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    Impact of Cation Type of Chloride Salts on Diffusion Behavior and Binding Capacity of Chloride Ions in Concrete Containing Sodium Nitrite and Disodium Hydrogen Phosphate

    Source: Journal of Materials in Civil Engineering:;2022:;Volume ( 034 ):;issue: 004::page 04022013
    Author:
    Jyotish Kumar Das
    ,
    Bulu Pradhan
    DOI: 10.1061/(ASCE)MT.1943-5533.0004145
    Publisher: ASCE
    Abstract: Chloride diffusion in concrete induces depassivation of steel reinforcement, which can jeopardize the service life of concrete structures subjected to aggressive environments. This paper investigates the effect of a cation type of chloride salts, sodium nitrite (SN) (NaNO2) and disodium hydrogen phosphate (DHP), on the diffusion behavior and binding capacity of chloride ions in concrete prepared from ordinary portland cement (OPC) and portland pozzolana cement (PPC) and exposed to different chloride salt solutions for an exposure period of 756 days. The results showed that the cation type of chloride salts and admixed NaNO2 and DHP have a significant effect on the chloride diffusion coefficient and chloride binding capacity of concrete. The apparent chloride diffusion coefficient (Dapp) of concrete decreased in the order Dapp: NaCl>CaCl2>MgCl2, whereas chloride binding capacity (R) decreased in the order R: CaCl2>MgCl2>NaCl. The microstructure of concrete examined through X-ray diffraction, Fourier transform infrared spectroscopy, and field emission scanning electron microscope analyses indicated the formation of nitrite- and phosphate-based compounds in concrete containing NaNO2 and DHP, respectively. The addition of NaNO2 or DHP decreased Dapp and increased chloride binding capacity of concrete. NaNO2 showed a lower chloride diffusion coefficient than Na2HPO4 (DHP). However, DHP exhibited a higher chloride binding capacity than NaNO2. This was due to the dominant effect of the formation of chlorapatite and a higher amount of Friedel’s salt in concrete containing DHP over the effect of a lower extent of physical binding of chloride ions due to the partial replacement of adsorbed nitrite ions from C─ S─ H by chloride ions. It was also due to the formation of a lower amount of Friedel’s salt due to the partial replacement of nitrite ions in nitrite–aluminate-ferrite-monosubstituent (AFm) by chloride ions in concrete containing NaNO2.
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      Impact of Cation Type of Chloride Salts on Diffusion Behavior and Binding Capacity of Chloride Ions in Concrete Containing Sodium Nitrite and Disodium Hydrogen Phosphate

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    http://yetl.yabesh.ir/yetl1/handle/yetl/4282020
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    contributor authorJyotish Kumar Das
    contributor authorBulu Pradhan
    date accessioned2022-05-07T20:07:38Z
    date available2022-05-07T20:07:38Z
    date issued2022-01-19
    identifier other(ASCE)MT.1943-5533.0004145.pdf
    identifier urihttp://yetl.yabesh.ir/yetl1/handle/yetl/4282020
    description abstractChloride diffusion in concrete induces depassivation of steel reinforcement, which can jeopardize the service life of concrete structures subjected to aggressive environments. This paper investigates the effect of a cation type of chloride salts, sodium nitrite (SN) (NaNO2) and disodium hydrogen phosphate (DHP), on the diffusion behavior and binding capacity of chloride ions in concrete prepared from ordinary portland cement (OPC) and portland pozzolana cement (PPC) and exposed to different chloride salt solutions for an exposure period of 756 days. The results showed that the cation type of chloride salts and admixed NaNO2 and DHP have a significant effect on the chloride diffusion coefficient and chloride binding capacity of concrete. The apparent chloride diffusion coefficient (Dapp) of concrete decreased in the order Dapp: NaCl>CaCl2>MgCl2, whereas chloride binding capacity (R) decreased in the order R: CaCl2>MgCl2>NaCl. The microstructure of concrete examined through X-ray diffraction, Fourier transform infrared spectroscopy, and field emission scanning electron microscope analyses indicated the formation of nitrite- and phosphate-based compounds in concrete containing NaNO2 and DHP, respectively. The addition of NaNO2 or DHP decreased Dapp and increased chloride binding capacity of concrete. NaNO2 showed a lower chloride diffusion coefficient than Na2HPO4 (DHP). However, DHP exhibited a higher chloride binding capacity than NaNO2. This was due to the dominant effect of the formation of chlorapatite and a higher amount of Friedel’s salt in concrete containing DHP over the effect of a lower extent of physical binding of chloride ions due to the partial replacement of adsorbed nitrite ions from C─ S─ H by chloride ions. It was also due to the formation of a lower amount of Friedel’s salt due to the partial replacement of nitrite ions in nitrite–aluminate-ferrite-monosubstituent (AFm) by chloride ions in concrete containing NaNO2.
    publisherASCE
    titleImpact of Cation Type of Chloride Salts on Diffusion Behavior and Binding Capacity of Chloride Ions in Concrete Containing Sodium Nitrite and Disodium Hydrogen Phosphate
    typeJournal Paper
    journal volume34
    journal issue4
    journal titleJournal of Materials in Civil Engineering
    identifier doi10.1061/(ASCE)MT.1943-5533.0004145
    journal fristpage04022013
    journal lastpage04022013-26
    page26
    treeJournal of Materials in Civil Engineering:;2022:;Volume ( 034 ):;issue: 004
    contenttypeFulltext
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