2018
DOI: 10.1016/j.jseaes.2018.04.005
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Genesis of giant Early Proterozoic magnesite and related talc deposits in the Mafeng area, Liaoning Province, NE China

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Cited by 12 publications
(5 citation statements)
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“…It is considered as a member of the calcite group of carbonate minerals that is a principal source of magnesium (Beyecha, 2016); Shand (2006). The mineral has the same crystal structure as calcite, a calcium carbonate with a hardness and texture similar to white magnesite and marble (Chen & Tao, 2004;Misch, 2012;Pluch, 2018;Siegesmund & Török, 2010). In its natural state, magnesite exists as a white, gray, or brown porous crystal (Chauke, 2020;Shand, 2006).…”
Section: Introductionmentioning
confidence: 99%
“…It is considered as a member of the calcite group of carbonate minerals that is a principal source of magnesium (Beyecha, 2016); Shand (2006). The mineral has the same crystal structure as calcite, a calcium carbonate with a hardness and texture similar to white magnesite and marble (Chen & Tao, 2004;Misch, 2012;Pluch, 2018;Siegesmund & Török, 2010). In its natural state, magnesite exists as a white, gray, or brown porous crystal (Chauke, 2020;Shand, 2006).…”
Section: Introductionmentioning
confidence: 99%
“…Differently from dolomite, magnesite mineralization only occurs at a relatively higher temperature (>60 • C) with elevating CO 2 pressure. On the other hand, talc mineralization mainly occurs in hydrothermal activities on dolomite and magnesite [14,15], where the silicate composition originates from the hydrothermal solution and the carbonate composition originates from dolomite and/or magnesite. Due to the geological characteristics, magnesite mineralization is mainly associated with carbonate rocks with talc as an accessory mineral, and thus, the commonly found gangue minerals are calcite, dolomite, and talc.…”
Section: Introductionmentioning
confidence: 99%
“…However, throughout talc applications, new requirements and/or new limitations appeared such as (i) the need of talc ore purity, particularly in cosmetic and pharmacologic uses; (ii) the difficulty to disperse talc in a water medium, and (iii) the need to use submicronic talc particles to develop polymer based nanocomposites (Usuki et al, 1993a, b;Kojima et al, 1993a, b). To satisfy these respective requirements, several possible ways were put forward: (i) the need of high purity talc was solved by the exploration of new highly pure talc deposit (Misch et al, 2018) and/or the improvements of techniques to purify talc ore (Baba et al, 2015;Castillo et al, 2014;Dumas et al, 2015a); (ii) talc dispersion in water medium was improved by using surface treatment such as pre-coating by carboxyl methyl cellulose adsorption, for example (Bonino et al, 2002;Bacchin et al, 2006); and (iii) the need of submicronic talc particles led to the development of grinding processes such as air jet milling, sonication, stirred ball milling and dry milling (Godet, 2001). However, using these top-down approaches, the results were not as successful since natural talc is difficult to ground homogeneously below 1 µm without leading to amorphization and structural disordering (Liao and Senna, 1992;Sanchez-Soto et al, 1997;Dellisanti et al, 2009;Cavaida et al, 2015;Borges et al, 2016).…”
Section: Introductionmentioning
confidence: 99%
“…shows the comparison between a natural pink talc from China (François Martin's collection), and a green synthetic talc whose Mg was replaced by Ni. The natural sample loses its color after grinding (like the colored talc samples studied byMisch et al (2018), this talc is very pure and contains no other associated mineral which could explain the pink color, which is probably due to the arrangement of crystallites in the bulk ore inducing light reflection phenomenon) while the synthetic Ni sample retains its green color. The paper of Dumas et al(2015b), based on the superior visibility of Ni in EXAFS spectroscopy with respect to Mg, aimed to first understand the genesis of Ni-rich talc from nucleation to crystal growth.…”
mentioning
confidence: 98%