全文获取类型
收费全文 | 72篇 |
免费 | 0篇 |
专业分类
化学 | 52篇 |
力学 | 4篇 |
数学 | 6篇 |
物理学 | 10篇 |
出版年
2022年 | 1篇 |
2021年 | 1篇 |
2019年 | 3篇 |
2018年 | 3篇 |
2017年 | 2篇 |
2016年 | 3篇 |
2015年 | 1篇 |
2014年 | 1篇 |
2013年 | 1篇 |
2012年 | 2篇 |
2011年 | 2篇 |
2010年 | 3篇 |
2009年 | 3篇 |
2007年 | 4篇 |
2006年 | 4篇 |
2005年 | 2篇 |
2004年 | 4篇 |
2003年 | 4篇 |
2002年 | 2篇 |
2000年 | 1篇 |
1999年 | 1篇 |
1993年 | 1篇 |
1991年 | 1篇 |
1990年 | 1篇 |
1989年 | 2篇 |
1985年 | 1篇 |
1984年 | 1篇 |
1983年 | 3篇 |
1982年 | 6篇 |
1978年 | 1篇 |
1977年 | 1篇 |
1975年 | 5篇 |
1974年 | 1篇 |
排序方式: 共有72条查询结果,搜索用时 328 毫秒
1.
The effect of calcinations on the silica surface groups and thereby on the activity of Ziegler-Natta catalysts in ethylene homopolymerisation has been studied. Silica was calcined at different temperatures and treated with MgR2 and HCl. Silica surface groups were identified by using 1H MAS NMR and 13C and 29Si CP MAS NMR techniques. Magnesium, titanium and chlorine were measured by elemental analysis. Ziegler-Natta catalysts were prepared from these supports and subsequently used in ethylene homopolymerisation. Maximum activity was obtained with the catalyst based on 590 °C calcined silica. The results indicate that MgR2 reacts with siloxane-groups (Si-O-Si) in the 300 °C calcined silica, leaving the hydrogen-bonded hydroxyl-groups unreacted. Low activity Si-O-Ti(Cl)2-O-Si species are formed after reacting with TiCl4. The higher activity in the catalyst based on 590 °C calcined silica can be explained by the formation of -Si(R)-O-Si-O-TiCl3 groups, originating from the siloxane bridges which cannot form in 300 °C calcined silica. Other explanations for the higher activity are a higher Mg/Ti ratio or small amounts of crystal water formed in the 590 °C calcined silica. 相似文献
2.
Born—Oppenheimer potential surfaces for a bridged three-site electron-transfer system are calculated. The adiabatic potentials depend upon both the vibrational sum and difference coordinates. Along the vibrational difference coordinate, the ground-state surface has single-minimun form when the through-bridge electronic coupling is strong, and double-minimum form for weak through-bridge coupling. The results are compared to those previously reported for two-site models. 相似文献
3.
L. M. Kustov O. K. Lebedeva D. Yu. Kultin N. V. Root V. B. Kazansky 《Doklady Chemistry》2016,470(2):297-301
The aim of this study was to synthesize low-concentration catalysts with a highly developed surface based on nanodispersed platinum deposited onto the steel surface electrochemically modified with the use of an ionic liquid. Sintered fibers of austenitic steel without pretreatment (steel 1) and etched with hydrochloric acid to remove surface oxides (steel 2) were used as substrates. 1-Butyl-4-methylimidazolium acetate [BMIM][Ac] ionic liquid was used. Variation of the current intensity and anodic treatment time leads to the formation of different structures at the steel surface. For steel 2, optimal conditions leading to self-organization, namely, formation of hexagonal structures, have been selected. It has been demonstrated that formation of nanostructures at the steel surface can occur without the participation of fluoride ions. Low-concentration (Pt/steel 2) catalysts with a uniform distribution of platinum nanoparticles over the surface were prepared via galvanostatic deposition from an aqueous solution of H2PtCl6. 相似文献
4.
Katharina Root Yves Wittwer Konstantin Barylyuk Ulrike Anders Renato Zenobi 《Journal of the American Society for Mass Spectrometry》2017,28(9):1863-1875
Native ESI-MS is increasingly used for quantitative analysis of biomolecular interactions. In such analyses, peak intensity ratios measured in mass spectra are treated as abundance ratios of the respective molecules in solution. While signal intensities of similar-size analytes, such as a protein and its complex with a small molecule, can be directly compared, significant distortions of the peak ratio due to unequal signal response of analytes impede the application of this approach for large oligomeric biomolecular complexes. We use a model system based on concatenated maltose binding protein units (MBPn, n = 1, 2, 3) to systematically study the behavior of protein mixtures in ESI-MS. The MBP concatamers differ from each other only by their mass while the chemical composition and other properties remain identical. We used native ESI-MS to analyze model mixtures of MBP oligomers, including equimolar mixtures of two proteins, as well as binary mixtures containing different fractions of the individual components. Pronounced deviation from a linear dependence of the signal intensity with concentration was observed for all binary mixtures investigated. While equimolar mixtures showed linear signal dependence at low concentrations, distinct ion suppression was observed above 20 μM. We systematically studied factors that are most often used in the literature to explain the origin of suppression effects. Implications of this effect for quantifying protein–protein binding affinity by native ESI-MS are discussed in general and demonstrated for an example of an anti-MBP antibody with its ligand, MBP. 相似文献
5.
6.
7.
William L. Root 《Applied Mathematics and Optimization》1982,8(1):293-307
The notion of system trajectory of a time-varying input-output, dynamical system is reviewed. By introducing a probability measure on a class of such systems a stochastic system, the randomized system, is defined. The randomized system has a trajectory induced by the trajectories of the original systems. A theorem is proved giving fairly general conditions under which the randomized system trajectory is generated by a strongly continuous semigroup of bounded linear operators in a Banach space. An example is presented for a system represented by a quadratic integral operator.Research supported in part by National Science Foundation under Grant No. ECS-8005960. 相似文献
8.
9.
The effect of the many-body potential on the structure of water is deduced assuming the MCY pair potential is a good approximate potential. 相似文献
10.
The reaction of NO with CO on Rh(111) has been studied with temperature programmed reaction (TPR). Comparisons are made with the reaction of O2 with CO and the reaction of NO with H2. The rate-determining step for both CO oxidation reactions is CO(a) + O(a) → CO2(g). Repulsive interactions between adsorbed CO and adsorbed nitrogen atoms lead to desorption of CO in a peak at 415 K which is in the temperature range where the reaction between CO(a) and O(a) produces CO2(g). Thus the extent of reaction of CO(a) with NO(a) is less than that between CO(a) and O(a) due to the lower coverage of CO caused by adsorbed N atoms and NO. A similar repulsive interaction between NO(a) and H(a) suppresses the NO + H2 reaction. CO + NO reaction behavior on Rh(111) is compared to that observed on Pt(111). 相似文献