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91.
The beam deflection phenomenon of a transverse-flow discharge-excited CO2 gas laser is studied by measuring the beam pattern with the rotating-wire method at gas velocities of 35-70 m/s, gas pressures of 5.3-10.6 kPa (103 N/m2), and laser powers of 50-700 W. The beam deflection distance increased with increasing laser power and gas pressure and with decreasing gas velocity. All the data points of beam deflection distances observed experimentally fell on one line when normalized by the gas pressure and plotted against the measured temperature gradient in the resonator. It is shown that the most important factor affecting the beam deflection is the refractive index variation of the gas produced by the gas temperature gradient in the resonator. Methods to reduce the beam-deflection distances are suggested 相似文献
92.
93.
The generation of a bipolarity solitary wave (soliton) is examined by using a transmission line containing gyromagnetic nonlinear inductors. The results indicate that a transmission line of the form shown here can be used in high-peak-power pulse-generating networks. 相似文献
94.
The evolution of the intelligent network (IN) is summarized, and its service creation requirements and provision environment are clarified. A prototype system called the ISDN development experimental system for advanced services (IDEA), which has been developed to validate the foregoing, is described. The evaluation of the system design and its future evolution are discussed 相似文献
95.
We propose a ray-tracing model that provides a clear physical picture and simple formulas for grating pair stretcher dispersion calculations. With this model we can easily demonstrate why and to what extent the stretcher and compressor are opposite quantitatively without using a Fourier transform. The dispersion calculation shows that the spherical aberration in the stretcher decreases fourth-order dispersion compared with an aberration-free stretcher. In a chirped pulse amplification system, this fourth order can help to reduce residual fourth-order dispersion. The effect of the finite beam size and the misalignment are also considered. 相似文献
96.
Infrared spectroscopy was applied to identify and determine microamounts of anionic surfactants contained in sewage or river waters. The surfactants tested were linear alkylbenzene sulfonate (LAS), branched alkylbenzene sulfonate (ABS), alpha olefine sulfonate (AOS), fatty alcohol sulfate (AS) and fatty alcohol ethoxy sulfate (AES).Anionic surfactants in waters were extracted by chloroform as methylene blue complexes and sulfate type surfactants, i.e. AS and AES were then removed by subsequent hydrolysis. Residual sulfonate type surfactants were first released from methylene blue complexes by ion exchange technique and then changed to sulfonyl chloride derivatives for infrared spectroscopy. Key bands for the identification of sulfonate type surfactants are 640, 618 and 524 cm−1 for LAS, ABS and AOS, respectively. Sulfate type surfactants was calculated from the difference of methylene blue active substance contents before and after hydrolysis. 相似文献
97.
I Pontén JM Sayer AS Pilcher H Yagi S Kumar DM Jerina A Dipple 《Canadian Metallurgical Quarterly》1999,38(3):1144-1152
Diastereomeric N6-substituted dAdo adducts (cis B[c]PhDE-2/1R and cis B[c]PhDE-2/1S) that correspond to cis-opening at C-1 of the enantiomeric benzo[c]phenanthrene 3,4-diol 1,2-epoxides in which the epoxide oxygen and the benzylic hydroxyl group are trans (DE-2) were synthetically incorporated into oligonucleotide 16-mers. Each adduct was placed at the fourth nucleotide from the 5'-end of each of two different oligonucleotide sequences derived from the E. coli supF gene. Each adduct was also placed in two additional oligonucleotide sequences that were constructed by interchanging the adduct site and the immediately adjacent nucleotides between the two original sequences. These oligonucleotides were designed for use in site-specific mutation studies, with a single-stranded bacteriophage M13mp7L2 vector, to determine if the effects of sequence context on types and frequencies of base substitution mutations are attributable only to nucleotides immediately adjacent to these polycyclic aromatic hydrocarbon diol epoxide-dAdo adducts, or whether more distant nucleotide residues also affect the mutagenic response. In SOS-induced Escherichia coli SMH77, total base substitution mutation frequencies for the cis B[c]PhDE-2/1R-dAdo adduct were relatively low (0.62-5.6%) compared with those for the cis B[c]PhDE-2/1S-dAdo adduct (11.9-56.5%). Depending on sequence context, cis B[c]PhDE-2/1R-dAdo gave predominantly A-->T or a more equal distribution of A-->T and A-->G mutations whereas cis B[c]PhDE-2/1S-dAdo gave either predominantly A-->T or predominantly A-->G base substitutions. Our results clearly indicate that nucleotides that are distal as well as those that are proximal to the adduct site are capable of influencing both the mutation frequency and the distribution of base substitution mutations. 相似文献
98.
By using the characteristics of a hydrogen-absorbing alloy, the hydrogen produced by catalytic dehydrogenation of saturated
compounds can be absorbed to form metal hydrides, and, vice versa, the resulting metal hydrides are able to hydrogenate efficiently
unsaturated compounds upon dehydriding. Gas-phase reactions between 2-butene and 2-propanol on a hydrogen-absorbing alloy
CaNi5 have been studied in the temperature range of 393–473 K. CaNi5 showed interesting characteristics as an active catalyst for the catalytic transfer hydrogenation of butene from propanol
as a hydrogen donor. 2-propanol was effectively dehydrogenated at 423 K to yield acetone in which the dissociated hydrogen
was completely absorbed by CaNi5 to form the metal hydride. When the alloy was hydrided to some extent, butene was hydrogenated by the absorbed hydrogen in
the metal hydride to produce butane. The overall reaction on CaNi5 was expressed as catalytic transfer hydrogenation of 2-butene from 2-propanol through intermediate formation of metal hydrides,
rather than the direct reaction between butene and propanol on the alloy. Thus, CaNi5 effectively repeated hydriding–dehydriding cycles: hydriding of CaNi5 by 2-propanol dehydrogenation with subsequent dehydriding for the hydrogenation of 2-butene. The use of hydrogen-absorbing
CaNi5 provides a novel reaction system for the catalytic transfer hydrogenation.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
99.
100.