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dc.contributor.advisorWiik, Kjell
dc.contributor.advisorDe Weerdt, Klaartje
dc.contributor.advisorMachner, Alisa
dc.contributor.authorHemstad, Petter
dc.date.accessioned2019-09-11T10:50:15Z
dc.date.created2018-03-09
dc.date.issued2018
dc.identifierntnudaim:18355
dc.identifier.urihttp://hdl.handle.net/11250/2615776
dc.description.abstractA new method for artificially leaching hydrated cement paste and studying how lowered pH in the pore solution affects chloride binding has been developed. Hydrated cement paste was exposed to a NaCl-solution before being acidified by adding small volumes of HCl in steps over several days, gradually lowering the pH. A pH-development curve was established, determining how the pH in the pore solution responded to increasing amounts of acid being added. The chloride binding of the cement paste as a function of the pH and free chloride concentration was then determined. For the range of pH from 12 to 13, decreasing pH increased chloride binding. At a pH of 11, the cement paste showed almost no chloride binding. The mechanisms of changes in chloride binding were investigated using TGA, XRD, SEM-EDS, ICP-MS and thermodynamic modelling. One of the main chloride binding phases, Friedel s salt, could not be detected with the applied techniques due to the cement paste being cured at 60 °C, therefore its influence could not be verified. Thermodynamic modelling does however confirm the possibility of Friedel s salt decomposing at pH 11. The increase in chloride binding from pH 13 to 12 is most likely related to the changes in the main hydrate phase C-S-H. The effect of pH on chloride binding should be accounted for in service life prediction models for concrete structures exposed to chlorides.en
dc.languageeng
dc.publisherNTNU
dc.subjectIndustriell kjemi og bioteknologi, Materialkjemi og energiteknologien
dc.titlepH-dependence of chloride binding in ordinary Portland cementen
dc.typeMaster thesisen
dc.source.pagenumber118
dc.contributor.departmentNorges teknisk-naturvitenskapelige universitet, Fakultet for naturvitenskap,Institutt for materialteknologinb_NO
dc.date.embargoenddate10000-01-01


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