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121.
Yong K. Park Ho K. Lee Nong M. Hwang Houk C. Kwon Jong C. Park Duk N. Yoon 《Journal of the American Ceramic Society》1988,71(6):297-C
Microstructures of Y-Ba-Cu-O superconductor were observed using a polarized microscope. Orthorhombic and tetragonal phases were easily distinguished by the optical etching with cross-polarized light. In the specimen cooled rapidly in oxygen, it was possible to see the path of oxygen diffusion by observing the variation of the twin concentration. At the boundary between transformed and untransformed materials, evidence for diffusion-driven transformation could be clearly seen. 相似文献
122.
Highly Efficient Overall Water Splitting Through Optimization of Preparation and Operation Conditions of Layered Perovskite Photocatalysts 总被引:1,自引:0,他引:1
Jindo Kim Dong Won Hwang Hyun Gyu Kim Sang Won Bae Jae Sung Lee Wei Li Se Hyuk Oh 《Topics in Catalysis》2005,35(3-4):295-303
The layered perovskite materials were found to give the high photocatalytic activity in water splitting reaction under UV
irradiation, where the electronic structure of perovskite slab constructing the layered structure (the total cation valency)
was the most crucial factor to the high photocatalytic activity. Both the excessive cation valency and the layered structure
were required for active photocatalysts, while the slab thickness of layered perovskites had an insignificant effect on water-splitting
activity. In order to identify key variables that affected photocatalytic activity and to optimize the performance of (110)
layered perovskite, La2Ti2O7 was modified by various methods. The optimum amount of loaded nickel had a great effect and the amount depended on the surface
area of the perovskite phase. When an alkaline-earth element such as Ba, Sr, and Ca was doped on La2Ti2O7, the photocatalytic activity was enhanced markedly. Introduction of an alkaline hydroxide into the reaction system as an
external additive enhanced the activity further showing extremely high quantum yields close to 50%. 相似文献
123.
Summary Poly[2-(2-(4-(trifluoromethyl)phenyl)ethenyl)-5-methoxy-1,4-phenylenevinylene] (PFEMPV) and a series of PPV copolymers containing 1,4-phenylenevinylene (PV) units were synthesized through a water-soluble precursor route, and their electrical and third-order nonlinear optical properties were studied. The PFEMPV films could not be doped with I2, but FeCl3-doped films showed an electrical conductivity of 5.0x10-4 S/cm. The conductivities of FeCl3-doped copolymer films ranged from 2.0x10-3 to 2.0 S/cm depending on their copolymer compositions. The third-order nonlinear optical susceptibility, (3)(–;,,–), was also investigated by the degenerate four wave mixing technique at 602 nm. The (3) value of PFEMPV was 6.9x10-11 esu. The photoluminescence spectrum of PFEMPV shows its emission maximum at 550 nm. 相似文献
124.
J.-F. Hwang J. A. Manson R. W. Hertzberg G. A. Miller L. H. Sperling 《Polymer Engineering and Science》1989,29(20):1466-1476
Epoxies toughened with two reactive liquid rubbers, an epoxy-terminated butadiene acrylonitrile rubber (ETBN) and an amino-terminated butadiene acrylonitrile rubber (ATBN), were prepared and studied in terms of their structure property relationships. A two-phase structure was formed, consisting of spherical rubber particles dispersed in an epoxy matrix. A broad distribution of rubber particles was observed in all the materials with most of the particles ranging in size from 1 to 4 μm, but some particles exceeding 20 μm were also found. Impact strength, plane strain fracture toughness (KIC), and fracture energy (GIC) were increased, while Young's modulus and yield strength decreased slightly with increasing rubber content and volume fraction of the dispersed phase. Both GIC and KIC were found to increase with increasing apparent molecular weight between crosslinks and decreasing yield strength. The increased size of the plastic zone at the crack tip associated with decreasing yield strength could be the cause of the increased toughness. An ATBN-toughened system containing the greatest amount of epoxy sub-inclusion in the rubbery phase demonstrated the best fracture toughness in this series. In the present systems, rubber-enhanced shear deformation of the matrix is considered to be the major toughening mechanism. Curing conditions and the miscibility between the liquid rubber and the epoxy resin determine the phase morphology of the resulting two-phase systems. Kerner's equation successfully describes the modulus dependence on volume fraction for the two-phase epoxy materials. 相似文献
125.
Shiang-Hua Wang Ford-Son Hwang Tseung-Yuen Tseng 《Journal of the American Ceramic Society》1990,73(9):2767-2770
High-Curie-point semiconducting barium-lead titanate positive temperature coefficient of resistivity (PTCR) ceramics of composition Ba0.897 Pb0.1 La0.003 TiO3 and Ba0.5 Pb0.5 La0.003 TiO3 were prepared. The starting powders were synthesized by reacting commercial BaTiO3 , PbO, and TiO2 . To avoid the nonstoichiometry due to the volatilization of Pb during the sintering process, a lead atmosphere sintering approach with PbTiO3 as packing powder was used. The samples being fabricated by this method show a PTCR effect of 3 to 4.5 orders of magnitude above the Curie point. The curie points were about 180°C for Ba0.897 Pb0.1 La0.003 TiO3 and about 360°C for Ba0.497 Pb0.5 La0.003 TiO3 . 相似文献
126.
The interfaces between metal organic chemical vapor deposited PbTiO3 thin films and various diffusion barrier layers deposited on Si substrates were investigated by transmission electron microscopy. Several diffusion barrier thin films such as polycrystalline TiO2 , amorphous TiO2 , ZrO2 , and TiN were deposited between the PbTiO3 thin film and Si substrate, because the deposition of PbTiO3 thin films on bare Si substrates produced Pb silicate layers at the interface irrespective of the deposition conditions. The TiO2 films were converted to PbTiO3 by their reaction with diffused Pb and O ions during PbTiO3 deposition at a gubstrate temperature of 410°C. Further diffusion of Pb and O induces formation of a Pb silicate layer at the interface. ZrO2 did not seem to react with Pb and O during PbTiO3 deposition at the same temperature, but the Pb and O ions that diffused through the ZrO2 layer formed a Pb silicate layer between the ZrO2 and Si substrate. The TiN films did not seem to react with Pb and O ions during the deposition of PbTiO3 at 410°C, but reacted with PbTiO3 to form a lead-deficient pyrochlore during postdeposition rapid thermal annealing at 700°C. However, TiN could effectively block the diffusion of Pb and O ions into the Si substrate and the formation of Pb silicate at the interface. 相似文献
127.
New microporous hybrid organic/inorganic materials were obtained by modification of zeolites using chlorination of their surface,
followed by treatment with a Grignard reagent. Loading of butyl groups and retained crystallinity of ZSM-5 type zeolites was
higher than for zeolites Y. In contrast to zeolites Y, the lattice parameters of zeolites ZSM-5 increased after surface modification.
The obtained hybrid materials on the basis of high-silica zeolites possess a high degree of crystallinity at increased hydrophobicity. 相似文献
128.
An increase in the depolymerization of chitosan was found with an increased concentration of sodium perborate. Acetic anhydride was added to reacetylated chitosan in a molar ratio per gulcosamine unit, and the amide I band of IR spectra changed with the addition of acetic anhydride. Sixteen chitosans with various molecular weights (MWs) and degrees of deacetylation (DODs) were prepared. X‐ray diffraction patterns indicated their amorphous and partially crystalline states. Increases in the chitosan MW and DOD increased the tensile strength (TS). TS of the chitosan films ranged from 22 to 61 MPa. However, the elongation (E) of chitosan films did not show any difference with MW. TS of chitosan films decreased with the reacetylation process. However, E of chitosan films was not dependent on DOD. The water vapor permeabilities (WVPs) of the chitosan films without a plasticizer were between 0.155 and 0.214 ng m/m2 s Pa. As the chitosan MW increased, the chitosan film WVP increased, but the values were not significantly different. Moreover, the WVP values were not different from low DOD to high DOD. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 89: 3476–3484, 2003 相似文献
129.
The manufacture of polymer composites through resin transfer molding (RTM) or structural reaction injection molding (SRIM) involves the impregnation of a fibrous reinforcement in a mold cavity with a reactive polymer resin. The design of RTM and SRIM operations requires an understanding of the various parameters, such as materials properties, mold geometry, and mold filling conditions, that affect the resin impregnation process. Modeling provides a potential tool for analyzing the relationships among the important parameters. The present work provides the physical model and finite element formulations for simulating the mold filling stage. Resin flow through the fibers is modeled using two-dimensional Darcian flow. Simultaneous resin reaction and heat transfer among resin, mold walls, and fibers are considered in the model. The proposed technique emphasizes the use of the least squares finite element method to solve the convection dominated mass and energy equations for the resin. Excellent numerical stability of the proposed technique provides a powerful numerical method for the modeling of polymer processing systems characterized by convection dominated transport equations. Results from example numerical studies for SRIM of polyurethane/glass fiber composites were presented to illustrate the application of the proposed model and numerical scheme. 相似文献
130.
Sang Hern Kim Won Keun Son Yong Joo Kim Eu‐Gene Kang Dong‐Won Kim Chang Woo Park Whan‐Gi Kim Hyung‐Joong Kim 《应用聚合物科学杂志》2003,88(3):595-601
A polystyrene (PS)/poly(butyl acrylate) (PBA) composite emulsion was produced by seeded emulsion polymerization of butyl acrylate (BA) with PS seed particles which were prepared by emulsifier‐free polymerization of styrene with potassium persulfate (KPS) under a nitrogen atmosphere at 70°C for 24 h with stirring at 60 rpm and swelled with the BA monomer in an ethanol/water medium. The structure of the PS/PBA composite particles was confirmed by the presence of the characteristic absorption band attributed to PS and PBA from FTIR spectra. The particles for pure PS and PS/PBA with a low content of the BA monomer were almost spherical and regular. As the BA monomer content was increased, the particle size of the PS/PBA composite particles became larger, and more golf ball‐like particles were produced. The surface morphology of the PS/PBA composite particles was investigated by AFM and SEM. The Tg's attributed to PS and PBA in the PS/PBA composite particles were found at 110 and ?49°C, respectively. The thermal degradation of the pure PS and PS/PBA composite particles occurred in one and two steps, respectively. With an increasing amount of PBA, the initial thermal decomposition temperature increased. On the contrary the residual weight at 450°C decreased with an increasing amount of PBA. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 88: 595–601, 2003 相似文献