The pH of concrete-based material is a key parameter for the assessment of its stability and durability, since a change in pH is usually associated with major types of chemical degradation such as carbonation, leaching and acid attacks. Conventional surface pH measurements with potentiometric flat surface electrodes have low spatial resolution, whereas optical pH visualization with indicator dyes (phenolphthalein) only indicates the areas with higher or lower pH than the pKa of the indicator. In this regard, it is key to develop wide-range imaging systems, enabling accurate and spatially resolved determination of pH variability for an advanced knowledge of degradation mechanisms. This contribution presents the enhancements made for a high-resolution optical pH imaging system based on fluorescent aza-BODIPY indicator dyes. The measurement range was increased to 6 pH units (pH 6.5 to pH 12.5) by a combination of two indicator dyes. Moreover, background scattering effects were sufficiently eliminated. With the improved sensor foils steep pH gradients (up to 3 pH units within 2 mm) were successfully recorded in various concrete specimens using a macro lens reaching a resolution of down to 35 µm per pixel.
Many (inter)national standards exist to evaluate the resistance of mortar and concrete to carbonation. When a carbonation coefficient is used for performance comparison of mixtures or service life prediction, the applied boundary conditions during curing, preconditioning and carbonation play a crucial role, specifically when using latent hydraulic or pozzolanic supplementary cementitious materials (SCMs). An extensive interlaboratory test (ILT) with twenty two participating laboratories was set up in the framework of RILEM TC 281-CCC ‘Carbonation of Concrete with SCMs’. The carbonation depths and coefficients determined by following several (inter)national standards for three cement types (CEM I, CEM II/B-V, CEM III/B) both on mortar and concrete scale were statistically compared. The outcomes of this study showed that the carbonation rate based on the carbonation depths after 91 days exposure, compared to 56 days or less exposure duration, best approximates the slope of the linear regression and those 91 days carbonation depths can therefore be considered as a good estimate of the potential resistance to carbonation. All standards evaluated in this study ranked the three cement types in the same order of carbonation resistance. Unfortunately, large variations within and between laboratories complicate to draw clear conclusions regarding the effect of sample pre-conditioning and carbonation exposure conditions on the carbonation performance of the specimens tested. Nevertheless, it was identified that fresh and hardened state properties alone cannot be used to infer carbonation resistance of the mortars or concretes tested. It was also found that sealed curing results in larger carbonation depths compared to water curing. However, when water curing was reduced from 28 to 3 or 7 days, higher carbonation depths compared to sealed curing were observed. This increase is more pronounced for CEM I compared to CEM III mixes. The variation between laboratories is larger than the potential effect of raising the CO
2
concentration from 1 to 4%. Finally, concrete, for which the aggregate-to-cement factor was increased by 1.79 in comparison with mortar, had a carbonation coefficient 1.18 times the one of mortar.
Supplementary Information
The online version contains supplementary material available at 10.1617/s11527-022-01927-7.
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