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101.
采用溶胶-凝胶方法在Si(111)上制备了LSMO(x=0.17)薄膜.研究了块体材料和不同厚度薄膜R -T曲线、红外光谱和X射线衍射.结果表明,LSMO薄膜属于正交晶体结构,薄膜取向与膜厚度 有关,当膜厚度为450nm或680nm时,主要取向〈200〉,而膜厚度为900nm时取向为〈020〉 :根据离子对相互作用能和谐振子模型,得到了红外吸收与Mn—O—Mn键长和键角关系式,6 00cm-1附近红外吸收与晶格常数b的变化有关;块体与薄膜的金属—绝缘体转变 温度(TMI)存在较大差别,薄膜转变温度显著低于块体,并与厚度有一定关系. 认为是LSMO薄膜中的应力诱导了晶格常数变化,引起键角改变及JT效应是转变温度变化的主 要原因.
关键词:
单晶硅
晶格常数
金属—绝缘体转变温度
应力诱导 相似文献
102.
Dilip H. Dagade Rajendra R. KumbharSandip R. Sabale Kesharsingh J. Patil 《Fluid Phase Equilibria》2007
In the present communication, we report the studies concerning liquid–liquid–solid equilibria for the ternary system sodium thiosulphate (Na2S2O3) + ethanol + water at ambient pressure and at room temperature (303 ± 2 K). The solubility data of Na2S2O3 are reported for solutions in water, ethanol and solutions of varying concentrations of ethanol in water. The phase diagram for the said system is developed, described and compared with similar system K2CO3 + methanol + water. These results have been explained in terms of structural properties of aqueous ethanol solutions and further discussed in terms of the effect of ions to cause phase separation. 相似文献
103.
B. Rustem 《Journal of Optimization Theory and Applications》1993,76(3):429-453
In this paper, we consider two algorithms for nonlinear equality and inequality constrained optimization. Both algorithms utilize stepsize strategies based on differentiable penalty functions and quadratic programming subproblems. The essential difference between the algorithms is in the stepsize strategies used. The objective function in the quadratic subproblem includes a linear term that is dependent on the penalty functions. The quadratic objective function utilizes an approximate Hessian of the Lagrangian augmented by the penalty functions. In this approximation, it is possible to ignore the second-derivative terms arising from the constraints in the penalty functions.The penalty parameter is determined using a strategy, slightly different for each algorithm, that ensures boundedness as well as a descent property. In particular, the boundedness follows as the strategy is always satisfied for finite values of the parameter.These properties are utilized to establish global convergence and the condition under which unit stepsizes are achieved. There is also a compatibility between the quadratic objective function and the stepsize strategy to ensure the consistency of the properties for unit steps and subsequent convergence rates.This research was funded by SERC and ESRC research contracts. The author is grateful to Professors Laurence Dixon and David Mayne for their comments. The numerical results in the paper were obtained using a program written by Mr. Robin Becker. 相似文献
104.
通过实验分析确立了把光纤电阻作为衡量气密性碳涂覆光纤通过2%应变筛选的过渡标准。要拉制2%应变筛选的碳涂覆光纤,其电阻值应小于30kΩ/cm。 相似文献
105.
For structural parameters with uncertainties, interval mathematics can, in the case where the probabilistic distribution density
of uncertain variables is unavailable, deal with the influence of uncertainties in structural parameters on the response of
structures. In order to evaluate the region containing natural frequencies of structures with interval parameters, the interval
parameter perturbation method is presented in this paper. The advantage of the present method is its computational efficiency
in evaluating the region containing natural frequencies. A numerical example is used to illustrate the efficiency of the method
proposed.
The project is supported by National Youth Natural Science Foundation of China and National Outstanding Youth Science Foundation
of China. 相似文献
106.
用脉冲回波重叠法测量了钛合金(TC-6)的二阶、三阶弹性常数。实验中发现dμ/dp<0(p<0.17 GPa),dμ/dp>0(p>0.17 GPa)。 相似文献
107.
本文以二苯基甲酮的KBr压片为标样,在Bruker IFS 120HR付里叶变换红外光谱仪上系统考察了该仪器折一些重要操作参数(光源光栏、切趾函数、扫描速度)对光谱质量(信噪比,分辨率)的影响。从而获得了测样时的优化操作条件。 相似文献
108.
The solubilities of o-, m- and p-xylene in water were measured at 25.0°C up to 250, 385, and 50 MPa, respectively. The solubility increased with increasing pressure up to 120 MPa (50 MPa for p-xylene) and then decreased. The reaction volumes, Vo accompanying the dissolution at 0.1 MPa were estimated as –3.6±0.5, –3.4±0.5, and –4.1±0.5 cm3-mol–1 for o-, m-, and p-xylene, respectively, from the pressure dependences of the solubilities. The limiting partial molar volumes, of p- and o-xylene in water under high pressure were estimated from Vo and the molar volume of the xylene. The partial molar volumes decreased with increasing pressure. The reaction volume for the formation of intra-molecular pairwise hydrophobic interaction between the methyl groups, as proposed by Ben-Naim, is discussed for the Vo of p- and o-xylene at 0.1 MPa. 相似文献
109.
110.