Hostname: page-component-586b7cd67f-2brh9 Total loading time: 0 Render date: 2024-11-26T05:10:17.882Z Has data issue: false hasContentIssue false

Smoky, blue, greenish yellow, and other irradiation-related colors in quartz

Published online by Cambridge University Press:  05 July 2018

K. Nassau
Affiliation:
Bell Laboratories, Murray Hill, New Jersey 07974
B. E. Prescott
Affiliation:
Bell Laboratories, Murray Hill, New Jersey 07974

Summary

Almost 400 specimens of natural and synthetic quartz were γ-irradiated and then heated. Polarized absorption spectroscopy, EPR, and spectrochemical analysis were used to investigate the various colors produced.

A blue color originated from absorption by the A1 and A2 bands at 1·85 and 2·55 eV. The substitutional A1 EPR hole-type center usually considered to be the cause of the color in smoky quartz does not correlate with A1 and A2, but with A3, a previously unreported absorption band at 2·90 eV. The A1 and A2 absorptions bleach at temperatures as low as 280 °C and as high as 360 °C the range for A3 being 140 to 380 °C. The B band at 3·95 eV was previously reported only in irradiated fused silica.

Greenish-yellow colors (appearing yellow when of low intensity) were observed after irradiation (followed by heating in some instances) in many specimens of natural and synthetic quartz; the color originates from the tail of a strong absorption band in the ultraviolet. The bleaching temperature range is the same as that for A2.

The wide variation in color of natural and irradiated smoky quartz can be explained by combinations of the smoky (A3), blue (A1 and A2), and greenish yellow absorption features.

Type
Research Article
Copyright
Copyright © The Mineralogical Society of Great Britain and Ireland 1977

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Ballman, (A. A.), Laudise, (R. A.), and Rudd, (D. W.), 1966. Appl. Phys. Lett 8, 53–4.CrossRefGoogle Scholar
Barry, (T. I.), McNamara, (P.), and Moore, (W. J.), 1965. J. Chem. Phys. 42, 2599-2606.CrossRefGoogle Scholar
Chentsova, (L. G.), Tsinober, (L. I.), and Samoilovich, (M. I.), 1966. Soviet Phys.—Crystallogr. 11, 219-23 (transl. o. Kristallografiya, 11, 236–44, 1966).Google Scholar
Cohen, (A. J.), 1956. Am. Mineral. 41, 874–91.Google Scholar
Cohen, (A. J.), 1975. Ibid. 60, 338–9.CrossRefGoogle Scholar
Frondel, (C), 1962. The System of Mineralogy (John Wiley and Sons, Inc., New York), 7th edn., 3, 137–42 and 171-86.Google Scholar
Griffiths, (J. H. E.), Owen, (J.), and Ward, (I. M.), 1954. Nature, 173, 439–40.CrossRefGoogle Scholar
Halperin, (A.) and Ralph, (J. E.), 1963. J. Chem. Phys. 39, 63–73.CrossRefGoogle Scholar
Heising, (R. A.), 1946. Quartz Crystals for Electrical Circuits (D. Van Nostrand Co., Inc., New York), 104 and 106.Google Scholar
Kelly, (K. L.) and Judd, (D. B.), 1965. The ISCC-NBS Method of Designating Color and a Dictionary of Color Names (including the supplement: ISCC-NBS Color Name Charts Illustrated with Centroid Colors). Circular 533, 2nd edit. Natl. Bur. Stand. U.S. Govt. Printing Office, Washington, D.C.Google Scholar
Laudise, (R. A.), 1962. Hydrothermal Synthesis of Single Crystals. In Cotton, F. A., Ed.. Progress in Inorganic Chemistry, 3, 1–47 (Interscience Publishers, New York).Google Scholar
Lehmann, (G.), 1971. Phys. stat. solids, B48, K65-7.Google Scholar
Lehmann, (G.), 1975. Am. Mineral. 60, 335–7.Google Scholar
Lehmann, (G.) and Bambauer, (H. U.), 1973. Angew. Chem. Int. Ed. 12, 283–91.CrossRefGoogle Scholar
Lell, (E.), 1962. Radiation Effects in Doped Fused Silica. Phys. and Chem. Glasses, 3, 84–94.Google Scholar
Lell, (E.), Kreidl, (N. J.), and Heusler, (J. R.), 1966. Radiation Effects in Quartz, Silica and Glasses. In Burke, J. E., Ed. Prog. Ceram. Sci. 4, 1–93 (Pergamon Press, New York).Google Scholar
Mackey, (J. H., Jr.), 1963. J. Chem. Phys. 39, 74–83.CrossRefGoogle Scholar
Mitchell, (E. W. J.) and Paige, (E. G. S.), 1956. Phil. Mag. 1, 1085-1115.CrossRefGoogle Scholar
Mitchell, (E. W. J.) and Paige, (E. G. S.), 1964. Proc. Phys. Soc. STB, 262-4.Google Scholar
Nassau, (K.), 1974, Lapidary Journal, 28, 1064-74, 1084.Google Scholar
Nassau, (K.) and Prescott, (B. E.), 1975. Phys. stat. solids, A29, 659-63.CrossRefGoogle Scholar
Nelson, (C. M.) and Weeks, (R. A.), 1961. J. Appl. Phys. 32, 883–6.CrossRefGoogle Scholar
O'Brien, (M. C. M.), 1955. Proc. R. Soc. A231, 404-14.Google Scholar
Rose, (H.) and Lietz, (J.). 1954. Naturwiss. 41, 448.CrossRefGoogle Scholar
Samoilovich, (M. I.), Tsinober, (L. I.), Khadzhi, (V. E.), and Lelekova, (M. V.), 1968. Soviet Phys—Crystallogr. 13, 734–6 (transl. o. Kristallografiya, 13, 850–3, 1968).Google Scholar
Sawyer, (B.), U.S. Patent 3,837,826, 24 September 1974.Google Scholar
Sawyer, (B.), U.S. Patent 3,936,188, 3 February 1976.Google Scholar
Schnadt, (R.) and Rauber, (A.), 1971. Solid State Commun. 9, 159–61.CrossRefGoogle Scholar
Schnadt, (R.) and Schneider, (J.), 1970. Phys. kondens. Mater. 11, 19–42.Google Scholar
Shternberg, (A. A.), Gordienko, (L. A.), and Tsinober, (L. I.), 1970. Soviet Phys.—Crystallogr. 14, 728–32 (transl. o. Kristallografiya, 14, 845–51, 1969).Google Scholar
Tsinober, (L. I.), 1962. Soviet Phys.—Crystallogr. 7, 113–14 (transl. of Kristallografiya, 7, 138–9, 1962).Google Scholar
Tsinober, (L. I.), Samoilovich, (M. I.), Gordienko, (L. A.), and Chentsova, (L. G.), 1967. Soviet Phys.—Crystallogr. 12, 53–6 (transl. o. Kristallografiya, 12, 65–9, 1967).Google Scholar