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Anglesite

Anglesite is a secondary lead mineral with the PbSO₄, typically forming transparent to translucent, colorless to white crystals with an luster in the , and it arises as an oxidation product of primary ores like in weathered zones of lead deposits. Named in 1832 by François Sulpice Beudant after its type locality at Parys Mountain in , —where it was first identified in 1783 by —anglesite exhibits a Mohs hardness of 2.5 to 3, a high specific of 6.3 to 6.4 due to its lead content, and may show tints of gray, yellow, green, blue, or other colors, while remaining colorless in transmitted light. It often occurs as prismatic or tabular crystals, sometimes in radiating clusters or as coatings, and is commonly associated with other secondary lead minerals such as and, less frequently, . As one of the most common secondary lead minerals, anglesite serves primarily as an of lead, which is extracted for use in batteries, shielding, and other industrial applications, though its soft nature and perfect cleavage limit its use as a to rare, faceted specimens prized for their high and brilliance comparable to . Notable occurrences include in , Touissit in , Broken Hill in , and Los Lamentos in , where gem-quality crystals have been found, making it a sought-after item for collectors. Due to its lead content, handling anglesite requires caution to avoid of , as it poses health risks.

Etymology and history

Discovery

Anglesite was first described in 1783 by Reverend from specimens collected at , , . Withering characterized it as a novel lead mineralized by vitriolic and iron, present in vast quantities within the copper mines. Initial observations noted its occurrence as a white, earthy alteration product of in lead mines, forming through oxidation processes in the upper zones of ore deposits. In the early , chemical analyses by mineralogists such as François Sulpice Beudant and others confirmed anglesite as a distinct , separate from lead carbonates like and other compounds, through solubility tests and compositional breakdowns establishing its lead nature.

Naming

The anglesite was officially named in 1832 by the French mineralogist François Sulpice Beudant, who proposed the term to honor its type locality at the Parys Mine on the Isle of in . This naming occurred nearly five decades after its initial identification in 1783 by , reflecting the gradual formalization of mineral descriptions during that era. Anglesite's recognition as a member of the group stems from its isomorphous relationships with (barium sulfate) and celestine ( sulfate), sharing the same orthorhombic and anion composition. These structural similarities, first systematically explored in the early , allowed for substitutions among lead, , and in the sulfate series, influencing its classification within the group. In the early 19th century, mineralogical naming conventions emphasized locality-based terms, especially for species identified in prominent mining districts, as seen in Beudant's comprehensive treatises like his 1832 revision of Traité élémentaire de minéralogie, where he coined numerous names to standardize the field amid rapid discoveries. This approach contrasted with earlier 18th-century practices that often relied on descriptive or chemical terms, promoting a more systematic and geographic that persists in modern .

Physical properties

Appearance and crystal habit

Anglesite typically forms prismatic orthorhombic crystals characterized by sharp edges and vertical striations along the prism faces, particularly on {210} and {100} planes. These crystals often exhibit a rhomboidal cross-section and may be elongated along the c-axis, with pointed terminations enhancing their distinct . Common habits include thin to thick tabular crystals on {001}, sometimes with rhomboidal outlines formed by {210} and {101} faces, as well as equant or pyramidal forms involving {111} and {211}. It also occurs in massive, granular, compact, nodular, or stalactitic aggregates, reflecting its variable growth conditions in lead-rich deposits. Transparent, gemmy crystals are rare but can reach several centimeters in length, such as prismatic specimens up to 2.4 from select localities. Twinning is uncommon in anglesite, though substrate-induced coalescence can produce rare twins on {110} or {021}.

Hardness, density, and fracture

Anglesite exhibits a Mohs of 2.5–3, rendering it relatively soft and susceptible to scratching by common materials such as a fingernail or . This low value places it among softer minerals, limiting its use in applications requiring durability. The specific gravity of anglesite ranges from 6.37 to 6.39, significantly higher than many common minerals due to its substantial lead content in the PbSO₄. This makes anglesite feel unusually heavy for its size, a characteristic often noted in hand samples from lead deposits. Anglesite displays a and possesses brittle , meaning it breaks irregularly under stress without significant plastic deformation. These properties contribute to its tendency to shatter rather than bend, consistent with its orthorhombic .

Optical properties

Color, luster, and streak

Anglesite typically exhibits a colorless to white body color, though it is commonly tinted gray, and less frequently , , , , or rarely , due to trace impurities from associated in its formation environment. These color variations arise primarily from inclusions or oxidation products in lead-bearing deposits, with the mineral appearing colorless under transmitted . The luster of anglesite is predominantly adamantine to resinous or vitreous, imparting a brilliant, gem-like sheen to well-formed crystals that enhances its visual appeal. In earthy or massive varieties, however, the luster can transition to dull, resulting from altered surface textures or finer-grained aggregates. Regardless of its body color or luster variations, anglesite produces a consistent streak when powdered, a that aids in its identification .

Transparency and refractive indices

Anglesite exhibits varying degrees of transparency depending on its form, ranging from transparent in well-formed to translucent or opaque in massive varieties. Clear, colorless are prized for their optical clarity, allowing light to pass through with minimal scattering, while earthy or massive aggregates appear opaque due to internal impurities and grain boundaries. The mineral's optical behavior is characterized by its refractive indices, which are α = 1.877, β = 1.883, and γ = 1.894, indicating a . This results in a weak of δ = 0.017 (γ - α), producing subtle double that is not strongly pronounced in most specimens. Anglesite displays strong with a value of 0.044 (r < v), comparable to that of , which separates white light into spectral colors. Combined with its high refractive indices, this property imparts a fiery brilliance to faceted gemstones, enhanced further by the mineral's luster.

Chemical properties

Composition and formula

Anglesite is a lead with the PbSO₄. The ideal elemental composition by weight consists of 68.32% lead (Pb), 10.57% (S), and 21.11% (O). In terms of oxide equivalents, it corresponds to 73.60% PbO and 26.40% SO₃. Although rare due to differences in ionic radii, minor isomorphous substitutions can occur in the baryte group, with strontium (Sr) or barium (Ba) replacing lead (Pb) at low levels, as seen in varieties such as barytoanglesite.

Stability and solubility

Anglesite exhibits very low solubility in water, with a reported value of approximately 0.004 g/100 mL at 25°C, rendering it effectively insoluble under typical environmental conditions. However, it dissolves in concentrated sulfuric acid, particularly when hot, forming lead hydrogen sulfate, and is also soluble in ammonium acetate solutions at concentrations of 6 mol/L or higher. This selective solubility influences its behavior in geochemical processes, where it remains stable in sulfate-dominated, acidic settings but can dissolve under specific chemical treatments. Under surface oxidation conditions, anglesite is thermodynamically stable, commonly forming as a secondary in the weathered zones of lead deposits. In carbonate-rich environments, however, it undergoes alteration to (PbCO₃), driven by the reaction with dissolved carbonate ions, which favors the more stable carbonate phase in mildly acidic to basic conditions. This transformation is prevalent in oxidized lead ores exposed to or atmospheric CO₂, highlighting anglesite's limited persistence in settings. In its pure, crystalline form, anglesite presents low due to its insolubility, which limits and direct leaching of lead ions in neutral aqueous systems. Nonetheless, the high lead content (approximately 68% by weight) introduces significant environmental hazards in and processing contexts, where mechanical disturbance can generate respirable dust or facilitate lead mobilization into soils and water, contributing to broader lead contamination risks. Such exposures are associated with neurotoxic effects and disruption, necessitating careful handling protocols in extraction operations.

Crystal structure

Symmetry and unit cell

Anglesite crystallizes in the with Pnma (equivalent to Pbnm in some settings). This results in crystals exhibiting three perpendicular axes of unequal length, consistent with the observed prismatic and tabular habits. The contains four formula units (Z = 4) and has dimensions a = 6.9549(9) , b = 8.472(1) , c = 5.3973(8) , yielding a volume of approximately 318.03 ³. These parameters reflect the refined structure from single-crystal data on natural anglesite specimens. In the , isolated SO₄ tetrahedra are linked through Pb²⁺ cations, each of which is coordinated to 12 oxygen atoms from six surrounding groups, forming a distorted polyhedron due to the stereochemically active on lead. The tetrahedra themselves are nearly rigid, with S–O bond lengths averaging about 1.47 and O–S–O angles close to the ideal tetrahedral value of 109.5°, exhibiting minimal distortion influenced by the cation . This arrangement creates a where the tetrahedra share no edges or corners directly, but are bridged solely by the lead coordination.

Polymorphism

Anglesite represents the orthorhombic polymorph of lead(II) sulfate (PbSO₄), characterized by the space group Pnma. This structure aligns it within the barite group of minerals. While anglesite lacks common polymorphs under ambient conditions, experimental studies have identified high-pressure phases. A reversible phase transition occurs above approximately 23 GPa, transforming the barite-type structure (Pnma) to a denser post-barite-type polymorph with space group P2₁2₁2₁. This high-pressure form has been observed through in situ X-ray diffraction and Raman spectroscopy, reverting to the orthorhombic phase upon decompression, though the transition can be kinetically hindered in certain media. Anglesite is isostructural with barite (BaSO₄) and celestine (SrSO₄), sharing the orthorhombic sulfate framework that facilitates solid solutions, particularly in the BaSO₄-PbSO₄ series where complete miscibility has been demonstrated experimentally through of zoning-free crystals. , with the formula Pb₂(SO₄)O, is a monoclinic lead oxysulfate related to anglesite but distinct in composition and structure, often occurring as an associated secondary mineral in lead deposits.

Occurrence and formation

Geological formation processes

Anglesite primarily forms as a secondary through the oxidation of primary minerals, such as (), within the zone of lead-bearing deposits. This process occurs near the Earth's surface where hypogene sulfides are exposed to , leading to the chemical transformation of into lead () as the end product. The reaction is driven by the interaction of with atmospheric oxygen, producing ions that combine with dissolved lead to precipitate anglesite. The formation requires the circulation of oxygenated meteoric waters through fractured ore bodies, which facilitate the and transport of lead and species under relatively acidic conditions ( typically 0.4–5.0). These waters, often derived from rainfall or , introduce oxygen and maintain moisture essential for ongoing oxidation, while ions—sourced from the breakdown of or associated sulfides—enable precipitation. This alteration is favored in arid to semi-arid or temperate climates, where stability is preserved before potential conversion to more soluble carbonates in highly humid environments. A characteristic feature of anglesite formation is its pseudomorphic replacement of crystals, where anglesite inherits and preserves the original cubic of the host , often forming rims or infills along planes and boundaries. This replacement highlights the low-temperature, near-surface nature of the process, typically below 100 °C, and results in visually distinctive specimens that retain the structural outline of the precursor .

Associated minerals

Anglesite commonly occurs in association with , the primary from which it often forms through oxidation, remaining as unaltered remnants in oxidized zones. , a , frequently accompanies anglesite as a product of further alteration in carbonate-rich environments. Other secondary lead minerals such as and mimetite are typical associates, forming in lead-bearing oxidation zones where or ions are present. Hemimorphite, a zinc , is also commonly found alongside anglesite in polymetallic deposits involving lead and sulfides. In the oxidation zones of copper-lead deposits, anglesite may coexist with copper minerals including and , particularly where mixed ores have weathered. Associations with silver-bearing species, such as native silver or argentite, are rare, though trace silver can occasionally substitute in anglesite crystals. The paragenetic sequence typically involves early oxidation of to anglesite, followed by later transformation to under increasing carbonation conditions.

Distribution and localities

Type locality

The type locality of anglesite is (Mynydd Parys), near on the , , , a prominent volcanogenic massive deposit rich in , lead, and ores. Mining at this site dates back to the around 4,000 years ago, with indications of activity, though it flourished as one of the world's largest copper producers during the . The lead-bearing zones, including primary (PbS), underwent oxidation to form secondary minerals like anglesite in the gossan cap overlying the lodes. In the late , during operations targeting the oxidized gossan, early specimens of anglesite were identified from lead workings, appearing as white coatings on crystals in the zone. These discoveries, documented around 1783 and later formalized as a new in 1832, highlighted the site's role in early , with anglesite forming through the acidic alteration of under surface conditions. Parys Mountain reached peak production in the late 1700s, yielding over 3,300 tons of annually, while the lead deposits provided the initial anglesite material circa 1790–1800, though specimens are now rare due to extensive historical extraction. Today, the site is preserved as an industrial heritage area, managed for its geological and historical value, with no active mining.

Major global deposits

Anglesite occurs in several significant global deposits, primarily as a secondary mineral in the oxidized zones of lead-bearing ore bodies. One of the most renowned localities is the Touissit-Bou Beker district in , where gemmy, transparent crystals up to several centimeters in size have been extracted, prized for their clarity and luster. Similarly, the Tsumeb Mine in has yielded exceptional specimens, including large, well-formed prismatic crystals often associated with other secondary lead minerals, contributing to its status as a world-class site for collector material. In the United States, notable occurrences include the Grand Reef Mine in , which has produced attractive, tabular crystals in vugs within a complex polymetallic deposit. The Bunker Hill Mine in , is another key site, where blocky to tabular anglesite crystals up to 5 cm have been found in the oxidized portions of lead-zinc veins. Other important localities encompass in , Australia, known for massive and crystalline anglesite in silver-lead-zinc deposits; the Monteponi Mine on , Italy, yielding prismatic crystals; Los Lamentos in Chihuahua, Mexico, noted for gem-quality crystals; and regions in , Russia, such as , where it forms in association with primary lead sulfides. Global production of anglesite remains minor, typically extracted as a byproduct during lead operations rather than as a primary target, with most output derived from the of in environments.

Uses and significance

As a lead ore

Anglesite, a lead (PbSO₄), functions as a minor in the extraction of lead, typically forming in the oxidized zones of primary deposits where (PbS) weathers. While galena dominates global lead production, anglesite supplements the supply in secondary enriched deposits, contributing to the overall recovery of lead from complex polymetallic ores. Its high lead content, approximately 68% by weight, makes it viable for industrial processing when concentrated. Beneficiation of anglesite-bearing ores begins with crushing and grinding to liberate the mineral from , followed by physical separation techniques. separation, using jigs or shaking tables, exploits the difference between anglesite (specific gravity ~6.3) and lighter materials, often as a preliminary step to remove coarse fractions. For finer particles and mixtures with , is employed, where collectors such as xanthates or hydroxamic acids selectively float lead minerals into a concentrate grading 50-70% lead, while depressants suppress unwanted sulfides. These methods yield a mixed lead concentrate suitable for , with recovery rates typically exceeding 80% in optimized operations. The processed concentrate undergoes roasting at temperatures around 800-1000°C to decompose anglesite into (PbO) and (SO₃), which can further decompose to (SO₂), via the reaction PbSO₄ → PbO + SO₃, regenerating sulfur for production and avoiding direct issues. The resulting is then charged into a along with and fluxes, where carbon reduction yields molten lead: PbO + C → Pb + . This two-stage thermal process integrates anglesite into conventional lead , minimizing waste. Lead from such anglesite-bearing deposits bolsters global output, which reached about 12.3 million tonnes of refined lead in 2023 (as of 2024 data), primarily fueling lead-acid batteries (over 80% of consumption) and alloys for cables, shielding, and .

Gemological and collectible value

Anglesite is rarely faceted into gemstones due to its relative softness, with a Mohs of 2.5 to 3, and its perfect in three directions, which make it prone to chipping and difficult to cut and effectively. Despite these challenges, high-quality rough from select localities, such as and , yields attractive faceted stones that exhibit exceptional brilliance and a diamond-like owing to the mineral's high of 0.044 and adamantine luster. These gems are typically small, ranging from 1 to 6 carats, and are prized by collectors for their rarity and optical appeal rather than everyday jewelry use. In the gem market, faceted anglesite commands prices of approximately $30 to $80 per , varying by color—colorless stones at the lower end, with deeper or tinted varieties fetching higher values—reflecting its and the skill required to facet it successfully. As a collectible , anglesite is highly regarded for its specimens, particularly the large, transparent, prismatic crystals that can reach up to 10 cm in length, often displaying gemmy clarity and a vitreous to sheen. These specimens, sourced primarily from historic deposits like in and Touissit in , are valued for their aesthetic qualities, including well-formed habits and associations with other lead minerals. Market values for such cabinet-sized pieces typically range from $50 to $500, depending on crystal size, transparency, and overall aesthetics, with exceptional examples exceeding this range.

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