Manufacture of rich-sulfoaluminate belite cement at low temperature from waste mixture by dry and hydrothermal processes

2022 ◽  
Vol 314 ◽  
pp. 125641
Author(s):  
Faiza Nabila Bouha ◽  
Larbi Kacimi ◽  
Angeles G. De la Torre
2021 ◽  
Author(s):  
Giovanni Baccolo ◽  
Barbara Delmonte ◽  
Paul Niles ◽  
Giannantonio Cibin ◽  
Elena Di Stefano ◽  
...  

<p>On Earth, jarosite is a weathering product forming in acidic-oxidative environments from the alteration of iron-bearing minerals in presence of liquid water. Typical settings where this iron-potassium hydrated sulphate is found, are weathering zones of pyrite-rich deposits, evaporative basins and fumaroles. Jarosite is not only known on Earth, it also occurs on Mars, where it was firstly identified by the Opportunity rover. The mineral was in fact recognized in the finely layered formations outcropping at Meridiani Planum and that were accurately investigated by the rover (Klingelhöfer et al. 2004). Since jarosite requires liquid water to form, its occurrence on Mars has been regarded as an evidence for the presence of liquid water in the geologic past of Mars (Elwood-Madden et al., 2004). Since then, many models have been proposed to describe the environments where the precipitation of Martian jarosite took place. The most accepted ones deal with evaporative basins similar to Earth’s playas, others concern volcanic activity and hydrothermal processes. An alternative proposal predicted that jarosite may have formed as a consequence of weathering of mineral dust trapped in massive ice deposits, i.e. the ice-weathering model (Niles & Michalsky, 2009). The hypothesis that jarosite formed on Mars because of low-temperature, acidic and water limited weathering, is not new (Burns, 1987), but until now no direct evidences were available to support it.</p><p>A potential Earth analogue to investigate such processes is deep Antarctic ice. We present a first investigation of deep ice samples from the Talos Dome ice core (East Antarctica) aimed at the identification of englacial jarosite, so as to support the ice-weathering model. Evidences gathered through independent techniques showed that jarosite is actually present in deep Antarctic ice and results from the weathering of dust trapped into ice. The process is controlled by the re-crystallization of ice grains and the concurrent re-location of impurities at grain-junctions, which both depend on ice depth. This study demonstrates that the deep englacial environment is suitable for jarosite precipitation. Our findings support the hypothesis that, as originally predicted by the ice-weathering model, paleo ice-related processes have been important in the geologic and geochemical history of Mars.</p><p> </p><p><strong>References</strong></p><p>Burns, R. Ferric sulfates on Mars. <em>J. Geophys. Res.</em> <strong>92</strong>, E570-E574 (1987).</p><p>Elwood-Madden et al., 2004. Jarosite as an indicator of water-limited chemical weathering on Mars. <em>Nature</em> <strong>431</strong>, 821-823 (2004).</p><p>Klingelhöfer, G. et al. Jarosite and Hematite at Meridiani Planum from Opportunity's Mössbauer Spectrometer. <em>Science</em> <strong>306</strong>, 1740-1745 (2004).</p><p>Niles, P. B. & Michalski, J. M. Meridiani Planum sediments on Mars formed through weathering in massive ice deposits. <em>Nat. Geosci.</em> <strong>2</strong>, 215-220 (2009).</p>


Minerals ◽  
2020 ◽  
Vol 10 (5) ◽  
pp. 392 ◽  
Author(s):  
Katarzyna Gros ◽  
Ewa Słaby ◽  
Petras Jokubauskas ◽  
Jiří Sláma ◽  
Gabriela Kozub-Budzyń

Allanite is one of the main rare earth elements (REE)-rich accessory minerals in composite dykes from the granitoid pluton of Karkonosze. These dykes differ in composition from the bulk of the pluton by elevated rare earth elements (REE), Y, Zr, and alkali contents, suggesting contribution of an additional component. Allanite exhibits complex alteration textures, which can be divided into two stages. The first stage is represented by allanite mantles, formed by fluid infiltration into previously crystallized magmatic allanite. These zones have low totals, are Ca-, Al-, Mg-, and light REE (LREE)-depleted, and Y-, heavy REE (HREE)-, Th-, Ti-, and alkali-enriched. The fractionation between LREE and HREE was caused by different mobility of complexes formed by these elements in aqueous fluids. The second stage includes recrystallized LREE-poor, Y-HREE-rich allanite with variable Ca, Al, Mg, and REE-fluorocarbonates. The alteration products from both stages demonstrate higher Fe3+/(Fe2+ + Fe3+) ratios and a negative Ce anomaly. These features point to the alkaline, low-temperature, and oxidized nature of the fluids. The differences in mobility and solubility of respective ligands show that the fluids from the first stage may have been dominated by Cl, whereas those of the second stage may have been dominated by F and CO2 (and PO4 in case of one sample). The inferred chemistry of the fluids resembles the overall geochemical signature of the composite dykes, indicating a major contribution of the hydrothermal processes to their geochemical evolution.


Nanomaterials ◽  
2021 ◽  
Vol 11 (8) ◽  
pp. 2038
Author(s):  
Suhdi Suhdi ◽  
Sheng-Chang Wang

Recently, the conversion of biomass into carbon nanofibers has been extensively studied. In this study, carbon nanofibers (CNFs) were prepared from rubber fruit shell (RFS) by chemical activation with H3PO4, followed by a simple hydrothermal process at low temperature and without a vacuum and gas catalyst. XRD and Raman studies show that the structure formed is an amorphous graphite formation. From the thermal analysis, it is shown that CNFs have a high thermal stability. Furthermore, an SEM/TEM analysis showed that CNFs’ morphology varied in size and thickness. The obtained results reveal that by converting RFS into an amorphous carbon through chemical activation and hydrothermal processes, RFS is considered a potential biomass source material to produce carbon nanofibers.


2021 ◽  
Vol 105 ◽  
pp. 102929
Author(s):  
Luis C. Escobar-Arenas ◽  
Maria I. Marín-Cerón ◽  
Sergio A. Restrepo-Moreno ◽  
José M. Jaramillo ◽  
Robert E. Márquez-Romero ◽  
...  

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