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Hellandite.

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—Hellandite[43] is a mixed silicate of rare earths with lime, magnesia, alumina, ferric and manganic oxides, with considerable quantities of water. The formula approximates to 3H₂O,2R´´O,3R´´´´₂O₃,4SiO₂, where R´´ = (Ca,Mg,Th2)—Thorium being able to replace two atoms of calcium or magnesium—and R´´´ = (Al,Fe´´´,Mn´´´ and rare earth metals). This may be written as a basic orthosilicate, R´´₂[R´´´´(OH)]₆(SiO₄)₄, a basic salt of the acid H₁₆Si₄O₁₆ (= 4H₄SiO₄). This composition puts it in the class containing topaz and some rarer silicates.

[43] Brögger, Zeitsch. Kryst. Min. 1906, 42, 417.

The mineral is crystalline, the crystals being well developed, but often dull and opaque by alteration (hydration).

Crystal system—Monoclinic, holosymmetric, a: b: c = 2·0646: 1: 2·507. β = 109° 45´. Habit usually prismatic, with {100}, {010}, and several prisms {hko}, terminated by various pyramid forms.

Angles (100) ∧ (001) = 70° 32´; (100) ∧ (110) = 62° 22´; (010) ∧ (110) = 27° 14´; (110) ∧ (11̅0) = 125° 0´.

Twinned on (001), twin plane (001), forming knee-shaped twins. Hardness varies from 512 in the least altered to 1 in the most altered specimens; sp. gr. 3·70 in least altered specimens, decreasing with hydration. Colour of fresh crystals, reddish-brown; on alteration they become brownish-black, yellow, or even white.

The mineral dissolves easily in hydrochloric acid, with evolution of chlorine; it is less soluble in nitric and sulphuric acids. It readily fuses to a yellow mass.

It was first discovered by Brögger at Lindvikskollan, in 1903, and later, in larger quantities, at Kragerö in Norway. It occurs in pegmatite veins in granite.

The Rare Earths: Their Occurrence, Chemistry, and Technology

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