The differences between the hydration of Portland cements with single and with mixed sulfate carriers in the presence of triethanolamine (TEA) were investigated, and possible mechanisms were proposed. Without TEA, cements with different types of sulfate carriers (gypsum, hemihydrate, anhydrite, and mixture of these) have a comparable hydration process at the same molar amount of calcium sulfate. At a TEA dosage of 0.5 wt.%, the sample with a mixture of three sulfate carriers shows substantially stronger retardation of the C ₃ S (This publication uses the cement chemist notation: C ₃ S = Ca ₃ SiO ₅ , C ₂ S = Ca ₂ SiO ₄ , C ₃ A = Ca ₃ Al ₂ O ₆ , C ₄ AF = Ca ₂ (Al, Fe) ₂ O ₅ .) hydration than the cements with only one of these sulfate carriers, which is likely caused by the rapid formation of ettringite and the fast depletion of all sulfate carriers. These effects indicate that TEA influences the balance of sulfate carriers with aluminate‐containing clinker phases. On the one hand, TEA can disturb the original sulfate balance due to the accelerated dissolution of aluminate‐containing clinker phases, especially C ₄ AF. On the other hand, these effects are closely related to the types and amounts of the sulfate carriers in the cement. A higher amount of sulfate carriers can minimize the TEA‐related retardation of the C ₃ S hydration, and hemihydrate shows the strongest impact at the same calcium sulfate quantity.

The effect of triethanolamine (TEA) at various dosages on the early performance of cement paste was systematically evaluated through the techniques of rheological measurements, penetration tests, and ultrasonic pulse velocity. The correlation of early performance to the chemical hydration process was analyzed by calorimetry, zeta potential, in situ XRD, and pore solution analysis. It is found that the effect of TEA on the early performance of cement paste is strongly dependent on its dosage. With the TEA dosage below 0.1 wt%, the setting and microstructural development of cement paste are retarded. Meanwhile, the yield stress of fresh paste is decreased due to the increasing zeta potential of cement grains. The promoted formation of ettringite (AFt) and monosulfate (AFm) caused by TEA decreases the rheological retention ability. At dosages ≥0.2 wt%, the reaction of aluminate‐containing phases is greatly accelerated and a flash setting is observed. Besides, the importance of ferric phase on the reaction of cement with TEA is highlighted. At a low dosage, TEA prefers to accelerate the dissolution of tetracalcium aluminoferrite (C₄AF) first and increases the [Fe] in the pore solution of cement paste. In cement without C₄AF, the retardation of TEA on silicate phase hydration is significantly alleviated.

The effect of styrene-acrylate (SA) polymer latex on alkali-activated slag (AAS) was systematically studied in the aspects of hydration, hydration products, pore structure and mechanical properties through the combined analytical techniques including calorimetry, X-ray diffraction, thermogravimetric analysis, mercury intrusion porosimetry, and mechanical measurement. It was found that the addition of SA does not retard the AAS hydration, but slightly accelerates it, possibly due to the increasing ion diffusion through the loosely structured hydration products. Pore structure analysis indicates that the addition of polymer increases the cumulative pore volume and the portion of pores with size >100 nm in the hardened AAS paste. The addition of SA latex results in a continuous decrease of the compressive strength, but the flexural strength firstly increases and then decreases with the increase of polymer dosage. The polymer dosage of 2.5 wt % is optimal when applying polymer latex in the AAS system in this study.