一种通过聚丙烯酸稳定无定形碳酸钙球的碳酸盐控制添加方法。
A carbonate controlled-addition method for amorphous calcium carbonate spheres stabilized by poly(acrylic acid)s.
作者信息
Huang Shu-Chen, Naka Kensuke, Chujo Yoshiki
机构信息
Department of Polymer Chemistry, Graduate School of Engineering, Kyoto University, Katsura, Nishikyo-ku, Kyoto, Japan.
出版信息
Langmuir. 2007 Nov 20;23(24):12086-95. doi: 10.1021/la701972n. Epub 2007 Oct 27.
Stable amorphous calcium carbonate (ACC) composite particle with a size-controlled monodispersed sphere was obtained by a new simple carbonate controlled-addition method by using poly(acrylic acid) (PAA) (Mw = 5000), in which an aqueous ammonium carbonate solution was added into an aqueous solution of PAA and CaCl2 with a different time period. The obtained ACC composite products consist of about 50 wt % of ACC, 30 wt % of PAA, and H2O. Average particle sizes of the ACC spheres increased from (1.8 +/- 0.4) x 102 to (5.5 +/- 1.2) x 102 nm with an increase of the complexation time of the PAA-CaCl2 solution from 3 min to 24 h, respectively. The ACC formed from the complexation time for 3 min was stable for 10 days with gentle stirring as well as 3 months under a quiescent condition in the aqueous solution. Moreover, the ACC was also stable at 400 degrees C. Stability of the amorphous phase decreased with an increase of the complexation time of the PAA-CaCl2 solution. No ACC was obtained when the lower molar mass PAAs (Mw = 1200 and 2100) were used. In the higher molar mass case (Mw = 25 000), a mixture of the amorphous phase and vaterite and calcite crystalline product was produced. The present results demonstrate that the interaction and the reaction kinetics of the PAA-Ca2+-H2O complex play an important role in the mineralization of CaCO3.
采用一种新的简单的碳酸盐控制添加法,通过使用聚(丙烯酸)(PAA,Mw = 5000),获得了具有尺寸可控的单分散球形的稳定无定形碳酸钙(ACC)复合颗粒,其中在不同时间段将碳酸铵水溶液添加到PAA和CaCl2的水溶液中。所获得的ACC复合产物由约50 wt%的ACC、30 wt%的PAA和水组成。随着PAA - CaCl2溶液的络合时间从3分钟增加到24小时,ACC球体的平均粒径分别从(1.8±0.4)×102 nm增加到(5.5±1.2)×102 nm。由3分钟络合时间形成的ACC在水溶液中温和搅拌下可稳定10天,在静止条件下可稳定3个月。此外,ACC在400℃时也稳定。无定形相的稳定性随着PAA - CaCl2溶液络合时间的增加而降低。当使用较低摩尔质量的PAA(Mw = 1200和2100)时,未获得ACC。在较高摩尔质量的情况下(Mw = 25000),产生了无定形相和球霰石以及方解石晶体产物的混合物。目前的结果表明,PAA - Ca2+ - H2O络合物的相互作用和反应动力学在CaCO3矿化中起重要作用。