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101.
在Ni系ABO3和A2BO4型复合氧化物催化剂上NO吸附性能的研究 总被引:4,自引:1,他引:4
合成了具有钙钛石和类钙钛石结构的复合氧化物LaNiO3,La0.1Sr0.9NiO3,La2NiO4和LaSrNiO4。考察了它们对NO的吸附和NO直接分解反应的催化性能,结合比表面测定,化学分析,XRD和NO-TPD对催化剂的表征结果,探讨了该系列复合氧化物对NO的吸附规律。 相似文献
102.
还原温度对超细K-Co-Mo催化剂合成低碳醇性能的影响 总被引:2,自引:0,他引:2
用溶胶-凝胶法合成了K-Co-Mo催化剂.样品经不同温度还原后,用于低碳醇的合成.XRD和HRTEM结果表明,样品是超细粒子,粒子尺寸为2~5nm.考察了催化剂的还原温度和反应条件对催化剂性能的影响.实验结果表明,还原温度对催化剂的活性有较大的影响,最佳还原温度为500℃.最佳反应温度范围为310~330℃.升高压力和空速可以提高醇的收率和选择性.在空速14400h-1,压力6.0MPa和温度310℃的条件下,醇的选择性为55.8%,收率为520.0g/(kg·h),MeOH/C2+OH为0.27.催化剂稳定性良好,在200h的寿命实验中,活性基本不变.与文献中催化剂相比,超细K-Co-Mo催化剂对合成醇具有较高的活性和选择性,尤其是对C2+OH的合成明显高于其他合成醇催化剂体系. 相似文献
103.
氧鎓盐类化合物因具有较强的亲电性,在有机合成[1]及电照相体系[2]中存在着广泛的应用前景.由于它们还表现出较强的荧光发射能力[3],因而在作为激光工作材料[4,5]方面也受到重视.正因如此,这类化合物的光物理和光谱特性引起了许多化学家的兴趣.氧钠盐化合物溶液的荧 相似文献
104.
O. N. Babkina O. M. Chukanova E. E. Faingol"d N. M. Bravaya 《Russian Chemical Bulletin》2004,53(4):785-790
Quantitative characteristics of changes in the energy of charge transfer from -bonded ligands to metal are presented for the series of structurally similar ansa-metallocene complexes of IVB Group elements. The changes are caused by the solvation effect, replacement of -bonded chlorine ligands by methyl groups and of bridging ethylene groups by dimethylsilylene moieties, introduction of the methyl substituent into position 2 and phenyl substituent into position 4 of the indenyl system, variation of the transition metal in metallocene, and formation of complexes with polymethylalumoxane (MAO) at different AlMAO/Zr ratios. These effects are found to be additive. 相似文献
105.
耐硫催化剂上合成混合醇的研究 总被引:2,自引:1,他引:2
通过改进制备方法和添加助剂,用浸渍-热分解法制得了具有高活性和高选择性的MoS2-K-C型耐硫低碳混合醇催化剂。在8.0-11.0MPa,290-340℃,6000-12000h^-1,H2 S 浓度为100ppm 左右的条件下,在直流反应器中对催化剂进行了性能测试,结果表明,醇得率为0.14-0.47gROH(gcat·h)^-1,选择性为89-98%。同时,考察了操作条件对催化剂性能的影响。1042h的试验,证明催化剂具有很好的稳定性。 相似文献
106.
Two mixed oxide systems La2-xSrxCuO4±
λ (0.0⩽x⩽1. 0) and La2-xThxCuO4±
λ (O. O⩽x⩽ 0.4) with K2NiF4 structure were prepared by varyingx values. Their crystal structures were studied by means of XRD and IR spectra. The average valence of Cu ion at B site, nonstoichiometric
oxygen (λ) and the chemical composition in the bulk and on the surface of the catalysts were measured by means of chemical
analysis and XPS. The catalytic behavior in reaction CO+NO was investigated under the regular change of average valence of
Cu ion at B site and nonstoichiometric oxygen (λ). Meanwhile, the adsorption and activation of the small molecules NO and
the mixture of NO+CO over the mixed oxide catalysts were studied by means of MS-TPD. The catalytic mechanism of reaction NO+CO
over these oxide catalysts were proposed; and it has been found that, at lower temperatures the activation of NO is the rate
determining step and the catalytic activity is related to the lower valent metallic ion and its concentration, while at higher
temperatures the adsorption of NO is the rate determining step and the catalytic activity is related to the oxygen vacancy
and its concentration.
Project supported by the National Natural Science Foundation of China. 相似文献
107.
R. Cabrera‐Trujillo J. R. Sabin Y.
hrn E. Deumens 《International journal of quantum chemistry》2003,94(4):215-221
Under certain collision conditions, a swift ion projectile colliding with a target will gain rather than lose kinetic energy, contrary to the standard conception of stopping power. In this work, we consider the conditions for such a collision such that the energy loss is negative, that is, that there will be projectile kinetic energy gain. In particular, for a target initially in the ground state we find that the projectile gains kinetic energy only when charge exchange and de‐excitation processes are involved. This occurs when the electron affinity of the projectile is larger than the ionization potential of the target. Consequences of this effect are analyzed. © 2003 Wiley Periodicals, Inc. Int J Quantum Chem 94: 215–221, 2003 相似文献
108.
通过键合不同数量的H2PO4^-离子构造了H4P2O8^2-和H4P4O16^8-两种阴离子集 团。利用密度泛函理论对它们的构型进行优化并计算其振动频率和喇曼散射效率。 测量了固—液界面边界层的喇曼光谱并与理论计算结果进行对比分析,进一步研究 了阴离子集团的结构、聚合及脱水等过程。实验和理论研究均表明阴离子二聚体是 KDP晶体的生长基元,他们在固液界面将进一步形成多聚体分子集团,而离子集团 的脱水过程则发生在距KDP晶体表面约50μm的固—液界面边界层中。随着生长层向 界面的推进,这些分子集团将变得越来越有序。本文的研究结果对确定晶体生长界 面动力学过程、发展和完善晶体生长理论有重要意义。 相似文献
109.
The effect of Ni substitution for Mn on magnetic and transport properties has been investigated for layered manganese oxides LaSr2Mn2-xNixO7. Nickel doping hampered the canted antiferromagnetic (AFM) exchange at low temperature and their Neel temperature (TN) decreased from 138 K (x=0) to 102 K (x=0.3). Meanwhile, spin glass, charge ordering and metal-insulator transition are suppressed by Ni addition. The resistivity increases obviously with increasing x due to double exchange interaction channel broken by Ni2+ addition. The resistivity of all samples in low temperature range fits to the Mott′s variable rang hopping (VRH) model, while it fits to nearest neighbor hopping of small polarons model in high temperature range. 相似文献
110.
The influence of the pH of precipitation and the ionic medium nature on the composition, surface charge, and kinetic sorption characteristics of aluminum oxyhydroxides formed by alkaline hydrolysis of an aqueous solution of aluminum nitrate was studied. The methods of drop titration with alkali, argentometric titration, point of zero charge, and indicator reactions of heterogeneous hydrolysis were used. The composition of the freshly precipitated hydrogels of aluminum(iii) oxyhydroxide, rate constants of heterogeneous hydrolysis of the IrCl6
2– ions as indicator reactions, and the pH of the point of zero charge were determined. The rate of indicator reactions (as for other oxyhydroxide hydrogels) depends strongly on the pH of precipitation. However, it is lower than the rates characteristics of iron(iii) and chromium(iii) oxyhydroxides obtained under similar conditions. The pH of the point of zero charge for the alumogels in a chloride medium is 8.3 and that in a sulfate medium is 9.5. 相似文献