Difference between revisions of "Anatase"

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== Description ==
 
== Description ==
  
One of three naturally occuring isomorphic forms of [[titanium%20dioxide|titanium dioxide]]: anatase, rutile, and brookite. Anatase forms hard, transparent crystals. Deposits have been found in the Alps, Brazil, and the Ural Mountains; it is also formed by the weathering of titanite. Anatase was produced synthetically for use as a white paint pigment in 1906. It was a common white pigment in the early 20th century. Once the first commercially viable method for producing rutile was developed in 1938, production shifted to rutile because white paints with anatase pigments were subject to chalking and yellowing.
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One of three naturally occuring isomorphic forms of [[titanium%20dioxide|titanium dioxide]]: anatase, rutile, and brookite. Anatase forms translucent or transparent crystals (octahedrite) varying in color from black to reddish brown, yellowish brown, dark blue or gray. Deposits have been found in the Alps, Brazil, and the Ural Mountains; it is also formed by the weathering of titanite (sphene) and ilmenite. Mineral anatase is not a major component of artists' materials; however, it has been reported as a minor constituent (<2%)in white paints on ancient artifacts from diverse sites, as a mineral impurity in white clay-based pigments.
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Anatase was produced synthetically in the early 20th century for use as a white paint pigment with remarkable hiding power. The most successful processes were based on extraction from crushed and roasted ilmenite (iron titanate). The major problems in producing a white anatase pigment were to remove iron, a major element in the ilmenite starting material, and to prevent the formation of rutile during the final calcination step; the early experimental pigments typically were not bright white as they contained impurities such as residual iron as well as some rutile.  For at least a decade from about 1908 onward, laboratory research into possible purification and production methods was being conducted in Europe and the United States. Although the first commercial product was a less than pure pigment (the Prima X line, 83% TiO2) produced in Norway (Titan Company A/S) in 1918 to 1919, this was almost immediately replaced by a composite pigment containing calcium phosphate and barium sulfate in 1919; the early composites were described as the color of “old India ivory.”  In the United States (Titanium Pigment Company), pure pigment was only produced in small experimental batches until 1926 (Titanox A, 98% TiO2), and the pigments which were commercially available from 1916 until 1925 were composites with barium sulphate. The Americans eventually adopted the Norwegian technology and the two companies amalgamated in 1920.  In France, a process was discovered in 1920 to allow production of pure anatase titanium dioxide pigment, but only in 1923 did production of a 96-99% titanium dioxide pigment begin; the pure anatase had significantly greater hiding power than the composities.  Pigment purity continued to be a problem, however, and even by 1927 the pure anatase was described as slightly yellow. Because rutile had advantageous weathering properties (less chalking) and higher hiding power (up to 25% improvement over pure anatase), research to improve experimental rutile-based pigments that were patented in 1931 culminated in commercial production in Europe and in the United States in 1937.  
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== Synonyms and Related Terms ==
 
== Synonyms and Related Terms ==
  
octahedrite; titanium dioxide; anatase (Eng., Fr., Port., Nor.); anastase (sp); Anatas (Deut.); anatasio (It.); anatasa (Esp.); anataas (Ned.);
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octahedrite; titanium dioxide; anatase (Eng., Fr., Port., Nor.); anastase (sp); Anatas (Deut.); anatasio (It.); anatasa (Esp.); anataas (Ned.)
  
 
[[[SliderGallery rightalign|Anataseitaly1.jpg~Raman|MFA- Titanium dioxide (anatase).jpg~FTIR|PIG533.jpg~XRD|f533sem.jpg~SEM|f533edsbw.jpg~EDS]]]
 
[[[SliderGallery rightalign|Anataseitaly1.jpg~Raman|MFA- Titanium dioxide (anatase).jpg~FTIR|PIG533.jpg~XRD|f533sem.jpg~SEM|f533edsbw.jpg~EDS]]]
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== Other Properties ==
 
== Other Properties ==
  
Tetragonal crystal system. Particle size 0.2 - 0.5 micrometers.  
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Tetragonal crystal system.
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Optic sign uniaxial, negative.
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Particle size of modern pigment 0.2 - 0.5 micrometers.
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High birefringence under crossed polars.
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Non-fluorescent to weak white fluorescence (pigment).
  
At high temperatures anatase will convert to rutile
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At high temperatures (400-1200C) anatase will convert to rutile.
  
High birefringence under crossed polars.  Weak white fluorescence.
 
  
 
{| class="wikitable"
 
{| class="wikitable"
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|-
 
|-
 
! scope="row"| Melting Point
 
! scope="row"| Melting Point
| 1560
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| transforms to rutile
 
|-
 
|-
 
! scope="row"| Density
 
! scope="row"| Density
| 3.88-3.94
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| 3.7 (coated pigment)- 3.9
 
|-
 
|-
 
! scope="row"| Refractive Index
 
! scope="row"| Refractive Index
| 2.54 - 2.55
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| 2.54 - 2.55 (mineral, pure pigment)
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| 1.87 - 2.3 (composite pigment)
 
|}
 
|}
  
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Nontoxic. No significant hazards.
 
Nontoxic. No significant hazards.
  
Acts as photocatalysts when exposed to UV light
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Chemically inert, insoluble in water, organic solvents, aqueous alkalis; can be dissolved in sulfuric or hydrofluoric acid; slow to dry in oil without additives or surface treatment.
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Strong UV absorber, photochemically active and can cause deterioration of admixed media if exposed to ultraviolet light; early anatase pigments showed considerable tendency to chalk on exposure and could discolor.
  
 
== Additional Information ==
 
== Additional Information ==
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* Website address 1  Comment: Pigments Through the Ages at http://webexhibits.org/pigments : Refractive index: anatase: 2.3 - 2.65
 
* Website address 1  Comment: Pigments Through the Ages at http://webexhibits.org/pigments : Refractive index: anatase: 2.3 - 2.65
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* Buzgar et al., "The Raman Study of the White Pigment used in Cucuteni Pottery," Analele Stiintifice ale Universitatii “Al. I. Cuza” din Iasi Seria Geologie  59(2) 2013) 41–50; also http://geology.uaic.ro/auig/articole/2013%20no2/1_L03-Buzgar.pdf
  
  
  
 
[[Category:Materials database]]
 
[[Category:Materials database]]

Revision as of 17:21, 20 November 2016

Anatase particles

Description

One of three naturally occuring isomorphic forms of Titanium dioxide: anatase, rutile, and brookite. Anatase forms translucent or transparent crystals (octahedrite) varying in color from black to reddish brown, yellowish brown, dark blue or gray. Deposits have been found in the Alps, Brazil, and the Ural Mountains; it is also formed by the weathering of titanite (sphene) and ilmenite. Mineral anatase is not a major component of artists' materials; however, it has been reported as a minor constituent (<2%)in white paints on ancient artifacts from diverse sites, as a mineral impurity in white clay-based pigments.

Anatase was produced synthetically in the early 20th century for use as a white paint pigment with remarkable hiding power. The most successful processes were based on extraction from crushed and roasted ilmenite (iron titanate). The major problems in producing a white anatase pigment were to remove iron, a major element in the ilmenite starting material, and to prevent the formation of rutile during the final calcination step; the early experimental pigments typically were not bright white as they contained impurities such as residual iron as well as some rutile. For at least a decade from about 1908 onward, laboratory research into possible purification and production methods was being conducted in Europe and the United States. Although the first commercial product was a less than pure pigment (the Prima X line, 83% TiO2) produced in Norway (Titan Company A/S) in 1918 to 1919, this was almost immediately replaced by a composite pigment containing calcium phosphate and barium sulfate in 1919; the early composites were described as the color of “old India ivory.” In the United States (Titanium Pigment Company), pure pigment was only produced in small experimental batches until 1926 (Titanox A, 98% TiO2), and the pigments which were commercially available from 1916 until 1925 were composites with barium sulphate. The Americans eventually adopted the Norwegian technology and the two companies amalgamated in 1920. In France, a process was discovered in 1920 to allow production of pure anatase titanium dioxide pigment, but only in 1923 did production of a 96-99% titanium dioxide pigment begin; the pure anatase had significantly greater hiding power than the composities. Pigment purity continued to be a problem, however, and even by 1927 the pure anatase was described as slightly yellow. Because rutile had advantageous weathering properties (less chalking) and higher hiding power (up to 25% improvement over pure anatase), research to improve experimental rutile-based pigments that were patented in 1931 culminated in commercial production in Europe and in the United States in 1937.


Synonyms and Related Terms

octahedrite; titanium dioxide; anatase (Eng., Fr., Port., Nor.); anastase (sp); Anatas (Deut.); anatasio (It.); anatasa (Esp.); anataas (Ned.)

Raman

Anataseitaly1.jpg

FTIR

MFA- Titanium dioxide (anatase).jpg

XRD

PIG533.jpg

SEM

F533sem.jpg

EDS

F533edsbw.jpg


Other Properties

Tetragonal crystal system.

Optic sign uniaxial, negative.

Particle size of modern pigment 0.2 - 0.5 micrometers.

High birefringence under crossed polars.

Non-fluorescent to weak white fluorescence (pigment).

At high temperatures (400-1200C) anatase will convert to rutile.


Composition TiO2
Mohs Hardness 5.0 - 6.0
Melting Point transforms to rutile
Density 3.7 (coated pigment)- 3.9
Refractive Index 2.54 - 2.55 (mineral, pure pigment) 1.87 - 2.3 (composite pigment)

Hazards and Safety

Nontoxic. No significant hazards.

Chemically inert, insoluble in water, organic solvents, aqueous alkalis; can be dissolved in sulfuric or hydrofluoric acid; slow to dry in oil without additives or surface treatment.

Strong UV absorber, photochemically active and can cause deterioration of admixed media if exposed to ultraviolet light; early anatase pigments showed considerable tendency to chalk on exposure and could discolor.

Additional Information

° M.Laver, "Titanium Dioxide Whites", Artists Pigments, Volume 3, E. West FitzHugh (ed.), Oxford University Press: Oxford, 1997.

° Walter C. McCrone, "Polarized Light Microscopy in Conservation: A Personal Perspective" JAIC 33(2):101-14, 1994. (contains a table of dates on the history of titanium white as a pigment)

Comparisons

Characteristics of Common White Pigments


Sources Checked for Data in Record

  • Nicholas Eastaugh, Valentine Walsh, Tracey Chaplin, Ruth Siddall, Pigment Compendium, Elsevier Butterworth-Heinemann, Oxford, 2004
  • G.S.Brady, Materials Handbook, McGraw-Hill Book Co., New York, 1971 Comment: p. 815
  • R. J. Gettens, G.L. Stout, Painting Materials, A Short Encyclopaedia, Dover Publications, New York, 1966 Comment: Ref. Index = 2.5; density = 3.9
  • Dictionary of Building Preservation, Ward Bucher, ed., John Wiley & Sons, Inc., New York City, 1996
  • Thomas B. Brill, Light Its Interaction with Art and Antiquities, Plenum Press, New York City, 1980 Comment: Ref. index = 2.56, 2.49
  • Artists' Pigments: A Handbook of their History and Characteristics, Elisabeth West FitzHugh, Oxford University Press, Oxford, Vol. 3, 1997 Comment: M.Laver, "Titanium Dioxide Whites"
  • Richard S. Lewis, Hawley's Condensed Chemical Dictionary, Van Nostrand Reinhold, New York, 10th ed., 1993

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