{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Zheng H"],"funding":["National Natural Science Foundation of China"],"pagination":["12476-12483"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC8696962"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["11(21)"],"pubmed_abstract":["CaO derived naturally from limestone or dolomite is an inexpensive and widely available sorbent. Understanding the mechanisms of CaO carbonation at ambient temperature under the assistance of H<sub>2</sub>O is important for predicting the reaction of CaO in complex environments and designing novel CaO materials. In this study, we found that the reaction rate of alkali-activated slag is controlled by the CaCO<sub>3</sub> layer on a partially carbonized CaO alkali activator. The size of the sorbent increased after the adsorption reaction and the physically adsorbed water in the pores accelerated the carbonation. The carbonation process was governed by CO<sub>2</sub> diffusion. When the carbonation conversion rate reached 2-6%, the setting time increased rapidly with the increase in the carbo"],"journal":["RSC advances"],"pubmed_title":["Novel procedure of CO<sub>2</sub> capture of the CaO sorbent activator on the reaction of one-part alkali-activated slag."],"pmcid":["PMC8696962"],"funding_grant_id":["51768010"],"pubmed_authors":["Zheng H","He Y","Liu L","Zhu Y","Cui X"],"additional_accession":[]},"is_claimable":false,"name":"Novel procedure of CO<sub>2</sub> capture of the CaO sorbent activator on the reaction of one-part alkali-activated slag.","description":"CaO derived naturally from limestone or dolomite is an inexpensive and widely available sorbent. Understanding the mechanisms of CaO carbonation at ambient temperature under the assistance of H<sub>2</sub>O is important for predicting the reaction of CaO in complex environments and designing novel CaO materials. In this study, we found that the reaction rate of alkali-activated slag is controlled by the CaCO<sub>3</sub> layer on a partially carbonized CaO alkali activator. The size of the sorbent increased after the adsorption reaction and the physically adsorbed water in the pores accelerated the carbonation. The carbonation process was governed by CO<sub>2</sub> diffusion. When the carbonation conversion rate reached 2-6%, the setting time increased rapidly with the increase in the carbo","dates":{"release":"2021-01-01T00:00:00Z","publication":"2021 Mar","modification":"2025-04-22T10:01:03.308Z","creation":"2025-04-05T23:22:30.055Z"},"accession":"S-EPMC8696962","cross_references":{"pubmed":["35423813"],"doi":["10.1039/d1ra01353j"]}}