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1.
VK Tzitzios V Georgakilas TN Angelidis 《Journal of chemical technology and biotechnology (Oxford, Oxfordshire : 1986)》2005,80(6):699-704
A study of nitrous oxide (N2O) reduction with methane (CH4) and propene (C3H6) in the presence of oxygen (5%) over Ag/Al2O3, Rh/Al2O3 and Ag–Rh/Al2O3 catalysts, with Ag and Rh loadings of 5 wt% and 0.05 wt% respectively, has been performed. From the results, it was observed that the Ag–Rh bimetallic catalyst was the most active for both nitrous oxide removal (more than 95%) and hydrocarbon oxidation. This high activity seems to be connected with a synergistic effect between Ag and Rh. The findings from X‐ray diffraction and X‐ray photoelectron spectroscopy studies showed also, that there were no strong interactions (eg alloying) between Ag and Rh. Copyright © 2005 Society of Chemical Industry 相似文献
2.
A seed-growth method has been applied to synthesize gold (Au) and Au-silver (Ag) bimetallic nanoparticles (NP) by using 12-3-12, a cationic Gemini surfactant, as a capping agent as well as micellar template. A systematic increase in the [12-3-12] from pre- to post-micellar region (up to 5 times the critical micelle concentration, cmc) produces Au NP from spherical to large plate like structures. Keeping [12-3-12] constant (equal to 1 / 2 cmc) and increasing ascorbic acid (AA) concentration lead to the formation of core shell type Au-Ag bimetallic NP. At maximum AA concentration (i.e. [AA] = 5.6 mM), fused bimetallic Au-Ag NP are obtained. The anisotropic growth of such materials is a key factor for various applications in nanotechnology. 相似文献
3.
Pt NaY and Pt In NaY adsorption properties have been compared by using probes like H2, C4H10, 2-C4H8 and microcalorimetry. It appears that the addition of In to Pt does not change the initial heat of H2 chemisorption but decreases the initial heat of butane and butene chemisorption. 相似文献
4.
通过对AlSn20Cu/Steel双金属板(带)复合轧制过程变形区变形规律的分析,确定了轧制过程的总变形率与各分层变形率的关系,解决了实际生产中各分层原料的厚度匹配问题。 相似文献
5.
An anomalous rate enhancement with increasing conversion has been observed during the liquid phase hydrogenation of nitrobenzene and crotonaldehyde over Ge/Pd/C catalysts at ambient temperature and atmospheric pressure. Inductive coupled plasma atomic emission spectroscopy and electrochemical measurement of the oxidation state of catalysts during reaction revealed that the bimetallic particles were partially oxidized by the reactants, which resulted in Ge-dissolution and increased exposure of Pd on the surface. It is proposed that the surface and bulk composition of Ge/Pd catalysts are a function of their oxidation state. This behaviour is due to the unusually high mobility of Ge in the Pd lattice and to the good solubility of GeO2 in polar solvents. The influence of hydrogen transport on the corrosion process and the stability of other X/Pd type bimetallic catalysts during liquid phase hydrogenation are also discussed. 相似文献
6.
The partial oxidation of methane to synthesis gas was studied at atmospheric pressure and in the temperature range of 550–800°C over -Al2O3-supported bimetallic Pt–Co, and monometallic Pt and Co catalysts, respectively. Both methane conversion and CO selectivity over a bimetallic Pt0.5Co1 catalyst were higher than those over monometallic Pt0.5 and Co1 catalysts. Furthermore, the addition of platinum in Pt–Co bimetallic catalysts effectively improved their resistance to carbon deposition with no coking occurring on Pt0.5Co1 during 80 h reaction. The FTIR study of CO adsorption observed only linearly bonded CO on bimetallic Pt–Co catalysts. TPR and XPS showed enhanced formation of a cobalt surface phase (CSP) in bimetallic Pt–Co catalysts. The origins of the good coking resistivity of bimetallic Pt–Co catalysts were discussed. 相似文献
7.
以四氢呋喃为溶剂 ,合成了含Sn、Fe的环戊烯基二羰基铁的异核双金属化合物 ,并对配合物进行了元素分析、IR光谱分析 ,使用SimensP4单晶衍射仪测定了配合物的晶体结构。结构分析表明 ,该配合物属于三斜晶系 ,空间群P - 1。晶胞参数 :a =10 0 79(2 )A° ,b =10 975 0 (10 )A°,c =17 14 5 (3)A° ;a =82 0 30 (10 )° ,β =77 770 (10 )°,γ =6 3 70 0 (10 )° ,Z =2 相似文献
8.
以Al_2O_3、PdCl_2和RuCl_3为原料,采用水溶液浸渍法,通过控制固载顺序、制备流程以及焙烧温度等条件,制得系列负载型Ru Pd双金属催化剂,并用于对苯二甲酸二甲酯(DMT)制取1,4-环己烷二甲酸二甲酯(DMCD)的选择性加氢过程。其中,Ru和Pd的总负载量为0.3%(以催化剂总质量为基准,下同),且m(Ru)∶m(Pd)=1∶1。结果发现,采用先Ru后Pd(Ru-Pd)式固载顺序和浸渍-干燥-浸渍-干燥-焙烧(IDIDC)型制备流程,并在450℃下焙烧后,所得负载型Ru-Pd双金属催化剂的反应性能最佳,在6 MPa、180℃下,DMT转化率为89.6%,DMCD选择性为96.0%,DMCD产率为85.9%。这可能与Ru-Pd中大粒径粒子的形成受到抑制、粒径尺寸和分布更小、比表面积和总孔容更高、表面Pd原子摩尔分数较高以及Ru/Pd物质的量比较低有关。 相似文献
9.
项益智李小年 《中国化学工程学报》2005,13(5):696-700
Co and Mo bimetallic nitrides supported on Mg(Al)O, MgO and γ-Al2O3 were prepared in temperatureprogrammed reactions with NH3. The surface morphology, chemical composition and catalytic activity for NH3 decomposition on the supported Co and Mo bimetallic nitrides were studied by X-ray diffractometer (XRD), NH3 temperature-programmed desorption and mass spectrometer (NH3-TPD-MS), temperature-programmed desorption and mass spectrometer (TPD-MS), H2 temperature-programmed surface reaction (H2-TPSR) and activity test. The phases of Co3Mo3N and MoN could be formed on Mg(Al)O, MgO and Al2O3 during the nitridation, and they might be more uniformly dispersed on Mg(Al)O and MgO than on γ-Al2O3. Transition metallic nitrides are generally considered as potential catalysts for hydrogen-involving reactions due to the entrance of hydrogen atoms into subsurface and the lattice of metallic nitrides. The diffusion of nitrogen in the bulk and the structure transformation of Co and Mo nitride compounds occur during NH3-TPD, but the supported Co and Mo bimetallic nitrides are not easily reduced at H2 atmosphere. Co3Mo3N/Mg(Al)O catalyst exhibits the highest activity, while Co3Mo3N/Al2O3 exhibits the lowest activity for NH3 decomposition. Furthermore, the catalytic activity of Co and Mo bimetallic nitrides is not only much higher than that of supported single metallic nitride, but also highly dependent upon the surface acidity and BET surface area of support. 相似文献
10.
Hydrogen production by partial oxidation and steam reforming (POSR) of n‐octane was investigated over alumina‐supported Ni and Ni‐Pd catalysts. It showed that Ni‐Pd/Al2O3 had higher activity and hydrogen selectivity than the nickel catalyst under the experimental conditions, which indicated Ni‐Pd/Al2O3 could be an effective catalyst for the production of hydrogen from hydrocarbons. 相似文献