This paper studies hydration stages and phase transformation mechanism of the Sr 2? -doped calcium zirconium aluminate cement at room temperature. Features of different hydration stages of this cement paste are identified by X-ray diffraction, scanning electron microscopy, differential thermal analysis, thermogravimetric analysis, evolved gas analysis and heat evolution test. It was found that the partial isovalent substitution of Ca 2? for Sr 2? such as Ca 7-x Sr x ZrAl 6 O 18 , with x = 0.3, 0.6, 1.0, reduced the hydraulic reactivity of Ca 7 ZrAl 6 O 18 phase. The course of hydration of mixed oxides of the type 6CaOÁSrOÁ3Al 2 O 3 Á ZrO 2 documented using microcalorimetry was supported by investigations of the solid hydration products. Research showed that the hexagonal hydrates were stable at early and middle curing ages, an indication that including Sr in solid solution could effectively inhibit the conversion from both C 4 AH 13-19 and C 2 AH 8 to C 3 AH 6 and AH 3 . Calcium monocarboaluminate C 4 A CH 11 phases were also found in this system due to the carbonation process of C 4 AH 13 phase. Substitution of Ca 2? ions by Sr 2? ions in hexagonal calcium aluminate hydrates causes structural disorder and then contributes to the broadening of lines in the powder X-ray diffraction patterns of layered structures of metastable hydrates. At later curing ages, the formation of two hydrogarnet phases, one Sr-rich (C,Sr) 3 AH 6 and the other Ca-rich (C,Sr) 3 AH 6 , was proved.