Periodic Reporting for period 1 - CARS-CO2 (Carbonatation of Sulphates for CO2 sequestration)
Période du rapport: 2022-02-01 au 2024-01-31
The project had the following three objectives:
1. Improving our understanding of the crystallization processes of sulphates and carbonates.
2. Studying the mechanisms, kinetics and stability of the carbonatation of sulphates and the evaluation of sulphates as potential “sequestrators” of CO2.
3. Designing an effective strategy to use carbonatation of natural and waste sulphates to capture CO2.
The achievement of the third objective depended on the successful completion of the first two, making it the cornerstone of the project with the most significant societal impact. Leveraging insights gained from the initial objectives, a novel CO2 capture method was developed. This method utilizes powdered gypsum (CaSO4·2H2O) combined with carbonate solutions derived from CO2 capture. Mixing the powdered gypsum with these solutions yields a new carbonate mineral phase, namely vaterite (CaCO3), and sulfate-rich solutions, all achievable at ambient temperatures. Both resulting by-products hold industrial significance; vaterite finds applications in various sectors like cosmetics and pharmaceuticals, while the sulfate-rich solutions could be repurposed for synthesizing new gypsum or for agricultural fertilization. Consequently, the proposed approach aligns with the principles of the circular economy, wherein waste materials are converted into resources with renewed utility.
Furthermore, this project also provides a proof of concept for future endeavors, wherein waste gypsum produced by diverse industries would replace synthetic and natural gypsum, thereby extending the sustainability of the approach.
In this project, atomic force microscopy has been used to study the growth of gypsum on its main faces. We have been able to observe, for the first time, that the different faces have different growth mechanisms. A manuscript describing these results has been submitted for review to the journal Geochimica et Cosmochimica Acta.
The transformation of gypsum to bassanite in solutions with a high salt concentration, as well as the reverse reaction, i.e. the transformation of bassanite to gypsum, have also been studied using in situ Raman. These results, combined with results obtained in synchrotron experiments, have been published in the Journal of Cleaner Production.
Currently, we are finishing a third manuscript dealing with the transformation of gypsum into vaterite (a type of calcium carbonate used in different industries). This study, in which we have combined measurements made using an in situ Raman with measurements made ex situ, we have proposed a method of sulphate carbonation in which we use as raw material synthetic or natural gypsum and carbonate solutions, which were obtained by CO2 capture. This method therefore allows to capture CO2 and, at the same time, to obtain value-added by-products (i.e. vaterite and sulphate solutions).
During this period, additional side projects have focused on foliar fertilisation research, exploring various compounds pertinent to the project, such as sulphate solutions and carbonate particles. These efforts have resulted in remarkable findings that have been disseminated through publications in different journals.
Beyond its environmental benefits, this sulfate carbonation pathway yields materials of significant economic value. Vaterite, as a solid phase, holds promise across diverse industrial sectors such as cosmetics and pharmaceuticals, while sulfate-rich solutions offer avenues for gypsum resynthesis or serve as potent foliar fertilizers for agricultural cultivation. Thus, our method not only facilitates CO2 capture but also aligns with principles of circular economy by repurposing waste streams into valuable resources.
By showcasing the viability of our approach, this project sets the stage for future endeavours. We envision utilizing waste gypsum from various industries to bolster CO2 capture efforts, effectively addressing two environmental challenges while simultaneously generating industrial-grade by-products.