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Laura M. Russell Lloyd F. Johnson D. P. H. Hasselman Robert Ruh 《Journal of the American Ceramic Society》1987,70(10):226-C
The thermal conductivity and diffusivity of silicon carbide whisker reinforced mullite was shown to increase with whisker content. This effect was much greater for vapor-liquid-solid (VLS) whiskers than for rice-hull (RH) whiskers. This suggests that the thermal conductivity for the VLS whiskers was significantly higher than for the RH whiskers. Due to preferred orientation of the whiskers, thermal conductivity and diffusivity of the composite samples exhibited significant anisotropy. 相似文献
167.
A. R. Johnson A. C. Fogerty Judith A. Pearson F. S. Shenstone Audrey M. Bersten 《Lipids》1969,4(4):265-269
Hen liver preparations which desaturate stearic acid at the 9,10 position to form oleic acid have been found to desaturate
other saturated fatty acids of carbon chain length from 12 to 20 and 22. The 9,10-monoenoic fatty acid of the same chain length
as the substrate fatty acid is the major product formed. Minor amounts of the 10,11- and 11, 12-monoenoic acids are also formed.
Maximum desaturation occurred with the C14 fatty acid substrate and with the fatty acids C17 and C18, suggesting the presence of at least two desaturating systems. The cyclopropene fatty acids, sterculic and malvalic acids,
inhibited the desaturation of all thefatty acids at the 9,10 position but desaturation at the 10,11 and 11, 12 positions was
affected only slightly. The effect is not due to inhibition of the primary activating enzyme, the long chain acyl CoA synthetase.
Sterculic acid is a more effective inhibitor than either malvalic acid or sterculyl alcohol, probably because these cyclopropene
compounds do not block the desaturating site of the enzyme as completely as sterculic acid. 相似文献
168.
Wax esters were isolated from commercial orange roughy (Hoplostethus atlanticus) oil by column chromatography and fractionated by argentation thin layer chromatography. Following transesterification, the
resultant fatty acid methyl esters and fatty alcohols were analyzed by gas chromatography. both acyl- and alkyl-moieties were
mainly of the monoene structure within the 16∶1–22∶1 range. After derivatization, the positions of the double bonds of even
numbered fatty acid and fatty alcohol isomers were located by chromatography-mass spectrometry and compared.
Results of these positional analyses indicate that the primary desaturation reactions takes place in the Δ9 position of pre-existing
(C14 to C24) acyl chains. It is proposed that acyl components from 18∶1 are subjected to chain elongation to form a mixture of 24∶1 isomers
as the final product. Apart from the 24∶1 acyl moiety of the wax esters, in which the double bond was almost exclusively in
the Δ15 position, de novo biosynthetic reactions on acids and alcohols appear to yield related acyl- and alkyl-moieties of
resynthesized wax esters. 相似文献
169.
Raman spectra of Graphon carbon black 总被引:1,自引:0,他引:1
The Raman spectrum of Graphon carbon black has been recorded using rotating cell techniques. Angular dependence of scattering at 1360, 1580 and 2700 cm?1 are reported and these data suggest that the 1360 cm?1 line is associated with non-planar microstructure distortions. The excitation frequency dependence of the intensity ratio of the bands at 1360 (D) and 1580 cm?1 (G) is interpreted in terms of resonance (vibronic) interaction. This dependence is primarily the result of an increase in the intensity of the 1360 cm ?1 line. The disorder-associated line (D) exhibits a significant excitation-dependent shift from 1378 cmi?1 (457.9 nm Ar+) to 1330 cm?1 (647.1 nm Kr+). The “graphite” (G) line position is less sensitive to changes in excitation frequency. The spectral features are discussed in terms of factor group, C6v4, and layer site symmetry, C3v. Also the possible role of localized alkene-like structure in zones of structural distortion is considered. 相似文献
170.
H. J. Dutton S. B. Johnson F. J. Pusch M. S. F. Lie Ken Jie F. D. Gunstone R. T. Holman 《Lipids》1988,23(5):481-489
An approach to the analysis of 55 possible nonconjugated positional isomers of octadecadienoic acid is described and tested
with mixtures of individual synthetic methyl esters. In the first example, by ozonolysis a sevencomponent mixture consisting
ofcis,cis 5,12-, 6,10-, 6,11-, 6,12-, 7,12-, 8,12-, and 9,12-octadecadienoates was converted to aldehydes, aldehyde-esters and dialdehydes.
These fragments were separated on a 50 m×0.2 mm free fatty acid phase (FFAP) vitreous silica capillary column. Equations for
an arbitrarily restricted 12×15 matrix of linear simultaneous equations and a computer solution of the matrix provided the
composition of the initial methyl octadecadienoate mixture. The power and significance of this method became apparent with
the observation that only two of the seven isomers in the known mixture were resolved as single peaks by state-of-the-art
capillary gas chromatography, but all seven were identified and estimated with acceptable error by the ozonolysis-capillary
gas chromatography-computer procedure. In a generalized approach to the analysis of the 55 possible nonconjugated isomers,
a computer program selects the appropriate matrix of linear simultaneous equations based on the aldehyde data supplied by
the analyst. Twenty of 21 combinations of seven isomeric esters taken five at a time have been analyzed to assess the efficiency
of the method. To illustrate applicability at this stage of development, the method has been used to analyze the diene products
of the hydrazine reduction of γ-linolenic acid and the diene products from the biological desaturation of isomeric monoenes.
The possibility of distinguishing geometric and positional isomers of 18∶2 has been opened by the observed separation ofcis-andtrans-unsaturated aldehydes and aldehyde-esters.
Presented in part at the 16th World Congress of the International Society for Fat Research, October 4–7, 1983, in Budapest,
Hungary, and at the American Oil Chemists' Society Meeting, May 15, 1986, in Honolulu, Hawaii. 相似文献