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11.
12.
The dynamic moduli, E′ and E″, and tan δ for nylon–CR and PET–CR composites with unidirectional short fibers were studied as a function of temperature by using a Rheovibron. The temperature dependence of tan δ showed two dispersion peaks for nylon–CR composite. The peak at ?28°C corresponded to the main dispersion of CR and the peak at 100°C to the α-dispersion of nylon 6. For a PET-CR composite, in addition to the individual dispersion of CR and PET, a small and broad peak was observed at about 90°C. The angular dependence of E′ indicated that the short fibers assumed good orientation. The storage modulus for the composites was given by the parallel model as E′ = Vf′Ef + VmE′m., where E′c, E′f and E′m were the storage modulus for the composite, fiber, and matrix and Vf and Vm were the volume fraction of fiber and matrix, respectively. In the transverse direction of fiber, the peak values of tan δ at ?28°C were given by the following equation; tan δc = tan δm ? δVf, where tan δc and tan δm are the loss tangent for the composite and matrix, respectively, and α is coefficient depending on fiber type. The results indicated that a region with strong interaction was formed between fibers and CR matrix. 相似文献
13.
Crystals of ethyl p-chloro α-cyano-β-methyl-cis-cinnamate, C13H12NO2Cl, are orthorhombic, space group Pbcn, with eight molecules per unit cell, a = 17.31, b = 8.68 and c = 17.20 Å. The structure was solved by direct methods and refined subsequently by Fourier techniques. The benzene ring makes a dihedral angle of 60.0° with the ethylenic group. This suggests significant steric effects of the β-methyl group and of the carbonyl group on the orientation of the benzene ring. The conformation of the ethylene bond and the carbonyl group around the Cα? C bond is roughly cisoid and the angle of twist is 16.5°. Nearest-neighbour >C = C <groups make contact across a two-fold axis at a center-to-center distance of 4.33 Å. 相似文献
14.
Hitomi Natomi Toshihito Saitoh Kentaro Sugano Masao Iwamori Masahisa Fukayama Yoshitaka Nagai 《Lipids》1993,28(8):737-742
The composition of the glycosphingolipids of the human gastrointestinal tract was studied. The major neutral glycosphingolipids
were ceramide monohexosides (e.g., GalCer, GlcCer), LacCer, Gb3Cer, Gb4Cer and more polar ones with more than four sugars, whereas neither Gg3Cer nor Gg4Cer were present. The acidic glycosphingolipids consisted of sulfatides and gangliosides such as GM3, GM1, GD3 and GD1a. Also a large amount of sulfatides was found in the gastric mucosa and duodenum. The concentrations of sulfatides in the
fundic mucosa, antral mucosa and duodenum amounted to 416.0, 933.8 and 682.9 nmol/g of dry weight, respectively, exceeding
those in the gastric mucosa and kidney of other mammals. The major molecular species of the sulfatides were identified as
I3SO3-GalCer with hydroxylated longer-chain fatty acids based on the analyses by gas-liquid chromatography and negative ion fast-atom
bombardment mass spectrometry. In contrast, gangliosides in these regions showed a tendency to be lower than sulfatides, and
the molar ratios of sulfatides to gangliosides were about 2.0, whereas those in other parts were less than 0.5. A high content
of sulfatides in the gastric and duodenal mucosa, where mucosa is easily insulted by acid, pepsin and bile salts, may be closely
related to their roles in mucosal protection.
The nomenclature used for gangliosides and other glycosphingolipids follows the system of Svennerholm (Ref. 1) and the recommendation
of the IUPAC-IUB Commission (Ref. 2), respectively. 相似文献
15.
Yutaka Nagai Hiroshi Kondo Noriyuki Tatsumi 《Journal of Automated Methods and Management in Chemistry》2005,2005(4):235-239
Rapid and accurate analysis of platelet count plays an important role in evaluating hemorrhagic status. Therefore, we evaluated platelet counting performance of a hematology analyzer, Celltac F (MEK-8222, Nihon Kohden Corporation, Tokyo, Japan), that
features easy use with low reagent consumption and high throughput while occupying minimal space in the clinical laboratory. All blood samples were anticoagulated with dipotassium ethylenediaminetetraacetic acid (EDTA-2K). The samples were stored
at room temperature (18^C–22^C) and tested within 4 hours of phlebotomy. We evaluated the counting ability of the Celltac F hematology analyzer by comparing it with the platelet counts obtained by the flow cytometry method that ISLH and ICSH recommended, and also the manual visual method by Unopette (Becton Dickinson Vacutainer Systems). The ICSH/ISLH reference method is based on the fact that platelets can be stained with monoclonal antibodies to CD41 and/or CD61. The dilution ratio was optimized after the precision, coincidence events, and debris counts were confirmed by the reference method. Good correlation of platelet count between the Celltac F and the ICSH/ISLH reference method (r = 0.99, and the manual visual method (r= 0.93) were obtained. The regressions were y = 0.90 x+9.0 and y=1.11x+8.4, respectively. We conclude that the Celltac F hematology analyzer for platelet counting was well suited to the ICSH/ISLH reference method for rapidness and reliability. 相似文献
16.
17.
Porous carbon beads were prepared by carbonizing at 700 and 1000 °C under N2 (NN-series) or CO2 atmospheres (CO-series) and a subsequent oxidization with boiling nitric acid solution (13%, v/v) for 3 h (ANN- and ACO-series). BET surface area of both CO- and NN-series samples tends to increase with increasing carbonization temperature, but CO-series samples show higher BET surface areas (700 °C: 610 m2/g, 1000 °C: 780 m2/g) compared with those of NN-series samples (700 °C: 380 m2/g, 1000 °C: 580 m2/g). After acid oxidation, BET surface areas of NN-series samples increased from 580 to 650 m2/g, whereas those of CO-series samples decreased from 780 to 600 m2/g. On subsequent acid oxidation, acidic surface functional groups increased in both CO- and NN-series samples, but the CO-series samples tend to have much more acidic surface functional groups. Adsorption of halogenated methanes, such as tetra-, tri- and dichloromethanes, onto the samples of CO-, NN-, ACO- and ANN-series was thought to be driven initially by the basicity, but the acidic functional groups that could attract adsorbates via dipole-dipole interaction might hinder the adsorption of subsequently incoming adsorbates. 相似文献
18.
On fibrous carbon materials, including activated carbon fibers, sorption capacity for heavy oils, less viscous A-grade and more viscous C-grade, was determined. Sorption capacity depended strongly on their bulk density; the correlation was the same as that found previously on exfoliated graphite and carbonized fir fibers. On carbon fiber felts, excellent recycling performance was observed, though sorption capacity was not so high as on exfoliated graphite and carbonized fir fibers. By filtration under suction, about 90% of sorbed A-grade heavy oil could be recovered and no decrease in sorption capacity was detected even after eight cycles. By washing with solvents, n-hexane for A- and C-grade oils and A-grade oil for C-grade oil, almost 100% recovery with no marked reduction in sorption capacity was found for each cycle. For the felts of PAN-based carbon fibers, rather severe operations for oil recovery, centrifugation and squeezing with twisting, could be applied without pronounced decreases in sorption capacity and recovery ratio. 相似文献
19.
Micrinite and exudatinite in some Australian coals,and their relation to the generation of petroleum
Michio Shibaoka 《Fuel》1978,57(2):73-78
The occurrence and microscopic features of micrinite and exudatinite in some Australian coals are reported. The origin of these macerals and also the significance of their occurrence are discussed in connection with hydrocarbon genesis. In Australia, micrinite occurs in bituminous and sub-bituminous coals which are very rich in inertinite, and also in brown coal rich in inertinite. One of the possible progenitors of micrinite is oxidized porigelinite. There is little reason to conclude that micrinite was formed from resinite and other macerals at an early stage of coalification and that liquid hydrocarbons were formed during this process. Exudatinite occurs in sub-bituminous and high-volatile bituminous coals in the Gippsland Basin. There is no positive evidence of a genetic relation between liquid hydrocarbons, exudatinite, micrinite and liptinite macerals. The formation of liquid hydrocarbons from solid liptinite etc. may take place just before and during Teichmüller's so-called ‘2nd coalification jump’. 相似文献
20.
S. Watanabe S. Nakasato S. Hayano H. Kuwamura T. Nagai M. Negishi Y. Sasamoto H. Seino S. Shiraishi 《Journal of the American Oil Chemists' Society》1973,50(9):360-363
In this study known mixtures of four or five fatty acid methyl esters were analyzed collaboratively by gas chromatography
with flame ionization detectors. The experimental data was treated statistically to examine inter- and intralaboratory scattering.
More-over the effect of the use of correction factors was investigated. Even if only the specific analytical values that scattered
a little were chosen, the averages of such values did not always approach the actual values. In some laboratories a sort of
regularity was observed in the deviation of analytical values from real values throughout the analyses of four samples. The
application of correction factors to the analytical values obtained by these laboratories resulted in a considerable decrease
of interlaboratory scattering and deviation from the real values. When a constant amount of sample was injected, intralaboratory
scattering was decreased, whereas interlaboratory scattering was not. Injection of large sample sizes caused deviation. From
this collaborative study it was recommended that 0.5–1.0 μl of 20% solution be injected.
Presented at the JOCS-AOCS Joint Meeting, Los Angeles, April 1972. 相似文献