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1.
介绍了一种使用钢环和碳纤维复合材料环共同预紧方式的两面顶超高压模具,该结构在全钢环两面顶模具的基础上,使用一层碳纤维复合材料环代替最外层钢环,得到了一种具有碳纤维复合材料环的超高压模具。这种设计避免了大直径钢环难以制造加工的问题,形成一种以钢环与复合材料环共同对压缸预紧的新型预紧方式。数值分析表明:该模具结构设计具有可行性,可以在一定程度上减小压缸的周向应力、最大剪切应力和等效应力。此外,对碳纤维复合材料环进行了失效判别。  相似文献   
2.
A *-ring R is called a nil *-clean ring if every element of R is a sum of a projection and a nilpotent.Nil *-clean rings are the *-version of nil-clean rings introduced by Diesl.This paper is about the nil *-clean property of rings with emphasis on matrix rings.We show that a *-ring R is nil *-clean if and only if J(R) is nil and R/J(R) is nil*-clean.For a 2-primal *-ring R,with the induced involution given by (aij)* =(a*ij)T,the nil *-clean property of Mn(R) is completely reduced to that of Mn(Z2).Consequently,Mn(R) is not a nil *-clean ring for n =3,4,and M2(R) is a nil *-clean ring if and only if J(R) is nil,R/J(R) is a Boolean ring and a*-a ∈ J(R) for all a ∈ R.  相似文献   
3.
We construct the Grothendieck rings of a class of 2n2dimensional semisimple Hopf Algebras H2n2,which can be viewed as a generalization of the 8 dimensional Kac-Paljutkin Hopf algebra H8.All irreducible H2n2-modules are classified.Furthermore,we describe the Grothendieck rings r(H2n2)by generators and relations explicitly.  相似文献   
4.
The commonly used multi-center initiation methods always lead to the formation of quantities of homopolymer in the surface tailoring based on reverse atom transfer radical polymerization (ATRP) and reversible addition-fragmentation chain-transfer (RAFT) polymerization. In this study, a monocenter redox pair constructed of silica bearing tert-butyl hydroperoxide groups and ascorbic acid (SiO2-TBHP/AsAc) was applied to substitute the commonly used initiation method of R-supported RAFT grafting polymerization. All the propagating radicals were restricted on the surface of solid particles during the whole procedure theoretically, resulting in a higher grafting efficiency of 95.1% combined with the “controllable” feature at 10 h. This redox pair was also used to initiate the reverse ATRP in miniemulsion successfully with a grafting efficiency of 86.3% at 10 h. The grafting efficiency obtained under this monocenter initiation method was significantly higher than that of the frequently reported surface modification by reverse ATRP and RAFT polymerization. In addition, the high-efficient surface tailoring was traced and confirmed by nuclear magnetic resonance, Fourier transform infrared, X-ray photoelectron spectroscopy, thermogravimetric analysis, transmission electron microscopy, and other analysis tests. The advantage of this monocenter redox pair will open a new avenue for the potential “high-efficient” surface tailoring of various materials.  相似文献   
5.
Acridone as a new kind of visible light photocatalyst has been developed to catalyze metal free atom transfer radical polymerization (ATRP). The photocatalyst possess low excited state potential as can undergo an oxidative quenching pathway to initiate ATRP of vinyl monomers. Kinetic study and light on/off reaction demonstrate the “living”/controlled nature of the polymerization by light. Block copolymers can be achieved by using PMMA as macroinitiator to reinitiate polymerization of other vinyl monomers, which shows highly preserved Br chain-end functionality in the synthesized polymers. Moreover, the polymerization can be conducted under air atmosphere as most photocatalysts need anaerobic condition, which may give inspiration of further application of this kind of photocatalyst.  相似文献   
6.
One of the well-known ways of increasing the visible light absorption capability of semiconducting materials is cation doping. This study aims to use Gd doping to tailor the bandgap energy of K2Ta2O6 (KTO) for photocatalytic degradation of organic pollutants under visible light irradiation. Accordingly, the parent KTO and Gd-doped KTO with different Gd concentrations (K2-3xGdxTa2O6; x = 0.025, 0.05, 0.075 and 0.1 mol%) were synthesized by hydrothermal and facile ion-exchange methods, respectively. The powder XRD, FT-IR, SEM-EDS, TEM-SAED, N2 adsorption-desorption, XPS, UV–Vis DRS, PL and ESR techniques were used to investigate the effect of Gd dopant concentration on the structural and photocatalytic properties of KTO. The photocatalytic activity of these samples was investigated for the photocatalytic degradation of methylene blue (MB) dye in an aqueous solution at room temperature under visible light irradiation. The experimental results show that all Gd-doped KTO samples exhibit enhanced photocatalytic activity compared with parent KTO toward MB degradation. In particular, Gd-KTO obtained by doping of 0.075 mol% shows the highest photocatalytic activity among the Gd-doped samples and the degradation efficiency of MB was 79% after 180 min of visible light irradiation, which is approximately 1.5 times as high as that by parent KTO (53%). In addition, trapping experiments and electron spin resonance (ESR) analysis demonstrated that the hydroxyl radicals (?OH) have played a crucial role in the photocatalytic degradation of MB. The reusability and stability of Gd doped-KTO with a Gd content of 0.075 mol% against MB degradation were examined for five cycles. Based on the present study results, a visible light induced photocatalytic mechanism has been proposed for Gd0075-KTO sample.  相似文献   
7.
A detailed study of the geometry, aromatic character, electronic and magnetic properties for a series of positively charged N-doped polycyclic aromatic hydrocarbons (PAHs) was performed. Magnetic properties of the examined molecules were analyzed by means of the magnetically induced current density calculated using the diamagnetic-zero version of the continuous transformation of origin of current density (CTOCD-DZ) method. The comparative study of the local aromaticity of the studied molecules was performed using several different indices: energy effect (ef), harmonic oscillator model of aromaticity (HOMA) index, six centre delocalization index (SCI) and nucleus independent chemical shifts (NICS). The presence of N-atoms in the inner rings was found to cause a planarity distortion in the studied N-doped systems. The geometric changes and charged nature of the studied N-doped systems do not significantly influence the current density and the local aromaticity distribution in comparison with the corresponding parent benzenoid hydrocarbons. The present study demonstrates how quantum chemical calculations can be used for rational design of novel PAHs and for fine tuning of their properties.  相似文献   
8.
We consider the dynamics and formation of vortices from ring dark solitons in a two-dimensional Bose–Einstein condensate with the Rashba spin–orbit coupling based on the time-dependent coupled Gross–Pitaevskii equation. Compared with previous results, the system exhibits complex dynamical behaviors in the presence of the spin–orbit coupling. With the modulation of the spin–orbit coupling, not only the lifetime of ring dark solitons is greatly prolonged, but also their attenuation kinetics is significantly affected. For two shallow ring dark solitons with the equal strength of the spin–orbit coupling, the radius of ring dark solitons increases to a maximum value over time and then shrinks into a minimum value. Due to the effect of the snake instability, ring dark solitons split into a series of ring-like clusters of vortex pairs, which perform complex oscillations. This indicates that the system is strongly dependent on the presence of the spin–orbit coupling. Furthermore, the effect of different initial modulation depths on the dynamics of ring dark solitons is investigated.  相似文献   
9.
王楠  周宇齐  姜子叶  吕田钰  林进  宋洲  朱丽华 《化学进展》2022,34(12):2667-2685
全/多卤代有机污染物大多具有生态毒性、生物蓄积性、环境持久性及长距离迁移性,不仅危害环境与生态安全,而且可经食物链传递威胁人类健康。由于卤原子是吸电子基团且取代数目多,这类物质的最高占据分子轨道能较低,难于被氧化降解,相反较易被还原法脱卤降解。随卤原子取代数减少,脱卤产物难被进一步还原,而其毒性甚至高于母体污染物。注意到低卤代有机物更容易发生氧化降解,一些研究构建了还原-氧化接力降解体系,即先利用还原法将全/多卤代有机污染物还原为低卤代产物,再利用氧化法降解这些中间产物,从而实现深度/完全脱卤和矿化。本文根据催化反应类型对还原-氧化联用法进行了归纳,分类介绍了基于传统化学催化、光催化、电化学、光电化学及机械化学等构建还原-氧化协同降解体系的原理及应用,以期为开发高效的处置技术提供思路和建议。  相似文献   
10.
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