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排序方式: 共有4396条查询结果,搜索用时 15 毫秒
121.
A.H Moreira A.V BenedettiP.T.A Sumodjo J.A GarridoP.L Cabot 《Electrochimica acta》2002,47(17):2823-2831
The electrochemical corrosion and passivation of Al5Zn1.7Mg0.23Cu0.053Nb alloys, submitted to different heat treatments (cold-rolled, annealed, quenched and aged, and quenched in two steps and aged), in sulphate-containing chloride solutions, has been studied by means of cyclic polarization, electrochemical impedance spectroscopy (EIS), scanning electron microscopy (SEM), energy-dispersive X-ray (EDX), and X-ray photoelectron spectroscopy (XPS). The cyclic polarization curves showed that sulphate addition to the chloride solution produced a poor reproducible shift of the breakdown potential to more positive potentials. The repassivation potentials, much more reproducible, and practically separating the passive from the pitting potential region, were slightly displaced in the negative direction with that addition. When the alloys were potentiodynamically polarized in the passive potential region, sulphate was incorporated in the oxide film, thus precluding chloride ingress. In addition, Zn depletion was favoured, whereas Mg losses were avoided. Different equivalent circuits corresponding to different alloys and potentials in the passive and pitting regions were employed to account for the electrochemical processes taking place in each condition. This work shows that sulphate makes these alloys more sensitive to corrosion, increasing the fracture properties of the surface layer and favouring the pitting attack over greater areas than chloride alone. 相似文献
122.
Hui Gu Rowland M. Cannon Hans J. Seifert Michael J. Hoffmann Isao Tanaka 《Journal of the American Ceramic Society》2002,85(1):25-32
The nitrogen solubility in the SiO2 -rich liquid in the metastable binary SiO2 -Si3 N4 system has been determined by analytical TEM to be 1%–4% of N/(O + N) at 1973–2223 K. Analysis of the near edge structure of the electron energy loss peak indicates that nitrogen is incorporated into the silicate network rather than being present as molecular N2 . A regular solution model with a positive enthalpy of mixing for the liquid was used to match the data for the metastable solubility of N in the presence of crystalline Si3 N4 and to adjust the computed phase diagram. The solubility of Si3 N4 in fused SiO2 is far less than reported in liquid silicates also containing Al, Mg, and/or Y. Apparently, these cations act as modifiers that break anion bridges in the silicate network and, thereby, allow further incorporation of Si3 N4 without prohibitive amounts of network cross-linking. Finally, indications emerged regarding the diffuse nature of the Si3 N4 -SiO2 interface that leads to amorphous regions of higher N content. 相似文献
123.
Calcium hexa-aluminate (CaO·6Al2 O3 ) has been prepared from calcium nitrate and aluminum sulfate solutions in the temperature range of 1000°–1400°C. A 0.3 mol/L solution of aluminum sulfate was prepared, and calcium nitrate was dissolved in it in a ratio that produced 6 mol of Al2 (SO4 )3 ·16H2 O for each mole of Ca(NO3 )2 ·4H2 O. It was dried over a hot magnetic stirrer at ∼70°C and fired at 1000°–1400°C for 30–360 min. The phases formed were determined by XRD. It was observed that CaO·Al2 O3 and CaO·2Al2 O3 were also formed as reaction intermediates in the reaction mix of CaO·6Al2 O3 . The kinetics of the formation of CaO·6Al2 O3 have been studied using the phase-boundary-controlled equation 1 − (1 − x )1/3 = K log t and the Arrhenius plot. The activation energy for the low-temperature synthesis of CaO·6Al2 O3 was 40 kJ/mol. 相似文献
124.
Yoshiyuki Abe Kazuyuki Kakegawa Yoshinori Sasaki 《Journal of the American Ceramic Society》1992,75(1):234-236
A complex perovskite of Sr(Cu x Zn1- x )1/2 W1/2 O3 (SCZW) is synthesized by a new combination of wet and dry processess. Mixed oxides containing Cu2+ and Zn2+ (CZ) are prepared by the wet process (coprecipitate method). SCZW is obtained by the dry process (mixed-oxide method) from a mixture of CZ, SrCO3 , and WO3 . SCZW has practically no compositional, unlike solid solutions prepared by the conventional dry method. The wet–dry process method is useful because the wet process is applied to only B-site cations having the same valence. 相似文献
125.
Youren Xu Avigdor Zangvil Martine Landon François Thevenot 《Journal of the American Ceramic Society》1992,75(2):325-333
A flexural strength of up to 1 GPa was achieved in SiC-AIN materials and is attributed to a dense, equiaxial grain structure of the 2H(δ) SiC-AIN solid solution, with a relatively uniform grain size of ∼ 1 μm. The strength was found to decrease with increasing grain size. While the β→α phase transformation and the formation of various metastable polytypes make microstructural control difficult in SiC materials, excellent control is facilitated in SiC-AIN materials as a result of the stable 2H solid solution. Several mechanisms of grain refinement during the β→ 2H transition were observed, most notably the direct formation of several 2H grains from a single β grain. In addition, grain growth is limited by the diffusion-controlled nature of the transition. These mechanisms could be utilized to achieve even higher strength values, with potentially higher reliability of the materials in structural applications. 相似文献
126.
Activities of NiO were measured in the oxide and spinel solutions of the system MnO–NiO–Al2 O3 at 1300° and 1400° C with the aim of deriving information on the thermodynamic properties of the spinel phases. Synthetic samples in selected phase assemblages of the system were equilibrated with metallic nickel and a gas phase of known oxygen partial pressures at a total pressure of 1 atm. The data on NiO activities and directions of conjugation lines between coexisting oxide and spinel phases were used to establish the activity–composition relations in spinel solid solutions at 1300° and 1400°C. The MnAl2 O4 –NiAl2 O4 solid solutions exhibit considerable negative deviations from ideality at these temperatures. The free energy of formation of MnAl2 O4 from its oxide components (MnO + Al2 O3 ) at 1300° and 1400°C is calculated to be −24.97 and −26.56 kJ. mol−1 , respectively. The activities determined in the stoichiometric spinel solid solutions are more negative as compared with those predicted from cation distribution models. 相似文献
127.
The equilibrium reaction 3'(Fe, Co)O'( ss ) +1/2O2 ( g ) ⇄ (Fe, Co)3 O4 ( ss ) was studied in the temperature range 970 to 1370 K for seven different total compositions of molar ratios 0.5 < Fe/(Fe + Co) ≤ 1.0. The equilibrium pressures of oxygen were determined by using galvanic cells incorporating calcia stabilized zirconia as solid electrolyte and the Fe/Co ratios in the solid-solution phases by wavelength dispersive spectrometry microprobe analyses. The activities of 'FeO' in the cobaltowüstite phase were then derived from the experimental results obtained. 相似文献
128.
Masatomo Yashima Nobuo Ishizawa Masahiro Yoshimura 《Journal of the American Ceramic Society》1992,75(6):1541-1549
Oxygen vacancies can be introduced into zirconia solid solution ZrO2 –MO u ( u = 1 and 1.5) to maintain electroneutrality. Recently, the local structures around Zr4+ and M2 u + ions in ZrO2 –MO u solid solutions have been studied through EXAFS spectroscopy, diffuse scattering analysis, and single-crystal structure analysis. The present study constructs an ion-packing model for zirconia solid solutions based on some defect cluster models. The decrease of cell volume with the occurrence of vacancies is assumed to be expressed by decreasing the coordination number (CN) of cations around the vacancy. The distribution of CNs in a solid solution was calculated from a certain defect cluster model. The average interatomic distances, the average CN, and the short-range order parameters were calculated using this distribution of CNs. The local structures calculated from the model were compared with experimental data in the systems ZrO2 –MO1.5 (M = Y, Gd, Yb, and Ca). In the ZrO2 –YO1.5 system, the r (s–O) interatomic distance, where s represents Zr4+ or Y3+ and O represents O2− , decreased with Y content and therefore vacancy content. The probability of finding Y3+ around a vacancy increases with increasing yttria content from a comparison of the calculated results with the ones from recent EXAFS studies. The present model can qualitatively explain compositional and size dependences of the dopant on various local structures. 相似文献
129.
利用三角降次公式及留数解决了第一类Dirichlet积分问题,即给出了第一类Dirichlet积分的公式解。利用所得结果,定义了Dirichlet数Dn,证明了其一般性质。 相似文献
130.
Investigation of transport phenomena in a hybrid ion exchange-electrodialysis system for the removal of copper ions 总被引:2,自引:0,他引:2
A. Mahmoud L. Muhr S. Vasiluk A. Aleynikoff F. Lapicque 《Journal of Applied Electrochemistry》2003,33(10):875-884
Hybrid ion exchange electrodialysis processes allow the removal of metal ions from dilute waste liquids and the recovery of more concentrated solutions. The work reported here was aimed at investigating the two steps in the treatment process, namely, adsorption of metal ions onto the packed bed of resin and electromigration (i.e., the transport of these ions in the complex system under the applied electrical field). The case of copper sulfate was investigated. Dowex resins with a cross-linking degree of 2 and 8% were used. The flux of copper through the resin bed and the current efficiency for ion transfer to the cathode compartment were determined as a function of potential gradient and copper ionic fraction in the bed. Apparent diffusion coefficients of Cu2+ in the overall system were deduced from the experimental data. 相似文献