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21.
Motonobu Yoshikawa Hiroshi Nakajima Takeshi Inada Yasushi Harada Masahiko Amano Yuji Nakata 《Electrical Engineering in Japan》1995,115(7):29-39
A new practical method is proposed which gives a quasi-optimal solution of the dynamic load-dispatching problem formulated by a multiconstraint multiobjective optimization problem. Here, the multiple constraints are rate reserve constraints and power flow ones, and the multiple objectives are fuel cost and CO2 emission. The proposed method is an integration of the following three techniques: (1) “Group Dispatch Scheme,” which is developed by the authors, is used to satisfy a violated constraint easily. This scheme consists of three steps. The first step is to classify all generators into two groups. One is the group which should be more loaded to satisfy the violated constraint, and the other is the should-be less loaded group. The second step is to add some load to the former group, and to subtract the same load from the latter. The third step is to dispatch each group load to each groups generators, respectively; (2) the dynamic load-dispatching algorithm is used which provides, in practical time, quasi-optimal generation trajectories; (3) the conventional weighting parametric method is used to obtain a Pareto optimal solution of multiobjective problems. The effectiveness of the method is clarified by a computer simulation on the actual power system of Kansai Electric Power Company. 相似文献
22.
Kenta Miura Takeshi Tanemura Shunya Yamamoto Masaki Sugimoto 《Nuclear instruments & methods in physics research. Section B, Beam interactions with materials and atoms》2007,263(2):532-534
We fabricated fused-silica substrates which emit blue light by using Si-ion implantation and high-temperature annealing. Photoluminescence peak wavelengths are around 400 nm, and the peak intensities can be remarkable after annealing above 1150 °C. 相似文献
23.
Nobuo Ishizawa Atsushi Saiki Takeshi Yagi Nobuyasu Mizutani Masanori Kato 《Journal of the American Ceramic Society》1986,69(2):18-C-
Crystals of yttria partially stabilized zirconia were grown by the arc-image floating-zone technique and studied by transmission electron microscopy. Crystals annealed at 1700°C consist of tetragonal precipitates and a cubic matrix. The platelike domains in a precipitate are twin-related tetragonal variants stacked alternately parallel to the (011) twin plane. The axial relations between the tetragonal precipitate and the cubic matrix are [100]tetragonal |[100]cubic , [011]tetragonal |[011]cubic . 相似文献
24.
Kazuko Satake Ai Katayama Hideki Ohkoshi Takeshi Nakahara Takashi Takeuchi 《Sensors and actuators. B, Chemical》1994,20(2-3):111-117
Oxide semiconductors have been examined to develop NOx sensors for exhaust monitoring. Titania doped with trivalent elements, such as Al3+, Sc3+, Ga3+ or In3+, has a good sensitivity and selectivity to NO between 450 and 550 °C, and shows rapid response. A sensor probe for monitoring exhaust NOx has been fabricated. Many kinds of interference gases, such as C3H6, CO and SO2, have been found to have only a slight influence on the sensor response to NO. The influence of O2 and H2O is also negligible, except for the cases of 0% H2O and fuel-rich conditions. In accordance with these results, the sensor probe operates satisfactority in the exhaust gas of various combustion conditions without interference from the various kinds of gas species in the exhaust gases. 相似文献
25.
Takeshi Kikuchi Yoshizo Kitami Masato Yokoyama Hiroshi Sakai 《Journal of Materials Science》1989,24(12):4275-4278
The phase equilibria in the pseudo-binary system Bi2O3-TeO2 at 600° 950° C in air were examined by solid-state reaction techniques and X-ray powder diffraction method. Four pseudo-binary compounds appeared, i.e., -Bi2O3 type solid solution having a compositional range of (1-x)Bi2O3·xTeO2 wherex=0 0.4 a new compound Bi6Te2O15 which has an orthorhombic cell of a=2.27(4) nm, b=1.06(1) nm and c = 0.539(8) nm, 2Bi2O3 · 3TeO2, and an unidentified phase Bi2O3·2TeO2. The formation of the phase Bi6Te2O15, in which all the Te ions are hexavalent, was confirmed by the thermogravimetry and by the Mössbauer spectra. The liquidus curves for whole system were determined by DTA method. 相似文献
26.
Takeshi Yagi Kazuo Shinozaki Nobuo Ishizawa Nobuyasu Mizutani Masanori Kato Akihiko Tsuge 《Journal of the American Ceramic Society》1988,71(7):334-C
The thermal diffusivity of AlN ceramics was significantly decreased by the addition of SiO2 . The AlN ceramics with 4 wt% SiO2 could not be densified by pressureless sintering in the temperature range 1400° to 1800°C. The thermal diffusivity of these samples was very low because of their porous structure. The AlN ceramics containing 2, 4, and 8 wt% SiO2 were densified by hot-pressing and also had low thermal diffusivity. In these samples, the grains of the 27R polytype that resulted from the reaction between AlN and SiO2 were dispersed, obstructing the conduction of heat. The relation between the amount of 27R polytype and the thermal diffusivity of the AlN ceramics was determined. 相似文献
27.
A physicochemical parameter, represented by the symbol Σs*, based on molar solubility in water and molar attraction constants of Small, has been developed to express quantitatively the relative hydrophobicity, or nonpolar character, of the hydrocarbon molecule. The value of Σs* can be calculated for a hydrocarbon from its chemical structure. The scale of Σs* is consistent within each group of aromatic, cyclic, and noncyclic hydrocarbons. Reverse osmosis data have been obtained at 250 psig for single-solute aqueous feed solution systems involving low concentrations of 39 different hydrocarbons (including 13 aromatics, 10 cyclic, and 16 noncyclic compounds) and several samples of cellulose acetate membranes of different surface porosities. The effect of operating pressure on membrane performance has also been studied for two aromatic hydrocarbon solutes. The values of Σs* for the solutes used were in the range of 425 to 924 for aromatic hydrocarbons, 521 to 931 for cyclic hydrocarbons, and 369 to 960 for noncyclic hydrocarbons. The reverse osmosis data have been correlated with Σs* for each group of hydrocarbons studied. In all cases, positive solute separations were obtained, and the ratio [PR]/[PWP] was less than 1. With respect to each film, solute separation increased with increase in Σs*, and decreased with increase in operating pressure. Also, solute separation decreased in the order aromatic hydrocarbon > cyclic hydrocarbon > noncyclic hydrocarbon at any given value of Σs*. At a given operating pressure, for low values of Σs* (~500 or less) solute separation increased with progressive decrease in average pore size on the membrane surface. For high values of Σs* (~800 or more), solute separation initially increased with decrease in average pore size, then passed through a maximum and minimum with further decrease in average pore size, and again increased with still further decrease in average pore size. The results are discussed on the basis of preferential sorption of solute at the membrane–solution interface under the experimental conditions studied. 相似文献
28.
Reverse osmosis separations of eight polyethylene glycol (PEG) solutes in the average molecular weight range of 200 to 6750 in single-solute dilute aqueous solutions have been studied using porous cellulose acetate membranes at the operating pressures of 50, 75, and 100 psig. Diffusivity data for the above PEG solutes have also been obtained from experimental data on intrinsic viscosities. From an analysis of all experimental data, numerical values for the parameters representing the polar (?ΔΔG/RT), steric (δ*ΣEs), and nonpolar (ω*Σs*) forces governing reverse osmosis separations of PEG solutes have been generated. These numerical values are useful for precise characterization of cellulose acetate membranes for whose specifications sodium chloride is not the appropriate reference solute because of its low or practically negligible separation under reverse osmosis operating conditions. This work also illustrates that solute separation in reverse osmosis can predictably increase or decrease with increase in operating pressure depending on experimental conditions. 相似文献
29.
Reverse osmosis separations of phenol (9.4 to 108 ppm), p-cresol (108 ppm), and p-chlorophenol (129 ppm) were studied using Loeb-Sourirajan-type porous cellulose acetate membranes, and single-solute aqueous feed solutions at 500 psig and the indicated solute concentrations. It was found that, by dissociating the solute by changing the pH of the feed solution, all the above phenols could be separated by reverse osmosis. Solute separation increased with increase in the degree of dissociation of the solute in the feed solution; and, by the appropriate choice of pore size on the membrane surface, separations of phenol approaching the degree of dissociation of phenol in the feed solution could be obtained under the operating conditions used. Similar experiments using aniline (93 ppm) as the solute showed that dissociation of solute molecules in the feed solution could be a technique generally applicable for the reverse osmosis separation of nonionic solutes in aqueous solution. The effects of operating pressure in the range 250 to 1500 psig and pore size on the membrane surface on the separation of un-ionized phenol and p-chlorophenol showed that, with respect to single-solute aqueous feed solutions of phenols, the component whose relative acidity was greater was preferentially sorbed at the cellulose acetate membrane—aqueous solution interface, and the solute concentration in the membrane-permeated product solution was a function of the extent and mobility of each of the sorbed species. 相似文献
30.
Hakoshima Toshio; Tanaka Masahiro; Itoh Takeshi; Tomita Ken-khi; Amisaki Takashi; Nishikawa Satoshi; Morioka Hiroshi; Uesugi Sei-ichi; Ohtsuka Eiko; Ikehara Morio 《Protein engineering, design & selection : PEDS》1991,4(7):793-799
Hydrophobic effects on binding of ribonuclease Tl to guaninebases of several ribonucleotides have been proved by mutatinga hydrophobic residue at the recognition site and by measuringthe effect on binding. Mutation of a hydrophobic surface residueto a more hydrophobic residue (Tyr45 Trp) enhances thebinding to ribonucleotides, including mononucleotide inhibitorand product, and a synthetic substrate-analog trinudeotide aswell as the binding to dinucleotide substrates and RNA. Enhancementson binding to non-substrate ribonucleotides by the mutationhave been observed with free energy changes ranging from 2.2 to 3 .9 kJ/mol. These changes are in good agreementwith that of substrate binding, 2.3 kJ/mol, which iscalculated from Michaelis constants obtained from kinetic studies.It is shown, by comparing the observed and calculated changesin binding free energy with differences in the observed transferfree energy changes of the amino acid side chains from organicsolvents to water, that the enhancement observed on guaninebinding comes from the difference in the hydrophobic effectsof the side chains of tyrosine and tryptophan. Furthermore,a linear relationship between nucleolytic activities and hydrophobicityof the residues (Ala, Phe, Tyr, Trp) at position 45 is observed.The mutation could not change substantially the base specificityof RNase Tl, which exhibits a prime requirement for guaninebases of substrates. 相似文献