Department of Applied Chemistry, Faculty of Engineering, Osaka Institute of Technology, 5-16-1 Ohmiya, Asahi-ku, Osaka, 535-8585, Japan.
Langmuir. 2012 Feb 7;28(5):2436-47. doi: 10.1021/la204324f. Epub 2012 Jan 18.
A range of near-monodisperse, multimicrometer-sized polymer particles has been coated with ultrathin overlayers of polypyrrole-palladium (PPy-Pd) nanocomposite by chemical oxidative polymerization of pyrrole using PdCl(2) as an oxidant in aqueous media. Good control over the targeted PPy-Pd nanocomposite loading is achieved for 5.2 μm diameter polystyrene (PS) particles, and PS particles of up to 84 μm diameter can also be efficiently coated with the PPy-Pd nanocomposite. The seed polymer particles and resulting composite particles were extensively characterized with respect to particle size and size distribution, morphology, surface/bulk chemical compositions, and conductivity. Laser diffraction studies of dilute aqueous suspensions indicate that the polymer particles disperse stably before and after nanocoating with the PPy-Pd nanocomposite. The Fourier transform infrared (FT-IR) spectrum of the PS particles coated with the PPy-Pd nanocomposite overlayer is dominated by the underlying particle, since this is the major component (>96% by mass). Thermogravimetric and elemental analysis indicated that PPy-Pd nanocomposite loadings were below 6 wt %. The conductivity of pressed pellets prepared with the nanocomposite-coated particles increased with a decrease of particle diameter because of higher PPy-Pd nanocomposite loading. "Flattened ball" morphologies were observed by scanning/transmission electron microscopy after extraction of the PS component from the composite particles, which confirmed a PS core and a PPy-Pd nanocomposite shell morphology. X-ray diffraction confirmed the production of elemental Pd and X-ray photoelectron spectroscopy studies indicated the existence of elemental Pd on the surface of the composite particles. Transmission electron microscopy confirmed that nanometer-sized Pd particles were distributed in the shell. Near-monodisperse poly(methyl methacrylate) particles with diameters ranging between 10 and 19 μm have been also successfully coated with PPy-Pd nanocomposite, and stable aqueous dispersions were obtained. The nanocomposite particles functioned as an efficient catalyst for the aerobic oxidative homocoupling reaction of 4-carboxyphenylboronic acid in aqueous media for the formation of carbon-carbon bonds. The composite particles sediment in a short time (<several tens of minutes) by gravity alone and hence recycling of this catalyst is easy.
一系列具有近单分散性、多微米尺寸的聚合物颗粒已通过在水溶液中使用 PdCl2 作为氧化剂,通过吡咯的化学氧化聚合被涂覆有超薄的聚吡咯-钯(PPy-Pd)纳米复合材料层。对于 5.2μm 直径的聚苯乙烯(PS)颗粒,可以很好地控制目标 PPy-Pd 纳米复合材料的负载量,并且高达 84μm 直径的 PS 颗粒也可以有效地用 PPy-Pd 纳米复合材料进行涂覆。种子聚合物颗粒和所得复合颗粒在颗粒尺寸和尺寸分布、形态、表面/体化学组成和电导率方面进行了广泛的表征。对稀释的水性悬浮液的激光衍射研究表明,在涂覆 PPy-Pd 纳米复合材料之前和之后,聚合物颗粒都能稳定分散。涂覆有 PPy-Pd 纳米复合材料覆盖层的 PS 颗粒的傅里叶变换红外(FT-IR)光谱主要由基础颗粒主导,因为这是主要成分(>质量的 96%)。热重分析和元素分析表明,PPy-Pd 纳米复合材料的负载量低于 6wt%。由于较高的 PPy-Pd 纳米复合材料负载量,用纳米复合材料涂覆的颗粒制备的压片的电导率随着颗粒直径的减小而增加。从复合颗粒中萃取 PS 成分后,通过扫描/透射电子显微镜观察到“扁平球”形态,这证实了 PS 核和 PPy-Pd 纳米复合材料壳的形态。X 射线衍射证实了元素 Pd 的生成,X 射线光电子能谱研究表明复合颗粒表面存在元素 Pd。透射电子显微镜证实纳米尺寸的 Pd 颗粒分布在壳中。直径在 10 到 19μm 之间的近单分散性聚甲基丙烯酸甲酯(PMMA)颗粒也已成功涂覆 PPy-Pd 纳米复合材料,并获得了稳定的水性分散体。纳米复合材料颗粒在水介质中用作对羧基苯硼酸的有氧氧化偶联反应的有效催化剂,用于形成碳-碳键。复合颗粒通过重力在短时间内(<数十分钟)沉淀,因此这种催化剂易于回收。