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101.
102.
(Bi1-xSbx)2Te3 thermoelectric thin films were deposited on stainless steel discs in 1 M perchloric acid and 0.1 M tartaric acid by pulse electrodeposition in order to optimize the grain growth. The influence of the electrolyte composition, the cathodic current density and the cathodic pulse time on film stoichiometry were studied. The results show that it is necessary to increase the Sb content in the electrolyte to obtain the (Bi0.25Sb0.75)2Te3 film stoichiometry. Pulse plating reduced the grain size and the roughness, compared with continuous plating. Thermoelectric and electrical properties were also studied and it was found that the Seebeck coefficient and electrical resistivity were related to two parameters: the cathodic pulse current density and the films thickness.  相似文献   
103.
During industrial electrolysis, for hydrogen, dichloride or aluminium production, there is bubbles creation at one or two electrodes which imply a great hydrodynamic acceleration but also a quite important electrical field disturbance. This disturbance can lead to the modification of the local current density and to anode effects for example. There is few works concerning the local modelling of coupled electro active species transport and electrochemical processes in a biphasic electrolyte. There are also few local experimental measurements in term of chemical composition, temperature or current density which would allow the numerical calculations validation. Nevertheless, effects like the anode effect, particularly expensive on the point of the process efficiency, should need a better understanding. Nowadays, the respective roles of the local temperature increases, the electro active specie composition or the transport properties modification due to bubbles are not known.The goal of the present work is the modelling and the numerical simulation of the vertical electrode configuration for a biphasic electrolysis process. Bubbles presence is supposed to modify the electrical properties, and then the electro active species diffusive transport and the current density. Bubbles are also motion sources for the electrolysis cell flow, and then hydrodynamic properties are strongly coupled with species transport and electrical field. The present work shows hydrodynamic and electrical properties in a laboratory scale electrolysis cell with a vertical electrode. The numerical algorithm used was the finite volume used in the computational fluid dynamic software Fluent®.  相似文献   
104.
Granular Matter - The prediction quality of discrete element method (DEM) models for railway ballast can be expected to depend on three points: the geometry representation of the single particles,...  相似文献   
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106.
Particulate matter (PM) is a significant contributor to death and disease globally. This paper summarizes the work of an international expert group on the integration of human exposure to PM into life cycle impact assessment (LCIA), within the UNEP/SETAC Life Cycle Initiative. We review literature-derived intake fraction values (the fraction of emissions that are inhaled), based on emission release height and "archetypal" environment (indoor versus outdoor; urban, rural, or remote locations). Recommended intake fraction values are provided for primary PM(10-2.5) (coarse particles), primary PM(2.5) (fine particles), and secondary PM(2.5) from SO(2), NO(x), and NH(3). Intake fraction values vary by orders of magnitude among conditions considered. For outdoor primary PM(2.5), representative intake fraction values (units: milligrams inhaled per kilogram emitted) for urban, rural, and remote areas, respectively, are 44, 3.8, and 0.1 for ground-level emissions, versus 26, 2.6, and 0.1 for an emission-weighted stack height. For outdoor secondary PM, source location and source characteristics typically have only a minor influence on the magnitude of the intake fraction (exception: intake fraction values can be an order of magnitude lower for remote-location emission than for other locations). Outdoor secondary PM(2.5) intake fractions averaged over respective locations and stack heights are 0.89 (from SO(2)), 0.18 (NO(x)), and 1.7 (NH(3)). Estimated average intake fractions are greater for primary PM(10-2.5) than for primary PM(2.5) (21 versus 15), owing in part to differences in average emission height (lower, and therefore closer to people, for PM(10-2.5) than PM(2.5)). For indoor emissions, typical intake fraction values are ~1000-7000. This paper aims to provide as complete and consistent an archetype framework as possible, given current understanding of each pollutant. Values presented here facilitate incorporating regional impacts into LCIA for human health damage from PM.  相似文献   
107.
    
The aim of this study was to underscore that seed treatment by the fog of ozonated water constitutes a promising alternative tool, in terms of health and environmental gains, regarding traditional ozone treatment. In order to obtain a clear vision of this performance, the technology was implemented on an industrial scale (malting industry). Under an exposition of barley seeds to 9.8 ppm of dissolved ozone into water, our results showed a significant disinfection effect of 80% for Fusarium sp. and 70% for Aspergillus sp., but no effect was established on Alternaria sp.  相似文献   
108.
    
The self-assembly method of layer-by-layer deposition of oppositely charged polyelectrolytes is used to insert J-aggregates of the dye tetrachloro-diethyl-disulfobutyl-benzimido-carbocyanine (TDBC) into thin polymeric films. The J-aggregates are characterized by a narrow absorption- and fluorescence band with its maximum at 590 nm, which is red-shifted with respect to the monomeric transition at 515 nm. The dyes are either coadsorbed with the polyelectrolytes poly(allylamine hydrochloride (PAH) and poly(styrene sulfonate) (PSS), or alternately deposited with the precursor of poly(phenylene vinylene) (pre-PPV). The optical properties of the aggregates are not changed significantly by the deposition process. The pre-PPV/TDBC films are heated under vacuum to convert the PPV to its conjugated form. The resulting films can be used for the fabrication of light-emitting devices. The optical properties such as fluorescence and electroluminescence are dominated by the J-aggregates. The excitation energy of PPV is transferred to the dye aggregates with an efficiency of 100%. The electroluminescence is not very stable and shows a very slow turn-on time. However, the combination of self-assembled PPV/TDBC layers with a spin-coated film of PPV results in stable electroluminescence emission under ambient conditions. In this case, light is emitted from both species, the PPV and the J-aggregates, whereas the ratio of the two intensities strongly depends on temperature.  相似文献   
109.
    
On‐line mixing of the resin with its curing agents prior to injection into a mold is a common industrial technique for fabricating composite parts. For vinyl‐ester resins that cure via free radical polymerization, the concentrations of retarder, accelerator, and initiator are pre‐selected and cannot be changed during the injection. Hence, the resin that enters the mold the earliest has cured longer than the resin that enters the mold later, since the gel time for the resin is the same, owing to the fixed ratio of the curing agents. This approach leads to inhomogeneous cure of the resin and consequently to longer residence time of the resin in the mold. It requires an additional 50 to 75 percent of the filling time before a part can be de‐molded. In this study, it is shown that by adjusting the concentration of curing agents during the injection, a more homogeneous gel time throughout the mold can be achieved. The time to de‐mold is reduced to 18‐24 percent of the filling time. Sensors that measure the conductivity of the resin were used to detect the location and monitor the cure of vinyl‐ester. This approach could be extended to other resin systems to control the spatial curing of the resin in the mold.  相似文献   
110.
    
The effect of pressure on carbon dioxide solubility in water is significantly smaller than that of temperature under hydrate–liquid water (HLw) equilibrium. As a result, experimental values of carbon dioxide solubility in the water rich liquid phase under HLw equilibrium are often inconclusive and in some cases contradictory. This work proposes a theoretical derivation, based on fundamental thermodynamics, of the gas hydrate former solubility dependency on pressure for any binary system under two‐phase equilibrium. The obtained expression is applied to the carbon dioxide–water system under both hydrate–liquid water and vapour–liquid water equilibrium. It is shown that the solubility of carbon dioxide in the water rich liquid phase increases with increasing pressure under HLw equilibrium. The predicted trend is then compared to the limited experimental data available in the literature.  相似文献   
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