Abstract

Magnesium carbonate powders are essential in the manufacture of basic refractories capable of withstanding extremely high temperatures and for special types of cement and powders used in the paper, rubber, and pharmaceutical industries. A novel synthesis route is based on CO2 absorption/sequestration by minerals. This combines the global challenge of climate change with materials development. Carbon dioxide has the fourth highest composition in earth’s atmosphere next to nitrogen, oxygen and argon and plays a big role in global warming due to the greenhouse effect. Because of the significant increase of CO2 emissions, mineral carbonation is a promising process in which carbon oxide reacts with materials with high metal oxide composition to form chemically stable and insoluble metal carbonate. The formed carbonate has long-term stability and does not influence the earth’s atmosphere. Therefore, it is a feasible and safe method to bind carbon dioxide in carbonate compounds such as magnesite. The subject of this work is the carbonation of an olivine (Mg2SiO4) and synthetic magnesia sample (>97 wt% MgO) under high pressure and temperature in an autoclave. Early experiments have studied the influence of some additives such as sodium bicarbonate, oxalic acid and ascorbic acid, solid/liquid ratio, and particle size on the carbonation efficiency. The obtained results for carbonation of olivine have confirmed the formation of magnesium carbonate in the presence of additives and complete carbonation of the MgO sample in the absence of additives.

Highlights

  • The significance of the results coming from greenhouse gas (GHG) emissions to both the atmosphere and our lives has already been urged and is nowadays well-known

  • Carbon capture and utilization (CCU) is considered as the most promising technique in order to use the product in cement, transforming it into insoluble carbonate, that is able to remain stable in a geological timeframe [1]

  • Synthesis of magnesium carbonate was studied via carbonation of olivine using different size fractions with different solid/liquid ratios of 1:15 and 1:5; at 175 ◦ C and pressure of CO2 (117 bar) in an autoclave in the presence and in the absence of additives

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Summary

Introduction

The significance of the results coming from greenhouse gas (GHG) emissions to both the atmosphere and our lives has already been urged and is nowadays well-known. Optimal addition of additives are reported by Bearat et al [13] in studies about the mechanism that limits aqueous olivine carbonation reactivity under the optimum sequestration reaction conditions observed as follows: 1 M NaCl + 0.64 M NaHCO3 , at 185 ◦ C and P (CO2 ) about 135 bar. Daval et al [15] reported about high influence of amorphous silica layer formation on the dissolution rate of olivine at 90 ◦ C and elevated pressure of carbon dioxide. This passivating layer may either built up from non-stoichiometric dissolution, precipitation of amorphous silica on forsterite particles or a combination of both. Plasma Optical Emission Spectroscopy ICP-OES in order to determine the concentration of nickel, iron, magnesium and cobalt

Experimental
Advance with
Results and Discussion
Product Characterization–XRD Analysis of Product after Carbonation
Analysis of Water Solution after Carbonation of an Olivine
Carbonation Extent
Conclusion
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