全文获取类型
收费全文 | 5545篇 |
免费 | 1129篇 |
国内免费 | 669篇 |
专业分类
化学 | 6476篇 |
晶体学 | 50篇 |
力学 | 51篇 |
综合类 | 22篇 |
数学 | 28篇 |
物理学 | 716篇 |
出版年
2024年 | 14篇 |
2023年 | 96篇 |
2022年 | 152篇 |
2021年 | 206篇 |
2020年 | 342篇 |
2019年 | 248篇 |
2018年 | 246篇 |
2017年 | 188篇 |
2016年 | 332篇 |
2015年 | 364篇 |
2014年 | 405篇 |
2013年 | 564篇 |
2012年 | 356篇 |
2011年 | 323篇 |
2010年 | 274篇 |
2009年 | 299篇 |
2008年 | 348篇 |
2007年 | 293篇 |
2006年 | 272篇 |
2005年 | 242篇 |
2004年 | 240篇 |
2003年 | 204篇 |
2002年 | 150篇 |
2001年 | 141篇 |
2000年 | 123篇 |
1999年 | 126篇 |
1998年 | 102篇 |
1997年 | 110篇 |
1996年 | 91篇 |
1995年 | 90篇 |
1994年 | 60篇 |
1993年 | 51篇 |
1992年 | 57篇 |
1991年 | 38篇 |
1990年 | 29篇 |
1989年 | 19篇 |
1988年 | 18篇 |
1987年 | 20篇 |
1986年 | 21篇 |
1985年 | 12篇 |
1984年 | 12篇 |
1983年 | 8篇 |
1982年 | 9篇 |
1981年 | 11篇 |
1980年 | 9篇 |
1979年 | 5篇 |
1978年 | 7篇 |
1975年 | 3篇 |
1974年 | 4篇 |
1972年 | 3篇 |
排序方式: 共有7343条查询结果,搜索用时 156 毫秒
51.
用溶胶-凝胶方法制备了钠快离子导体Na_5YSi_4O_(12)(简称NYS)的纯相,应用交流阻抗谱技术测定了样品的离子电导和离子导电活化能,用扫描电子显微镜对用不同方法制备的样品烧结体表面进行了观察。与传统固相反应法制备的NYS离子导体相比,用溶胶-凝胶方法制备的NYS烧结体具有较好的界面效应。 相似文献
52.
Laurence E. Strong Christopher L. Brummel Robert Ryther John R. Radford Alan D. Pethybridge 《Journal of solution chemistry》1988,17(12):1145-1167
Precision molar conductances of benzoic, o-toluic, 2,6-dimethylbenzoic, 2,3,6-trimethylbenzoic, and, o-fluorobenzoic acids have been determined in aqueous solution as a function of temperature and of concentration up to near saturation (<0.035 M). At the higher concentrations molar conductances are found to be less than anticipated for the simple dissociation of a 1-1 electrolyte. Although the deviations are only 1% or less they have been interpreted to show that these acids are dimerized in solution. The interpretation includes an assumption that the dimer ionizes to produce a triple ion. Increasing numbers of methyl groups lead to increasing dimerization. For those acids with two ortho groups the dimerization increases with increasing temperature while the other three show decreasing dimerization with increasing temperature. Temperature functions have been determined for the dimerization constants and from these functions standard changes in enthalpy, entropy, and heat capacity have been determined. Comparisons are made with dimerization studies in non-aqueous solvents. From these as well as the behavior of benzene in water it is concluded that a major factor driving the dimerization is hydrophobic interaction. To provide a limiting conductance of the triple ion needed in the dimerization calculations a conductance study was also made for o-Phenylbenzoic acid on the assumption that its anion provides an approximate model of the triple ion. 相似文献
53.
S. M. A. Shibli V. S. Dilimon V. S. Saji 《Journal of Solid State Electrochemistry》2007,11(2):201-208
It has been recently proved that RuO2 can act as an effective surface activator of aluminum alloy sacrificial anodes. TiO2 has the property of stabilizing RuO2 coating and resisting biofouling on metal surfaces. Hence, a mixed oxide catalytic coating of TiO2 and RuO2 can enhance the galvanic performance of aluminum alloy sacrificial anodes and resists biofouling on the anode surface. In the present work RuO2–TiO2 mixed oxide was coated on aluminum alloy sacrificial anodes. The large and uniform porous nature of the coating was found to facilitate efficient ion diffusion. The coating was found to persist on the anode even after 3 months of galvanic exposure. The anode having an optimum combination of the mixed oxide had 70% TiO2 as the major component in the coating. The catalytic coating significantly improved the performance of the anodes to a large extent. 相似文献
54.
Thomas C. Amu 《Journal of solution chemistry》1981,10(1):69-78
Interdiffusion coefficient have been measured for 1,1,2,2-tetrabromoethane in 21 organic solvents in order to ascertain the influence of shape, size, viscosity, nature and degree of branching, of the solvent molecules on transport properties. None of the existing correlations for diffusion in binary liquid systems appear to fit all the experimental data. Steric effects due to the solvent molecules are shown to be very important in the interpretation of the diffusion process. 相似文献
55.
Using flow microcalorimetry, the ion association reaction M2+(aq)+Fe(CN)
6
4–
(aq)=MFe(CN)
6
2–
(aq) (M=Ca, Mg) has been studied at 25°C over the ionic strength range 0.02 to 0.08 mol-dm–3. Analyses of the data to obtain Ho, the enthalpy change at infinite dilution, are described. The value obtained for Ho is sensitive to the kind of functions used to correct for non-ideal behavior. 相似文献
56.
粘土矿物的结构特征及其应用研究 总被引:2,自引:0,他引:2
阐述了贮量巨大、用途广泛的粘土矿物,其充分开发应用的关键,在于根据其结构特征,并通过适当的物理、化学方法加以改造、以适应各种不同工业应用的要求。并以我们对粘土矿物进行活化、改性、层间插入及其工业应用产品开发的初步研究成果,阐明利用粘土硅酸盐多层次结构的可变性,开拓新的应用性能的可能性及粘土矿物充分开发应用的途径。 相似文献
57.
A new technique, called modulated thermogravimetry, is introduced as a tool for obtaining continuous kinetic information for
decomposition and volatilization reactions. The approach makes use of an oscillatory temperature program to obtain kinetic
parameters during a mass loss. MTGA™ may be used under quasi-isothermal conditions to observe a single mass loss or may be
combined with linear heating rate or Hi-Res™ controlled rate thermogravimetry to scan from one mass loss region to another.
Results obtained are in agreement with those obtained by other kinetic methods.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
58.
This is the second part of a paper which deals with the advantages and disadvantages of relative instrumental neutron activation
analysis concerning traceability and uncertainty, and the current scope and possible future extensions of neutron activation
analysis as a primary ratio method. The first part of this paper has been published in this Journal [1].
Received: 19 March 2001 Accepted: 2 October 2001 相似文献
59.
Recently the hydrogen-bond activated reactions have attracted much attention.1 Takemoto2 reported a highly enantioselective Michael addition of manolate to nitroolefins catalyzed by a bifunctional organocatalyst with tertiary amine and thiourea moiety. As we known,stereoselective conjugate additions of thiols are interesting due to the standpoint of biological and synthetic importance, however, only very limited good results have been obtained except for the works of Shibasaki3, Kanemasa4 and Deng5 et al.In this letter, we report an efficient catalytic asymmetric Michael reactions of thiols to a,a-unsaturated carbonyl compounds promoted by bifunctional organocatalysts. A series of organocatalysts with chiral amine and thiourea structures were designed and synthesized and have been successfully applied in the conjugated additions of thiols to a,a-unsaturated imides and enones.The reactions got quantitative yields and the ee values were up to 84%. It is noteworthy that the a-asymmetric protonation (up to 43% ee) also could be achieved.The Michael addition between aromatic thiols and a,a-unsaturated carbonyl compounds isdescribed as follows:Works to further increase the enantioselectivity is under investigation in our laboratory. 相似文献
60.