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991.
We present a simple and fast algorithm to test the thermodynamic stability and determine the necessary chemical environment for the production of a multiternary material, relative to competing phases and compounds formed from the constituent elements. If the material is found to be stable, the region of stability, in terms of the constituent elemental chemical potentials, is determined from the intersection points of hypersurfaces in an (n−1)-dimensional chemical potential space, where n is the number of atomic species in the material. The input required is the free energy of formation of the material itself, and that of all competing phases. Output consists of the result of the test of stability, the intersection points in the chemical potential space and the competing phase to which they relate, and, for two- and three-dimensional spaces, a file which may be used for visualization of the stability region. We specify the use of the program by applying it both to a ternary system and to a quaternary system. The algorithm automates essential analysis of the thermodynamic stability of a material. This analysis consists of a process which is lengthy for ternary materials, and becomes much more complicated when studying materials of four or more constituent elements, which have become of increased interest in recent years for technological applications such as energy harvesting and optoelectronics. The algorithm will therefore be of great benefit to the theoretical and computational study of such materials. 相似文献
992.
The effectiveness of an active shutter-glasses stereoscopic display (SD) and a passive polarised SD was evaluated in a live robot-teleoperation task and a simulated indirect-vision driving task in various terrains. Overall, participants completed their tasks significantly faster with the SDs in three-dimensional (3D) mode than with the SDs in the baseline 2D mode. They also navigated more accurately with the SDs in 3D mode. When the effectiveness of the two types of SDs was examined separately, results showed that the active shutter-glasses SD resulted in faster responses and task completion times than the passive polarised SD, though most of the differences failed to reach statistical significance. Perceived workload when interacting with the two SD systems did not differ significantly between the active versus passive display types or between the 3D and 2D modes of operation; however, participants reported more severe discomfort after interacting with the passive polarised SD. 相似文献
993.
Fidelis O. Okafor 《Cement and Concrete Research》1988,18(6):901-910
These concrete mixes of widely differing water/cement ratios were made using palm kernel shell as course aggregate. The properties tested include the physical properties of the shell, the compressive, flexural and tensile splitting strengths of the concrete. These properties were compared with those of similar concrete specimens made with crushed granite as course aggregate. Results of the tests suggest that palm kernel shell cannot produce concrete with compressive strength above 30 MPa. However, for concrete grade 25 and below, the material was found to compare favourably with other conventional aggregate such as crushed granite. 相似文献
994.
995.
Ovsyannikov V. G. Voronina O. B. D'yachenko V. F. Sarychev B. A. Prishchepova T. K. Loginova L. T. 《Refractories and Industrial Ceramics》2002,43(1-2):6-9
Tests of periclase-carbon blocks for the converter's steel-tapping channel available from the Kombinat Magnezit JSC were carried out in an oxygen-converter shop at the Magnitogorskii Metal-and-Steel Works JSC. The new refractory materials are shown to have a higher endurance as compared to the conventional periclase blocks, which made it possible to increase the operational efficiency of converters. 相似文献
996.
A new type of ion implantation technique is used to create a non-equilibrium Pt-Sn(IMP) near-surface alloy with ca. 8.6 at%
Sn. The surface composition was determined by low-energy ion-scattering (LEIS). The kinetics of the electrooxidation of CO
and 2% CO/H2 mixtures on Pt-Sn(IMP) is essentially identical to that of Pt3Sn(110). The fact that any non-equilibrium composition can be easily prepared by this implantation method opens an interesting
practical opportunity to create a new Pt-Sn alloy fuel cell catalyst having an otherwise unobtainable surface composition
of Sn. This method also appears to have general utility in alloy catalysis as a means of exploring compositions in thermodynamically
unfavorable regions of the bulk phase diagram.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
997.
V.A. de la Peña O’Shea M.C. Alvarez-Galvan J. M. Campos-Martin J. L. G. Fierro 《Catalysis Letters》2005,100(1-2):105-116
A 10 wt% Co/SiO2 catalyst was prepared by the incipient wet-impregnation method and tested in Fischer–Tropsch synthesis in a slurry reactor under conditions approaching industrial practice. The catalyst precursor was investigated by X-ray diffraction (XRD), temperature-programmed reduction (TPR), transmission electron microscopy (TEM) and photoelectron spectroscopy (XPS). The XPS and XRD techniques revealed the presence of a crystalline Co3O4 spinel-type phase, while-in addition-TEM and XPS analyses pointed to the formation of another amorphous Co3O4 spinel phase, both species interacting weakly with the silica substrate. The influence of total pressure on the conversion, selectivity and stability of the catalyst was studied. Upon increasing the overall pressure from 20 to 40 bar, not only activity increased but also the catalyst are not deactivating. These results are explained in terms of an increase of gases solubility in the solvent, this increment of CO concentration in the liquid phase favours carbonyl species formation and the cobalt particles segregation that implies an increase in the metal surface area. 相似文献
998.
Composite sheets composed of biodegradable polymers (BP) and paper were prepared, and their physical and biodegradable properties were investigated. The paper sheets were soaked in BP emulsions and cured at 100°C for 20 min. The wet strength of composite sheets with the same basis weight increased significantly with increasing BP content, although dry strength increased only moderately. A 0.5% addition of a common wet paper‐strengthening agent, poly(amidoamine‐epichlorohydrin) (PAE) resin, enhanced the wet strength, which reached 9.3 MPa, of composite sheets consisting of a BP : paper ratio of 20 : 80. Further enhancement was achieved by the addition of polyvinylamines (PVAm). The wet tensile strength of composite sheets consisting of BP and paper (20 : 80) increased by 27% with the addition of 0.2% PVAm and 0.5% PAE, whereas it was enhanced by only 3–4% with the addition of 0.7% PAE. The biodegradability of the composite sheets was somewhat retarded by the addition of PAE and PVAm. However, a 90% weight loss was observed 60 days after placing composite sheet samples in soil. A similar weight loss was observed after 45 days for composites without additives and after 30 days for base paper alone. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 96: 861–866, 2005 相似文献
999.
C. Gauthier O. Sindt G. Vigier A. Guyot H. A. S. Schoonbrood M. Unzue J. M. Asua 《应用聚合物科学杂志》2002,84(9):1686-1700
In the context of a European union‐supported network on “Reactive Surfactants for Heterophase Polymerization,” different polymerizable surfactants (surfmers) have been synthesized and engaged in the emulsion polymerization of styrene, butyl acrylate, and acrylic acid. The thermomechanical properties of films cast from these different latices are reported in this article. The evolution of the mechanical properties with temperature and the effect of water molecules on these properties are studied. We observed that the studied surfactants do not influence the properties of the dry films. However, some differences due to grafting of reactive surfactants appeared when the films were wet. The amount of water uptake is drastically decreased when only reactive surfactants are present in the film. Concerning the mechanical behavior of the wet films, a decrease of the plastic flow stress is observed for all the samples whatever the nature of the surfactant (reactive or conventional). Hence, calorimetric measurements and dynamic mechanical analysis are used to identify the possible mechanisms that induce the change in the mechanical behavior of the latex films. In the case of reactive surfactant grafted to the polymer, the very low value of water uptake is accompanied by a plasticization of the polymer. In contrast, no plasticizing effect is observed in the case of nonreactive surfactant, even if the amount of water is very large. Finally, the tensile behavior of the styrene–butyl acrylate copolymer versus temperature is analyzed in the frame of the quasi point defects (qpd) model. Both rubber elasticity and chain orientation effects are taken into account to describe the behavior laws at large extensions (i.e., ? ≈ 1.2). © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 84: 1686–1700, 2002; DOI 10.1002/app.10548 相似文献
1000.
The crystallization kinetics of the running filament in melt spinning have been studied for three cases: isothermal crystallization of an isotropic melt, non-isothermal crystallization of an isotropic melt, and non-isothermal crystallization of a non-isotropic melt. Both the temperature and the orientation dependences of nucleation rate and growth rate are estimated for polypropylene. Calculated curves for non-isothermal crystallization of a non-isotropic melt with partial high orientation closely approximate the experimental data. In particular, the experimental data are best explained by crystallization with two-dimensional growth. The crystallization processes in melt spinning may be governed by localized molecular orientation of the supercooled melt in the initial stage. 相似文献