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51.
Eighteen compositions of MoO3-Te at 800 °C and seven of each of MoO3-Cd (at 500 °C) and MoO3-Sb (at 600 °C) were heat treated in vacuum-sealed quartz ampules. The phases of the heat-treated compositions were analyzed using x-ray diffraction (XRD) patterns. The interactions in the three systems are summarized. Three phases in equilibrium are (1) in the MnO3-Te system at 800 °C, Te, Mo4O11, TeMo4O13—(0<xMoO 3<0 889) and MoO3, Mo4O11, TeMo4O13—(0.889<xMoO 3<1); (2) in the MoO3_Cd system at 500 °C, Cd, MoO2, CdMoO4—(0<xMoO 3<0.6667) and MoO3, MoO2, CdMoO4—(0.6667<xMoO 3<1); and (3) in the MoO3-Sb system at 600 °C, Sb, MoO2, Sb4Mo10O31—(0<xMoO 3<0.734) and MoO3+MoO2+Sb4Mo10O31 (0.734<xMoO 3<1). The results lead to construction of ternary phase diagrams: Te-MoO3-TeMo4O13, Cd-MoO3-CdMoO4, and Sb-MoO3-Sb4Mo10O31.  相似文献   
52.
Economic dispatch is carried out at the energy control center to find out the optimal output of thermal generating units such that power balance criterion is met, unit operating limits are satisfied and the fuel cost is minimized. With growing environmental awareness and strict government regulations throughout the world, it has become essential to optimize not only the total fuel cost but also the harmful emissions, both, under static as well as dynamic conditions. The static environment economic dispatch finds the optimal output of generating units for a fixed load demand at a given time, while the dynamic environmental economic dispatch schedules the output of online generators with changing power demands over a certain time period (normally one day) so as to minimize these two conflicting objectives, simultaneously. In this paper, the price penalty factor approach is employed for simultaneous minimization of cost and emission. The generator ramp rate constraints, non-convex and discontinuous nature of cost function and the large number of generators in practical power plants, make this problem very difficult to solve. Here, a fuzzy ranking approach is employed to identify the solution which offers the best compromise between cost and emission objectives.  相似文献   
53.
A numerical technique for the full-wave analysis of shielded, passive microstrip components on a two-layer substrate is presented. The distinct feature of the technique is an efficient formulation for establishing the system matrix in the moment method procedure which allows the derivation of the elements of any large matrix by a linear combination of elements in a precomputed index table. The table is obtained from a two-dimensional discrete fast Fourier transform. In the moment method procedure, the two-dimensional surface current is represented by locally defined rooftop functions. The effect of the resonant modes associated with the metallic enclosure on the numerical procedure is examined. In order to demonstrate the features and the accuracy of the technique, numerical results for a microstrip open end and for a right-angle bend with and without the compensated corner are computed by using the resonant technique and are compared with other published computational and experimental data  相似文献   
54.
In the present study, storage proteins from five different wheat cultivars were extracted, fractionated and evaluated for their accumulation at different stages of development. SDS–PAGE analysis revealed that the accumulation of high molecular weight glutenin subunits was cultivar and stage dependent. However, low molecular weight glutenin subunits’ accumulation was not altered significantly after 16 days post anthesis in any of the cultivars. The rheological parameters (storage- and loss-modulus) of dough and gluten showed close association with either gliadins or glutenins. Peptidyl prolyl cis–trans isomerase (PPIase) activity, measured at different stages of grains development, showed variability with both the developmental stage and cultivar, and appeared to be primarily due to cyclophilins. Principal component analysis revealed the association of PPIase activity with either gliadin or total proteins, suggesting their significant role in the deposition of storage proteins in wheat.  相似文献   
55.
Stoichiometric magnesium aluminate spinel was synthesized by reaction sintering of alumina with caustic and sintered magnesia. The volume expansion of 5–7% during MgAl2O4 formation was utilized to identify the starting temperature of spinel formation and densification by high temperature dilatometry. The magnesia reactivity was determined by measurement of crystallite size and specific surface area. Caustic magnesia and sintered magnesia behave differently vis-à-vis phase formation and densification of spinel. Densification of stoichiometric Mag-Al spinel was carried out between 1650 and 1750 °C. Attempts were made to correlate the MgO reactivity with microstructure and densification of spinel.  相似文献   
56.
57.
Time-resolved spectroscopic experiments have been performed with protein in solution and in crystalline form using a newly designed microspectrophotometer. The time-resolution of these experiments can be as good as two nanoseconds (ns), which is the minimal response time of the image intensifier used. With the current setup, the effective time-resolution is about seven ns, determined mainly by the pulse duration of the nanosecond laser. The amount of protein required is small, on the order of 100 nanograms. Bleaching, which is an undesirable effect common to photoreceptor proteins, is minimized by using a millisecond shutter to avoid extensive exposure to the probing light. We investigate two model photoreceptors, photoactive yellow protein (PYP), and α-phycoerythrocyanin (α-PEC), on different time scales and at different temperatures. Relaxation times obtained from kinetic time-series of difference absorption spectra collected from PYP are consistent with previous results. The comparison with these results validates the capability of this spectrophotometer to deliver high quality time-resolved absorption spectra.  相似文献   
58.
The extractant‐impregnated polymeric beads (EIPBs), containing Di(2‐ethylhexyl) phosphonic acid (D2EHPA) as an extractant and polyethersulfone as base polymer, were prepared by phase‐inversion method. These beads were characterized by fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), and scanning electron microscope (SEM) analysis to gain insight into the composition and morphology of beads. The beads exhibited good acid stability as no significant structural deformation or leaching out of the extractant was observed in 6M HNO3 solution, up to the studied equilibration time of 15 days. The synthesized EIPBs were evaluated, for their ability to absorb uranium from aqueous solution, at different concentration and pH values. The kinetics measurement showed that about 90 min of equilibration time was enough to remove saturation amount of uranium from the solution. Kinetic modeling analysis of the extraction results was carried out using pseudo‐first‐order, pseudo‐second‐order, and intraparticle diffusion equations and the corresponding rate constants were determined. The equilibrium data were fitted into different isotherm models and were found to be represented well by the Freundlich isotherm equation. Reusability of the beads was also established by multiple sorption–desorption experiments. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 130: 3355–3364, 2013  相似文献   
59.
In the present work, results on the physico-chemical properties of the silica aerogels prepared by sol–gel process using mixtures of TMOS and MTMS as precursor are reported. The wide range of precursor mixture was studied with ratio of MTMS/TMOS in precursor mixtures as 0:100, 25:75, 50:50, 75:25, and 100:0 by volume. The gels with these precursor mixtures were successfully prepared using two step acid–base catalysis for gelation. Acetic acid (0.001 M) and NH4OH (1.5 M) were used for catalysis and resulting alcogels were subsequently dried by supercritical solvent extraction method. FTIR spectroscopy revealed that the aerogels show more intense peak at 1,260 and 790 cm−1 attributed to Si–CH3 resulting in more hydrophobic nature and these results were concurrent with adsorbed water content measurements made using Karl Fischer’s titration technique. The resulted aerogels were characterized using differential thermal analysis, thermo gravimetric analysis and surface area measurements. The surface area measurements showed an interesting trend that the surface area increased from 395 to 1,037 m2/g with increase in MTMS content in the precursor mixture from 0 to 50% and then again decreased to 512 m2/g for further increase in MTMS content from 50 to 100% in the precursor mixture. It was observed from our studies that silica aerogels prepared using a starting mixture of 50% TMOS and 50% MTMS resulted in high moisture resistance (adsorbed water content of 0.721% w/w), low density of 90 kg/m3 and the highest surface area of 1,037 m2/g, which has great potential for catalysis support applications.  相似文献   
60.
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