TY - JOUR
T1 - Phase transition and morphology evolution of precipitated calcium carbonate (PCC) in the CO2 mineralization process
AU - Mei, Xiaohui
AU - Zhao, Qing
AU - Li, Yumeng
AU - Min, Yi
AU - Liu, Chengjun
AU - Saxén, Henrik
AU - Zevenhoven, Ron
N1 - Funding Information:
The authors gratefully acknowledge supports by the National Natural Science Foundation of China (No. 52074078 ), and the Fundamental Research Funds for the Central Universities (No. N2125034, N2201023, and N2025035).
Publisher Copyright:
© 2022 Elsevier Ltd
PY - 2022/11/15
Y1 - 2022/11/15
N2 - The indirect CO2 mineralization by using Ca/Mg-containing industrial alkaline by-products or wastes is a promising way for mitigation of CO2 emissions and valorization of wastes, although plagued by the utilization of precipitated calcium carbonate (PCC) if low-value product is obtained. It is difficult to acquire specific PCC with targeted morphology for commercial use since many parameters change in the gas–liquid carbonation process. In this work, the phase transition and morphology evolution behavior of PCC precipitated during carbonation of 0.1 mol·L−1 NH4Cl Ca-rich solution were studied. Results show that the polymorph transformation from rhombohedral calcite to spherical vaterite was found during the gas–liquid carbonation process, which is different from the traditional carbonation process (aqueous carbonation of lime). A promising result is that pure spherical vaterite of industrial interest was obtained under the studied conditions. In addition, to achieve conversion of CO2(g) into desired morphology of PCC, the feasibility of introducing additives (ethylene glycol and citric acid) into the gas–liquid carbonation system was also evaluated in terms of CO2(g) adsorption and PCC polymorphs control. Finally, the mechanism of additives on the growth and morphology of crystalline CaCO3 was investigated by FTIR and interpreted at the atomic level.
AB - The indirect CO2 mineralization by using Ca/Mg-containing industrial alkaline by-products or wastes is a promising way for mitigation of CO2 emissions and valorization of wastes, although plagued by the utilization of precipitated calcium carbonate (PCC) if low-value product is obtained. It is difficult to acquire specific PCC with targeted morphology for commercial use since many parameters change in the gas–liquid carbonation process. In this work, the phase transition and morphology evolution behavior of PCC precipitated during carbonation of 0.1 mol·L−1 NH4Cl Ca-rich solution were studied. Results show that the polymorph transformation from rhombohedral calcite to spherical vaterite was found during the gas–liquid carbonation process, which is different from the traditional carbonation process (aqueous carbonation of lime). A promising result is that pure spherical vaterite of industrial interest was obtained under the studied conditions. In addition, to achieve conversion of CO2(g) into desired morphology of PCC, the feasibility of introducing additives (ethylene glycol and citric acid) into the gas–liquid carbonation system was also evaluated in terms of CO2(g) adsorption and PCC polymorphs control. Finally, the mechanism of additives on the growth and morphology of crystalline CaCO3 was investigated by FTIR and interpreted at the atomic level.
KW - Precipitated calcium carbonate (PCC)
KW - CO2 mineralization
KW - Phase transition
KW - Morphology evolution
KW - Organic molecule
UR - http://www.scopus.com/inward/record.url?scp=85134303760&partnerID=8YFLogxK
U2 - 10.1016/j.fuel.2022.125259
DO - 10.1016/j.fuel.2022.125259
M3 - Article
AN - SCOPUS:85134303760
SN - 0016-2361
VL - 328
JO - Fuel
JF - Fuel
M1 - 125259
ER -