Clinkering-free cementation by fly ash carbonation. (January 2018)

• Record Type: Journal Article
• Authors: Wei, Zhenhua; Wang, Bu; Falzone, Gabriel; La Plante, Erika Callagon; Okoronkwo, Monday Uchenna; She, Zhenyu; Oey, Tandre; Balonis, Magdalena; Neithalath, Narayanan; Pilon, Laurent; Sant, Gaurav
• Is Part Of: Journal of CO₂ utilization. Volume 23(2018)
• Page Start: 117
• Page End: 127
• Publication Date: 2018-01
• Subjects: Fly ash -- Cementation -- CO2 -- Upcycling -- Strength -- Concrete; Carbon dioxide -- Periodicals; Carbon dioxide -- Environmental aspects -- Periodicals; Carbon dioxide mitigation -- Periodicals; Carbon dioxide; Carbon dioxide -- Environmental aspects; Carbon dioxide mitigation; Periodicals; 628.53205
• DOI: 10.1016/j.jcou.2017.11.005
• Languages: English
• ISSNs: 2212-9820

Abstract

Highlights: Fly ashes can be readily carbonated in dilute CO2 streams ("flue gas"). The carbonated solids offer robust cementation in relation to their mobile Ca-content. Carbonation is readily facilitated at sub-boiling temperatures—e.g., by using the waste heat contained in flue gas—thereby creating low-energy pathways for cementation. Abstract: The production of ordinary portland cement (OPC) is a CO2 intensive process. Specifically, OPC clinkering reactions not only require substantial energy in the form of heat, but they also result in the release of CO2 ; i.e., from both the decarbonation of limestone and the combustion of fuel to provide heat. To create alternatives to this CO2 intensive process, this paper demonstrates a new route for clinkering-free cementation by the carbonation of fly ash; i.e., a by-product of coal combustion. It is shown that in moist environments and at sub-boiling temperatures, Ca-rich fly ashes react readily with gas-phase CO2 to produce robustly cemented solids. After seven days of exposure to vapor-phase CO2 at 75 °C, such formulations achieve a compressive strength of around 35 MPa and take-up 9% CO2 (i.e., by mass of fly ash solids). On the other hand, Ca-poor fly ashes due to their reduced alkalinity (i.e., low abundance of mobile Ca- or Mg-species), show limited potential for CO2 uptake and strength gain—although this deficiency can be somewhat addressed by the provision of supplemental/extrinsic Ca agents. The roles of CO2 concentration and processing temperature are discussed, and linked to the progress of reactions and the development of microstructure. The outcomes create new pathways for achieving clinkering-free cementation while enabling the beneficial utilization ("upcycling") of emitted CO2 and fly ash; i.e., two abundant, but underutilized industrial by-products.