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1.
Stanisic B.R. Verghese N.K. Rutenbar R.A. Carley L.R. Allstot D.J. 《Solid-State Circuits, IEEE Journal of》1994,29(3):226-238
This paper describes new techniques for the simulation and power distribution synthesis of mixed analog/digital integrated circuits considering the parasitic coupling of noise through the common substrate. By spatially discretizing a simplified form of Maxwell's equations, a three-dimensional linear mesh model of the substrate is developed. For simulation, a macromodel of the fine substrate mesh is formulated and a modified version of SPICE3 is used to simulate the electrical circuit coupled with the macromodel. For synthesis, a coarse substrate mesh, and interconnect models are used to couple linear macromodels of circuit functional blocks. Asymptotic Waveform Evaluation (AWE) is used to evaluate the electrical behavior of the network at every iteration in the synthesis process. Macromodel simulations are significantly faster than device level simulations and compare accurately to measured results. Synthesis results demonstrate the critical need to constrain substrate noise and simultaneously optimize power bus geometry and pad assignment to meet performance targets 相似文献
2.
A. F. Carley 《Catalysis Today》1992,12(4):413-419
During the past 15 years the advent of laboratory microcomputers has had a dramatic effect on the information we can extract from spectroscopic data. In this paper we take a brief look at the historical development of this field, consider some of the techniques being currently researched, and comment on possible future trends. 相似文献
3.
Jennifer K. Edwards Adrian Thomas Benjamin E. Solsona Philip Landon Albert F. Carley Graham J. Hutchings 《Catalysis Today》2007,122(3-4):397-402
The direct synthesis of hydrogen peroxide from H2 and O2 using a range of supported Au–Pd alloy catalysts is compared for different supports using conditions previously identified as being optimal for hydrogen peroxide synthesis, i.e. low temperature (2 °C) using a water–methanol solvent mixture and short reaction time. Five supports are compared and contrasted, namely Al2O3, -Fe2O3, TiO2, SiO2 and carbon. For all catalysts the addition of Pd to the Au only catalyst increases the rate of hydrogen peroxide synthesis as well as the concentration of hydrogen peroxide formed. Of the materials evaluated, the carbon-supported Au–Pd alloy catalysts give the highest reactivity. The results show that the support can have an important influence on the synthesis of hydrogen peroxide from the direct reaction. The effect of the methanol–water solvent is studied in detail for the 2.5 wt% Au–2.5 wt% Pd/TiO2 catalyst and the ratio of methanol to water is found to have a major effect on the rate of hydrogen peroxide synthesis. The optimum mixture for this solvent system is 80 vol.% methanol with 20 vol.% water. However, the use of water alone is still effective albeit at a decreased rate. The effect of catalyst mass was therefore also investigated for the water and water–methanol solvents and the observed effect on the hydrogen peroxide productivity using water as a solvent is not considered to be due to mass transfer limitations. These results are of importance with respect to the industrial application of these Au–Pd catalysts. 相似文献
4.
Gang Li Dan I. Enache Jennifer Edwards Albert F. Carley David W. Knight Graham J. Hutchings 《Catalysis Letters》2006,110(1-2):7-13
The oxidation of benzyl alcohol to benzaldehyde has been investigated in the absence of solvent using zeolite-supported Au
and Au–Pd catalysts. Three zeolites were investigated, ZSM-5, zeolite β and zeolite Y, and these were contrasted with the
titanoslicalite TS-1 and TiO2 as supports. For the Au catalysts the best results are obtained with zeolite β as the support and the conversions were comparable
or better than those observed with TiO2 in terms of turn over frequencies. However, the selectivities observed with the acidic zeolites were lower than the non-acidic
TS-1 and TiO2. This is due to the subsequent reaction of benzaldehyde via acid catalysed reactions to give benzyl benzoate and its dibenzyl
acetal, and, in some cases dibenzylether. Initial catalysts were evaluated with a gold loading of 2 wt% and increasing this
to 4 wt% showed the expected increase in activity, indicating that there is scope to improve the performance of these catalysts.
The most active catalysts were prepared by impregnation and catalysts prepared by deposition precipitation were considerably
less active. Introduction of Pd into the catalyst improved the activity without significantly affecting the selectivity. 相似文献
5.
Saleh Al-Sayari Albert F. Carley Stuart H. Taylor Graham J. Hutchings 《Topics in Catalysis》2007,44(1-2):123-128
The preparation of Au/ZnO and Au/Fe2O3 catalysts using two coprecipitation methods is investigated to determine the important factors that control the synthesis
of high activity catalysts for the oxidation of carbon monoxide at ambient temperature. In particular, the factors involved
in the preparation of catalysts that are active without the need for a calcination step are evaluated. The two preparation
methods differ in the manner in which the pH is controlled during the precipitation, either constant pH throughout or variable
pH in which the pH is raised from an initial low value to a defined end point. Non-calcined Au/ZnO catalysts prepared using
both methods are very sensitive to pH and ageing time, and catalysts prepared at a maximum pH = 5 with a short ageing time
(ca. 0–3 h) exhibit high activity. Catalysts prepared at higher pH give lower activity. However, all catalysts require a short
operation period during which the oxidation activity increases. In contrast, the calcined catalysts are not particularly sensitive
to the preparation conditions. Non-calcined Au/Fe2O3 catalysts exhibit high activity when prepared at pH ≥ 5. Calcined Au/Fe2O3 prepared using the controlled pH method retain high activity, whereas calcined catalysts prepared using the variable pH method
are inactive. The study shows the immense sensitivity of the catalyst performance to the preparation methods. It is therefore
not surprising that marked differences in the performance of supported Au catalysts for CO oxidation that are apparent in
the extensive literature on this subject, particularly the effect of calcination, can be expected if the preparation parameters
are not carefully controlled and reported. 相似文献
6.
Carbon dioxide and carbon monoxide undergo reactive chemisorption with cesium modified Cu(110) and Cu(110)-O surfaces and via the anionic intermediate CO
2
–
(a) form a surface carbonate. The CO
2
–
(a) species was characterised by VEELS and XPS at low temperature (80 K) and the surface carbonate at 295 K. For cesium modified Cu(110) surfaces chemisorption of carbon monoxide gives rise to electron energy loss peaks (v
co) as low as 1450 cm–1 at 295 K. 相似文献
7.
Nikolaos Dimitratos Jose Antonio Lopez-Sanchez David Morgan Albert Carley Laura Prati Graham J. Hutchings 《Catalysis Today》2007,122(3-4):317-324
Solvent free oxidation of benzyl alcohol was investigated in the absence of a base using Au catalysts prepared by sol immobilization on titania and carbon supports. Comparison between the Au supported catalysts revealed that activity and distribution of products was dependent on the nature of support and heat treatment. Specifically, heat pre-treatment of the Au catalysts has a beneficial effect in terms of activity, but is detrimental in terms of selectivity to the benzaldehyde. We conclude that sol immobilization is a suitable technique for preparing gold catalysts with small particle size and narrow particle size distributions and very high activity and selectivity for benzyl alcohol oxidation. 相似文献
8.
The direct synthesis of hydrogen peroxide from H2 and O2 using zeolite-supported Au catalysts is described and their activity is contrasted with silica- and alumina-supported Au catalysts. Two zeolites were investigated, ZSM-5 and zeolite Y. The effect of calcination of these catalysts is studied and it is found that for uncalcined catalysts high rates of hydrogen peroxide formation are observed, but these catalysts are unstable and lose Au during use. Consequently, reuse of these catalysts leads to lower rates of hydrogen peroxide formation. However, catalysts calcined at 400 °C are more stable and can be reused without loss of gold. The use of zeolites as a support for Au gives comparable rates of hydrogen peroxide formation to alumina-supported Au catalysts and higher rates when compared with silica-supported catalysts. prepared using a similar method. Zeolite Y-supported catalysts are more active than ZSM-5-supported catalysts for the stable calcined materials. It is considered that the overall activity of these supported catalysts may be related to the aluminium content as the activity increases with increasing aluminium content. 相似文献
9.
This paper is concerned with establishing the conditions of stability of a cantilevered tube conveying a compressible fluid. Solutions to Niordson's eigenvalue problem associated with the equations of motion are computed using Muller's method. The effects on critical velocity of compressibility which are accommodated by specifying the tube aspect ratio and fluid sonic velocity are parametrically studied. Aspect ratio is found to have a more pronounced effect on critical velocity than sonic velocity over the parameter range that was considered. 相似文献
10.