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651.
Oxide-dispersion-strengthened (ODS) steels are attractive materials for application as fuel cladding in fast reactors and first-wall material of fusion blanket. Recent studies have focused more on high-chromium ferritic (12–18 wt% Cr) ODS steels with attractive corrosion resistance properties. However, they have poor material workability, require complicated heat treatments for recrystallization, and possess anisotropic microstructures and mechanical properties. On the other hand, low-chromium ferritic/martensitic (8–9 wt% Cr) ODS steels have no such limitations; nonetheless, they have poor corrosion resistance properties. In our work, we developed a corrosion-resistant coating technique for a low-chromium ferritic/martensitic ODS steel. The ODS steel was coated with the 304 or 430 stainless steel, which has better corrosion resistances than the low-chromium ferritic/martensitic ODS steels. The 304 or 430 stainless steel was coated by changing the canning material from mild steel to stainless steel in the conventional material processing procedure for ODS steels. Microstructural observations and micro-hardness tests proved that the stainless steels were successfully coated without causing a deterioration in the mechanical property of the low-chromium ferritic/martensitic ODS steel.  相似文献   
652.
We have developed a novel process for recovering metals from alloy-wastes by using a mechanochemical (MC) reaction. The process consists of co-grinding both alloy and polyvinyl chloride (PVC) samples, followed by washing with water and filtration. The co-grinding of the wastes causes a solid-state MC reaction to form metal chlorides and hydrocarbon in the product. The former products are soluble in water, so they can be recovered from the wastes by washing with water, followed by filtration. The PVC waste plays a significant role as a chlorine source in the MC reaction. After filtration, the solid residue can be used as a fuel, due to the absence of chlorine in the product, and the filtrate is subjected to hydrometallurgical process to extract metals from the solution.  相似文献   
653.
In this work, a detailed coupled equilibrium model is presented for predicting the ensemble average probability of hybridization error per chip-hybridized input strand, providing the first ensemble average method for estimating postannealing microarray/TAT system error rates. Following a detailed presentation of the model and implementation via the software package NucleicPark, under a mismatched statistical zipper model of duplex formation, error response is simulated for both mean-energy and randomly encoded TAT systems versus temperature and input concentration. Limiting expressions and simulated model behavior indicate the occurrence of a transition in hybridization error response, from a logarithmically convex function of temperature for excess inputs (high-error behavior), to a monotonic, log-linear function of temperature for dilute inputs (low-error behavior), a novel result unpredicted by uncoupled equilibrium models. Model scaling behavior for random encodings is investigated versus system size and strand-length. Application of the model to TAT system design is also undertaken, via the in silico evolution of a high-fidelity 100-strand TAT system, with an error response improved by nine standard deviations over the performance of the mean random encoding  相似文献   
654.
Local lattice strains of semiconductor devices have been so far examined using higher order Laue zone (HOLZ) line patterns of convergent-beam electron diffraction (CBED). Recently, strain analyses in highly strained regions near interfaces have been reported using split HOLZ line patterns. In the present paper, it is demonstrated for arsenic-doped silicon that the use of CBED rocking curves of low-order reflections provides a promising new tool for the determination of strain distributions of highly strained specimen areas. That is, the anomalous intensity increase in the CBED rocking curves of low-order reflections is explained using a model structure with a strain gradient in the electron beam direction, which is similar to the models used for the split HOLZ line patterns.  相似文献   
655.
Diamond-like carbon (DLC) films have been attractive materials because of their excellent mechanical properties such as high hardness, low friction coefficient, high wear resistance and more. In order to spread the application of the DLC coatings for polymer materials, it is necessary to make the temperature go down during the coating process.Our group has been studying DLC coatings on several materials with bipolar pulse type PBII (plasma based ion implantation) systems, which consist of positive and negative (or bipolar) pulse generators and a timing controller. Recently we have introduced a new bipolar pulse generator, whose slew-rate is several times larger than that of previous generators, and a controller which can make a very short pulse less than 1 μs. Using the pulse generator and controller, we have tried to make Si incorporated DLC (Si-DLC) coatings on fluoro rubber, which is widely used in many industries, at low temperature.Using the new pulse generator and controller, we can make very short width positive pulse of about 1 μs, and reduce the temperature during Si-DLC coating to about 30 K. The lower temperature makes fewer folds on the sample surface. By using optical indentation microscope system, Meyer hardness (HM) of uncoated and Si-DLC coated fluoro rubber was obtained and the value of HM for Si-DLC coated rubber is about 1.4 times larger than that of uncoated rubber. Coefficient of friction of Si-DLC coated rubber was 0.2 to 0.25 and drastically decreased from 1.3 to 1.9 of uncoated rubber. Wear of uncoated fluoro rubber is apparent, however, wear of Si-DLC coated rubber cannot be observed, except for the creep effect of fluoro rubber substrate. The counter SUJ2 ball surfaces also showed almost no wear. Si-DLC coating can make the tribological property of fluoro rubber to low friction and less wear. Si-DLC coatings are very useful in many applications.  相似文献   
656.
To understand the enzymatic degradation behavior of crosslinked polylactide (PLA), the preparation and enzymatic degradation of both thermoplastic (linear) and crosslinked PLAs that have pore structures with different dimensions were carried out. The porous structures of the linear PLA samples were of micro and nanoporous nature, and prepared by batch foaming with supercritical CO2 and compared with the porous structures of crosslinked PLA (Lait-X) created by the salt leaching method. The surface and cross-sectional morphologies of the porous structures were investigated by using scanning electron microscopy. The morphological analysis of porous Lait-X showed a rapid loss of physical features within 120 h of exposure to proteinase-K enzymatic degradation at 37 °C. Due to the higher affinity for water, enhanced enzymatic activity as compared to the linear PLA porous structures in the micro and nanoporous range was observed.  相似文献   
657.
Surface-initiated atom transfer radical polymerization (ATRP) of (2-methacryloyloxyethyl)trimethylammonium chloride (MTAC), 3-(N-2-methacryloyloxyethyl-N,N-dimethyl) ammonatopropanesulfonate) (MAPS), and 2-methacryloyloxyethyl phosphorylcholine (MPC) was carried out in 2,2,2-trifluoroethanol (TFE) containing a small amount of 1-hexyl-3-methylimidazolium chloride at 60 °C to produce well-defined ionic polymer brushes and the corresponding free polymers with predictable number-average molecular weight (Mn, 1×104−3×105 g mol−1) and narrow molecular weight dispersity (Mw/Mn<1.2). A first-order kinetic plot for ATRP of MTAC and MAPS revealed a linear relationship between the monomer conversion index (ln([M]0/[M])) and polymerization time. Reduction in polymerization rates was observed with an increase in ionic liquid concentration. The Mn of both poly(MTAC) and poly(MAPS) increased in proportion to the conversion. The sequential polymerization of MAPS initiated with the chain ends of poly(MAPS) produced the postpolymer with quantitative efficiency. The thickness of the polymer brush was controllable from 5 to 100 nm based on the Mn of the polymer. These results suggest the successful control of the polymerization of sulfobetaine-type methacrylates owing to the TFE and ionic liquids. In particular, the high affinity of TFE for the sulfobetaine monomers and polymers yielded a homogeneous polymerization media to improve surface-initiated polymerization generating the polymer brushes on the substrate surface as well as the free polymers formed in the solution. The effect on ATRP of the chemical structure of ionic liquids and ligands for copper catalyst was also investigated.  相似文献   
658.
In this study, polymethylmethacrylate-based composite cements containing 40–55.6 wt% micron-sized titania (titanium oxide) particles were developed, and their mechanical, setting, and biological properties evaluated. Three types of composite cement containing 40, 50, and 55.6 wt% silanized titania were designated ST2-40c, ST2-50c, and ST2-56c, respectively. In animal experiments, ST2-50c and ST2-56c were implanted into rat tibiae and solidified in situ. An affinity index was used to evaluate osteoconductivity. Compressive and bending strength of ST2-56c was 147.7 ± 3.2 and 69.3 ± 7.4; those of the other cements exceeded 100 MPa and 50 MPa, respectively. The affinity indices of ST2-56c were 42.1 ± 12.9 at six weeks and 53.4 ± 16.6 at 12 weeks, and were significantly higher than for ST2-50c and a commercial PMMA bone cement within 12 weeks. Our data indicate that bone cement containing micron-sized titania particles can be applied to prosthesis fixation as well as vertebroplasty, and ST2-56c is a good candidate cement.  相似文献   
659.
660.
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