Experiments and modelling to understand FeCO3 cement formation mechanism: time-evolution of CO2-species, dissolved-Fe, and pH during CO2-induced dissolution of Fe(0)

https://doi.org/10.1016/j.conbuildmat.2022.128281Get rights and content
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Highlights

  • Solution-pH increased with increased [Fe]. Possibly a surface controlled reaction.

  • Lower temperatures (T): Consistently higher [H+] and lower Fe-dissolution.

  • Higher CO2-pressures (P): Consistently higher [H+] and higher Fe-dissolution.

  • At 1 barg P: pHmeasured pHmodelled. At 10 barg P: pHmeasured 1.3 * pHmodelled.

  • Underlying influences of CO2-depressurization on experiment and model discussed.

Abstract

FeCO3 cement can be produced by reacting CO2(aq) and particulate-Fe(0). Process conditions and solution compositions influence cement properties through kinetics of Fe-dissolution and FeCO3-precipitation. This study investigates Fe-dissolution in dilute systems (water(wt.)/Fe(wt.) = 1000) at 30/60 °C, and 1/10 barg CO2-pressures. Experimentally, time-evolution of solution composition shows increased [Fe] and solution-pH. As a proxy for high-pressure in-situ experiments, a modeling approach is developed to quantify with [Fe]-increase, the: decreased [H+], increased [HCO3-]/[OH]/[CO32-], and undisturbed [CO2(aq)]/[H2CO3]. Fe-dissolution rates increase with: (a) pH-decrease with increased CO2-pressure, and (b) faster kinetics at higher temperatures, even with higher pH. Experimental and modeled pH are comparable at 1 bar, two causes are discussed for it being ∼ 1.2 times at 10 barg: CO2-depressurization, and Fe-precipitation. Lower CO2-mediated dissolution activation energies of ∼ 30 (1 barg) and ∼ 20 kJ/mol (10 barg) compared to strong acids (∼60 kJ/mol) are attributed to buffering action of CO2(aq).

Keywords

Accelerated carbonation
Siderite (FeCO3)-cement
CO2-corrosion
Fe-dissolution
Carbonate cement
CO2-utilization

Data availability

Data will be made available on request.

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