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111.
Positron lifetimes have been measured as a function of temperature in 4-butyloxybenzal-4′-ethylaniline (BEA). BEA has been previously reported to have two liquidcrystalline phases (smectic and nematic) with transition temperatures as follows: solid → smectic, 40.5° C; smectic → nematic, 51.0° C; and nematic → isotropic liquid, 65.5° C. Positron life time spectra were resolved into two components, with the shorter component τ1 remaining approximately constant in all phases, and τ2 exhibiting reversible changes at all of the above transitions. In addition, an irreversible discontinuity in the τ2 lifetime was observed in the vicinity of 28° C, indicating the presence of a new phase (phase X) of BEA. The τ2 andI 2 values obtained for the various phases of BEA are: solid (1.25 nsec, 7.1%), phase X (1.97 nsec, 26.2%), smectic (2.36 nsec, 23.6%), nematic (2.72 nsec, 28.3%), and isotropic liquid (2.69 nsec, 29.8%). 相似文献
112.
The nuclear quadrupole tensor for 27Al in yttrium ortho-aluminate has been measured between 30°C and ?150°C. The coupling constant varies linearly from 1.44 to 1.56 MHz over this range, whereas the asymmetry parameter η drops rapidly from 0.748 toward an asymptotic value of 0.663. 相似文献
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115.
Bailey Bennett W. J. Mueller Richard A. Nathan 《Journal of polymer science. Part A, Polymer chemistry》1973,11(7):1589-1600
Four pure hydroperoxides were evaluated as initiators for the polymerization of styrene–butadiene rubber (SBR) at 5°C. These materials were the meta and para isomers of mono- and dihydroperoxy-diisopropylbenzene. Results showed that the monohydroperoxides produced somewhat faster reactions than a control hydroperoxide, p-menthane hydroperoxide. Response to mercaptan level adjustments was good, providing polymer with a Mooney viscosity in the 50 to 60 range. The reaction rate with the dihydroperoxides was slower, but again provided polymer with a satisfactory viscosity. Basic physical property measurements on polymers prepared with the pure hydroperoxides or control hydroperoxides showed only minor differences. It is anticipated that these differences can be eliminated by small adjustments in the compound recipe. 相似文献
116.
Q-values for the (p, t), (p, 3He) and (p, d) reactions for twenty-five isobaric analog states in the shell have been accurately measured. The corresponding experimental displacement energies are compared with recent model predictions. 相似文献
117.
Crosson GS Choi S Chorover J Amistadi MK O'Day PA Mueller KT 《The journal of physical chemistry. B》2006,110(2):723-732
The weathering of a specimen kaolinite clay was studied over the course of 369 d via solid-state 29Si magic angle spinning (MAS) nuclear magnetic resonance (NMR) spectroscopy and high-field 27Al MAS NMR. The chosen baseline solution conditions (0.05 mol kg-1 of Al, 2 mol kg-1 of Na+, 1 mol kg-1 of NO3-, 1 mol kg-1 of OH-, and pH approximately 13.8) approximate those of solutions leaking from waste tanks at the Hanford Site in Richland, WA. Nonradioactive Cs and Sr cations were added to this synthetic tank waste leachate (STWL) solution at concentrations of 10(-3), 10(-4), and 10(-5) molal (m) to represent their radionuclide counterparts. The transformations of silicon- and aluminum-containing solid phase species were monitored quantitatively by using NMR spectroscopy, with the resulting spectra directly reporting the influence of the initial Cs and Sr on formation and transformation of the neo-formed solids. At the lowest concentration of Cs and Sr employed (10(-5) m in each cation) peaks consistent with the formation of zeolite-like minerals were detected via 29Si and 27Al MAS NMR as early as 33 d. At concentrations of 10(-3) m in each cation, new silicon species are not detected until 93 d, although neophases containing four-coordinate aluminum were detectable at earlier reaction times via 27Al MAS NMR. At the highest magnetic field strengths employed in this NMR study, deconvolutions of resonances detected in the tetrahedral region of the 27Al MAS spectra yielded multiple components, indicating the existence of at least four new aluminum-containing phases. Two of these phases are identified as sodalite and cancrinite through comparison with diffuse-reflectance infrared (DRIFT) spectra and powder X-ray diffraction (XRD) results, while a third phase may correlate with a previously detected aluminum-rich chabazite phase. All measurable solid reaction products have been quantified via their 27Al MAS resonances acquired at high magnetic field strengths (17.6 T), and the quantitative nature of the 27Al NMR data shows that cancrinite growth increases while sodalite reaches a steady state with respect to total aluminum in the solid phases. The data also relate the coupling of Cs sorption to the ripening of feldspathoid phases in this heterogeneous system as a function of time, and illustrate the important influence of co-contaminants on the environmental reaction kinetics studied here. 相似文献
118.
Hybrid specimens of metal and fibre-reinforced polymer are applied in automotive and aerospace industry. The simulation and analysis of damage of such engineering structures is the focus of this research. The investigation includes a computation of the extension of single lap tensile specimen, produced by ultrasonic metal welding. The specimen is manufactured from CF-PA66 - fibre-reinforced polymer and AlMg3 (AA5754), which is used as a metallic joining partner. The aluminium substrate is treated as an elastoplastic material. The polymer composite generally shows an orthotropic elastic behaviour. The interface material has been numerically modeled as an elastoplastic material with linear hardening, coupled with Lemaitre-type damage. The finite element method is used for the investigation of so-called interface elements. The geometry of the interface is a consequence of the welding sonotrode geometry. The behaviour of specimens with square and ring interface geometry are analysed. The influence of the interface geometry on the mechanical properties of the joint is shown. The increase of the damage parameter and the development of failure are described for both cases. (© 2010 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim) 相似文献
119.
Rolf W. B. Russow Michael Intorp Christian Mueller C. Florian Stange 《Isotopes in environmental and health studies》2013,49(3):257-262
To determine the 13C abundance of combustion and break down products formed in cigarette smoke, especially CO and CO2, a simple and fast analytical method is needed. Taking into account the knowledge about the determination of the natural 13C abundance in air, an online method—based on gas chromatography-reaction-continuous flow mass spectrometry (GC-R-CF-MS)—has been developed, which enables the determination of the 13C abundance of CO and CO2 in the vapour phase of cigarette smoke with a relative standard deviation of≤0.5% in one analytical run. Additionally, in a second step, the 13C abundance of total volatile carbon can be determined. 相似文献