首页 | 本学科首页   官方微博 | 高级检索  
文章检索
  按 检索   检索词:      
出版年份:   被引次数:   他引次数: 提示:输入*表示无穷大
  收费全文   278781篇
  免费   1605篇
  国内免费   802篇
化学   127856篇
晶体学   4139篇
力学   16873篇
综合类   10篇
数学   53285篇
物理学   79025篇
  2021年   1971篇
  2020年   2008篇
  2019年   2568篇
  2018年   13890篇
  2017年   13702篇
  2016年   10757篇
  2015年   3149篇
  2014年   4564篇
  2013年   8857篇
  2012年   10484篇
  2011年   18257篇
  2010年   11941篇
  2009年   12532篇
  2008年   14027篇
  2007年   16095篇
  2006年   6879篇
  2005年   7149篇
  2004年   7093篇
  2003年   7067篇
  2002年   6122篇
  2001年   5825篇
  2000年   4409篇
  1999年   3267篇
  1998年   2877篇
  1997年   2891篇
  1996年   2730篇
  1995年   2322篇
  1994年   2399篇
  1993年   2315篇
  1992年   2573篇
  1991年   2704篇
  1990年   2602篇
  1989年   2679篇
  1988年   2589篇
  1987年   2608篇
  1986年   2469篇
  1985年   3080篇
  1984年   3147篇
  1983年   2631篇
  1982年   2604篇
  1981年   2567篇
  1980年   2381篇
  1979年   2752篇
  1978年   2708篇
  1977年   2890篇
  1976年   2889篇
  1975年   2680篇
  1974年   2614篇
  1973年   2736篇
  1972年   2104篇
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
41.
This is a review paper of basic knowledge and recent advances in the area of spatial solitons in Kerr and Kerr-like media. We consider spatial bright and dark solitons, solitons in waveguide geometries, optical bullets, vortex solitons and, briefly, dissipative cases. In our treatment, we use a Hamiltonian approach when considering stability issues.  相似文献   
42.
Flowing and static gas-phase samples of HNO3 in O2 and N2 were analyzed by long-path ultraviolet/visible (UV/VIS) spectroscopy to reveal the presence of both NO2 and NO3, the concentrations of which were calculated using differential absorption cross sections. NO2 is produced predominantly by the heterogeneous decomposition of HNO3, whereas NO3 is generated in the gas phase by the thermal decomposition of N2O5, a product of the self-disproportionation of liquid HNO3. © 1993 John Wiley & Sons, Inc.  相似文献   
43.
We study the fractal properties of a convolution of two Cantor distributions. By using the method of characteristic functions, we establish sufficient conditions for the singularity of the convolution of an arbitrary finite number of distributions of random variables with independent s-adic digits. We disprove the hypothesis on the validity of a “singular analog” of the Jessen-Wintner theorem for anomalously fractal distributions. Translated from Ukrainskii Matematicheskii Zhurnal, Vol. 50, No. 8, pp. 1082–1088, August, 1998. The present work was partially supported by the International Soros Program of Educational Support in Exact Sciences (grant No. APU 061086).  相似文献   
44.
The gauge compensation fields induced by the differential operators of the Stueckelberg-Schrödinger equation are discussed, as well as the relation between these fields and the standard Maxwell fields; An action is constructed and the second quantization of the fields carried out using a constraint procedure. The properties of the second quantized matter fields are discussed.  相似文献   
45.
46.
We show that the modified method for finite-dimensional approximation of solutions of Fredholm integral equations of the first kind presented in this paper is more economical than traditional methods for finite-dimensional approximation. Institute of Mathematies, Ukrainian Academy of Science, Kiev. Translated from Ukrainskii Matematicheskii Zhurnal, Vol. 49, No. 2, pp. 289–295, February, 1997.  相似文献   
47.
The fracture behavior of a core-shell rubber (CSR) modified epoxy is investigated using both fracture mechanics and microscopy tools. The CSR-modified epoxy is found to be toughened via numerous line-array cavitations of the CSR particles, followed by plastic flow of the epoxy matrix. The toughening effect via the above craze-like damage process is found to be as effective as that of the well-known widespread rubber cavitation/matrix shear yielding mechanisms. The conditions for triggering the craze-like damage appear to be both stress state and rubber concentration dependent. The type of rubber tougheners utilized also plays a critical role in triggering this rather unusual craze-like damage in epoxy systems. © 1993 John Wiley & Sons, Inc.  相似文献   
48.
49.
Supramolecular block‐random copolymers containing [Ir(terpy)2]3+ in the side chain were synthesized via postfunctionalization of a P(S‐b‐ACterpy) block copolymer. Absorbance and emission spectra compared to a model compound show that the polymer backbone has a minor effect on the polymer absorbance but produces a larger shift for the phosphorescence signals to higher wavelength. Dynamic light scattering of the metal complex containing copolymer studied in various solvents showed monomodal aggregation with decreasing aggregate size as the solvent dielectric constant increased. The copolymer precursor P(S‐b‐ACterpy) shows multimodal aggregation in different solvents with the major population consisting of single chains. This difference in behavior between the two polymers is attributed to the electrolytic nature of the complex and the amphiphilicity induced by the charged metal complex. Supramolecular copolymers like these will continue to have interesting self‐organizational properties and may find applications in multicomponent systems for photoinduced charge separation processes. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 1109–1121, 2007  相似文献   
50.
In this work, we propose that retardation in vinyl acetate polymerization rate in the presence of toluene is due to degradative chain transfer. The transfer constant to toluene (Ctrs) determined using the Mayo method is equal to 3.8 × 10?3, which is remarkably similar to the value calculated from the rate data, assuming degradative chain transfer (2.7 × 10?3). Simulations, including chain‐length‐dependent termination, were carried out to compare our degradative chain transfer model with experimental results. The conversion–time profiles showed excellent agreement between experiment and simulation. Good agreement was found for the Mn data as a function of conversion. The experimental and simulation data strongly support the postulate that degradative chain transfer is the dominant kinetic mechanism. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 3620–3625, 2007  相似文献   
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号