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51.
基于系统最优原则,将计划车流看成是对路网能力提出的要求,把路网上车流径路的优化问题,采用分层次考虑的办法进行分析,并给出一复杂度为O(n5)的多项式算法  相似文献   
52.
A novel method via a semibatch process in the absence of surfactant has been adopted to prepare pH- and temperature-sensitive nanogels. The shape, charge distribution, temperature, and pH-induced volume phase transition behavior of the latexes were investigated by scanning electronic microscopy, zeta potentials, dynamic laser light scattering, and UV/vis spectroscopy. It was found that, in the absence of surfactant, with increasing the amount of AAc from 5 to 20 mol% of N-isopropylacrylamide (NIPAM), the hydrodynamic diameters (DH) decrease from 230 to 60 nm. With increasing pH value from 3 to 11, the DH values increase slightly, which is different than the dramatic increase seen when using a conventional batch method with a range from 680 to 1700 nm. However, at pH 3, the turbidity curves of these kinds of particles increase dramatically at temperatures between 33 and 37 °C, while remaining constant at first and then increasing directly at pH 11. Furthermore, the distribution of carboxylic groups located not only on the interior but also on the exterior of colloidal particles as a result of adoption of the semibatch method, other than simple surface distribution of poly(NIPAM-co-AAc) latexes via the batch method.  相似文献   
53.
开洞集装箱房屋结构纵向刚度分析   总被引:3,自引:0,他引:3  
针对目前广泛使用的集装箱房屋,研究了开洞集装箱在外荷载作用下的纵向刚度.首先,利用蒙皮理论对其进行了力学分析,初步得出了开洞箱体刚度的计算方法,并通过算例阐述了具体的计算过程.然后,利用非线性有限元软件ABAQUS对其建立了有限元模型,并进行了基于开洞面积和洞口高长比的参数分析,得出了各参数对开洞箱体刚度的影响规律,并给出了相应的设计建议.最后,进行了5种开洞箱体刚度的试验研究,并将理论分析和有限元模拟的结果与试验数据进行了对比验证,吻合良好.本研究不仅可为目前广泛使用的集装箱房屋提供设计和施工参考,更可为相应的规范编制提供借鉴.  相似文献   
54.
结合K近邻、核学习方法、特征线重心法和LDA算法,提出了用于情感识别的LDA+kernel-KNNFLC方法.首先针对先验样本特征造成的计算量庞大问题,采用重心准则学习样本距离,改进了核学习的K近邻方法;然后加入LDA对情感特征向量进行优化,在避免维度冗余的情况下,更好地保证了情感信息识别的稳定性.最后,通过对特征空间再学习,结合LDA的kernel-KNNFLC方法优化了情感特征向量的类间区分度,适合于语音情感识别.对包含120维全局统计特征的语音情感数据库进行仿真实验,对降维方案、情感分类器和维度参数进行了多组对比分析.结果表明,LDA+kernel-KNNFLC方法在同等条件下性能提升效果最显著.  相似文献   
55.
A new form of charged particle energy analyser is proposed. It is broadly based on the 180° magnetic spectrograph, but is intended to detect charged particles moving out of the dispersion plane with a helical motion. The analyser has the capability to acquire charged particle energy spectra over a large energy range, similar to those acquired in Auger electron spectroscopy, ca. 2500 eV and large angular range, up to 90°, in parallel. These conditions are more favourable for surface analysis by electron spectroscopy at high vacuum, where for example an electron energy resolution of 0.2% to 0.5% is typical. Expressions showing how the landing positions of the charged particles on the detector vary as a function of energy and polar take off angle are determined as well as the conditions for optimum energy resolution at a range of polar take off angles. The equations reveal that in general, the device obtains the highest resolution at angles of revolution greater than 180°. The design is simple and could be easily put into practice using available material and technologies and be used to analyse the energies of electrons emitted from a sample placed in a scanning electron microscope. It can be made to function with a primary electron beam of any desired energy and could fit in to the small space between the sample and the end of an electron column. However, the device is difficult to retrofit into existing SEMs and ideally an SEM column needs to be designed to work in association with the analyser. The direction of the magnetic field of the analyser is coincident with the axis of the electron gun so that the primary beam is little influenced by the magnetic field and symmetry can be maintained in the primary beam electron column. Because the device is intended to acquire electron spectra in parallel, any movement of the primary beam on the sample because of a ramping field in the analyser is avoided. The field of view and the effect of the analyser upon the operation of the SEM are discussed. Spectra including elastic and Auger peaks reveal an energy resolution of ~4 eV at 900‐eV electron energy. Copyright © 2016 John Wiley & Sons, Ltd.  相似文献   
56.
Compounds with diketopyrrolopyrrole (DPP) and thiophene moieties have attracted considerable attention because of their promising charge transport properties. The molecular conformation and self‐assembly of 2,5‐dihexadecyl‐3,6‐di(thiophen‐2‐yl)‐2,5‐dihydropyrrolo[3,4‐c]pyrrole‐1,4‐dione (TDPP‐C16) molecule have been investigated by scanning tunneling microscopy and density functional theory alculation. The TDPP‐C16 molecules adsorb with their optimized S‐shaped conformation and form a zipper‐like pattern on highly oriented pyrolytic graphite surface. R and S rotated structures are observed. The nanostructure is dominated by intermolecular double hydrogen bonds between C═O of the DPP units and hydrogen atom of thiophene rings in the neighboring molecules in each row. Atomic force microscopy and density functional theory calculation also display the existence of strong intermolecular hydrogen bonding. The results provide molecular evidence for the intermolecular interactions of the surface structure, which could benefit to the design of the organic semiconducting materials and understanding of underlying principle of charge transfer process. Copyright © 2017 John Wiley & Sons, Ltd.  相似文献   
57.
The microcapsules with interpenetrating polymer network (IPN) structure based on crosslinked poly (N-isopropylacrylamide) (PNIPAM) and crosslinked poly (acrylic acid) (PAA) were fabricated in a three-step process. Firstly, silica/PNIPAM core/shell composite particles were synthesized by thermo-initiated seed precipitation polymerization using 3-(trimethoxysilyl)propyl methacrylate modified silica colloidal particles as seeds and N-isopropylacrylamide and N,N′-methylenebisacrylamide (MBA) as monomer and crosslinker, respectively. Secondly, PAA network was incorporated into the shell of the composite particles by redox-initiated polymerization of acrylic acid and MBA entrapped in the PNIPAM network. Finally, the silica core of the composite particles was removed using hydrofluoric acid under certain condition to produce the microcapsules. The chemical compositions, their mass ratio, and particle sizes of the particles formed in each step were determined by Fourier transformation infrared spectroscopy, thermogravimetry, and dynamic laser light scattering (DLLS), respectively. The IPN structure of the microcapsules was identified by transmission electron microscopy (TEM) using uranyl acetate staining method, and their hollow structure was evidenced by TEM and scanning electron microscopy. Their temperature- or pH-dependent hydrodynamic diameters were measured by DLLS, and the results showed that the microcapules had both pH- and temperature-responsive properties, and the temperature-responsive component and the pH-responsive component inside the microcapsule shell had little interference with each other.  相似文献   
58.
The chemical investigation of the aerial parts of Pteris semipinnata resulted in the isolation of three illudalane sesquiterpenoids, namely (2R)‐norpterosin B ( 1 ), (2R)‐12‐Oβ‐D ‐glucopyranosylnorpterosin B ( 2 ), and semipterosin A ( 3 ), along with three known compounds. The structures of 1 – 3 were established by spectroscopic methods, including extensive 2D‐NMR and CD analyses.  相似文献   
59.
The present paper mainly studied the phase formation and reaction pathway of the Al–Ti–Si system in detail by thermal analysis combined with XRD and SEM observations. The phase formation sequence in Al–Ti–Si system from starting mixtures to final products with increasing temperature can be described as following: Al(l) + Ti(s) + Si(s) → (Al–Si)(l) + Ti(s) + Si(s) → Ti(Al,Si)3(s) + Si(s)Ti5(Si,Al)3 + Al(l). More importantly, the solubility of Si in Ti(Al,Si)3 decreased gradually while that of Al in Ti5(Si,Al)3 increased with temperature increasing, suggesting the transportation of Si atoms from intermediate aluminides Ti(Al,Si)3 to final stable silicides Ti5(Si,Al)3 and hence further confirming the formation of Ti5(Si,Al)3 at the expense of Ti(Al,Si)3.  相似文献   
60.
Decabromodiphenyl ether (BDE209) is poorly absorbed by mammals, and little information is available on the toxicokinetics of BDE209 and its metabolites in fish. In the present study, rainbow trout (Oncorhynchus mykiss) were administered to 100 ng/g and 500 ng/g body wet weight of BDE209 via a single intraperitoneal injection and parent BDE209 and its metabolites were sequentially monitored for 28 days. The results showed that toxicokinetic profiles of BDE209 could be described by the one-compartment model. In the higher dose group (500 ng/g wet weight), the calculated half-life (t 1/2) and elimination rate (k e) were 17.7 d and 0.039/d in the liver, and 100.3 d and 0.007/d in the muscle, respectively. Three major methoxylated brominated diphenyl ethers (MeO-BDEs) were detected with 2,2′,4,4′-tetrabromo-5-methoxydiphenyl ether (5-MeO-BDE47) being detected in all tissue samples. There was no significant temporal change of 5-MeO-BDE47 concentration in the muscle, whereas an exponential increase was observed in the liver. Therefore, the metabolism rate of BDE209 depended on the administered dose. BDE209 was hardly accumulated in the muscle of rainbow trout, while the liver was a primary metabolic organ. MeO-BDEs were formed via metabolism of BDE209, which probably played a significant role in fish toxicology as a potential indicator.  相似文献   
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