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911.
Ammonia volatilization, denitrification loss and total nitrogen (N) loss (unaccounted-for N) have been investigated from N fertilizer applied to a calcareous sandy loam fluvo-aquic soil at Fengqiu in the North China Plain. Ammonia volatilization was measured by the micrometeorological mass balance method, denitrification by the acetylene inhibition – soil core incubation technique, and total N loss by 15N-balance technique. Ammonia loss was an important pathway of N loss from N fertilizer applied to rice (30–39% of the applied N) and maize (11–48%), but less so for wheat (1–20%). The amounts of unaccounted-for fertilizer N were in the order of rice > maize > wheat. Deep placement greatly reduced ammonia volatilization and total N loss. Temperature, wind speed, and solar radiation (particular for rice), and source of N fertilizer also affect extent and pattern of ammonia loss. Denitrification (its major gas products are N2 and N2O) usually was not a significant pathway of N loss from N fertilizer applied to maize and wheat. The amount of N2O emission (N2O is an intermediate product from both nitrification and denitrification) was comparable to denitrification loss for maize and wheat, and it was not significant in the economy of fertilizer N in agronomical terms, but it is of great concern for the environment.  相似文献   
912.
The study of heat exchanger fouling using supersaturated calcium sulphate solutions has been widely reported. In this study fouling was investigated in a larger-scale heat exchange apparatus using stainless-steel pipe, and data were obtained at different flow rates, concentrations and temperature differences. The deposits were examined using a scanning electron microscope, X-ray diffraction and conventional photography. In a novel approach, wood pulp fibers were added to the fouling solution at various concentrations to mitigate fouling. Heat transfer enhancement above the solution-alone was observed initially and the onset of fouling delayed. When fouling eventually developed the final asymptotic level was lower than the fiber-free case for the experimental conditions specified. At a fiber concentration of 0.15% heat transfer augmentation occurred for 11 days. However, at 0.25% fiber concentration, heat transfer augmentation (no fouling) was sustained over the experimental duration of 45 days. It can be concluded that the service-life cycle of a heat exchanger can be prolonged with the addition of asymmetric, flexible, natural fibers. In this work it is argued that fibers modify the onset of deposition by boundary layer scavenging, and interact with turbulent eddies to reduce the rate of mass transfer of the foulant to the heated surface. When scale forms, the crystalline structure of the scale is interrupted by the fibers, which appear to roughen the heat transfer surface initially and increase the heat transfer coefficient. However, the scale deposit continues to build up very slowly, causing the thermal resistance to eventually override the turbulence augmented heat transfer effect of the fibers.  相似文献   
913.
Three MgO surfaces of different structures have been employed as models for study of the acid-base properties of MgO. Surface spectroscopies including XPS, UPS, and ISS were used to determine the nature and the absolute coverage of surface intermediates, and the nature of bonding sites upon adsorption of Brønsted acid molecules on these surfaces. Different behavior patterns of the Brønsted acid molecules with varying strengths on the three model surfaces provide insights into the site requirements for dissociation of Brønsted acids on MgO. The base-catalyzed Cannizzaro reaction of formaldehyde was observed on these model surfaces under UHV conditions.  相似文献   
914.
The texture of a polymer (on fiber) is effectively developed by heat and stress. In this article, the chief material studied is acrylics, usually polyacrylonitile copolymer (PAC fiber) produced by Jingshan Jinglun Fiber Production Plant. In industry, the Jinglun acrylic fiber is heat treated, using saturated steam, at a temperature of 120–130°C to enhance its loop strength, reduce shrinkage, and stabilize crimp. At 140°C, the fiber becomes tacky and its good textile properties seem to deteriorate. At 150–160°C, the texture of the fiber seems to be deeply modified. Tested by differential scanning calorimetry (DSC) with the fiber immersed in a swelling agent (usually termed swelling DSC, abbreviated as SDSC), in addition to the entanglement peaks situated on the latter part of the thermogram of the Jinglun fiber, a new endothermic peak before the crystalline peak (actually, paracrystalline in the case of acrylic fiber) was discovered. The elastic recovery properties of the treated fiber under partially swelling conditions were improved. This seems to indicate that this preparacrystalline peak might also be concerned with entanglements.  相似文献   
915.
Methodology was developed for the synthesis of novel 2-substituted o-nitrobenzyl chromophores, which were derivatized as the tosylate esters. The thermal stabilities of these new tosylates fell within the range predicted from an empirical model. Lithographic sensitivities of deep UV resists made from these new esters and poly(4-(tert-butoxycarbonyloxy)styrene-sulfone) ranged from 45 to 90 mJ/cm2.  相似文献   
916.
Formulation effects on the distribution of pigment particles in paints   总被引:2,自引:0,他引:2  
Modern water-borne paints are widely used in different areas of applications ranging from high-gloss lacquers to flat, scrub-resistant interior paints. From this point of view, the pigment volume concentration (PVC) is one key-parameter adjusting the desired application properties. In high-gloss paints, for example, a low PVC is required to accommodate the proper surface roughness to achieve a high gloss. Consequently, a high concentration of TiO2 is needed to obtain a good hiding power at the same time. Flat paints nonetheless are highly filled due to cost reasons preferentially by CaCO3 and the pigment binding capacity of the binder is crucial. In this work, paint formulations differing in PVC, and the type of binder or dispersing agent were investigated by various techniques concerning the distribution and aggregation of pigment particles, e.g. TiO2. To get a detailed insight into the structure of the liquid paints and the corresponding dried paint films, suitable analytical tools were applied for characterization. The structure of the liquid paints was analyzed by remission light spectroscopy (RLS), disc centrifugation, cryogenic-replication transmission electron microscopy (Cryo-replica TEM) and cryogenic-scanning electron microscopy (Cryo-SEM). The pigment distribution in the corresponding dried paint films was examined by means of atomic force microscopy (AFM), TEM and RLS. The tendency of the TiO2-pigments to form aggregates was found to depend on both: first on the type of binder used in the formulation and second on the employed dispersing agent. It is shown that only by adjusting the properties of the binder in combination with common dispersants, it is possible to get well-distributed TiO2 particles within the paint. Correlation of application properties, e.g. gloss and blocking to the microscopic structure is presented.  相似文献   
917.
This paper describes the methodology for simulating a reprographic ink with a ceramic ink based on a commercially available zirconia powder for direct ceramic ink-jet printing. Of over-riding importance was matching viscosity and this was tested systematically by using a mineral oil–hexane binary system. Of secondary importance was adjustment of the pressure defect behind the nozzle to compensate for small differences in surface tension. The inks tested in the wide array print-head were based on low electrical conductivity liquids to avoid damage to the electroding system. The organic binder for the zirconia ink was paraffin wax and the dispersant was a hydroxystearic acid based polyester.  相似文献   
918.
X. Dupain  R. Madon  M. Makkee  J.A. Moulijn 《Fuel》2003,82(13):1559-1569
A paraffinic hydrowax feed spiked with naphthalene, anthracene, and phenanthrene was cracked in a once-through microriser reactor at 575 °C and with a catalyst-to-oil (CTO) ratio of 4.8 gcat goil−1. The conversion by cracking reactions is limited to the paraffinic fraction of the feed and the alkyl groups associated with the benzene ring in aromatic compounds; the aromatic probes did not crack under the applied conditions, and in fact an additional amount of naphthalene was formed by complex dealkylation and hydrogen transfer reactions. The ‘uncrackabilty’ of aromatics was directly demonstrated by processing an aromatic gas oil, containing 33.3 wt% aromatics. Experiments were performed with residence times between 0.05 and 8.2 s, keeping the temperature (525 °C) and CTO ratio (5.5 gcat goil−1) constant. The data was interpreted with a simplified first-order five-lump kinetic model, where approximately 19 wt% of the feed was found to be uncrackable. HCO (feedstock) conversion took mainly place during the first two seconds and coke was only formed during the first 50 ms of catalyst-oil contact. Gasoline was not overcracked to gas. Approximately 50 wt% of the LCO fraction was formed during this 50 ms and did not change thereafter.  相似文献   
919.
L.X. Zhou  F. Wang  J. Zhang 《Fuel》2003,82(13):1579-1586
A unified second-order moment (USM) turbulence-chemistry model is used to simulate methane-air swirling combustion and NO formation for different swirl numbers. The simulation results are compared with those using the EBU-Arrhenius (E-A) combustion model, the simplified PDF model of NO formation in turbulent flows and the corresponding experimental results. The comparison indicates that the USM model is obviously better than the E-A model and the simplified PDF model. The E-A model cannot reasonably simulate the finite-rate kinetics, while the simplified PDF model, using a product of two single-variable PDF's instead of a joint PDF, remarkably under-predicts the NO reaction rate. The USM model gives the best agreement with the experimental results. Predictions show that as the swirl number increases the total NO formation at first decreases and then increases, which is in agreement with the experimental results.  相似文献   
920.
W.X Chen  L.Y Wang  Z.D Xu 《Carbon》2003,41(2):215-222
Ni-P-carbon nanotube (CNT) composite coating and carbon nanotube/copper matrix composites were prepared by electroless plating and powder metallurgy techniques, respectively. The effects of CNTs on the tribological properties of these composites were evaluated. The results demonstrated that the Ni-P-CNT electroless composite coating exhibited higher wear resistance and lower friction coefficient than Ni-P-SiC and Ni-P-graphite composite coatings. After annealing at 673 K for 2 h, the wear resistance of the Ni-P-CNT composite coating was improved. Carbon nanotube/copper matrix composites revealed a lower wear rate and friction coefficient compared with pure copper, and their wear rates and friction coefficients showed a decreasing trend with increasing volume fraction of CNTs within the range from 0 to 12 vol.% due to the effects of the reinforcement and reduced friction of CNTs. The favorable effects of CNTs on the tribological properties are attributed to improved mechanical properties and unique topological structure of the hollow nanotubes.  相似文献   
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