Department of Chemistry and Materials Technology, Graduate School of Science and Technology, Kyoto Institute of Technology , Goshokaido-cho, Matsugasaki, Sakyo-ku, Kyoto 606-8585, Japan.
Langmuir. 2013 Dec 23;29(51):15888-97. doi: 10.1021/la403193e. Epub 2013 Dec 11.
Vaterite composite particles with a size-controlled sphere were obtained by a carbonate controlled-addition method by using a carboxylate-terminated poly(amidoamine) (PAMAM)-type polyhedral oligomeric silsesquioxane (POSS)-core dendrimer. An aqueous ammonium carbonate solution was added to an aqueous solution of the dendrimer and CaCl2 at different times (3 min, 30 min, and 1 h) and stirred for 1 h at 30 °C. When the complexation time of the POSS-core dendrimer-CaCl2 solution was increased from 3 min to 1 h, the average particle sizes of the spheres increased from 0.71 ± 0.08 to 1.86 ± 0.22 μm, respectively. However, the average particle sizes decreased with decreasing temperature. Particles with minimum sizes of 70 ± 6 nm were obtained when COONa to calcium ion molar ratio was 16 and the complexation time was 3 min at 20 °C. Incubation of the vaterite composite particles in distilled water for 3 days led to complete phase transition to calcite. Negative zeta potential values, ranging from -30 to -10 mV, were detected for the vaterite particles, indicating that the POSS-core dendrimers were exposed on the CaCO3 particles. The CaCO3 particle surfaces were successfully coated with poly(diallyldimethylammonium chloride) (PDDA) in aqueous dispersions by adding a controlled concentration of the polymer. Alternate vaterite composite particles and polyelectroyte multilayer films were prepared by a layer-by-layer method. The obtained (PDDA/vaterite)10(PDDA) multilayer films were incubated in distilled water at 30 °C. Incubation for 5 days led to complete phase transition to calcite, as estimated by Fourier transform infrared (FTIR) spectroscopic and XRD analyses. The SEM observation of the sample after 5 days of incubation showed a granular network structure of irregularly shaped calcite particles. Although some patches and pores were present in the films, the SEM image clearly demonstrated that large-area and continuous CaCO3 films were formed.
采用碳酸根离子控制添加法,利用末端为羧酸盐的聚酰胺-胺(PAMAM)型多面体低聚倍半硅氧烷(POSS)核树枝状大分子合成了粒径可控的方解石复合粒子。将碳酸铵水溶液在不同时间(3 min、30 min 和 1 h)下滴加到树枝状大分子和 CaCl2 的水溶液中,并在 30℃下搅拌 1 h。当 POSS 核树枝状大分子-CaCl2 溶液的络合时间从 3 min 增加到 1 h 时,球体的平均粒径分别从 0.71±0.08μm 增加到 1.86±0.22μm。然而,平均粒径随温度的降低而减小。当 COONa 与钙离子的摩尔比为 16,络合时间为 3 min,温度为 20℃时,得到了最小粒径为 70±6nm 的粒子。在蒸馏水中共孵育 3 天后,水碳酸钙复合粒子完全相变为方解石。水碳酸钙粒子的zeta 电位值为-30 至-10 mV,表明 POSS 核树枝状大分子暴露在 CaCO3 粒子上。通过加入可控浓度的聚合物,在水溶液中成功地将聚二烯丙基二甲基氯化铵(PDDA)涂覆在 CaCO3 粒子表面。通过层层自组装法制备交替的水碳酸钙复合粒子和聚电解质多层膜。所得(PDDA/水碳酸钙)10(PDDA)多层膜在 30℃的蒸馏水中孵育。FTIR 光谱和 XRD 分析表明,孵育 5 天后,样品完全相变为方解石。孵育 5 天后的样品 SEM 观察显示出不规则形状的方解石颗粒的颗粒状网络结构。尽管膜中存在一些斑点和孔隙,但 SEM 图像清楚地表明形成了大面积且连续的 CaCO3 膜。