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Siderite
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Siderite is a composed of iron(II) carbonate (FeCO3). Its name comes from the word (), meaning "iron". A valuable , it consists of 48% and lacks and . , , and commonly substitute for the iron, resulting in the siderite-, siderite-, and siderite- series.

Siderite has Mohs hardness of 3.75 to 4.25, a of 3.96, a white streak and a or pearly luster. Siderite is antiferromagnetic below its Néel temperature of that can assist in its identification.

It crystallizes in the trigonal crystal system; crystals are in shape, typically with curved and striated faces. It also occurs in masses. Color ranges from yellow to dark brown or black, the latter being due to the presence of manganese.

Siderite is commonly found in hydrothermal veins, and is associated with , , , and others. It is also a common mineral in and , where it sometimes forms , which can encase three-dimensionally preserved . In , siderite commonly forms at shallow burial depths and its elemental composition is often related to the depositional environment of the enclosing sediments. In addition, a number of recent studies have used the of sphaerosiderite (a type associated with ) as a proxy for the composition of shortly after deposition. Evidence of the presence of siderite on Mars is being interpreted as a possible indicator of the presence of abundant water early in the climate history of that planet.Janice Bishop and M. Lane, Catching a glimpse of ancient Mars, , Vol. 388, April 18, 2025, p. 251. doi: 10.1126/science.adw4889 Benjamin Tutolo et al., Carbonates identified by the Curiosity rover indicate a carbon cycle operated on ancient Mars, Science, Vol. 388, April 18, 2025, p. 292. doi: 10.1126/science.ado9966 Grossman, Lisa, A NASA rover finally found Mars’ missing carbon: The finding could help explain why Mars lost its habitable climate, , April 17, 2025


Carbonate iron ore
Although iron ores, such as siderite, have been economically important for steel production, they are far from ideal as an ore.

Their hydrothermal mineralisation tends to form them as small , often following steeply dipping . This keeps them from being amenable to , and increases the cost of working them by mining with horizontal . As the individual ore bodies are small, it may also be necessary to duplicate or relocate the pit head machinery, , and pumping engine, between these bodies as each is worked out. This makes mining the ore an expensive proposition compared to typical or opencasts.

The recovered ore also has drawbacks. The carbonate ore is more difficult to than a haematite or other oxide ore. Driving off the carbonate as carbon dioxide requires more energy and so the ore 'kills' the if added directly. Instead the ore must be given a preliminary roasting step. Developments of specific techniques to deal with these ores began in the early nineteenth century, largely with the work of Sir Thomas Lethbridge in . His 'Iron Mill' of 1838 used a three-chambered concentric roasting furnace, before passing the ore to a separate reducing furnace for smelting. Details of this mill were the invention of Charles Sanderson, a steel maker of Sheffield, who held the patent for it.

These differences between spathic ore and haematite have led to the failure of a number of mining concerns, notably the Brendon Hills Iron Ore Company.

Spathic iron ores are rich in manganese and have negligible phosphorus. This led to their one major benefit, connected with the . Although the first demonstrations by Bessemer in 1856 were successful, initial attempts by others to replicate his method infamously failed to produce good steel. Work by the metallurgist Robert Forester Mushet showed that the reason for the discrepancy was the nature of the Swedish ores that Bessemer had innocently used; they were very low in phosphorus. Using a typical European high-phosphorus ore in Bessemer's converter gave a poor quality steel. To produce high quality steel from a high-phosphorus ore, Mushet realised that he could operate the Bessemer converter for longer, burning off all the steel's impurities including the unwanted phosphorus, but also the carbon (which is an essential ingredient in steel), and then re-adding carbon, along with manganese, in the form of a previously obscure ferromanganese ore with no phosphorus, . This created a sudden demand for spiegeleisen. Although it was not available in sufficient quantity as a mineral, steelworks such as that at Ebbw Vale in South Wales soon learned to make it from the spathic siderite ores. For a few decades, spathic ores were therefore in demand and this encouraged their mining. In time though, the original 'acidic' liner of the Bessemer converter, made from siliceous sandstone or , was replaced by a 'basic' liner in the newer Gilchrist Thomas process. This removed the phosphorus impurities as produced by chemical reaction with the liner, and no longer required spiegeleisen. From the 1880s, demand for the ores fell once again and many of their mines, including those of the , closed soon after.


Gallery
Siderite late 1800s Redruth.jpg|Siderite from , Cornwall, England Galena-Quartz-Siderite-oldeuro-56c.jpg|Siderite crystals with galena and quartz. Size: Chalcopyrite-Siderite-gha7a.jpg|Disc-shaped, brown siderite crystals perched upon chalcopyrites SideriteTaillée.jpg|Cut siderite from Minas Gerais, Brazil. Size: Siderite-64328.jpg|Colorado siderite, with sharp blades of olive-brown and minor accenting quartz Siderite Concretion Carboniferous.JPG|Fossiliferous siderite concretion from the Lower Carboniferous


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