乙二醇水热还原法制备纳米银

利用乙二醇在高温下的还原特性,在水热条件下制备了纳米银粒子,并通过透射电镜、X射线衍射、紫外吸收光谱对其结构进行了表征.研究结果表明:所制备的纳米银具有面心立方相的多晶结构,平均粒径在30nm左右,紫外吸收峰的位置在380 nm左右.分散剂和体系中含水量对纳米银的粒径有一定影响.     

纳米CeO2单晶的制备与热处理对粒径的影响

以Ce(NO3)3·6H2O为铈源、NH3·H2O为沉淀剂,用化学沉淀法通过对陈化时间的控制,制备了单分散的单晶纳米CeO2粒子,并用XRD、TEM、ED、BET、TG-DTA等测试手段对产物的物相结构、形貌和纳米尺度进行了表征.XRD分析表明,制得的纳米CeO2粒子为萤石结构且晶型比较完整. 通过控制热处理的温度和陈化时间可以控制粒子的大小.TEM和ED分析表明产物颗粒基本为球形,分散性较好且为单晶. 通过TG-DTA结果可以断定所制备的前驱体结构式为CeO2·1/2H2O.     

Role of platinum in the Na2SO4-Induced hot corrosion resistance of aluminum duffusion coatings

Electrochemical corrosion measurements have been carried out with Pt-containing and Pt-free Al-diffusion coatings on IN 738 LC in a 90Na₂SO₄+ 10K₂SO₄ (mol%) melt at 1173 K. Pt improves the resistance to basic fluxing while there are no significant differences between both coating types in their resistance to acidic fluxing. The corrosion resistance of the Pt-containing coating is also higher in the passive potential region where protective scales rich in Al₂O₃ are formed. The reason for the different behavior of both coating types appears to be related to the high corrosion resistance of the Pt-rich surface layer of the coating and an increased Al₂O₃ content in the scale of the Pt-containing type.     

Synthesis and characterization of La0.8Sr0.2MO3−δ (M=Mn, Fe, or Co) cathode materials by induction plasma technology

In this work, nanopowders of perovskite cathode materials (La_0.8Sr_0.2MnO_3−δ, La_0.8Sr_0.2FeO_3−δ, and La_0.8Sr_0.2CoO_3−δ), for use in solid oxide fuel cells (SOFC), were successfully synthesized, using induction plasma techniques. Their compositions, structures, morphology, particle size distributions, and BET specific surface areas were determined for comparison with their counterparts prepared by the Pechini method and by the glycine-nitrate combustion (GNC) technique. The particle sizes of the plasma-synthesized powders are mostly around 63 nm. These plasma-synthesized powders are generally globular, their BET specific surface areas being about 26 m²g⁻¹, approximately twice those of powders prepared by the GNC and Pechini methods. These plasma-synthesized powders are readily reproducible and are not agglomerated. Their individual particle sizes and distributions are very independent of their composition.     

超声和微波作用下制备纳米氧化铜

以氢氧化铜为前驱体，在超声和微波作用下制备纳米氧化铜。借助透射电镜（TEM）、X射线衍射（XRD）、粒度分析等手段，研究了超声、分散剂、微波等制备条件的影响。结果表明：采用该法可以制备粒径小（15nm）、分散良好的纳米氧化铜粉体；超声可使前驱体Cu（OH）2转变为CuO，并粉碎颗粒间形成的团聚；分散剂通过表面修饰抑制颗粒的团聚；微波加热促进了前驱体的转化，并抑制颗粒的长大。     

The influence of platinum on the maintenance of α-Al2O3 as a protective scale

The influence of externally located platinum on the isothermal stability of -Al₂O₃ scales formed at high temperatures has been examined. It has been observed that a nickel-base alloy forms an external scale of -Al₂O₃ during oxidation at 1200°C, but this scale breaks down isothermally, enabling a faster-growing Cr₂O₃-rich scale to develop. However, in the presence of platinum metal alongside the specimen in the furnace hot zone, the breakdown of the -Al₂O₃ scale is postponed for a substantial period of time. It appears that platinum, as the volatile species PtO₂, is incorporated into the growing -Al₂O₃ scale where it either influences the stress relief mechanism at temperature or reduces oxidation growth stress generation and thus significantly enhances the isothermal stability of the scale.     

基于纳米金颗粒放大的电化学传感器用于三聚氰胺的检测

三聚氰胺与胸腺嘧啶（T）之间能够通过三个氢键结合,以富T的DNA探针为识别元件,结合DNA修饰的纳米金颗粒放大技术,以电活性物质钌胺作为信号分子,发展了一种高灵敏检测三聚氰胺的电化学传感器,该传感器具有良好的特异性和灵敏度,检测下限低至0．5nmol／L。     

Three-dimensional automated nanoparticle tracking using Mie scattering in an optical microscope

The forward scattering of light in a conventional inverted optical microscope by nanoparticles ranging in diameter from 10 to 50nm has been used to automatically and quantitatively identify and track their location in three-dimensions with a temporal resolution of 200ms. The standard deviation of the location of nominally stationary 50-nm-diameter nanoparticles was found to be about 50nm along the light path and about 5nm in the plane perpendicular to the light path. The method is based on oscillating the microscope objective along the light path using a piezo actuator and acquiring images with the condenser aperture closed to a minimum to enhance the effects of diffraction. Data processing in the time and spatial domains allowed the location of particles to be obtained automatically so that the technique has potential applications both in the processing of nanoparticles and in their use in a variety of fields including nanobiotechnology, pharmaceuticals and food processing where a simple optical microscope maybe preferred for a variety of reasons.     

基于纳米银修饰电极的电位型铬（Ⅵ）传感器研究

纳米银修饰过的石墨电极在铬酸盐溶液中活化处理后,可制成一种新型的电位型铬传感器。将该传感器用于铬（Ⅵ）的测定,实验结果表明：此传感器对铬（Ⅵ）具有灵敏的电位响应,其线性范围较宽,为1．0×10^-7～1．0×10^-2mol·L^-1,检出限为4×10^-8mol·L^-1。应用于水样中铬（Ⅵ）的测定,结果符合分析要求。     

The application of inductively coupled plasma mass spectrometry in clinical pharmacological oncology research

Metal-based anticancer agents are frequently used in the treatment of a wide variety of cancer types. The monitoring of these anticancer agents in biological samples is important to understand their pharmacokinetics, pharmacodynamics, and metabolism. In addition, determination of metals originating from anticancer agents is relevant to assess occupational exposure of health care personnel working with these drugs. The high sensitivity of inductively coupled plasma mass spectrometry (ICP-MS) has resulted in an increased popularity of this technique for the analysis of metal-based anticancer drugs. In addition to the quantitative analysis of the metal of interest in a sample, ICP-MS can be used as an ultrasensitive metal selective detector in combination with speciation techniques such as liquid chromatography. In the current review we provide a systematic survey of publications describing the analysis of platinum- and ruthenium-containing anticancer agents using ICP-MS, focused on the determination of total metal concentrations and on the speciation of metal compounds in biological fluids, DNA- and protein-adducts, and environmental samples. We conclude that ICP-MS is a powerful tool for the quantitative analysis of metal-based anticancer agents from multiple sample sources.