全文获取类型
收费全文 | 182篇 |
免费 | 5篇 |
专业分类
化学 | 111篇 |
力学 | 3篇 |
数学 | 16篇 |
物理学 | 57篇 |
出版年
2023年 | 1篇 |
2022年 | 2篇 |
2021年 | 4篇 |
2020年 | 4篇 |
2019年 | 4篇 |
2018年 | 3篇 |
2017年 | 1篇 |
2016年 | 8篇 |
2015年 | 4篇 |
2014年 | 3篇 |
2013年 | 9篇 |
2012年 | 8篇 |
2011年 | 20篇 |
2010年 | 9篇 |
2009年 | 5篇 |
2008年 | 15篇 |
2007年 | 10篇 |
2006年 | 19篇 |
2005年 | 7篇 |
2004年 | 10篇 |
2003年 | 10篇 |
2002年 | 11篇 |
2001年 | 3篇 |
2000年 | 1篇 |
1999年 | 1篇 |
1998年 | 2篇 |
1997年 | 1篇 |
1994年 | 1篇 |
1993年 | 1篇 |
1991年 | 1篇 |
1990年 | 1篇 |
1989年 | 1篇 |
1988年 | 2篇 |
1987年 | 1篇 |
1986年 | 2篇 |
1981年 | 2篇 |
排序方式: 共有187条查询结果,搜索用时 15 毫秒
101.
The validity of the diffusion approximation for the intensity of multiply scattered waves is tested with numerical simulations in a strongly scattering 2D medium of finite extent. We show that the diffusion equation underestimates the intensity and attribute this to both the neglect of recurrent scattering paths and interference within diffusion theory. We present a theory to quantify this discrepancy based on counting all possible scattering paths between point scatterers. Interference phenomena, due to loop paths, are incorporated in a way similar to coherent backscattering. 相似文献
102.
Concentrated suspensions of model colloidal hard spheres at a wall were studied in real space by means of time-resolved fluorescence confocal scanning microscopy. Both structure and dynamics of these systems differ dramatically from their bulk analogs (i.e., far away from a wall). In particular, systems that are a glass in the bulk show significant hexagonal order at a wall. Upon increasing the volume fraction of the colloids, a reentrant melting transition involving a hexatic structure is observed. The last observation points to two-dimensional behavior of matter at walls. 相似文献
103.
Jie Jian Dr. Roel Hammink Prof. Dr. Christine J. McKenzie Prof. Dr. F. Matthias Bickelhaupt Prof. Dr. Jordi Poater Prof. Dr. Jasmin Mecinović 《Chemistry (Weinheim an der Bergstrasse, Germany)》2022,28(9):e202104044
Boronic acids are Lewis acids that exist in equilibrium with boronate forms in aqueous solution. Here we experimentally and computationally investigated the Lewis acidity of 2,6-diarylphenylboronic acids; specially designed phenylboronic acids that possess two flanking aromatic rings with tunable aromatic character. Hammett analysis of 2,6-diarylphenylboronic acids reveals that their Lewis acidity remains unchanged upon the introduction of EWG/EDG at the distant para position of the flanking aromatic rings. Structural and computational studies demonstrate that polar-π interactions and solvation effects contribute to the stabilization of boronic acids and boronate forms by aromatic rings. Our physical-organic chemistry work highlights that boronic acids and boronates can be stabilized by aromatic systems, leading to an important molecular knowledge for rational design and development of boronic acid-based catalysts and inhibitors of biomedically important proteins. 相似文献
104.
Incipient-wetness impregnation of gamma-Al(2)O(3) with HAuCl(4) and subsequent removal of chlorine with NaOH, and deposition-precipitation of HAuCl(4) on TiO(2) at pH 7 resulted in supported Au(3+) species. Time-resolved in situ XAS at the Au L(3) edge showed that the Al(2)O(3)-supported oxidic or hydroxidic species were reduced in hydrogen at 440 K to yield small metallic gold clusters. The Au(3+) precursor decomposed to metallic gold in inert atmosphere at 573 K and in oxidizing atmosphere above 623 K. In all atmospheres, initially small clusters were formed that gradually grew with increasing temperature. The TiO(2)-supported species were considerably less stable. In hydrogen and carbon monoxide, Au(0) clusters of 1 to 1.5 nm were formed at room temperature, which was the lowest temperature studied. In inert and oxidizing atmosphere, the Au(3+) precursor decomposed fully to metallic gold at 530 K, as shown by XAS and temperature-programmed experiments. Large clusters were obtained already in the initial stage of reduction. Residual chlorine inhibited the reduction and led to sintering of the gold clusters. Exposure of the TiO(2)-supported catalyst precursor to light or the X-ray beam led to partial reduction, and STEM showed that storage of the reduced gold clusters under ambient conditions led to agglomeration and bimodal cluster-size distributions. 相似文献
105.
The durability of topcoats is dependent on a large number of factors as polymer composition, stabilization package and the conditions during the weathering process. For obvious reasons prediction of the long-term (5-10 year) durability of coatings is very important. The rate-determining factor for the degradation of PUR coatings is photo-oxidation. The photo-oxidation rate is controlled by the polymer structure but also stabilizers as HALS has a large influence. The prediction of the durability of clearcoats is based on tracing of the photo-oxidation rate and of the HALS longevity during exposure. The photo-oxidation rate is measured using FTIR-PAS. The results show that degradation can be detected much earlier compared with classical methods as gloss loss. Moreover detection of differences between systems after short exposure times as well as prediction of the long-term durability are possible. 相似文献
106.
Job Jan C. Samson Peter J. Bosman Günter Weickert K. Roel Westerterp 《Journal of polymer science. Part A, Polymer chemistry》1999,37(2):219-232
This paper presents an experimental kinetic study of the polymerization of propylene in liquid monomer with a high activity catalyst. The influences of the concentration of hydrogen and the molar ratios of the catalyst, cocatalyst, and electron donor on the activation period, the maximum activity, the yield, and the decay behavior have been investigated at a temperature of 42°C using a relatively simple kinetic model. On the basis of the experimental data, the reaction rate has been modeled as a function of the hydrogen concentration, the molar ratio of cocatalyst and titanium, and the molar ratio of the electron donor and the cocatalyst. © 1999 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 37: 219–232, 1999 相似文献
107.
Surfactants such as quaternary ammonium salts (QAS) have been in increasing demand, for emerging new applications. Recent attempts at process intensification of their production have disclosed the need for a better understanding of QAS thermal stability. This work aims to determine the degradation kinetics of various QASs and the associated solvent effects. The degradation kinetics of four methyl carbonate QASs were determined in various polar solvents in stainless steel batch autoclaves. H NMR spectrometry was employed for offline analysis of the reaction mixtures. The kinetic parameters were then used to compare the thermal stability of the four compounds in the polar solvents. Water showed no degradation, and methanol (MeOH) was the solvent that provided the second-best stability. Water–MeOH mixtures may provide an overall optimum. Moreover, and longer long-chain substituents increased the degradation rate. Thermogravimetric analysis was used to obtain the thermal stability in a solid state, that is, solventless environment. Isoconversional analysis showed that no reliable kinetic parameters could be determined. Nevertheless, the data did allow for a comparison of the thermal stability of 14 different QASs. Furthermore, the relative instability of the compounds in the solid state demonstrated the challenges of solventless QAS production. 相似文献
108.
109.