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131.
Anders A. Anders S. Hantzsche E. 《IEEE transactions on plasma science. IEEE Nuclear and Plasma Sciences Society》1989,17(5):653-656
Validity conditions for complete and partial local thermodynamic equilibrium (CLTE and PLTE) of homogeneous, time-dependent, and optically thin plasmas are derived. For Cu I, electron densities of n e⩾(5×1022-5×1023 ) m-3 are required for the establishment of CLTE. For Cu I and Cu II, n e⩾(5×1021-5×1021 -5×1022) m-3 is necessary for PLTE (for electron temperatures of 1-2 eV). Application to low-current copper vapor arcs in vacuum shows that CLTE can be expected for r <200-600 μm (r =distance from the cathode spot). A further limitation follows for temperatures of 2 eV or higher if diffusion effects are taken into consideration. Consequently, the use of the LTE formulas in plasma spectroscopy of low-current vacuum arcs is very limited 相似文献
132.
The cathode processes of electric ares on cleaned Cu cathodes were investigated in the transition region between vacuum and atmospheric pressure (argon). The plasma density in the cathode plane was estimated by probe measurements to be n = r are current, r – distance from the spot). It was observed that several cathode spot parameters have an extremum at p ~ 104 Pa. The crater diameter has a minimum independently of the cathode temperature. The diffusion constant of the chaotic motion determined by framing photographs was found to have a maximum. Some additional, large displacements occurred at that pressure. The diameter of the bright plasma cloud obtained by open-shutter photographs showed a maximum, the current per spot was found to decrease from 20 A in vacuum to 10 A at atmospheric pressure. It is thus concluded that the spot with the smallest crater radius and a low current per spot, occurring at ~ 104 Pa, represents the single spot, whereas the spot at higher pressures, and probably also in vacuum, has a complicated nature where the large craters are formed by a cooperation of single spots. 相似文献
133.
Targeted analysis of protein citrullination using chemical modification and tandem mass spectrometry
Maria Stensland Anders Holm Andrea Kiehne Burkhard Fleckenstein 《Rapid communications in mass spectrometry : RCM》2009,23(17):2754-2762
Protein citrullination originates from enzymatic deimination of polypeptide‐bound arginine and is involved in various biological processes during health and disease. However, tools required for a detailed and targeted proteomic analysis of citrullinated proteins in situ, including their citrullination sites, are limited. A widely used technique for detection of citrullinated proteins relies on antibody staining after specific derivatization of citrulline residues by 2,3‐butanedione and antipyrine. We have recently reported on the details of this reaction. Here, we show that this chemical modification can be utilized to specifically detect and identify citrullinated peptides and their citrullination sites by liquid chromatography/tandem mass spectrometry (LC/MS/MS) analysis. Using model compounds, we demonstrate that in collision‐induced dissociation (CID) a specific, modification‐derived fragment ion appears as the dominating signal at m/z 201.1 in the MS/MS spectra. When applying electron transfer dissociation (ETD), however, the chemical modification of citrulline remained intact and extensive sequence coverage allowed identification of peptides and their citrullination sites. Therefore, LC/MS/MS analysis with alternating CID and ETD has been performed, using CID for specific, signature ion‐based detection of derivatized citrullinated peptides and ETD for sequence determination. The usefulness of this targeted analysis was demonstrated by identifying citrullination sites in myelin basic protein deiminated in vitro. Combining antibody‐based enrichment of chemically modified citrulline‐containing peptides with specific mass spectrometric detection will increase the potential of such a targeted analysis of protein citrullination in the future. Copyright © 2009 John Wiley & Sons, Ltd. 相似文献
134.
In this paper, the long-run dynamics of a resonant converter is studied. The modelling of the resonant converter can be done using various approximations and the long-run dynamics of the two dimensional cases were earlier analysed. In this paper, we discuss results that can be extended to the three dimensional case. It seems that limit cycles describe the long-run dynamics in important situations in the three dimensional case, too. Our objective is to relate the limit cycles found previously in the two-dimensional case to those found now in the three dimensional approximation. 相似文献
135.
Total Domination in Graphs with Given Girth 总被引:1,自引:0,他引:1
A set S of vertices in a graph G without isolated vertices is a total dominating set of G if every vertex of G is adjacent to some vertex in S. The minimum cardinality of a total dominating set of G is the total domination number γ
t
(G) of G. In this paper, we establish an upper bound on the total domination number of a graph with minimum degree at least two in
terms of its order and girth. We prove that if G is a graph of order n with minimum degree at least two and girth g, then γ
t
(G) ≤ n/2 + n/g, and this bound is sharp. Our proof is an interplay between graph theory and transversals in hypergraphs.
Michael A. Henning: Research supported in part by the South African National Research Foundation and the University of KwaZulu-Natal. 相似文献
136.
We study the three point genus zero Gromov-Witten invariants on the Grassmannians which parametrize non-maximal isotropic
subspaces in a vector space equipped with a nondegenerate symmetric or skew-symmetric form. We establish Pieri rules for the
classical cohomology and the small quantum cohomology ring of these varieties, which give a combinatorial formula for the
product of any Schubert class with certain special Schubert classes. We also give presentations of these rings, with integer
coefficients, in terms of special Schubert class generators and relations. 相似文献
137.
J. L. Kleinschmidt E. Anders Bodenbender E. Sostmannn C. Scheibler und Dubrunfaut 《Fresenius' Journal of Analytical Chemistry》1867,6(1):462-471
Ohne Zusammenfassung 相似文献
138.
Federico Chiariotti Israel Leyva-Mayorga edomir Stefanovi Anders E. Kalr Petar Popovski 《Entropy (Basel, Switzerland)》2021,23(6)
Wireless mobile networks from the fifth generation (5G) and beyond serve as platforms for flexible support of heterogeneous traffic types with diverse performance requirements. In particular, the broadband services aim for the traditional rate optimization, while the time-sensitive services aim for the optimization of latency and reliability, and some novel metrics such as Age of Information (AoI). In such settings, the key question is the one of spectrum slicing: how these services share the same chunk of available spectrum while meeting the heterogeneous requirements. In this work we investigated the two canonical frameworks for spectrum sharing, Orthogonal Multiple Access (OMA) and Non-Orthogonal Multiple Access (NOMA), in a simple, but insightful setup with a single time-slotted shared frequency channel, involving one broadband user, aiming to maximize throughput and using packet-level coding to protect its transmissions from noise and interference, and several intermittent users, aiming to either to improve their latency-reliability performance or to minimize their AoI. We analytically assessed the performances of Time Division Multiple Access (TDMA) and ALOHA-based schemes in both OMA and NOMA frameworks by deriving their Pareto regions and the corresponding optimal values of their parameters. Our results show that NOMA can outperform traditional OMA in latency-reliability oriented systems in most conditions, but OMA performs slightly better in age-oriented systems. 相似文献
139.
In situ ion beam sputter deposition and X‐ray photoelectron spectroscopy (XPS) of multiple thin layers under computer control for combinatorial materials synthesis 下载免费PDF全文
Thomas A. Wilson Anders J. Barlow Michael L. Foster Mariela Bravo Sanchez Jose F. Portoles Naoko Sano Peter J. Cumpson Ian W. Fletcher 《Surface and interface analysis : SIA》2017,49(1):18-24
Deposition of ultra‐thin layers under computer control is a frequent requirement in studies of novel sensors, materials screening, heterogeneous catalysis, the probing of band offsets near semiconductor junctions and many other applications. Often large‐area samples are produced by magnetron sputtering from multiple targets or by atomic layer deposition (ALD). Samples can then be transferred to an analytical chamber for checking by X‐ray photoelectron spectroscopy (XPS) or other surface‐sensitive spectroscopies. The ‘wafer‐scale’ nature of these tools is often greater than is required in combinatorial studies, where a few square centimetres or even millimetres of sample is sufficient for each composition to be tested. The large size leads to increased capital cost, problems of registration as samples are transferred between deposition and analysis, and often makes the use of precious metals as sputter targets prohibitively expensive. Instead we have modified a commercial sample block designed to perform angle‐resolved XPS in a commercial XPS instrument. This now allows ion‐beam sputter deposition from up to six different targets under complete computer control. Ion beam deposition is an attractive technology for depositing ultra‐thin layers of great purity under ultra‐high vacuum conditions, but is generally a very expensive technology. Our new sample block allows ion beam sputtering using the ion gun normally used for sputter depth‐profiling of samples, greatly reducing the cost and allowing deposition to be done (and checked by XPS) in situ in a single instrument. Precious metals are deposited cheaply and efficiently by ion‐beam sputtering from thin metal foils. Samples can then be removed, studied and exposed to reactants or surface treatments before being returned to the XPS to examine and quantify the effects. Copyright © 2016 The Authors Surface and Interface Analysis Published by John Wiley & Sons Ltd. 相似文献
140.
Georgios M. Kontogeorgis Ioannis Tsivintzelis Nicolas von Solms Andreas Grenner David Bøgh Michael Frost Anders Knage-Rasmussen Ioannis G. Economou 《Fluid Phase Equilibria》2010
Association theories such as the CPA (cubic-plus-association), NRHB (non-random hydrogen bonding) equations of state and the various variants of SAFT (statistical associating fluid theory) have been extensively applied to phase equilibrium calculations. Such models can also be used for estimating the monomer fraction of hydrogen bonding compounds and their mixtures. Monomer fraction data are obtained from spectroscopic measurements and they are available for a few compounds such as pure water and alcohols as well as for some alcohol–alkane and similar mixtures. These data are useful for an understanding of the capabilities and limitations of association models. The purpose of this work is two-fold: (i) to compare the performance of three models, CPA, NRHB and sPC-SAFT, in predicting the monomer fraction of water, alcohols and mixtures of alcohol-inert compounds and (ii) to investigate whether “improved” model parameters can be obtained if monomer fraction data are included in the parameter estimation together with vapor pressures and liquid densities. The expression “improved” implies parameters which can represent several pure compound properties as well as monomer fraction data for pure compounds and mixtures. The accuracy of experimental monomer fraction data is discussed, as well as the role of monomer fraction data in clarifying which association scheme should be used in these equations of state. The results reveal that the investigated association models (CPA, sPC-SAFT and NRHB) can predict, at least qualitatively correct, monomer fractions of associating compounds and mixtures. Only, small differences are observed between the models. In addition, it has been shown that, using a suitable association scheme, a single set of parameters can describe satisfactorily vapor pressures, liquid densities and monomer fractions of water and alcohols. The 4C scheme is the best choice for water, while for methanol there is small difference between the 2B and 3B association schemes. 相似文献