The crystallinity, morphology, structure, shape and molecule size of precipitated calcium carbonate were directly influenced by the stirring action during the carbonation process. As depicted in the Fig. 1, SEM images of nano CaCO3 precipitated at different stirring rate varied from 700, 800, 900, 1000, 1100 and 1200 rpm had shown significant differences in morphology structure influenced by agitation rate, respectively. Results revealed that in Fig. 1 (a) and (b) the particle morphology was tended to rhombic-calcite. Meanwhile, Fig. 1 (c) and (d) showed structured more likely to needlelike-aragonite and Fig. 1 (e) and (f) were indicating to spherical-vaterite. This can be explicated from the perspective of the co-effects of micro-macro mixing and mass transfer theory. At low multiple impeller stirring rotation speed, the level of supersaturation had a wide variety of different local areas in the interface region between particle and agitation medium. Meanwhile, when the multiple impeller stirring rotation speed was excessively high, the micro-macro mixing was significantly increased, and the CO2 transfer coefficient was additionally intensified into the system. Higher multiple impeller stirring rotation speed also will provide a better homogeneity and heterogeneity of nucleation of nano-precipitated CaCO3. This finding was supported by previous researchers' work such as M. Wang et. al., Laifeng et. al. and Martin Back et. al. which described and discussed deeply about the transformation of CaCO3 morphology, influenced by numerous parameters
The crystallinity, morphology, structure, shape and molecule size of precipitated calcium carbonate were directly influenced by the stirring action during the carbonation process. As depicted in the Fig. 1, SEM images of nano CaCO3 precipitated at different stirring rate varied from 700, 800, 900, 1000, 1100 and 1200 rpm had shown significant differences in morphology structure influenced by agitation rate, respectively. Results revealed that in Fig. 1 (a) and (b) the particle morphology was tended to rhombic-calcite. Meanwhile, Fig. 1 (c) and (d) showed structured more likely to needlelike-aragonite and Fig. 1 (e) and (f) were indicating to spherical-vaterite. This can be explicated from the perspective of the co-effects of micro-macro mixing and mass transfer theory. At low multiple impeller stirring rotation speed, the level of supersaturation had a wide variety of different local areas in the interface region between particle and agitation medium. Meanwhile, when the multiple impeller stirring rotation speed was excessively high, the micro-macro mixing was significantly increased, and the CO2 transfer coefficient was additionally intensified into the system. Higher multiple impeller stirring rotation speed also will provide a better homogeneity and heterogeneity of nucleation of nano-precipitated CaCO3. This finding was supported by previous researchers' work such as M. Wang et. al., Laifeng et. al. and Martin Back et. al. which described and discussed deeply about the transformation of CaCO3 morphology, influenced by numerous parameters