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151.
152.
Chang Soo Kim Stephen J. Lombardo Robert A. Winholtz 《Journal of the American Ceramic Society》2005,88(8):2064-2070
Ceramic beams are induced in situ to form complex shapes at elevated temperature without the application of an external stress. This process has been demonstrated for thin alumina substrates coated with a layer of magnesia. The internal strain causing the substrates to deform at elevated temperature arises as a consequence of strain mismatch accompanying the penetration of the coating into the substrate. The magnitude of the deformation depends on the amount of coating applied, on the thickness of the substrate, on the density of the substrate, and on the temperature. During exposure of the beams to elevated temperature, the magnesia coating reacts with the alumina substrate to form the spinel phase; the resulting volume change accompanying the phase transformation is likely the predominant driving force for deformation. 相似文献
153.
Three-dimensionally ordered long-range macroporous carbon structures were prepared using commercially available phenolic resin
by utilizing sacrificial colloidal silica crystalline arrays as templates that were subsequently removed by HF etching after
pyrolysis in an argon atmosphere. SEM, TEM, and BET were employed to characterize the morphology and the surface area of the
porous carbon structures. The pore size (150–1000 nm) and BET surface area, which reflect pore volume (298.6 m2/g (1.32 cm3/g) ∼ 93.7 m2/g (0.12 cm3/g)), of the macroporous carbon structures produced were approximately proportional to the size (150–1000 nm) of the sacrificial
silica sphere templates used (annealing temp. 550°C). The achieved 550 nm porous carbon structures were examined to function
as potential catalyst carriers and were successfully impregnated with Ag or Pt-Ru on their inner walls after borohydride reduction
at room temperature. In addition, porous carbon patterns were fabricated using the ‘micromolding in capillary’ technique,
which has potential applications in the microreaction technology. 相似文献
154.
155.
J. G. M. de Jong H. N. Stein J. M. Stevels 《Journal of chemical technology and biotechnology (Oxford, Oxfordshire : 1986)》1969,19(1):25-28
Amorphous silica influences tricalcium aluminate (C3A) hydration both in pastes and in suspensions. Two heat peaks are found by isothermal calorimetry during the paste hydration of C3A. The addition of amorphous silica causes the second heat peak to shift towards shorter reaction times and become more pronounced. In suspensions, the change in ion concentration in the water phase is not influenced by the presence of amorphous silica except that the change in concentration occurs more quickly. Quantitative X-ray analysis shows that more 3CaO.Al2O3.6H2O is present in suspensions containing amorphous silica than in silica-free suspensions at equal hydration times. 相似文献
156.
This study is to investigate the factors influencing the alcohol production byKluyveromyces fragilis using the juice of Jerusalem Artichoke tubers.
The cell growth rate and ethanol production rate were stimulated by aeration and by the addition of unsaturated fatty acids
and the cell mass production and the ethanol production were substantially improved.
It was found that oxygen and unsaturated fatty acids added played a decisive role on the increase of alcohol tolerance of
yeast. 相似文献
157.
PdOx/MnO2 has been examined as a catalyst for CO oxidation using a conventional flow reactor at reaction temperatures between 50 and 150°C. In the reaction conditions of GHSV (gashourlyspacevelocity) of 1.22 × 105/h and CO concentration of 2000 ppm, PdOx/MnO2 showed higher catalytic activity compared with PdOx/Mn2O3, which had been previously reported as an effective catalyst due to the cooperative action of Pd and Mn2O3 for this reaction. The reason for higher activity of PdOx/MnO2 than PdOx/Mn2O3 has been investigated using TPR (temperatureprogrammed reduction) and XPS studies. TPR showed that PdOx/MnO2 could be reduced by CO at much lower temperature than PdOx/Mn2O3. During the experiment of reduction and oxidation, XPS showed that the valence of Mn in the PdOx/MnO2 was between 4+ and 3+, which is higher than that of Mn in the PdOx/Mn2O3 catalyst of which the valence has been reported to be between 3+ and 2+. It is known that in this catalyst system the support supplies oxygen onto Pd, where the oxidation occurs with adsorbed CO, and the ability of the support to provide oxygen improves the performance of the catalyst. Therefore, it was concluded that the readiness of MnO2 to be reduced with maintaining a higher oxidation state showed higher CO oxidation activity than Mn2O3 as support for PdOx. 相似文献
158.
159.
Summary New biodegradable hydrophobic polyurethane (PU)/hydrophilic poly (ethylene glycol) diacrylate (PEGDA) IPN was simultaneously synthesized with changing the molecular weight of PEGDA to investigate the effect of crosslinking density on the degree of phase separation. PU was modified using biodegradable poly(-caprolactone)diol and the hydroxy group of PEG was substituted to crosslinkable acrylate group having double bond, which induce photo-polymerization. The sturucture of PEGDA was confirmed by NMR. Because the reaction rate of PEGDA was faster than that of PU, the continuous matrix of the micro-separated PU/PEGDA IPNs having amphiphilic character was made of hydrophilic PEGDA-rich phase. All IPNs have sea-island morphology resulting from the suppressed phase separation. The effect of the degree of phase separation on blood compatibility was investigated. 相似文献
160.
The onset of hydrodynamical instability induced by impulsive spin-down to rest in a cylinder containing a Newtonian fluid
is analyzed by using propagation theory. It is well-known that the primary transient swirl flow is laminar, but with initial
high velocities secondary motion sets in at a certain time. The dimensionless critical time Τc to mark the onset of instability is presented here as a function of the Reynolds number Re. Available experimental data indicate
that for large Re deviation of the velocity profiles from their momentum diffusion occurs starting from a certain time Τ≈4Τc. This means that secondary motion is detected at this characteristic time. It seems evident that during Τc⪯Τ⪯4Τc, secondary motion is relatively very weak and the primary diffusive momentum transfer is dominant. 相似文献