全文获取类型
收费全文 | 323434篇 |
免费 | 2463篇 |
国内免费 | 796篇 |
专业分类
化学 | 169625篇 |
晶体学 | 5289篇 |
力学 | 15674篇 |
综合类 | 13篇 |
数学 | 34202篇 |
物理学 | 101890篇 |
出版年
2021年 | 2777篇 |
2020年 | 2929篇 |
2019年 | 3511篇 |
2018年 | 4854篇 |
2017年 | 4874篇 |
2016年 | 6740篇 |
2015年 | 3590篇 |
2014年 | 6162篇 |
2013年 | 13689篇 |
2012年 | 10824篇 |
2011年 | 12921篇 |
2010年 | 9815篇 |
2009年 | 9970篇 |
2008年 | 12323篇 |
2007年 | 12012篇 |
2006年 | 11115篇 |
2005年 | 9961篇 |
2004年 | 9323篇 |
2003年 | 8554篇 |
2002年 | 8406篇 |
2001年 | 10136篇 |
2000年 | 7497篇 |
1999年 | 5689篇 |
1998年 | 4484篇 |
1997年 | 4599篇 |
1996年 | 4273篇 |
1995年 | 3842篇 |
1994年 | 3949篇 |
1993年 | 3676篇 |
1992年 | 4374篇 |
1991年 | 4579篇 |
1990年 | 4315篇 |
1989年 | 4371篇 |
1988年 | 4223篇 |
1987年 | 4238篇 |
1986年 | 3967篇 |
1985年 | 5002篇 |
1984年 | 5099篇 |
1983年 | 4194篇 |
1982年 | 4156篇 |
1981年 | 3979篇 |
1980年 | 3798篇 |
1979年 | 4375篇 |
1978年 | 4439篇 |
1977年 | 4565篇 |
1976年 | 4478篇 |
1975年 | 4200篇 |
1974年 | 4150篇 |
1973年 | 4247篇 |
1972年 | 3095篇 |
排序方式: 共有10000条查询结果,搜索用时 0 毫秒
101.
102.
T. Beda 《Journal of Polymer Science.Polymer Physics》2007,45(13):1713-1732
A constitutive phenomenological model completing the Gent‐Thomas concept is carried out to formulate laws governing the hyperelastic behavior of incompressible rubber materials. It is shown that the phenomenological Gent‐Thomas model (1958) and the constrained chain model (1992) give similar precise results at small to moderate deformation. On the other hand, comparisons of the outcome of the proposed model with that of the molecular model from the combined concepts of Flory‐Erman and Boyce‐Arruda (2000), and with those of the phenomenological models of Ogden (1982), Yeoh‐Fleming (1997), Pucci‐Saccomandi (2002) and Beda (2005) are made. Residual inconveniences raised by attractive continuum models in rubber elasticity literature have been successfully overcome. Results from both the statistical and phenomenological mechanics concepts are compared with the data of some useful classical materials (rubbers of Treloar, Rivlin‐Saunders, Pak‐Flory and Yeoh‐Fleming). The results permit one to see salient equivalence of the two theories for a more reliable prediction of stress‐stretch response for all states of any mode of deformation. A complete and exhaustive analysis of the Mooney plot that combines small and very large extension‐compression has been quite essential in assessing the validity of models. A method of identification of material parameters is presented and data of the simple tension suffice for the determination of the parameter values. It is shown that the ordinary identification procedures, such as the usual least squares, a very much used numerical method in materials investigation, can be unsuitable in some cases of hyperelastic modeling. © 2007 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 45: 1713–1732, 2007 相似文献
103.
The kinetics of hydrogen peroxide decomposition in a guaiacol solution, catalyzed by potassium hexacyanoferrate(II), were studied. The reaction mainly follows the pathway of guaiacol hydroxylation. The reaction order is 1 with respect to H2O2, 0.5 with respect to hexacyanoferrate, and from 0.4 to 0 with respect to guaiacol (the latter parameter decreases with increasing guaiacol concentration). The apparent activation energy is 105 kJ mol-
1. A kinetic scheme of the process was proposed. An expression consistent with the experiment was obtained for the rate of hydrogen peroxide decomposition in the presence of guaiacol, catalyzed by hexacyanoferrate(II). 相似文献
104.
Nikulin S. S. Akatova I. N. Kondrat'eva N. A. 《Russian Journal of Applied Chemistry》2003,76(4):652-655
The influence of the charge of a metal cation and the nature of a coagulant on the recovery of butadiene-styrene rubber and properties of rubber stocks and vulcanizates was examined. 相似文献
105.
N. Dolbilin 《Discrete and Computational Geometry》1995,13(1):405-414
If a given finite protoset, together with a given finite matching rule, gives rise to at most countably many different tilings
ofd-dimensional space, then at least one of them is periodic.
This research was supported in part by the SFB 343 “Diskrete Strukturen in der Mathematik” at Bielefeld University and the
Russian Foundation for Fundamental Research. 相似文献
106.
N. B. Voznesensky E. V. Gavrilov A. P. Zhevlakov V. K. Kirillovskiĭ P. V. Orlov 《Technical Physics》2007,52(2):271-275
Methods and schemes to inspect the EUV mirror shape are developed on the basis of a point diffraction interferometer with computer processing of interferograms. A measurement accuracy to within 0.001 of a wavelength in the visual range is achieved. 相似文献
107.
V. V. AntiĆ M. P. AntiĆ M. N. Govedarica P. R. DvorniĆ 《Journal of polymer science. Part A, Polymer chemistry》2007,45(11):2246-2258
The kinetics of the formation of poly(carbosiloxane), as well as of alkyl-substituted poly(siloxane), by Karstedt's catalyst catalyzed hydrosilylation were investigated. Linear poly(carbosiloxane), poly[(1,1,3,3-tetramethyldisiloxanyl)ethylene], (PTMDSE), was obtained by hydrosilylation of 1,3-divinyltetramethyldisiloxane (DVTMDS) and 1,1,3,3-tetramethyldisiloxane (TMDS), while alkyl-substituted poly(siloxane), poly(methyldecylsiloxane), (PMDS), was synthesized by hydrosilylation of poly(methylhydrosiloxane) (PMHS) and 1-decene. To investigate the kinetics of PTMDSE formation, two series of experiments were performed at reaction temperatures ranging from 25 to 56 °C and with catalyst concentrations ranging from 7.0 × 10−6 to 3.1 × 10−5 mol Pt/mol CHCH2. A series of experiments was performed at reaction temperatures ranging from 28 to 48 °C, with catalyst concentrations of 7.0 ×10−6 mol of Pt per mol of CHCH2, when kinetics of PMDS formation was investigated. All reactions were carried out in bulk, with equimolar amounts of the reacting Si H and CHCH2 groups. The course of the reactions was monitored by following the disappearance of the Si H bands using quantitative infrared spectroscopy. The results obtained showed typical first order kinetics for the PTMDSE formation, consistent with the proposed reaction mechanism. In the case of PMDS an induction period occurred at lower reaction temperatures, but disappeared at 44 °C and the rate of Si H conversion also started to follow the first-order kinetics. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 2246–2258, 2007 相似文献
108.
N. M. Bogoliubov 《Journal of Mathematical Sciences》2007,143(1):2729-2737
We consider random walks of two essentially different classes of random walkers, namely, of vicious and friendly ones, on
one-dimensional lattices with periodic boundary conditions. The walkers are called vicious since, arriving at a lattice site,
they annihilate not only one another but all the remaining walkers as well. On the contrary, an arbitrary number of friendly
walkers can share the same lattice sites. It is shown that a natural model describing the behavior of friendly walkers is
an integrable model of the boson type. A representation of the generating function for the number of the lattice paths performed
by a fixed number of friendly walkers for a certain number of steps is obtained. Bibliography: 22 titles.
__________
Translated from Zapiski Nauchnykh Seminarov POMI, Vol. 335, 2006, pp. 59–74. 相似文献
109.
110.
Raman scattering in glasses is investigated theoretically. The experimental Raman spectra of glasses exhibit a low-frequency peak (at ~10 cm?1) that, as a rule, is attributed to vibrational modes of nanometer-sized structural units (nanocrystallites). It is established that the elastic moduli of nanocrystallites must necessarily be dependent on their sizes due to the Laplace pressure effect. A theory of the low-frequency peak is constructed using a realistic size distribution function of nanocrystallites with allowance made for the Laplace pressure effect and the dissipation of vibrational energy. Within this theory, the shape of the low-frequency peak and its evolution with temperature can be analyzed quantitatively. The proposed approach offers a physical interpretation of the experimental data and provides insight into the relation of the characteristic nanocrystallite sizes to the elastic moduli and surface tension coefficients of materials. 相似文献