.; Alianelli, L.; Moignard, B.; Pichon, L.; Calligaro, T.; et al. Microanalysis study of archaeological mural samples containing Maya blue pigment. Spectrochim. Acta Part B At. Spectrosc. 2004, 59, 1619–1625. [Google Scholar] [CrossRef]
  13. Hradil, D.; Hradilova, J.; Bezdicka, P.; Serendan, C. Late Gothic/early Renaissance gilding technology and the traditional poliment material “Armenian bole”: Truly red clay, or rather bauxite? Appl. Clay Sci. 2017, 135, 271–281. [Google Scholar] [CrossRef]
  14. Mazzocchin, G.A.; Agnoli, F.; Mazzocchin, S.; Colpo, I. Analysis of pigments from Roman wall paintings found in Vicenza. Talanta 2003, 61, 565–572. [Google Scholar] [CrossRef] [PubMed]
  15. Kugler, V.; Bean, S.; Spring, M. Quantitative EDX Analysis of Smalt Pigment in Sixteenth and Eighteenth Century Paintings. Microsc. Microanal. 2013, 19, 1428–1429. [Google Scholar] [CrossRef]
  16. Samanian, K. Identification of Green Pigment Used in Persian Wall Paintings (ad1501-1736) Using PLM, FT-IR, SEM/EDX and GC-MS Techniques. Archaeometry 2015, 57, 740–758. [Google Scholar] [CrossRef]
  17. Freitas, R.P.; Felix, V.S.; Pereira, M.O.; Santos, R.S.; Oliveira, A.L.; Gonçalves, E.A.; Ferreira, D.S.; Pimenta, A.R.; Pereira, L.O.; Anjos, M.J. Micro-XRF analysis of a Brazilian polychrome sculpture. Microchem. J. 2019, 149, 6. [Google Scholar] [CrossRef]
  18. Bell, I.M.; Clark, R.J.; Gibbs, P.J. Raman spectroscopic library of natural and synthetic pigments (pre- approximately 1850 AD). Spectrochim. Acta Part A Mol. Biomol. Spectrosc. 1997, 53A, 2159–2179. [Google Scholar] [CrossRef]
  19. Franquelo, M.L.; Duran, A.; Herrera, L.K.; de Haro, M.C.J.; Perez-Rodriguez, J.L. Comparison between micro-Raman and micro-FTIR spectroscopy techniques for the characterization of pigments from Southern Spain Cultural Heritage. J. Mol. Struct. 2009, 924, 404–412. [Google Scholar] [CrossRef]
  20. Lang, P.L.; Keefer, C.D.; Juenemann, J.C.; Tran, K.V.; Peters, S.M.; Huth, N.M.; Joyaux, A.G. The infrared microspectroscopic and energy dispersive X-ray analysis of paints removed from a painted, medieval sculpture of Saint Wolfgang. Microchem. J. 2003, 74, 33–46. [Google Scholar] [CrossRef]
  21. Perez-Alonso, M.; Castro, K.; Madariaga, J.M. Investigation of degradation mechanisms by portable Raman spectroscopy and thermodynamic speciation: The wall painting of Santa Maria de Lemoniz (Basque Country, North of Spain). Anal. Chim. Acta 2006, 571, 121–128. [Google Scholar] [CrossRef] [PubMed]
  22. Svarcova, S.; Cermakova, Z.; Hradilova, J.; Bezdicka, P.; Hradil, D. Non-destructive micro-analytical differentiation of copper pigments in paint layers of works of art using laboratory-based techniques. Spectrochim. Acta Part A Mol. Biomol. Spectrosc. 2014, 132, 514–525. [Google Scholar] [CrossRef] [PubMed]
  23. Stanzani, E.; Bersani, D.; Lottici, P.P.; Colomban, P. Analysis of artist’s palette on a 16th century wood panel painting by portable and laboratory Raman instruments. Vib. Spectrosc. 2016, 85, 62–70. [Google Scholar] [CrossRef]
  24. Wang, X.; Zhen, G.; Hao, X.; Zhou, P.; Wang, Z.; Jia, J.; Gao, Y.; Dong, S.; Tong, H. Micro-Raman, XRD and THM-Py-GC/MS analysis to characterize the materials used in the Eleven-Faced Guanyin of the Du Le Temple of the Liao Dynasty, China. Microchem. J. 2021, 171, 106828. [Google Scholar] [CrossRef]
  25. Kurouski, D.; Zaleski, S.; Casadio, F.; Van Duyne, R.P.; Shah, N.C. Tip-Enhanced Raman Spectroscopy (TERS) for in Situ Identification of Indigo and Iron Gall Ink on Paper. J. Am. Chem. Soc. 2014, 136, 8677–8684. [Google Scholar] [CrossRef]
  26. Orsini, S.; Parlanti, F.; Bonaduce, I. Analytical pyrolysis of proteins in samples from artistic and archaeological objects. J. Anal. Appl. Pyrolysis 2017, 124, 643–657. [Google Scholar] [CrossRef]
  27. Stenberg, C.; Svensson, M.; Johansson, M. Study of the drying of linseed oils with different fatty acid patterns using RTIR-spectroscopy and chemiluminescence (CL). Ind. Crop. Prod. 2005, 21, 263–272. [Google Scholar] [CrossRef]
  28. Wang, Y.; Wang, Q.; Artz, W.E.; Padua, G.W. Fourier transform infrared spectra of drying oils treated by irradiation. J. Agric. Food Chem. 2008, 56, 3043–3048. [Google Scholar] [CrossRef]
  29. Oakley, L.H.; Dinehart, S.A.; Svoboda, S.A.; Wustholz, K.L. Identification of Organic Materials in Historic Oil Paintings Using Correlated Extractionless Surface-Enhanced Raman Scattering and Fluorescence Microscopy. Anal. Chem. 2011, 83, 3986–3989. [Google Scholar] [CrossRef]
  30. Vandenabeele, P.; Ortega-Aviles, M.; Castilleros, D.T.; Moens, L. Raman spectroscopic analysis of Mexican natural artists’ materials. Spectroc. Acta Pt A Molec. Biomolec. Spectr. 2007, 68, 1085–1088. [Google Scholar] [CrossRef]
  31. Vandenabeele, P.; Wehling, B.; Moens, L.; Edwards, H.; De Reu, M.; Van Hooydonk, G. Analysis with micro-Raman spectroscopy of natural organic binding media and varnishes used in art. Anal. Chim. Acta 2000, 407, 261–274. [Google Scholar] [CrossRef]
  32. Cipriani, G.; Salvini, A.; Dei, L.; Macherelli, A.; Cecchi, F.S.; Giannelli, C. Recent advances in swollen-state NMR spectroscopy for the study of drying oils. J. Cult. Herit. 2009, 10, 388–395. [Google Scholar] [CrossRef]
  33. Van den Berg, J.D.J.; van den Berg, K.J.; Boon, J.J. Determination of the degree of hydrolysis of oil paint samples using a two-step derivatisation method and on-column GC/MS. Prog. Org. Coat. 2001, 41, 143–155. [Google Scholar] [CrossRef]
  34. Echard, J.P.; Benoit, C.; Peris-Vicente, J.; Malecki, V.; Gimeno-Adelantado, J.V.; Vaiedelich, S. Gas chromatography/mass spectrometry characterization of historical varnishes of ancient Italian lutes and violin. Anal. Chim. Acta 2007, 584, 172–180. [Google Scholar] [CrossRef]
  35. Gimeno-Adelantado, J.; Mateo-Castro, R.; Doménech-Carbó, M.; Bosch-Reig, F.; Doménech-Carbó, A.; Casas-Catalán, M.; Osete-Cortina, L. Identification of lipid binders in paintings by gas chromatography—Influence of the pigments. J. Chromatogr. A 2001, 922, 385–390. [Google Scholar] [CrossRef]
  36. Kouloumpi, E.; Vandenabeele, P.; Lawson, G.; Pavlidis, V.; Moens, L. Analysis of post-Byzantine icons from the Church of the Assumption in Cephalonia, Ionian islands, Greece: A multi-method approach. Anal. Chim. Acta 2007, 598, 169–179. [Google Scholar] [CrossRef]
  37. Hao, X.; Schilling, M.R.; Wang, X.; Khanjian, H.; Heginbotham, A.; Han, J.; Auffret, S.; Wu, X.; Fang, B.; Tong, H. Use of THM-PY-GC/MS technique to characterize complex, multilayered Chinese lacquer. J. Anal. Appl. Pyrolysis 2019, 140, 339–348. [Google Scholar] [CrossRef]
  38. Chiantore, O.; Riedo, C.; Scalarone, D. Gas chromatography-mass spectrometric analysis of products from on-line pyrolysis/silylation of plant gums used as binding media. Int. J. Mass Spectrom. 2009, 284, 35–41. [Google Scholar] [CrossRef]
  39. De la Cruz-Canizares, J.; Domenech-Carbo, M.T.; Gimeno-Adelantado, J.V.; Mateo-Castro, R.; Bosch-Reig, F. Study of Burseraceae resins used in binding media and varnishes from artworks by gas chromatography-mass spectrometry and pyrolysis-gas chromatography-mass spectrometry. J. Chromatogr. A 2005, 1093, 177–194. [Google Scholar] [CrossRef]
  40. Niimura, N. Determination of the type of lacquer on East Asian lacquer ware. Int. J. Mass Spectrom. 2009, 284, 93–97. [Google Scholar] [CrossRef]
  41. Gard, F.S.; Santos, D.M.; Daizo, M.B.; Freire, E.; Reinoso, M.; Halac, E.B. Pigments analysis of an Egyptian cartonnage by means of XPS and Raman spectroscopy. Appl. Phys. A Mater. Sci. Process 2020, 126, 218. [Google Scholar] [CrossRef]
  42. Cosano, D.; Esquivel, D.; Costa, C.M.; Jimenez-Sanchidrian, C.; Ruiz, J.R. Identification of pigments in the Annunciation sculptural group (Cordoba, Spain) by micro-Raman spectroscopy. Spectroc. Acta Pt A Molec. Biomolec. Spectr. 2019, 214, 139–145. [Google Scholar] [CrossRef] [PubMed]
  43. Carter, E.A.; Perez, F.R.; Garcia, J.M.; Edwards, H.G.M. Raman spectroscopic analysis of an important Visigothic historiated manuscript. Philos. Trans. R. Soc. A Math. Phys. Eng. Sci. 2016, 374, 2082. [Google Scholar] [CrossRef]
  44. Klisinska-Kopacz, A. Non-destructive characterization of 17th century painted silk banner by the combined use of Raman and XRF portable systems. J. Raman Spectrosc. 2015, 46, 317–321. [Google Scholar] [CrossRef]
  45. Liu, J.-H.; He, Y.; Ke, W.; Hwang, M.-c.; Chen, K.Y. Cinnabar use in Anyang of bronze age China: Study with micro-raman spectroscopy and X-ray fluorescence. J. Archaeol. Sci. Rep. 2022, 43, 103460. [Google Scholar] [CrossRef]
  46. Frost, R.L.; Martens, W.N.; Rintoul, L.; Mahmutagic, E.; Kloprogge, J.T. Raman spectroscopic study of azurite and malachite at 298 and 77 K. J. Raman Spectrosc. 2002, 33, 252–259. [Google Scholar] [CrossRef]
  47. Singh, M.; Mani, B.R. Historical Note: Characterization of Pigments and Binders in Mural Painting Fragments from Bezeklik, China. Indian J. Hist. Sci. 2019, 54, 348–360. [Google Scholar] [CrossRef]
  48. Kalinina, K.B.; Bonaduce, I.; Colombini, M.P.; Artemieva, I.S. An analytical investigation of the painting technique of Italian Renaissance master Lorenzo Lotto. J. Cult. Herit. 2012, 13, 259–274. [Google Scholar] [CrossRef]
  49. Coccato, A.; Bersani, D.; Coudray, A.; Sanyova, J.; Moens, L.; Vandenabeele, P. Raman spectroscopy of green minerals and reaction products with an application in Cultural Heritage research. J. Raman Spectrosc. 2016, 47, 1429–1443. [Google Scholar] [CrossRef]
  50. Marcaida, I.; Maguregui, M.; Morillas, H.; Prieto-Taboada, N.; de Vallejuelo, S.F.-O.; Veneranda, M.; Madariaga, J.M.; Martellone, A.; De Nigris, B.; Osanna, M. In situ non-invasive characterization of the composition of Pompeian pigments preserved in their original bowls. Microchem. J. 2018, 139, 458–466. [Google Scholar] [CrossRef]
  51. Liu, Z.; Wang, J.; Han, L.; Zhou, X. Raman Spectra of Some Mineral Pigments Used in Ancient Chinese Artworks (II). J. Artic. 2013, 25, 170–175. [Google Scholar] [CrossRef]
  52. Nusimovici, M.A.; Meskaoui, A. Raman Scattering by Alpha-HgS (CINNABAR). Phys. Status Solidi (b) 1973, 58, 121–125. [Google Scholar] [CrossRef]
  53. Karapanagiotis, I.; Lampakis, D.; Konstanta, A.; Farmakalidis, H. Identification of colourants in icons of the Cretan School of iconography using Raman spectroscopy and liquid chromatography. J. Archaeol. Ence 2013, 40, 1471–1478. [Google Scholar] [CrossRef]
  54. Ha, T.; Lee, H.; Sim, K.I.; Kim, J.; Jo, Y.C.; Kim, J.H.; Baek, N.Y.; Kang, D.-I.; Lee, H.H. Optimal methodologies for terahertz time-domain spectroscopic analysis of traditional pigments in powder form. J. Korean Phys. Soc. 2017, 70, 866–871. [Google Scholar] [CrossRef]
  55. Petrova, O.; Pankin, D.; Povolotckaia, A.; Borisov, E.; Krivul’ko, T.; Kurganov, N.; Kurochkin, A. Pigment palette study of the XIX century plafond painting by Raman spectroscopy. J. Cult. Herit. 2019, 37, 233–237. [Google Scholar] [CrossRef]
  56. Vigouroux, J.P.; Husson, E.; Calvarin, G.; Dao, N.Q. Etude par spectroscopié vibrationnelle des oxydes Pb3O4, SnPb2O4 et SnPb(Pb2O4)2. Spectrochim. Acta Part A Mol. Spectrosc. 1982, 38, 393–398. [Google Scholar] [CrossRef]
  57. Guo, X.L.; Shi, H.S.; Dick, W.A. Compressive strength and microstructural characteristics of class C fly ash geopolymer. Cem. Concr. Compos. 2010, 32, 142–147. [Google Scholar] [CrossRef]
  58. Nastova, I.; Grupče, O.; Minčeva-Šukarova, B.; Turan, S.; Yaygingol, M.; Ozcatal, M.; Martinovska, V.; Jakovlevska-Spirovska, Z. Micro-Raman spectroscopic analysis of inks and pigments in illuminated medieval old-Slavonic manuscripts. J. Raman Spectrosc. 2012, 43, 1729–1736. [Google Scholar] [CrossRef]
  59. Arjonilla, P.; Dominguez-Vidal, A.; Correa-Gomez, E.; Jose Domene-Ruiz, M.; Jose Ayora-Canada, M. Raman and Fourier transform infrared microspectroscopies reveal medieval Hispano-Muslim wood painting techniques and provide new insights into red lead production technology. J. Raman Spectrosc. 2019, 50, 1537–1545. [Google Scholar] [CrossRef]
  60. Dallongeville, S.; Garnier, N.; Rolando, C.; Tokarski, C. Proteins in Art, Archaeology, and Paleontology: From Detection to Identification. Chem. Rev. 2016, 116, 2–79. [Google Scholar] [CrossRef]
  61. Wang, X.; Zhen, G.; Hao, X.; Tong, T.; Tong, H. Spectroscopic investigation and comprehensive analysis of the polychrome clay sculpture of Hua Yan Temple of the Liao Dynasty. Spectrochim. Acta Part A Mol. Biomol. Spectrosc. 2020, 240, 118574. [Google Scholar] [CrossRef] [PubMed]
  62. Carbini, M.; Stevanato, R.; Rovea, M.; Traldi, P.; Favretto, D. Curie-point pyrolysis-gas chromatography/mass spectrometry in the art field. 2—The characterization of proteinaceous binders. Rapid Commun. Mass Spectrom. RCM 1996, 10, 1240–1242. [Google Scholar] [CrossRef]
  63. Whiton, R.S. Trace Analysis of Biopolymer Components by Capillary Gas Chromatography-Mass Spectrometry (PYROLYSIS). Ph.D. Thesis, University of South Carolina, Columbia, SC, USA, 1985. [Google Scholar]
  64. Calvano, C.D.; Rigante, E.; Picca, R.A.; Cataldi, T.R.I.; Sabbatini, L. An easily transferable protocol for in-situ quasi-non-invasive analysis of protein binders in works of art. Talanta 2020, 215, 120882. [Google Scholar] [CrossRef]
  65. Wei, S.; Song, G.; He, Y. The identification of binding agent used in late Shang Dynasty turquoise-inlayed bronze objects excavated in Anyang. J. Archaeol. Sci. 2015, 59, 211–218. [Google Scholar] [CrossRef]
  66. Wang, N.; Zhang, T.; Min, J.; Li, G.; Ding, Y.; Liu, J.; Gu, A.; Kang, B.; Li, Y.; Lei, Y. Analytical investigation into materials and technique: Carved lacquer decorated panel from Fuwangge in the Forbidden City of Qianlong Period, Qing Dynasty. J. Archaeol. Sci. Rep. 2018, 17, 529–537. [Google Scholar] [CrossRef]
  67. Lu, R.; Kamiya, Y.; Miyakoshi, T. Applied analysis of lacquer films based on pyrolysis-gas chromatography/mass spectrometry. Talanta 2006, 70, 370–376. [Google Scholar] [CrossRef]
  68. Vicente, J.P.; Adelantado, J.V.G.; Carbo, M.T.D.; Castro, R.M.; Reig, F.B. Identification of drying oils used in pictorial works of art by liquid chromatography of the 2-nitrophenylhydrazides derivatives of fatty acids. Talanta 2004, 64, 326–333. [Google Scholar] [CrossRef]
  69. Song, Y.; Gao, F.; Nevin, A.; Guo, J.; Zhou, X.; Wei, S.; Li, Q. A technical study of the materials and manufacturing process used in the Gallery wall paintings from the Jokhang temple, Tibet. Herit. Sci. 2018, 6, 18. [Google Scholar] [CrossRef]
  70. Wang, N.; He, L.; Zhao, X.; Simon, S. Comparative analysis of eastern and western drying-oil binding media used in polychromic artworks by pyrolysis-gas chromatography/mass spectrometry under the influence of pigments. Microchem. J. 2015, 123, 201–210. [Google Scholar] [CrossRef]
  71. Peifan, Q.; Deqi, Y.; Qi, M.; Aijun, S.; Jingqi, S.; Zengjun, Z.; Jianwei, H. Study and Restoration of the Yi Ma Wu Hui Layer of the Ancient Coating on the Putuo Zongcheng Temple. Int. J. Archit. Herit. 2021, 15, 1707–1721. [Google Scholar] [CrossRef]
Figure 1. Puren Temple: (a) location map of Puren Temple; (b) floor plan of Puren Temple; (c) the main hall, Ciyun Puyin Hall, in the Puren Temple; (d) color painting on ancient wooden architecture; (e) ceiling painting.
Figure 1. Puren Temple: (a) location map of Puren Temple; (b) floor plan of Puren Temple; (c) the main hall, Ciyun Puyin Hall, in the Puren Temple; (d) color painting on ancient wooden architecture; (e) ceiling painting.
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Figure 2. Optical microscopic images of samples.
Figure 2. Optical microscopic images of samples.
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Figure 3. (a,b) Raman spectra for the Red pigments (a: P1; b: P2); (c,d) X-ray diffraction spectra of the Red pigments (c: P1; d: P2).
Figure 3. (a,b) Raman spectra for the Red pigments (a: P1; b: P2); (c,d) X-ray diffraction spectra of the Red pigments (c: P1; d: P2).
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Figure 4. (a,b) Raman spectra for the blue pigments (a: P3; b: P4); (c,d) Xray diffraction spectra of the blue pigments (c: P3; d: P4).
Figure 4. (a,b) Raman spectra for the blue pigments (a: P3; b: P4); (c,d) Xray diffraction spectra of the blue pigments (c: P3; d: P4).
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Figure 5. (a,b) Raman spectra for the green pigments (a: P5; b: P6); (c,d) Xray diffraction spectra of the green pigments (c: P5; d: P6).
Figure 5. (a,b) Raman spectra for the green pigments (a: P5; b: P6); (c,d) Xray diffraction spectra of the green pigments (c: P5; d: P6).
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Figure 6. (a,b) Raman spectra for the white pigments (a: P7; b: P8); (c,d) Xray diffraction spectra of the white pigments (c: P7; d: P8).
Figure 6. (a,b) Raman spectra for the white pigments (a: P7; b: P8); (c,d) Xray diffraction spectra of the white pigments (c: P7; d: P8).
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Figure 7. (a) Raman spectra for the yellow pigment (P9); (b) Xray diffraction spectra of the yellow pigment (P9).
Figure 7. (a) Raman spectra for the yellow pigment (P9); (b) Xray diffraction spectra of the yellow pigment (P9).
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Figure 8. py-GC/MS results of the samples ((a1): P1; (a2): P2; (b1): P3; (b2): P4; (c1): P5; (c2): P6; (d1): P7; (d2): P8; (e): P9).
Figure 8. py-GC/MS results of the samples ((a1): P1; (a2): P2; (b1): P3; (b2): P4; (c1): P5; (c2): P6; (d1): P7; (d2): P8; (e): P9).
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Figure 9. Relative concentrations of fatty acids of samples ((a1): P1; (a2): P2; (b1): P3; (b2): P4; (c1): P5; (c2): P6; (d1): P7; (d2): P8; (e): P9).
Figure 9. Relative concentrations of fatty acids of samples ((a1): P1; (a2): P2; (b1): P3; (b2): P4; (c1): P5; (c2): P6; (d1): P7; (d2): P8; (e): P9).
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Table 1. The main hall Ciyun Puyin.samples position.
Table 1. The main hall Ciyun Puyin.samples position.
Samples PositionSamples Images
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Table 2. Information regarding the color samples.
Table 2. Information regarding the color samples.
SampleColorSource of SampleElements
P1RedBeam paintingHg (51.27%), Pb (10.59%), Ca (10.42%), Si (9.36%), Fe (7.41%)
P2Ceiling paintingHg (50.42%), Pb (11.22%), Si (10.78%), Ca (9.88%), Fe (7.13%)
P3BlueBeam paintingCa (21.2%), Si (18.35%), Fe (12.24%), Cu (8.46%), As (7.98%)
P4Ceiling paintingSi (26.62%), Ca (19.9%), Fe (13.15%), As (11.31%), Cu (7.38%)
P5GreenBeam paintingCu (55.05%), Si (13.84%), Ca (10.63%), Pb (10.43%), K (3.55%)
P6Ceiling paintingCu (57.79%), Cl (12.06%), Ca (11.82%), Pb (2.98%), Fe (2.48%)
P7WhiteBeam paintingPb (72.44%), Ca (16.23%), Si (4.37%), Fe (2.98%), K (2.24%)
P8Ceiling paintingPb (74.95%), Ca (8.56%), Si (6.52%), K (4.57%), Fe (2.02%)
P9YellowCeiling paintingAs (30.59%), S (28.16%), Ca (21.17%), Si (3.52%), Fe (1.02%)
Table 3. The P/S and A/P values of the color painting samples.
Table 3. The P/S and A/P values of the color painting samples.
SampleA/PP/SThe Type of Substance Contained
P14.091.02Heat-bodied tung oil (the presence of APAs)
P23.751.19Heat-bodied tung oil (the presence of APAs)
P32.771.17Heat-bodied tung oil (the presence of APAs)
P43.411.97Heat-bodied tung oil (the presence of APAs)
P58.990.52Raw tung-oil
P62.652.55Raw tung-oil
P76.991.17Raw tung-oil
P85.900.94Raw tung-oil
P95.010.90Heat-bodied tung oil (the presence of APAs)
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Teri, G.; Han, K.; Huang, D.; Li, Y.; Tian, Y.; Chao, X.; Jia, Z.; Fu, P.; Li, Y. A Study on the Materials Used in the Ancient Architectural Paintings from the Qing Dynasty Tibetan Buddhist Monastery of Puren, China. Materials 2023, 16, 6404. https://0-doi-org.brum.beds.ac.uk/10.3390/ma16196404

AMA Style

Teri G, Han K, Huang D, Li Y, Tian Y, Chao X, Jia Z, Fu P, Li Y. A Study on the Materials Used in the Ancient Architectural Paintings from the Qing Dynasty Tibetan Buddhist Monastery of Puren, China. Materials. 2023; 16(19):6404. https://0-doi-org.brum.beds.ac.uk/10.3390/ma16196404

Chicago/Turabian Style

Teri, Gele, Kezhu Han, Dan Huang, Yanli Li, Yuxiao Tian, Xiaolian Chao, Zhihui Jia, Peng Fu, and Yuhu Li. 2023. "A Study on the Materials Used in the Ancient Architectural Paintings from the Qing Dynasty Tibetan Buddhist Monastery of Puren, China" Materials 16, no. 19: 6404. https://0-doi-org.brum.beds.ac.uk/10.3390/ma16196404

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