Argon oxygen decarburization stainless steel slag (AOD slag) has high mineral carbonation activity. AOD slag carbonation has both the resource utilization of metallurgical waste slag and the carbon reduction effect of CO2 storage. This paper aimed to study carbonation reaction characteristics of AOD slag. Under the slurry-phase accelerated carbonation route, the effect of stirring speed (r) and reaction temperature (T) on AOD slag’s carbonation was studied by controlling the reaction conditions. Mineral composition analysis and microscopic morphology analysis were used to explore the mineral phase evolution of AOD slag during the carbonation process. Based on the unreacted core model, the kinetic model of the carbonation reaction of AOD slag was analyzed. The results showed that the carbonation ratio of AOD slag reached its maximum value of 66.7% under the reaction conditions of a liquid to solid ratio (L/S) of 8:1, a CO2 partial pressure of 0.2 MPa, a stirring speed of 450 r·min−1, and a reaction temperature of 80 °C. The carbonation reaction of AOD slag was controlled by internal diffusion, and the calculated apparent activation energy was 22.28 kJ/mol.
EAF stainless steel slag (EAF slag) is one kind of chromium-bearing metallurgical solid waste, which belongs to alkaline steel slag, and contains a large number of alkaline mineral phases. The carbonation activity of these minerals gives EAF slag the capability to effectively capture CO2. In this paper, EAF slag samples with different carbonation degrees were prepared by the slurry-phase accelerated carbonation route. The mineralogical identification analysis was used to qualitatively and semi-quantitatively determine the types and contents of the carbonatable mineral phases in the EAF slag. The sequential leaching test was used to study the chromium leachabilities in EAF slags with different carbonation degrees. The results showed that the main minerals with carbonation activity in EAF slag were Ca3Mg(SiO4)2 and Ca2SiO4, with mass percentages of 56.9% and 23%, respectively. During the carbonation process, Ca2SiO4 was the main reactant and calcite was the main product. As the degree of carbonation increased, the pH of the EAF slags’ leachate gradually decreased while the redox potential (Eh) gradually increased. At the same time, a large amount of Ca2+ in the EAF slag combined with CO2 to form slightly soluble calcium carbonate, which led to a significant decrease in the conductivity of the leachate. With the gradual increase in carbonation ratio, the leachability of chromium in the EAF slag first decreased and then increased, and reached its lowest value when the CO2 uptake ratio was 11.49%.
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