全文获取类型
收费全文 | 152篇 |
免费 | 10篇 |
专业分类
化学 | 106篇 |
力学 | 5篇 |
数学 | 13篇 |
物理学 | 38篇 |
出版年
2023年 | 3篇 |
2022年 | 8篇 |
2021年 | 4篇 |
2020年 | 5篇 |
2019年 | 6篇 |
2018年 | 10篇 |
2017年 | 5篇 |
2016年 | 12篇 |
2015年 | 4篇 |
2014年 | 4篇 |
2013年 | 15篇 |
2012年 | 10篇 |
2011年 | 6篇 |
2010年 | 9篇 |
2009年 | 7篇 |
2008年 | 3篇 |
2007年 | 5篇 |
2006年 | 1篇 |
2005年 | 2篇 |
2004年 | 5篇 |
2003年 | 6篇 |
2002年 | 3篇 |
2001年 | 2篇 |
2000年 | 1篇 |
1998年 | 3篇 |
1996年 | 2篇 |
1995年 | 2篇 |
1993年 | 2篇 |
1991年 | 1篇 |
1988年 | 3篇 |
1987年 | 2篇 |
1985年 | 1篇 |
1982年 | 1篇 |
1980年 | 3篇 |
1975年 | 1篇 |
1973年 | 1篇 |
1963年 | 1篇 |
1959年 | 1篇 |
1958年 | 1篇 |
1957年 | 1篇 |
排序方式: 共有162条查询结果,搜索用时 296 毫秒
1.
2.
In developing a method for possible low level isotopic enrichment, which uses to advantage the equilibrium isotope effect
observed during U(1V)-U(VI) electron exchange reaction in sulphate solutions, details of a solvent extraction process involving
high concentration of a mixture of U(IV) and U(VI) and at low acid concentrations, are described. The extraction behaviour
of uranium under these conditions is discussed. During the extraction with amines, U(IV) tended to get oxidised in sulphate
solutions. 相似文献
3.
K. L. N. Rao J. P. Shukla B. Venkataramani 《Journal of Radioanalytical and Nuclear Chemistry》1995,189(1):107-114
Ammonium molybdophosphate (AMP) was irradiated with electrons up to a dose of 1 MGy. X-ray diffraction patterns and FT-IR of irradiated and control AMP samples were recorded. Uptake of137Cs from nitric acid in the range of 0.2 to 10 mol·dm–3 was estimated by a batch equilibration technique. AMP undergoes perceptible changes in its physico-chemical characteristics on irradiation with electrons. Uptake of137Cs from nitric acid by irradiated AMP was nearly the same as the control AMP in the nitric acid concentration range of 6 to 10 mol·dm–3 and relatively higher in the range of 0.2 to 6 mol·dm–3. The results are discussed in terms of available information on the physicochemical properties of 12-heteropoly acids and their salts. 相似文献
4.
5.
In this work, we prove the weak and strong convergence of a sequence generated by a modified S-iteration process for finding a common fixed point of two G-nonexpansive mappings in a uniformly convex Banach space with a directed graph. We also give some numerical examples for supporting our main theorem and compare convergence rate between the studied iteration and the Ishikawa iteration. 相似文献
6.
Barium Manganate Oxidation in Organic Synthesis: Part—IV: Oxidation of Aldehydes to Carboxylic Acids
The oxidation of aldehydes to corresponding carboxylic acids by barium manganate under heterogeneous conditions is described. Aromatic aldehydes were smoothly converted to carboxylic acids while aliphatic aldehydes underwent polymerisation. 相似文献
7.
The oxidative cyclisation of bsenzylideneamino anilines, phenols and thiophenols to benzimidazoles, benzoxazoles and benzthiazoles respectively using barium manganate is described. 相似文献
8.
Sharma Deepika Radha Anu Kumar Pretam Kumar Sandeep Jassal Amanpreet K. Lata Suman Vikas Pandey Sushil K. 《Transition Metal Chemistry》2020,45(8):531-544
Transition Metal Chemistry - Nickel(II) complexes with octahedral coordination stabilized by N-donor ligands corresponds to [{(ArO)2PS2}2Ni·L2] [Ar = 4-(C2H5)C6H4 (3), and... 相似文献
9.
Kinetics of oxidation of ethylene glycol and glycerol by acidic solution of N-bromoacetamide (NBA) in the presence of ruthenium (III) chloride as a homogeneous catalyst and mercuric acetate as scavenger in the temperature range of 30–50°C have been reported. The reactions follow identical kinetics, being zero-order in substrate and first-order in Ru(III). First order dependence of the reaction on NBA at its low concentrations tends to zero order in the higher concentration range. Positive effect of [H?] and [Cl?] has been observed. A negative effect of acetamide and ionic strength of the medium is observed while D2O and mercuric acetate show zero effect on the reaction velocity. Various activation parameters have been computed. The main product of the oxidation is corresponding acid. (H2OBr)+ has been postulated as the oxidizing species. A suitable mechanism in conformity with the kinetic data has been proposed. 相似文献
10.
Semen B. Kharchenko Rangaramanujam M. Kannan Jeff J. Cernohous Shivshankar Venkataramani Gaddam N. Babu 《Journal of Polymer Science.Polymer Physics》2001,39(21):2562-2571
With the increase in sophisticated synthesis methods, it appears that polymer architecture may be a tunable property. Therefore, the role of architecture in rheological and processing properties has received renewed attention, mainly because of dendrimer synthesis and metallocene‐catalyst technology. Linear polymers and hyperbranched polymers represent two ends of branching complexity. Some previous studies have suggested that hyperbranched polymers may behave like unentangled polymers, whereas others have proposed that they exhibit the properties of soft colloids. In an effort to compare the responses of linear and hyperbranched polymers, we synthesized starlike hyperbranched polystyrenes (HBPSs) of various branch lengths and numbers of branches. The HBPSs used in this study were unentangled or weakly entangled, allowing us to study the effect of branch density more readily. Two linear polystyrene (L‐PS) melts and two HBPSs were studied. Using a custom‐built rheooptical apparatus, we characterized the rheology and flow birefringence of these materials. To our knowledge, these are the first flow birefringence measurements on highly branched polymer melts. Our results suggest that the flow behavior of HBPS is significantly different from that of L‐PS: (1) HBPS shows nonterminal behavior in the low‐frequency rheological response; (2) when the stress‐optical rule (SOR) holds, the stress‐optical coefficient of HBPS is much lower than those of analogous linear polymers; and (3) when the branch density is high and the branch length is sufficiently low, the SOR fails for these homopolymer melts. A significant increase in the birefringence for a given amount of stress in the low‐frequency region suggests that there may be a soft core in these materials due to the strong preferential radial orientation of chain segments near the center of a molecule versus those near the periphery. The predominantly elastic response of the soft structures may be responsible for the enhanced form birefringence. Our preliminary results indicate that these materials may exhibit both polymeric and soft‐colloid natures. © 2001 John Wiley & Sons, Inc. J Polym Sci Part B: Polym Phys 39: 2562–2571, 2001 相似文献