Department of Materials Science and Engineering, McMaster University, Hamilton, Ontario, Canada.
J Colloid Interface Sci. 2012 Aug 15;380(1):8-15. doi: 10.1016/j.jcis.2012.04.077. Epub 2012 May 11.
Bio-inspired chemical approach has been developed for the surface modification and electrophoretic deposition of manganese dioxide and zirconia nanoparticles, prepared by chemical precipitation methods. Caffeic acid, trans-cinnamic acid, p-coumaric acid, and 2,4-dihydroxycinnamic acid were investigated for the surface modification of the nanoparticles. The influence of the structure of the organic molecules on their adsorption on the oxide nanoparticles has been investigated. The mechanism of caffeic acid adsorption was similar to that of natural catecholic amino acid, L-3,4-dihydroxyphenylalanine. The use of caffeic acid allowed for agglomerate-free synthesis, efficient dispersion, charging, electrophoretic deposition and co-deposition of manganese dioxide and zirconia nanoparticles. The deposition yield data, coupled with the results of thermogravimetric analysis, X-ray diffraction analysis, and Fourier transform infrared spectroscopy, showed that surface chemistry, rather than the crystal structure, determined the adsorption behavior. Electron microscopy and energy dispersive spectroscopy investigations showed the formation of nanostructured oxide films and composites. The deposit composition can be varied.
已经开发出一种仿生化学方法,用于通过化学沉淀法制备的二氧化锰和氧化锆纳米粒子的表面改性和电泳沉积。研究了咖啡酸、反式肉桂酸、对香豆酸和 2,4-二羟基肉桂酸对纳米粒子的表面改性。考察了有机分子结构对其在氧化物纳米粒子上吸附的影响。咖啡酸的吸附机制与天然儿茶酚氨基酸 L-3,4-二羟基苯丙氨酸相似。使用咖啡酸可以实现无团聚体的合成、有效分散、充电、电泳沉积和二氧化锰和氧化锆纳米粒子的共沉积。沉积产率数据,结合热重分析、X 射线衍射分析和傅里叶变换红外光谱的结果表明,表面化学而非晶体结构决定了吸附行为。电子显微镜和能谱分析研究表明形成了纳米结构的氧化物薄膜和复合材料。沉积物的组成可以改变。