US Environmental Protection Agency, 919 Kerr Research Drive, Ada, OK 74820, USA.
J Colloid Interface Sci. 2011 Nov 1;363(1):84-91. doi: 10.1016/j.jcis.2011.06.085. Epub 2011 Jul 14.
This study investigated the sedimentation and aggregation kinetics of titanium dioxide (TiO(2)) nanoparticles with varying material properties (i.e., crystallinity, morphology, and chemical composition). Used in the study were various types of commercially available TiO(2) nanoparticles: three spherical anatase (nominal diameters of 5, 10, and 50 nm) and two rutile nanoparticles (10×40 and 30×40 nm). The 50 nm anatase and 10×40 nm rutile showed higher stability in deionized water and 5 mM NaCl solutions at pH 7 than the 5, and 10 nm anatase nanoparticles in sedimentation experiments. In aggregation experiments, critical coagulation concentration values for the 50 nm anatase were the highest, followed by the 10×40 nm rutile and the 5 nm anatase nanoparticles in NaCl and CaCl(2) solutions. The aggregation kinetics was fitted reasonably well with the Derjaguin-Landau-Verwey-Overbeek (DLVO) equations for the TiO(2) nanoparticles tested. Results showed that crystallinity and morphology are not influential factors in determining the stability of TiO(2) nanoparticle suspensions; however, the differences in their chemical compositions, notably, the varying concentrations of impurities (i.e., silicon and phosphorus) in the pristine materials, determined the surface charge and therefore the sedimentation and aggregation of TiO(2) nanoparticles in the aqueous phase.
本研究考察了具有不同材料特性(即结晶度、形态和化学成分)的二氧化钛(TiO2)纳米粒子的沉降和聚集动力学。研究中使用了各种市售的 TiO2 纳米粒子:三种球形锐钛矿(名义直径为 5、10 和 50nm)和两种金红石纳米粒子(10×40 和 30×40nm)。在沉降实验中,50nm 锐钛矿和 10×40nm 金红石在去离子水和 pH7 的 5mMNaCl 溶液中的稳定性高于 5nm 和 10nm 锐钛矿纳米粒子。在聚集实验中,在 NaCl 和 CaCl2 溶液中,50nm 锐钛矿的临界聚沉浓度值最高,其次是 10×40nm 金红石和 5nm 锐钛矿纳米粒子。对于所测试的 TiO2 纳米粒子,聚集动力学与德加古因-兰德劳-韦尔拜(DLVO)方程拟合得相当好。结果表明,结晶度和形态不是决定 TiO2 纳米粒子悬浮液稳定性的影响因素;然而,它们化学成分的差异,特别是原始材料中杂质(即硅和磷)的浓度不同,决定了 TiO2 纳米粒子在水相中的表面电荷,从而决定了其沉降和聚集。