碳纤维经氧等离子/KH550处理后的表面形态和结构

碳纤维(CF)表面经氧等离子、KH550和 LiAlH_4处理后,其物理和化学性能得以改善.由于提高了 CF 和树脂间的联结,使 CF 复合材料的层间剪切强度提高50%以上,在湿热下的强度保留率达94%以上.使用纤维接触角测定仪,SEM 和 XPS 等对 CF 表面的浸润性、形态和化学组成进行了研究.实验指出:CF 经等离子和 KH550处理后,其临界表面能有了提高;CF 本身仅受氧离子刻蚀,故其拉伸强度的损失小于其他处理方法.     

大型空分制氧站DCS调试技术

以宝钢集团浦钢60000 Nm3/h的大型空分制氧站DCS调试为基础,结合以往大型空分制氧站DCS调试经验,探讨了大型空分制氧站DCS调试的特点、施工组织、调试工艺及方法,并对控制回路试验、离心式压缩机防喘振控制组态、压缩机起停及控制逻辑、紧急停车及重要安全回路调试、组态临时变更管理等重点、难点及关键环节的调试技术进行了详细的总结、说明,旨在为其他同类工程提供参考与借鉴.     

双阳煤在PKM气化炉试烧总结

介绍了在PKM气化炉中弱粘结性双阳煤的试烧情况,并给出了主要工艺参数控制范围。试烧结果表明:依兰煤中配入50%双阳煤,汽氧比6.0:1时,气化炉工况良好。     

On the nature of the active state of silver during catalytic oxidation of methanol

Under the applied high reaction temperatures (900 K) the Ag surface is restructured and a tightly held oxygen species is formed on the surface (O) apart from O atoms dissolved in the bulk (O). Methanol oxidation to formaldehyde proceeds through this O species as demonstrated by application of a variety of spectroscopic techniques.     

High catalytic activity of PdOx/MnO2 for CO oxidation and importance of oxidation state of Mn

PdO_x/MnO₂ has been examined as a catalyst for CO oxidation using a conventional flow reactor at reaction temperatures between 50 and 150°C. In the reaction conditions of GHSV (gashourlyspacevelocity) of 1.22 × 10⁵/h and CO concentration of 2000 ppm, PdO_x/MnO₂ showed higher catalytic activity compared with PdO_x/Mn₂O₃, which had been previously reported as an effective catalyst due to the cooperative action of Pd and Mn₂O₃ for this reaction. The reason for higher activity of PdO_x/MnO₂ than PdO_x/Mn₂O₃ has been investigated using TPR (temperatureprogrammed reduction) and XPS studies. TPR showed that PdO_x/MnO₂ could be reduced by CO at much lower temperature than PdO_x/Mn₂O₃. During the experiment of reduction and oxidation, XPS showed that the valence of Mn in the PdO_x/MnO₂ was between 4+ and 3+, which is higher than that of Mn in the PdO_x/Mn₂O₃ catalyst of which the valence has been reported to be between 3+ and 2+. It is known that in this catalyst system the support supplies oxygen onto Pd, where the oxidation occurs with adsorbed CO, and the ability of the support to provide oxygen improves the performance of the catalyst. Therefore, it was concluded that the readiness of MnO₂ to be reduced with maintaining a higher oxidation state showed higher CO oxidation activity than Mn₂O₃ as support for PdO_x.     

介体型水质BOD生物电化学传感器研究进展

生物化学需氧量(BOD)是目前国际上用来衡量水质有机物污染的重要指标之一。由于水体中氧的溶解度非常低,以电子媒介体代替溶解氧为电子受体的介体型BOD生物电化学传感器以其快速、准确、稳定等优点得到了较快的发展。论述了介体型水质BOD生物电化学传感器的发展现状及研究动态,重点讨论了介体型水质BOD生物电化学传感器的工作原理、构成及类型,分析了不同类型传感器的优缺点,并对其核心部分-微生物膜的制备方法做了比较详细的介绍。     

磁氧分析仪在焦化回收系统的应用

分析磁氧分析仪在实际生产中存在的问题,并提出改造措施,以提高电捕焦油器的安全性和稳定性。     

The reduction/oxidation behaviour of MnAPO-5 as studied by ESR spectroscopy

It is shown by ESR spectroscopy that Mn²⁺ ions in MnAPO-5 are oxidized to Mn³⁺ during calcination atT475 K. Mn²⁺ occupies variously distorted tetrahedral positions within the framework and in extra-lattice sites. Octahedrally coordinated Mn²⁺ presumably located in the channels becomes detectable after adsorption of water. The ESR spectra of reduced MnAPO-5 show line-narrowing due to spin exchange interactions. The material behaves reversible in redox cycles at temperatures near 500 K.     

Electrochemical and microstructural characterization of cyclic redox behaviour of SOFC anodes

The oxidation of Ni to NiO in solid oxide fuel cell (SOFC) anode will result in large bulk volume change, which may change the interfaces of the two phases in the anode cermet and thus may cause significant performance degradation. The reduction and oxidation (redox) of the Ni/YSZ cermet were studied at 800 ℃. Anodic polarization measurements were performed before and after redox cycles. The anode current density at an overpotential of 100 mV kept decreasing during the whole redox treatment. It decreased from 19.11 to 7.95 mA·cm-2 after two redox cycles. Anode supported unit cell was assembled for cell's discharge measurements. Cell performance declined after each redox cycle. The maximum power density decreased from 126.28 to 40.32 mW·cm-2 . The microstructural changes after redox cycling were recorded using scanning electron microscopy (SEM). The results reveal that after re-oxidation, the Ni gets coarse and has a higher porosity; the nickel network structure turns to be desultory.     

High-temperature oxidation of SiC in a glow-discharge oxygen plasma

The oxidation kinetics and structure of the oxide scales formed on high-density SiC were studied in molecular oxygen at 740 Torr and in a glow-discharge oxygen plasma at 0.1 Torr at temperatures of 1000, 1100, and 1200°C. The monatomic oxygen formed by the glow discharge markedly increased the reaction rate and the vaporization of some of the oxidation products. The marked differences in kinetics suggest that the rate-controlling step during oxidation in molecular oxygen is the dissociation of adsorbed diatomic oxygen to the monatomic species. Films formed in molecular oxygen were mostly amorphous SiO₂ with small inclusions of SiC and graphite, whereas films formed in dissociated oxygen were primarily amorphous SiO₂ containing SiO, S₂O₃, and the coesite form of SiO₂.