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991.
响应量在临近破坏时呈现出临界幂律奇异性加速特征,是一种被广泛证实的灾变破坏前兆,并被火山、滑坡和岩石破坏实验等后验预测结果证实为一种对破坏时间进行短临期预测的可行方法.但是,奇异性指数测量值的较大分散性导致了对其具体取值的争议和预测效果的不确定性.因此,理解奇异性指数取值特征及其内在物理控制因素,成为了一个核心问题.本文基于连续介质损伤力学和材料时间相关失效特征,构建了刻画损伤加速发展通向破坏过程的力学模型.导出了恒名义应力蠕变加载和控制名义应力随时间线性增大两种典型加载方式下,损伤和应变率加速发展通向破坏的临界幂律奇异性前兆特征.阐明了临界幂律奇异性指数取值依赖于材料损伤与承受真应力之间的非线性关系这一内在物理根源,表明了实际测量中奇异性指数的分散性不完全归结于测量数据误差,而是有着内在物理控制因素.针对破坏前奇异性指数的不确定性,建议了在未知奇异性指数条件下预测破坏时间的方法,并基于花岗岩脆性蠕变破坏实验进行了验证和说明. 相似文献
992.
993.
Q. Paula Lei I. Jonathan Amster 《Journal of the American Society for Mass Spectrometry》1996,7(8):722-730
A systematic investigation of the gas-phase reactions of Cu+ and Fe+ with the 20 common amino acids is reported. Metal ions are formed by laser ablation of a metal target and are trapped in the analyzer cell of a Fourier transform mass spectrometer. By using quadrupolar excitation to axialize the metal ions, tens of thousands of thermalizing collisions occur prior to their reactions with laser-desorbed amino acid neutral molecules. Amino acids with nonpolar side chains are found to be more reactive toward Cu+ and Fe+ than amino acids with polar side chain. Many of the nonpolar amino acids are found to undergo dissociative metal attachment with a neutral loss of 46 u. A 13C-labeling experiment shows that the carboxyl group is lost during dissociative metal attachment to amino acids. Together these results suggest that these metal ions interact primarily with the carboxyl functional group in these molecules. 相似文献
994.
The Cu/SiO2 catalyst prepared by incipient wetness method exhibited very high activity and selectivity for the vapor-phase synthesis of JV-butylaniline from aniline and 1-butanol. When Cu loading was 0.70 mmol/g-SiO2 and the catalyst precursor was calcined at 500 ℃, 1-butanol conversion reached 99%, and the selectivity of JV-butylaniline exceeded 97%. 相似文献
995.
996.
采用不同合成方法制备了4种组成为Ce0.5Zr0.5O2的铈锆固溶体.通过XRD,BET,H2-TPR,HREM以及SEAD等表征手段,研究了微观晶相结构对铈锆固溶体还原性能的影响规律,以及对固溶体储放氧能力的影响.分析结果表明,在同一组成下,不同制备方法得到截然不同的晶相组成,4种固溶体包含4种不同的晶相组合.通过对微观晶相结构的定量分析,发现立方相的形成对促进固溶体的还原性能起到重要作用.其中,反相微乳法制得的铈锆固溶体能够形成完整的立方相结构,在H2-TPR还原过程中耗氢量最大,表明其具有优良的可还原性及储放氧能力,适合作为TWC,POX等催化剂载体. 相似文献
997.
Dr. Hua Bai Can Du Aijuan Zhang Prof. Lei Li 《Angewandte Chemie (International ed. in English)》2013,52(47):12240-12255
A breath figure (BF) is the water droplet array that forms when moisture comes in contact with a cold substrate. This water droplet array has been widely utilized in the past two decades as a versatile soft template for the fabrication of polymeric porous films. Accordingly, the ordered pores on the polymer films formed with such a method are named a breath figure array (BFA).The BF templating technique is undergoing rapid development. Several unconventional BF processes have been established to prepare porous films with unique morphologies or primary materials, and various newly developed functionalization techniques have significantly improved the performance of polymeric films with BFA, leading to novel applications, including templates, biosensors, and separation membranes. These recent achievements will be described in this Minireview. 相似文献
998.
999.
A new sandwiched polyoxometalate [HK11Cd4Cl2(PW9034)2]·18H2O (1), incor- porating a unique hybrid tetranuclear cadmium cluster (abbreviated to {Cd4}) with two trivacant polyanions [B-α-PW9O34]9-, has been hydrothermally synthesized and structurally characterized by elemental analyses, IR spectroscopy, UV-vis, and single-crystal X-ray diffraction analysis. Crystal data for 1: monoclinic, space group C2/c, a = 19.2997(4), b = 13.8014(3), c = 31.9819(8) A, β = 102.764(2)°, V= 8308.3(3) A3, Z = 4, P2O86Cl2K11Cd4W18H37, Mr = 5735.13, Dc = 4.584 mg-mm-3, F(000) = 10084, μ = 26.579 mm-1, the final R = 0.0378 and wR = 0.0989 for 6558 observed reflections (I〉 2σ(I)). X-ray crystallographic study shows that the molecular structure of 1 contains four cadmium atoms. Two CdO6 distorted octahedra and two CdOsC1 distorted octahedra combine with each other in turn via edge-sharing, resulting in a regular rhomb-like cluster sandwiched between two {B-a-PW9034} units. Further, the sandwich-type polyoxoanions were connected by K+ ions to form a complicated 3-D open-framework through connecting with each terminal O atom of the [Cd4C12(PW9O34)2]12- polyoxoanions. In addition, compound 1 exhibits photoluminescence property at room temperature and the band gap can be assessed at 3.25 eV. 相似文献
1000.