Sequestration of carbon dioxide by steelmaking slag was studied in an atmospheric three-phase system containing industrial slag particles, water, and CO 2 gas. Batch-type reactors were used to measure the rate of aqueous alkaline leaching and slag particle carbonization independently. Four sizes of slag particles were tested for the Ca leaching rate in deionized water at a constant 7.5 pH in an argon atmosphere and for carbonate conversion with CO 2 bubbled through an aqueous suspension. Conversion data (fraction of Ca leached or converted to carbonate) were evaluated to determine the rate-limiting step based on the shrinking core model. For Ca leaching, the chemical reaction is the controlling mechanism during the initial period of time, which then switches to diffusion through the developed porous layer as the rate-limiting step. Carbonate conversion proceeded much slower than leaching conversion and was found to be limited by diffusion through the product calcium carbonate layer. The calculated value of diffusivity was found to be 5 · 10 -9 cm 2 /s, which decreased by an order of magnitude with increasing carbonization conversion as a result of changing density of the product layer. The experimental data fit the shrinking core model well after correction for the particle specific surface area.
Clogging of tundish and submerged entry nozzles (SENs) adversely impacts productivity and quality in the continuous casting of aluminum-killed steels. Clogging results from an accretion layer that develops on the inside surface of the nozzle and restricts steel flow. Current nozzle refractories often react with molten steel to form solid by products that promote clogging. Nozzle materials that are inert with the liquid steel or react with accretions to form liquid reaction products could inhibit or eliminate clogging. Static experiments were conducted to investigate the stability between calciumbased materials and aluminum-killed steel. The results indicate that both calcium titanate and calcium zirconate react with alumina to form calcium aluminates. However, only the reaction between alumina and calcium titanate yielded calcium aluminate chemistries that were molten at steel casting temperatures. Liquid reaction products are preferred since they would be removed from the nozzle by the steel flow, thereby preventing accretion formation and clogging.
The clogging of submerged entry nozzles (SENs) and tundish well nozzles is a common problem in the continuous casting of aluminum-killed steels. Clogging occurs when alumina attaches to the inside of the nozzle restricting the flow. This article explores the use of new nozzle materials that could prevent accretion growth through the formation of liquid phases at the inclusionrefractory interface. Casting simulation experiments were conducted using three nozzle refractory formulations: calcium titanate, calcium zirconate, and a 2:1 calcium titanate to calcium zirconate molar mixture. Nozzles fabricated from these materials cast more aluminum-killed steel without clogging than typical industrial alumina graphite nozzles. However, the nozzles constructed of calcium titanate dramatically outperformed alumina graphite, calcium zirconate, and the mixed nozzles. Microscopy investigation of spent nozzles found no accretion formation in the calcium titanate nozzles. The performance difference was due to the formation of a liquid calcium aluminum titanate phase, which prevented alumina accretions.
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