Corrosion behavior of the reinforcement in chloride-contaminated alkali-activated fly ash pore solution

Author(s):  
Zhangmin Zhang ◽  
Rui Chen ◽  
Jie Hu ◽  
Yangyang Wang ◽  
Haoliang Huang ◽  
...  
2018 ◽  
Vol 761 ◽  
pp. 65-68 ◽  
Author(s):  
Yi Bing Zuo ◽  
Marija Nedeljković ◽  
Guang Ye

Pore solution of hardened alkali-activated fly ash paste was extracted by the steel-die method. The aqueous phase composition of pore solution was analyzed using ICP-OES analysis technique. The results show that the concentrations of Si, Al, Ca, K and OH- decrease with curing time regardless of the curing temperatures (40°C/60°C) and alkaline activators (sodium hydroxide with/without sodium silicate). On the contrary, the concentration of S increases with curing time. A higher temperature curing decreases the solubility of Si, Al, Ca and K in the alkali-activated fly ash, while it doesn’t show much influence on the solubility of S. The plot of the concentration of Al versus the concentration of Si displays a quasi-linear logarithmic relationship. This relationship implies congruent removal of Si and Al from the frameworks of fly ash.


2021 ◽  
Vol 11 (4) ◽  
pp. 1908
Author(s):  
Giulia Masi

Alkali activated materials as possible sustainable alternative to cementitious binders showed competitive performances in terms of mechanical and durability properties and high temperature stability. For this reason, light weight fly-ash based mortars have already been optimized as passive fire protective coating for steel structures. However, a lack of information about the durability of these innovative systems in terms of steel corrosion resistance is still present. Thus, this study aims at investigating the durability of steel coated with a 20-mm thick light weight mortar layer in a neutral environment (tap water) and in presence of chloride-containing solution (0.2 M NaCl). In addition, the influence of pore solution chemistry and pH was discussed through electrochemical testing in leachate pore solution and NaOH aqueous solutions at different concentrations. It was found that almost complete protection ability of light weight mortar was obtained when coated steel is exposed to neutral solution for 60 days, while in presence of chlorides, steel is more susceptible to corrosion already after 40 days of exposure. In addition, the developed open porosity of the light weight mortars, it was found that pH and the chemistry of the pore solution in contact with steel strongly influenced the steel corrosion resistance.


2018 ◽  
Vol 761 ◽  
pp. 148-151
Author(s):  
Marija Nedeljković ◽  
Yi Bing Zuo ◽  
Kamel Arbi ◽  
Guang Ye

Carbonation of the pore solution in alkali-activated materials (AAMs) produces alkali and/or alkali-earth carbonates. When the carbonate solubility in the water is very high (case of the most alkali carbonates), it is very hard to determine the carbonation depth in AAMs with the phenolphthalein indicator frequently used in Ordinary Portland Cement (OPC)-based materials. Carbonation gradually decreases the alkalinity of the pore solution, while the color after spraying phenolphthalein changes from colorless to pink when pH< 13 and changes back to colorless when pH< 8.2. The color change with phenolphthalein indicator may still exist in the less alkaline areas where carbonation may have already occurred. Therefore, using the indicator test is likely to underestimate the depth to which carbonation reaction has occurred in AAMs and more complete assessment is required. This study investigates the carbonation front in alkali-activated fly ash (FA) and blast furnace slag (BFS) pastes in natural laboratory conditions. Monitoring carbonation front in the samples after one year of exposure has been carried out under polarized light microscope (PLM), and environmental scanning electron microscope (ESEM). The carbonation products were sharply distinguished from the other constituents of the paste, by their crystallographic and optical characteristics under PLM, and characterized by X-Ray diffraction (XRD).


2019 ◽  
Vol 116 ◽  
pp. 146-158 ◽  
Author(s):  
Marija Nedeljković ◽  
Bahman Ghiassi ◽  
Sieger van der Laan ◽  
Zhenming Li ◽  
Guang Ye

2021 ◽  
Vol 11 (9) ◽  
pp. 4054
Author(s):  
Juan Bosch ◽  
Ulises Martin ◽  
Jacob Ress ◽  
Keston Klimek ◽  
David M. Bastidas

In this study the effect of thermomechanical treatments in chloride induced pitting corrosion is presented for carbon steel rebars exposed to synthetic fly ash (FA) pore solution. Due to the likely phase transformations that steel reinforcements in concrete experience during the event of a fire, the understanding of the corrosion behavior of such phases is key in predicting the stability of the structure. The motivation for this study arrives from the scarce literature regarding the corrosion behavior of thermomechanically treated steel reinforcements in FA environments and the need for further investigation to understand its mechanism. In order to better understand the effects on the corrosion behavior electrochemical measurements including cyclic potentiodynamic polarization curves (CPP) and electrochemical impedance spectroscopy (EIS) were used. It was found that quenched specimens showed enhanced corrosion kinetics as their icorr values were higher, being of 3.18 × 10−5 and 2.20 × 10−5 A/cm2 for water and oil quenched compared to 2.13 × 10−6 A/cm2 for the as-received. Furthermore, the effective capacitance of the double layer (Ceff,dl) showed the lower stability of the passive film for the quenched specimens, with values of 1.11 × 10−3 µF/cm2 for the as-receive sample that decreased to 8.12 × 10−4 µF/cm2 for the water quenched sample. The anodic charge transfer coefficient in the synthetic FA alkaline pore solution changes from 0.282 to 0.088, for the as-received and water quenched rebars specimens, respectively. These results indicate a lower energy barrier for the anodic dissolution reaction of quenched specimens, indicating that martensite and bainite microstructures promote corrosion process. Enhanced corrosion was found on quenched samples presenting martensite and bainite microstructure as showed by the increased pith depth, with values of 5 μm compared to 1 μm observed in the as-received samples.


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