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Two composite supports with a mixed inorganic–organic structure were synthesized: BTAl and UTAl. Hydrophilic–hydrophobic dual properties of the supports were suitable for preparing egg-shell-supported metal catalysts for selective hydrogenation reactions. The catalysts were characterized by ICP, XRD, OM, TEM, EPMA, XPS and TGA. Their mechanical resistance was assessed. Activity and selectivity were tested with the hydrogenation of 2,3-butanedione (diacetyl) to 3-hydroxy-2-butanoneacetoin (acetoin). The same order of increasing metal particle size was found for the two tested supports: Pt < Ru < Pd. The XPS analysis showed that the metal/composite catalysts reduced in H2 at 503 K had two kinds of active sites: reduced (Me°) and electron-deficient (Me+). It was rationalized that the hydrogen bond cleavage was performed on the Me° active sites, while reactant adsorption occurred on the Me+ sites. The differences in activity and selectivity between the composite catalysts were attributed to electronic effects on the different metals and to different adsorptive properties of the different polymers. The high selectivity to acetoin was attributed to the preferential adsorption of diacetyl as compared to the adsorption of acetoin. The BTAl catalysts were slightly more active and selective than the UTAl ones. This was attributed to electronic effects caused by remnant organic groups on the composite supports (urethane or biphenyl on UTAl or BTAl, respectively). Pd-BTAl was the most active and selective catalyst, a fact related to electronic effects of both palladium and the support. 相似文献
114.
Evgeny Yu. Taran Yury V. Pridatchenko Vera A. Gryaznova 《Comptes Rendus Mecanique》2004,332(4):279-284
The problem of rotary motion of rigid axially symmetric elongated particles in the Couette flow of dilute suspension with anisotropic carrier fluid is solved. It is shown that the stable stationary solutions of the dynamical set of ordinary differential equations describing the particles rotary motion are possible in the case of forming the stationary anisotropy in the carrier fluid of the suspension. It allows us to detect the stationary orientation of suspended particles and formation of stable anisotropic liquid-crystalline structures in the considered suspension under the action of hydrodynamic forces. The study of rheological properties of such a structured suspension shows that it behaves as a viscoelastic quasi-Newtonian anisotropic liquid medium. To cite this article: E.Yu. Taran et al., C. R. Mecanique 332 (2004). 相似文献
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Daiane P. Torres Ingrid M. Dittert Vera L.A. Frescura Adilson J. Curtius 《Microchemical Journal》2010,96(1):32-699
A simple method for the determination of mercury in gasoline samples diluted with ethanol by graphite furnace atomic absorption spectrometry (GF AAS) after cold vapor (CV) generation, pre-concentration in a gold column and trapping on a graphite tube is proposed. The methodology is based upon conventional analytical processes that can be performed by any laboratory with a chemical generation and gold amalgamation systems coupled to the atomic absorption spectrometer. The GF AAS temperature was optimized, being the retention, pyrolysis and atomization temperatures, respectively, 100 °C, 150 °C and 800 °C. Gasoline samples were prepared simply by forming a 2-fold diluted solution in ethanol. The mercury formed vapors by reacting the sample with the reducing agent were pre-concentrated in a gold column and further retained on a graphite tube, coated with gold as permanent modifier. Five samples from different gas stations around the UFSC Campus (Florianópolis, Brazil) were analyzed and the Hg concentrations were found to be in the range from 0.40 µg L− 1 to 0.90 µg L− 1. Calibration against aqueous standard solutions in acidic medium was carried out. The standard solutions had about the same viscosity as the gasoline diluted in ethanol. The relative standard deviations were lower than 2.4% for the samples. The limits of detection in the samples were 0.08 and 0.14 µg L− 1, with and without pre-concentration in the gold column, respectively. The accuracy of the method was estimated by applying the recovery test and recovery values between 92 and 100% were obtained. A sample throughput of 4 h− 1 was achieved. Simplicity and high detection capability are some of the qualities of the method. 相似文献
117.
Vera Vasylyeva 《Journal of fluorine chemistry》2010,131(3):446-4255
The influence of fluorine substituents on the crystallisation behaviour of pyridine was investigated by crystal structure determinations. The low melting compounds 2-fluoropyridine, 2,6-difluoropyridine and 2,4,6-trifluoropyridine were crystallised by in situ crystallisation directly on the single crystal X-ray diffractometer. 相似文献
118.
Keiser T Höllriegl V Giussani A Oeh U 《Isotopes in environmental and health studies》2011,47(2):238-252
Thermal ionisation mass spectrometry (TIMS) method has been developed for the simultaneous detection of different cerium isotopes in biological samples (i.e., blood and urine) at very low concentrations. The work has been done in the frame of a biokinetic study, where different stable cerium isotopes have been administered orally and intravenously as tracers to the human body. In order to develop an appropriate detection method for the tracers in the biological samples, an optimum sample preparation technique has been set and adapted to the specific requirements of the analysis technique used, i.e., TIMS. For sample evaporation and ionisation, the double tantalum filament technique showed the best results. The ions produced were simultaneously collected on a secondary electron multiplier so that the isotopic ratios of the cerium isotopes in the biological samples could be measured. The technique has been optimised for the determination of cerium down to 1?ng loaded on the evaporation filament corresponding to cerium concentrations of down to 1?ng?ml(-1) in the blood or urine samples. It has been shown that the technique is reliable in application and enables studies on cerium metabolism and biokinetics in humans without employing radioactive tracers. 相似文献
119.
Spatial distribution of AT- and GC-rich DNA within interphase cell nuclei of Triatoma infestans Klug
Alvarenga EM Mondin M Martins JA Rodrigues VL Vidal BC Rincones J Carazzolle MF Andrade LM Mello ML 《Micron (Oxford, England : 1993)》2011,42(6):568-578
Heterochromatin bodies in single- and multichromocentered interphase cell nuclei of Triatoma infestans, a vector of Chagas disease, have been suggested to contain AT-rich DNA, based on their positive response to Q-banding and Hoechst 33248 treatment. No information exists on whether GC-rich DNA is also present in these nuclei and whether it plays a role on chromatin condensation. Considering that methodologies more precise than those previously used to determine DNA base composition in situ are currently available, and that the spatial distribution of chromatin areas differing in composition in interphase cell nuclei of different species is a matter of interest, the localization of AT- and GC-rich DNA in T. infestans nuclei is revisited here. The methodologies used included DAPI/AMD and CMA(3)/Distamycin differential staining, Feulgen-DNA image analysis following Msp I and Hpa II enzymatic digestion, 5-methylcytidine immunodetection, AgNOR response, confocal microscopy, and the 5-aza-2'-deoxycytidine (5-AZA) demethylation assay. The results identified the presence of AT-rich/GC-poor DNA in chromocenters and evenly distributed AT and GC sequences in euchromatin. A GC-rich DNA zone encircling the chromocenters was also found but it could not be associated with NOR regions. To corroborate the DNA AT-richness in T. infestans nuclei, bioinformatic analyses were also performed. Methylated cytosine was evident at some points of the chromocenters' edge in single- and multichromocentered nuclei and at the euchromatin of multichromocentered nuclei and could be transiently affected by the 5-AZA treatment. The present results suggest that in the particular case of chromocenters of the hemipteran T. infestans, cytosine methylation is not a relevant factor involved in chromatin condensation. 相似文献
120.
Real-time holographic recording and an improvement of the response time in ruthenium (Ru)-doped Bi(12)SiO(20) (BSO) crystal at 1064 nm is obtained. Using green light pre-exposure, a significant operation speed of 60 ms is achieved. In addition, the ability for image reconstruction is demonstrated in Ru-doped BSO, supporting further applications as reversible media for real-time image processing at the near-IR spectral range. 相似文献