Microanalysis of clay-based pigments in painted artworks by the
means of Raman spectroscopy

J 2013

Microanalysis of clay-based pigments in painted artworks by the means of Raman spectroscopy

KOŠAŘOVÁ, Veronika; David HRADIL; Ivan NĚMEC; Petr BEZDIČKA; Viktor KANICKÝ et al.

Základní údaje

Originální název

Microanalysis of clay-based pigments in painted artworks by the means of Raman spectroscopy

Autoři

KOŠAŘOVÁ, Veronika; David HRADIL; Ivan NĚMEC; Petr BEZDIČKA a Viktor KANICKÝ

Vydání

Journal of Raman Spectroscopy, Wiley, 2013, 0377-0486

Další údaje

Jazyk

angličtina

Typ výsledku

Článek v odborném periodiku

Obor

10402 Inorganic and nuclear chemistry

Stát vydavatele

Spojené státy

Utajení

není předmětem státního či obchodního tajemství

Odkazy

URL

Impakt faktor

Impact factor: 2.519

Označené pro přenos do RIV

Ano

Kód RIV

RIV/00216224:14310/13:00071643

Organizační jednotka

Přírodovědecká fakulta

DOI

https://doi.org/10.1002/jrs.4381

UT WoS

000330107900015

Klíčová slova anglicky

Raman spectroscopy; clay based pigments; clay minerals; iron oxides; microanalysis of paintings

Štítky

AKR

Příznaky

Mezinárodní význam, Recenzováno

Změněno: 6. 1. 2016 11:02, Mgr. Veronika Kohútová, Ph.D.

Anotace

V originále

FT Raman spectroscopy and micro-Raman spectroscopy with lasers of three different wavelengths (1064 nm, 785nm and 532 nm) were used for analysis of reference samples of natural clay pigments including white clay minerals (kaolinite, illite, montmorillonite), green earths (glauconite and celadonite) and red earths (natural mixtures of white clay minerals with hematite). In addition, eight micro-samples obtained from historical paintings containing clay pigments in ground and colour layers have been examined. Powder X-ray diffraction and micro-diffraction were used as supplementary methods. It was found that laser operating at 1064nm provided the best quality Raman spectra for distinguishing different white clay minerals, but the spectra of green and red earths were affected by strong fluorescence caused by the presence of iron. Green earth minerals could be easily distinguished by 532 or 785nm excitation lasers, even in small concentrations in the paint layers. On the other hand, when anatase (TiO2) or iron oxides (such as hematite) were present as admixtures (both are quite common, particularly in red earths), the collection of characteristic spectra of clay minerals which form the main component of the layer was hindered or even prevented. Another complicating factor was the fluorescence produced by organic binders when analysing the micro-samples of artworks. In those cases, it is always necessary to use powder X-ray micro-diffraction to avoid misleading interpretations of the pigment’s composition.

Citovat

KOŠAŘOVÁ, Veronika; David HRADIL; Ivan NĚMEC; Petr BEZDIČKA a Viktor KANICKÝ. Microanalysis of clay-based pigments in painted artworks by the means of Raman spectroscopy. Journal of Raman Spectroscopy. Wiley, 2013, roč. 44, č. 11, s. 1570-1577. ISSN 0377-0486. Dostupné z: https://doi.org/10.1002/jrs.4381.

@article{1162016,
   author = {Košařová, Veronika and Hradil, David and Němec, Ivan and Bezdička, Petr and Kanický, Viktor},
   article_number = {11},
   doi = {https://doi.org/10.1002/jrs.4381},
   keywords = {Raman spectroscopy; clay based pigments; clay minerals; iron oxides; microanalysis of paintings},
   language = {eng},
   issn = {0377-0486},
   journal = {Journal of Raman Spectroscopy},
   title = {Microanalysis of clay-based pigments in painted artworks by the means of Raman spectroscopy},
   url = {http://onlinelibrary.wiley.com/doi/10.1002/jrs.4381/abstract},
   volume = {44},
   year = {2013}
}

TY  - JOUR
ID  - 1162016
AU  - Košařová, Veronika - Hradil, David - Němec, Ivan - Bezdička, Petr - Kanický, Viktor
PY  - 2013
TI  - Microanalysis of clay-based pigments in painted artworks by the means of Raman spectroscopy
JF  - Journal of Raman Spectroscopy
VL  - 44
IS  - 11
SP  - 1570-1577
EP  - 1570-1577
PB  - Wiley
SN  - 03770486
KW  - Raman spectroscopy
KW  - clay based pigments
KW  - clay minerals
KW  - iron oxides
KW  - microanalysis of paintings
UR  - http://onlinelibrary.wiley.com/doi/10.1002/jrs.4381/abstract
L2  - http://onlinelibrary.wiley.com/doi/10.1002/jrs.4381/abstract
N2  - FT Raman spectroscopy and micro-Raman spectroscopy with lasers of three different wavelengths (1064 nm, 785nm and 532 nm) were used for analysis of reference samples of natural clay pigments including white clay minerals (kaolinite, illite, montmorillonite), green earths (glauconite and celadonite) and red earths (natural mixtures of white clay minerals with hematite). In addition, eight micro-samples obtained from historical paintings containing clay pigments in ground and colour layers have been examined. Powder X-ray diffraction and micro-diffraction were used as supplementary methods. It was found that laser operating at 1064nm provided the best quality Raman spectra for distinguishing different white clay minerals, but the spectra of green and red earths were affected by strong fluorescence caused by the presence of iron. Green earth minerals could be easily distinguished by 532 or 785nm excitation lasers, even in small concentrations in the paint layers. On the other hand, when anatase (TiO2) or iron oxides (such as hematite) were present as admixtures (both are quite common, particularly in red earths), the collection of characteristic spectra of clay minerals which form the main component of the layer was hindered or even prevented. Another complicating factor was the fluorescence produced by organic binders when analysing the micro-samples of artworks. In those cases, it is always necessary to use powder X-ray micro-diffraction to avoid misleading interpretations of the pigment’s composition.
ER  -

KOŠAŘOVÁ, Veronika; David HRADIL; Ivan NĚMEC; Petr BEZDIČKA a Viktor KANICKÝ. Microanalysis of clay-based pigments in painted artworks by the means of Raman spectroscopy. \textit{Journal of Raman Spectroscopy}. Wiley, 2013, roč.~44, č.~11, s.~1570-1577. ISSN~0377-0486. Dostupné z: https://doi.org/10.1002/jrs.4381.

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