Chloride adsorption by calcined layered double hydroxides in hardened Portland cement paste

Citation data:

Materials Chemistry and Physics, ISSN: 0254-0584, Vol: 145, Issue: 3, Page: 376-386

Publication Year:
2014
Usage 99
Abstract Views 99
Captures 26
Readers 25
Exports-Saves 1
Citations 15
Citation Indexes 15
Repository URL:
http://hdl.handle.net/10754/597775
DOI:
10.1016/j.matchemphys.2014.02.026
Author(s):
Yoon, Seyoon; Moon, Juhyuk; Bae, Sungchul; Duan, Xiaonan; Giannelis, Emmanuel P.; Monteiro, Paulo M.
Publisher(s):
Elsevier BV
Tags:
Materials Science; Physics and Astronomy; A. Composite material; D. Adsorption; D. Corrosion; D. Diffusion
article description
This study investigated the feasibility of using calcined layered double hydroxides (CLDHs) to prevent chloride-induced deterioration in reinforced concrete. CLDHs not only adsorbed chloride ions in aqueous solution with a memory effect but also had a much higher binding capacity than the original layered double hydroxides (LDHs) in the cement matrix. We investigated this adsorption in hardened cement paste in batch cultures to determine adsorption isotherms. The measured and theoretical binding capacities (153 mg g − 1 and 257 mg g − 1, respectively) of the CLDHs were comparable to the theoretical capacity of Friedel's salt (2 mol mol − 1 or 121 mg g − 1 ), which belongs to the LDH family among cementitious phases. We simulated chloride adsorption by CLDHs through the cement matrix using the Fickian model and compared the simulation result to the X-ray fluorescence (XRF) chlorine map. Based on our results, it is proposed that the adsorption process is governed by the chloride transport through the cement matrix; this process differs from that in an aqueous solution. X-ray diffraction (XRD) analysis showed that the CLDH rebuilds the layered structure in a cementitious environment, thereby demonstrating the feasibility of applying CLDHs to the cement and concrete industries.