Shen Zhi-Gang, Chen Jian-Feng, Zou Hai-kui, Yun Jimmy
Research Center of the Ministry of Education for High Gravity Engineering and Technology, Beijing University of Chemical Technology, Beijing 100029, People's Republic of China.
J Colloid Interface Sci. 2004 Jul 1;275(1):158-64. doi: 10.1016/j.jcis.2003.12.025.
The colloidal stability of nanosized barium titanate (BaTiO3) aqueous suspensions with ammonium polyacrylate (PAA-NH4) at different pH values has been investigated by means of zeta potential, adsorption isotherm, sedimentation, and rheology characterization. The isoelectric point of BaTiO3 powders is at pH 2.5 and the value of zeta potential is at its maximum near pH 10. The amount of leached barium ion decreases with increasing pH, but the change decreases with increasing initial pH. Adsorption of PAA-NH4 onto the surface of BaTiO3 decreases its zeta potential. Results show that PAA-NH4 adsorption follows Langmuir monolayer adsorption isotherms and the amount of PAA-NH4 required to stabilize nanosized BaTiO3 suspensions decreases as the pH increases. The mechanism of stabilization of BaTiO3 is shown to be electrosteric under the experimental conditions. Good agreement between zeta potential, sedimentation, and rheological tests is found, which identifies an optimum pH value of about 10 and an optimum dispersant concentration of about 2.0 wt%, independent of the solids volume fraction of suspensions.
通过zeta电位、吸附等温线、沉降和流变学表征研究了纳米钛酸钡(BaTiO3)水悬浮液与聚丙烯酸铵(PAA-NH4)在不同pH值下的胶体稳定性。BaTiO3粉末的等电点在pH 2.5,zeta电位值在pH 10附近达到最大值。浸出钡离子的量随pH值升高而减少,但随着初始pH值升高,这种变化减小。PAA-NH4在BaTiO3表面的吸附降低了其zeta电位。结果表明,PAA-NH4的吸附遵循朗缪尔单层吸附等温线,稳定纳米BaTiO3悬浮液所需的PAA-NH4量随pH值升高而减少。在实验条件下,BaTiO3的稳定机制显示为电空间稳定。发现zeta电位、沉降和流变学测试之间具有良好的一致性,确定了约10的最佳pH值和约2.0 wt%的最佳分散剂浓度,与悬浮液的固体体积分数无关。