Abstract

AbstractThe new mineral torrecillasite (IMA2013-112), Na(As,Sb)43+O6Cl, was found at the Torrecillas mine, Iquique Province, Chile, where it occurs as a secondary alteration phase in association with anhydrite, cinnabar, gypsum, halite, lavendulan, magnesiokoritnigite, marcasite, quartz, pyrite, scorodite, wendwilsonite and other potentially new As-bearing minerals. Torrecillasite occurs as thin colourless prisms up to 0.4 mm long in jack-straw aggregates, as very thin fibres in puff balls and as massive intergrowths of needles. Prisms are elongated on [100] with diamond-shaped cross-section and irregular terminations. Crystals are transparent, with adamantine lustre and white streak. The Mohs hardness is 2½, tenacity is brittle and fracture is irregular. Cleavage on (001) is likely. The calculated density is 4.056 g cm−3. Optically, torrecillasite is biaxial (−) with α = 1.800(5), β = 1.96(1), γ = 2.03(calc.) (measured in white light). The measured 2V is 62.1(5)°, no dispersion or pleochroism were observed, the optical orientation isX=c,Y=b,Z=a. The mineral is very slowly soluble in H2O, slowly soluble in dilute HCl and rapidly soluble in concentrated HCl. The empirical formula, determined from electron-microprobe analyses, is (Na1.03Mg0.02)∑1.05(As3.39Sb0.62)∑4.01O6.07Cl0.93. Torrecillasite is orthorhombic,Pmcn, a= 5.2580(9),b= 8.0620(13),c= 18.654(3) Å,V= 790.7(2) Å3andZ= 4. The eight strongest X-ray powder diffraction lines are [dobsÅ(I)(hkl)]: 4.298(33)(111), 4.031(78)(014,020), 3.035(100)(024,122), 2.853(39)(115,123), 2.642(84)(124,200), 2.426(34)(125), 1.8963(32)(225) and 1.8026(29)(0·1·10,233). The structure, refined toR1= 4.06% for 814Fo>4σFreflections, contains a neutral, wavy As2O3layer parallel to (001) consisting of As3+O3pyramids that share O atoms to form six-membered rings. Successive layers are flipped relative to one another and successive interlayer regions contain alternately either Na or Cl atoms. Torrecillasite is isostructural with synthetic orthorhombic NaAs4O6Br.

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