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排序方式: 共有5085条查询结果,搜索用时 250 毫秒
91.
采用Al2O3基料,添加第二相(ZrO2,Si3N4)和纤维相(ZrO2,(f),以热压法制成Al2O3-Si3N4-ZrO2多相复合材料。研究表明,新材料在青静态和动态试验中表现出良好的综合性能:1073K时的高温电阴率p=1.24×17^7Ω.cm;静态熔渣最大腐蚀速率Vs=0.16μm/h;动态最大腐蚀速率Vd=0.449μm/h。与Al2O3陶瓷相比,室温抗弯强度提高93%,抗热震临界... 相似文献
92.
Edward J. Rode Paul E. Gee Linda N. Marquez Tetsuji Uemura Mohammad Bazargani 《Catalysis Letters》1991,9(1-2):103-113
Alkali metal zeolites and metal oxides were used for the aldol condensation of n-butanal to 2-ethyl-2-hexenal. The order of activity at 150 °C and 1 atm. was: CsNaY > NaY > LiNaY > MgO >Al2O3. Selectivity to 2-ethyl-2-hexenal was 100% for both pure and mixed isomer feed. Infrared spectroscopic studies showed that stable catalysts were produced by propene pretreatments which blocked Lewis acid sites. Adsorption of ammonia and carbon dioxide on CsNaY during aldol condensation of n-butanal causes a decrease in rate. This result, along with the order of activity, suggests that the presence of both acid and basic sites produce higher activity than strongly basic MgO.Work performed at San Jose State University. 相似文献
93.
SiC晶须增强陶瓷基复合材料的研究 总被引:2,自引:0,他引:2
用不同的Al_2O_3粉料,采用SiC晶须补强以及加入第三相SiC粒子弥散增韧的方式,研究了SiC晶须Al_2O_3基复合材料的力学性能,得到强度σ_f=780MPa,K_(Ic)=7.6MPa·m~(1/2)的结果。通过不同的分敌途径,对晶须分散效果进行了实验观察和探讨;并讨论了晶须的分散均匀性对力学性能的影响。同时,就晶须团聚体在增韧过程中所起的作用提出了一种新的、可能的增韧机制,合理地解释了实验结果。最后,就三元复合系统中晶须补强和弥散增韧两种途径的迭加效果进行了讨论。 相似文献
94.
Yangyang Ji Jingkui Liang Zhan Chen Sishen Xie 《Journal of the American Ceramic Society》1991,74(2):444-446
The phase relations at a temperature below "subsolidus" in the system Al2 O3 –B2 O3 –Nd2 O3 are reported. Specimens were prepared from various compositions of Al2 O3 , B2 O3 , and Nd2 O3 of purity 99.5%, 99.99%, and 99.9%, respectively, and fired at 1100°C. There are six binary compounds and one ternary compound in this system. The ternary compound, NdAl3 (BO3 )4 (NAB), has a phase transition at 950°C ± 15°C. The high-temperature form of NAB has a second harmonic generation (SHG) efficiency of KH2 PO4 (KDP) of the order of magnitude of the form which has been used as a good self-activated laser material, and the low-temperature form of NAB has no SHG efficiency. 相似文献
95.
The crystal-growth process and growth conditions of β-alumina (Na2 O · Al2 O3 ) were investigated using the Na2 B4 O7 -Na3 AlF6 flux method. β-Alumina (electric fusion brick) was used as both nutrient and seed. Weight loss of the flux varied widely for various runs: ≅ 10 wt% of flux evaporated at 100 h, ≅ 17 wt% at 150 h, and 43 wt% at 600 h. When β-alumina crystal was grown, only 20 wt% Na2 B4 O7 was added to the Na3 AlF6 flux. The linear growth rates of the β-alumina single crystal grown by an Na3 AlF6 -20 wt% Na2 B4 O7 flux method at 1040°C and Δ t = 18°C were ≅ 1.0 × 10−3 mm/h ( a face) and ≅0.3 × 10−3 mm/h ( c face). The β-alumina single crystals grown were bounded by only c [001] and a [100] and were colorless and transparent. 相似文献
96.
Carlos G. Levi Eric Sommer Scott G. Terry Amalia Catanoiu Manfred Rühle 《Journal of the American Ceramic Society》2003,86(4):676-85
The microstructure of Al2 O3 formed by oxidation of a model NiCrAlY alloy during electron-beam physical vapor deposition of ZrO2 –7.6 mol% YO1.5 is examined and compared with that formed on the bare substrate. The growth rate, morphology, and chemical composition of the oxide vary among the different constituents of the alloy surface and are further influenced by the O2 partial pressure and the physical presence of the thermal barrier coating (TBC) layer. These differences, however, are largely limited to the outer oxide layer. The interplay between the TBC and the growing oxide leads to the formation of a fine-grain Al2 O3 –ZrO2 "mixed zone" within the thermally grown oxide. A mechanism is outlined to explain this behavior, based on the dissolution of ZrO2 in a transient Al2 O3 structure growing by outward diffusion of Al, and its subsequent reprecipitation when the metastable phase transforms to the stable α-Al2 O3 form. 相似文献
97.
Rising Crack-Growth-Resistance (R-Curve) Behavior of Toughened Alumina and Silicon Nitride 总被引:2,自引:0,他引:2
Nageswaran Ramachandran Dinesh K. Shetty 《Journal of the American Ceramic Society》1991,74(10):2634-2641
R -curves for a sinter/HIPed SiC(whisker)-reinforced alumina and a sintered silicon nitride were assessed by direct measurements of lengths of cracks associated with Vickers indentation flaws. The fracture toughness measurements based on (a) initial (as-indented) crack lengths, (b) equilibrium growth of cracks during increasing far-field loading, and (c) crack lengths corresponding to unstable fracture showed definitive trends of R -curves for both materials. The fracture mechanics analyses employed an indenter-material constant that was independently estimated using a physical model for the residual driving force and a free surface correction factor that accounted for the effects of size and shape of the cracks on stress intensity. It is shown that R -curve estimations based on crack length measurements have the intrinsic advantage that crack length dependence of fracture toughness is not assumed a priori as is done in conventional analysis based on strength. The measured fracture toughness of SiC(whisker)-reinforced alumina was in agreement with the prediction of a toughening model based on crack bridging by partially debonded whiskers. 相似文献
98.
Víctor Valcárcel Carmen Cerecedo Francisco Guitián 《Journal of the American Ceramic Society》2003,86(10):1683-1690
α-alumina (α-Al2 O3 , corundum) fibers exhibit high thermal and chemical stability, as well as good mechanical properties, even at high temperatures. Such characteristics make them good candidates for use in composites. Nevertheless, very few methods of producing α-Al2 O3 fibers are available. In the present work, we describe a method that uses aluminum pieces deposited on SiO2 powder, in an argon atmosphere, at temperatures in the range 1300°–1600°C. The α-Al2 O3 fibers are obtained via vapor-liquid-solid deposition. The novel addition of nickel and cobalt (or their oxides) allows the use of temperatures >1500°C, resulting in improved fiber production. We demonstrate that the metals do not contaminate the fibers produced in this way. Finally, we also estimate the tensile strength of the Al2 O3 fibers produced through this method. 相似文献
99.
The preparation of near stoichiometric spinel and alumina-rich spinel composites from Al2 O3 and MgO powders with the addition of Na3 AlF6 up to 4 wt% in the temperature range 700°–1600°C was studied; 98 wt% spinel containing 72 wt% Al2 O3 can be produced from the mixture of 72 wt% (50 at.%) Al2 O3 + 28 wt% (50 at.%) MgO powders with the addition of 1 wt% Na3 AlF6 fired at 1300°C for 1 h. Spinels containing 81–85 wt% Al2 O3 can be produced from either the mixture of 90 wt% (78 at.%) Al2 O3 + 10 wt% (22 at.%) MgO or the mixture of 95 wt% (88 at.%) Al2 O3 + 5 wt% (12 at.%) MgO powders with the addition of 4 wt% Na3 AlF6 in the temperature range 1300°–1600°C by using a torch-flame firing for 3 min, followed by quenching in water, while the same system under slow cooling in a furnace results in spinel containing 74–76 wt% Al2 O3 . Microscopic studies indicate that the alumina-rich spinel composites consist of a continuous majority spinel phase and an isolated minority corundum phase, regardless of slow cooling in a furnace or quenching in water. 相似文献
100.
Mesoporous Ni–alumina catalysts (Ni–alumina-pre and Ni–alumina-post) were synthesized by one-step sol–gel method using micelle
complex comprising lauric acid and nickel ion as a template with metal source and using aluminum sec-butoxide as an aluminum source. The Ni–alumina catalysts showed relatively high surface areas (303 m2/g for Ni–alumina-pre and 331 m2/g for Ni–alumina-post) and narrow pore size distributions centered at ca. 4 nm. Highly dispersed Ni particles were observed
in the Ni–alumina catalysts (ca. 5.2 nm for Ni–alumina-pre and ca. 6.8 nm for Ni–alumina-post) after reduction at 550 °C,
while a catalyst prepared without a template (NiAl-comp) exhibited inferior porosity with large metal particles (ca. 12.3 nm).
Mesoporous Ni–alumina catalysts with different porosity were obtained by employing different hydrolysis step of aluminum source.
When aluminum source was hydrolyzed under the presence of micelle complex, a supported Ni catalyst with highly developed framework
mesoporosity was obtained (Ni–alumina-post). On the other hand, when aluminum source was pre-hydrolyzed followed by mixing
with micelle solution, the resulting catalyst (Ni–alumina-pre) retained high portion of textural porosity. It was revealed
that the hydrolysis method employed in this research affected not only textural properties but also metal-support interaction
in the Ni–alumina catalysts. It was also found that the Ni–alumina-pre catalyst exhibited weaker interaction between nickel
and alumina than the Ni–alumina-post, leading to higher degree of reduction in the Ni–alumina-pre catalyst. In the hydrodechlorination
of o-dichlorobenzene, the Ni–alumina catalysts exhibited better catalytic performance than the NiAl-comp catalyst, which was attributed
to higher metal dispersion in the Ni–alumina catalysts. In particular, the Ni–alumina-pre catalyst showing 1.5 times higher
degree of reduction and larger amounts of o-dichlorobenzene adsorption exhibited better catalytic performance than the Ni–alumina-post catalyst. 相似文献