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991.
Comparison of multicomponent fuel droplet vaporization experiments in forced convection with the Sirignano model 总被引:2,自引:0,他引:2
A. Daï f M. Bouaziz X. Chesneau A. Ali Ch rif 《Experimental Thermal and Fluid Science》1998,18(4):282-290
The vaporization of multicomponent fuel droplets was studied experimentally in a heated flow and the results were compared to the model proposed by Abramzon and Sirignano. The droplet was suspended on a permanent holder which was set up in a thermal wind-tunnel. This wind-tunnel was fitted with a video recording system and an infra-red camera. The period during which the droplet was suspended on the holder before the opening of the hot air flow damper was recorded. This first sequence corresponds to the droplet vaporization in natural convection, whose initial experiment conditions, especially diameter, temperature, composition of the droplet, are well known. Then the damper was turn on, and the sequence of forced convection begun. The initial diameter of the droplet was recorded by the video system. The other initial conditions of this second sequence cannot be determined experimentally. The distribution of temperature in the droplet and the surface temperature, the mass fraction distribution in the droplet and the surface mass fraction were unknown. These unknown parameters were determined by coupling our experiment with a model using “the film concept” in natural convection. Experimental results were compared with the calculations and found satisfactory, in natural convection as well as in forced convection initiated by this method. The method was tested in the case of a fuel mixture droplets (heptane–decane) for different initial concentrations and variable durations of the sequence in natural convection. 相似文献
992.
A general nonlinear theory for the dynamics of elastic anisotropic plates undergoing moderate-rotation vibrations is presented. The theory fully accounts for geometric nonlinearities (moderate rotations and displacements) by using local stress and strain measures and an exact coordinate transformation, which result in nonlinear curvatures and strain-displacement expressions that contain the von Karman strains as a special case. The theory accounts for transverse shear deformations by using a third-order theory and for extensionality and changes in the configuration due to in-plane and transverse deformations. Five third-order nonlinear partial-differential equations of motion describing the extension-extension-bending-shear-shear vibrations of plates are obtained by an asymptotic analysis, which reveals that laminated plates display linear elastic and nonlinear geometric couplings among all motions. 相似文献
993.
994.
Norouzi Parviz Ganjali Mohammad Reza Qomi Mahnaz Nemati Kharat Ali Zamani Hassan Ali 《中国化学》2010,28(7):1133-1139
A continuous cyclic voltammetric study of letrozole at gold microelectrode was carried out. The drug in phosphate buffer (pH 2.0) is adsorbed at ?200 mV, giving rise to change in the current of well‐defined oxidation peak of gold in the flow injection system. The proposed detection method has some of advantages, the greatest of which are as follows: first, it is no more necessary to remove oxygen from the analyte solution and second, this is a very fast and appropriate technique for determination of the drug compound in a wide variety of chromatographic analysis methods. Signal‐to‐noise ratio has significantly increased by application of discrete Fast Fourier Transform (FFT) method, background subtraction and two‐dimensional integration of the electrode response over a selected potential range and time window. Also in this work some parameters such as sweep rate, eluent pH, and accumulation time and potential were optimized. The linear concentration range was of 1.0×10?7?1.0×10?10 mol/L (r=0.9975) with a limit of detection and quantitation 0.08 nmol/L and 0.15 nmol/L, respectively. The method has the requisite accuracy, sensitivity, precision and selectivity to assay letrozol in tablets. The influences of pH of eluent, accumulation potential, sweep rate, and accumulation time on the determination of the letrozol were considered. 相似文献
995.
Bamoharram Fatemeh F Roshani Mina Heravi Majid M Mahdavi Masoumeh Javid Ali Emampour Jalal Sh 《中国化学》2010,28(6):974-976
Isoxazolo[5,4‐d]pyrimidine‐4,6(5H,7H)diones 2a – 2f have been synthesized from the reaction of ethyl 5‐amino‐3‐methyl‐4‐isoxazole carboxylate ( 1 ) with aryl isocyanates in the presence of Keggin heteropolyacid H3[PW12O40] as a green solid acid catalyst at room temperature in a one‐pot process in good yields. 相似文献
996.
Mohammad Nikpassand Manouchehr Mamaghani Mohammad Ali Zanjanchi Nosrat Olah Mahmoodi Massomeh Mirzaeinejad 《中国化学快报》2010,21(1):5-8
<正>A facile and convenient protocol was developed for the synthesis of 1,5-diarylpyrazoles using Baylis-Hillman adducts in the presence of HY-zeolite as an efficient recyclable heterogeneous catalyst in reasonable reaction times(1.5-2.5 h) and high yields (78-90%). 相似文献
997.
Ali Nakhaei Pour Mohammad Reza Housaindokht Sayyed Faramarz Tayyari Jamshid Zarkesh 《天然气化学杂志》2010,19(3):333-340
A nano-structured iron catalyst for syngas conversion to hydrocarbons in Fischer-Tropsch synthesis (FTS) was prepared by micro-emulsion method. Compositions of bulk iron phase and phase transformations of carbonaceous species during catalyst deactivation in FTS reaction were characterized by temperature-programmed surface reaction with hydrogen (TPSR-H2), and XRD techniques. Many carbonaceous species on surface and bulk of the nano-structured iron catalysts were completely identified by combined TPSR-H2 and XRD spectra and which were compared with those recorded on conventional co-precipitated iron catalyst. The results reveal that the catalyst deactivation results from the formation of inactive carbide phases and surface carbonaceous species like graphite, and it will be increased when the particle size of iron oxides was reduced in FTS iron catalyst. 相似文献
998.
The effects of Mg, La and Ca promoters on primary and secondary CO_2 and H_2O formation pathways during Fischer-Tropsch synthesis on precipitated Fe/Cu/SiO_2 catalysts are investigated. The chemisorbed oxygen atoms in the primary pathway formed in the CO dissociation steps reacted with co-adsorbed hydrogen or carbon monoxide to produce H_2O and CO_2 , respectively. The secondary pathway was the water-gas shift reaction. The results indicated that the CO_2 production led to an increase in both primary and secondary pathways, and H_2 O production
decreased when surface basicity of the catalyst increased in the order Ca >Mg >La. 相似文献
999.
Lotf Ali Saghatforoush Robabeh Mehdizadeh Firoozeh Chalabian 《Transition Metal Chemistry》2010,35(8):903-910
The Ni(II) complexes [Ni(L)2](ClO4)2 (1) and [Ni(L)2(NO3)2] (2), where L is the Schiff base ligand of 4,5,9,13,14-pentaaza-benzo[b] triphenylene, were synthesized and characterized by physico-chemical and spectroscopic methods. Nano-sized particles of (1) were prepared both by sonochemistry (3) and solvothermal (4) methods. NiO nanoparticles were obtained by calcination of the nano-structure complexes at 500 °C. The structures of the nano-sized compounds were characterized by X-ray powder diffraction and scanning electron microscopy. The thermal stabilities of the bulk complexes (1–2) and nano-sized particles (3–4) were studied by thermogravimetric and differential scanning calorimetry. The catalytic activities of complexes of (1–4) are reported. The free Schiff base and its Ni(II) complexes have been screened for antibacterial activities against three Gram-positive bacteria. The metal complexes are more active than the free Schiff base. Electrochemical studies show that the Ni complexes undergo irreversible reduction in MeCN solution. 相似文献
1000.
Hossein Eshtiagh-Hosseini Mohammad Reza Housaindokht Mohammad Chahkandi Ali Morsali 《Transition Metal Chemistry》2010,35(8):939-947