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991.
采用正交设计实验方法分析了SnO2、MnCO3、B i2O3和A l2O3添加量对BST/MgO系铁电移相材料微波电性能影响。实验结果表明:SnO2的引入促进样品烧结,有助于降低低频和微波损耗,但过多的加入会产生第二相,会使微波损耗上升。Mn受主取代Ti产生空穴等缺陷,不利于微波损耗的降低,而等价取代类似SnO2的情况,有助于降低微波损耗,但过多的加入会产生第二相,也会使微波损耗上升。B i2O3对材料微波电性能有显著的影响,从离子半径匹配角度,B i2O3一般出现在晶粒间,形成玻璃相,一方面促进烧结,使致密化提高,低频损耗变小;另一方面低熔点的玻璃相引起微波损耗急剧上升。A l2O3对材料电性能影响不显著。 相似文献
992.
993.
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
994.
Three different polyethylene/polypropylene (PE/PP) blends were microcellular foamed and their crystallinities and melt strengths were investigated. The relationship between crystallinity, melt strength, and cellular structure was studied. Experimental results showed that the three blends had similar variation patterns in respect of crystallinity, melt strength, and cellular structure, and these variation patterns were correlative for each blend. For all blends, the melt strength and PP melting point initially heightened and then lowered, the PP crystallinity first decreased, and then increased as the PE content increased. At PE content of 30%, the melt strength and PP melting point were highest and the PP crystallinity was least. The blend with lower PP crystallinity and higher melt strength had better cellular structure and broader microcellular foaming temperature range. So, three blends had best cellular structure at PE content of 30%. Furthermore, when compared with PE/homopolymer (hPP) blend, the PE/copolymer PP (cPP) blend had higher melt strength, better cellular structure, and wider microcellular foaming temperature range, so it was more suited to be microcellular foamed. Whereas LDPE/cPP blend had the broadest microcellular foaming temperature range because of its highest melt strength within three blends. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 104: 4149–4159, 2007 相似文献
995.
We have synthesized a series of fully aliphatic polyimides (APIs) from bicyclo[2,2,2]oct‐7‐ene‐2,3,5,6‐tetracarboxylic dianhydride (BOCA) and various aliphatic diamines, including linear aliphatic, flexible alicyclic, and rigid adamantyl diamines. We performed the polymerization reactions using one‐step syntheses in m‐cresol at elevated temperatures without the isolation of poly(amic) acid. The chemical composition and structure of the polymers were characterized by nuclear magnetic resonance (NMR) and infrared (IR) spectrometry. The characterization data are reported from analyses using gel permeation chromatography (GPC), thermogravimetric analysis (TGA), differential scanning calorimeter (DSC), and wide‐angle X‐ray diffraction (WXAD) measurements. The polyimides are also subjected to solubility, solution viscosity, tensile strength, transparency, and dielectric constant measurements. The resultant polyimides possess well‐controlled molecular weight, reasonable intrinsic viscosity, good transparency, enhanced solubility, low dielectric constants, and high glass transition temperature, together with marginal thermal and mechanical stability. These properties were enhanced in copolyimides containing equimolar amounts of rigid and flexible moieties. These rigid‐rod APIs derived from the alicyclic dianhydride and aliphatic diamines are promising candidates as advanced materials for future applications in micro‐ and photoelectronic devices. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 3316–3326, 2006 相似文献
996.
997.
998.
Radiation‐induced simultaneous grafting of styrene onto polytetrafluoroethylene (PTFE) films and the subsequent sulfonation in the chlorosulfonic acid/dichloroethane were investigated. The effects of the main radiation grafting conditions, such as the type of solvents, irradiation dose, dose rate, the styrene concentrations, etc., on the degree of grafting (DOG) were studied. To elucidate the influence of both the grafting and sulfonation conditions on the properties of the PTFE‐g‐polystyrene‐sulfonic acid (PSSA) membranes, the sulfonation conditions, including the sulfonation temperature and the concentration of the ClSO3H with respect to the DOG, were systematically evaluated. The grafted and sulfonated membranes were characterized by FTIR–ATR spectra, ion‐exchange capacity (IEC), water uptake, thickness measurement, etc. The as‐prepared PTFE‐g‐PSSA membranes in this work showed a good combination of a high IEC (0.85–2.75 meq g?1), acceptable water uptake (8.86–56.9 wt %), low thickness, and volume expansion and/or contraction. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 99: 1415–1428, 2006 相似文献
999.
Jian Guo Li Fang Jiao HuaTang Yuan Li Qin Wang Hai Xia Li Ming Zhang Yong Mei Wang 《Electrochimica acta》2006,51(28):6275-6280
Layered Li[Ni(1−x)/3Mn(1−x)/3Co(1−x)/3Crx]O2 materials with x = 0, 0.01, 0.02, 0.03, 0.05 are prepared by a solid-state pyrolysis method. The oxide compounds were calcined with various Cr-doped contents, which result in greater difference in morphological (shape, particle size and specific surface area) and the electrochemical (first charge profile, reversible capacity and rate capability) differences. The Li[Ni(1−x)/3Mn(1−x)/3Co(1−x)/3Crx]O2 powders were characterized by means of X-ray diffraction (XRD), charge/discharge cycling, cyclic voltammetry, and SEM. XRD experiment revealed that the Li[Ni(1−x)/3Mn(1−x)/3Co(1−x)/3Crx]O2 (x = 0, 0.01, 0.02, 0.03, 0.05) were crystallized to well layered -NaFeO2 structure. The first specific discharge capacity and coulombic efficiency of the electrode of Cr-doped materials were higher than that of pristine material. When x = 0.02, the sample showed the highest first discharge capacity of 241.9 mAh g−1 at a current density of 30 mA g−1 in the voltage range 2.3–4.6 V, and the Cr-doped samples exhibited higher discharge capacity and better cycleability under medium and high current densities at room temperature. 相似文献
1000.
Ming Li Zbigniew Twardowski Felix Mok Norbert Tam 《Journal of Applied Electrochemistry》2007,37(4):499-504
Sodium dichromate is commonly used in sodium chlorate production to maintain high current efficiency; however, it is also
a well documented carcinogen. To reduce the environmental impact, identification of a suitable alternative with similar buffering
characteristics to dichromate and without adverse effect on the electrolytic performance of sodium chlorate production is
important; sodium molybdate is a good candidate. Molybdate ion and its conjugated acid work as a buffer pair at pH 5–6, a
lower and slightly narrower pH window than the typical buffer region of dichromate. Nonetheless, the molybdate buffer works
effectively during the electrolytic process by maintaining pH at 5.9. Although the use of molybdate buffer will lower the
overpotential of hydrogen evolution reaction (HER) by 100 mV, the average off-gas oxygen content is noticeably compromised
at 3.6–4.6%, measured using a pilot cell operated at 3 kA m−2and 80 °C during a 3-day trial. The resulting current efficiency of 91 92% is significantly lower than when dichromate is
employed as the process additive (> 96%). Mixtures of different dichromate and molybdate ratio were also investigated in terms
of the resulting cathode surface potential. 相似文献