hackmanite

 


Chemical formula: See SODALITE

Family: Silicates

Status: NON APPR

Crystal system : Isometric

Display mineral: OUI

 

Luminescence:

Longwave UV (365nm) colors:

              


Orange , Orangy yellow , Orange Red ,

Intensity LW:Strong

Frequency LW:Always

Midwave UV (320nm) colors:

         


Orange , Orangy yellow ,

Shortwave UV (254nm) colors:

                             


Orangy yellow , Bluish White , Yellowish White , Orangy yellow , Orange , Yellowish ,

Intensity SW:Medium

Frequency SW:Very often


Daylight picture


Longwave (365nm) picture


hackmanite under UVLW,
Photo and Copyright: James Hamblen
Site of the author
Used with permission of the author

 

Pictures Galery:

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Phosphorescence (in the common sense of the term) observable with the naked eye:

Type d'UV

Couleur

Intensité

Fréquence d'observation

UV longs (365nm):

Bluish White Medium

UV moyens (320 nm):

Bluish White Very Strong

UV courts (254 nm):

Bluish White Very Strong
 

Tenebrescence: OUI


hackmanite, up after and down before exposition to SW (tenebrescence);
Koksha Valley, Badakhshan Province, Afghanistan; ;
Col. G.Barmarin; Photo: G. Barmarin

Thermoluminescence: OUI

Comments:

A sulfide rich sodalite and should not be regarded as a separate species.

Activator(s) and spectrum:

Activator(s): S2-,

Peaks in the spectrum (nm):

S2-  : (566),(610), 625, 647, 664, (695), (723), (751nm)


Col. G. Barmarin; Spectre: G. Barmarin

Spectrum Galery:

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Comments on spectrum and activators:

O. Ivan Lee investigated what he calls the reversible photosensitivity of hackmanite from Bancroft (Ontario) and his response to different UV sources as early as 1936. He presented the phenomenon for the 50th Anniversary Celebration Banquet of the New York Mineralogical Club, in November 18, 1936 at the American Museum of Natural History. It seems that it was the first observation and the first public announcement and publication (American Mineralogist vol 21) about photochromism (tenebrescence) in mineralogy.

Chemical analyses revealed that the mineral contains a certain amount of sulfur as a substitute for chlorine in the crystal structure. The FTIR spectra of hackmanite showed that the samples contain water. The stretching vibration peak of water of crystallization (H2O) occurs at 3438 cm-1 and the bending peak is at 1623 cm-1. Its tenebrescence is caused by hole color centers which are contributed to the presence of sulfur (S2-)) and to some negatively charged chlorine atoms being missing in the crystal structure of hackmanite. (source: http://www.geology.com.cn/Geology-Journals/article-35765.html)

Crystals of Hackmanite of Koksha Valley in Afghanistan are usually found in a matrix constituted by non-fluorescing Winchite and/or marble.

Synthetic sodalites containing sulfur and showing considerable photochromic activity have been investigated by ESR. The center responsible for the color has been shown to be an electron trapped at a chlorine vacancy. The origin of the electron which is reversibly transferred during the processes of coloration and bleaching is believed to be the ion S2-). (see William G. Hodgson, Jacob S. Brinen, and Emil F. Williams, Electron Spin Resonance Investigation of Photochromic Sodalites, The Journal of Chemical Physics 47, 3719 , 1967)

Best localities for fluorescence (*):

(*)The data are not exhaustive and are limited to a few remarkable localities for fluorescence

Bibliographic reference for luminescence:

Reference for luminescence on the Internet:

Mineralogical reference on the Internet:

  http://www.mindat.org/show.php?name=Hackmanite

  http://webmineral.com/data/Hackmanite.shtml

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