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71.
铀(Ⅵ)的二溴水杨醛缩二胺类双希夫碱及溶剂三元配合物的合成和表征 总被引:1,自引:0,他引:1
Nine new complexes [UO2(Dbsal-o-Phdn)L][UO2(Dbsalen)L] and [UO2(Dbsalpn)L] [Dbsal-o-PhdnH 2=N,N′-o-phenylenebis-(3,5-dibromosalicylideneimine), DbsalenH2=N,N′-ethylenebis (3,5-dibromosalicylideneimine), DbsalpnH2=N,N′-1,2-propanylenebis (3,5-dibromosalicylideneimine), L=MeOH, EtOH, py] have been synthesized and characterized by elemental analysis, IR, UV, TG-DTA and molar conductance analysis. These complexes are proposed to have seven coordinate environment. 相似文献
72.
73.
Influence of hydrostatic pressure and temperature on electronic band parameters for zinc-blende AlxGa1–xAs was investigated by means of pseudopotential calculations. The agreement between our results and the available experimental data is generally satisfactory. Our results showed that the effect of pressure leads to a decrease of the crossing point and the optical bowing parameter. However, the temperature effect was found to be insignificant on both crossing point and bowing parameter. 相似文献
74.
We consider quadratic diophantine equations of the shape
for a polynomial Q(X1, ..., Xs) Z[X1, ..., Xs] of degree 2.Let H be an upper bound for the absolute values of the coefficientsof Q, and assume that the homogeneous quadratic part of Q isnon-singular. We prove, for all s 3, the existence of a polynomialbound s(H) with the following property: if equation (1) hasa solution x Zs at all, then it has one satisfying
For s = 3 and s = 4 no polynomial bounds s(H) were previouslyknown, and for s 5 we have been able to improve existing boundsquite significantly. 2000 Mathematics Subject Classification11D09, 11E20, 11H06, 11P55. 相似文献
75.
Parallel to the study of finite-dimensional Banach spaces, there is a growing interest in the corresponding local theory of operator spaces. We define a family of Hilbertian operator spaces , , generalizing the row and column Hilbert spaces and , and we show that an atomic subspace that is the range of a contractive projection on is isometrically completely contractive to an -sum of the and Cartan factors of types 1 to 4. In particular, for finite-dimensional , this answers a question posed by Oikhberg and Rosenthal. Explicit in the proof is a classification up to complete isometry of atomic w-closed -triples without an infinite-dimensional rank 1 w-closed ideal.
76.
In this paper, new codes of dimension 8 are presented which give improved bounds on the maximum possible minimum distance of ternary linear codes. These codes belong to the class of quasi-twisted (QT) codes, and have been constructed using a stochastic optimization algorithm, tabu search. Twenty three codes are given which improve or establish the bounds for ternary codes. In addition, a table of upper and lower bounds for d
3(n, 8) is presented for n 200. 相似文献
77.
在Ag38.5Cu33.4Ge28.1三元共晶合金的深过冷实验中,获得的最大过冷度为175 K(0.22TE). XRD分析表明,不同过冷条件下其共晶组织均由(Ag),(Ge)和η(Cu3Ge)三相组成. 在小过冷条件下,三个共晶相协同生长,凝固组织粗大.随着过冷度的增大,共晶组织明显细化,(Ge)相与其他两相分离,以初生相方式生长,而(Ag)相与η相始终呈二相层片共晶方式共生生长. 当过冷度超过80 K时,初生相(Ge)由小过冷时的块状转变为具有小面相特征的枝晶方式生长. 部分小面相(Ge)枝晶出现规则的花状,花瓣数介于5—8之间,并且过冷度越大(Ge)相越容易分瓣. 花状(Ge)枝晶的晶体表面为{111}晶面簇,择优生长方向为〈100〉晶向族.
关键词:
三元共晶
晶体形核
深过冷
快速凝固 相似文献
78.
The liquid to solid transformation of ternary Ag42.4Cu21.6Sb36 eutectic alloy was accomplished in an ultrasonic field with a frequency of 35 kHz, and the growth mechanism of this ternary eutectic was examined. Theoretical calculations predict that the sound intensity in the liquid phase at the solidification interface increases gradually as the interface moves up from the sample bottom to its top. The growth mode of (ε θ Sb) ternary eutectic exhibits a transition of "divorced eutectic- mixture of anomalous and regular structures-regular eutectic" along the sample axis due to the inhomogeneity of sound field distribution. In the top zone with the highest sound intensity, the cavitation effect promotes the three eutectic phases to nucleate independently, while the acoustic streaming efficiently suppresses the coupled growth of eutectic phases. In the meantime, the ultrasonic field accelerates the solute transportation at the solid-liquid interface, which reduces the solute solubility of eutectic phases. 相似文献
79.
The rapid solidification of Sb60Ag20Cu20 ternary alloy was realized by high undercooling method, and the maximum undercooling is up to 142 K (0.18TL). Within the wide undercooling range of 40-142 K, the solidified microstructures are composed of (Sb), θand ε phases. High undercooling enlarges the solute solubility of (Sb) phase, which causes its crystal lattice to expand and its crystal lattice constants to increase. Primary (Sb) phase grows in two modes at small undercoolings non-faceted dendrite growth is the main growth form; whereas at large undercoolings faceted dendrite growth takes the dominant place. The remarkable difference of crystal structures between (Sb) and θphases leads to (θ Sb) pseudobinary eutectic hard to form, whereas strips of θform when the alloy melt reaches the (θ Sb) pseudobinary eutectic line. The cooperative growth of θand ε phases contributes to the formation of (ε θ) pseudobinary eutectic easily. In addition, the crystallization route has been determined via microstructural characteristic analysis and DSC experiment. 相似文献
80.
Hongwei Lu Yusheng Qin Xianhong Wang Xiangguang Yang Suobo Zhang Fosong Wang 《Journal of polymer science. Part A, Polymer chemistry》2011,49(17):3797-3804
Recently, rare earth ternary coordination catalyst represented as Y(CCl3OO)3‐Glycerin‐ZnEt2 has been used for producing poly(propylene carbonate) (PPC, an alternating copolymer of carbon dioxide and propylene oxide) in industry scale, but its catalytic activity needs further improvement. One reason for the relatively low catalytic activity lied in that only 11.7% of active center was efficient due to possible embedding of active center in the heterogeneous catalyst. In this report, supporting strategy was developed, where Y(CCl3OO)3‐Glycerin‐ZnEt2 was supported on various inorganic oxides. Two supporting methods were carried out. One way was to mix Y(CCl3OO)3‐Glycerin with inorganic oxide first and then ZnEt2 was dropped to form the supported catalyst, and the other was to make Y(CCl3OO)3‐Glycerin‐ZnEt2 at first and then mixing with inorganic oxides. The former showed decreasing catalytic activity compared with corresponding unsupported rare earth ternary catalyst, while an improvement of 16–36% in catalytic activity was realized in the latter. PPC with an average number molecular weight (Mn) of over 100 kg/mol and carbonate unit (CU) content of higher than 96% was prepared by both supported catalysts. The catalytic activity of the supported catalyst depended significantly on the supports, which increased in the following order: α‐Al2O3 < MgO < ZnO ≈ SiO2 <γ‐Al2O3. γ‐Al2O3 was the best support for rare earth ternary catalyst, which showed a remarkable 36% increase in catalytic activity, corresponding to the utilization of 17% of active center. Although MgO supported catalyst gave only an 8% increase in catalytic activity, the Mn and CU content of PPC were raised to about 143 kg/mol and 99%, whereas the PPC from common rare earth ternary catalyst was about 108 kg/mol and 97%, respectively. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011 相似文献