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941.
This paper outlines the first known examination of the forces required to jettison a simulated exit used during helicopter underwater egress training (HUET). To capture the forces placed on the simulated cabin exit, a purpose build force plate was designed to replace an existing simulator exit used during HUET. A 25-point map was created to identify specific jettison forces required across the entire exit surface. Ten participants completed a total of 120 underwater egress sequences in–air and in-water from a normal flight and fully compressed crash attenuating seat position. The results indicate that the force required to jettison the simulated exit is significantly different in relationship to location on the exit surface. From the results, it can be concluded that helicopter underwater egress training protocols should ensure that offshore candidates are informed of the different force requirements as well as have the opportunity to practice jettisoning a high physical fidelity exit from a fully compressed crash attenuating seat. 相似文献
942.
Mark I. Jones Hideki Hyuga Kiyoshi Hirao Yukihiko Yamauchi 《Journal of the American Ceramic Society》2004,87(4):714-716
Novel Lu-α-SiAlON ceramics were produced by hot pressing mixtures of Si3 N4 , Lu2 O3 , AlN, and Al2 O3 at 1950°C for 2 h in a nitrogen atmosphere. The resultant SiAlON was fully dense and possessed a uniform, equiaxed microstructure with a grain size of ∼1 μm, which resulted in a high hardness of >19 GPa. In addition to high hardness, the sample showed very high optical transparency in the visible light region, with >70% transmission at higher wavelengths. This high transparency was attributed to the uniform, dense microstructure and lack of residual grain-boundary phase. 相似文献
943.
Ping-Hua Xiang Xian-Lin Dong Chu-De Feng Yong-Ling Wang 《Journal of the American Ceramic Society》2003,86(9):1631-1634
NiO nanoparticle-coated lead zirconate titanate (PZT) powders are successfully fabricated by the heterogeneous precipitation method using PZT, Ni(NO3 )2 ·6H2 O, and NH4 HCO3 as the starting materials. The amorphous NiCO3 ·2Ni(OH)2 ·2H2 O are uniformly coated on the surface of PZT particles. XRD analysis and the selected-area diffraction (SAD) pattern indicate that the amorphous coating layer is crystallized to NiO after being calcined at 400°C for 2 h. TEM images show that the NiO particles of ∼8 nm are spherical and weakly agglomerated. The thickness of the nanocrystalline NiO coating layer on the surface of PZT particle is ∼30 nm. 相似文献
944.
Masashi Shou Hiroyuki Takekawa Dong-Ying Ju Tokio Hagiwara Da-ling Lu Ken-ichi Tanaka 《Catalysis Letters》2006,108(3-4):119-124
Catalytic activity of a 1 wt% Au/TiO2 catalyst is markedly improved by loading a large amount of FeOx, on which the oxidation of CO in excess H2 is selectively promoted at temperature lower than 60 °C. Oxidation of CO with O2 on the FeOx/Au/TiO2 catalyst is markedly enhanced by H2, and H2O moisture also enhances the oxidation of CO but its effect is not so large as the promotion by H2. We deduced that activation of Au/TiO2 catalyst by loading FeOx is not caused by the size effect of Au particles but a new reaction path via hydroxyl carbonyl intermediate is responsible
for the superior activity of the FeOx/Au/TiO2 catalyst. 相似文献
945.
Esterification of acrylic acid with methanol by reactive chromatography: Experiments and simulations
The esterification of acrylic acid with methanol using Amberlyst 15 as a stationary phase has been investigated using a chromatographic reactor. Several experimental runs at various operating conditions have been conducted on a batch column. A classical reactive chromatography model including lumped kinetics, a linear driving force transport model and a heterogeneous kinetic model for the catalytic reaction has been developed. The additional dispersion of concentration fronts due to density gradient effects has been accounted for in the model. The model parameters have been determined in a fast and reliable way by directly fitting the batch column experiments. In general, a good agreement between experimental and calculated results is obtained. The evaluation of the covariance of the fitted model parameters reveals important insights about the system behavior.Based on the detailed batch column model, a complete model of a simulated-moving-bed reactor has been implemented and its optimal point of operation for the synthesis of methyl acrylate from acrylic acid has been determined. Particularly when considering the low-operating temperature, we can regard this process as a possible competition for current technologies. 相似文献
946.
Propylene epoxidation over Ti/MCM-41 catalysts prepared by chemical vapor deposition 总被引:3,自引:0,他引:3
Ti-containing mesoporous catalysts were prepared by chemical vapor deposition (CVD) of TiCl4 on silica MCM-41 in the 700–900 °C temperature range. These samples were characterized (with XRD, ICP, nitrogen adsorption, FT-IR, ESCA, and TEM) and evaluated for the epoxidation of propylene with two alkyl hydroperoxides. The increase of CVD temperature resulted in the decrease of titanium content, catalyst hydroxyl population, crystallinity, and surface area. Catalyst selectivity to the desired product – propylene oxide – was highly sensitive to the deposition temperature. The best Ti/MCM-41 catalyst was prepared at the temperature of 800 °C, which had the maximum propylene oxide yield of 94.3%. 相似文献
947.
M. Pérez-Luna A. Cosultchi J. A. Toledo-Antonio C. Angeles-Chavez E. M. Arce-Estrada 《Catalysis Letters》2006,107(1-2):103-110
Three Ni/ZrO2–SO4=/Al2O3 catalysts with different concentrations of platinum (0.2, 0.3 and 0.4 wt%) were prepare and tested for n-butane isomerization reaction at 338 K, in absence and in presence of hydrogen. The results shown that, at low temperature,
platinum contributes to the olefin or butyl ion formation and the reaction follows a bimolecular pathway. However, when the
reaction occurs in the presence of hydrogen, the formation of butyl ions is inhibited. The main feature of platinum addition
is the stabilization of the catalytic activity, which is indicated by the slow deactivation constants compared to that of
the unpromoted catalyst. 相似文献
948.
Recent studies of self-condensation and co-condensation of melamine-formaldehyde resins; cure at low temperatures 总被引:1,自引:0,他引:1
Self-condensation: recent research on the chemical pathways by which alcoholated melamine-formaldehyde (MF) resins react with themselves and on the product structures is summarized. Model compound studies suggest that
bridges are less stable than widely thought unless they are in hexahydro-1,3,5-triazine ring structures. In acyclic structures they are probably less stable than
bridges. Co-condensation: studies of how the composition of MF resins influences the rates of reaction with poly(ol) co-reactant show that MF resins that contain very low levels of
and/or
functionality are quite reactive. Reactivities of a variety of poly(ester) and acrylic coreactants were studied. By combining reactive MF resins with reactive co-reactants one can formulate high solids enamels that cure by co-condensation in 30 min at 50 to 65 °C with 0.5 parts per hundred (phr) of p-toluenesulfonic acid (p-TSA) catalyst. Cure at 25 °C appears feasible with higher catalyst levels. 相似文献
949.
An isothermal model for hydrodemetallation (HDM) of crude oils in catalytic fixed-bed reactors is proposed. This model involves a consecutive reaction mechanism, which is capable of accounting for particle deposit profiles with interior maxima. Consistent with the fact that HDM catalysts are conglomerates formed by precipitation, the porous catalyst itself is modeled as randomly overlapping spheres of equal size. The metal is deposited as growing metal sulfide crystallites on the inner surface of the catalyst. These crystallites originate from a certain number of randomly scattered nuclei and increase in size as the deposition proceeds. The random sphere model for the catalyst and the deposit provides the changes in the catalyst pore structure—local porosity and surface area.
The mass transport within the domain of the particle is due to restricted liquid diffusion, since the diameter of the metal bearing compound (porphyrin) and the intermediate are comparable to the pore size. The diffusion restrictions taken into account are the enhanced drag imposed on a molecule by adjacent pore walls and steric partitioning.
Since the deposition process is much slower than diffusion and reaction, the pseudo-steady-state assumption can be justified. The equations of conservation for mass are solved by orthogonal collocation on finite elements. Based on this solution technique a computer simulation program of HDM is designed that allows two modes of operation: constant temperature and constant conversion. The simulation program “SIMULA” is highly flexible with regard to reaction kinetics, catalyst structure, reactor design, and operating conditions. In comparison to a base case with uniform activity, the effect of intraparticle (radial) and bed (axial) activity profiles on the conversion rate is discussed. For the case investigated, a radial distribution of activity higher at the center of the particle than at the edge can increase catalyst life by 25%, but axial distribution was less successful. 相似文献
The mass transport within the domain of the particle is due to restricted liquid diffusion, since the diameter of the metal bearing compound (porphyrin) and the intermediate are comparable to the pore size. The diffusion restrictions taken into account are the enhanced drag imposed on a molecule by adjacent pore walls and steric partitioning.
Since the deposition process is much slower than diffusion and reaction, the pseudo-steady-state assumption can be justified. The equations of conservation for mass are solved by orthogonal collocation on finite elements. Based on this solution technique a computer simulation program of HDM is designed that allows two modes of operation: constant temperature and constant conversion. The simulation program “SIMULA” is highly flexible with regard to reaction kinetics, catalyst structure, reactor design, and operating conditions. In comparison to a base case with uniform activity, the effect of intraparticle (radial) and bed (axial) activity profiles on the conversion rate is discussed. For the case investigated, a radial distribution of activity higher at the center of the particle than at the edge can increase catalyst life by 25%, but axial distribution was less successful. 相似文献
950.
Walter Brockmann 《The Journal of Adhesion》1989,29(1):53-61
Adequate adhesion between metals and polymers is primarily the result of chemical bonds in the boundary layer. This region, however, is subject to degradation by moisture. Three modes of deterioration are observed. The first is a largely reversible weakening effect in the polymer layer near the metal oxide surface. The structure of this layer differs from that of the bulk and is influenced by the chemical and physical properties of the surface. The second is a slow transformation of the oxide by hydration and a diffusion of oxide constituents into the polymer. This process is irreversible and is influenced by the state of the surface and chemical properties of the polymer. The third is a fast deterioration of the oxide by primary corrosion usually initiating at an unprotected edge but occasionally arising within the body of a joint. 相似文献