Laurentthomasite, Mg2K(Be2Al)Si12O30: a new milarite-group-type member from the Ihorombe region, Fianarantsoa Province, Madagascar
Abstract
Laurentthomasite, ideally Mg2K(Be2Al)Si12O30, is a new milarite-group member found within quartz-syenite pegmatites from the Ihorombe region, Fianarantsoa Province, Madagascar. It occurs as euhedral {0001} hexagonal crystals, maximum 15 mm large and 5 mm thick. The crystals show a very strong dichroism with cobalt blue and green-yellow colours when observed along [0001] and [1000], respectively. The mineral is transparent, uniaxial (+) and its lustre is vitreous. The hardness is about 6 (Mohs scale), showing a poor {0001} cleavage, irregular to conchoidal fracture, and a measured density of 2.67(8) g cm-3. Laurentthomasite is hexagonal, space group P6/mcc (no. 192), with a=9.95343(6) Å, c=14.15583(8) Å, V=1214.54(1) Å3 and Z=2. The strongest nine lines in the X-ray powder diffraction pattern [d in Å - (I) - hkl] are 3.171 - (10) - 211, 4.064 - (8) - 112, 2.732 - (8) - 204, 4.965 - (6) - 110, 2.732 - (4) - 204, 3.533 - (3) - 004, 7.055 - (2) - 002, 4.302 - (2) - 200 and 3.675 - (2) - 202. Chemical analyses by electron microprobe and several spectroscopies (inductively coupled plasma, ICP; optical emission, OES; mass, MS; and Mössbauer) give the following empirical formula based on 30 anions per formula unit: (Mg0.86 Sc0.54 Fe0.352+ Mn0.26)∑=2.01(K0.89 Na0.05 Y0.02 Ca0.01 Ba0.01)∑=0.98[(Be2.35 Al0.50 Mg0.11 Fe0.033+)∑=2.99(Si11.90 Al0.10)O30]; the simplified formula is (Mg, Sc)2(K, Na)[(Be, Al, Mg)3(Si, Al)12O30]. The crystal structure was refined to an R index of 1.89 % based on 430 reflections with Io > 2σ(I) collected on a four-circle diffractometer with CuKα radiation. By comparison with the general formula of the milarite group, A2B2C[T(2)3T(1)12O30](H2O) x (0<x<n, with n<2 pfu, per formula unit), the laurentthomasite structure consists of a beryllo-alumino-silicate framework in which the T(1) site is occupied by Si and minor Al and forms [Si12O30] cages linked by the T(2) site mainly occupied by (Be + Al). The A and C sites occur in the interstices of the framework while the B site is vacant. The origin of the strong dichroism is related to a charge transfer process between Fe2+ and Fe3+ in octahedral A sites and tetrahedral T(2) sites, respectively.
- Publication:
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European Journal of Mineralogy
- Pub Date:
- June 2020
- DOI:
- 10.5194/ejm-32-355-2020
- Bibcode:
- 2020EJMin..32..355F