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991.
Piezoelectric cable is a commercial electronic sensor that incorporates the piezoelectric polymer polyvinylidene fluoride. This paper investigated a potential application of piezoelectric cable for energy harvesting. A method for testing the electrical output using the tensile load was developed and used to determine the output properties of the cable. A design for a piezoelectric cable fiber composite is presented, along with recommendations for potential applications and further research. Copyright © 2014 John Wiley & Sons, Ltd.  相似文献   
992.
We report the preparation of a polypyrrole/graphene oxide/zinc oxide nanocomposite on a nickel foam using a simple and rapid single‐step electrochemical deposition process under ambient conditions. A free‐standing flexible supercapacitor was fabricated by sandwiching a polyvinyl alcohol hydrogel polymer electrolyte between two layers of the as‐prepared ternary nanocomposite electrodes. The electrochemical properties of the free‐standing supercapacitor were analyzed using a two‐electrode system. The supercapacitor achieved a specific capacitance of 123.8 F/g at 1 A/g, which was greater than its single (39.1 F/g) and binary (81.3 F/g) counterparts. This suggests that ZnO acts as a spacer and support that hinders the ternary structure from collapsing and subsequently enhances the diffusion of ions within the matrix. The flexible supercapacitor exhibited remarkable electrochemical stability when subjected to bending at various angles. The cycling stability of the ternary nanocomposite showed a favorable specific capacitance retention of more than 90% after 1000 cycles for mild alkaline electrolytes compared with strong alkali electrolytes. The presence of glycerin in the polymer electrolyte enabled the supercapacitor to perform better under the vigorous cycling condition. The potential of the as‐fabricated supercapacitor for real applications was manifested by its ability to light up a light‐emitting diode after being charged. Copyright © 2014 John Wiley & Sons, Ltd.  相似文献   
993.
The greatest challenge for a feasible hydrogen economy lies on the production of pure hydrogen and the materials for its storage with controlled release at ambient conditions. Hydrogen with its great abundance, high energy density and clean exhaust is a promising candidate to meet the current global challenges of fossil fuel depletion and green house gases emissions. Extensive research on hollow glass microspheres (HGMs) for hydrogen storage is being carried out world‐wide, but the right material for hydrogen storage is yet underway. But many other characteristics, such as the poor thermal conductivity etc. of the HGMs, restrict the hydrogen storage capacity. In this work, we have attempted to increase the thermal conductivity of HGMs by ZnO doping. The HGMs with Zn weight percentage from 0 to 10 were prepared by flame spheroidization of amber‐colored glass powder impregnated with the required amount of zinc acetate. The prepared HGMs samples were characterized using field emission‐scanning electron microscope (FE‐SEM), environmental SEM (ESEM), high‐resolution transmission electron microscopy (HRTEM), Fourier transform infrared spectroscopy and X‐ray diffraction (XRD) techniques. The deposition of ZnO on the microsphere walls was observed using FE‐SEM, ESEM and HRTEM which was further confirmed using the XRD and ultraviolet–visible absorption data. The hydrogen storage studies done on these samples at 200 °C and 10‐bar pressure for 5 h showed that the hydrogen storage increased when the Zn percentage in the sample increased from 0 to 2%. The percentage of zinc beyond 2, in the microspheres, showed a decline in the hydrogen storage capacity. The closure of the nanopores due to the ZnO nanocrystal deposition on the microsphere surface reduced the hydrogen storage capacity. The hydrogen storage capacity of HAZn2 was found 3.26 wt% for 10‐bar pressure at 200 °C. Copyright © 2015 John Wiley & Sons, Ltd.  相似文献   
994.
Lead sulfide (PbS) thin films with 150 nm thickness were prepared onto ultra-clean quartz substrate by the RF-sputtering deposition method. Deposited thin films of PbS were annealed at different temperatures 100 °C, 150 °C, 200 °C, 250 °C and 300 °C. X-ray diffraction pattern of thin films revealed that thin films crystallized at 150 °C. Crystalline thin films had cubic phase and rock salt structure. The average crystallite size of crystalline thin films was 22 nm, 28 nm and 29 nm for 150 °C, 200 °C and 250 °C respectively. From 150 °C to 250 °C increase in annealing temperature leads to increase in crystallite arrangement. FESEM images of thin films revealed that crystallite arrangement improved by increasing annealing temperature up to 250 °C. Increase in DC electrical conductivity by increasing temperature confirmed the semiconductor nature of crystalline thin films. Increase in dark current by increasing annealing temperature showed the effect of crystallite arrangement on carrier transport. Photosensitivity decreased by increasing annealing temperature for crystalline thin films that it was explained at the base of thermal quenching of photoconductivity and adsorption of oxygen at the surface of thin films that leads to the formation of PbO at higher temperatures.  相似文献   
995.
Undoped and fluorine doped ZnO thin films were deposited onto glass substrates using successive ionic layer adsorption and reaction (SILAR) technique and then annealed at 350 °C in vacuum ambience. The F doping level was varied from 0 to 15 at% in steps of 5 at%. The XRD analysis showed that all the films are polycrystalline with hexagonal wurtzite structure and preferentially oriented along the (002) plane. Crystallite sizes were found to increase when 5 at% of F is doped and then decreased with further doping. It was seen from the SEM images that the doping causes remarkable changes in the surface morphology and the annealing treatment results in well-defined grains with an improvement in the grain size irrespective of doping level. All the films exhibit good transparency (>70%) after vacuum annealing. Electrical resistivity of the film was found to be minimum (1.32×10−3 Ω cm) when the fluorine doping level was 5 at%.  相似文献   
996.
Class I hydrophobin Vmh2, a peculiar surface active and versatile fungal protein, is known to self‐assemble into chemically stable amphiphilic films, to be able to change wettability of surfaces, and to strongly adsorb other proteins. Herein, a fast, highly homogeneous and efficient glass functionalization by spontaneous self‐assembling of Vmh2 at liquid–solid interfaces is achieved (in 2 min). The Vmh2‐coated glass slides are proven to immobilize not only proteins but also nanomaterials such as graphene oxide (GO) and quantum dots (QDs). As models, bovine serum albumin labeled with Alexa 555 fluorophore, anti‐immunoglobulin G antibodies, and cadmium telluride QDs are patterned in a microarray fashion in order to demonstrate functionality, reproducibility, and versatility of the proposed substrate. Additionally, a GO layer is effectively and homogeneously self‐assembled onto the studied functionalized surface. This approach offers a quick and simple alternative to immobilize nanomaterials and proteins, which is appealing for new bioanalytical and nanobioenabled applications.  相似文献   
997.
The quality of recycled process water is an important issue in the flotation of Cu–Mo ores. Processing of Cu–Mo ores includes two steps: a bulk flotation where molybdenite is recovered together with Cu sulfides, and a subsequent selective flotation step where molybdenite is separated from depressed copper sulfides. Flocculants are usually employed in the middling thickeners in the copper plant, and in the Cu–Mo bulk concentrate ahead of the molybdenite plant. However, the floatability of molybdenite, similarly to other naturally hydrophobic minerals, is highly sensitive to the presence of both natural and synthetic polymers. In this work flotation tests demonstrate that conventional flocculants, high-molecular weight anionic polyacrylamides (PAM), are strong molybdenite depressants. Low-molecular weight shear degraded polyacrylamides in spite of losing flocculation efficiency maintain depressing ability for molybdenite. Also a non-ionic flocculant, polyethylene oxide (PEO), has been studied in this project. Our results indicate that PEO is an efficient flocculant for molybdenite suspensions in a wide pH range. However, similarly to polyacrylamides, the PEO flocculant also depresses molybdenite flotation.  相似文献   
998.
We investigate the fluid mechanics of cleaning viscous drops attached to a flat inclined surface using thin gravity-driven film flows. We focus on the case where the drop cannot be detached either partially or completely from the surface by the mechanical forces exerted by the cleaning fluid on the drop surface. Instead a convective mass transfer establishes across the drop–film interface and the fluid in the drop dissolves into the cleaning film flow, which then transports it away. The characteristic time scale of dissolution is much longer than the advection time scale in the film flow. Thus, the shape and size of the drop can be considered as quasi-steady. To assess the impact of the shape and size of the drop on the velocity of the cleaning fluid, we have developed a novel experimental technique based on particle image velocimetry. We show the velocity distribution at the film surface in the situations both where the film is flowing over a smooth surface, and where it is perturbed by a solid obstacle representing a very viscous drop. We find that at intermediate Reynolds numbers the acceleration of the starting film is overestimated by a plane model using the lubrication approximation. In the perturbed case, the streamwise velocity is strongly affected by the presence of the obstacle. The upstream propagation of the disturbance is limited, but the disturbance extends downstream for distances larger than 10 obstacle diameters. Laterally, we observe small disturbances in both the streamwise and lateral velocities, owing to stationary capillary waves. The flow also exhibits a complex three-dimensional converging pattern immediately below the obstacle.  相似文献   
999.
In the present work, transparent and conductive Nd doped SnO2 thin films were deposited via spray pyrolysis. Crystallographic, morphological, optical and electrical characterizations of SnO2 were researched as a function of Nd doping. The XRD analysis indicated the films had tetragonal cassiterite tin oxide structure and (211) preferential direction for NdTO-0, NdTO-1, NdTO-2 and NdTO-3 samples changed to (110) plane for NdTO-4 and NdTO-5 samples. The crystalline size and strain analysis were made by using a Williamson–Hall method. The SEM micrographs showed that all films had homogenously scattered pyramidal and small densely nanoparticles. The optical analysis indicated optical band gap value of undoped film increased with 1 at% Nd doping and then it decreased with more Nd content. The Hall measurements indicated that the highest electrical conductivity was obtained for 2 at% Nd doping content.  相似文献   
1000.
In the current study, graphene oxide (GO) was prepared using green chemistry with modified Hummer's method without incorporating sodium nitrate (NaNO3). Solvent casting was employed to fabricate GO-doped poly(ethylene oxide) (PEO), that is, PEO/GO composites with various proportion of Na2SO4 and were then subjected to characterization via advanced spectroscopic techniques for different physicochemical aspects to estimate their potential applications as marketable products. XRD analysis explored that fabricated composites are more crystalline than neat PEO. PEO/GO/Na2SO4 composite films offered maximum crystallinity. SEM displayed the same trend. TG/DTA thermogram exposed better thermal stability than pristine polymer. FTIR studies confirmed complexation among hybrid's components. Elongation-at-break and Young's modulus displayed an enhancing behavior with an incremental loading of salt and filler. In terms of mechanical performance, composite of PEO with 0.37 wt % GO and 0.08 g salt was found to be an ideal composition during the course of study. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 48376.  相似文献   
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