全文获取类型
收费全文 | 319篇 |
免费 | 15篇 |
国内免费 | 6篇 |
专业分类
电工技术 | 1篇 |
综合类 | 11篇 |
化学工业 | 200篇 |
金属工艺 | 28篇 |
机械仪表 | 3篇 |
能源动力 | 37篇 |
轻工业 | 9篇 |
石油天然气 | 4篇 |
无线电 | 13篇 |
一般工业技术 | 13篇 |
冶金工业 | 10篇 |
原子能技术 | 8篇 |
自动化技术 | 3篇 |
出版年
2024年 | 1篇 |
2023年 | 9篇 |
2022年 | 8篇 |
2021年 | 8篇 |
2020年 | 3篇 |
2019年 | 14篇 |
2018年 | 5篇 |
2017年 | 5篇 |
2016年 | 4篇 |
2015年 | 3篇 |
2014年 | 11篇 |
2013年 | 9篇 |
2012年 | 7篇 |
2011年 | 16篇 |
2010年 | 15篇 |
2009年 | 21篇 |
2008年 | 20篇 |
2007年 | 18篇 |
2006年 | 19篇 |
2005年 | 17篇 |
2004年 | 6篇 |
2003年 | 8篇 |
2002年 | 17篇 |
2001年 | 9篇 |
2000年 | 13篇 |
1999年 | 8篇 |
1998年 | 14篇 |
1997年 | 2篇 |
1996年 | 8篇 |
1995年 | 5篇 |
1994年 | 13篇 |
1993年 | 8篇 |
1992年 | 5篇 |
1991年 | 5篇 |
1990年 | 3篇 |
1989年 | 1篇 |
1988年 | 1篇 |
1986年 | 1篇 |
排序方式: 共有340条查询结果,搜索用时 15 毫秒
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.
Exchange and oxidation of C16O were investigated at 450°C on 18O-predosed Rh and Pt catalysts supported on A12O3, CeO2 and CeO2-Al2O3. In all cases, a rapid exchange of C16O with the surface can be observed. CO oxidation leads to C16O2, C16O18O and C18O2. Significant formation of C16O2 is due to the relatively high 16O coverage in reaction resulting from the C16O exchange and from an exchange between O surface species and 16O internal atoms. Hydrogen is also formed via a water-gas shift reaction (CO + surface OH) in higher proportion on CeO2-containing catalysts than on A12O3. Chlorine inhibits all the reactions (exchange, oxidation and WGS) and particularly the internal exchange. 相似文献
3.
介绍了铂铑包覆钼合金搅拌器的结构与技术要求,以及搅拌器的制作与使用效果。研制结果表明,国产搅拌器达到了日本同类产品的水平。 相似文献
4.
The adsorption of ethene and propene on titania and titania-supported rhodium has been studied, observing a continuous adsorption even after 24 h. The samples have been reduced at 623 or 773 K, but no difference was observed, whichever the reduction temperature or the presence of rhodium, on the amount of gas adsorbed per unit of surface area of the solid. A study of the polymerization has been done following the equal reactivity hypothesis, and it has been concluded that the role played by the rhodium particles is to facilitate adsorption of the gaseous molecule, that is then transfered to the surface of the support, where it polymerizes. 相似文献
5.
Cobalt catalysts supported on silica aerogel have been prepared using sol–gel chemistry followed by drying under supercritical ethanol conditions. Three different loadings of cobalt were synthesized: 2, 6, and 10% by weight. Transmission electron micrographs indicate that the metallic cobalt exists as discrete particles 50–70 nm in diameter for the 2 and 6% loadings. The 10% catalyst shows long needles of cobalt. BET and BJH measurements indicate that the catalysts retain the silica aerogel properties of high surface area (∼800 m2/g), large pore volume (∼5 cm3/g), and an average pore diameter in the mesoporous regime (∼25 nm). The catalysts were evaluated for Fischer–Tropsch activity in a laboratory-scale packed bed reactor. All three catalysts were active with the 10% Co catalyst achieving more than 20% CO conversion which corresponds to a rate of 1.53 g CO per g-cat per hour. The catalysts were selective for the C10+ hydrocarbons with more than 50% of the carbon contained within this fraction. A significant portion of the C9–C15 hydrocarbon product was observed as 1-olefins which reflects the enhanced mass transport within the very porous aerogel support. 相似文献
6.
K. Juodkazis J. Juodkazyt? T. Juodien? V. Šukien? I. Savickaja 《Electrochimica acta》2006,51(27):6159-6164
The idea of underpotential oxidation of water, taking place on the surface of noble metals in the range of potentials preceding molecular oxygen evolution, is more than 40-years old. Chemisorbed oxygen atom—Ochem is considered to be the main intermediate in the underpotential oxidation of H2O, leading eventually to chemical oxidation of noble metals and formation of anhydrous surface oxides of MeO type. This concept is still used for the evaluation of the real surface area of the noble metal electrodes and also for the interpretation of new experimental results.The existence of reversible metal-oxide electrodes demonstrated experimentally for Pt, Pd, Rh, Ir and Au electrodes, oxidized anodically in the range of potentials preceding O2 evolution, shows that noble metals do have electrochemistry of their own. Nanometric layers of amorphous, slightly soluble hydroxides, hydrous oxides or oxides can form electrochemically on the electrode surface during the anodic process and be reduced during the cathodic one. Such alternative concept admits the reversibility of anodic and cathodic processes and changes essentially the understanding and interpretation of the phenomena of anodic oxidation of noble metals. 相似文献
7.
8.
Bozena Silberova Hilde J. Venvik John C. Walmsley Anders Holmen 《Catalysis Today》2005,100(3-4):457-462
Partial oxidation and oxidative steam reforming of propane were investigated over 0.01 wt.% Rh/Al2O3 foam catalysts. High selectivity to hydrogen was obtained for both reactions, but addition of steam to the reactant mixture gave higher selectivity to hydrogen. Stability tests over 7 h revealed that the catalytic activity of Rh was quite stable under partial oxidation conditions. Higher loss in Rh activity was observed when steam was present in the reactant mixture. FE-SEM images showed that Rh particle size and distribution are modified under partial oxidation and oxidative steam reforming conditions. However, these changes were more distinct on the catalyst used for oxidative steam reforming. 相似文献
9.
Sub-monolayer quantities of metal oxides are found to influence CO hydrogenation, CO2 hydrogenation, acetone hydrogenation, ethylene hydroformylation, ethylene hydrogenation, and ethane hydrogenolysis over Rh foils. The metal oxides investigated include AlOx, TiOx, VOx, FeOx, ZrOx, NbOx, TaOx, and WOx. Only those reactions involving the hydrogenation of C-O bonds are enhanced by the oxide overlayers. The coverage at which maximum rate enhancement occurs is approximately 0.5 ML for each oxide promoter. Titanium, niobium, and tantalum oxides are the most effective promoters. XPS measurements after reaction show that of the oxides studied titanium, niobium, and tantalum oxide overlayers are stable in the highest oxidation states. The trend in promotion effectiveness is attributed to the direct relationship between oxidation state and Lewis acidity. For the oxide promoters, bonding at the metal oxide/metal interface between the O-end of adsorbed CO and the Lewis acidic oxide is postulated to facilitate C-O bond dissociation and subsequent hydrogenation. 相似文献
10.
本文以对氯苯酚(4-cP)、对硝基苯酚(4-NP)和罗丹明B(RhB)为模型有机物(以4-CP和4-NP为小分子模型有机物,以RhB为大分子模型有机物),分别研究了185nmUV对水中这3种模型有机物的降解规律、性能和效果.研究结果表明,185nmUV直接对水中4-CP、4-NP和RhB有很好的降解效果.研究内容包括:185nmUV降解模型有机物的浓度、TOC(Totalorganic carbon)浓度、185nmUV降解模型有机物过程中溶液pH及电导率变化、以及降解模型有机物过程中产生的无机离子等几个方面. 相似文献