排序方式: 共有12条查询结果,搜索用时 223 毫秒
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涡轮叶尖泄漏流动对涡轮通道内流动损失有着显著影响,叶顶冷气射流对控制叶尖泄漏流动和改善涡轮叶尖气热性能有重要意义。本文利用数值模拟方法,研究了叶顶冷气喷射位置和喷射流量对高压涡轮凹槽叶顶间隙泄漏流动控制的影响。文中重点分析了泄漏流动结构及涡轮气动效率的变化,探讨了冷气对刮削涡这一间隙内主控流动结构演化的影响。研究表明,冷气孔位置的变化对间隙内刮削涡的演化造成了一定影响,但并未造成涡轮整体效率的较大变化;而冷气喷射流量不仅影响到刮削涡结构演化,而且导致了涡轮级效率近0.5%的变化。 相似文献
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溶剂化金属原子浸渍法制备Pd-Cu/γ-Al2O3低温CO氧化催化剂 总被引:5,自引:0,他引:5
Nano-particle Pd/γ-Al2O3 monometallic and Pd-Cu/γ-Al2O3 bimetallic catalysts were prepared by solvated metal atom impregnation (SMAI) method. The results of XRD measurement indicated that Pd- Cu alloy was formed in the bimetallic catalysts and the crystalline particle size of the alloy increased as Cu contents increased with av-erage diameters < 6.0nm for all the samples. XPS and Auger spectra showed that Pd was in zero- valent state, Cu existed mainly in zero- valent state and partially in monovalent state Cu+. The Pd/γ-Al2O3 and Pd-Cu/γ-Al2O3 catalysts exhibited higher activity for CO oxidation at low temperature. The activity of Pd-Cu/γ-Al2O3 bimetallic catalyst was higher than that of Pd/γ-Al2O3 monometallic catalyst. The Pd-Cu/γ-Al2O3 catalyst with Pd/Cu atomic ratio of 1∶1 showed the highest activity. 相似文献
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采用浸渍化学还原法制备羟基硅酸镁纳米管(MgSNTs)负载非晶态钴硼催化剂(Co-B/MgSNTs)。应用X衍射技术(XRD),透射电子显微镜(TEM),X射线光电子能谱仪(XPS),元素分析(ICP)和比表面积(BET)分析等手段对催化剂进行了表征。研究了催化剂对于环己烯氢甲酰化反应的催化活性及循环使用。研究结果表明,具有高比表面积(250 m2·g-1)、较强耐受性和稳定性的MgSNTs可以有效的分散金属粒子,防止活性中心团聚和流失,催化环己烯的转化率为75.8%,醛的选择性为65.8%,实验重复3次以上,催化剂依然保持良好的催化活性和选择性。 相似文献
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不同方法掺杂Au对纳米α-Fe2O3气敏性能的影响 总被引:1,自引:0,他引:1
分别采用共沉淀法、浸渍法、紫外辐照法制备了掺杂不同Au含量的α-Fe2O3纳米粉体,并制作了旁热式厚膜型气敏元件.用XRD、TG-DTA和TEM技术对纳米晶的晶型、晶粒大小及形貌进行了表征.考察了掺杂方法、Au含量及焙烧温度对α-Fe2O3气敏性能的影响.结果表明,采用三种方法掺杂适量Au后,都使α-Fe2O3的气敏性有了显著提高,其中采用共沉淀法,在400℃焙烧的Au质量分数为1.5%的α-Fe2O3的气敏性最佳. 相似文献
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Hong-Yan Wu Hong Li Bao-Lin Zhu Shu-Rong Wang Shou-Min Zhang Shi-Hua Wu Wei-Ping Huang 《Transition Metal Chemistry》2008,33(1):9-15
Two new blue luminescent Zn(II) complexes, [ZnL2(H2O)]Cl2 · H2O (1) and [ZnL2Cl][ZnLCl2] · NO3 (2) (L = 2-aminomethylbenzimidazole) have been synthesized and characterized spectroscopically and crystallographically. The
structure of complex (1) can be described as a square pyramid. In the complex (2), there are two units [ZnLCl2] (a), and [ZnL2Cl]+ (b), which have a distorted tetrahedral geometry and a slightly distorted trigonal bipyramidal coordination geometry, respectively.
In these complexes, significant multiple inter- and intra-molecular hydrogen bonding and π–π stacking interactions are shown.
These contacts lead to aggregation and supramolecular assembly of complexes (1) and (2) into 3D and 2D frameworks, respectively. Fluorescent analysis in the dilute DMF solution and solid state shows that both
complexes exhibit intense emission in blue region. They display high blue luminescence quantum efficiency due to a metal-to-ligand
charge transfer (MLCT) and have a bathochromic shift of the emission energy compared with the free ligand L. The emission
intensity of complex (2) is higher than that of complex (1). 相似文献
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钛酸盐纳米管与二硫化碳修饰钛酸盐纳米管的合成、表征及其去除重金属离子性能 总被引:1,自引:0,他引:1
在水热法制备钛酸盐纳米管的基础上, 通过形成黄原酸基反应合成了CS2修饰的钛氧纳米管. 采用粉末X射线衍射(XRD)、透射电镜(TEM)、红外光谱(FTIR)和拉曼光谱(Raman)等技术对产物进行了表征. 以水溶液中铅离子、铜离子和银离子作为目标重金属离子, 分别用纯钛酸盐纳米管和CS2修饰后的钛氧纳米管对其进行反应和吸附, 通过一系列对比性实验, 评价了不同形式纳米管去除重金属的能力. 实验结果表明, 与文献报道的吸附剂对重金属离子的吸附量相比, 纯钛酸盐纳米管和CS2修饰的钛氧纳米管吸附重金属离子的容量非常大, 尤其是经CS2修饰后的钛氧纳米管去除铅离子的能力明显增强, 它们去除重金属离子的能力还与重金属盐的阴离子、溶液的pH值相关. 在相同的pH条件下, 钛酸盐纳米管去除铅离子、铜离子和银离子的能力分别为599.37, 163.22和474.73 mg/g; CS2修饰的钛氧纳米管去除铅离子、铜离子和银离子的能力分别为663.37, 160.21和423.05 mg/g. 相似文献
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Shu-Ping Wang Xiao-Ying Wang Xiu-Cheng Zheng Shu-Rong Wang Shou-Min Zhang Wei-Ping Huang Shi-Hua Wu 《Reaction Kinetics and Catalysis Letters》2006,89(1):37-44
Summary Copper oxide catalysts supported on Ce0.8Zr0.2O2 were prepared via an impregnation method and characterized by XRD and H2-TPR techniques. The catalytic activity of the samples for low-temperature CO oxidation was investigated by means of a microreactor-GC
system. The influence of calcination temperature, calcination time and different CuO content on the catalytic activity was
studied. TPR analysis indicated that well-dispersed CuO was responsible for the low-temperature CO oxidation. The results
of the investigation showed that the calcination temperature and CuO loadings had larger influence than the calcination time. 相似文献
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