Viridian

Artificial inorganic pigment

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Composition and Properties of Viridian

Viridian is hydrated chromium oxide Cr2O3 • 2 H2O. This form of chromium oxide contains water molecules in its crystal structure and is of vivid color with a bluish tint. It is called viridian in English and vert émeraude in French.

The pigment chromium oxide green with the formula of Cr2O3 is similar to hydrated chromium oxide but does not contain water molecules in its crystal structure. Its appearance is rather dull and more in the direction of olive green.

Both variants are chemically stable and resistant against boiling acids and alkalis. Chemical stability and general permanence are some of the most important advantages of these pigments which are also compatible with all other pigments.

Video: 'Watercolor Viridian' by Jo MacKenzie

Viridian-crystals

Pigment

viridian-painted-swatch

Painted swatch

Names of Viridian

Alternative names

Emeraude green, Pannetier’s green, Guignet’s green

Color Index

PG 18, CI 77289

Word origin

From Latin virid, stem of viridis “green, blooming, vigorous”
From Online Etymology Dictionary

Spain Flag

Chromoxidhydratgrün

German

Spain Flag

Vert émeraude

French

Spain Flag

Verde di Guignet

Italian

Spain Flag

Verde de Guignet, óxhidrato de cromo

Spanish

Preparation of Viridian

Hydrated chromium oxide can be prepared by heating a mixture of potassium dichromate and boric acid.

Preparation of the Pigment in the Lab

Attention: All chromates and dichromates are highly toxic chemicals and should not be handled by people not trained to do so.

 

One part of potassium dichromate and two parts boric acid are homogenized in a porcelain mortar and are placed into a crucible.

preparation of hydrated chromium oxide 1

preparation of hydrated chromium oxide 2

The crucible is placed into an oven and heated for 6 hours at a temperature of 500° C.

preparation of hydrated chromium oxide 3

preparation of hydrated chromium oxide 2

After the completion of the reaction, the still hot crucible is grasped by forceps and thrown into a beaker filled with cold water. After cooling the hard material can be taken out of the crucible by scrapping and/or breaking the crucible and then dried and homogenized in a mortar.

preparation of hydrated chromium oxide 5

References

(1) Claudia Pelosi, Giorgia Agresti, Ulderico Santamaria, Elisabetta Mattei, Artificial Yellow Pigments: Production and Spectroscopic Characterization, e-PS, 2010, 7, 108-115

(2) Dik, J., Scientific analysis of historical paint and the implications for art history and art conservation. The case studies of naples yellow and discoloured smalt. Thesis, University of Amsterdam, 2003 (available as pdf).

(3) Henk Schenk, J. Dik, R. Peschar, The Production History of Naples Yellow and the Discoloration of the Blue Pigment Smalt, Acta Cryst. (2005). A61, C494

(4) L. Chiarantini1, F. Gallo, V. Rimondi, M. Benvenuti, P. Costagliola and A. Dini, Early Renaissance Production Recipes for Naples Yellow Pigment: A Mineralogical and Lead Isotope Study of Italian Majolica from Montelupo (Florence), Archeometry, 28 Nov 2014, DOI: 10.1111/arcm.12146.

(5) Robin J. H. Clark, Lucas Cridland, Benson M. Kariuki, Kenneth D. M. Harris and Robert Withnall, Synthesis, structural characterisation and Raman spectroscopy of the inorganic pigments lead tin yellow types I and II and lead antimonate yellow: their identification on medieval paintings and manuscripts. J. Chem. Soc., Dalton Trans., 1995, 2577-2582. DOI: 10.1039/DT9950002577.

(6) Joris Dik, E. Hermens, R Peschar, H Schenk, Early Production Recipes for Lead Antimonate Yellow in Italian Art, Archaeometry 08/2005; 47(3). DOI:10.1111/j.1475-4754.2005.00221.x. Available as pdf.

(7) Agresti G., Baraldi P., Pelosi C. and Santamaria U.,Yellow pigments based on lead, tin, and antimony: Ancient recipes, synthesis, characterization, and hue choice in artworks, Color Research and Application 41 (3) 2016. https://doi.org/10.1002/col.22026

History of Use 

The element chromium was discovered in 1797 and the use of chromium oxide greens goes back to the first half of the nineteenth century. Viridian was first prepared by Pannetier around 1838 in Paris and subsequently patented by the French chemist Guignet in 1859 (1).

References

(1) Newman, R., Chromium Oxide Greens, in  Artists’ Pigments, A Handbook of Their History and Characteristics, Vol 3: E.W. Fitzhugh (Ed.) Oxford University Press 1997, p. 273 – 286.  Available as pdf from the National Gallery of Art.

Examples of use

Pierre-Auguste Renoir, La Yole, ca 1879

Pierre-Auguste_Renoir, La_Yole

 

Renoir used viridian mixed with chrome yellow and lead white for the green rushes in the foreground.

Pierre-Auguste_Renoir, La_Yole, detail

 

Identification

Fiber Optics Reflectance Spectra (FORS)
Infrared Spectrum

1. IR Spectrum of viridian in the ATR-FT-IR spectra of different pure inorganic pigments, University of Tartu, Estonia

2. IR Spectrum by S. Vahur, Database of ATR-IR spectra of materials related to paints and coatings, University of Tartu, Estonia

 

IR-Spectrum of chromium oxide green in linseed oil

IR-Spectrum of chromium oxide green in linseed oil

Raman Spectrum

 raman spectrum of viridian

Spectrum by Ian M. Bell, Robin J.H. Clark and Peter J. Gibbs, Raman Spectroscopic Library
University College of London

X-Ray Fluorescence Spektrum (XRF)

XRF Spectrum in the Free XRF Spectroscopy Database of Pigments Checker, CHSOS website.

References

(1) Brown, D. A., Cunningham, D., & Glass, W. K., The infrared and Raman spectra of chromium (III) oxide. Spectrochimica Acta Part A: Molecular Spectroscopy, 24(8), (1968) 965–968. doi:10.1016/0584-8539(68)80115-1

viridian-microphotograph

Microphotograph

image © Volker Emrath

Further Reading

References

(1) Newman, R., Chromium Oxide Greens, in  Artists’ Pigments, A Handbook of Their History and Characteristics, Vol 3: E.W. Fitzhugh (Ed.) Oxford University Press 1997, p. 273 – 286.  Available as pdf from the National Gallery of Art.

(2) S. Muntwyler, J. Lipscher, HP. Schneider, Das Farbenbuch, 2nd. Ed., 2023, alataverlag Elsau, pp. 104-105.