Table 1 shows the area and perimeter phase fractions for two different fields of view for the cement shown in Figure 3. It should be noted that the perimeter fractions will be a stronger function of image resolution than the area fractions. In both cases, the bulk area fractions are quite similar to the volume fractions computed using the Bogue equations [9 ]. Since most of the larger silicate particles are C3 S, the C3S particles generally have a lower surface area to volume (or perimeter to area) ratio than the C2S particles. Thus, the C 2S occupies a larger fraction of the phase perimeter than its area fraction. The C2S generally reacts at a slower rate than the C3 S suggesting that this cement might hydrate at a slower rate than a cement with the same bulk phase fractions but a proportional distribution of the two silicates on its surfaces. Since the gypsum is generally present as smaller discrete particles, it too occupies a larger perimeter fraction than its area fraction.
Scrivener has computed the area and surface fractions of silicates and interstitial phases and in general found that the interstitial phases occupied a larger fraction of the surfaces than their area fraction [2]. For this particular cement, we actually observe the opposite trend, as the interstitial phases (ferrite and aluminate) occupy a smaller perimeter fraction than their area fraction. This can be directly observed in Figure 3, where many of the C 3A regions are part of much larger polymineralic particles and have much of their perimeter in contact with C3S instead of porosity.
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Table 1 |
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Area and Perimeter Phase Fractions for a Type I Portland Cement |
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Image 1 |
Image 2 |
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Bogue |
Area |
Perimeter |
Area |
Perimeter |
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| C3S | 0.618 | 0.637 | 0.397 | 0.648 | 0.445 |
| C2S | 0.127 | 0.115 | 0.322 | 0.121 | 0.316 |
| C3A | 0.145 | 0.177 | 0.157 | 0.144 | 0.124 |
| C4AF | 0.058 | 0.018 | 0.013 | 0.044 | 0.021 |
| Gypsum | 0.051 | 0.053 | 0.111 | 0.043 | 0.093 |