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81.
在常温常压下采用新型旋转电极等离子体反应器,对辉光等离子体作用下的甲烷偶联反应制C2烃进行了研究。结果表明,甲烷偶联反应的主要产物为C2H2,占C2烃的80%以上,能量效率在5.6%~11.2%之间;增加H2含量可以提高CH4转化率和C2烃收率;在500~2200kJ•mol−1的能量密度范围内,CH4转化率随能量密度的增大而线性增加,C2烃收率随着能量密度的增加呈峰形变化趋势。 相似文献
82.
利用气体放电双探针法研究了等离子体的I-V曲线中的电流I相对于电压V轴交点的不对称性,并提出2种可能的解释:一认为是由于两探针表面积不同引起的;二认为是由于探针所在处等离子体电位不等引起的.本文利用仪器的工艺误差和调换放电管电压的方法,对提出的2种可能原因分别进行验证,并指出第二种解释的合理性,并对其进行了理论分析. 相似文献
83.
由Q-Nd:YAG脉冲激光(波长1.06μm,脉宽10 ns)烧蚀Al靶产生等离子体.观测了在低气压和直流电场条件下的Al等离子体发射光谱.研究了激光功率密度和直流电场对各谱线强度的影响,分析了谱线半高全宽与外加电压,等离子体电子温度与激光能量的变化规律.结果表明,直流电场对铝原子谱线强度有显著的增强,铝原子谱线的半高全宽与直流电场的外加电压基本上呈线性关系. 相似文献
84.
Wieczorek-Ciurowa K. Gamrat K. Paryło M. Shirokov Ju. G. 《Journal of Thermal Analysis and Calorimetry》2002,70(1):165-172
The physical mixtures of hydroxocarbonates of Cu and Ni with aluminium were activated using a laboratory planetary mill. The
chemical reactions and alloy formations as the effects of grinding were followed by the phase analysis of solid products based
on the thermogravimetry and X-ray diffractometry. Experimental evidence indicates that the nature of reactions and products
of mechanical activation was dependent on the amount of aluminium and time of grinding.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
85.
The features of interaction of a spherical metallic particle with a rarefied thermal plasma flow due to the presence o charges-electrons and ions in the gaseous phase-are considered. Analytical expressions describing charge, momentum, and energy exchange between the plasma and the particle für the cases of strong and weak Debye screening are obtained. It is illustrated that the efficiency of particle heating in the plasma considerably grows as compared with a hot molecular gas due to participation of electrons and ions in file transfer processes. 相似文献
86.
87.
88.
O. D. Greenwood S. Tasker J. P. S. Badyal 《Journal of polymer science. Part A, Polymer chemistry》1994,32(13):2479-2486
Dielectric barrier air discharge treatment of polyethylene, polypropylene, polyisobutylene, polystyrene, and polyisoprene substrates has been characterized by x-ray photoelectron spectroscopy (XPS). The relative reactivities of these polymers towards silent discharge oxidation are rationalized in terms of ozone molecules interacting with an excited surface. © 1994 John Wiley & Sons, Inc. 相似文献
89.
Summary Oblique propagating magnetohydrodynamic waves with various wave forms and amplitudes are observed both at the Earth's foreshock
and at comets. The possibility of interpreting some observational results in terms of nonlinear evolution of one- and two-dimensional
hydromagnetic waves is investigated. For this purpose both analytical and numerical techniques are employed. It is found that
an initial monochromatic wave changes its polarization giving origin to magnetosonic shocks and rotational discontinuities;
the time evolution of density-magnetic-field correlation is studied, as a function of the plasma parameters and of the propagation
angle. In the two-dimensional case both a transverse instability and a self-focusing effect may take place. Moreover, a two-dimensional
magnetosonic solution is found, in which the density fluctuations are driven by the total pressure fluctuation as in a one-dimensional
simple wave. These theoretical predictions compare well with the features observed in the solar-wind waves.
Paper presented at the V Cosmic Physics National Conference, S. Miniato, November 27–30, 1990. 相似文献
90.
Andrzej Kaim 《Journal of polymer science. Part A, Polymer chemistry》2007,45(2):232-241
The competitiveness of the combination and disproportionation reactions between a 1‐phenylpropyl radical, standing for a growing polystyryl macroradical, and a 2,2,6,6‐tetramethyl‐1‐piperidinyloxy (TEMPO) radical in the nitroxide‐mediated free‐radical polymerization of styrene was quantitatively evaluated by the study of the transition geometry and the potential energy profiles for the competing reactions with the use of quantum‐mechanical calculations at the density functional theory (DFT) UB3‐LYP/6‐311+G(3df, 2p)//(unrestricted) Austin Model 1 level of theory. The search for transition geometries resulted in six and two transition structures for the radical combination and disproportionation reactions, respectively. The former transition structures, mainly differing in the out‐of‐plane angle of the N? O bond in the transition structure TEMPO molecule, were correlated with the activation energy, which was determined to be in the range of 8.4–19.4 kcal mol?1 from a single‐point calculation at the DFT UB3‐LYP/6‐311+G(3df, 2p)//unrestricted Austin Model 1 level. The calculated activation energy for the disproportionation reaction was less favorable by a value of more than 30 kcal mol?1 in comparison with that for the combination reaction. The approximate barrier difference for the TEMPO addition and disproportionation reaction was slightly smaller for the styrene polymerization system than for the acrylonitrile polymerization system, thus indicating that a β‐proton abstraction through a TEMPO radical from the polymer backbone could diminish control over the radical polymerization of styrene with the nitroxide even more than in the latter system. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 232–241, 2007 相似文献