n-Al2O3P/Ni复合刷镀层的组织和摩擦磨损特性

研究了镍基纳米Al2O3复合电刷镀层（n-Al2O3^p/Ni）的组织特征及擦磨损特性，并与快镍刷镀（Ni)进行了比较。结果表明：n-Al2O3^p/Ni复合刷镀层表面粗糙度更小，组织更致密，镀层摩擦系数随镀液中纳米粒子含量增加稍有增大；n-Al2O3在复合刷镀层中弥散分布，与基相良好结合；复合镀的耐磨性能明显优于Ni刷镀层，镀液中n-Al2O3含量为20g/L时，复合刷镀层具有最佳耐磨性能。     

宽带激光熔覆WCP/Ni基合金梯度复合涂层组织与摩擦磨损特性

研究了铸造WC_P/Ni基合金梯度复合涂层组织与摩擦磨损特性。结果表明,梯度复合涂层与基材实现了良好的冶金结合,涂层内有γ-Ni枝晶组织,γ-Ni＋M₂₃C 6共晶组织以及凝固结晶析出的M₆C、M₂₃C₆、M₇C₃等块状或条状组织;随着铸造WC_P体积分数的增加,复合涂层摩擦系数减小,耐磨性增加。19-4试样的耐磨性最高值为4.61,是基材的3倍以上。梯度涂层的磨损机理为磨粒磨损与粘着磨损的复合作用。     

Determination of Discrete-Structure Parameters of Coatings with Allowance for Residual Stresses

The authors suggest that the dimensions of a discrete section of a coating should be chosen on the basis of calculation of the critical crack spacing in cohesion cracking. This approach allows for residual stresses in the coating. The reliability of the calculation method has been verified experimentally by direct measurement of the crack spacing.     

长输管道不停输防腐层大修技术

东河塘至轮南输油管道,经过12年的运行,钢管外石油沥青玻璃布防腐层已严重老化甚至剥离。在不停输的情况下,对输油管道防腐层大修,特别像东—轮线输油管道,地处沙漠边缘、戈壁地带,没有成熟的施工经验可以借鉴。文章根据东—轮线输油管道防腐层大修的施工实践,详细介绍了长输管道不停输防腐层大修的施工工艺和质量保证措施。     

薄膜包衣技术及应用

对薄膜包衣技术及其在制剂生产中应用的研究进展作一综述。     

Synthesis and Evaluation of Blends Formed by Polymeric Crown Ethers and a Fullerene-Containing Primary Ammonium Salt in Organic Thin Films

The synthesis of a series of polymers and cyclopolymers bearing crown ethers of differing structure and affinities towards primary ammonium ions is discussed. These polymers have been tested in their efficiency to form structurally homogeneous thin films when blended with an amphiphilic C₆₀ compound containing a primary ammonium ion functional group. The X-ray reflectivity characterization of the films revealed that the polymer bearing the crown ether with the least affinity for primary ammonium ions, but having the highest degree of polymerization, is the most effective in forming structurally homogeneous thin films.     

Thermal Conductivity Measurement of an Electron-Beam Physical-Vapor-Deposition Coating

An industrial ceramic thermal-barrier coating designated PWA 266, processed by electron-beam physical-vapor deposition, was measured using a steady-state thermal conductivity technique. The thermal conductivity of the mass fraction 7 % yttria-stabilized zirconia coating was measured from 100 °C to 900 °C. Measurements on three thicknesses of coatings, 170 μm, 350 μm, and 510 μm resulted in thermal conductivity in the range from 1.5 W/(m·K) to 1.7 W/(m·K) with a combined relative standard uncertainty of 20 %. The thermal conductivity is not significantly dependent on temperature.     

Ideally selective diisocyanate building blocks: New perspectives for dendrimers and coating binders

Using zirconium (IV) salts as catalyst, the reaction of a diisocyanate carrying one tertiary and one primary isocyanate group (IMCI, DIMP) with alcohols can be conducted with complete regioselectivity. This unique selectivity enables the use of a diisocyanate building block in unprecedented ways. Incomplete regioselectivity of diisocyanates, as commonly encountered in currently commercial ones like IPDI and TDI, inevitably leads to polydisperse products in reaction with polyols. The ultimate monodisperse polymer architecture, dendrimers, can now be made in a facile, straightforward manner using IMCI as the ideal diisocyanate building block. Coating applications of this unique building block are not restricted to these perfect branching polymers, but also include isocyanate-functional coating resins. Without any increase in polydispersity, a hydroxyl-functional polyester can be end-capped with the IMCI diisocyanate and subsequently serve as a crosslinker in powder coatings.     

In situ polymerization and characterization of polyester‐based polyurethane/nano‐silica composites

Polyester‐based polyurethane/nano‐silica composites were obtained via in situ polymerization and investigated by Fourier‐transform infrared spectroscopy (FTIR), or FTIR coupled with attenuated total reflectance (FTIR‐ATR), Transmission electron microscopy (TEM), atomic force microscopy (AFM), an Instron testing machine, dynamic mechanical analysis (DMA) and ultraviolet‐visible spectrophotometry (UV‐vis). FTIR analysis showed that in situ polymerization provoked some chemical reactions between polyester molecules and nano‐silica particles. FTIR‐ATR, TEM and AFM analyses showed that both surface and interface contained nano‐silica particles. Instron testing and DMA data showed that introducing nano‐silica particles into polyurethane enhanced the hardness, glass temperature and adhesion strength of polyurethane to the substrate, but also increased the resin viscosity. UV‐vis spectrophotometry showed that nano‐silica obtained by the fumed method did not shield UV radiation in polyurethane films. Copyright © 2003 Society of Chemical Industry