A crystal-chemical investigation of clinozoisite synthesized along the join Ca2Al3Si3O12(OH)-Ca2Al2CrSi3O12(OH)

Cr3+-bearing clinozoisite along the join Ca2Al3Si3O12(OH)-Ca2Al2Cr3+Si3O12(OH) was synthesized using cold-seal pressure vessels at P-H2O = 0.35 to 0.40 GPa and T = 500 degrees C and a piston-cylinder apparatus at P-H2O = 0.8 to 1.5 GPa and T = 500 to 800 degrees C. Gel-starting materials of Ca2Al3-qCrq3+Si3O12.5 composition with q = 1.00, 0.75, 0.50, and 0.25 were employed to maximize the yields of clinozoisite. Mass fractions of clinozoisite in the experimental products with q = 0.50, 0.75, and I were about 70 to 90% along with lesser amounts of eskolaite, garnet, and quartz. Clinozoisite crystallized from the gel with q = 0.25 was associated only with zoisite. The crystal structures of clinozoisite in four runs, containing 0.28, 0.49, 0.50, and 0.62 Cr apfu were refined using X-ray powder diffraction data and the Rietveld method. The amount of Cr3+ at the octahedral M3 and M1 sites ranged from 0.37(1)-0.16(1) to 0.25(1)-0.12(1) apfu, respectively. Corresponding K-D = (Cr3+/Al)(M1)/(Cr3+/Al)(M3) values range between 0.57 and 0.73. The M2 site contained only Al. The K-D values, and published results for intracrystalline partitioning in epidote and piemontite, show that the preference of Cr3+ for M1 is stronger than that of Fe3+ and Mn3+ in spite of the fact that most Cr3+ is partitioned into M3. Unit-cell parameters of clinozoisite increase with increasing Cr3+. Variations in macroscopic Unit-cell parameters can be related to variations in the local M3-Oi and M1-Oi distances.