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31.
Journal d'Analyse Mathématique - 相似文献
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Experimental Techniques - 相似文献
33.
We have measured the transmission and extinction properties of a large aperture (10 × 10 mm) CdTe Pockels cell crystal. The crystal has been used for single pulse selection from a mode-locked CO2 laser and results show that it is superior to GaAs for this purpose. 相似文献
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Adhesion of (CH)x film prepared by the Luttinger method to glass can be improved by silylation in order to more closely match dispersive surface energies. Treatment of n-type (CH) films with NiBr2/HMPA/THF affords (CH)x -supported N° which shows selectivity in hydrogenation of phenyl acetylene. 相似文献
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F. Grandjean Gary J. Long Dimitri Hautot Dennis L. Whitney 《Hyperfine Interactions》1998,116(1-4):105-115
The iron57 Mössbauer spectra of three different samples of the Jilin meteorite have been measured at 78 and 295 K. Five iron containing major components are identified, two magnetic components, kamacite and troilite, and three nonmagnetic components, olivine, pyroxene, and an iron(III) component. The relative absorption areas of these five components show that sample A contains a larger fraction of magnetic components, ca. 50 percent, than samples B and C, which contain ca. 30 percent. This difference indicates a significant compositional inhomogeneity in the Jilin meteorite. The fit of the troilite component sextet is extensively discussed in the paper and requires the adjustment of not only the isomer shift and hyperfine field, but also of the quadrupole interaction, the asymmetry parameter of the electric field gradient tensor, and the orientation of the hyperfine field in the principal axes of the electric field gradient tensor. The smaller isomer shift and hyperfine field of the kamacite mineral in sample B indicate that this sample contains less nickel than the kamacite in samples A and C, in which the amount of nickel is estimated to be ca. 9 percent. On the basis of its hyperfine parameters, the iron(III) component is assigned to iron(III) substituted on the M1 site of pyroxene. 相似文献
38.
Karim K Klasson KT Drescher SR Ridenour W Borole AP Al-Dahhan MH 《Applied biochemistry and biotechnology》2007,142(3):231-242
Anaerobic digestion kinetics study of cow manure was performed at 35°C in bench-scale gas-lift digesters (3.78 l working volume)
at eight different volatile solids (VS) loading rates in the range of 1.11–5.87 g l−1 day−1. The digesters produced methane at the rates of 0.44–1.18 l l−1 day−1, and the methane content of the biogas was found to increase with longer hydraulic retention time (HRT). Based on the experimental
observations, the ultimate methane yield and the specific methane productivity were estimated to be 0.42 l CH4 (g VS loaded)–1 and 0.45 l CH4 (g VS consumed)–1, respectively. Total and dissolved chemical oxygen demand (COD) consumptions were calculated to be 59–17% and 78–43% at 24.4–4.6 days
HRTs, respectively. Maximum concentration of volatile fatty acids in the effluent was observed as 0.7 g l–1 at 4.6 days HRT, while it was below detection limit at HRTs longer than 11 days. The observed methane production rate did
not compare well with the predictions of Chen and Hashimoto’s [1] and Hill’s [2] models using their recommended kinetic parameters. However, under the studied experimental conditions, the predictions of
Chen and Hashimoto’s [1] model compared better to the observed data than that of Hill’s [2] model. The nonlinear regression analysis of the experimental data was performed using a derived methane production rate
model, for a completely mixed anaerobic digester, involving Contois kinetics [3] with endogenous decay. The best fit values for the maximum specific growth rate (μ
m) and dimensionless kinetic parameter (K) were estimated as 0.43 day–1 and 0.89, respectively. The experimental data were found to be within 95% confidence interval of the prediction of the derived
methane production rate model with the sum of residual squared error as 0.02. 相似文献
39.
The combination of shot noise-limited direct absorption spectroscopy with long-path-length slit supersonic discharges has been used to obtain first high-resolution infrared spectra for jet-cooled CH2F radicals in the symmetric (nu1) and antisymmetric (nu5) CH2 stretching modes. Spectral assignment has yielded refined lower- and upper-state rotational constants and fine-structure parameters from least-squares fits to the sub-Doppler line shapes for individual transitions. The rotational constants provide indications of large amplitude vibrational averaging over a low-barrier double minimum inversion-bending potential. This behavior is confirmed by high-level coupled cluster singles/doubles/triples calculations extrapolated to the complete basis set limit and adiabatically corrected for zero point energy. The calculations predict a nonplanar equilibrium structure (theta approximately 29 degrees, where theta is defined to be 180 degrees minus the angle between the C-F bond and the CH2 plane) with a 132 cm(-1) barrier to planarity and a vibrational bend frequency (nu(bend) approximately 276 cm(-1)), in good agreement with previous microwave estimates (nu(bend) = 300 (30) cm(-1)) by Hirota and co-workers [Y. Endo et al., J. Chem. Phys. 79, 1605 (1983)]. The nearly 2:1 ratio of absorption intensities for the symmetric versus antisymmetric bands is in good agreement with density functional theory calculations, but in sixfold contrast with simple local mode CH2 bond dipole predictions of 1:3. This discrepancy arises from a surprisingly strong dependence of the symmetric stretch intensity on the inversion bend angle and provides further experimental support for a nonplanar equilibrium structure. 相似文献
40.
Karthik Vikram Siva Shanmugam J. Scott Parent Ralph A. Whitney 《European Polymer Journal》2012,48(4):841-849
Solid-state rheometry and model compound reactions are used to investigate free radical reactions of N-arylmaleimide coagents with saturated and unsaturated polymers. N,N′-m-phenylene dimaleimide (BMI) is shown to provide superior cross-link densities over diacrylate and diallyl coagents for all of the polymers studied, including linear low density polyethylene (LLDPE), poly(ethylene oxide) (PEO), cis-poly(butadiene) (PBD) and cis-poly(isoprene) (PIP). Studies of the N-phenylmaleimide (NPM) + cis-cyclooctane system show that C–H bond addition to yield N-aryl-2-alkylsuccimide grafts is the predominant reaction pathway, as opposed to maleimide homopolymerization. In contrast, peroxide-initiated reactions of cis-cyclooctene with small NPM concentrations generate highly alternating poly(cycloctene-alt-N-phenylmaleimide) in high yield, indicating that unsaturated mers in materials such as PBD engage maleimides in an efficient alternating copolymerization between electron-rich and electron-deficient monomer pairs. Factors that affect the reactivity of different polymers in these C–H bond additions and alternating copolymerizations are discussed. 相似文献