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A series of A‐modified hexaaluminates, ANiAl11O19-δ (A = Ca, Sr, Ba and La) as new catalysts for carbon dioxide reforming of methane to synthesis gas, were prepared by decomposition
of nitrates and calcination at high temperature. Nickel ions as active component were inlayed in the hexaaluminate lattices
to substitute part of Al ions. The structure and properties of these samples were characterized using XRD, XPS, TPR and TGA
techniques. The series of hexaaluminates exhibited significantly catalytic activity and stability at high temperature, for
instance at 780°C for 18 h, the conversion of CH4 and CO2 was kept over 91.0 and 93.7%, respectively, meanwhile no Ni sintering, phase transformation and catalyst deactivation due
to carbon deposition were found. Besides, the modifier A in the mirror plane layer of the lattices showed different effects
on reducibility and catalytic activity of transition metal Ni in the hexaaluminate lattices.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
106.
(Z)-11-Octadecenyl acetate (Z11–18Ac) and (Z)-11-eicosenyl acetate (Z11–20Ac) were identified as the aggregation pheromones ofDrosophila ananassae, andZ11–20Ac was identified as the aggregation pheromone ofDrosophila bipectinata. Z11–18Ac andZ11–20Ac were not attractive alone; however, in combination with fermenting food odors, the acetates attracted flies of both sexes in a wind-tunnel olfactometer. The pheromones were present in the ejaculatory bulb of sexually mature male flies and transferred to the female during mating. MaleD. bipectinata released little if anyZ11–20Ac to the food; however, recently mated females releasedZ11–20Ac to the surrounding surfaces in just a few hours after mating.D. ananassae males, on the other hand, appeared to release moreZ11–18Ac andZ11–20Ac to the surroundings than mated females. AlthoughD. bipectinata males had noZ11–18Ac, flies were as attracted toZ11–18Ac as to an equal quantity ofZ11–20Ac.D. ananassae were attracted toZ11–18Ac but not toZ11–16Ac orZ11–20Ac. However,Z11–20Ac in combination withZ11–18Ac was significantly more attractive thanZ11–18Ac alone. 相似文献
107.
A monolayer of Keggin-type heteropolyanion [SiNi(H2O)W11O39]6− was fabricated by electrodepositing [SiNi(H2O)W11O39]6− on cysteamine modified gold electrode. The monolayer of [SiNi(H2O)W11O39]6− modified gold electrode was characterized by atomic force microscopy (AFM) and electrochemical method. AFM results showed the [SiNi(H2O)W11O39]6− uniformly deposited on the electrode surface and formed a porous monolayer. Cyclic voltammetry exhibited one oxidation peak and two reduction peaks in 1.0 M H2SO4 in the potential range of −0.2 to 0.7 V. The constructed electrode could exist in a large pH (0-7.6) range and showed good catalytic activity towards the reduction of bromate anion (BrO3−) and nitrite (NO2−), and oxidation of ascorbic acid (AA) in acidic solution. The well catalytic active of the electrode was ascribed to the porous structure of the [SiNi(H2O)W11O39]6− monolayer. 相似文献
108.
通过对TC11钛合金进行不同表面改性实验(微弧氧化、N+离子注入、DLC多层膜),得到不同表面改性膜层。利用扫描电子显微镜(SEM),X射线衍射(XRD)和Raman光谱研究表面改性层的相组成和微结构。在模拟海水环境下,采用SRV-IV微动磨损试验机评价TC11合金及不同表面改性膜层的微动磨损性能(摩擦系数、磨损量及磨损机制),并比较抗微动防护效果。结果表明,TC11经改性后摩擦系数呈现不同程度下降,磨损量的降低则非常明显,其中DLC多层膜抗微动防护效果最显著。海水介质中各摩擦系数显著比纯水中低。海水中钛合金的磨损量小于纯水中的数值,腐蚀与磨损呈"负交互作用"规律,而改性层磨损较纯水中略高。 相似文献
109.
采用真空电子束焊对Ti3Al合金与TC11合金进行焊接,研究焊接电流对Ti3Al /TC11焊缝区组织及合金元素扩散的影响。结果表明,随焊接电流增大,焊缝区组织明显粗化,且晶粒尺寸差异逐渐减小;当焊接电流增大至25 mA时,焊缝区组织为粗大β柱状晶。焊接电流对焊缝区各合金元素含量影响较小,但对其均匀性影响较显著,这与焊缝区显微组织形貌有关。随焊接电流的增大,焊缝区合金元素含量均匀性变差。 相似文献
110.
The effect of an NiAl microcrystalline coating prepared by magnetron sputtering on the high-temperature oxidation behavior of NiAl–28Cr–5Mo–1Hf was investigated in static air at 1000–1150°C. The additions of Cr, Mo, and Hf changed the single 11gq7454214v154/xxlarge946.gif" alt="beta" align="MIDDLE" BORDER="0">-phase structure into a multiphase structure [11gq7454214v154/xxlarge946.gif" alt="beta" align="MIDDLE" BORDER="0">-NiAl, 11gq7454214v154/xxlarge945.gif" alt="agr" align="BASELINE" BORDER="0">-Cr(Mo), and Heusler phase]. The NiAl–28Cr–5Mo–1Hf alloy formed a nonprotective mixed scale of Al2O3+Cr2O3+HfO2 and exhibited relatively large weight gains. The large weight gains were attributed to extensive internal oxidation. The sputtered NiAl microcrystalline coating remarkably improved the oxidation resistance of NiAl–28Cr–5Mo–1Hf due to the formation of a compact and adherent Al2O3 scale at all test temperatures. It was found that the 11gq7454214v154/xxlarge952.gif" alt="theta" align="BASELINE" BORDER="0">-11gq7454214v154/xxlarge945.gif" alt="agr" align="BASELINE" BORDER="0">-Al2O3 transformation caused the anomalous behavior of the oxidation–kinetics curves of the NiAl microcrystalline coating in the temperature range 1000–1150°C. A change in the morphology of scales occurred with the transformation. 相似文献