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排序方式: 共有662条查询结果,搜索用时 31 毫秒
1.
The most promising next generation Image Velocimtry (IV) is the high-speed Dynamic PIV. It requires the development of innovative
high-speed video camera sensors. We started by specifying the required performance of these new sensors, for measurements
in air and water flows. These criteria founded on the most recent developments in PIV algorithms and incorporate results from
a large questionnaire survey of users of high-speed video cameras in Japan. The results suggest that the followings are required:
(1) frame rate of 1,000,000 fps, (2) pixel count of 1,000,000 pixels, (3) frame storage capacity of 100–200 frames for tracing
a single event and 10,000 frames for turbulent measurements, (4) gray levels of 4–8 bits for PTV; 12 bits for observation.
Finally, we reviewed the state of the art of high-speed video-image sensors. Currently the standard parallel-readout sensors
can operate at 1 Kfps with a pixel count of approximately 1 Kpixels. The In-situ Storage Image Sensor (ISIS) developed by
the authors has recently achieved frame rates of 1 Mfps. 相似文献
2.
The self-restoration properties in VWP networks are investigated with optimization about spare wavelength by simulations. Rapid restoration can be achieved by selection of rerouting path with long delay and no delay-limitation for new routes. 相似文献
3.
Yong Lee Kazuhiko Hosomi Hiroyuki Uchiyama Toshio Katsuyama Shinya Kominami Tomoyoshi Mishima 《Optical Review》2003,10(1):38-42
An InGaAsP slab-type asymmetric-coupled-waveguide-based dispersion compensator with a mode selector has been designed and fabricated. The mode selector is necessary to select either a symmetric [with a positive group-velocity dispersion (GVD)] or antisymmetric (with a negative GVD) supermode. These supermodes exist simultaneously in the dispersion-compensation region of the device. Pulse-compression experiments were used to test the dispersion compensator, evaluating the function of the mode selector. A theoretical study of the experimental results shows that the mode selector obtains a very strong selectivity (nearly 100%) for the antisymmetric supermode. 相似文献
4.
H. Kuramochi J. Okabayashi F. Takano M. Mizuguchi T. Manago H. Akinaga 《Surface science》2004,550(1-3):192-198
Strong magnetic poles at characteristic rectangular defects have been observed using a magnetic force microscope on a MnAs(
1 0 0) thin film with the thickness of 30 nm. The MnAs thin film was epitaxially grown on a GaAs(0 0 1) substrate. The magnetic poles were in one-arranging direction, being independent of the magnetization direction of the film. The poles were pinned at the edges of the rectangular defects until just below the Curie temperature, and formed a stable magnetic-field loop on the MnAs surface. The stability of the magnetic pole pinning shows the distinctive feature of the magnetic domain structure on the surface with a strong anisotropy, which was built in the heterostructure of MnAs and GaAs. 相似文献
5.
Hiroshi Sakurai Fumitake Itoh Katsuyoshi Takano Hiromi Oike 《Journal of Physics and Chemistry of Solids》2004,65(12):2083-2088
A novel technique of measuring a magnetic Compton profile using the grazing angle geometry against a sample surface (Grazing Incidence Magnetic Compton Profile) has been successively developed. Measurements of a magnetic moment and a magnetic Compton profile are possible for a Fe 200 nm film on a thick glass substrate. The estimated thinnest limit for measurements is 100 nm for a Fe film. 相似文献
6.
Iron speciation related to color of Jurassic sedimentary rocks in Turpan Basin, northwest China 总被引:1,自引:0,他引:1
Guodong Zheng Bihong Fu Yi Duan Qi Wang M. Matsuo B. Takano 《Journal of Radioanalytical and Nuclear Chemistry》2004,260(2):421-427
Mesozoic-Cenozoic reddish and green beds are widely distributed in northwest China. Mössbauer spectroscopy revealed that the composition of iron species varies with color in the middle-upper Jurassic sedimentary rocks from the Turpan Basin. Three main kinds of iron species were identified: (1) ferric iron of hematite (hem-Fe3+), (2) paramagnetic ferric iron (para-Fe3+), and (3) paramagnetic ferrous iron (para-Fe2+). Pyrite iron (pyr-Fe2+) was revealed only in a few samples. In general, there is a direct correlation between rock color, iron species and total iron content, however, in detail, this relationship is more complicated. The reddish rocks contain higher contents of total iron and hem-Fe3+, whereas the gray rocks contain much more para-Fe2+. However, relatively low hematite content cannot give red color to rocks, probably due to suppression by other pigments such as organic matter in black or chlorite in green. The dark or green rocks normally contain either only paramagnetic Fe2+ and paramagnetic Fe3+ species or these two species associated with hematite Fe3+, but the relative content of hematite species is lower. The variations of different iron species control lithological properties such as color and also may reflect the sedimentary conditions. Moreover, iron speciation in these rocks is one of the main factors, which result the color features of rocks in remote sensing imagery.This revised version was published online in November 2005 with corrections to the Cover Date. 相似文献
7.
8.
Rijssenbeek JT Saito T Malo S Azuma M Takano M Poeppelmeier KR 《Journal of the American Chemical Society》2005,127(2):675-681
The related parameters of cation size and valence that control the crystallization of Sr(3)CaRu(2)O(9) into a 1:2 B-site-ordered perovskite structure were explored by cationic substitution at the strontium and calcium sites and by the application of high pressure. At ambient pressures, Sr(3)MRu(2)O(9) stoichiometries yield multiphasic mixtures for M = Ni(2+), Mg(2+), and Y(3+), whereas pseudocubic perovskites result for M = Cu(2+) and Zn(2+). For A-site substitutions, an ordered perovskite structure results for Sr(3-x)Ca(x)CaRu(2)O(9), with 0 = x = 1.5. In contrast, Ba(2+) substitution for Sr(2+) is accompanied by a phase change to a hexagonal BaTiO(3) structure type. At high pressures and temperatures, a 1:2 B-site-ordered perovskite structure is stabilized for Sr(3-x)Ba(x)CaRu(2)O(9), with 0 = x = 3. The scarcity of B-site-ordered perovskite ruthenates at ambient pressure and the metastable nature of the high-pressure phases underscore the strict size and valence requirements that must be met by the constituent cations to achieve these uncommon ordered structures. 相似文献
9.
A simple and selective route to the Strychnos framework containing 19,20-double bond has been developed employing the thio-Claisen rearrangement. 相似文献
10.
Shigeru Matsuo Tomoyoshi Murakami Ryuichi Takasawa 《Journal of polymer science. Part A, Polymer chemistry》1993,31(13):3439-3446
Crystalline poly(arylene ether nitrile) could be prepared by the polycondensation of 2,6-dihalobenzonitrile with resorcinol at 200°C in N-methylpyrrolidone in the presence of sodium carbonate. A reaction temperature of at least 200°C was necessary to attain high molecular weight polymer. Spectral data indicated that the polymer had the structure of a poly(meta-phenylene ether) with pendent nitrile groups on every other phenylene unit. Despite this structure, the crystallinity and the crystallization rate of the polymer were greater than those of the corresponding polymer with a para-linked structure. The glass transition temperature and the melting temperature of the polymer were almost the same as those of poly(etheretherketone) (PEEKTM). A series of other new poly(arylene ether nitriles) were also examined. The polymers derived from 4,4′-biphenol, dihydroxytetra-phenylmethane, dihydroxydiphenylsulfone, and 1,5-isoquinolinediol had high glass transition temperatures. The poly(arylene ether nitriles) exhibited excellent tensile strength compared with the corresponding ketone- or sulfone-containing polymers. Comparing the three different kinds of polymers containing the same bisphenol units, the order of glass transition temperature was found to be sulfone- > nitrile- > ketone-containing polymers, while the order of tensile strength was nitrile- > ketone- > sulfone-containing polymers. The excellent mechanical properties are attributable to dipole-dipole interactions of nitrile groups. © 1993 John Wiley & Sons, Inc. 相似文献