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Assessment of co2 capture via mineralization using coal fly ash

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dc.contributor.advisor Kawnish Kirtania, Dr.
dc.contributor.author Jahirul Islam, Md.
dc.date.accessioned 2024-12-21T03:54:49Z
dc.date.available 2024-12-21T03:54:49Z
dc.date.issued 2024-02-07
dc.identifier.uri http://lib.buet.ac.bd:8080/xmlui/handle/123456789/6926
dc.description.abstract Amid growing concerns about anthropologically induced climate change, the search for effective strategies to mitigate CO2 emission become paramount.CO2mineralization using fly ash can be a promising method to address this environmentally significantchallenge, especially in industries which emit substantial amount of CO2 and produce a huge amount of fly ash by product. The present study aimed at assessing the potential of coal fly ash as a source of carbon mineralization through ex-situ mineral carbonation. The study investigated the impact of solid to liquid ratio, reaction time, and temperature on the CO2 sequestration capacity and it compares the sequestration capacities between direct and indirect aqueous carbonation routes.The results indicate that sequestration capacity increases with reaction time, albeit with a decreasing carbonation rate over time. The optimum solid to liquid ratio was found to be 100 g/L, at which maximum sequestration occurred. Temperature has a marginal effect on sequestration capacity, with only a slight increase observed as temperature rises.In the direct aqueous route, maximum sequestration capacity reaches 12.25 g CO2/kg fly ash, while the pH swing method attains a sequestration capacity of 93.48 g CO2/kg fly ash.The presence and quantification of calcium carbonate in the carbonated product are verified through TGA, XRD, and SEM-EDS analysis. en_US
dc.language.iso en en_US
dc.publisher Department of Chemical Engineering, BUET en_US
dc.subject Coal technology en_US
dc.title Assessment of co2 capture via mineralization using coal fly ash en_US
dc.type Thesis-MSc en_US
dc.contributor.id 0421022008 en_US
dc.identifier.accessionNumber 119720
dc.contributor.callno 662.62/JAH/2024 en_US


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