研究生: |
張滙婷 Chang, Hui-Ting |
---|---|
論文名稱: |
以拉曼光譜技術鑑定東方繪畫顏料的實際與應用 Identification and Application of Oriental Painting Pigments by Raman Spectroscopy |
指導教授: |
林震煌
Lin, Cheng-Huang |
口試委員: |
林震煌
Lin, Cheng-Huang 呂家榮 Lu, Chia-Jung 丁望賢 Ding, Wang-Hsien |
口試日期: | 2021/06/11 |
學位類別: |
碩士 Master |
系所名稱: |
化學系 Department of Chemistry |
論文出版年: | 2021 |
畢業學年度: | 109 |
語文別: | 中文 |
論文頁數: | 88 |
中文關鍵詞: | 顏料 、拉曼光譜 、表面增強拉曼散射 、LabVIEW |
英文關鍵詞: | pigments, Raman spectroscopy, surface enhanced Raman scattering, LabVIEW |
DOI URL: | http://doi.org/10.6345/NTNU202100510 |
論文種類: | 學術論文 |
相關次數: | 點閱:173 下載:0 |
分享至: |
查詢本校圖書館目錄 查詢臺灣博碩士論文知識加值系統 勘誤回報 |
本研究以拉曼散射光譜儀分析顏料的拉曼指紋圖譜,做為標準參考物質顏料,建立鑑定維護或修復畫作時所需的標準拉曼光譜圖。再使用本實驗室開發的LabVIEW程式擷取背景螢光的功能,擷取螢光背景光譜圖分析,另一方面也使用表面增強拉曼散射技術,藉著增強拉曼訊號並降低螢光背景的方法,解決螢光干擾的問題。
利用上述方法技術,以螢光光譜區分方解末及胡粉兩種碳酸鈣顏料和辰砂及鉛丹兩種無機顏料;而LabVIEW程式無法解決的背景螢光問題,以表面增強拉曼散射技術,增強拉曼訊號並解決螢光干擾的問題,藉著添加奈米銀及使用拉曼光譜儀分析,解決紅色有機顏料強烈的背景螢光問題。
本研究分析顏料標準品的拉曼光譜圖,實際將表面增強拉曼散射技術應用於東方畫作未知樣品上,成功降低拉曼光譜中的螢光干擾,並與顏料之標準拉曼光譜比較,分析出未知樣品1中之成分顏料為鉛丹,未知樣品2中之成分顏料為鉛丹和鉛白,透過分析未知樣品的例子,證明本研究方法能成功應用於東方畫作顏料的鑑定上。
In this work, various color of pigments were selected, including inorganic and organic pigments, as standard reference material. These pigments were analyzed by Raman scattering spectrometer to establish the reference spectra for identification and restoration of paintings.
Using the LabVIEW program to retrieve the Raman and fluorescence spectrum separately. On the other hand, utilizing the surface enhanced Raman scattering (SERS) to enhance the Raman signal and reduce the fluorescence background to solve the problem on fluorescent interference.
By the LabVIEW program, distinguishing two of the calcium carbonate pigments and two of the red inorganic pigments. When fluorescence background couldn’t be solved with the LabVIEW program, the SERS was used for the identification of red organic pigments.
Analyzing the fingerprint spectrum of the Raman spectroscopy to apply on the unknown samples of oriental paintings which used SERS to reduce the fluorescence interference. The results of unknown 1 and 2 have successfully confirmed. The composition of unknown 1 is red lead, and unknown 2 is red lead and white lead. Successfully proved that this work has been applied for the identification of oriental painting pigments.
1. C. Anselmi, M. Vagnini, L. Cartechini, C. Grazia, R. Vivani, A. Romani, F. Rosi, A. Sgamellotti, C. Miliani, Spectroc. Acta Pt. A-Molec. Biomolec. Spectr. 173 (2017) 439-444.
2. H. Airi, A. Yoshinari, V.L. Annelies, D.K. Nouchka, N. Petria, V. Frederik, J. Koen, T. Kriengkamol, T. Kazuo, N. Izumi, Microchem J. 138 (2018) 266-272.
3. P.O. Autran, C. Dejoie, P. Bordet, J.L. Hodeau, C. Dugand, M. Gervason, M. Anne, P. Martinetto, Anal. Chem. 93 (2021) 1135-1142.
4. C. Vlachou-Mogire, P. Moretti, L. Monico, A. Chieli, M. Iwanicka, P. Targowski, V. Detalle, E. Bourguignon, K. Laclavetine, F. Mirambet, T. Tong, S. Pinchin, Microchem J. 156 (2020) 104797.
5. A. Abdrabou, M. Abdallah, H.M. Kamal, Conservar Património 26 (2017) 51-63.
6. T. Arlt, H. E. Mahnke, T. Siopi, E. Menei, C. Aibéo, R. R. Pausewein, I. Reiche, I. Manke, V. Lepper, J. Cult. Herit. 39 (2019) 13-20.
7. F. Gabrieli, K.A. Dooley, M. Facini, J.K. Delaney, Sci. Adv. 5 (2019) eaaw7794.
8. E. Pięta, J. Olszewska-Świetlik, C. Paluszkiewicz, A. Zając, W.M. Kwiatek, Vib. Spectrosc. 103 (2019)
9. C. Pelosi, G. Capobianco, G. Agresti, G. Bonifazi, F. Morresi, S. Rossi, U. Santamaria, S. Serranti, Spectroc. Acta Pt. A-Molec. Biomolec. Spectr. 198 (2018) 92-106.
10. C. Biron, G. Le Bourdon, J. Perez-Arantegui, L. Servant, R. Chapoulie, F. Daniel, Anal. Bioanal. Chem. 410 (2018) 7043-7054.
11. A. Daveri, M. Malagodi, M. Vagnini, J. Anal. Methods Chem. 2018 (2018) 6595643.
12. L. Rampazzi, V. Brunello, F. P. Campione, C. Corti, L. Geminiani, S. Recchia, M. Luraschi, Microchem J. 157 (2020) 105017.
13. L. Nodari and P. Ricciardi, Herit. Sci. 7 (2019)
14. S.P. Best, R.J.H. Clark, R. Withnall, Endeavour 16 (1992) 66-73.
15. A. Derbyshire and R. Withnall, J. Raman Spectrosc. 30 (1999) 185-188.
16. F. Rosi, M. Paolantoni, C. Clementi, B. Doherty, C. Miliani, B.G. Brunetti, A. Sgamellotti, J. Raman Spectrosc. 41 (2009) 452-458.
17. G. Marucci, A. Beeby, A.W. Parker, C.E. Nicholson, Anal. Methods 10 (2018) 1219-1236.
18. T. Christiansen, D. Buti, K. N. Dalby, P. E. Lindelof, K. Ryholt, A. Vila, J. Archaeol. Sci. Rep. 14 (2017) 208-219.
19. A. Botteon, C. Colombo, M. Realini, C. Castiglioni, A. Piccirillo, P. Matousek, C. Conti, J. Raman Spectrosc. 51 (2020) 2016-2021.
20. N. Grechukha, K. Gorshkova, M. Panov, I. Tumkin, E. Kirillova, V. Lukianov, N. Kirillova, V. Kochemirovsky, Appl. Sci. 7 (2017) 991.
21. X. Jiang, Y. Ma, Y. Chen, Y. Li, Q. Ma, Z. Zhang, C. Wang, Y. Yang, Spectroc. Acta Pt. A-Molec. Biomolec. Spectr. 190 (2018) 61-67.
22. O. Petrova, D. Pankin, A. Povolotckaia, E. Borisov, T. Krivul’ko, N. Kurganov, A. Kurochkin, J. Cult. Herit. 37 (2019) 233-237.
23. P. Colomban, Y. Zhang, B. Zhao, Ceram. Int. 43 (2017) 12079-12088.
24. S. Steger, H. Stege, S. Bretz, O. Hahn, J. Cult. Herit. 38 (2019) 20-28.
25. C. Miliani, F. Rosi, B. G. Brunetti, A. Sgamellotti, Accounts Chem. Res. 43 (2010) 728-738.
26. D. Mancini, A. Percot, L. Bellot-Gurlet, P. Colomban, P. Carnazza, Talanta 227 (2021) 122159.
27. M. Leona, F. Casadio, M. Bacci, M. Picollo, J. Am. Inst. Conserv. 43 (2004) 39-54.
28. M. Fleischmann, P.J. Hendra, A.J. McQuillan, Chem. Phys. Lett. 26 (1974) 163-166.
29. E. Garcia-Rico, R.A. Alvarez-Puebla, L. Guerrini, Chem. Soc. Rev. 47 (2018) 4909-4923.
30. W. Nam, X. Ren, S.A.S. Tali, P. Ghassemi, I. Kim, M. Agah, W. Zhou, Nano Lett. 19 (2019) 7273-7281.
31. V. Moisoiu, A. Socaciu, A. Stefancu, S.D. Iancu, I. Boros, C.D. Alecsa, C. Rachieriu, A.R. Chiorean, D. Eniu, N. Leopold, C. Socaciu, D.T. Eniu, Appl. Sci. 9 (2019) 806.
32. R. Pilot, J. Raman Spectrosc. 49 (2018) 954-981.
33. J. Soto, E. Imbarack, I. López-Tocón, S. Sánchez-Cortés, J. C. Otero, P. Leyton, RSC Adv. 9 (2019) 14511-14519.
34. Y. Jiang, J. Wang, L. Malfatti, D. Carboni, N. Senes, P. Innocenzi, Appl. Surf. Sci. 450 (2018) 451-460.
35. A.M.C.A.N. 80, Anal. Methods 9 (2017) 4338-4340.
36. \ V.M. Nardo, F. Aliotta, M.A. Mastelloni, R.C. Ponterio, F. Saija, S. Trusso, C.S. Vasi, Atti. Accad. Naz. Lin. 95 (2017) A5.
37. F. Pozzi, J.R. Lombardi, M. Leona, Herit. Sci. 1 (2013) 23.
38. E.V. Shabunya-Klyachkovskaya, O.S. Kulakovich, S.V. Gaponenko, Spectroc. Acta Pt. A-Molec. Biomolec. Spectr. 222 (2019) 117235.
39. A. Cesaratto, Y.B. Luo, H.D. Smith, M. Leona, Herit. Sci. 6 (2018)
40. F. Pozzi, K.J. van den Berg, I. Fiedler, F. Casadio, J. Raman Spectrosc. 45 (2014) 1119-1126.
41. E. Casanova‐González, A. García‐Bucio, J.L. Ruvalcaba‐Sil, V. Santos‐Vasquez, B. Esquivel, T. Falcón, E. Arroyo, S. Zetina, M.L. Roldán, C. Domingo, J. Raman Spectrosc. 43 (2012) 1551-1559.
42. C. Sessa, R. Weiss, R. Niessner, N.P. Ivleva, H. Stege, Microchem J. 138 (2018) 209-225.
43. S. Bruni, V. Guglielmi, F. Pozzi, J. Raman Spectrosc. 41 (2010) 175-180.
44. M.L. de Souza and P. Corio, Vib. Spectrosc. 54 (2010) 137-141.
45. W.C. Lin, S.H. Huang, C.L. Chen, C.C. Chen, D.P. Tsai, H.P.Chiang, Appl. Phys. A-Mater. Sci. Process. 101 (2010) 185-189.
46. M.H. Cho, Y.S. Paik, T.R. Hahn, J. Agric. Food Chem. 48 (2000) 3917-3921.
47. L. Burgio, R.J.H. Clark, R.R. Hark, Proc. Natl. Acad. Sci. U.S.A. 107 (2010) 5726-5731.
48. J.G. Shapter, M.H. Brooker, W.M. Skinner, Int. J. Miner. Process. 60 (2000) 199-211.
49. M. Jeršek and S. Kramar, J. Raman Spectrosc. 45 (2014) 1000-1005.
50. F. Casadio, A. Bezúr, I. Fiedler, K. Muir, T. Tradc, S. Maccagnola, J. Raman Spectrosc. 43 (2012) 1761-1771.
51. W.J.B. Dufresne, C.J. Rufledt, C.P. Marshall, J. Raman Spectrosc. 49 (2018) 1999-2007.
52. P. Vandenabeele, P.D. Paepe, L. Moens, J. Raman Spectrosc. 39 (2008) 1099-1103.
53. N. Prieto-Taboada, O. Gomez-Laserna, I. Martinez-Arkarazo, M.A. Olazabal, J.M. Madariaga, Anal. Chem. 86 (2014) 10131-7.
54. T. Schmid, R. Jungnickel, P. Dariz, Minerals 10 (2020)
55. S.V. Gotoshia and L.V. Gotoshia, J. Phys. D-Appl. Phys. 41 (2008)
56. L. Burgio, R.J.H. Clark, S. Firth, Analyst 126 (2001) 222-227.
57. F.J. Owens and J. Orosz, Solid State Commun. 138 (2006) 95-98.
58. D.L.A. de Faria and F.N. Lopes, Vib. Spectrosc. 45 (2007) 117-121.
59. Y. Wang, Spectroc. Acta Pt. A-Molec. Biomolec. Spectr. 247 (2021) 119117.
60. G.D. Ventura, F. Capitelli, M. Sbroscia, A. Sodo, J. Raman Spectrosc. 51 (2019) 1513-1521.
61. R.L. Frost, W.N. Martens, L. Rintoul, E. Mahmutagic, J.T. Kloprogge, J. Raman Spectrosc. 33 (2002) 252-259.
62. M. Vermeulen, S. Saverwyns, A. Coudray, K. Janssens, J. Sanyova, Dyes Pigment. 149 (2018) 290-297.
63. C. Defeyt, P. Vandenabeele, B. Gilbert, J.V. Pevenage, R. Clootse, D. Strivay, J. Raman Spectrosc. 43 (2012) 1772-1780.
64. S. Lin, (2015) Investigation into the Use of Surface-Enhanced Raman Spectroscopy (SERS) for Organic Dye Analysis. (Bachelor's degree, Massachusetts Institute of Technology) Retrieved from: http://hdl.handle.net/1721.1/98657.
65. Y. Zhang, C. Zhao, G. Tian, C. Lu, Y. Li, L. He, H. Xiao, J. Zheng, Food Chem. 240 (2018) 743-750.
66. T. Bayerová, Stud. Conserv. 63 (2017) 171-188.
67. K. Retko, P. Ropret, R.C. Korošec, J. Raman Spectrosc. 45 (2014) 1140-1146.
68. M.V. Cañamares, J.V. Garcia-Ramos, C. Domingo, S. Sanchez-Cortes, J. Raman Spectrosc. 35 (2004) 921-927.
69. S. Bruni, V. Guglielmi, F. Pozzi, J. Raman Spectrosc. 42 (2011) 1267-1281.
70. M.V. Cañamares, M.G. Mieites‐Alonso, M. Leona, J. Raman Spectrosc. 51 (2020) 903-909.
71. A. Amat, F. Rosi, C. Miliani, A. Sgamellotti, S. Fantacci, J. Mol. Struct. 993 (2011) 43-51.
72. A. Baran, A. Fiedler, H. Schulz, M. Baranska, Anal. Methods 2 (2010) 1372-1376.
73. A.M. Hofmeister, T.C. Hoering, D. Virgo, Phys. Chem. Miner. 14 (1987) 205-224.