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排序方式: 共有1921条查询结果,搜索用时 15 毫秒
81.
主要研究了碳酸钠、氢氧化钠、硅酸钠三种碱与稠油的界面张力和碱液-稠油乳状液的特性,讨论了乳状液的驱油机理。结果表明,这三种碱液与稠油的界面张力在一定条件下均能达到10~2mN/m数量级以下;高油水体积比下的碱水-稠油乳液类型由碱浓度决定。 相似文献
82.
The synthesis of higher alcohols, obtained from CO hydrogenation over transition metals, is an alternative for the production of chemical commodities and less pollutant renewable fuels nowadays. In this work, the influence of different alkali metals (Li, Na, K, Cs) over the formation of active phases of supported catalysts, based on cobalt and copper, as well as the performance of these solids in the reaction of CO hydrogenation under a 50 bar pressure were studied. The solids were prepared by continuous coprecipitation of sodium carbonate with metal nitrate solutions (Al–Co, Al–Cu or Al–Co–Cu) promoted with the alkali metals with dry impregnation. Characterization studies by atomic absorption spectrophotometry, BET, XPS and also the results of catalytic tests show that physico-chemical properties of the obtained catalyst are similar to those of the industrial catalyst used as reference (I). 相似文献
83.
Z. Jovanovi? M. De FrancescoS. Tosti A. Pozio 《International Journal of Hydrogen Energy》2011,36(23):15364-15371
The influence of surface oxidation and hydrogen upload into the Pd0.79Ag0.21 membrane on hydrogen permeation was examined by measuring the permeation of: 1) gas-phase H2 sent from the electrode back-side and 2) electrolytic H2 produced on electrolyte side. It was verified that hydrogen upload into PdAg lattice has positive effect i.e. increases hydrogen permeation, while surface oxides formed during and after electrolysis cycles are the main factors acting on decrease of hydrogen permeation. Particularly, silver oxides are identified as permeation-blocking species. Consequently, several treatments were proposed aiming to reduce electrode deactivation; beside wet chemistry treatments applicable after electrolysis, the in situ electrode reactivation by ultrasonic pulses was presented. 相似文献
84.
Ana S.V. FerreiraCátia M.C. Soares Filipe M.H.L.R. FigueiredoFernando M.B. Marques 《International Journal of Hydrogen Energy》2011,36(5):3704-3711
Composite ionic conductors for fuel cells were produced by combination of one ceria-based ceramic electrolyte and various mixtures of Na and Li carbonates, using several processing routes. These materials were characterized by impedance spectroscopy, scanning electron microscopy with energy dispersive spectroscopy, X-ray diffraction and Fourier transform infrared spectroscopy with attenuated total reflectance. The chemical composition of the mixed carbonates and the processing route were influential in the development of impressive conductivity levels (close to 0.1 S/cm) at modest temperatures (below 600 °C), suggesting a complex role of chemical composition (Na/Li ratio), phase composition (solid/liquid ratio), processing route (mechanothermal history) and microstructure. Furthermore, exposure to humidity showed formation of OH groups. Such hydrogenated species are believed to increase the complexity of the global surface processes and charge transport mechanisms where several native and foreign species may play a significant role. 相似文献
85.
86.
Gvozden S. Tasić Uroš Lačnjevac Marijana M. Tasić Milica Marčeta Kaninski Vladimir M. Nikolić Dragana L. Žugić Vladimir D. Jović 《International Journal of Hydrogen Energy》2013
In this study, different Ni–W coatings, obtained by cheap and technologically simple electrodeposition method, were examined as potential electrocatalysts for the hydrogen evolution reaction (HER). All electrodepositions were done on a Ni mesh substrate from ammoniacal-citrate bath containing different concentrations of Na2WO4. The influence of deposition parameters, such as deposition current density, pH and composition of ammoniacal-citrate bath on electrocatalytic activity of obtained Ni–W coatings toward HER was examined by polarization curve measurements in 6 M KOH at room temperature. The morphology and tungsten content of the Ni–W coatings were investigated by means of SEM and EDS analysis. All investigated electrodes have shown high electrocatalytic activity for the HER. The samples obtained at higher deposition current densities had the lowest overvoltage for the HER. It has been shown that the plating bath pH value is very important parameter in obtaining active coatings. Results of the analysis of polarization curves, morphology of deposited Ni–W coatings and the content of tungsten in the coatings, indicate that the surface roughness of the coatings is responsible for their catalytic activity towards HER. 相似文献
87.
Experimental study on the external electrical thermal and dynamic power characteristics of alkaline water electrolyzer
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As hydrogen production with a water electrolyzer is an effective way for renewable energy consumption, understanding the external electrical characteristics of water electrolyzer is of great significance for the modeling and simulation, system configuration, and control strategy of the system for hydrogen production by renewable energy. However, there are relatively fewer studies in this area. This paper presents the establishment of an experimental platform to conduct an experimental study on the static and dynamic voltage‐current characteristics and analyze the adjustability of the electric power of the traditional alkaline water electrolyzer, the relationship between the electrical characteristics and the electrolyte temperature, and operating point of the alkaline water electrolyzer. In addition, the mathematical fitting problem of the electrical characteristics of the alkaline water electrolyzer is discussed. The work could supply a reference to alkaline water electrolyzer intergrated application in renewable energy. 相似文献
88.
In preparing low-temperature fuel cell electrodes, a polymer binder is essential to bind discrete catalyst particles to form a porous catalyst layer that simultaneously facilitates the transfer of ions, electrons, and reactants/products. For two types of polymer binder, namely, an A3-an anion conducting ionomer and a PTFE-a neutral polymer, an investigation is made of the effect of the content of each binder in the anode catalyst layer on the performance of an alkaline direct ethanol fuel cell (DEFC) with an anion-exchange membrane and non-platinum (non-Pt) catalysts. Experiments are performed by feeding either ethanol (C2H5OH) solution or ethanol–potassium hydroxide (C2H5OH–KOH) solution. The experimental results for the case of feeding C2H5OH solution without added KOH indicate that the cell performance varies with the A3 ionomer content in the anode catalyst layer, and a content of 10 wt.% exhibits the best performance. When feeding C2H5OH–KOH solution, the results show that: (i) in the region of low current density, the best performance is achieved for a membrane electrode assembly without any binder in the anode catalyst layer; (ii) in the region of high current density, the performance is improved with incorporation of PTFE binder in the anode catalyst layer; (iii) the PTFE binder yields better performance than does the A3 binder. 相似文献
89.
Nanoparticles of Pd-Sn were prepared under various conditions by applying ultrasonic irradiation, and their electrocatalytic activity for oxygen reduction was evaluated in 0.5 M KOH. The average size of Pd-Sn nanoparticles thus prepared was about 3-5 nm. The Pd in Pd-Sn nanoparticles was found to be mostly in the metallic state. The electrocatalytic activity of the Pd-Sn nanoparticles for the oxygen reduction reaction (ORR) is greater than Pt or Pd nanoparticles in alkaline media. The molar ratio of Pd to Sn metal ions in the synthesizing solution, their initial concentrations, the concentration of ethanol, which increases primary hydrogen radicals during sonolysis, and the concentration of citric acid were found to affect the size distribution of the Pd-Sn nanoparticles, and therefore, those factors controlled the electrocatalytic activity for ORR. Particularly, the concentration of citric acid was found to be important for controlling the surface property on Pd-Sn particles to adjust the electrocatalytic activity for ORR. 相似文献
90.
可充碱性锌锰电池进展 总被引:2,自引:0,他引:2
本文综合介绍了可充碱锰电池的最新进展,重点论述了目前国际上正在研制开发的两种可充二氧化锰电极,即奥地利kordesch的加压式二氧化锰电极和美国Ford公司的改性二氧化锰电极,对各自的特性进行了分析对比,阐明了可充碱锰电池的发展方向。 相似文献