Difference between revisions of "Phthalocyanine blue"
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| − | == | + | == Physical and Chemical Properties == |
| − | Slowly turns yellow then dissolves in concentrated sulfuric acid | + | * Slowly turns yellow then dissolves in concentrated sulfuric acid |
| − | + | * Insoluble in organic solvents, water and alkalies. | |
| − | Insoluble in organic solvents, water and alkalies. | + | * Fine grain translucent to opaque particles with moderate to strong birefringence |
| − | + | * Crystal type I appears deep red through Chelsea filter and crystal type II appears black | |
| − | Fine grain translucent to opaque particles with moderate to strong birefringence | + | * Composition = C32H16N8Cu |
| − | + | * CAS = 147-14-8 | |
| − | + | * Density = 1.6 | |
| − | + | * Refractive Index = 1.38 | |
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== Hazards and Safety == | == Hazards and Safety == | ||
Revision as of 11:39, 12 June 2020
== Description ==
A synthetic organic colorant composed of copper phthalocyanine that was first synthesized in 1933 by R.P.Linstead. In 1935, copper phthalocyanine was marketed as a paint pigment called Monastral blue [ICI]. The organic colorant is usually adsorbed on an aluminum hydrate base to form a deep blue color. Other colors are achieved by varying the formulation, i.e., chlorinated copper phthalocyanine produces a green colorant. Phthalocyanine blue is a permanent pigment which is unaffected by light, heat, and chemicals. It is used as a colorant in inks, enamels, plastics, paints, chalks, leather, pencils, and photographs. In industry, phthalocyanine blue has replaced all other blue pigments for use in coatings because it is lightfast as well as resistant to chemicals and clumping.
Synonyms and Related Terms
Pigment Blue 15; CI 74160; Heliogenblau (Deut.); bleu héliogène (Fr.); bleu de phtalocyanine (Fr.); Phtalocyaninblau (Deut.); azul de ftalocianina (Esp.); blu ftalo (It.); phtalocyanine blauw (Ned.); azul de ftalocianina (Port.); phthalo blue; copper phthalocyanine blue; Monastral Fast Blue; Winsor blue; Bocour blue; Talens Rembrandt blue; Thalo blue; Heliogen blue
Comparisons
| Pigment number | Manufacture | Pigment name | Manufacture CI number | Comments |
|---|---|---|---|---|
| PB15:1 | Kremer | phthalo blue, primary | 23050 | |
| PB15:1 | Sun | phthalocyanine blue red shade | 248-3745 | |
| PB15:3 | Kremer | unspecified | 23060 | |
| PB15:3 | Sun | phthalocyanine green shade beta | 249-1282 | |
| PB15:3 | Magruder | phthalocyanine blue g_s | bl1301-dc |
Physical and Chemical Properties
- Slowly turns yellow then dissolves in concentrated sulfuric acid
- Insoluble in organic solvents, water and alkalies.
- Fine grain translucent to opaque particles with moderate to strong birefringence
- Crystal type I appears deep red through Chelsea filter and crystal type II appears black
- Composition = C32H16N8Cu
- CAS = 147-14-8
- Density = 1.6
- Refractive Index = 1.38
Hazards and Safety
Suspected carcinogen, teratogen. May be contaminated with traces of PCB.
Fisher Scientific: MSDS
Comparisons
Characteristics of Common Blue Pigments
Sources Checked for Data in Record
- Nicholas Eastaugh, Valentine Walsh, Tracey Chaplin, Ruth Siddall, Pigment Compendium, Elsevier Butterworth-Heinemann, Oxford, 2004
- R. J. Gettens, G.L. Stout, Painting Materials, A Short Encyclopaedia, Dover Publications, New York, 1966 Comment: ...was first introduced to the pigment trade under the name 'Monastral blue' at an exhibition in London, November 1935.
- Reed Kay, The Painter's Guide To Studio Methods and Materials, Prentice-Hall, Inc., Englewood Cliffs, NJ, 1983
- Ralph Mayer, A Dictionary of Art Terms and Techniques, Harper and Row Publishers, New York, 1969 (also 1945 printing) Comment: Phthalocyanine blue was put on the market in Britain in 1935 and in America in 1936.
- Art and Architecture Thesaurus Online, http://www.getty.edu/research/tools/vocabulary/aat/, J. Paul Getty Trust, Los Angeles, 2000
- The Dictionary of Art, Grove's Dictionaries Inc., New York, 1996 Comment: "Pigments"
- Hermann Kuhn, Conservation and Restoration of Works of Art and Antiquities, Butterworths, London, 1986
- Michael McCann, Artist Beware, Watson-Guptill Publications, New York City, 1979
- Website address 1 Comment: www.handprint.com - R. Linstead analyzed and named the molecule in 1933...it was commercially introduced in 1935
- Sigma Dyes, Stains and Natural Pigments, Infrared Library, Nicolet, 1991-1995 Comment: OMNIC: formula= C32H16N8Cu, CAS= 147-14-8